Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57636 |
| ensemblid | ENSG00000275832.5 |
| hgncid | 29293 |
| symbol | ARHGAP23 |
| name | Rho GTPase activating protein 23 |
| refseq_nuc | NM_001199417.2 |
| refseq_prot | NP_001186346.1 |
| ensembl_nuc | ENST00000622683.5 |
| ensembl_prot | ENSP00000481862.1 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 38428464 |
| end | 38512385 |
| strand | + |
| ver | v1.2 |
| region | chr17:38428464-38512385 |
| region5000 | chr17:38423464-38517385 |
| regionname0 | ARHGAP23_chr17_38428464_38512385 |
| regionname5000 | ARHGAP23_chr17_38423464_38517385 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1491 | 267 | 68 | 58 | 91 | 14 | 35 | 63 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | MNGVA others(1486): Show |
chr17 | 38423464 | 38517385 |
| a0002 | 0/0 | 352 | 8 | 1 | 2 | 4 | 0 | 1 | 4 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | MNGVA others(347): Show |
chr17 | 38423464 | 38517385 |
| a0003 | 0/0 | 1491 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | MNGVA others(1486): Show |
chr17 | 38423464 | 38517385 |
| a0004 | 0/0 | 1491 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | MNGVA others(1486): Show |
chr17 | 38423464 | 38517385 |
| a0005 | 0/0 | 1491 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | MNGVA others(1486): Show |
chr17 | 38423464 | 38517385 |
| a0006 | 0/0 | 1491 | 2 | 1 | 0 | 1 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | MNGVA others(1486): Show |
chr17 | 38423464 | 38517385 |
| a0007 | 0/0 | 1491 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | MNGVA others(1486): Show |
chr17 | 38423464 | 38517385 |
| a0008 | 0/0 | 1491 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | MNGVA others(1486): Show |
chr17 | 38423464 | 38517385 |
| a0009 | 0/0 | 1491 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | MNGVA others(1486): Show |
chr17 | 38423464 | 38517385 |
| a0010 | 0/0 | 1491 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | MNGVA others(1486): Show |
chr17 | 38423464 | 38517385 |
| a0011 | 0/0 | 1491 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | MNGVA others(1486): Show |
chr17 | 38423464 | 38517385 |
| a0012 | 0/0 | 1491 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | MNGVA others(1486): Show |
chr17 | 38423464 | 38517385 |
| a0013 | 0/0 | 1491 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | MNGVA others(1486): Show |
chr17 | 38423464 | 38517385 |
| a0014 | 0/0 | 1491 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | MNGVA others(1486): Show |
chr17 | 38423464 | 38517385 |
| a0015 | 0/0 | 1491 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | MNGVA others(1486): Show |
chr17 | 38423464 | 38517385 |
| a0016 | 0/0 | 1491 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | MNGVA others(1486): Show |
chr17 | 38423464 | 38517385 |
| a0017 | 0/0 | 1491 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | MNGVA others(1486): Show |
chr17 | 38423464 | 38517385 |
| a0018 | 0/0 | 1491 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | MNGVA others(1486): Show |
chr17 | 38423464 | 38517385 |
| a0019 | 0/0 | 1491 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | MNGVA others(1486): Show |
chr17 | 38423464 | 38517385 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 4473 | 128 | 17 | 32 | 53 | 10 | 15 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0001c0002 | 0/0 | 4473 | 24 | 1 | 4 | 10 | 0 | 9 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0001c0003 | 0/0 | 4473 | 21 | 0 | 6 | 10 | 1 | 4 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0001c0004 | 0/0 | 4473 | 20 | 10 | 6 | 1 | 2 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0001c0005 | 0/0 | 4473 | 17 | 16 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0001c0006 | 0/0 | 4473 | 7 | 0 | 0 | 7 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0001c0007 | 0/0 | 4473 | 6 | 2 | 2 | 1 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0001c0008 | 0/0 | 4473 | 5 | 0 | 1 | 2 | 1 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0001c0009 | 0/0 | 4473 | 5 | 4 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0001c0010 | 0/0 | 4473 | 5 | 3 | 2 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0001c0011 | 0/0 | 4473 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0001c0012 | 0/0 | 4473 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0001c0016 | 0/0 | 4473 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0001c0018 | 0/0 | 4473 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0001c0020 | 0/0 | 4473 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0001c0024 | 0/0 | 4473 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0001c0025 | 0/0 | 4473 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0001c0027 | 0/0 | 4473 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0001c0031 | 0/0 | 4473 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0001c0032 | 0/0 | 4473 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0001c0037 | 0/0 | 4473 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0001c0040 | 0/0 | 4473 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0001c0042 | 0/0 | 4473 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0001c0043 | 0/0 | 4473 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0001c0045 | 0/0 | 4473 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0001c0048 | 0/0 | 4473 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0001c0051 | 0/0 | 4473 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0001c0052 | 0/0 | 4473 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0001c0054 | 0/0 | 4473 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0002c0015 | 0/0 | 4474 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4469): Show |
chr17 | 38423464 | 38517385 | ||
| a0002c0022 | 0/0 | 4474 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4469): Show |
chr17 | 38423464 | 38517385 | ||
| a0002c0023 | 0/0 | 4474 | 2 | 0 | 0 | 1 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4469): Show |
chr17 | 38423464 | 38517385 | ||
| a0002c0035 | 0/0 | 4474 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4469): Show |
chr17 | 38423464 | 38517385 | ||
| a0002c0036 | 0/0 | 4474 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4469): Show |
chr17 | 38423464 | 38517385 | ||
| a0003c0013 | 0/0 | 4473 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0003c0014 | 0/0 | 4473 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0003c0028 | 0/0 | 4473 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0003c0038 | 0/0 | 4473 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0004c0017 | 0/0 | 4473 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0004c0019 | 0/0 | 4473 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0004c0055 | 0/0 | 4473 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0005c0033 | 0/0 | 4473 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0005c0041 | 0/0 | 4473 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0005c0053 | 0/0 | 4473 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0006c0049 | 0/0 | 4473 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0006c0050 | 0/0 | 4473 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0007c0021 | 0/0 | 4473 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0008c0029 | 0/0 | 4473 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0009c0026 | 0/0 | 4473 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0010c0046 | 0/0 | 4473 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0011c0059 | 0/0 | 4473 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0012c0039 | 0/0 | 4473 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0013c0047 | 0/0 | 4473 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0014c0056 | 0/0 | 4473 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0015c0044 | 0/0 | 4473 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0016c0057 | 0/0 | 4473 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0017c0034 | 0/0 | 4473 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0018c0058 | 0/0 | 4473 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 | ||
| a0019c0030 | 0/0 | 4473 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | ATGAA others(4468): Show |
chr17 | 38423464 | 38517385 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5911 | 122 | 16 | 31 | 51 | 9 | 14 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0001c0001t0003 | 0/0 | 5911 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0001c0001t0007 | 0/0 | 5911 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0001c0001t0008 | 0/0 | 5911 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0001c0001t0009 | 0/0 | 5911 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0001c0001t0011 | 0/0 | 5911 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0001c0001t0014 | 0/0 | 5911 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0001c0002t0002 | 0/0 | 5911 | 23 | 1 | 4 | 10 | 0 | 8 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0001c0002t0012 | 0/0 | 5911 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0001c0003t0001 | 0/0 | 5911 | 20 | 0 | 6 | 9 | 1 | 4 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0001c0003t0007 | 0/0 | 5911 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0001c0004t0001 | 0/0 | 5911 | 19 | 9 | 6 | 1 | 2 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0001c0004t0006 | 0/0 | 5907 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5902): Show |
chr17 | 38423464 | 38517385 |
| a0001c0005t0001 | 0/0 | 5911 | 16 | 15 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0001c0005t0006 | 0/0 | 5907 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5902): Show |
chr17 | 38423464 | 38517385 |
| a0001c0006t0002 | 0/0 | 5911 | 7 | 0 | 0 | 7 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0001c0007t0003 | 0/0 | 5911 | 4 | 1 | 2 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0001c0007t0013 | 0/0 | 5911 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0001c0007t0015 | 0/0 | 5911 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0001c0008t0001 | 0/0 | 5911 | 5 | 0 | 1 | 2 | 1 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0001c0009t0003 | 0/0 | 5911 | 5 | 4 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0001c0010t0001 | 0/0 | 5911 | 5 | 3 | 2 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0001c0011t0001 | 0/0 | 5911 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0001c0011t0006 | 0/0 | 5907 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5902): Show |
chr17 | 38423464 | 38517385 |
| a0001c0012t0003 | 0/0 | 5911 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0001c0016t0003 | 0/0 | 5911 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0001c0018t0001 | 0/0 | 5911 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0001c0020t0005 | 0/0 | 5911 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0001c0024t0001 | 0/0 | 5911 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0001c0025t0002 | 0/0 | 5911 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0001c0027t0005 | 0/0 | 5911 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0001c0031t0003 | 0/0 | 5911 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0001c0032t0001 | 0/0 | 5911 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0001c0037t0003 | 0/0 | 5911 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0001c0040t0002 | 0/0 | 5911 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0001c0042t0001 | 0/0 | 5911 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0001c0043t0001 | 0/0 | 5911 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0001c0045t0001 | 0/0 | 5911 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0001c0048t0002 | 0/0 | 5911 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0001c0051t0003 | 0/0 | 5911 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0001c0052t0001 | 0/0 | 5911 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0001c0054t0002 | 0/0 | 5911 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0002c0015t0001 | 0/0 | 5912 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5907): Show |
chr17 | 38423464 | 38517385 |
| a0002c0022t0001 | 0/0 | 5912 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5907): Show |
chr17 | 38423464 | 38517385 |
| a0002c0022t0010 | 0/0 | 5912 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5907): Show |
chr17 | 38423464 | 38517385 |
| a0002c0023t0001 | 0/0 | 5912 | 2 | 0 | 0 | 1 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5907): Show |
chr17 | 38423464 | 38517385 |
| a0002c0035t0001 | 0/0 | 5912 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5907): Show |
chr17 | 38423464 | 38517385 |
| a0002c0036t0003 | 0/0 | 5912 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5907): Show |
chr17 | 38423464 | 38517385 |
| a0003c0013t0001 | 0/0 | 5911 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0003c0014t0001 | 0/0 | 5911 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0003c0028t0001 | 0/0 | 5911 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0003c0038t0001 | 0/0 | 5911 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0004c0017t0004 | 0/0 | 5908 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5903): Show |
chr17 | 38423464 | 38517385 |
| a0004c0019t0004 | 0/0 | 5908 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5903): Show |
chr17 | 38423464 | 38517385 |
| a0004c0055t0004 | 0/0 | 5908 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5903): Show |
chr17 | 38423464 | 38517385 |
| a0005c0033t0001 | 0/0 | 5911 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0005c0041t0001 | 0/0 | 5911 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0005c0053t0001 | 0/0 | 5911 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0006c0049t0001 | 0/0 | 5911 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0006c0050t0003 | 0/0 | 5911 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0007c0021t0003 | 0/0 | 5911 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0008c0029t0001 | 0/0 | 5911 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0009c0026t0001 | 0/0 | 5911 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0010c0046t0003 | 0/0 | 5911 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0011c0059t0001 | 0/0 | 5911 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0012c0039t0001 | 0/0 | 5911 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0013c0047t0001 | 0/0 | 5911 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0014c0056t0001 | 0/0 | 5911 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0015c0044t0001 | 0/0 | 5911 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0016c0057t0001 | 0/0 | 5911 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0017c0034t0001 | 0/0 | 5911 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0018c0058t0002 | 0/0 | 5911 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| a0019c0030t0001 | 0/0 | 5911 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | GCAGA others(5906): Show |
chr17 | 38423464 | 38517385 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0001g0302 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0007g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0008g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0009g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0011g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0001t0014g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0002t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0002t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0002t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0002t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0002t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0002t0012g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0003t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0003t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0003t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0003t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0003t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0003t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0003t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0003t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0003t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0003t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0003t0007g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0004t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0004t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0004t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0004t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0004t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0004t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0004t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0004t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0004t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0004t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0004t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0004t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0004t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0004t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0004t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0004t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0004t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0004t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0004t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0004t0006g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0005t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0005t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0005t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0005t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0005t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0005t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0005t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0005t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0005t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0005t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0005t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0005t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0005t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0005t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0005t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0005t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0005t0006g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0006t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0006t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0006t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0006t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0006t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0006t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0006t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0007t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0007t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0007t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0007t0003g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0007t0013g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0007t0015g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0008t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0008t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0008t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0008t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0008t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0009t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0009t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0009t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0009t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0009t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0010t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0010t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0010t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0010t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0010t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0011t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0011t0006g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0011t0006g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0012t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0012t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0012t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0016t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0016t0003g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0018t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0018t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0020t0005g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0020t0005g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0024t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0024t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0025t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0025t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0027t0005g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0027t0005g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0031t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0032t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0037t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0040t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0042t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0043t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0045t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0048t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0051t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0052t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0001c0054t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0002c0015t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0002c0015t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0002c0022t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0002c0022t0010g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0002c0023t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0002c0023t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0002c0035t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0002c0036t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0003c0013t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0003c0013t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0003c0013t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0003c0014t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0003c0014t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0003c0028t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0003c0028t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0003c0038t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0004c0017t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0004c0017t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0004c0019t0004g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0004c0019t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0004c0055t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0005c0033t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0005c0041t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0005c0053t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0006c0049t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0006c0050t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0007c0021t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0007c0021t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0008c0029t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0008c0029t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0009c0026t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0009c0026t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0010c0046t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0011c0059t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0012c0039t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0013c0047t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0014c0056t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0015c0044t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0016c0057t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0017c0034t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0018c0058t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| a0019c0030t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0008 | t0001 | g0198 | EUR | GBR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0231 | EUR | GBR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0205 | EUR | GBR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0271 | EUR | GBR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0232 | EUR | FIN | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0246 | EUR | FIN | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0203 | EUR | FIN | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG00323 | hp2 | a0001 | c0004 | t0001 | g0071 | EUR | FIN | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG00544 | hp1 | a0001 | c0007 | t0003 | g0112 | EAS | CHS | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG00558 | hp1 | a0001 | c0006 | t0002 | g0175 | EAS | CHS | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | CHS | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG00597 | hp2 | a0001 | c0003 | t0007 | g0078 | EAS | CHS | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG00609 | hp1 | a0001 | c0025 | t0002 | g0183 | EAS | CHS | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG00621 | hp1 | a0001 | c0006 | t0002 | g0177 | EAS | CHS | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG00733 | hp1 | a0001 | c0005 | t0001 | g0036 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG00733 | hp2 | a0010 | c0046 | t0003 | g0029 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG00735 | hp2 | a0001 | c0040 | t0002 | g0137 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG00741 | hp2 | a0002 | c0015 | t0001 | g0240 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01070 | hp1 | a0001 | c0004 | t0001 | g0171 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01071 | hp1 | a0001 | c0004 | t0001 | g0170 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01071 | hp2 | a0001 | c0004 | t0001 | g0194 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01074 | hp2 | a0001 | c0010 | t0001 | g0169 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01081 | hp1 | a0001 | c0020 | t0005 | g0011 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01099 | hp2 | a0011 | c0059 | t0001 | g0024 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01109 | hp1 | a0001 | c0003 | t0001 | g0065 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01109 | hp2 | a0001 | c0051 | t0003 | g0267 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01169 | hp1 | a0001 | c0002 | t0002 | g0015 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01175 | hp1 | a0001 | c0004 | t0001 | g0182 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01243 | hp1 | a0001 | c0007 | t0003 | g0277 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01243 | hp2 | a0004 | c0019 | t0004 | g0060 | AMR | PUR | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01255 | hp2 | a0012 | c0039 | t0001 | g0186 | AMR | CLM | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0027 | AMR | CLM | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0028 | AMR | CLM | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01261 | hp1 | a0001 | c0003 | t0001 | g0014 | AMR | CLM | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01261 | hp2 | a0001 | c0001 | t0008 | g0256 | AMR | CLM | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01346 | hp2 | a0001 | c0003 | t0001 | g0023 | AMR | CLM | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01358 | hp1 | a0001 | c0032 | t0001 | g0201 | AMR | CLM | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01361 | hp1 | a0002 | c0035 | t0001 | g0234 | AMR | CLM | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0251 | AMR | CLM | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01433 | hp2 | a0001 | c0004 | t0001 | g0133 | AMR | CLM | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0295 | EUR | IBS | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0219 | EUR | IBS | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01884 | hp1 | a0001 | c0005 | t0001 | g0052 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01884 | hp2 | a0003 | c0014 | t0001 | g0074 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01891 | hp1 | a0001 | c0004 | t0001 | g0054 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01891 | hp2 | a0013 | c0047 | t0001 | g0018 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01952 | hp1 | a0001 | c0008 | t0001 | g0197 | AMR | PEL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01952 | hp2 | a0001 | c0003 | t0001 | g0115 | AMR | PEL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01981 | hp2 | a0001 | c0003 | t0001 | g0259 | AMR | PEL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01993 | hp1 | a0001 | c0010 | t0001 | g0168 | AMR | PEL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02040 | hp1 | a0001 | c0003 | t0001 | g0111 | EAS | KHV | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02055 | hp1 | a0001 | c0004 | t0001 | g0031 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02055 | hp2 | a0001 | c0005 | t0001 | g0033 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02071 | hp1 | a0001 | c0006 | t0002 | g0176 | EAS | KHV | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02071 | hp2 | a0001 | c0024 | t0001 | g0098 | EAS | KHV | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0241 | EAS | KHV | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02132 | hp1 | a0001 | c0002 | t0002 | g0252 | EAS | KHV | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02135 | hp1 | a0015 | c0044 | t0001 | g0192 | EAS | KHV | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02145 | hp1 | a0007 | c0021 | t0003 | g0070 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02145 | hp2 | a0003 | c0028 | t0001 | g0017 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02148 | hp1 | a0001 | c0004 | t0001 | g0199 | AMR | PEL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02148 | hp2 | a0001 | c0007 | t0003 | g0020 | AMR | PEL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0166 | EAS | CDX | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CDX | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02165 | hp2 | a0016 | c0057 | t0001 | g0278 | EAS | CDX | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02257 | hp2 | a0001 | c0005 | t0001 | g0158 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02258 | hp1 | a0001 | c0005 | t0001 | g0050 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02258 | hp2 | a0001 | c0011 | t0006 | g0073 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02280 | hp1 | a0005 | c0053 | t0001 | g0128 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02280 | hp2 | a0007 | c0021 | t0003 | g0072 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02293 | hp1 | a0001 | c0003 | t0001 | g0193 | AMR | PEL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02451 | hp2 | a0001 | c0010 | t0001 | g0163 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02572 | hp1 | a0001 | c0005 | t0006 | g0035 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0122 | SAS | PJL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02602 | hp2 | a0001 | c0054 | t0002 | g0227 | SAS | PJL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02622 | hp1 | a0001 | c0004 | t0001 | g0164 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02622 | hp2 | a0001 | c0009 | t0003 | g0173 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02630 | hp2 | a0017 | c0034 | t0001 | g0039 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02647 | hp1 | a0001 | c0012 | t0003 | g0045 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02647 | hp2 | a0001 | c0004 | t0001 | g0055 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02723 | hp1 | a0001 | c0005 | t0001 | g0038 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02723 | hp2 | a0001 | c0031 | t0003 | g0067 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02735 | hp1 | a0001 | c0007 | t0015 | g0266 | SAS | PJL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0026 | SAS | PJL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0226 | SAS | PJL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02738 | hp2 | a0002 | c0023 | t0001 | g0236 | SAS | PJL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02809 | hp2 | a0001 | c0009 | t0003 | g0172 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02818 | hp1 | a0001 | c0004 | t0006 | g0010 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02818 | hp2 | a0001 | c0005 | t0001 | g0044 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02886 | hp1 | a0001 | c0005 | t0001 | g0041 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02886 | hp2 | a0001 | c0016 | t0003 | g0047 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02895 | hp2 | a0003 | c0013 | t0001 | g0129 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02896 | hp1 | a0003 | c0014 | t0001 | g0068 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02896 | hp2 | a0003 | c0013 | t0001 | g0132 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02922 | hp1 | a0003 | c0038 | t0001 | g0160 | AFR | ESN | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02922 | hp2 | a0001 | c0027 | t0005 | g0146 | AFR | ESN | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02965 | hp1 | a0001 | c0004 | t0001 | g0131 | AFR | ESN | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02970 | hp1 | a0004 | c0019 | t0004 | g0063 | AFR | ESN | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02970 | hp2 | a0001 | c0018 | t0001 | g0042 | AFR | ESN | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03017 | hp1 | a0001 | c0008 | t0001 | g0030 | SAS | PJL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0123 | SAS | PJL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03041 | hp1 | a0001 | c0004 | t0001 | g0059 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03098 | hp2 | a0001 | c0005 | t0001 | g0037 | AFR | MSL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03130 | hp1 | a0001 | c0001 | t0011 | g0064 | AFR | ESN | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ESN | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ESN | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03139 | hp2 | a0004 | c0017 | t0004 | g0140 | AFR | ESN | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03195 | hp1 | a0001 | c0007 | t0003 | g0053 | AFR | ESN | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03195 | hp2 | a0001 | c0011 | t0006 | g0076 | AFR | ESN | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03209 | hp1 | a0004 | c0017 | t0004 | g0141 | AFR | MSL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03209 | hp2 | a0001 | c0012 | t0003 | g0051 | AFR | MSL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03225 | hp1 | a0001 | c0018 | t0001 | g0046 | AFR | MSL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03225 | hp2 | a0001 | c0009 | t0003 | g0161 | AFR | MSL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03453 | hp1 | a0001 | c0005 | t0001 | g0049 | AFR | MSL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03453 | hp2 | a0001 | c0037 | t0003 | g0139 | AFR | MSL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03486 | hp1 | a0003 | c0013 | t0001 | g0130 | AFR | MSL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03486 | hp2 | a0001 | c0004 | t0001 | g0061 | AFR | MSL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0125 | SAS | PJL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03516 | hp1 | a0001 | c0012 | t0003 | g0048 | AFR | ESN | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03516 | hp2 | a0001 | c0004 | t0001 | g0062 | AFR | ESN | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03540 | hp2 | a0001 | c0010 | t0001 | g0162 | AFR | GWD | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03579 | hp1 | a0001 | c0009 | t0003 | g0057 | AFR | MSL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03579 | hp2 | a0001 | c0005 | t0001 | g0159 | AFR | MSL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0254 | SAS | PJL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0239 | SAS | PJL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03688 | hp1 | a0018 | c0058 | t0002 | g0202 | SAS | STU | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03688 | hp2 | a0001 | c0009 | t0003 | g0190 | SAS | STU | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03710 | hp1 | a0001 | c0004 | t0001 | g0283 | SAS | PJL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03710 | hp2 | a0001 | c0002 | t0012 | g0108 | SAS | PJL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0284 | SAS | BEB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03927 | hp1 | a0001 | c0048 | t0002 | g0113 | SAS | BEB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03927 | hp2 | a0001 | c0003 | t0001 | g0022 | SAS | BEB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0116 | SAS | BEB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | STU | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG04115 | hp2 | a0001 | c0042 | t0001 | g0257 | SAS | STU | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG04184 | hp1 | a0001 | c0003 | t0001 | g0101 | SAS | BEB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG04199 | hp1 | a0019 | c0030 | t0001 | g0167 | SAS | STU | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG04199 | hp2 | a0001 | c0003 | t0001 | g0229 | SAS | STU | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | STU | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG04228 | hp2 | a0001 | c0003 | t0001 | g0185 | SAS | STU | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18522 | hp1 | a0001 | c0010 | t0001 | g0016 | AFR | YRI | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18522 | hp2 | a0001 | c0005 | t0001 | g0043 | AFR | YRI | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18747 | hp1 | a0001 | c0025 | t0002 | g0212 | EAS | CHB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18906 | hp1 | a0003 | c0028 | t0001 | g0299 | AFR | YRI | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18906 | hp2 | a0001 | c0005 | t0001 | g0040 | AFR | YRI | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18940 | hp1 | a0008 | c0029 | t0001 | g0285 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18940 | hp2 | a0008 | c0029 | t0001 | g0181 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18943 | hp1 | a0001 | c0002 | t0002 | g0087 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18943 | hp2 | a0001 | c0002 | t0002 | g0303 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18944 | hp1 | a0001 | c0003 | t0001 | g0082 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18948 | hp2 | a0001 | c0006 | t0002 | g0088 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18957 | hp1 | a0001 | c0006 | t0002 | g0204 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0118 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18960 | hp1 | a0001 | c0052 | t0001 | g0287 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18963 | hp1 | a0006 | c0049 | t0001 | g0262 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18963 | hp2 | a0001 | c0006 | t0002 | g0210 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18966 | hp2 | a0001 | c0001 | t0009 | g0005 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18970 | hp1 | a0009 | c0026 | t0001 | g0099 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18975 | hp1 | a0001 | c0024 | t0001 | g0105 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18979 | hp1 | a0001 | c0001 | t0007 | g0106 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18979 | hp2 | a0001 | c0003 | t0001 | g0289 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0086 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18983 | hp1 | a0001 | c0008 | t0001 | g0195 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18985 | hp1 | a0002 | c0015 | t0001 | g0189 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18985 | hp2 | a0001 | c0043 | t0001 | g0178 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18995 | hp2 | a0001 | c0003 | t0001 | g0206 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18998 | hp2 | a0001 | c0003 | t0001 | g0119 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA18999 | hp2 | a0001 | c0003 | t0001 | g0107 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA19004 | hp1 | a0001 | c0003 | t0001 | g0191 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA19030 | hp1 | a0001 | c0011 | t0001 | g0069 | AFR | LWK | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA19030 | hp2 | a0005 | c0041 | t0001 | g0032 | AFR | LWK | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA19043 | hp1 | a0002 | c0036 | t0003 | g0179 | AFR | LWK | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA19043 | hp2 | a0001 | c0007 | t0013 | g0148 | AFR | LWK | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA19054 | hp1 | a0001 | c0003 | t0001 | g0109 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA19058 | hp1 | a0001 | c0002 | t0002 | g0110 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA19058 | hp2 | a0001 | c0002 | t0002 | g0225 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA19062 | hp1 | a0002 | c0022 | t0010 | g0253 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA19062 | hp2 | a0002 | c0022 | t0001 | g0097 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA19065 | hp1 | a0009 | c0026 | t0001 | g0280 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA19067 | hp1 | a0001 | c0002 | t0002 | g0092 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA19067 | hp2 | a0001 | c0045 | t0001 | g0096 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA19077 | hp2 | a0001 | c0006 | t0002 | g0209 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA19079 | hp2 | a0001 | c0003 | t0001 | g0012 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA19087 | hp1 | a0001 | c0008 | t0001 | g0188 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA19090 | hp1 | a0002 | c0023 | t0001 | g0180 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA19091 | hp1 | a0001 | c0004 | t0001 | g0300 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0157 | AFR | YRI | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA19240 | hp2 | a0001 | c0005 | t0001 | g0147 | AFR | YRI | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ASW | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA20129 | hp2 | a0001 | c0004 | t0001 | g0056 | AFR | ASW | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0220 | EUR | TSI | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0174 | EUR | TSI | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA20805 | hp1 | a0001 | c0004 | t0001 | g0276 | EUR | TSI | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA20805 | hp2 | a0001 | c0003 | t0001 | g0275 | EUR | TSI | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA20905 | hp1 | a0001 | c0001 | t0014 | g0270 | SAS | GIH | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | GIH | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02109 | hp1 | a0006 | c0050 | t0003 | g0138 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02109 | hp2 | a0014 | c0056 | t0001 | g0013 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02486 | hp1 | a0004 | c0055 | t0004 | g0298 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG02486 | hp2 | a0001 | c0005 | t0001 | g0144 | AFR | ACB | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | MSL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG03471 | hp2 | a0001 | c0020 | t0005 | g0143 | AFR | MSL | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | USA | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| HG06807 | hp2 | a0005 | c0033 | t0001 | g0075 | AFR | USA | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA20300 | hp2 | a0001 | c0016 | t0003 | g0297 | AFR | USA | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA21309 | hp1 | a0001 | c0005 | t0001 | g0142 | AFR | LWK | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| NA21309 | hp2 | a0001 | c0027 | t0005 | g0155 | AFR | LWK | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0302 | REF | REF | ARHGAP23_chr17_38423464_38517385 | ARHGAP23 | chr17 | 38423464 | 38517385 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:38458241 | C | T | 1 | a0011 | 1 | HG01099.hp2 | missense_variant | MODERATE | c.203C>T | p.Ser68Leu | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/24 | 225/5911 | 203/4476 | 68/1491 | chr17 | 38458241 | |||
| chr17:38462857 | C | T | 1 | a0018 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.265C>T | p.Arg89Trp | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 4/24 | 287/5911 | 265/4476 | 89/1491 | chr17 | 38462857 | |||
| chr17:38462864 | G | A | 1 | a0019 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.272G>A | p.Arg91His | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 4/24 | 294/5911 | 272/4476 | 91/1491 | chr17 | 38462864 | |||
| chr17:38466282 | G | A | 1 | a0017 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.599G>A | p.Arg200Gln | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/24 | 621/5911 | 599/4476 | 200/1491 | chr17 | 38466282 | |||
| chr17:38466480 | C | T | 1 | a0007 | 2 | HG02145.hp1 HG02280.hp2 |
missense_variant | MODERATE | c.797C>T | p.Thr266Met | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/24 | 819/5911 | 797/4476 | 266/1491 | chr17 | 38466480 | |||
| chr17:38466571 | A | AC | 1 | a0002 | 8 | HG00741.hp2 HG01361.hp1 HG02738.hp2 others(5): Show |
frameshift_variant | HIGH | c.892dupC | p.Arg298fs | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/24 | 915/5911 | 893/4476 | 298/1491 | INFO_REALIGN_3_PRIME | chr17 | 38466571 | ||
| chr17:38466804 | G | T | 1 | a0008 | 2 | NA18940.hp1 NA18940.hp2 |
missense_variant | MODERATE | c.1121G>T | p.Arg374Leu | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/24 | 1143/5911 | 1121/4476 | 374/1491 | chr17 | 38466804 | |||
| chr17:38466879 | G | A | 1 | a0015 | 1 | HG02135.hp1 | missense_variant | MODERATE | c.1196G>A | p.Gly399Glu | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/24 | 1218/5911 | 1196/4476 | 399/1491 | chr17 | 38466879 | |||
| chr17:38466942 | G | A | 1 | a0010 | 1 | HG00733.hp2 | missense_variant | MODERATE | c.1259G>A | p.Arg420Gln | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/24 | 1281/5911 | 1259/4476 | 420/1491 | chr17 | 38466942 | |||
| chr17:38467128 | C | T | 1 | a0007 | 2 | HG02145.hp1 HG02280.hp2 |
missense_variant | MODERATE | c.1445C>T | p.Ala482Val | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/24 | 1467/5911 | 1445/4476 | 482/1491 | chr17 | 38467128 | |||
| chr17:38467266 | G | A | 1 | a0012 | 1 | HG01255.hp2 | missense_variant | MODERATE | c.1583G>A | p.Arg528His | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/24 | 1605/5911 | 1583/4476 | 528/1491 | chr17 | 38467266 | |||
| chr17:38471937 | T | G | 1 | a0013 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.2049T>G | p.Asp683Glu | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/24 | 2071/5911 | 2049/4476 | 683/1491 | chr17 | 38471937 | |||
| chr17:38477679 | C | T | 1 | a0016 | 1 | HG02165.hp2 | missense_variant | MODERATE | c.2219C>T | p.Ala740Val | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/24 | 2241/5911 | 2219/4476 | 740/1491 | chr17 | 38477679 | |||
| chr17:38477718 | C | T | 1 | a0014 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.2258C>T | p.Ala753Val | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/24 | 2280/5911 | 2258/4476 | 753/1491 | chr17 | 38477718 | |||
| chr17:38491417 | G | A | 1 | a0006 | 2 | HG02109.hp1 NA18963.hp1 |
missense_variant | MODERATE | c.3161G>A | p.Arg1054Gln | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/24 | 3183/5911 | 3161/4476 | 1054/1491 | chr17 | 38491417 | |||
| chr17:38510370 | G | C | 1 | a0005 | 3 | HG02280.hp1 HG06807.hp2 NA19030.hp2 |
missense_variant | MODERATE | c.3874G>C | p.Ala1292Pro | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 3896/5911 | 3874/4476 | 1292/1491 | chr17 | 38510370 | |||
| chr17:38510613 | C | T | 1 | a0009 | 2 | NA18970.hp1 NA19065.hp1 |
missense_variant | MODERATE | c.4117C>T | p.Arg1373Cys | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 4139/5911 | 4117/4476 | 1373/1491 | chr17 | 38510613 | |||
| chr17:38510616 | C | G | 1 | a0003 | 8 | HG01884.hp2 HG02145.hp2 HG02895.hp2 others(5): Show |
missense_variant | MODERATE | c.4120C>G | p.Leu1374Val | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 4142/5911 | 4120/4476 | 1374/1491 | chr17 | 38510616 | |||
| chr17:38510947 | C | T | 1 | a0004 | 5 | HG01243.hp2 HG02486.hp1 HG02970.hp1 others(2): Show |
missense_variant | MODERATE | c.4451C>T | p.Ala1484Val | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 4473/5911 | 4451/4476 | 1484/1491 | chr17 | 38510947 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:38462898 | T | C | 1 | a0001c0031 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.306T>C | p.Asn102Asn | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 4/24 | 328/5911 | 306/4476 | 102/1491 | chr17 | 38462898 | |||
| chr17:38466205 | G | A | 4 | a0001c0011 a0001c0032 a0003c0014 others(1): Show |
7 | HG01358.hp1 HG01884.hp2 HG02258.hp2 others(4): Show |
synonymous_variant | LOW | c.522G>A | p.Pro174Pro | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/24 | 544/5911 | 522/4476 | 174/1491 | chr17 | 38466205 | |||
| chr17:38466241 | C | G | 31 | a0001c0001 a0001c0002 a0001c0003 others(28): Show |
219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
synonymous_variant | LOW | c.558C>G | p.Pro186Pro | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/24 | 580/5911 | 558/4476 | 186/1491 | chr17 | 38466241 | |||
| chr17:38466469 | G | A | 1 | a0001c0043 | 1 | NA18985.hp2 | synonymous_variant | LOW | c.786G>A | p.Ser262Ser | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/24 | 808/5911 | 786/4476 | 262/1491 | chr17 | 38466469 | |||
| chr17:38466661 | C | T | 1 | a0007c0021 | 2 | HG02145.hp1 HG02280.hp2 |
synonymous_variant | LOW | c.978C>T | p.Pro326Pro | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/24 | 1000/5911 | 978/4476 | 326/1491 | chr17 | 38466661 | |||
| chr17:38466898 | G | A | 6 | a0001c0016 a0001c0024 a0001c0037 others(3): Show |
10 | HG02071.hp2 HG02886.hp2 HG03139.hp2 others(7): Show |
synonymous_variant | LOW | c.1215G>A | p.Pro405Pro | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/24 | 1237/5911 | 1215/4476 | 405/1491 | chr17 | 38466898 | |||
| chr17:38466916 | G | A | 5 | a0001c0005 a0001c0012 a0001c0018 others(2): Show |
24 | HG00733.hp1 HG01884.hp1 HG02055.hp2 others(21): Show |
synonymous_variant | LOW | c.1233G>A | p.Leu411Leu | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/24 | 1255/5911 | 1233/4476 | 411/1491 | chr17 | 38466916 | |||
| chr17:38469295 | C | T | 3 | a0001c0016 a0001c0037 a0004c0017 |
5 | HG02886.hp2 HG03139.hp2 HG03209.hp1 others(2): Show |
synonymous_variant | LOW | c.1800C>T | p.Asp600Asp | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 8/24 | 1822/5911 | 1800/4476 | 600/1491 | chr17 | 38469295 | |||
| chr17:38479480 | C | T | 50 | a0001c0001 a0001c0002 a0001c0003 others(47): Show |
287 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(284): Show |
synonymous_variant | LOW | c.2481C>T | p.Asn827Asn | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 13/24 | 2503/5911 | 2481/4476 | 827/1491 | chr17 | 38479480 | |||
| chr17:38482624 | C | T | 1 | a0001c0042 | 1 | HG04115.hp2 | synonymous_variant | LOW | c.2853C>T | p.Ser951Ser | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/24 | 2875/5911 | 2853/4476 | 951/1491 | chr17 | 38482624 | |||
| chr17:38490133 | C | T | 1 | a0004c0055 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.3018C>T | p.Arg1006Arg | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 18/24 | 3040/5911 | 3018/4476 | 1006/1491 | chr17 | 38490133 | |||
| chr17:38490145 | G | A | 4 | a0001c0032 a0001c0040 a0001c0048 others(1): Show |
4 | HG00735.hp2 HG01358.hp1 HG01361.hp1 others(1): Show |
synonymous_variant | LOW | c.3030G>A | p.Ala1010Ala | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 18/24 | 3052/5911 | 3030/4476 | 1010/1491 | chr17 | 38490145 | |||
| chr17:38510093 | G | A | 1 | a0001c0051 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.3597G>A | p.Lys1199Lys | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 3619/5911 | 3597/4476 | 1199/1491 | chr17 | 38510093 | |||
| chr17:38510126 | G | A | 1 | a0001c0052 | 1 | NA18960.hp1 | synonymous_variant | LOW | c.3630G>A | p.Gln1210Gln | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 3652/5911 | 3630/4476 | 1210/1491 | chr17 | 38510126 | |||
| chr17:38510222 | C | T | 1 | a0001c0054 | 1 | HG02602.hp2 | synonymous_variant | LOW | c.3726C>T | p.Asp1242Asp | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 3748/5911 | 3726/4476 | 1242/1491 | chr17 | 38510222 | |||
| chr17:38510315 | T | C | 47 | a0001c0001 a0001c0002 a0001c0004 others(44): Show |
261 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(258): Show |
synonymous_variant | LOW | c.3819T>C | p.Asp1273Asp | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 3841/5911 | 3819/4476 | 1273/1491 | chr17 | 38510315 | |||
| chr17:38510375 | G | A | 7 | a0001c0002 a0001c0006 a0001c0025 others(4): Show |
37 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(34): Show |
synonymous_variant | LOW | c.3879G>A | p.Ala1293Ala | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 3901/5911 | 3879/4476 | 1293/1491 | chr17 | 38510375 | |||
| chr17:38510504 | C | T | 2 | a0001c0020 a0001c0027 |
4 | HG01081.hp1 HG02922.hp2 HG03471.hp2 others(1): Show |
synonymous_variant | LOW | c.4008C>T | p.Gly1336Gly | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 4030/5911 | 4008/4476 | 1336/1491 | chr17 | 38510504 | |||
| chr17:38510783 | C | A | 1 | a0001c0025 | 2 | HG00609.hp1 NA18747.hp1 |
synonymous_variant | LOW | c.4287C>A | p.Gly1429Gly | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 4309/5911 | 4287/4476 | 1429/1491 | chr17 | 38510783 | |||
| chr17:38510786 | C | T | 10 | a0001c0007 a0001c0009 a0001c0012 others(7): Show |
22 | HG00544.hp1 HG00733.hp2 HG01109.hp2 others(19): Show |
synonymous_variant | LOW | c.4290C>T | p.Pro1430Pro | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 4312/5911 | 4290/4476 | 1430/1491 | chr17 | 38510786 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:38428471 | C | G | 1 | a0001c0007t0015 | 1 | HG02735.hp1 | 5_prime_UTR_variant | MODIFIER | c.-15C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/24 | 15 | chr17 | 38428471 | ||||||
| chr17:38511244 | C | T | 1 | a0001c0001t0014 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*272C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 272 | chr17 | 38511244 | ||||||
| chr17:38511384 | C | A | 1 | a0001c0001t0008 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*412C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 412 | chr17 | 38511384 | ||||||
| chr17:38511428 | AGAG | A | 6 | a0001c0004t0006 a0001c0005t0006 a0001c0011t0006 others(3): Show |
9 | HG01243.hp2 HG02258.hp2 HG02486.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*461_*463delAGG | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 461 | INFO_REALIGN_3_PRIME | chr17 | 38511428 | |||||
| chr17:38511523 | T | C | 6 | a0001c0004t0006 a0001c0005t0006 a0001c0011t0006 others(3): Show |
9 | HG01243.hp2 HG02258.hp2 HG02486.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*551T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 551 | chr17 | 38511523 | ||||||
| chr17:38511671 | A | C | 1 | a0001c0007t0013 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*699A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 699 | chr17 | 38511671 | ||||||
| chr17:38511690 | A | G | 1 | a0001c0002t0012 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*718A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 718 | chr17 | 38511690 | ||||||
| chr17:38511743 | GT | G | 3 | a0001c0004t0006 a0001c0005t0006 a0001c0011t0006 |
4 | HG02258.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*772delT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 772 | chr17 | 38511743 | ||||||
| chr17:38511744 | T | G | 3 | a0004c0017t0004 a0004c0019t0004 a0004c0055t0004 |
5 | HG01243.hp2 HG02486.hp1 HG02970.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*772T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 772 | chr17 | 38511744 | ||||||
| chr17:38511846 | C | T | 1 | a0001c0001t0008 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*874C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 874 | chr17 | 38511846 | ||||||
| chr17:38511861 | G | A | 1 | a0001c0001t0009 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*889G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 889 | chr17 | 38511861 | ||||||
| chr17:38511867 | G | A | 8 | a0001c0002t0002 a0001c0002t0012 a0001c0006t0002 others(5): Show |
37 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*895G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 895 | chr17 | 38511867 | ||||||
| chr17:38511960 | G | A | 1 | a0002c0022t0010 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*988G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 988 | chr17 | 38511960 | ||||||
| chr17:38512057 | C | G | 1 | a0001c0001t0011 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1085C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 1085 | chr17 | 38512057 | ||||||
| chr17:38512060 | G | A | 22 | a0001c0001t0003 a0001c0002t0002 a0001c0002t0012 others(19): Show |
62 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*1088G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 1088 | chr17 | 38512060 | ||||||
| chr17:38512117 | C | A | 2 | a0001c0020t0005 a0001c0027t0005 |
4 | HG01081.hp1 HG02922.hp2 HG03471.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1145C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 1145 | chr17 | 38512117 | ||||||
| chr17:38512182 | A | T | 2 | a0001c0001t0007 a0001c0003t0007 |
2 | HG00597.hp2 NA18979.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1210A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 24/24 | 1210 | chr17 | 38512182 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:38428861 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.63+313G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38428861 | |||||||
| chr17:38428900 | C | A | 1 | a0001c0001t0001g0007 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.63+352C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38428900 | |||||||
| chr17:38429027 | C | A | 1 | a0001c0001t0001g0008 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.63+479C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38429027 | |||||||
| chr17:38429080 | G | A | 1 | a0001c0001t0001g0009 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.63+532G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38429080 | |||||||
| chr17:38429209 | C | T | 1 | a0001c0002t0002g0303 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.63+661C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38429209 | |||||||
| chr17:38429370 | C | A | 166 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0021 others(163): Show |
167 | HG00323.hp2 HG00544.hp1 HG00597.hp2 others(164): Show |
intron_variant | MODIFIER | c.63+822C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38429370 | |||||||
| chr17:38429402 | G | T | 6 | a0001c0004t0001g0170 a0001c0004t0001g0171 a0001c0009t0003g0172 others(3): Show |
6 | HG01070.hp1 HG01071.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+854G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38429402 | |||||||
| chr17:38429545 | C | T | 6 | a0001c0004t0001g0170 a0001c0004t0001g0171 a0001c0009t0003g0172 others(3): Show |
6 | HG01070.hp1 HG01071.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+997C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38429545 | |||||||
| chr17:38429586 | T | C | 60 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(57): Show |
60 | HG00733.hp1 HG00733.hp2 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.63+1038T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38429586 | |||||||
| chr17:38429717 | G | C | 1 | a0001c0001t0011g0064 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.63+1169G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38429717 | |||||||
| chr17:38429827 | C | T | 1 | a0019c0030t0001g0167 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.63+1279C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38429827 | |||||||
| chr17:38429997 | C | G | 1 | a0001c0001t0001g0002 | 2 | NA18945.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.63+1449C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38429997 | |||||||
| chr17:38430151 | C | T | 6 | a0001c0001t0001g0058 a0001c0004t0001g0059 a0001c0004t0001g0061 others(3): Show |
6 | HG01243.hp2 HG02451.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+1603C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38430151 | |||||||
| chr17:38430232 | T | C | 61 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(58): Show |
61 | HG00733.hp1 HG00733.hp2 HG01070.hp1 others(58): Show |
intron_variant | MODIFIER | c.63+1684T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38430232 | |||||||
| chr17:38430280 | G | A | 2 | a0001c0004t0006g0010 a0001c0020t0005g0011 |
2 | HG01081.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.63+1732G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38430280 | |||||||
| chr17:38430339 | G | T | 3 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0001g0056 |
3 | HG01891.hp1 HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.63+1791G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38430339 | |||||||
| chr17:38430354 | G | A | 4 | a0001c0006t0002g0175 a0001c0006t0002g0176 a0001c0006t0002g0177 others(1): Show |
4 | HG00558.hp1 HG00621.hp1 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+1806G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38430354 | |||||||
| chr17:38430476 | G | C | 2 | a0001c0001t0001g0066 a0001c0031t0003g0067 |
2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.63+1928G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38430476 | |||||||
| chr17:38430522 | G | A | 1 | a0002c0036t0003g0179 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.63+1974G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38430522 | |||||||
| chr17:38430610 | A | G | 233 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(230): Show |
234 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.63+2062A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38430610 | |||||||
| chr17:38430755 | A | T | 1 | a0001c0002t0002g0166 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.63+2207A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38430755 | |||||||
| chr17:38430920 | C | T | 1 | a0002c0015t0001g0240 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.63+2372C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38430920 | |||||||
| chr17:38430940 | C | T | 1 | a0001c0001t0001g0301 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.63+2392C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38430940 | |||||||
| chr17:38431274 | G | T | 6 | a0001c0004t0001g0170 a0001c0004t0001g0171 a0001c0009t0003g0172 others(3): Show |
6 | HG01070.hp1 HG01071.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+2726G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38431274 | |||||||
| chr17:38431295 | C | G | 1 | a0001c0007t0003g0053 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.63+2747C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38431295 | |||||||
| chr17:38431394 | A | G | 3 | a0001c0005t0001g0050 a0001c0005t0001g0052 a0001c0012t0003g0051 |
3 | HG01884.hp1 HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.63+2846A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38431394 | |||||||
| chr17:38431455 | G | C | 2 | a0001c0004t0006g0010 a0001c0020t0005g0011 |
2 | HG01081.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.63+2907G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38431455 | |||||||
| chr17:38431489 | C | T | 1 | a0001c0004t0001g0300 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.63+2941C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38431489 | |||||||
| chr17:38432070 | C | T | 75 | a0001c0001t0001g0034 a0001c0001t0001g0058 a0001c0001t0001g0066 others(72): Show |
75 | HG00733.hp1 HG01070.hp1 HG01071.hp1 others(72): Show |
intron_variant | MODIFIER | c.63+3522C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38432070 | |||||||
| chr17:38432140 | C | G | 1 | a0001c0001t0001g0165 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.63+3592C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38432140 | |||||||
| chr17:38432258 | C | T | 1 | a0001c0008t0001g0030 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.63+3710C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38432258 | |||||||
| chr17:38432259 | G | A | 2 | a0001c0001t0001g0058 a0001c0004t0001g0031 |
2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.63+3711G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38432259 | |||||||
| chr17:38432419 | C | T | 2 | a0001c0005t0001g0049 a0001c0012t0003g0048 |
2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.63+3871C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38432419 | |||||||
| chr17:38432517 | T | G | 1 | a0001c0002t0002g0241 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.63+3969T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38432517 | |||||||
| chr17:38432591 | A | T | 1 | a0006c0050t0003g0138 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.63+4043A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38432591 | |||||||
| chr17:38432631 | A | G | 1 | a0001c0001t0001g0296 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.63+4083A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38432631 | |||||||
| chr17:38432635 | C | T | 3 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0001g0056 |
3 | HG01891.hp1 HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.63+4087C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38432635 | |||||||
| chr17:38432651 | T | C | 75 | a0001c0001t0001g0034 a0001c0001t0001g0058 a0001c0001t0001g0066 others(72): Show |
75 | HG00733.hp1 HG01070.hp1 HG01071.hp1 others(72): Show |
intron_variant | MODIFIER | c.63+4103T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38432651 | |||||||
| chr17:38432851 | A | T | 4 | a0001c0004t0001g0164 a0001c0009t0003g0057 a0001c0010t0001g0162 others(1): Show |
4 | HG02451.hp2 HG02622.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+4303A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38432851 | |||||||
| chr17:38432931 | T | A | 69 | a0001c0001t0001g0034 a0001c0001t0001g0058 a0001c0001t0001g0066 others(66): Show |
69 | HG00733.hp1 HG01081.hp1 HG01109.hp1 others(66): Show |
intron_variant | MODIFIER | c.63+4383T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38432931 | |||||||
| chr17:38432954 | C | T | 69 | a0001c0001t0001g0034 a0001c0001t0001g0058 a0001c0001t0001g0066 others(66): Show |
69 | HG00733.hp1 HG01081.hp1 HG01109.hp1 others(66): Show |
intron_variant | MODIFIER | c.63+4406C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38432954 | |||||||
| chr17:38433509 | G | A | 75 | a0001c0001t0001g0034 a0001c0001t0001g0058 a0001c0001t0001g0066 others(72): Show |
75 | HG00733.hp1 HG01070.hp1 HG01071.hp1 others(72): Show |
intron_variant | MODIFIER | c.63+4961G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38433509 | |||||||
| chr17:38433627 | T | C | 6 | a0001c0005t0001g0142 a0001c0016t0003g0297 a0001c0020t0005g0143 others(3): Show |
6 | HG03139.hp2 HG03209.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+5079T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38433627 | |||||||
| chr17:38433633 | A | G | 1 | a0001c0040t0002g0137 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.63+5085A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38433633 | |||||||
| chr17:38433857 | G | T | 1 | a0001c0002t0002g0239 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.63+5309G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38433857 | |||||||
| chr17:38433860 | G | A | 2 | a0001c0011t0001g0069 a0003c0014t0001g0068 |
2 | HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.63+5312G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38433860 | |||||||
| chr17:38433872 | G | A | 4 | a0001c0001t0003g0174 a0001c0003t0001g0012 a0001c0003t0001g0014 others(1): Show |
4 | HG01261.hp1 HG02109.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+5324G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38433872 | |||||||
| chr17:38433981 | T | G | 6 | a0001c0004t0001g0170 a0001c0004t0001g0171 a0001c0009t0003g0172 others(3): Show |
6 | HG01070.hp1 HG01071.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+5433T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38433981 | |||||||
| chr17:38434204 | C | T | 4 | a0001c0001t0001g0235 a0001c0001t0001g0237 a0001c0001t0001g0238 others(1): Show |
4 | HG00639.hp2 HG02004.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+5656C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38434204 | |||||||
| chr17:38434265 | G | T | 1 | a0001c0009t0003g0161 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.63+5717G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38434265 | |||||||
| chr17:38434492 | G | A | 71 | a0001c0001t0001g0034 a0001c0001t0001g0058 a0001c0001t0001g0066 others(68): Show |
71 | HG00733.hp1 HG01070.hp1 HG01071.hp1 others(68): Show |
intron_variant | MODIFIER | c.63+5944G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38434492 | |||||||
| chr17:38434591 | G | A | 9 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0244 others(6): Show |
9 | HG00280.hp2 HG01106.hp2 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+6043G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38434591 | |||||||
| chr17:38434825 | C | T | 1 | a0002c0035t0001g0234 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.63+6277C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38434825 | |||||||
| chr17:38434947 | G | C | 65 | a0001c0001t0001g0034 a0001c0001t0001g0058 a0001c0001t0001g0066 others(62): Show |
65 | HG00733.hp1 HG01081.hp1 HG01109.hp1 others(62): Show |
intron_variant | MODIFIER | c.63+6399G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38434947 | |||||||
| chr17:38434985 | G | A | 2 | a0001c0004t0006g0010 a0001c0020t0005g0011 |
2 | HG01081.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.63+6437G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38434985 | |||||||
| chr17:38434990 | G | C | 2 | a0001c0004t0006g0010 a0001c0020t0005g0011 |
2 | HG01081.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.63+6442G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38434990 | |||||||
| chr17:38435060 | A | C | 1 | a0001c0001t0001g0295 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.63+6512A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38435060 | |||||||
| chr17:38435145 | G | C | 6 | a0001c0005t0001g0142 a0001c0016t0003g0297 a0001c0020t0005g0143 others(3): Show |
6 | HG03139.hp2 HG03209.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+6597G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38435145 | |||||||
| chr17:38435302 | G | A | 1 | a0001c0004t0001g0059 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.63+6754G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38435302 | |||||||
| chr17:38435302 | G | GGAGA | 63 | a0001c0001t0001g0034 a0001c0001t0001g0058 a0001c0001t0001g0066 others(60): Show |
63 | HG00733.hp1 HG01081.hp1 HG01109.hp1 others(60): Show |
intron_variant | MODIFIER | c.63+6754_63+6755ins others(4): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38435302 | |||||||
| chr17:38435354 | A | G | 4 | a0001c0004t0001g0061 a0001c0004t0001g0062 a0004c0019t0004g0060 others(1): Show |
4 | HG01243.hp2 HG02970.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+6806A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38435354 | |||||||
| chr17:38435620 | C | T | 2 | a0001c0009t0003g0172 a0001c0009t0003g0173 |
2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.63+7072C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38435620 | |||||||
| chr17:38435748 | T | C | 2 | a0001c0004t0006g0010 a0001c0020t0005g0011 |
2 | HG01081.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.63+7200T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38435748 | |||||||
| chr17:38435791 | G | A | 159 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0021 others(156): Show |
160 | HG00323.hp2 HG00544.hp1 HG00597.hp2 others(157): Show |
intron_variant | MODIFIER | c.63+7243G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38435791 | |||||||
| chr17:38435802 | T | C | 2 | a0001c0004t0006g0010 a0001c0020t0005g0011 |
2 | HG01081.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.63+7254T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38435802 | |||||||
| chr17:38435872 | A | G | 1 | a0001c0003t0001g0065 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.63+7324A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38435872 | |||||||
| chr17:38435881 | G | A | 7 | a0001c0002t0002g0241 a0001c0005t0001g0142 a0001c0016t0003g0297 others(4): Show |
7 | HG02074.hp1 HG03139.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+7333G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38435881 | |||||||
| chr17:38435890 | C | T | 149 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0021 others(146): Show |
150 | HG00323.hp2 HG00544.hp1 HG00597.hp2 others(147): Show |
intron_variant | MODIFIER | c.63+7342C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38435890 | |||||||
| chr17:38436075 | G | A | 1 | a0001c0004t0006g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.63+7527G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38436075 | |||||||
| chr17:38436084 | C | T | 160 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0021 others(157): Show |
161 | HG00323.hp2 HG00544.hp1 HG00597.hp2 others(158): Show |
intron_variant | MODIFIER | c.63+7536C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38436084 | |||||||
| chr17:38436110 | C | T | 160 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0021 others(157): Show |
161 | HG00323.hp2 HG00544.hp1 HG00597.hp2 others(158): Show |
intron_variant | MODIFIER | c.63+7562C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38436110 | |||||||
| chr17:38436162 | C | T | 79 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0021 others(76): Show |
80 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.63+7614C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38436162 | |||||||
| chr17:38436396 | C | CA | 105 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0019 others(102): Show |
106 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.63+7856dupA | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38436396 | ||||||
| chr17:38436396 | C | CAA | 7 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0080 others(4): Show |
7 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+7855_63+7856dup others(2): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38436396 | ||||||
| chr17:38436397 | A | C | 3 | a0001c0004t0006g0010 a0001c0020t0005g0011 a0001c0020t0005g0143 |
3 | HG01081.hp1 HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.63+7849A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38436397 | |||||||
| chr17:38436559 | G | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.63+8011G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38436559 | |||||||
| chr17:38436774 | C | T | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(188): Show |
196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.63+8226C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38436774 | |||||||
| chr17:38436873 | C | T | 1 | a0018c0058t0002g0202 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.63+8325C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38436873 | |||||||
| chr17:38437036 | C | T | 3 | a0001c0010t0001g0016 a0001c0011t0001g0069 a0003c0014t0001g0068 |
3 | HG02896.hp1 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.63+8488C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38437036 | |||||||
| chr17:38437121 | A | G | 1 | a0001c0010t0001g0016 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.63+8573A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38437121 | |||||||
| chr17:38437208 | A | AT | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
176 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.63+8675dupT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38437208 | ||||||
| chr17:38437208 | A | ATT | 25 | a0001c0001t0001g0250 a0001c0005t0001g0036 a0001c0005t0001g0037 others(22): Show |
25 | HG00733.hp1 HG01884.hp1 HG01981.hp1 others(22): Show |
intron_variant | MODIFIER | c.63+8674_63+8675dup others(2): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38437208 | ||||||
| chr17:38437247 | C | T | 14 | a0001c0001t0001g0301 a0001c0003t0001g0259 a0001c0004t0001g0071 others(11): Show |
14 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.63+8699C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38437247 | |||||||
| chr17:38437270 | A | G | 9 | a0001c0001t0001g0058 a0001c0001t0001g0165 a0001c0010t0001g0016 others(6): Show |
9 | HG02451.hp1 HG02572.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+8722A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38437270 | |||||||
| chr17:38437411 | C | T | 1 | a0001c0004t0001g0059 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.63+8863C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38437411 | |||||||
| chr17:38437486 | G | A | 3 | a0001c0010t0001g0016 a0001c0011t0001g0069 a0003c0014t0001g0068 |
3 | HG02896.hp1 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.63+8938G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38437486 | |||||||
| chr17:38437559 | G | C | 1 | a0004c0019t0004g0060 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.63+9011G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38437559 | |||||||
| chr17:38437622 | AC | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(118): Show |
126 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.63+9082delC | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38437622 | ||||||
| chr17:38437631 | A | C | 1 | a0001c0001t0001g0165 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.63+9083A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38437631 | |||||||
| chr17:38437738 | T | G | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(118): Show |
126 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.63+9190T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38437738 | |||||||
| chr17:38437795 | A | AG | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
186 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.63+9255dupG | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38437795 | ||||||
| chr17:38437799 | G | GA | 31 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0001g0056 others(28): Show |
31 | HG00733.hp1 HG01884.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.63+9251_63+9252ins others(1): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38437799 | |||||||
| chr17:38437831 | A | C | 1 | a0001c0001t0001g0165 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.63+9283A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38437831 | |||||||
| chr17:38437866 | T | C | 77 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0021 others(74): Show |
77 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.63+9318T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38437866 | |||||||
| chr17:38437913 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.63+9365G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38437913 | |||||||
| chr17:38437968 | G | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(137): Show |
145 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.63+9420G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38437968 | |||||||
| chr17:38437987 | A | AAGGCTTC | 11 | a0001c0001t0001g0301 a0001c0003t0001g0259 a0001c0004t0001g0071 others(8): Show |
11 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.63+9441_63+9447dup others(7): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38437987 | ||||||
| chr17:38438212 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.63+9664T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38438212 | |||||||
| chr17:38438213 | T | C | 1 | a0001c0001t0001g0093 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.63+9665T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38438213 | |||||||
| chr17:38438215 | G | A | 1 | a0001c0010t0001g0016 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.63+9667G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38438215 | |||||||
| chr17:38438244 | C | T | 1 | a0001c0004t0001g0164 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.63+9696C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38438244 | |||||||
| chr17:38438321 | C | CA | 121 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(118): Show |
121 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.63+9793dupA | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38438321 | ||||||
| chr17:38438321 | C | CAA | 55 | a0001c0001t0001g0005 a0001c0001t0001g0058 a0001c0001t0001g0077 others(52): Show |
55 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.63+9792_63+9793dup others(2): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38438321 | ||||||
| chr17:38438321 | CAAAAAAA others(2): Show |
C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(94): Show |
102 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.63+9785_63+9793del others(9): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38438321 | ||||||
| chr17:38438402 | G | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(93): Show |
101 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.63+9854G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38438402 | |||||||
| chr17:38438522 | C | G | 1 | a0001c0001t0001g0034 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.63+9974C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38438522 | |||||||
| chr17:38438655 | G | GA | 70 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(67): Show |
70 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.63+10110dupA | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38438655 | ||||||
| chr17:38438710 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.63+10162G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38438710 | |||||||
| chr17:38438771 | G | T | 1 | a0006c0050t0003g0138 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.63+10223G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38438771 | |||||||
| chr17:38438966 | T | C | 1 | a0001c0009t0003g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.63+10418T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38438966 | |||||||
| chr17:38439125 | C | T | 41 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0095 others(38): Show |
41 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.63+10577C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38439125 | |||||||
| chr17:38439190 | A | G | 1 | a0001c0004t0001g0059 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.63+10642A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38439190 | |||||||
| chr17:38439415 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.63+10867C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38439415 | |||||||
| chr17:38439465 | C | T | 1 | a0001c0042t0001g0257 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.63+10917C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38439465 | |||||||
| chr17:38439535 | T | G | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(109): Show |
117 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.63+10987T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38439535 | |||||||
| chr17:38439570 | C | T | 1 | a0001c0004t0001g0199 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.63+11022C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38439570 | |||||||
| chr17:38439633 | A | C | 2 | a0007c0021t0003g0070 a0007c0021t0003g0072 |
2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.63+11085A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38439633 | |||||||
| chr17:38439644 | C | T | 4 | a0001c0016t0003g0297 a0001c0037t0003g0139 a0004c0017t0004g0140 others(1): Show |
4 | HG03139.hp2 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+11096C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38439644 | |||||||
| chr17:38439659 | A | G | 11 | a0001c0001t0001g0126 a0001c0001t0001g0301 a0001c0003t0001g0259 others(8): Show |
11 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.63+11111A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38439659 | |||||||
| chr17:38439684 | T | G | 3 | a0001c0004t0001g0062 a0004c0019t0004g0060 a0004c0019t0004g0063 |
3 | HG01243.hp2 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.63+11136T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38439684 | |||||||
| chr17:38439777 | CT | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(93): Show |
101 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.63+11244delT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38439777 | ||||||
| chr17:38439866 | A | C | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(223): Show |
231 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.63+11318A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38439866 | |||||||
| chr17:38439889 | C | A | 3 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 |
3 | HG01256.hp2 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.63+11341C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38439889 | |||||||
| chr17:38439916 | G | T | 67 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(64): Show |
67 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.63+11368G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38439916 | |||||||
| chr17:38440264 | C | T | 1 | a0001c0012t0003g0045 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.63+11716C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38440264 | |||||||
| chr17:38440324 | T | C | 3 | a0001c0010t0001g0016 a0001c0011t0001g0069 a0003c0014t0001g0068 |
3 | HG02896.hp1 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.63+11776T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38440324 | |||||||
| chr17:38440587 | C | A | 1 | a0001c0001t0001g0058 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.63+12039C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38440587 | |||||||
| chr17:38440590 | G | A | 7 | a0001c0004t0006g0010 a0001c0010t0001g0016 a0001c0011t0001g0069 others(4): Show |
7 | HG01081.hp1 HG02071.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+12042G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38440590 | |||||||
| chr17:38440824 | C | T | 3 | a0001c0004t0006g0010 a0001c0020t0005g0011 a0001c0020t0005g0143 |
3 | HG01081.hp1 HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.63+12276C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38440824 | |||||||
| chr17:38440926 | C | T | 10 | a0001c0001t0001g0301 a0001c0003t0001g0259 a0001c0004t0001g0071 others(7): Show |
10 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.63+12378C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38440926 | |||||||
| chr17:38441001 | C | A | 1 | a0001c0009t0003g0190 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.63+12453C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38441001 | |||||||
| chr17:38441103 | C | T | 4 | a0001c0016t0003g0297 a0001c0037t0003g0139 a0004c0017t0004g0140 others(1): Show |
4 | HG03139.hp2 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+12555C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38441103 | |||||||
| chr17:38441128 | G | A | 2 | a0001c0024t0001g0105 a0002c0022t0001g0097 |
2 | NA18975.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.63+12580G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38441128 | |||||||
| chr17:38441244 | C | T | 1 | a0001c0003t0001g0065 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.63+12696C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38441244 | |||||||
| chr17:38441347 | G | A | 2 | a0001c0001t0007g0106 a0001c0002t0002g0303 |
2 | NA18943.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.63+12799G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38441347 | |||||||
| chr17:38441355 | T | C | 1 | a0001c0009t0003g0172 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.63+12807T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38441355 | |||||||
| chr17:38441432 | C | G | 10 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0126 others(7): Show |
10 | HG00733.hp2 HG01081.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.63+12884C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38441432 | |||||||
| chr17:38441484 | C | T | 1 | a0001c0031t0003g0067 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.63+12936C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38441484 | |||||||
| chr17:38441489 | G | C | 9 | a0001c0001t0001g0095 a0001c0001t0001g0261 a0001c0001t0007g0106 others(6): Show |
9 | HG00597.hp2 NA18943.hp2 NA18944.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+12941G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38441489 | |||||||
| chr17:38441496 | A | C | 1 | a0001c0007t0003g0020 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.63+12948A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38441496 | |||||||
| chr17:38441537 | C | T | 68 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(65): Show |
68 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.63+12989C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38441537 | |||||||
| chr17:38441554 | A | C | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(234): Show |
242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.63+13006A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38441554 | |||||||
| chr17:38441662 | G | T | 1 | a0005c0033t0001g0075 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.63+13114G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38441662 | |||||||
| chr17:38441738 | G | A | 5 | a0001c0016t0003g0047 a0001c0016t0003g0297 a0001c0037t0003g0139 others(2): Show |
5 | HG02886.hp2 HG03139.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+13190G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38441738 | |||||||
| chr17:38441846 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.63+13298G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38441846 | |||||||
| chr17:38441936 | C | G | 1 | a0001c0001t0001g0058 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.63+13388C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38441936 | |||||||
| chr17:38441946 | C | T | 2 | a0007c0021t0003g0070 a0007c0021t0003g0072 |
2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.63+13398C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38441946 | |||||||
| chr17:38441951 | C | T | 2 | a0001c0001t0001g0124 a0001c0002t0002g0125 |
2 | HG01175.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.63+13403C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38441951 | |||||||
| chr17:38441966 | C | CT | 9 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0001g0056 others(6): Show |
9 | HG01891.hp1 HG02647.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+13426dupT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38441966 | ||||||
| chr17:38442031 | A | G | 25 | a0001c0005t0001g0033 a0001c0005t0001g0036 a0001c0005t0001g0037 others(22): Show |
25 | HG00733.hp1 HG01884.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.63+13483A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38442031 | |||||||
| chr17:38442250 | T | C | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.63+13702T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38442250 | |||||||
| chr17:38442254 | C | T | 10 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0126 others(7): Show |
10 | HG00733.hp2 HG01081.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.63+13706C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38442254 | |||||||
| chr17:38442381 | T | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
163 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.63+13833T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38442381 | |||||||
| chr17:38442559 | A | G | 8 | a0001c0004t0001g0071 a0001c0004t0001g0170 a0001c0004t0001g0171 others(5): Show |
8 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+14011A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38442559 | |||||||
| chr17:38442726 | C | T | 1 | a0001c0005t0001g0044 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.63+14178C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38442726 | |||||||
| chr17:38442957 | G | A | 1 | a0001c0004t0001g0031 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.63+14409G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38442957 | |||||||
| chr17:38443004 | A | G | 1 | a0001c0031t0003g0067 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.63+14456A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38443004 | |||||||
| chr17:38443024 | C | A | 1 | a0002c0022t0001g0097 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.63+14476C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38443024 | |||||||
| chr17:38443150 | A | G | 4 | a0001c0004t0001g0059 a0001c0031t0003g0067 a0007c0021t0003g0070 others(1): Show |
4 | HG02145.hp1 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+14602A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38443150 | |||||||
| chr17:38443189 | T | G | 54 | a0001c0001t0001g0165 a0001c0004t0001g0054 a0001c0004t0001g0055 others(51): Show |
54 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.63+14641T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38443189 | |||||||
| chr17:38443767 | C | T | 1 | a0009c0026t0001g0280 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.64-14335C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38443767 | |||||||
| chr17:38443768 | G | A | 1 | a0001c0004t0001g0059 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.64-14334G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38443768 | |||||||
| chr17:38443918 | G | A | 52 | a0001c0001t0001g0165 a0001c0004t0001g0054 a0001c0004t0001g0055 others(49): Show |
52 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.64-14184G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38443918 | |||||||
| chr17:38443935 | T | C | 52 | a0001c0001t0001g0165 a0001c0004t0001g0054 a0001c0004t0001g0055 others(49): Show |
52 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.64-14167T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38443935 | |||||||
| chr17:38443938 | C | T | 52 | a0001c0001t0001g0165 a0001c0004t0001g0054 a0001c0004t0001g0055 others(49): Show |
52 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.64-14164C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38443938 | |||||||
| chr17:38443962 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.64-14140G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38443962 | |||||||
| chr17:38444100 | C | T | 1 | a0001c0003t0001g0229 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.64-14002C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38444100 | |||||||
| chr17:38444201 | G | A | 8 | a0001c0004t0001g0071 a0001c0004t0001g0170 a0001c0004t0001g0171 others(5): Show |
8 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-13901G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38444201 | |||||||
| chr17:38444256 | C | T | 30 | a0001c0001t0001g0165 a0001c0005t0001g0033 a0001c0005t0001g0036 others(27): Show |
30 | HG00733.hp1 HG01358.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.64-13846C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38444256 | |||||||
| chr17:38444257 | G | A | 1 | a0014c0056t0001g0013 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.64-13845G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38444257 | |||||||
| chr17:38444321 | C | A | 2 | a0001c0001t0001g0281 a0002c0022t0010g0253 |
2 | NA19062.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.64-13781C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38444321 | |||||||
| chr17:38444333 | C | T | 3 | a0001c0004t0006g0010 a0001c0020t0005g0011 a0001c0020t0005g0143 |
3 | HG01081.hp1 HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.64-13769C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38444333 | |||||||
| chr17:38444430 | G | A | 52 | a0001c0001t0001g0165 a0001c0004t0001g0054 a0001c0004t0001g0055 others(49): Show |
52 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.64-13672G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38444430 | |||||||
| chr17:38444486 | T | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.64-13616T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38444486 | |||||||
| chr17:38444625 | G | T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(97): Show |
105 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.64-13477G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38444625 | |||||||
| chr17:38444820 | AT | A | 49 | a0001c0001t0001g0165 a0001c0001t0001g0203 a0001c0001t0001g0243 others(46): Show |
49 | HG00323.hp1 HG00323.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.64-13268delT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38444820 | ||||||
| chr17:38444860 | C | G | 2 | a0001c0001t0001g0203 a0001c0001t0001g0205 |
2 | HG00140.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.64-13242C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38444860 | |||||||
| chr17:38444880 | T | C | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(234): Show |
242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.64-13222T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38444880 | |||||||
| chr17:38445209 | G | A | 52 | a0001c0001t0001g0165 a0001c0004t0001g0054 a0001c0004t0001g0055 others(49): Show |
52 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.64-12893G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38445209 | |||||||
| chr17:38445303 | TA | T | 75 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(72): Show |
75 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.64-12776delA | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38445303 | ||||||
| chr17:38445303 | TAA | T | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(100): Show |
108 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.64-12777_64-12776d others(4): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38445303 | ||||||
| chr17:38445303 | TAAA | T | 12 | a0001c0001t0001g0165 a0001c0001t0001g0249 a0001c0002t0002g0157 others(9): Show |
12 | HG01167.hp2 HG01891.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.64-12778_64-12776d others(5): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38445303 | ||||||
| chr17:38445303 | TAAAA | T | 41 | a0001c0004t0001g0059 a0001c0004t0001g0071 a0001c0004t0001g0170 others(38): Show |
41 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.64-12779_64-12776d others(6): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38445303 | ||||||
| chr17:38445432 | A | G | 52 | a0001c0001t0001g0165 a0001c0004t0001g0054 a0001c0004t0001g0055 others(49): Show |
52 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.64-12670A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38445432 | |||||||
| chr17:38445491 | T | A | 8 | a0001c0004t0001g0071 a0001c0004t0001g0170 a0001c0004t0001g0171 others(5): Show |
8 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-12611T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38445491 | |||||||
| chr17:38445639 | CT | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
153 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.64-12450delT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38445639 | ||||||
| chr17:38445751 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.64-12351C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38445751 | |||||||
| chr17:38445757 | C | T | 51 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0001g0056 others(48): Show |
51 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.64-12345C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38445757 | |||||||
| chr17:38445820 | G | T | 1 | a0006c0050t0003g0138 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.64-12282G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38445820 | |||||||
| chr17:38445885 | C | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(99): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.64-12217C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38445885 | |||||||
| chr17:38446020 | CT | C | 142 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0019 others(139): Show |
142 | HG00140.hp2 HG00544.hp1 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.64-12066delT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38446020 | ||||||
| chr17:38446020 | CTT | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(85): Show |
93 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.64-12067_64-12066d others(4): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38446020 | ||||||
| chr17:38446020 | CTTT | C | 50 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0001g0056 others(47): Show |
50 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.64-12068_64-12066d others(5): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38446020 | ||||||
| chr17:38446061 | C | G | 51 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0001g0056 others(48): Show |
51 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.64-12041C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38446061 | |||||||
| chr17:38446181 | AT | A | 72 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(69): Show |
72 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.64-11898delT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38446181 | ||||||
| chr17:38446181 | ATT | A | 14 | a0001c0001t0001g0102 a0001c0001t0001g0165 a0001c0002t0002g0092 others(11): Show |
14 | HG01243.hp2 HG01256.hp2 HG02040.hp1 others(11): Show |
intron_variant | MODIFIER | c.64-11899_64-11898d others(4): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38446181 | ||||||
| chr17:38446181 | ATTT | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(121): Show |
128 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.64-11900_64-11898d others(5): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38446181 | ||||||
| chr17:38446181 | ATTTT | A | 16 | a0001c0001t0001g0003 a0001c0001t0001g0211 a0001c0001t0001g0284 others(13): Show |
17 | HG00609.hp1 HG01891.hp1 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.64-11901_64-11898d others(6): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38446181 | ||||||
| chr17:38446181 | ATTTTT | A | 11 | a0001c0004t0001g0059 a0001c0004t0001g0071 a0001c0004t0001g0170 others(8): Show |
11 | HG00323.hp2 HG00735.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.64-11902_64-11898d others(7): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38446181 | ||||||
| chr17:38446244 | A | G | 10 | a0001c0004t0001g0071 a0001c0004t0001g0170 a0001c0004t0001g0171 others(7): Show |
10 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-11858A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38446244 | |||||||
| chr17:38446273 | C | A | 51 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0001g0056 others(48): Show |
51 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.64-11829C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38446273 | |||||||
| chr17:38446280 | C | T | 1 | a0001c0031t0003g0067 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.64-11822C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38446280 | |||||||
| chr17:38446316 | C | T | 4 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(1): Show |
4 | HG01256.hp2 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-11786C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38446316 | |||||||
| chr17:38446609 | A | AT | 7 | a0001c0001t0001g0127 a0001c0001t0001g0263 a0001c0002t0002g0028 others(4): Show |
7 | HG00438.hp1 HG01258.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-11474dupT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38446609 | ||||||
| chr17:38446609 | AT | A | 8 | a0001c0001t0011g0064 a0001c0002t0002g0110 a0001c0002t0012g0108 others(5): Show |
8 | HG00544.hp1 HG03130.hp1 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-11474delT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38446609 | ||||||
| chr17:38446609 | ATTT | A | 48 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0001g0056 others(45): Show |
48 | HG00733.hp1 HG00735.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.64-11476_64-11474d others(5): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38446609 | ||||||
| chr17:38446672 | C | T | 3 | a0001c0004t0001g0062 a0004c0019t0004g0060 a0004c0019t0004g0063 |
3 | HG01243.hp2 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.64-11430C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38446672 | |||||||
| chr17:38446673 | G | A | 1 | a0004c0055t0004g0298 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.64-11429G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38446673 | |||||||
| chr17:38446675 | G | A | 30 | a0001c0005t0001g0033 a0001c0005t0001g0036 a0001c0005t0001g0037 others(27): Show |
30 | HG00733.hp1 HG01358.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.64-11427G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38446675 | |||||||
| chr17:38446782 | C | A | 1 | a0008c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.64-11320C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38446782 | |||||||
| chr17:38446833 | T | C | 39 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0001g0056 others(36): Show |
39 | HG00733.hp1 HG01358.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.64-11269T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38446833 | |||||||
| chr17:38447040 | T | G | 1 | a0001c0004t0001g0059 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.64-11062T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38447040 | |||||||
| chr17:38447271 | A | G | 51 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0001g0056 others(48): Show |
51 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.64-10831A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38447271 | |||||||
| chr17:38447276 | C | T | 51 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0001g0056 others(48): Show |
51 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.64-10826C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38447276 | |||||||
| chr17:38447303 | G | A | 2 | a0001c0011t0001g0069 a0003c0014t0001g0068 |
2 | HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.64-10799G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38447303 | |||||||
| chr17:38447334 | C | T | 9 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0001g0056 others(6): Show |
9 | HG01891.hp1 HG02647.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-10768C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38447334 | |||||||
| chr17:38447398 | C | T | 1 | a0001c0001t0001g0248 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.64-10704C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38447398 | |||||||
| chr17:38447437 | G | GA | 37 | a0001c0001t0001g0006 a0001c0001t0001g0120 a0001c0001t0001g0135 others(34): Show |
37 | HG00639.hp2 HG00642.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.64-10637dupA | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38447437 | ||||||
| chr17:38447437 | G | GAA | 20 | a0001c0004t0001g0133 a0001c0005t0001g0038 a0001c0005t0001g0040 others(17): Show |
20 | HG01358.hp1 HG01433.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.64-10638_64-10637d others(4): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38447437 | ||||||
| chr17:38447437 | G | GAAA | 7 | a0001c0001t0003g0174 a0001c0005t0001g0033 a0001c0005t0001g0036 others(4): Show |
7 | HG00733.hp1 HG02055.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-10639_64-10637d others(5): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38447437 | ||||||
| chr17:38447437 | G | GAAAAAAA others(3): Show |
1 | a0001c0001t0011g0064 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.64-10646_64-10637d others(12): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38447437 | ||||||
| chr17:38447437 | G | GAAAAAAA others(4): Show |
10 | a0001c0001t0001g0095 a0001c0002t0002g0015 a0001c0002t0002g0110 others(7): Show |
10 | HG01169.hp1 HG03017.hp2 HG03492.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-10647_64-10637d others(13): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38447437 | ||||||
| chr17:38447437 | G | GAAAAAAA others(5): Show |
24 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0079 others(21): Show |
24 | HG00597.hp2 HG01106.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.64-10648_64-10637d others(14): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38447437 | ||||||
| chr17:38447437 | G | GAAAAAAA others(6): Show |
14 | a0001c0001t0001g0058 a0001c0001t0001g0080 a0001c0001t0001g0100 others(11): Show |
14 | HG00621.hp2 HG00733.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.64-10649_64-10637d others(15): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38447437 | ||||||
| chr17:38447437 | G | GAAAAAAA others(7): Show |
4 | a0001c0001t0001g0021 a0001c0002t0002g0252 a0001c0048t0002g0113 others(1): Show |
4 | HG01081.hp2 HG02109.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-10650_64-10637d others(16): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38447437 | ||||||
| chr17:38447437 | GA | G | 10 | a0001c0001t0001g0149 a0001c0001t0001g0165 a0001c0001t0001g0261 others(7): Show |
10 | HG02055.hp1 HG02572.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.64-10637delA | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38447437 | ||||||
| chr17:38447437 | GAAAAAAA others(3): Show |
G | 1 | a0001c0003t0001g0259 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.64-10646_64-10637d others(12): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38447437 | ||||||
| chr17:38447437 | GAAAAAAA others(7): Show |
G | 2 | a0001c0003t0001g0111 a0001c0007t0003g0112 |
2 | HG00544.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.64-10650_64-10637d others(16): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38447437 | ||||||
| chr17:38447439 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.64-10663A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38447439 | |||||||
| chr17:38447453 | A | AAAAAAAA others(6): Show |
1 | a0001c0001t0001g0121 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.64-10645_64-10633d others(15): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38447453 | ||||||
| chr17:38447574 | C | A | 5 | a0001c0016t0003g0047 a0001c0016t0003g0297 a0001c0037t0003g0139 others(2): Show |
5 | HG02886.hp2 HG03139.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-10528C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38447574 | |||||||
| chr17:38447740 | T | C | 51 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0001g0056 others(48): Show |
51 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.64-10362T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38447740 | |||||||
| chr17:38447795 | A | AG | 51 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0001g0056 others(48): Show |
51 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.64-10303dupG | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38447795 | ||||||
| chr17:38447876 | T | G | 1 | a0001c0001t0001g0244 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.64-10226T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38447876 | |||||||
| chr17:38448083 | C | T | 5 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0001g0056 others(2): Show |
5 | HG01891.hp1 HG02647.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-10019C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38448083 | |||||||
| chr17:38448212 | A | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(165): Show |
173 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.64-9890A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38448212 | |||||||
| chr17:38448229 | T | C | 4 | a0001c0001t0003g0174 a0001c0003t0001g0014 a0001c0007t0003g0020 others(1): Show |
4 | HG01261.hp1 HG02109.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-9873T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38448229 | |||||||
| chr17:38448242 | G | A | 1 | a0001c0002t0002g0125 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.64-9860G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38448242 | |||||||
| chr17:38448364 | G | A | 1 | a0001c0031t0003g0067 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.64-9738G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38448364 | |||||||
| chr17:38448366 | C | T | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(106): Show |
114 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.64-9736C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38448366 | |||||||
| chr17:38448538 | T | C | 30 | a0001c0005t0001g0033 a0001c0005t0001g0036 a0001c0005t0001g0037 others(27): Show |
30 | HG00733.hp1 HG01358.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.64-9564T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38448538 | |||||||
| chr17:38448633 | C | G | 3 | a0001c0004t0001g0062 a0004c0019t0004g0060 a0004c0019t0004g0063 |
3 | HG01243.hp2 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.64-9469C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38448633 | |||||||
| chr17:38448641 | G | GT | 63 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0080 others(60): Show |
63 | HG00323.hp2 HG00621.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.64-9439dupT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38448641 | ||||||
| chr17:38448641 | G | GTT | 8 | a0001c0004t0001g0056 a0001c0004t0001g0059 a0001c0005t0001g0033 others(5): Show |
8 | HG01884.hp2 HG02055.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-9440_64-9439dup others(2): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38448641 | ||||||
| chr17:38448641 | GT | G | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(97): Show |
105 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.64-9439delT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38448641 | ||||||
| chr17:38448801 | A | ATCCCCGA others(317): Show |
2 | a0001c0011t0001g0069 a0003c0014t0001g0068 |
2 | HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.64-9285_64-9284ins others(324): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38448801 | ||||||
| chr17:38448801 | A | ATCCCCGA others(318): Show |
5 | a0001c0004t0001g0054 a0001c0004t0001g0056 a0001c0004t0001g0061 others(2): Show |
5 | HG01891.hp1 HG03486.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-9285_64-9284ins others(325): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38448801 | ||||||
| chr17:38448801 | A | ATCCCCGA others(319): Show |
2 | a0001c0004t0001g0055 a0001c0009t0003g0161 |
2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.64-9285_64-9284ins others(326): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38448801 | ||||||
| chr17:38448858 | C | CT | 7 | a0001c0001t0001g0079 a0001c0001t0001g0228 a0001c0004t0001g0031 others(4): Show |
7 | HG01243.hp1 HG01346.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-9227dupT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38448858 | ||||||
| chr17:38448858 | C | CTTTTT | 36 | a0001c0004t0001g0071 a0001c0004t0001g0170 a0001c0004t0001g0171 others(33): Show |
36 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.64-9231_64-9227dup others(5): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38448858 | ||||||
| chr17:38448858 | C | CTTTTTTT | 7 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0001g0056 others(4): Show |
7 | HG01891.hp1 HG02647.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-9233_64-9227dup others(7): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38448858 | ||||||
| chr17:38448858 | C | T | 2 | a0007c0021t0003g0070 a0007c0021t0003g0072 |
2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.64-9244C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38448858 | |||||||
| chr17:38448911 | G | T | 3 | a0001c0004t0001g0062 a0004c0019t0004g0060 a0004c0019t0004g0063 |
3 | HG01243.hp2 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.64-9191G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38448911 | |||||||
| chr17:38449157 | C | T | 51 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0001g0056 others(48): Show |
51 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.64-8945C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38449157 | |||||||
| chr17:38449246 | G | A | 59 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(56): Show |
59 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.64-8856G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38449246 | |||||||
| chr17:38449314 | G | A | 5 | a0001c0011t0006g0073 a0001c0011t0006g0076 a0001c0032t0001g0201 others(2): Show |
5 | HG01358.hp1 HG01884.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-8788G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38449314 | |||||||
| chr17:38449412 | C | T | 1 | a0001c0007t0003g0053 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.64-8690C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38449412 | |||||||
| chr17:38449417 | C | G | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
232 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.64-8685C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38449417 | |||||||
| chr17:38449475 | G | A | 51 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0001g0056 others(48): Show |
51 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.64-8627G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38449475 | |||||||
| chr17:38449550 | C | A | 51 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0001g0056 others(48): Show |
51 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.64-8552C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38449550 | |||||||
| chr17:38449650 | C | T | 51 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0001g0056 others(48): Show |
51 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.64-8452C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38449650 | |||||||
| chr17:38449895 | T | G | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
172 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.64-8207T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38449895 | |||||||
| chr17:38449903 | C | T | 51 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0001g0056 others(48): Show |
51 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.64-8199C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38449903 | |||||||
| chr17:38449947 | C | G | 1 | a0001c0024t0001g0105 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.64-8155C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38449947 | |||||||
| chr17:38449988 | C | T | 51 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0001g0056 others(48): Show |
51 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.64-8114C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38449988 | |||||||
| chr17:38450101 | C | T | 2 | a0001c0002t0002g0226 a0001c0054t0002g0227 |
2 | HG02602.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.64-8001C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38450101 | |||||||
| chr17:38450181 | C | T | 1 | a0001c0007t0003g0053 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.64-7921C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38450181 | |||||||
| chr17:38450347 | G | T | 4 | a0001c0011t0006g0073 a0001c0011t0006g0076 a0003c0014t0001g0074 others(1): Show |
4 | HG01884.hp2 HG02258.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-7755G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38450347 | |||||||
| chr17:38450444 | C | T | 1 | a0001c0031t0003g0067 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.64-7658C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38450444 | |||||||
| chr17:38450471 | A | AATGGCGT others(1): Show |
12 | a0001c0004t0001g0059 a0001c0004t0001g0071 a0001c0004t0001g0170 others(9): Show |
12 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-7629_64-7628ins others(8): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38450471 | ||||||
| chr17:38450472 | A | G | 9 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(6): Show |
9 | HG02071.hp2 HG02074.hp2 NA18943.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-7630A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38450472 | |||||||
| chr17:38450617 | G | A | 51 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0001g0056 others(48): Show |
51 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.64-7485G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38450617 | |||||||
| chr17:38450778 | T | G | 1 | a0001c0009t0003g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.64-7324T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38450778 | |||||||
| chr17:38451064 | T | G | 1 | a0001c0001t0001g0114 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.64-7038T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38451064 | |||||||
| chr17:38451239 | G | A | 8 | a0001c0004t0001g0071 a0001c0004t0001g0170 a0001c0004t0001g0171 others(5): Show |
8 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-6863G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38451239 | |||||||
| chr17:38451322 | T | A | 1 | a0001c0001t0001g0114 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.64-6780T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38451322 | |||||||
| chr17:38451343 | G | A | 51 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0001g0056 others(48): Show |
51 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.64-6759G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38451343 | |||||||
| chr17:38451364 | A | G | 1 | a0001c0001t0001g0265 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.64-6738A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38451364 | |||||||
| chr17:38451453 | C | A | 1 | a0001c0001t0001g0114 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.64-6649C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38451453 | |||||||
| chr17:38451458 | C | T | 1 | a0002c0036t0003g0179 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.64-6644C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38451458 | |||||||
| chr17:38451498 | C | T | 1 | a0001c0001t0001g0295 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.64-6604C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38451498 | |||||||
| chr17:38451534 | G | C | 2 | a0001c0004t0001g0031 a0004c0055t0004g0298 |
2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.64-6568G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38451534 | |||||||
| chr17:38451662 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.64-6440T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38451662 | |||||||
| chr17:38451846 | C | G | 1 | a0001c0001t0001g0114 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.64-6256C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38451846 | |||||||
| chr17:38451847 | G | C | 1 | a0001c0001t0001g0114 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.64-6255G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38451847 | |||||||
| chr17:38451887 | C | T | 3 | a0001c0008t0001g0188 a0001c0008t0001g0195 a0002c0015t0001g0189 |
3 | NA18983.hp1 NA18985.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.64-6215C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38451887 | |||||||
| chr17:38451966 | C | A | 1 | a0001c0001t0001g0165 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.64-6136C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38451966 | |||||||
| chr17:38452083 | C | A | 3 | a0001c0004t0006g0010 a0001c0020t0005g0011 a0001c0020t0005g0143 |
3 | HG01081.hp1 HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.64-6019C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38452083 | |||||||
| chr17:38452141 | C | T | 2 | a0001c0004t0001g0031 a0004c0055t0004g0298 |
2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.64-5961C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38452141 | |||||||
| chr17:38452247 | C | T | 1 | a0001c0002t0002g0123 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.64-5855C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38452247 | |||||||
| chr17:38452292 | C | G | 6 | a0001c0001t0001g0279 a0001c0004t0001g0170 a0001c0004t0001g0171 others(3): Show |
6 | HG01070.hp1 HG01071.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-5810C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38452292 | |||||||
| chr17:38452392 | C | A | 1 | a0001c0003t0001g0115 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.64-5710C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38452392 | |||||||
| chr17:38452433 | T | C | 286 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(283): Show |
291 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.64-5669T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38452433 | |||||||
| chr17:38452438 | C | T | 1 | a0002c0023t0001g0236 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.64-5664C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38452438 | |||||||
| chr17:38452555 | A | G | 28 | a0001c0001t0001g0165 a0001c0004t0001g0054 a0001c0004t0001g0055 others(25): Show |
28 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.64-5547A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38452555 | |||||||
| chr17:38452896 | C | T | 28 | a0001c0001t0001g0165 a0001c0004t0001g0054 a0001c0004t0001g0055 others(25): Show |
28 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.64-5206C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38452896 | |||||||
| chr17:38452916 | T | C | 28 | a0001c0001t0001g0165 a0001c0004t0001g0054 a0001c0004t0001g0055 others(25): Show |
28 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.64-5186T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38452916 | |||||||
| chr17:38452945 | C | T | 1 | a0001c0031t0003g0067 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.64-5157C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38452945 | |||||||
| chr17:38453021 | T | G | 3 | a0001c0004t0001g0062 a0004c0019t0004g0060 a0004c0019t0004g0063 |
3 | HG01243.hp2 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.64-5081T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38453021 | |||||||
| chr17:38453037 | T | A | 2 | a0001c0004t0001g0031 a0004c0055t0004g0298 |
2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.64-5065T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38453037 | |||||||
| chr17:38453040 | A | G | 9 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0001g0056 others(6): Show |
9 | HG01891.hp1 HG02647.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-5062A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38453040 | |||||||
| chr17:38453107 | G | T | 1 | a0001c0001t0001g0058 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.64-4995G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38453107 | |||||||
| chr17:38453244 | T | G | 16 | a0001c0001t0001g0165 a0001c0004t0001g0054 a0001c0004t0001g0055 others(13): Show |
16 | HG01358.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.64-4858T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38453244 | |||||||
| chr17:38453261 | T | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(125): Show |
133 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.64-4841T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38453261 | |||||||
| chr17:38453359 | A | T | 2 | a0001c0001t0001g0019 a0001c0001t0003g0174 |
2 | HG04184.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.64-4743A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38453359 | |||||||
| chr17:38453382 | TTCTC | T | 28 | a0001c0001t0001g0165 a0001c0004t0001g0054 a0001c0004t0001g0055 others(25): Show |
28 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.64-4718_64-4715del others(4): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453382 | ||||||
| chr17:38453415 | ATGCG | A | 3 | a0001c0009t0003g0172 a0001c0009t0003g0173 a0001c0040t0002g0137 |
3 | HG00735.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.64-4680_64-4677del others(4): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453415 | ||||||
| chr17:38453418 | CGTGCGT | C | 7 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0001g0056 others(4): Show |
7 | HG01891.hp1 HG02647.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-4680_64-4675del others(6): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453418 | ||||||
| chr17:38453418 | CGTGCGTG others(3): Show |
C | 3 | a0001c0004t0006g0010 a0001c0020t0005g0011 a0001c0020t0005g0143 |
3 | HG01081.hp1 HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.64-4680_64-4671del others(10): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453418 | ||||||
| chr17:38453418 | CGTGCGTG others(5): Show |
C | 2 | a0001c0031t0003g0067 a0007c0021t0003g0072 |
2 | HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.64-4680_64-4669del others(12): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453418 | ||||||
| chr17:38453418 | CGTGCGTG others(7): Show |
C | 6 | a0001c0011t0006g0073 a0001c0011t0006g0076 a0001c0032t0001g0201 others(3): Show |
6 | HG01358.hp1 HG01884.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-4680_64-4667del others(14): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453418 | ||||||
| chr17:38453419 | G | A | 5 | a0001c0016t0003g0047 a0001c0016t0003g0297 a0001c0037t0003g0139 others(2): Show |
5 | HG02886.hp2 HG03139.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-4683G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38453419 | |||||||
| chr17:38453422 | C | CGT | 23 | a0001c0001t0001g0066 a0001c0001t0001g0093 a0001c0001t0001g0094 others(20): Show |
23 | HG00558.hp1 HG01071.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.64-4642_64-4641dup others(2): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453422 | ||||||
| chr17:38453422 | C | CGTGT | 4 | a0001c0001t0001g0281 a0001c0004t0001g0133 a0003c0028t0001g0017 others(1): Show |
4 | HG01433.hp2 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-4644_64-4641dup others(4): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453422 | ||||||
| chr17:38453422 | C | CGTGTGT | 3 | a0001c0004t0001g0276 a0001c0006t0002g0176 a0001c0010t0001g0016 |
3 | HG02071.hp1 NA18522.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.64-4646_64-4641dup others(6): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453422 | ||||||
| chr17:38453422 | C | T | 3 | a0001c0004t0001g0170 a0001c0004t0001g0171 a0001c0010t0001g0169 |
3 | HG01070.hp1 HG01071.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.64-4680C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38453422 | |||||||
| chr17:38453422 | CGT | C | 17 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0077 others(14): Show |
17 | HG00099.hp1 HG00741.hp1 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.64-4642_64-4641del others(2): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453422 | ||||||
| chr17:38453422 | CGTGT | C | 27 | a0001c0001t0001g0058 a0001c0001t0001g0081 a0001c0001t0001g0095 others(24): Show |
27 | HG00609.hp2 HG00642.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.64-4644_64-4641del others(4): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453422 | ||||||
| chr17:38453422 | CGTGTGT | C | 21 | a0001c0001t0001g0025 a0001c0001t0001g0080 a0001c0001t0001g0100 others(18): Show |
21 | HG00621.hp2 HG01175.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.64-4646_64-4641del others(6): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453422 | ||||||
| chr17:38453422 | CGTGTGTG others(1): Show |
C | 10 | a0001c0001t0007g0106 a0001c0001t0011g0064 a0001c0003t0001g0115 others(7): Show |
10 | HG00597.hp2 HG01952.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-4648_64-4641del others(8): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453422 | ||||||
| chr17:38453422 | CGTGTGTG others(3): Show |
C | 3 | a0001c0002t0002g0015 a0001c0002t0002g0251 a0001c0003t0001g0014 |
3 | HG01169.hp1 HG01261.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.64-4650_64-4641del others(10): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453422 | ||||||
| chr17:38453422 | CGTGTGTG others(5): Show |
C | 9 | a0001c0002t0002g0116 a0001c0002t0002g0123 a0001c0002t0002g0303 others(6): Show |
9 | HG02886.hp2 HG03017.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.64-4652_64-4641del others(12): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453422 | ||||||
| chr17:38453450 | TGTGTGTG others(5): Show |
T | 2 | a0001c0001t0001g0213 a0001c0004t0001g0059 |
2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.64-4650_64-4639del others(12): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453450 | ||||||
| chr17:38453452 | TGTGTGTG others(3): Show |
T | 1 | a0001c0001t0001g0152 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.64-4648_64-4639del others(10): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453452 | ||||||
| chr17:38453456 | TGTGTGC | T | 23 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0084 others(20): Show |
25 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.64-4644_64-4639del others(6): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453456 | ||||||
| chr17:38453458 | T | C | 58 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(55): Show |
58 | HG00597.hp2 HG00621.hp2 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.64-4644T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38453458 | |||||||
| chr17:38453458 | TGTGC | T | 23 | a0001c0001t0001g0008 a0001c0001t0001g0151 a0001c0001t0001g0203 others(20): Show |
23 | HG00280.hp1 HG00323.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.64-4642_64-4639del others(4): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453458 | ||||||
| chr17:38453460 | T | C | 62 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(59): Show |
62 | HG00597.hp2 HG00621.hp2 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.64-4642T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38453460 | |||||||
| chr17:38453460 | TGC | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(44): Show |
50 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.64-4631_64-4630del others(2): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453460 | ||||||
| chr17:38453462 | C | T | 45 | a0001c0001t0001g0034 a0001c0001t0001g0066 a0001c0001t0001g0085 others(42): Show |
45 | HG00140.hp1 HG00558.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.64-4640C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38453462 | |||||||
| chr17:38453524 | G | A | 20 | a0001c0001t0001g0001 a0001c0001t0001g0213 a0001c0001t0001g0214 others(17): Show |
22 | HG00280.hp2 HG00639.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.64-4578G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38453524 | |||||||
| chr17:38453649 | C | T | 2 | a0001c0004t0001g0031 a0004c0055t0004g0298 |
2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.64-4453C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38453649 | |||||||
| chr17:38453708 | C | T | 1 | a0001c0004t0001g0059 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.64-4394C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38453708 | |||||||
| chr17:38453715 | C | A | 1 | a0001c0010t0001g0016 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.64-4387C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38453715 | |||||||
| chr17:38453796 | TCCGGGGG others(32): Show |
T | 1 | a0001c0031t0003g0067 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.64-4297_64-4259del others(39): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 38453796 | ||||||
| chr17:38453815 | C | T | 1 | a0001c0043t0001g0178 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.64-4287C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38453815 | |||||||
| chr17:38453866 | G | T | 1 | a0001c0001t0001g0264 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.64-4236G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38453866 | |||||||
| chr17:38453955 | C | T | 3 | a0001c0004t0006g0010 a0001c0020t0005g0011 a0001c0020t0005g0143 |
3 | HG01081.hp1 HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.64-4147C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38453955 | |||||||
| chr17:38454152 | G | A | 1 | a0005c0041t0001g0032 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.64-3950G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38454152 | |||||||
| chr17:38454306 | G | T | 23 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0001g0056 others(20): Show |
23 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.64-3796G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38454306 | |||||||
| chr17:38454435 | G | A | 1 | a0001c0007t0003g0020 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.64-3667G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38454435 | |||||||
| chr17:38454436 | T | A | 5 | a0001c0011t0006g0073 a0001c0011t0006g0076 a0001c0032t0001g0201 others(2): Show |
5 | HG01358.hp1 HG01884.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-3666T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38454436 | |||||||
| chr17:38454514 | G | T | 1 | a0001c0003t0001g0101 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.64-3588G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38454514 | |||||||
| chr17:38454625 | C | A | 50 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0077 others(47): Show |
50 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.64-3477C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38454625 | |||||||
| chr17:38454663 | G | A | 5 | a0001c0016t0003g0047 a0001c0016t0003g0297 a0001c0037t0003g0139 others(2): Show |
5 | HG02886.hp2 HG03139.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-3439G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38454663 | |||||||
| chr17:38454732 | G | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(79): Show |
87 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.64-3370G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38454732 | |||||||
| chr17:38454779 | C | T | 1 | a0001c0007t0003g0053 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.64-3323C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38454779 | |||||||
| chr17:38454784 | G | C | 5 | a0001c0001t0001g0187 a0001c0001t0001g0222 a0001c0001t0001g0231 others(2): Show |
5 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-3318G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38454784 | |||||||
| chr17:38454838 | G | A | 5 | a0001c0011t0006g0073 a0001c0011t0006g0076 a0001c0032t0001g0201 others(2): Show |
5 | HG01358.hp1 HG01884.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-3264G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38454838 | |||||||
| chr17:38455031 | C | T | 1 | a0001c0001t0001g0009 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.64-3071C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38455031 | |||||||
| chr17:38455045 | G | A | 6 | a0001c0001t0001g0081 a0001c0001t0001g0102 a0001c0001t0001g0103 others(3): Show |
6 | HG00642.hp2 HG01256.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-3057G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38455045 | |||||||
| chr17:38455169 | A | G | 3 | a0001c0008t0001g0197 a0001c0008t0001g0198 a0001c0010t0001g0168 |
3 | HG00099.hp1 HG01952.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.64-2933A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38455169 | |||||||
| chr17:38455207 | G | A | 3 | a0001c0002t0002g0116 a0001c0002t0002g0123 a0001c0002t0012g0108 |
3 | HG03017.hp2 HG03710.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.64-2895G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38455207 | |||||||
| chr17:38455469 | A | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.64-2633A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38455469 | |||||||
| chr17:38455487 | G | C | 3 | a0001c0004t0001g0062 a0004c0019t0004g0060 a0004c0019t0004g0063 |
3 | HG01243.hp2 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.64-2615G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38455487 | |||||||
| chr17:38455560 | G | T | 1 | a0016c0057t0001g0278 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.64-2542G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38455560 | |||||||
| chr17:38455618 | T | C | 1 | a0012c0039t0001g0186 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.64-2484T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38455618 | |||||||
| chr17:38455721 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.64-2381G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38455721 | |||||||
| chr17:38455727 | G | T | 1 | a0001c0009t0003g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.64-2375G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38455727 | |||||||
| chr17:38455741 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.64-2361G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38455741 | |||||||
| chr17:38455755 | C | T | 1 | a0001c0010t0001g0016 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.64-2347C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38455755 | |||||||
| chr17:38455815 | G | A | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(123): Show |
131 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.64-2287G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38455815 | |||||||
| chr17:38456054 | C | T | 1 | a0001c0001t0001g0295 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.64-2048C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38456054 | |||||||
| chr17:38456080 | G | T | 1 | a0001c0004t0001g0300 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.64-2022G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38456080 | |||||||
| chr17:38456118 | G | A | 1 | a0001c0032t0001g0201 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.64-1984G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38456118 | |||||||
| chr17:38456249 | C | G | 21 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0001g0056 others(18): Show |
21 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.64-1853C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38456249 | |||||||
| chr17:38456297 | C | G | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(98): Show |
106 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.64-1805C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38456297 | |||||||
| chr17:38456345 | A | C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(98): Show |
106 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.64-1757A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38456345 | |||||||
| chr17:38456590 | G | A | 7 | a0001c0004t0001g0071 a0001c0004t0001g0170 a0001c0004t0001g0171 others(4): Show |
7 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-1512G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38456590 | |||||||
| chr17:38456602 | G | C | 1 | a0001c0001t0001g0083 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.64-1500G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38456602 | |||||||
| chr17:38456632 | T | G | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(98): Show |
106 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.64-1470T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38456632 | |||||||
| chr17:38456694 | C | T | 27 | a0001c0004t0006g0010 a0001c0005t0001g0033 a0001c0005t0001g0036 others(24): Show |
27 | HG00733.hp1 HG01081.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.64-1408C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38456694 | |||||||
| chr17:38456704 | C | A | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(156): Show |
164 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.64-1398C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38456704 | |||||||
| chr17:38456829 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.64-1273C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38456829 | |||||||
| chr17:38457018 | T | G | 2 | a0007c0021t0003g0070 a0007c0021t0003g0072 |
2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.64-1084T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38457018 | |||||||
| chr17:38457019 | C | G | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(98): Show |
106 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.64-1083C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38457019 | |||||||
| chr17:38457101 | G | C | 1 | a0001c0007t0003g0053 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.64-1001G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38457101 | |||||||
| chr17:38457364 | T | G | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(101): Show |
109 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.64-738T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38457364 | |||||||
| chr17:38457492 | G | T | 30 | a0001c0004t0001g0059 a0001c0005t0001g0033 a0001c0005t0001g0036 others(27): Show |
30 | HG00733.hp1 HG01884.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.64-610G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38457492 | |||||||
| chr17:38457496 | T | C | 1 | a0001c0009t0003g0161 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.64-606T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38457496 | |||||||
| chr17:38457566 | G | A | 4 | a0001c0001t0001g0002 a0001c0001t0001g0083 a0001c0001t0001g0084 others(1): Show |
5 | HG02132.hp2 HG02165.hp1 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-536G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38457566 | |||||||
| chr17:38457768 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.64-334A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38457768 | |||||||
| chr17:38457893 | G | C | 1 | a0001c0032t0001g0201 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.64-209G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | chr17 | 38457893 | |||||||
| chr17:38458280 | G | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(96): Show |
104 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.225+17G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38458280 | |||||||
| chr17:38458319 | C | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(98): Show |
106 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.225+56C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38458319 | |||||||
| chr17:38458387 | C | T | 1 | a0001c0032t0001g0201 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.225+124C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38458387 | |||||||
| chr17:38458455 | A | G | 24 | a0001c0005t0001g0033 a0001c0005t0001g0036 a0001c0005t0001g0037 others(21): Show |
24 | HG00733.hp1 HG01884.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.225+192A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38458455 | |||||||
| chr17:38458486 | G | C | 1 | a0015c0044t0001g0192 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.225+223G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38458486 | |||||||
| chr17:38458605 | G | A | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(98): Show |
106 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.225+342G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38458605 | |||||||
| chr17:38458637 | CT | C | 5 | a0001c0001t0001g0288 a0001c0001t0001g0290 a0001c0001t0001g0291 others(2): Show |
5 | NA18960.hp1 NA18979.hp2 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.225+375delT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38458637 | |||||||
| chr17:38458763 | C | T | 3 | a0001c0004t0001g0062 a0004c0019t0004g0060 a0004c0019t0004g0063 |
3 | HG01243.hp2 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.225+500C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38458763 | |||||||
| chr17:38458806 | C | T | 7 | a0001c0004t0001g0071 a0001c0004t0001g0170 a0001c0004t0001g0171 others(4): Show |
7 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.225+543C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38458806 | |||||||
| chr17:38458807 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.225+544G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38458807 | |||||||
| chr17:38458819 | A | G | 1 | a0001c0003t0001g0109 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.225+556A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38458819 | |||||||
| chr17:38459190 | A | G | 1 | a0001c0002t0002g0303 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.225+927A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38459190 | |||||||
| chr17:38459208 | G | C | 2 | a0007c0021t0003g0070 a0007c0021t0003g0072 |
2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.225+945G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38459208 | |||||||
| chr17:38459331 | T | C | 1 | a0001c0004t0001g0031 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.225+1068T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38459331 | |||||||
| chr17:38459338 | T | C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(98): Show |
106 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.225+1075T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38459338 | |||||||
| chr17:38459389 | C | T | 4 | a0001c0004t0001g0059 a0001c0004t0001g0062 a0004c0019t0004g0060 others(1): Show |
4 | HG01243.hp2 HG02970.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+1126C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38459389 | |||||||
| chr17:38459460 | G | C | 1 | a0001c0004t0001g0059 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.225+1197G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38459460 | |||||||
| chr17:38459649 | A | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(104): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.226-1256A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38459649 | |||||||
| chr17:38459723 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(111): Show |
119 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.226-1182A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38459723 | |||||||
| chr17:38459740 | T | G | 25 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0001g0056 others(22): Show |
25 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.226-1165T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38459740 | |||||||
| chr17:38459815 | T | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(125): Show |
133 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.226-1090T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38459815 | |||||||
| chr17:38459822 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.226-1083C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38459822 | |||||||
| chr17:38459845 | C | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(150): Show |
158 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.226-1060C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38459845 | |||||||
| chr17:38459955 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.226-950G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38459955 | |||||||
| chr17:38459983 | T | C | 2 | a0001c0002t0002g0239 a0001c0003t0001g0185 |
2 | HG03669.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.226-922T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38459983 | |||||||
| chr17:38460222 | G | T | 3 | a0001c0001t0001g0208 a0015c0044t0001g0192 a0016c0057t0001g0278 |
3 | HG02135.hp1 HG02165.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.226-683G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38460222 | |||||||
| chr17:38460314 | C | T | 1 | a0018c0058t0002g0202 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.226-591C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38460314 | |||||||
| chr17:38460472 | G | A | 1 | a0001c0002t0002g0118 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.226-433G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38460472 | |||||||
| chr17:38460582 | C | T | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG02165.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.226-323C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38460582 | |||||||
| chr17:38460583 | G | A | 1 | a0006c0050t0003g0138 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.226-322G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38460583 | |||||||
| chr17:38460621 | C | T | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(232): Show |
240 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.226-284C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38460621 | |||||||
| chr17:38460692 | G | A | 7 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0001g0056 others(4): Show |
7 | HG01891.hp1 HG02647.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.226-213G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38460692 | |||||||
| chr17:38460704 | G | A | 1 | a0001c0007t0015g0266 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.226-201G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38460704 | |||||||
| chr17:38460766 | C | T | 4 | a0001c0004t0001g0059 a0001c0004t0001g0062 a0004c0019t0004g0060 others(1): Show |
4 | HG01243.hp2 HG02970.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.226-139C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38460766 | |||||||
| chr17:38460832 | C | T | 3 | a0001c0004t0006g0010 a0001c0020t0005g0011 a0001c0020t0005g0143 |
3 | HG01081.hp1 HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.226-73C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 2/23 | chr17 | 38460832 | |||||||
| chr17:38460966 | G | A | 111 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0019 others(108): Show |
111 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.253+34G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 3/23 | chr17 | 38460966 | |||||||
| chr17:38461183 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.253+251C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 3/23 | chr17 | 38461183 | |||||||
| chr17:38461234 | G | C | 7 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0001g0056 others(4): Show |
7 | HG01891.hp1 HG02647.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.253+302G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 3/23 | chr17 | 38461234 | |||||||
| chr17:38461480 | G | A | 2 | a0003c0028t0001g0299 a0004c0055t0004g0298 |
2 | HG02486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.253+548G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 3/23 | chr17 | 38461480 | |||||||
| chr17:38461565 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.253+633C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 3/23 | chr17 | 38461565 | |||||||
| chr17:38461584 | G | A | 11 | a0001c0001t0001g0034 a0001c0001t0001g0145 a0001c0001t0001g0149 others(8): Show |
11 | HG02145.hp2 HG02280.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.253+652G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 3/23 | chr17 | 38461584 | |||||||
| chr17:38461710 | CT | C | 274 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(271): Show |
279 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.253+780delT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr17 | 38461710 | ||||||
| chr17:38461782 | T | A | 1 | a0001c0008t0001g0030 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.253+850T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 3/23 | chr17 | 38461782 | |||||||
| chr17:38462040 | C | A | 2 | a0007c0021t0003g0070 a0007c0021t0003g0072 |
2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.254-806C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 3/23 | chr17 | 38462040 | |||||||
| chr17:38462046 | G | A | 24 | a0001c0005t0001g0033 a0001c0005t0001g0036 a0001c0005t0001g0037 others(21): Show |
24 | HG00733.hp1 HG01884.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.254-800G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 3/23 | chr17 | 38462046 | |||||||
| chr17:38462199 | C | T | 24 | a0001c0005t0001g0033 a0001c0005t0001g0036 a0001c0005t0001g0037 others(21): Show |
24 | HG00733.hp1 HG01884.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.254-647C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 3/23 | chr17 | 38462199 | |||||||
| chr17:38462247 | CT | C | 21 | a0001c0001t0001g0268 a0001c0001t0011g0064 a0001c0002t0002g0116 others(18): Show |
21 | HG01071.hp2 HG01081.hp1 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.254-575delT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr17 | 38462247 | ||||||
| chr17:38462247 | CTT | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(199): Show |
207 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.254-576_254-575del others(2): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr17 | 38462247 | ||||||
| chr17:38462247 | CTTT | C | 35 | a0001c0001t0001g0084 a0001c0001t0001g0114 a0001c0001t0001g0214 others(32): Show |
35 | HG00733.hp1 HG01256.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.254-577_254-575del others(3): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr17 | 38462247 | ||||||
| chr17:38462247 | CTTTT | C | 7 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0001g0056 others(4): Show |
7 | HG01891.hp1 HG02647.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.254-578_254-575del others(4): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr17 | 38462247 | ||||||
| chr17:38462546 | A | G | 274 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(271): Show |
279 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.254-300A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 3/23 | chr17 | 38462546 | |||||||
| chr17:38462744 | C | T | 2 | a0001c0001t0001g0286 a0006c0049t0001g0262 |
2 | NA18963.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.254-102C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 3/23 | chr17 | 38462744 | |||||||
| chr17:38462794 | T | C | 1 | a0001c0010t0001g0016 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.254-52T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 3/23 | chr17 | 38462794 | |||||||
| chr17:38462960 | C | T | 1 | a0001c0001t0001g0281 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.349+19C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 4/23 | chr17 | 38462960 | |||||||
| chr17:38462985 | C | G | 1 | a0001c0004t0001g0059 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.349+44C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 4/23 | chr17 | 38462985 | |||||||
| chr17:38463214 | C | T | 7 | a0001c0004t0001g0071 a0001c0004t0001g0170 a0001c0004t0001g0171 others(4): Show |
7 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.428+18C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 5/23 | chr17 | 38463214 | |||||||
| chr17:38463277 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.429-51C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 5/23 | chr17 | 38463277 | |||||||
| chr17:38463540 | C | T | 10 | a0001c0001t0001g0003 a0001c0001t0001g0211 a0001c0001t0001g0230 others(7): Show |
11 | HG00609.hp1 HG02040.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.483+158C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38463540 | |||||||
| chr17:38463650 | C | T | 2 | a0003c0028t0001g0299 a0004c0055t0004g0298 |
2 | HG02486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.483+268C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38463650 | |||||||
| chr17:38463750 | G | A | 5 | a0001c0016t0003g0047 a0001c0016t0003g0297 a0001c0037t0003g0139 others(2): Show |
5 | HG02886.hp2 HG03139.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.483+368G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38463750 | |||||||
| chr17:38464062 | C | T | 53 | a0001c0001t0001g0154 a0001c0004t0001g0054 a0001c0004t0001g0055 others(50): Show |
53 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.483+680C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38464062 | |||||||
| chr17:38464086 | C | T | 2 | a0007c0021t0003g0070 a0007c0021t0003g0072 |
2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.483+704C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38464086 | |||||||
| chr17:38464107 | A | G | 2 | a0007c0021t0003g0070 a0007c0021t0003g0072 |
2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.483+725A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38464107 | |||||||
| chr17:38464228 | C | T | 7 | a0001c0004t0001g0071 a0001c0004t0001g0170 a0001c0004t0001g0171 others(4): Show |
7 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.483+846C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38464228 | |||||||
| chr17:38464258 | G | A | 7 | a0001c0004t0001g0071 a0001c0004t0001g0170 a0001c0004t0001g0171 others(4): Show |
7 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.483+876G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38464258 | |||||||
| chr17:38464290 | C | CCA | 35 | a0001c0001t0001g0154 a0001c0001t0001g0279 a0001c0001t0014g0270 others(32): Show |
35 | HG00733.hp1 HG01358.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.483+926_483+927dup others(2): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr17 | 38464290 | ||||||
| chr17:38464290 | CCA | C | 5 | a0001c0016t0003g0047 a0001c0016t0003g0297 a0001c0037t0003g0139 others(2): Show |
5 | HG02886.hp2 HG03139.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.483+926_483+927del others(2): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr17 | 38464290 | ||||||
| chr17:38464354 | C | T | 1 | a0001c0002t0002g0241 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.483+972C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38464354 | |||||||
| chr17:38464355 | G | A | 1 | a0002c0023t0001g0236 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.483+973G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38464355 | |||||||
| chr17:38464384 | C | T | 1 | a0001c0012t0003g0051 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.483+1002C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38464384 | |||||||
| chr17:38464424 | T | G | 7 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0001g0056 others(4): Show |
7 | HG01891.hp1 HG02647.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.483+1042T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38464424 | |||||||
| chr17:38464526 | T | G | 1 | a0013c0047t0001g0018 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.483+1144T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38464526 | |||||||
| chr17:38464592 | G | C | 2 | a0001c0001t0001g0100 a0001c0003t0001g0101 |
2 | HG03492.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.483+1210G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38464592 | |||||||
| chr17:38464593 | G | C | 1 | a0005c0041t0001g0032 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.483+1211G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38464593 | |||||||
| chr17:38464652 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.483+1270C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38464652 | |||||||
| chr17:38464679 | C | G | 274 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(271): Show |
279 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.483+1297C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38464679 | |||||||
| chr17:38464922 | A | G | 1 | a0001c0001t0001g0205 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.484-1245A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38464922 | |||||||
| chr17:38464927 | C | T | 1 | a0001c0048t0002g0113 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.484-1240C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38464927 | |||||||
| chr17:38464933 | G | A | 3 | a0001c0001t0001g0288 a0001c0003t0001g0289 a0001c0052t0001g0287 |
3 | NA18960.hp1 NA18979.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.484-1234G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38464933 | |||||||
| chr17:38464970 | C | A | 5 | a0001c0016t0003g0047 a0001c0016t0003g0297 a0001c0037t0003g0139 others(2): Show |
5 | HG02886.hp2 HG03139.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.484-1197C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38464970 | |||||||
| chr17:38464986 | C | T | 1 | a0001c0003t0001g0101 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.484-1181C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38464986 | |||||||
| chr17:38465034 | G | A | 1 | a0001c0037t0003g0139 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.484-1133G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38465034 | |||||||
| chr17:38465080 | C | G | 266 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(263): Show |
271 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.484-1087C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38465080 | |||||||
| chr17:38465165 | G | A | 2 | a0001c0001t0001g0100 a0001c0003t0001g0101 |
2 | HG03492.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.484-1002G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38465165 | |||||||
| chr17:38465204 | T | C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(95): Show |
103 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.484-963T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38465204 | |||||||
| chr17:38465271 | C | CCTGGGAC others(21): Show |
24 | a0001c0005t0001g0033 a0001c0005t0001g0036 a0001c0005t0001g0037 others(21): Show |
24 | HG00733.hp1 HG01884.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.484-895_484-868dup others(28): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr17 | 38465271 | ||||||
| chr17:38465315 | C | T | 274 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(271): Show |
279 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.484-852C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38465315 | |||||||
| chr17:38465318 | CTG | C | 45 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0001g0056 others(42): Show |
45 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.484-835_484-834del others(2): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr17 | 38465318 | ||||||
| chr17:38465339 | G | T | 1 | a0001c0003t0001g0101 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.484-828G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38465339 | |||||||
| chr17:38465363 | T | C | 274 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(271): Show |
279 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.484-804T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38465363 | |||||||
| chr17:38465685 | C | T | 2 | a0001c0001t0001g0079 a0001c0003t0001g0065 |
2 | HG01109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.484-482C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38465685 | |||||||
| chr17:38465794 | C | T | 6 | a0001c0016t0003g0047 a0001c0016t0003g0297 a0001c0031t0003g0067 others(3): Show |
6 | HG02723.hp2 HG02886.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.484-373C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38465794 | |||||||
| chr17:38465897 | T | G | 1 | a0001c0001t0001g0233 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.484-270T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38465897 | |||||||
| chr17:38465932 | A | G | 45 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0001g0056 others(42): Show |
45 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.484-235A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38465932 | |||||||
| chr17:38465950 | A | G | 1 | a0001c0001t0001g0247 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.484-217A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 6/23 | chr17 | 38465950 | |||||||
| chr17:38467361 | G | A | 274 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(271): Show |
279 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.1648+30G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | chr17 | 38467361 | |||||||
| chr17:38467393 | G | A | 2 | a0003c0028t0001g0299 a0004c0055t0004g0298 |
2 | HG02486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1648+62G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | chr17 | 38467393 | |||||||
| chr17:38467497 | G | A | 2 | a0007c0021t0003g0070 a0007c0021t0003g0072 |
2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1648+166G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | chr17 | 38467497 | |||||||
| chr17:38467557 | T | C | 3 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0001c0002t0002g0092 |
3 | NA18943.hp1 NA18980.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1648+226T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | chr17 | 38467557 | |||||||
| chr17:38467557 | T | TTATCCTT others(3): Show |
1 | a0001c0001t0001g0009 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1648+227_1648+236d others(12): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr17 | 38467557 | ||||||
| chr17:38467579 | C | T | 274 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(271): Show |
279 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.1648+248C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | chr17 | 38467579 | |||||||
| chr17:38467648 | C | T | 1 | a0001c0010t0001g0168 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1648+317C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | chr17 | 38467648 | |||||||
| chr17:38467758 | A | C | 1 | a0006c0050t0003g0138 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1648+427A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | chr17 | 38467758 | |||||||
| chr17:38467856 | T | C | 7 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0001g0056 others(4): Show |
7 | HG01891.hp1 HG02647.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.1648+525T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | chr17 | 38467856 | |||||||
| chr17:38468010 | G | T | 4 | a0001c0011t0006g0073 a0001c0011t0006g0076 a0003c0014t0001g0074 others(1): Show |
4 | HG01884.hp2 HG02258.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1648+679G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | chr17 | 38468010 | |||||||
| chr17:38468033 | C | A | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.1648+702C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | chr17 | 38468033 | |||||||
| chr17:38468249 | C | A | 2 | a0007c0021t0003g0070 a0007c0021t0003g0072 |
2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1649-895C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | chr17 | 38468249 | |||||||
| chr17:38468254 | G | A | 1 | a0004c0019t0004g0063 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1649-890G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | chr17 | 38468254 | |||||||
| chr17:38468355 | G | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(96): Show |
104 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1649-789G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | chr17 | 38468355 | |||||||
| chr17:38468367 | A | G | 2 | a0007c0021t0003g0070 a0007c0021t0003g0072 |
2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1649-777A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | chr17 | 38468367 | |||||||
| chr17:38468383 | TGA | T | 7 | a0001c0011t0001g0069 a0001c0011t0006g0073 a0001c0011t0006g0076 others(4): Show |
7 | HG01358.hp1 HG01884.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1649-757_1649-756d others(4): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr17 | 38468383 | ||||||
| chr17:38468587 | G | A | 2 | a0001c0005t0001g0038 a0017c0034t0001g0039 |
2 | HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1649-557G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | chr17 | 38468587 | |||||||
| chr17:38468614 | C | T | 1 | a0001c0001t0001g0008 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1649-530C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | chr17 | 38468614 | |||||||
| chr17:38468669 | A | G | 162 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0019 others(159): Show |
162 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.1649-475A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | chr17 | 38468669 | |||||||
| chr17:38469110 | C | T | 2 | a0007c0021t0003g0070 a0007c0021t0003g0072 |
2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1649-34C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | chr17 | 38469110 | |||||||
| chr17:38469505 | G | A | 7 | a0001c0004t0001g0071 a0001c0004t0001g0170 a0001c0004t0001g0171 others(4): Show |
7 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.1805-19G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 8/23 | chr17 | 38469505 | |||||||
| chr17:38469678 | C | A | 1 | a0001c0001t0001g0271 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1916+43C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 9/23 | chr17 | 38469678 | |||||||
| chr17:38469678 | C | T | 31 | a0001c0004t0001g0054 a0001c0004t0001g0055 a0001c0004t0001g0056 others(28): Show |
31 | HG00733.hp1 HG01884.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.1916+43C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 9/23 | chr17 | 38469678 | |||||||
| chr17:38469821 | C | T | 38 | a0001c0001t0001g0066 a0001c0004t0001g0054 a0001c0004t0001g0055 others(35): Show |
38 | HG00733.hp1 HG01243.hp2 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.1917-26C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 9/23 | chr17 | 38469821 | |||||||
| chr17:38469915 | C | A | 6 | a0001c0004t0001g0059 a0001c0004t0001g0062 a0004c0019t0004g0060 others(3): Show |
6 | HG01243.hp2 HG02145.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1974+11C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38469915 | |||||||
| chr17:38469998 | C | T | 1 | a0002c0035t0001g0234 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1974+94C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38469998 | |||||||
| chr17:38470057 | G | A | 1 | a0001c0011t0001g0069 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1974+153G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38470057 | |||||||
| chr17:38470066 | C | G | 1 | a0001c0001t0001g0264 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1974+162C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38470066 | |||||||
| chr17:38470201 | G | A | 1 | a0001c0043t0001g0178 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1974+297G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38470201 | |||||||
| chr17:38470352 | T | C | 2 | a0001c0001t0001g0231 a0001c0001t0001g0232 |
2 | HG00099.hp2 HG00280.hp1 |
intron_variant | MODIFIER | c.1974+448T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38470352 | |||||||
| chr17:38470605 | T | C | 2 | a0001c0001t0008g0256 a0001c0007t0003g0020 |
2 | HG01261.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1974+701T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38470605 | |||||||
| chr17:38470622 | C | T | 3 | a0001c0001t0001g0095 a0001c0003t0001g0107 a0001c0003t0001g0191 |
3 | NA18959.hp2 NA18999.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.1974+718C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38470622 | |||||||
| chr17:38470627 | C | T | 128 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(125): Show |
128 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.1974+723C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38470627 | |||||||
| chr17:38470682 | G | A | 1 | a0001c0042t0001g0257 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1974+778G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38470682 | |||||||
| chr17:38470725 | C | G | 4 | a0001c0007t0003g0053 a0003c0014t0001g0068 a0003c0028t0001g0299 others(1): Show |
4 | HG02486.hp1 HG02896.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1974+821C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38470725 | |||||||
| chr17:38470775 | G | C | 1 | a0001c0003t0001g0206 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1974+871G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38470775 | |||||||
| chr17:38470807 | G | A | 5 | a0001c0011t0001g0069 a0001c0011t0006g0073 a0001c0011t0006g0076 others(2): Show |
5 | HG01884.hp2 HG02258.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1974+903G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38470807 | |||||||
| chr17:38470826 | C | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(79): Show |
87 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.1974+922C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38470826 | |||||||
| chr17:38470895 | G | A | 134 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(131): Show |
134 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.1975-968G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38470895 | |||||||
| chr17:38470928 | C | T | 135 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(132): Show |
135 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.1975-935C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38470928 | |||||||
| chr17:38470941 | T | A | 7 | a0001c0004t0001g0071 a0001c0004t0001g0170 a0001c0004t0001g0171 others(4): Show |
7 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.1975-922T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38470941 | |||||||
| chr17:38470957 | C | CTT | 8 | a0001c0001t0001g0165 a0001c0004t0001g0054 a0001c0004t0001g0055 others(5): Show |
8 | HG01891.hp1 HG02572.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1975-894_1975-893d others(4): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr17 | 38470957 | ||||||
| chr17:38470972 | A | C | 4 | a0001c0004t0001g0059 a0001c0004t0001g0062 a0004c0019t0004g0060 others(1): Show |
4 | HG01243.hp2 HG02970.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1975-891A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38470972 | |||||||
| chr17:38471016 | G | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(111): Show |
119 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.1975-847G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38471016 | |||||||
| chr17:38471099 | T | C | 1 | a0002c0035t0001g0234 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1975-764T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38471099 | |||||||
| chr17:38471221 | G | A | 5 | a0001c0001t0001g0187 a0001c0001t0001g0222 a0001c0001t0001g0231 others(2): Show |
5 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(2): Show |
intron_variant | MODIFIER | c.1975-642G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38471221 | |||||||
| chr17:38471533 | C | T | 1 | a0001c0004t0001g0062 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1975-330C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38471533 | |||||||
| chr17:38471681 | C | T | 7 | a0001c0004t0001g0059 a0001c0007t0003g0053 a0003c0014t0001g0068 others(4): Show |
7 | HG02145.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1975-182C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38471681 | |||||||
| chr17:38471750 | G | A | 1 | a0001c0003t0001g0065 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1975-113G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 10/23 | chr17 | 38471750 | |||||||
| chr17:38472186 | G | T | 1 | a0001c0004t0001g0059 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2118+180G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38472186 | |||||||
| chr17:38472236 | G | A | 134 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(131): Show |
134 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.2118+230G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38472236 | |||||||
| chr17:38472429 | C | CGGGGGCT others(45): Show |
2 | a0001c0007t0003g0053 a0004c0055t0004g0298 |
2 | HG02486.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2118+426_2118+477d others(54): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr17 | 38472429 | ||||||
| chr17:38472643 | A | G | 2 | a0001c0003t0001g0111 a0001c0007t0003g0112 |
2 | HG00544.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.2118+637A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38472643 | |||||||
| chr17:38472958 | A | G | 2 | a0001c0001t0001g0203 a0001c0001t0001g0205 |
2 | HG00140.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.2118+952A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38472958 | |||||||
| chr17:38472999 | C | T | 49 | a0001c0001t0001g0005 a0001c0001t0001g0077 a0001c0001t0001g0081 others(46): Show |
49 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.2118+993C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38472999 | |||||||
| chr17:38473090 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2118+1084C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38473090 | |||||||
| chr17:38473103 | A | AT | 10 | a0001c0001t0001g0095 a0001c0001t0001g0268 a0001c0002t0002g0015 others(7): Show |
10 | HG00323.hp2 HG00735.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.2118+1117dupT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr17 | 38473103 | ||||||
| chr17:38473103 | AT | A | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(108): Show |
116 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.2118+1117delT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr17 | 38473103 | ||||||
| chr17:38473103 | ATT | A | 18 | a0001c0001t0001g0084 a0001c0001t0001g0152 a0001c0004t0001g0055 others(15): Show |
18 | HG01070.hp1 HG01071.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.2118+1116_2118+111 others(6): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr17 | 38473103 | ||||||
| chr17:38473347 | C | G | 6 | a0001c0001t0001g0156 a0001c0007t0013g0148 a0001c0012t0003g0045 others(3): Show |
6 | HG02145.hp2 HG02647.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2118+1341C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38473347 | |||||||
| chr17:38473371 | G | T | 1 | a0001c0001t0001g0152 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2118+1365G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38473371 | |||||||
| chr17:38473400 | T | C | 1 | a0001c0003t0001g0107 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2118+1394T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38473400 | |||||||
| chr17:38473424 | G | A | 2 | a0001c0001t0001g0149 a0001c0001t0001g0153 |
2 | HG02965.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2118+1418G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38473424 | |||||||
| chr17:38473487 | G | A | 4 | a0001c0004t0006g0010 a0001c0010t0001g0169 a0001c0020t0005g0143 others(1): Show |
4 | HG01074.hp2 HG02818.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2118+1481G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38473487 | |||||||
| chr17:38473523 | G | T | 2 | a0001c0002t0002g0157 a0001c0004t0001g0031 |
2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2118+1517G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38473523 | |||||||
| chr17:38473567 | A | G | 1 | a0001c0001t0001g0291 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2118+1561A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38473567 | |||||||
| chr17:38473582 | G | A | 1 | a0001c0048t0002g0113 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2118+1576G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38473582 | |||||||
| chr17:38473649 | C | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0034 others(118): Show |
123 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.2118+1643C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38473649 | |||||||
| chr17:38473778 | A | G | 27 | a0001c0001t0001g0025 a0001c0001t0001g0120 a0001c0001t0001g0134 others(24): Show |
27 | HG01099.hp2 HG01175.hp1 HG01361.hp2 others(24): Show |
intron_variant | MODIFIER | c.2118+1772A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38473778 | |||||||
| chr17:38474030 | T | C | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(255): Show |
263 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.2118+2024T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38474030 | |||||||
| chr17:38474161 | G | T | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(220): Show |
228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.2118+2155G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38474161 | |||||||
| chr17:38474200 | C | T | 1 | a0001c0007t0003g0053 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2118+2194C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38474200 | |||||||
| chr17:38474211 | G | A | 65 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(62): Show |
67 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.2118+2205G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38474211 | |||||||
| chr17:38474266 | G | A | 1 | a0001c0001t0014g0270 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2118+2260G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38474266 | |||||||
| chr17:38474270 | T | C | 25 | a0001c0001t0001g0114 a0001c0001t0001g0117 a0001c0001t0001g0121 others(22): Show |
25 | HG00735.hp1 HG01169.hp1 HG01433.hp1 others(22): Show |
intron_variant | MODIFIER | c.2118+2264T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38474270 | |||||||
| chr17:38474328 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2118+2322C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38474328 | |||||||
| chr17:38474353 | G | T | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(235): Show |
243 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.2118+2347G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38474353 | |||||||
| chr17:38474356 | G | A | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(235): Show |
243 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.2118+2350G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38474356 | |||||||
| chr17:38474471 | G | T | 4 | a0001c0001t0001g0058 a0001c0001t0001g0156 a0001c0001t0011g0064 others(1): Show |
4 | HG02451.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2118+2465G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38474471 | |||||||
| chr17:38474599 | A | T | 2 | a0001c0003t0001g0065 a0001c0007t0013g0148 |
2 | HG01109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2118+2593A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38474599 | |||||||
| chr17:38474656 | C | A | 7 | a0001c0001t0001g0217 a0001c0001t0001g0242 a0001c0001t0001g0243 others(4): Show |
7 | HG01106.hp2 HG01167.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.2118+2650C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38474656 | |||||||
| chr17:38474674 | T | A | 58 | a0001c0001t0001g0008 a0001c0001t0001g0066 a0001c0001t0001g0120 others(55): Show |
58 | HG00639.hp2 HG00733.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.2118+2668T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38474674 | |||||||
| chr17:38474757 | T | TG | 117 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0025 others(114): Show |
119 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.2118+2758dupG | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr17 | 38474757 | ||||||
| chr17:38475077 | T | G | 1 | a0001c0003t0001g0082 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2119-2502T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38475077 | |||||||
| chr17:38475286 | C | T | 1 | a0001c0042t0001g0257 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2119-2293C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38475286 | |||||||
| chr17:38475321 | G | T | 2 | a0001c0031t0003g0067 a0006c0050t0003g0138 |
2 | HG02109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2119-2258G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38475321 | |||||||
| chr17:38475730 | T | G | 7 | a0001c0011t0006g0073 a0001c0011t0006g0076 a0003c0014t0001g0068 others(4): Show |
7 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2119-1849T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38475730 | |||||||
| chr17:38475737 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2119-1842G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38475737 | |||||||
| chr17:38475933 | G | A | 1 | a0006c0049t0001g0262 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2119-1646G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38475933 | |||||||
| chr17:38475987 | C | T | 1 | a0001c0001t0001g0091 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2119-1592C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38475987 | |||||||
| chr17:38476229 | G | A | 1 | a0003c0028t0001g0017 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2119-1350G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38476229 | |||||||
| chr17:38476258 | C | A | 6 | a0001c0003t0001g0111 a0001c0024t0001g0098 a0001c0024t0001g0105 others(3): Show |
6 | HG02040.hp1 HG02071.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.2119-1321C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38476258 | |||||||
| chr17:38476282 | C | T | 29 | a0001c0001t0001g0114 a0001c0001t0001g0117 a0001c0001t0001g0121 others(26): Show |
29 | HG00735.hp1 HG01169.hp1 HG01433.hp1 others(26): Show |
intron_variant | MODIFIER | c.2119-1297C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38476282 | |||||||
| chr17:38476283 | G | A | 1 | a0001c0032t0001g0201 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2119-1296G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38476283 | |||||||
| chr17:38476568 | C | T | 1 | a0008c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2119-1011C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38476568 | |||||||
| chr17:38476569 | T | G | 1 | a0008c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2119-1010T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38476569 | |||||||
| chr17:38476588 | G | A | 1 | a0004c0017t0004g0140 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2119-991G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38476588 | |||||||
| chr17:38476610 | A | G | 1 | a0004c0055t0004g0298 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2119-969A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38476610 | |||||||
| chr17:38476791 | T | TTGTGCAA | 3 | a0001c0004t0001g0054 a0001c0004t0001g0061 a0001c0009t0003g0161 |
3 | HG01891.hp1 HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2119-784_2119-778d others(9): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr17 | 38476791 | ||||||
| chr17:38476808 | G | A | 1 | a0001c0005t0001g0040 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2119-771G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38476808 | |||||||
| chr17:38476869 | T | G | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(127): Show |
133 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.2119-710T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38476869 | |||||||
| chr17:38477146 | A | G | 1 | a0001c0001t0011g0064 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2119-433A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38477146 | |||||||
| chr17:38477172 | G | A | 1 | a0001c0003t0001g0115 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2119-407G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38477172 | |||||||
| chr17:38477268 | G | A | 2 | a0001c0004t0001g0054 a0001c0004t0001g0061 |
2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2119-311G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38477268 | |||||||
| chr17:38477365 | G | C | 1 | a0001c0007t0003g0053 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2119-214G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38477365 | |||||||
| chr17:38477445 | G | A | 1 | a0001c0004t0001g0283 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2119-134G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | chr17 | 38477445 | |||||||
| chr17:38477972 | C | A | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(74): Show |
80 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.2436+76C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38477972 | |||||||
| chr17:38478042 | A | T | 102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(99): Show |
105 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.2436+146A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38478042 | |||||||
| chr17:38478092 | C | T | 1 | a0001c0051t0003g0267 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2436+196C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38478092 | |||||||
| chr17:38478103 | G | A | 1 | a0001c0001t0011g0064 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2436+207G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38478103 | |||||||
| chr17:38478108 | G | T | 8 | a0001c0001t0001g0120 a0001c0001t0001g0134 a0001c0001t0001g0135 others(5): Show |
8 | HG00642.hp1 HG01175.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.2436+212G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38478108 | |||||||
| chr17:38478233 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2436+337G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38478233 | |||||||
| chr17:38478399 | G | A | 7 | a0001c0005t0001g0033 a0001c0005t0001g0037 a0001c0005t0001g0040 others(4): Show |
7 | HG02055.hp2 HG02886.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.2436+503G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38478399 | |||||||
| chr17:38478417 | A | AT | 97 | a0001c0001t0001g0008 a0001c0001t0001g0058 a0001c0001t0001g0066 others(94): Show |
97 | HG00642.hp1 HG00733.hp1 HG00733.hp2 others(94): Show |
intron_variant | MODIFIER | c.2436+536dupT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr17 | 38478417 | ||||||
| chr17:38478417 | A | ATT | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.2436+535_2436+536d others(4): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr17 | 38478417 | ||||||
| chr17:38478460 | G | A | 75 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(72): Show |
78 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.2436+564G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38478460 | |||||||
| chr17:38478700 | T | C | 103 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(100): Show |
106 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.2437-736T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38478700 | |||||||
| chr17:38478800 | C | G | 3 | a0001c0002t0002g0166 a0002c0023t0001g0180 a0008c0029t0001g0285 |
3 | HG02155.hp2 NA18940.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.2437-636C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38478800 | |||||||
| chr17:38478826 | G | T | 1 | a0008c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2437-610G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38478826 | |||||||
| chr17:38478830 | C | T | 1 | a0008c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2437-606C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38478830 | |||||||
| chr17:38478831 | C | A | 1 | a0008c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2437-605C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38478831 | |||||||
| chr17:38478832 | C | G | 1 | a0008c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2437-604C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38478832 | |||||||
| chr17:38478833 | A | T | 1 | a0008c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2437-603A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38478833 | |||||||
| chr17:38478834 | C | G | 1 | a0008c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2437-602C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38478834 | |||||||
| chr17:38478836 | C | G | 1 | a0008c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2437-600C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38478836 | |||||||
| chr17:38478837 | A | T | 1 | a0008c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2437-599A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38478837 | |||||||
| chr17:38478838 | A | T | 1 | a0008c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2437-598A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38478838 | |||||||
| chr17:38479043 | C | G | 25 | a0001c0001t0001g0114 a0001c0001t0001g0117 a0001c0001t0001g0121 others(22): Show |
25 | HG00735.hp1 HG01169.hp1 HG01433.hp1 others(22): Show |
intron_variant | MODIFIER | c.2437-393C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38479043 | |||||||
| chr17:38479044 | T | G | 103 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(100): Show |
106 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.2437-392T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38479044 | |||||||
| chr17:38479283 | G | A | 1 | a0001c0012t0003g0045 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2437-153G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38479283 | |||||||
| chr17:38479307 | C | G | 2 | a0001c0001t0001g0100 a0012c0039t0001g0186 |
2 | HG01255.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2437-129C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38479307 | |||||||
| chr17:38479407 | A | G | 3 | a0001c0010t0001g0016 a0001c0011t0001g0069 a0001c0012t0003g0051 |
3 | HG03209.hp2 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2437-29A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 12/23 | chr17 | 38479407 | |||||||
| chr17:38479559 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2498+62G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 13/23 | chr17 | 38479559 | |||||||
| chr17:38479583 | G | C | 1 | a0001c0001t0001g0089 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2498+86G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 13/23 | chr17 | 38479583 | |||||||
| chr17:38479732 | C | A | 1 | a0008c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2499-21C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 13/23 | chr17 | 38479732 | |||||||
| chr17:38479734 | C | A | 1 | a0008c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2499-19C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 13/23 | chr17 | 38479734 | |||||||
| chr17:38479736 | C | A | 1 | a0008c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2499-17C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 13/23 | chr17 | 38479736 | |||||||
| chr17:38479737 | C | T | 1 | a0008c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2499-16C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 13/23 | chr17 | 38479737 | |||||||
| chr17:38479738 | C | A | 1 | a0008c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2499-15C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 13/23 | chr17 | 38479738 | |||||||
| chr17:38479739 | T | G | 1 | a0008c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2499-14T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 13/23 | chr17 | 38479739 | |||||||
| chr17:38479742 | T | G | 1 | a0008c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2499-11T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 13/23 | chr17 | 38479742 | |||||||
| chr17:38479743 | T | C | 1 | a0001c0002t0002g0118 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2499-10T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 13/23 | chr17 | 38479743 | |||||||
| chr17:38479744 | C | T | 1 | a0008c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2499-9C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 13/23 | chr17 | 38479744 | |||||||
| chr17:38479943 | G | A | 1 | a0013c0047t0001g0018 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2629+60G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38479943 | |||||||
| chr17:38479952 | T | A | 1 | a0001c0001t0001g0208 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2629+69T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38479952 | |||||||
| chr17:38480034 | G | T | 1 | a0006c0049t0001g0262 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2629+151G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480034 | |||||||
| chr17:38480077 | G | A | 8 | a0001c0001t0001g0120 a0001c0001t0001g0134 a0001c0001t0001g0135 others(5): Show |
8 | HG00642.hp1 HG01175.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.2629+194G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480077 | |||||||
| chr17:38480086 | T | G | 4 | a0001c0001t0001g0058 a0001c0001t0001g0156 a0004c0055t0004g0298 others(1): Show |
4 | HG02451.hp1 HG02486.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2629+203T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480086 | |||||||
| chr17:38480255 | C | T | 72 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(69): Show |
75 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.2629+372C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480255 | |||||||
| chr17:38480322 | T | C | 74 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(71): Show |
77 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.2629+439T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480322 | |||||||
| chr17:38480399 | C | T | 1 | a0001c0004t0001g0194 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2629+516C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480399 | |||||||
| chr17:38480589 | G | A | 4 | a0001c0001t0001g0058 a0001c0001t0001g0156 a0001c0001t0011g0064 others(1): Show |
4 | HG02451.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2629+706G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480589 | |||||||
| chr17:38480678 | C | T | 1 | a0001c0002t0002g0122 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2629+795C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480678 | |||||||
| chr17:38480803 | C | CA | 22 | a0001c0001t0001g0089 a0001c0001t0001g0121 a0001c0001t0001g0208 others(19): Show |
22 | HG00438.hp2 HG00609.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.2629+941dupA | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr17 | 38480803 | ||||||
| chr17:38480826 | AAAG | A | 3 | a0001c0001t0001g0058 a0001c0001t0001g0156 a0001c0001t0011g0064 |
3 | HG02451.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2629+946_2629+948d others(5): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr17 | 38480826 | ||||||
| chr17:38480828 | A | G | 1 | a0005c0041t0001g0032 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2629+945A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480828 | |||||||
| chr17:38480829 | G | A | 1 | a0005c0041t0001g0032 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2629+946G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480829 | |||||||
| chr17:38480897 | C | CTGTCCCA others(3): Show |
1 | a0001c0001t0001g0095 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2629+1016_2629+101 others(14): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr17 | 38480897 | ||||||
| chr17:38480901 | G | T | 1 | a0001c0001t0001g0095 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2629+1018G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480901 | |||||||
| chr17:38480914 | C | A | 1 | a0001c0001t0001g0095 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2629+1031C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480914 | |||||||
| chr17:38480916 | T | A | 1 | a0001c0001t0001g0095 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2629+1033T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480916 | |||||||
| chr17:38480930 | T | G | 1 | a0001c0001t0001g0095 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2629+1047T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480930 | |||||||
| chr17:38480931 | G | C | 1 | a0001c0001t0001g0095 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2629+1048G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480931 | |||||||
| chr17:38480934 | A | C | 1 | a0001c0001t0001g0095 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2629+1051A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480934 | |||||||
| chr17:38480941 | T | A | 1 | a0001c0001t0001g0095 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2629+1058T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480941 | |||||||
| chr17:38480950 | T | C | 1 | a0001c0001t0001g0095 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2629+1067T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480950 | |||||||
| chr17:38480951 | A | T | 1 | a0001c0001t0001g0095 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2629+1068A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480951 | |||||||
| chr17:38480953 | A | C | 1 | a0001c0001t0001g0095 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1069A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480953 | |||||||
| chr17:38480958 | T | G | 1 | a0001c0001t0001g0095 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1064T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480958 | |||||||
| chr17:38480961 | T | C | 1 | a0001c0001t0001g0095 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1061T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480961 | |||||||
| chr17:38480963 | T | A | 1 | a0001c0001t0001g0095 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1059T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480963 | |||||||
| chr17:38480964 | C | A | 1 | a0008c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2630-1058C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480964 | |||||||
| chr17:38480964 | C | G | 1 | a0001c0001t0001g0095 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1058C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480964 | |||||||
| chr17:38480965 | C | G | 1 | a0001c0001t0001g0095 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1057C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480965 | |||||||
| chr17:38480966 | C | A | 1 | a0008c0029t0001g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2630-1056C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480966 | |||||||
| chr17:38480966 | C | G | 1 | a0001c0001t0001g0095 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1056C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480966 | |||||||
| chr17:38480967 | T | A | 1 | a0001c0001t0001g0095 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1055T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480967 | |||||||
| chr17:38480972 | A | C | 1 | a0001c0001t0001g0095 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1050A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480972 | |||||||
| chr17:38480973 | A | T | 1 | a0001c0001t0001g0095 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1049A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480973 | |||||||
| chr17:38480975 | A | T | 1 | a0001c0001t0001g0095 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1047A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480975 | |||||||
| chr17:38480976 | T | C | 1 | a0001c0001t0001g0095 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1046T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480976 | |||||||
| chr17:38480980 | T | C | 1 | a0001c0001t0001g0095 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1042T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480980 | |||||||
| chr17:38480984 | A | T | 1 | a0001c0001t0001g0095 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1038A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480984 | |||||||
| chr17:38480986 | A | T | 1 | a0001c0001t0001g0095 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1036A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480986 | |||||||
| chr17:38480988 | A | T | 1 | a0001c0001t0001g0095 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1034A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480988 | |||||||
| chr17:38480991 | A | T | 1 | a0001c0001t0001g0095 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1031A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480991 | |||||||
| chr17:38480995 | A | T | 1 | a0001c0001t0001g0095 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1027A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480995 | |||||||
| chr17:38480999 | A | T | 1 | a0001c0001t0001g0095 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1023A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38480999 | |||||||
| chr17:38481011 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1011A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38481011 | |||||||
| chr17:38481018 | T | C | 1 | a0001c0001t0001g0095 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-1004T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38481018 | |||||||
| chr17:38481035 | G | C | 1 | a0001c0001t0001g0095 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2630-987G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38481035 | |||||||
| chr17:38481154 | T | A | 1 | a0001c0003t0001g0014 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2630-868T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38481154 | |||||||
| chr17:38481307 | T | C | 1 | a0001c0001t0001g0290 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2630-715T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38481307 | |||||||
| chr17:38481310 | C | G | 1 | a0001c0001t0001g0290 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2630-712C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38481310 | |||||||
| chr17:38481313 | A | C | 1 | a0001c0001t0001g0290 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2630-709A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38481313 | |||||||
| chr17:38481318 | T | A | 1 | a0001c0001t0001g0290 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2630-704T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38481318 | |||||||
| chr17:38481442 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2630-580C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38481442 | |||||||
| chr17:38481446 | C | T | 1 | a0001c0002t0002g0123 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2630-576C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38481446 | |||||||
| chr17:38481450 | G | A | 4 | a0001c0001t0001g0058 a0001c0001t0001g0156 a0001c0001t0011g0064 others(1): Show |
4 | HG02451.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2630-572G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38481450 | |||||||
| chr17:38481600 | T | A | 2 | a0001c0001t0001g0008 a0001c0002t0002g0254 |
2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2630-422T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38481600 | |||||||
| chr17:38481747 | T | C | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(240): Show |
248 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.2630-275T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38481747 | |||||||
| chr17:38481881 | A | T | 1 | a0001c0002t0002g0118 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2630-141A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38481881 | |||||||
| chr17:38481905 | C | CAGAT | 75 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(72): Show |
78 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.2630-116_2630-115i others(6): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr17 | 38481905 | ||||||
| chr17:38481907 | T | C | 1 | a0001c0001t0001g0006 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2630-115T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38481907 | |||||||
| chr17:38481937 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2630-85C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38481937 | |||||||
| chr17:38481938 | G | A | 75 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(72): Show |
78 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.2630-84G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38481938 | |||||||
| chr17:38482014 | C | T | 109 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0025 others(106): Show |
111 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(108): Show |
splice_region_variant&intron_variant | LOW | c.2630-8C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | chr17 | 38482014 | |||||||
| chr17:38482147 | A | G | 75 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(72): Show |
78 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(75): Show |
splice_region_variant&intron_variant | LOW | c.2751+4A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 15/23 | chr17 | 38482147 | |||||||
| chr17:38482303 | C | T | 75 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(72): Show |
78 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.2751+160C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 15/23 | chr17 | 38482303 | |||||||
| chr17:38482454 | G | T | 75 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(72): Show |
78 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.2752-69G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 15/23 | chr17 | 38482454 | |||||||
| chr17:38482707 | A | G | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(265): Show |
273 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.2907+29A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | chr17 | 38482707 | |||||||
| chr17:38483039 | C | T | 1 | a0001c0001t0011g0064 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2907+361C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | chr17 | 38483039 | |||||||
| chr17:38483040 | G | A | 4 | a0001c0031t0003g0067 a0006c0050t0003g0138 a0007c0021t0003g0070 others(1): Show |
4 | HG02109.hp1 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.2907+362G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | chr17 | 38483040 | |||||||
| chr17:38483170 | G | A | 25 | a0001c0001t0001g0114 a0001c0001t0001g0117 a0001c0001t0001g0121 others(22): Show |
25 | HG00735.hp1 HG01169.hp1 HG01433.hp1 others(22): Show |
intron_variant | MODIFIER | c.2907+492G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | chr17 | 38483170 | |||||||
| chr17:38483212 | G | A | 2 | a0001c0001t0001g0079 a0013c0047t0001g0018 |
2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2907+534G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | chr17 | 38483212 | |||||||
| chr17:38483403 | C | T | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(73): Show |
79 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.2907+725C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | chr17 | 38483403 | |||||||
| chr17:38483696 | T | C | 113 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0025 others(110): Show |
115 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.2907+1018T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | chr17 | 38483696 | |||||||
| chr17:38483799 | T | C | 1 | a0001c0016t0003g0297 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2907+1121T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | chr17 | 38483799 | |||||||
| chr17:38484158 | C | T | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(73): Show |
79 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.2907+1480C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | chr17 | 38484158 | |||||||
| chr17:38484230 | A | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0025 others(84): Show |
89 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.2907+1552A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | chr17 | 38484230 | |||||||
| chr17:38484348 | C | T | 1 | a0001c0003t0001g0023 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2907+1670C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | chr17 | 38484348 | |||||||
| chr17:38484367 | A | G | 1 | a0001c0011t0001g0069 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2907+1689A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | chr17 | 38484367 | |||||||
| chr17:38484493 | C | T | 1 | a0001c0002t0002g0118 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2908-1569C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | chr17 | 38484493 | |||||||
| chr17:38484601 | AGGGCATT others(1): Show |
A | 17 | a0001c0001t0001g0114 a0001c0001t0001g0117 a0001c0001t0001g0121 others(14): Show |
17 | HG00735.hp1 HG01169.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.2908-1458_2908-145 others(12): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr17 | 38484601 | ||||||
| chr17:38484618 | A | G | 5 | a0001c0001t0001g0077 a0001c0001t0001g0261 a0001c0001t0001g0264 others(2): Show |
5 | HG00558.hp2 NA18960.hp2 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.2908-1444A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | chr17 | 38484618 | |||||||
| chr17:38484767 | T | C | 9 | a0001c0001t0001g0120 a0001c0001t0001g0134 a0001c0001t0001g0135 others(6): Show |
9 | HG00642.hp1 HG01175.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.2908-1295T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | chr17 | 38484767 | |||||||
| chr17:38484990 | T | C | 2 | a0001c0001t0001g0079 a0013c0047t0001g0018 |
2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2908-1072T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | chr17 | 38484990 | |||||||
| chr17:38485476 | C | T | 1 | a0001c0009t0003g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2908-586C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | chr17 | 38485476 | |||||||
| chr17:38485779 | A | G | 1 | a0012c0039t0001g0186 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2908-283A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | chr17 | 38485779 | |||||||
| chr17:38485847 | A | C | 1 | a0001c0004t0001g0059 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2908-215A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 16/23 | chr17 | 38485847 | |||||||
| chr17:38486232 | CT | C | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(255): Show |
263 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.2986+107delT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr17 | 38486232 | ||||||
| chr17:38486255 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2986+115T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38486255 | |||||||
| chr17:38486337 | C | G | 1 | a0001c0010t0001g0016 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2986+197C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38486337 | |||||||
| chr17:38486423 | G | T | 75 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(72): Show |
78 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.2986+283G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38486423 | |||||||
| chr17:38486452 | G | T | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(203): Show |
211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.2986+312G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38486452 | |||||||
| chr17:38486536 | C | CT | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0025 others(85): Show |
90 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.2986+416dupT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr17 | 38486536 | ||||||
| chr17:38486536 | C | CTT | 10 | a0001c0001t0001g0081 a0001c0001t0001g0104 a0001c0001t0001g0127 others(7): Show |
10 | HG00323.hp2 HG00642.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.2986+415_2986+416d others(4): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr17 | 38486536 | ||||||
| chr17:38486536 | CT | C | 84 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(81): Show |
87 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.2986+416delT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr17 | 38486536 | ||||||
| chr17:38486556 | T | A | 2 | a0001c0001t0001g0203 a0001c0001t0001g0205 |
2 | HG00140.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.2986+416T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38486556 | |||||||
| chr17:38486662 | A | G | 1 | a0004c0055t0004g0298 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2986+522A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38486662 | |||||||
| chr17:38486834 | C | T | 29 | a0001c0001t0001g0114 a0001c0001t0001g0117 a0001c0001t0001g0121 others(26): Show |
29 | HG00735.hp1 HG01169.hp1 HG01433.hp1 others(26): Show |
intron_variant | MODIFIER | c.2986+694C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38486834 | |||||||
| chr17:38486898 | T | C | 8 | a0001c0001t0001g0058 a0001c0001t0001g0156 a0001c0001t0011g0064 others(5): Show |
8 | HG01081.hp1 HG02451.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.2986+758T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38486898 | |||||||
| chr17:38486987 | A | G | 1 | a0003c0028t0001g0017 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2986+847A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38486987 | |||||||
| chr17:38487130 | A | G | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(204): Show |
212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.2986+990A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38487130 | |||||||
| chr17:38487213 | G | A | 2 | a0001c0001t0001g0269 a0001c0004t0001g0059 |
2 | HG00642.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2986+1073G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38487213 | |||||||
| chr17:38487215 | G | A | 2 | a0001c0001t0001g0021 a0001c0003t0001g0022 |
2 | HG01081.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.2986+1075G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38487215 | |||||||
| chr17:38487222 | C | T | 2 | a0001c0001t0001g0021 a0001c0003t0001g0022 |
2 | HG01081.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.2986+1082C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38487222 | |||||||
| chr17:38487289 | A | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(171): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.2986+1149A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38487289 | |||||||
| chr17:38487431 | A | G | 1 | a0001c0005t0001g0036 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2986+1291A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38487431 | |||||||
| chr17:38487435 | C | T | 1 | a0001c0010t0001g0169 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2986+1295C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38487435 | |||||||
| chr17:38487470 | G | A | 2 | a0001c0001t0001g0165 a0001c0004t0006g0010 |
2 | HG02572.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2986+1330G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38487470 | |||||||
| chr17:38487495 | G | T | 1 | a0001c0001t0001g0081 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2986+1355G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38487495 | |||||||
| chr17:38487563 | A | G | 44 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0114 others(41): Show |
44 | HG00735.hp1 HG01081.hp2 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.2986+1423A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38487563 | |||||||
| chr17:38487693 | G | A | 8 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0003g0174 others(5): Show |
8 | HG01081.hp2 HG01346.hp2 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.2986+1553G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38487693 | |||||||
| chr17:38487728 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2986+1588G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38487728 | |||||||
| chr17:38487731 | G | GCAC | 3 | a0001c0001t0001g0120 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | HG01361.hp2 HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.2986+1592_2986+159 others(7): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr17 | 38487731 | ||||||
| chr17:38487756 | A | T | 4 | a0001c0001t0001g0058 a0001c0001t0001g0156 a0001c0001t0011g0064 others(1): Show |
4 | HG02451.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2986+1616A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38487756 | |||||||
| chr17:38487784 | A | C | 1 | a0001c0002t0002g0122 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2986+1644A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38487784 | |||||||
| chr17:38487904 | A | G | 1 | a0013c0047t0001g0018 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2986+1764A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38487904 | |||||||
| chr17:38488054 | A | G | 1 | a0013c0047t0001g0018 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2986+1914A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38488054 | |||||||
| chr17:38488079 | A | T | 67 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(64): Show |
70 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.2986+1939A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38488079 | |||||||
| chr17:38488080 | T | A | 2 | a0004c0019t0004g0060 a0004c0019t0004g0063 |
2 | HG01243.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2986+1940T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38488080 | |||||||
| chr17:38488155 | G | A | 6 | a0001c0001t0001g0079 a0001c0020t0005g0011 a0001c0020t0005g0143 others(3): Show |
6 | HG01081.hp1 HG01891.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2987-1947G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38488155 | |||||||
| chr17:38488199 | C | T | 1 | a0001c0010t0001g0169 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2987-1903C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38488199 | |||||||
| chr17:38488343 | A | G | 4 | a0001c0020t0005g0011 a0001c0020t0005g0143 a0001c0027t0005g0146 others(1): Show |
4 | HG01081.hp1 HG02922.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2987-1759A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38488343 | |||||||
| chr17:38488362 | G | A | 4 | a0001c0020t0005g0011 a0001c0020t0005g0143 a0001c0027t0005g0146 others(1): Show |
4 | HG01081.hp1 HG02922.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2987-1740G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38488362 | |||||||
| chr17:38488421 | C | T | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(204): Show |
212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.2987-1681C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38488421 | |||||||
| chr17:38488422 | G | A | 7 | a0001c0011t0006g0073 a0001c0011t0006g0076 a0003c0014t0001g0068 others(4): Show |
7 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2987-1680G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38488422 | |||||||
| chr17:38488533 | A | T | 4 | a0001c0020t0005g0011 a0001c0020t0005g0143 a0001c0027t0005g0146 others(1): Show |
4 | HG01081.hp1 HG02922.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2987-1569A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38488533 | |||||||
| chr17:38488548 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2987-1554T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38488548 | |||||||
| chr17:38489007 | C | G | 4 | a0001c0020t0005g0011 a0001c0020t0005g0143 a0001c0027t0005g0146 others(1): Show |
4 | HG01081.hp1 HG02922.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2987-1095C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38489007 | |||||||
| chr17:38489020 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2987-1082C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38489020 | |||||||
| chr17:38489055 | T | C | 2 | a0001c0001t0001g0165 a0001c0004t0006g0010 |
2 | HG02572.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2987-1047T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38489055 | |||||||
| chr17:38489181 | A | G | 1 | a0001c0003t0001g0082 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2987-921A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38489181 | |||||||
| chr17:38489425 | C | T | 8 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0003g0174 others(5): Show |
8 | HG01081.hp2 HG01346.hp2 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.2987-677C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38489425 | |||||||
| chr17:38489449 | A | G | 1 | a0001c0001t0011g0064 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2987-653A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38489449 | |||||||
| chr17:38489581 | C | T | 2 | a0001c0001t0001g0079 a0013c0047t0001g0018 |
2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2987-521C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38489581 | |||||||
| chr17:38489688 | A | G | 12 | a0001c0001t0001g0058 a0001c0001t0001g0079 a0001c0001t0001g0156 others(9): Show |
12 | HG01081.hp1 HG01891.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.2987-414A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38489688 | |||||||
| chr17:38489726 | G | C | 67 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(64): Show |
70 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.2987-376G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38489726 | |||||||
| chr17:38489807 | C | T | 2 | a0005c0033t0001g0075 a0005c0053t0001g0128 |
2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2987-295C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38489807 | |||||||
| chr17:38489915 | G | A | 1 | a0001c0018t0001g0046 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2987-187G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38489915 | |||||||
| chr17:38490020 | G | A | 2 | a0001c0004t0001g0170 a0001c0004t0001g0171 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2987-82G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38490020 | |||||||
| chr17:38490050 | A | G | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(202): Show |
210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.2987-52A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38490050 | |||||||
| chr17:38490084 | G | A | 2 | a0001c0009t0003g0172 a0001c0009t0003g0173 |
2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2987-18G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | chr17 | 38490084 | |||||||
| chr17:38490290 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.3060+115C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 18/23 | chr17 | 38490290 | |||||||
| chr17:38490367 | G | A | 1 | a0001c0001t0001g0281 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.3061-95G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 18/23 | chr17 | 38490367 | |||||||
| chr17:38490579 | G | A | 2 | a0001c0010t0001g0016 a0001c0011t0001g0069 |
2 | NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3150+28G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 19/23 | chr17 | 38490579 | |||||||
| chr17:38490778 | C | T | 6 | a0001c0001t0001g0079 a0001c0020t0005g0011 a0001c0020t0005g0143 others(3): Show |
6 | HG01081.hp1 HG01891.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.3150+227C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 19/23 | chr17 | 38490778 | |||||||
| chr17:38490782 | C | T | 5 | a0001c0001t0001g0058 a0001c0001t0001g0156 a0001c0001t0011g0064 others(2): Show |
5 | HG02451.hp1 HG02647.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.3150+231C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 19/23 | chr17 | 38490782 | |||||||
| chr17:38490811 | G | A | 67 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(64): Show |
70 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.3150+260G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 19/23 | chr17 | 38490811 | |||||||
| chr17:38490889 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3150+338G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 19/23 | chr17 | 38490889 | |||||||
| chr17:38490991 | T | G | 1 | a0001c0002t0002g0303 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.3151-416T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 19/23 | chr17 | 38490991 | |||||||
| chr17:38490992 | T | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.3151-415T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 19/23 | chr17 | 38490992 | |||||||
| chr17:38491053 | G | A | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(203): Show |
211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.3151-354G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 19/23 | chr17 | 38491053 | |||||||
| chr17:38491080 | A | AT | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.3151-325dupT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr17 | 38491080 | ||||||
| chr17:38491083 | A | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.3151-324A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 19/23 | chr17 | 38491083 | |||||||
| chr17:38491748 | G | A | 72 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(69): Show |
75 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.3276+216G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38491748 | |||||||
| chr17:38491850 | G | A | 2 | a0005c0033t0001g0075 a0005c0053t0001g0128 |
2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3276+318G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38491850 | |||||||
| chr17:38492103 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3276+571C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38492103 | |||||||
| chr17:38492160 | G | A | 2 | a0001c0001t0001g0079 a0013c0047t0001g0018 |
2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.3276+628G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38492160 | |||||||
| chr17:38492162 | G | A | 5 | a0001c0001t0001g0058 a0001c0001t0001g0156 a0001c0001t0011g0064 others(2): Show |
5 | HG02451.hp1 HG02647.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.3276+630G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38492162 | |||||||
| chr17:38492212 | G | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.3276+680G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38492212 | |||||||
| chr17:38492262 | A | G | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.3276+730A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38492262 | |||||||
| chr17:38492446 | G | A | 5 | a0001c0001t0001g0058 a0001c0001t0001g0156 a0001c0001t0011g0064 others(2): Show |
5 | HG02451.hp1 HG02647.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.3276+914G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38492446 | |||||||
| chr17:38492449 | G | A | 11 | a0001c0011t0006g0073 a0001c0011t0006g0076 a0003c0013t0001g0129 others(8): Show |
11 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.3276+917G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38492449 | |||||||
| chr17:38492609 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3276+1077G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38492609 | |||||||
| chr17:38492851 | A | C | 1 | a0001c0001t0001g0058 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3276+1319A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38492851 | |||||||
| chr17:38492917 | C | G | 2 | a0001c0001t0001g0127 a0001c0001t0001g0263 |
2 | HG00438.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.3276+1385C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38492917 | |||||||
| chr17:38493194 | C | CT | 8 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0211 others(5): Show |
8 | HG01891.hp1 HG02074.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.3276+1671dupT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr17 | 38493194 | ||||||
| chr17:38493194 | CT | C | 5 | a0001c0001t0001g0058 a0001c0001t0001g0156 a0001c0001t0011g0064 others(2): Show |
5 | HG02451.hp1 HG02647.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.3276+1671delT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr17 | 38493194 | ||||||
| chr17:38493211 | TG | T | 4 | a0003c0013t0001g0129 a0003c0013t0001g0130 a0003c0013t0001g0132 others(1): Show |
4 | HG02895.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.3276+1680delG | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38493211 | |||||||
| chr17:38493212 | G | GT | 12 | a0001c0001t0001g0120 a0001c0001t0001g0124 a0001c0001t0001g0134 others(9): Show |
12 | HG00642.hp1 HG01175.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.3276+1690dupT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr17 | 38493212 | ||||||
| chr17:38493212 | GT | G | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(198): Show |
206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.3276+1690delT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr17 | 38493212 | ||||||
| chr17:38493250 | T | C | 1 | a0002c0036t0003g0179 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3276+1718T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38493250 | |||||||
| chr17:38493449 | C | T | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(203): Show |
211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.3276+1917C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38493449 | |||||||
| chr17:38493568 | G | A | 1 | a0001c0003t0001g0229 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3276+2036G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38493568 | |||||||
| chr17:38493578 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3276+2046G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38493578 | |||||||
| chr17:38493715 | C | T | 67 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(64): Show |
70 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.3276+2183C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38493715 | |||||||
| chr17:38493742 | C | G | 58 | a0001c0001t0001g0008 a0001c0001t0001g0066 a0001c0001t0001g0120 others(55): Show |
58 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.3276+2210C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38493742 | |||||||
| chr17:38493757 | G | A | 4 | a0001c0031t0003g0067 a0006c0050t0003g0138 a0007c0021t0003g0070 others(1): Show |
4 | HG02109.hp1 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.3276+2225G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38493757 | |||||||
| chr17:38494001 | A | C | 1 | a0004c0055t0004g0298 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3276+2469A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494001 | |||||||
| chr17:38494024 | CTG | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0025 others(83): Show |
88 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.3276+2498_3276+249 others(6): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr17 | 38494024 | ||||||
| chr17:38494104 | G | A | 2 | a0001c0004t0001g0056 a0001c0005t0001g0044 |
2 | HG02818.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3276+2572G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494104 | |||||||
| chr17:38494202 | A | G | 1 | a0001c0002t0002g0166 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3276+2670A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494202 | |||||||
| chr17:38494357 | G | A | 1 | a0001c0007t0013g0148 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3276+2825G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494357 | |||||||
| chr17:38494360 | G | A | 4 | a0001c0001t0001g0114 a0001c0001t0001g0117 a0001c0001t0001g0121 others(1): Show |
4 | HG02135.hp2 NA18944.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.3276+2828G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494360 | |||||||
| chr17:38494460 | G | A | 51 | a0001c0001t0001g0008 a0001c0001t0001g0066 a0001c0001t0001g0120 others(48): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.3276+2928G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494460 | |||||||
| chr17:38494485 | G | A | 1 | a0001c0003t0001g0107 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3276+2953G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494485 | |||||||
| chr17:38494492 | G | GGTGGGAG others(6): Show |
1 | a0006c0049t0001g0262 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3276+2964_3276+297 others(17): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr17 | 38494492 | ||||||
| chr17:38494520 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3276+2988C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494520 | |||||||
| chr17:38494521 | G | A | 10 | a0001c0001t0001g0008 a0001c0001t0001g0066 a0001c0001t0001g0124 others(7): Show |
10 | HG00639.hp2 HG00733.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.3276+2989G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494521 | |||||||
| chr17:38494559 | GAC | G | 5 | a0001c0001t0001g0019 a0001c0001t0003g0174 a0001c0003t0001g0193 others(2): Show |
5 | HG01981.hp2 HG02293.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.3276+3045_3276+304 others(6): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr17 | 38494559 | ||||||
| chr17:38494564 | A | G | 1 | a0001c0001t0001g0008 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3276+3032A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494564 | |||||||
| chr17:38494575 | C | A | 1 | a0001c0009t0003g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3276+3043C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494575 | |||||||
| chr17:38494577 | C | A | 1 | a0001c0009t0003g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3276+3045C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494577 | |||||||
| chr17:38494579 | A | C | 1 | a0001c0003t0001g0014 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3276+3047A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494579 | |||||||
| chr17:38494588 | T | A | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(204): Show |
212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.3276+3056T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494588 | |||||||
| chr17:38494594 | A | C | 1 | a0006c0049t0001g0262 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3276+3062A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494594 | |||||||
| chr17:38494703 | C | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.3277-3082C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494703 | |||||||
| chr17:38494735 | T | C | 5 | a0001c0003t0001g0111 a0001c0024t0001g0098 a0001c0024t0001g0105 others(2): Show |
5 | HG02040.hp1 HG02071.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.3277-3050T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494735 | |||||||
| chr17:38494782 | G | T | 2 | a0001c0001t0001g0079 a0013c0047t0001g0018 |
2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.3277-3003G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494782 | |||||||
| chr17:38494882 | C | T | 1 | a0001c0003t0001g0014 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3277-2903C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494882 | |||||||
| chr17:38494904 | T | G | 4 | a0001c0031t0003g0067 a0006c0050t0003g0138 a0007c0021t0003g0070 others(1): Show |
4 | HG02109.hp1 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.3277-2881T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494904 | |||||||
| chr17:38494940 | C | A | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.3277-2845C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494940 | |||||||
| chr17:38494941 | A | G | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.3277-2844A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38494941 | |||||||
| chr17:38495020 | A | G | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.3277-2765A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38495020 | |||||||
| chr17:38495032 | C | T | 9 | a0001c0001t0001g0145 a0001c0001t0001g0149 a0001c0001t0001g0150 others(6): Show |
9 | HG02622.hp1 HG02895.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.3277-2753C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38495032 | |||||||
| chr17:38495228 | CT | C | 56 | a0001c0001t0001g0008 a0001c0001t0001g0066 a0001c0001t0001g0120 others(53): Show |
56 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.3277-2536delT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr17 | 38495228 | ||||||
| chr17:38495228 | CTT | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(205): Show |
213 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.3277-2537_3277-253 others(6): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr17 | 38495228 | ||||||
| chr17:38495233 | T | C | 4 | a0001c0002t0002g0087 a0001c0003t0001g0289 a0003c0028t0001g0017 others(1): Show |
4 | HG02145.hp2 NA18943.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.3277-2552T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38495233 | |||||||
| chr17:38495234 | T | C | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(201): Show |
209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.3277-2551T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38495234 | |||||||
| chr17:38495235 | T | C | 52 | a0001c0001t0001g0008 a0001c0001t0001g0066 a0001c0001t0001g0120 others(49): Show |
52 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.3277-2550T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38495235 | |||||||
| chr17:38495426 | T | C | 1 | a0001c0001t0001g0268 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.3277-2359T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38495426 | |||||||
| chr17:38495724 | T | C | 1 | a0001c0004t0001g0054 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3277-2061T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38495724 | |||||||
| chr17:38495754 | T | A | 4 | a0001c0001t0001g0083 a0001c0001t0001g0200 a0001c0001t0001g0286 others(1): Show |
4 | HG02132.hp2 NA18963.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.3277-2031T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38495754 | |||||||
| chr17:38495791 | T | G | 1 | a0001c0001t0001g0184 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.3277-1994T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38495791 | |||||||
| chr17:38495903 | T | C | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.3277-1882T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38495903 | |||||||
| chr17:38495906 | AT | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0025 others(80): Show |
85 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.3277-1871delT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr17 | 38495906 | ||||||
| chr17:38496140 | C | T | 6 | a0001c0001t0001g0058 a0001c0001t0001g0156 a0001c0001t0011g0064 others(3): Show |
6 | HG02451.hp1 HG02647.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.3277-1645C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38496140 | |||||||
| chr17:38496145 | G | C | 1 | a0004c0055t0004g0298 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3277-1640G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38496145 | |||||||
| chr17:38496269 | T | C | 1 | a0004c0055t0004g0298 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3277-1516T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38496269 | |||||||
| chr17:38496309 | ATT | A | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(204): Show |
212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.3277-1464_3277-146 others(6): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr17 | 38496309 | ||||||
| chr17:38496358 | C | T | 1 | a0004c0055t0004g0298 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3277-1427C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38496358 | |||||||
| chr17:38496952 | GA | G | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(255): Show |
263 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.3277-819delA | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr17 | 38496952 | ||||||
| chr17:38497119 | A | G | 2 | a0001c0001t0001g0079 a0004c0055t0004g0298 |
2 | HG02486.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3277-666A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38497119 | |||||||
| chr17:38497135 | T | C | 21 | a0001c0003t0001g0065 a0001c0004t0001g0056 a0001c0005t0001g0033 others(18): Show |
21 | HG00733.hp1 HG01109.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.3277-650T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38497135 | |||||||
| chr17:38497169 | A | C | 54 | a0001c0001t0001g0058 a0001c0001t0001g0156 a0001c0001t0001g0222 others(51): Show |
54 | HG00733.hp1 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.3277-616A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38497169 | |||||||
| chr17:38497298 | G | T | 1 | a0001c0005t0001g0147 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3277-487G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38497298 | |||||||
| chr17:38497307 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3277-478G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38497307 | |||||||
| chr17:38497352 | G | A | 21 | a0001c0003t0001g0065 a0001c0004t0001g0056 a0001c0005t0001g0033 others(18): Show |
21 | HG00733.hp1 HG01109.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.3277-433G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38497352 | |||||||
| chr17:38497368 | T | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0021 others(82): Show |
87 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.3277-417T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38497368 | |||||||
| chr17:38497373 | C | A | 5 | a0001c0001t0001g0058 a0001c0001t0001g0156 a0001c0001t0011g0064 others(2): Show |
5 | HG02451.hp1 HG02647.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.3277-412C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38497373 | |||||||
| chr17:38497398 | C | T | 57 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(54): Show |
60 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.3277-387C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38497398 | |||||||
| chr17:38497414 | C | T | 54 | a0001c0001t0001g0058 a0001c0001t0001g0156 a0001c0001t0001g0222 others(51): Show |
54 | HG00733.hp1 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.3277-371C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38497414 | |||||||
| chr17:38497422 | C | T | 55 | a0001c0001t0001g0058 a0001c0001t0001g0156 a0001c0001t0001g0222 others(52): Show |
55 | HG00733.hp1 HG00735.hp1 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.3277-363C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38497422 | |||||||
| chr17:38497446 | C | T | 58 | a0001c0001t0001g0058 a0001c0001t0001g0156 a0001c0001t0001g0222 others(55): Show |
58 | HG00733.hp1 HG00735.hp1 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.3277-339C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38497446 | |||||||
| chr17:38497572 | C | G | 1 | a0001c0001t0001g0281 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.3277-213C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38497572 | |||||||
| chr17:38497586 | A | G | 3 | a0001c0001t0001g0079 a0001c0009t0003g0057 a0004c0055t0004g0298 |
3 | HG02486.hp1 HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3277-199A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38497586 | |||||||
| chr17:38497698 | G | A | 69 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(66): Show |
72 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.3277-87G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38497698 | |||||||
| chr17:38497748 | A | G | 49 | a0001c0001t0001g0222 a0001c0002t0002g0015 a0001c0002t0002g0026 others(46): Show |
49 | HG00733.hp1 HG00735.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.3277-37A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38497748 | |||||||
| chr17:38497753 | G | C | 49 | a0001c0001t0001g0222 a0001c0002t0002g0015 a0001c0002t0002g0026 others(46): Show |
49 | HG00733.hp1 HG00735.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.3277-32G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38497753 | |||||||
| chr17:38497763 | C | T | 52 | a0001c0001t0001g0222 a0001c0002t0002g0015 a0001c0002t0002g0026 others(49): Show |
52 | HG00733.hp1 HG00735.hp1 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.3277-22C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | chr17 | 38497763 | |||||||
| chr17:38497904 | C | T | 1 | a0001c0006t0002g0088 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3318+78C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 21/23 | chr17 | 38497904 | |||||||
| chr17:38497916 | C | T | 51 | a0001c0001t0001g0222 a0001c0002t0002g0015 a0001c0002t0002g0026 others(48): Show |
51 | HG00733.hp1 HG00735.hp1 HG01074.hp2 others(48): Show |
intron_variant | MODIFIER | c.3318+90C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 21/23 | chr17 | 38497916 | |||||||
| chr17:38498036 | G | A | 1 | a0001c0010t0001g0016 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3318+210G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 21/23 | chr17 | 38498036 | |||||||
| chr17:38498070 | AC | A | 44 | a0001c0001t0001g0008 a0001c0001t0001g0034 a0001c0001t0001g0066 others(41): Show |
44 | HG00323.hp2 HG00609.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.3318+247delC | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr17 | 38498070 | ||||||
| chr17:38498205 | C | G | 52 | a0001c0001t0001g0222 a0001c0002t0002g0015 a0001c0002t0002g0026 others(49): Show |
52 | HG00733.hp1 HG00735.hp1 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.3319-209C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 21/23 | chr17 | 38498205 | |||||||
| chr17:38498756 | C | T | 1 | a0004c0055t0004g0298 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3415+246C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 22/23 | chr17 | 38498756 | |||||||
| chr17:38498809 | T | C | 1 | a0002c0035t0001g0234 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3415+299T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 22/23 | chr17 | 38498809 | |||||||
| chr17:38498819 | G | T | 1 | a0001c0004t0001g0276 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3415+309G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 22/23 | chr17 | 38498819 | |||||||
| chr17:38498858 | C | T | 12 | a0001c0001t0001g0120 a0001c0001t0001g0124 a0001c0001t0001g0134 others(9): Show |
12 | HG00323.hp2 HG00639.hp2 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.3415+348C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 22/23 | chr17 | 38498858 | |||||||
| chr17:38499025 | C | A | 1 | a0001c0001t0001g0019 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3415+515C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 22/23 | chr17 | 38499025 | |||||||
| chr17:38499040 | C | T | 23 | a0001c0004t0001g0056 a0001c0005t0001g0033 a0001c0005t0001g0036 others(20): Show |
23 | HG00733.hp1 HG01884.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.3415+530C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 22/23 | chr17 | 38499040 | |||||||
| chr17:38499061 | G | A | 12 | a0001c0001t0001g0085 a0001c0001t0001g0219 a0001c0001t0001g0221 others(9): Show |
12 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.3415+551G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 22/23 | chr17 | 38499061 | |||||||
| chr17:38499177 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3415+667C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 22/23 | chr17 | 38499177 | |||||||
| chr17:38499199 | C | T | 1 | a0001c0002t0002g0254 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3415+689C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 22/23 | chr17 | 38499199 | |||||||
| chr17:38499312 | C | A | 6 | a0001c0001t0001g0145 a0001c0001t0001g0149 a0001c0001t0001g0150 others(3): Show |
6 | HG02895.hp1 HG02965.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.3415+802C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 22/23 | chr17 | 38499312 | |||||||
| chr17:38499366 | G | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0156 |
2 | HG02451.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3415+856G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 22/23 | chr17 | 38499366 | |||||||
| chr17:38499377 | C | T | 1 | a0001c0003t0001g0065 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3415+867C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 22/23 | chr17 | 38499377 | |||||||
| chr17:38499576 | C | G | 8 | a0001c0003t0001g0065 a0001c0018t0001g0042 a0001c0018t0001g0046 others(5): Show |
8 | HG01109.hp1 HG02630.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.3416-1021C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 22/23 | chr17 | 38499576 | |||||||
| chr17:38499785 | G | A | 1 | a0003c0013t0001g0130 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3416-812G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 22/23 | chr17 | 38499785 | |||||||
| chr17:38499839 | T | C | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
261 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.3416-758T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 22/23 | chr17 | 38499839 | |||||||
| chr17:38499906 | G | A | 1 | a0001c0005t0001g0142 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3416-691G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 22/23 | chr17 | 38499906 | |||||||
| chr17:38499943 | G | A | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(220): Show |
228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.3416-654G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 22/23 | chr17 | 38499943 | |||||||
| chr17:38500207 | C | A | 9 | a0001c0001t0001g0034 a0001c0004t0001g0055 a0001c0004t0001g0062 others(6): Show |
9 | HG02451.hp2 HG02647.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.3416-390C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 22/23 | chr17 | 38500207 | |||||||
| chr17:38500553 | T | C | 1 | a0001c0004t0001g0031 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3416-44T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 22/23 | chr17 | 38500553 | |||||||
| chr17:38500636 | T | C | 1 | a0001c0001t0001g0006 | 1 | HG03831.hp1 | splice_region_variant&intron_variant | LOW | c.3447+8T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38500636 | |||||||
| chr17:38500697 | G | A | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(90): Show |
96 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.3447+69G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38500697 | |||||||
| chr17:38500716 | T | A | 3 | a0001c0001t0001g0214 a0001c0001t0001g0219 a0001c0001t0001g0221 |
3 | HG00639.hp1 HG01256.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.3447+88T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38500716 | |||||||
| chr17:38500931 | G | A | 9 | a0001c0001t0001g0034 a0001c0004t0001g0055 a0001c0004t0001g0062 others(6): Show |
9 | HG02451.hp2 HG02647.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.3447+303G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38500931 | |||||||
| chr17:38500932 | C | T | 9 | a0001c0001t0001g0034 a0001c0004t0001g0055 a0001c0004t0001g0062 others(6): Show |
9 | HG02451.hp2 HG02647.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.3447+304C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38500932 | |||||||
| chr17:38501071 | T | C | 2 | a0001c0001t0001g0085 a0015c0044t0001g0192 |
2 | HG02135.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.3447+443T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38501071 | |||||||
| chr17:38501219 | T | TA | 5 | a0001c0001t0001g0025 a0001c0001t0001g0100 a0001c0001t0001g0126 others(2): Show |
5 | HG01099.hp1 HG01255.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.3447+596dupA | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38501219 | ||||||
| chr17:38501242 | A | T | 26 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0034 others(23): Show |
26 | HG00544.hp1 HG00733.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.3447+614A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38501242 | |||||||
| chr17:38501286 | GTTATTTT | G | 30 | a0001c0001t0001g0058 a0001c0001t0001g0156 a0001c0002t0002g0015 others(27): Show |
30 | HG00735.hp2 HG01169.hp1 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.3447+672_3447+678d others(9): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38501286 | ||||||
| chr17:38501473 | T | C | 28 | a0001c0001t0001g0058 a0001c0001t0001g0156 a0001c0002t0002g0015 others(25): Show |
28 | HG00735.hp2 HG01169.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.3447+845T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38501473 | |||||||
| chr17:38501534 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.3447+906C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38501534 | |||||||
| chr17:38501536 | C | T | 1 | a0001c0012t0003g0045 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3447+908C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38501536 | |||||||
| chr17:38501553 | GGCCTCC | G | 73 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(70): Show |
76 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.3447+927_3447+932d others(8): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38501553 | ||||||
| chr17:38501592 | C | T | 13 | a0001c0004t0001g0056 a0001c0005t0001g0033 a0001c0005t0001g0036 others(10): Show |
13 | HG00733.hp1 HG02055.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.3447+964C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38501592 | |||||||
| chr17:38502081 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3447+1453G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38502081 | |||||||
| chr17:38502199 | A | C | 96 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(93): Show |
99 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.3447+1571A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38502199 | |||||||
| chr17:38502472 | G | C | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(74): Show |
80 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.3447+1844G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38502472 | |||||||
| chr17:38502473 | C | T | 3 | a0001c0005t0001g0144 a0001c0005t0001g0158 a0001c0005t0001g0159 |
3 | HG02257.hp2 HG02486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3447+1845C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38502473 | |||||||
| chr17:38502729 | G | C | 92 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0025 others(89): Show |
94 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.3447+2101G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38502729 | |||||||
| chr17:38502811 | G | A | 2 | a0001c0001t0001g0005 a0001c0001t0009g0005 |
2 | NA18952.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.3447+2183G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38502811 | |||||||
| chr17:38503015 | T | G | 73 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(70): Show |
76 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.3447+2387T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38503015 | |||||||
| chr17:38503021 | C | A | 1 | a0001c0006t0002g0088 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3447+2393C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38503021 | |||||||
| chr17:38503049 | A | AAAAC | 3 | a0001c0001t0001g0058 a0001c0001t0001g0156 a0001c0004t0001g0059 |
3 | HG02451.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3447+2441_3447+244 others(8): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38503049 | ||||||
| chr17:38503079 | C | T | 4 | a0001c0020t0005g0011 a0001c0020t0005g0143 a0001c0027t0005g0146 others(1): Show |
4 | HG01081.hp1 HG02922.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.3447+2451C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38503079 | |||||||
| chr17:38503401 | C | T | 4 | a0001c0001t0001g0187 a0001c0001t0001g0215 a0001c0001t0001g0231 others(1): Show |
4 | HG00099.hp2 HG00280.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.3447+2773C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38503401 | |||||||
| chr17:38503545 | T | A | 25 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0066 others(22): Show |
25 | HG00544.hp1 HG00733.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.3447+2917T>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38503545 | |||||||
| chr17:38503648 | G | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0080 others(111): Show |
116 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.3447+3020G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38503648 | |||||||
| chr17:38503668 | T | G | 2 | a0004c0019t0004g0060 a0004c0019t0004g0063 |
2 | HG01243.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3447+3040T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38503668 | |||||||
| chr17:38503749 | AGGAGGCC others(19): Show |
A | 1 | a0001c0006t0002g0088 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3447+3123_3447+314 others(30): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38503749 | ||||||
| chr17:38503870 | A | G | 3 | a0001c0001t0001g0058 a0001c0001t0001g0156 a0001c0004t0001g0059 |
3 | HG02451.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3447+3242A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38503870 | |||||||
| chr17:38504085 | T | C | 1 | a0001c0009t0003g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3447+3457T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38504085 | |||||||
| chr17:38504256 | C | T | 4 | a0001c0001t0011g0064 a0004c0017t0004g0140 a0004c0017t0004g0141 others(1): Show |
4 | HG02486.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3447+3628C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38504256 | |||||||
| chr17:38504303 | C | T | 1 | a0015c0044t0001g0192 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3447+3675C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38504303 | |||||||
| chr17:38504360 | C | A | 1 | a0001c0009t0003g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3447+3732C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38504360 | |||||||
| chr17:38504402 | C | T | 4 | a0001c0001t0011g0064 a0004c0017t0004g0140 a0004c0017t0004g0141 others(1): Show |
4 | HG02486.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3447+3774C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38504402 | |||||||
| chr17:38504425 | G | A | 1 | a0001c0010t0001g0169 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3447+3797G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38504425 | |||||||
| chr17:38504442 | C | T | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(226): Show |
234 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.3447+3814C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38504442 | |||||||
| chr17:38504687 | C | G | 11 | a0001c0004t0001g0056 a0001c0005t0001g0033 a0001c0005t0001g0036 others(8): Show |
11 | HG00733.hp1 HG02055.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.3447+4059C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38504687 | |||||||
| chr17:38504740 | C | T | 27 | a0001c0002t0002g0015 a0001c0002t0002g0026 a0001c0002t0002g0027 others(24): Show |
27 | HG00735.hp2 HG01169.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.3447+4112C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38504740 | |||||||
| chr17:38504816 | C | T | 4 | a0001c0001t0011g0064 a0004c0017t0004g0140 a0004c0017t0004g0141 others(1): Show |
4 | HG02486.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3447+4188C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38504816 | |||||||
| chr17:38504976 | ATCTTTTT others(13): Show |
A | 1 | a0001c0001t0001g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3447+4350_3447+436 others(24): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504976 | ||||||
| chr17:38504978 | C | CT | 12 | a0001c0001t0001g0216 a0001c0001t0001g0281 a0001c0003t0001g0012 others(9): Show |
12 | HG00621.hp1 HG01993.hp2 HG03017.hp1 others(9): Show |
intron_variant | MODIFIER | c.3447+4395dupT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | ||||||
| chr17:38504978 | C | CTT | 10 | a0001c0001t0001g0250 a0001c0001t0001g0255 a0001c0001t0001g0269 others(7): Show |
10 | HG00609.hp1 HG00642.hp1 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.3447+4394_3447+439 others(6): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | ||||||
| chr17:38504978 | C | CTTT | 7 | a0001c0001t0001g0120 a0001c0001t0001g0135 a0001c0001t0001g0294 others(4): Show |
7 | HG01074.hp1 HG01361.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.3447+4393_3447+439 others(7): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | ||||||
| chr17:38504978 | C | CTTTT | 6 | a0001c0001t0001g0124 a0001c0003t0001g0193 a0001c0004t0001g0171 others(3): Show |
6 | HG01070.hp1 HG01074.hp2 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.3447+4392_3447+439 others(8): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | ||||||
| chr17:38504978 | C | T | 1 | a0001c0008t0001g0198 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3447+4350C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38504978 | |||||||
| chr17:38504978 | CT | C | 28 | a0001c0001t0001g0005 a0001c0001t0001g0080 a0001c0001t0001g0100 others(25): Show |
28 | HG00438.hp1 HG00621.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.3447+4395delT | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | ||||||
| chr17:38504978 | CTT | C | 23 | a0001c0001t0001g0001 a0001c0001t0001g0102 a0001c0001t0001g0103 others(20): Show |
23 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(20): Show |
intron_variant | MODIFIER | c.3447+4394_3447+439 others(6): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | ||||||
| chr17:38504978 | CTTT | C | 6 | a0001c0001t0001g0025 a0001c0001t0001g0083 a0001c0001t0001g0184 others(3): Show |
6 | HG01884.hp1 HG01943.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.3447+4393_3447+439 others(7): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | ||||||
| chr17:38504978 | CTTTTTTT | C | 7 | a0001c0001t0001g0002 a0001c0001t0001g0089 a0001c0001t0001g0187 others(4): Show |
7 | HG02280.hp1 HG03239.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.3447+4389_3447+439 others(11): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | ||||||
| chr17:38504978 | CTTTTTTT others(1): Show |
C | 29 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0077 others(26): Show |
29 | HG00735.hp1 HG01106.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.3447+4388_3447+439 others(12): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | ||||||
| chr17:38504978 | CTTTTTTT others(2): Show |
C | 33 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(30): Show |
33 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.3447+4387_3447+439 others(13): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | ||||||
| chr17:38504978 | CTTTTTTT others(3): Show |
C | 22 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(19): Show |
23 | HG00323.hp1 HG00544.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.3447+4386_3447+439 others(14): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | ||||||
| chr17:38504978 | CTTTTTTT others(4): Show |
C | 4 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0002t0002g0110 others(1): Show |
4 | HG00140.hp1 HG01256.hp1 HG02074.hp1 others(1): Show |
intron_variant | MODIFIER | c.3447+4385_3447+439 others(15): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | ||||||
| chr17:38504978 | CTTTTTTT others(5): Show |
C | 21 | a0001c0001t0001g0019 a0001c0001t0001g0221 a0001c0001t0001g0235 others(18): Show |
21 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.3447+4384_3447+439 others(16): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | ||||||
| chr17:38504978 | CTTTTTTT others(6): Show |
C | 35 | a0001c0001t0001g0008 a0001c0001t0001g0066 a0001c0001t0001g0079 others(32): Show |
35 | HG00735.hp2 HG01106.hp1 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.3447+4383_3447+439 others(17): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | ||||||
| chr17:38504978 | CTTTTTTT others(7): Show |
C | 6 | a0001c0001t0001g0153 a0001c0002t0002g0303 a0001c0031t0003g0067 others(3): Show |
6 | HG02145.hp1 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.3447+4382_3447+439 others(18): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | ||||||
| chr17:38504978 | CTTTTTTT others(8): Show |
C | 3 | a0001c0007t0013g0148 a0001c0010t0001g0168 a0012c0039t0001g0186 |
3 | HG01255.hp2 HG01993.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3447+4381_3447+439 others(19): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | ||||||
| chr17:38504978 | CTTTTTTT others(9): Show |
C | 6 | a0001c0009t0003g0173 a0004c0017t0004g0140 a0004c0017t0004g0141 others(3): Show |
6 | HG01243.hp2 HG02486.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.3447+4380_3447+439 others(20): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | ||||||
| chr17:38504978 | CTTTTTTT others(10): Show |
C | 5 | a0001c0001t0001g0165 a0001c0001t0011g0064 a0001c0009t0003g0172 others(2): Show |
5 | HG02572.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.3447+4379_3447+439 others(21): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | ||||||
| chr17:38504978 | CTTTTTTT others(11): Show |
C | 2 | a0001c0001t0001g0134 a0001c0004t0001g0031 |
2 | HG02055.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.3447+4378_3447+439 others(22): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | ||||||
| chr17:38504978 | CTTTTTTT others(12): Show |
C | 1 | a0001c0027t0005g0155 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3447+4377_3447+439 others(23): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | ||||||
| chr17:38504978 | CTTTTTTT others(13): Show |
C | 4 | a0001c0003t0001g0275 a0001c0020t0005g0011 a0001c0020t0005g0143 others(1): Show |
4 | HG01081.hp1 HG02922.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.3447+4376_3447+439 others(24): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | ||||||
| chr17:38504978 | CTTTTTTT others(15): Show |
C | 1 | a0001c0007t0015g0266 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3447+4374_3447+439 others(26): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | ||||||
| chr17:38504978 | CTTTTTTT others(17): Show |
C | 3 | a0001c0001t0001g0058 a0001c0001t0001g0156 a0001c0004t0001g0059 |
3 | HG02451.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3447+4372_3447+439 others(28): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38504978 | ||||||
| chr17:38505155 | C | A | 4 | a0001c0001t0011g0064 a0004c0017t0004g0140 a0004c0017t0004g0141 others(1): Show |
4 | HG02486.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3447+4527C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38505155 | |||||||
| chr17:38505184 | A | T | 34 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0066 others(31): Show |
34 | HG00544.hp1 HG00733.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.3447+4556A>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38505184 | |||||||
| chr17:38505375 | A | G | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
257 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.3448-4569A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38505375 | |||||||
| chr17:38505458 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3448-4486G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38505458 | |||||||
| chr17:38505658 | G | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0025 others(84): Show |
89 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.3448-4286G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38505658 | |||||||
| chr17:38505690 | A | G | 1 | a0001c0006t0002g0088 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3448-4254A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38505690 | |||||||
| chr17:38505746 | TG | T | 3 | a0001c0001t0001g0058 a0001c0001t0001g0156 a0001c0004t0001g0059 |
3 | HG02451.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3448-4196delG | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38505746 | ||||||
| chr17:38505824 | C | T | 4 | a0001c0020t0005g0011 a0001c0020t0005g0143 a0001c0027t0005g0146 others(1): Show |
4 | HG01081.hp1 HG02922.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.3448-4120C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38505824 | |||||||
| chr17:38505971 | C | G | 2 | a0001c0001t0001g0292 a0001c0002t0002g0225 |
2 | NA18952.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.3448-3973C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38505971 | |||||||
| chr17:38506004 | C | G | 2 | a0001c0018t0001g0042 a0001c0018t0001g0046 |
2 | HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3448-3940C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38506004 | |||||||
| chr17:38506045 | G | A | 3 | a0001c0001t0001g0058 a0001c0001t0001g0156 a0001c0004t0001g0059 |
3 | HG02451.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3448-3899G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38506045 | |||||||
| chr17:38506162 | A | G | 9 | a0001c0003t0001g0065 a0003c0013t0001g0129 a0003c0013t0001g0130 others(6): Show |
9 | HG01109.hp1 HG01884.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.3448-3782A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38506162 | |||||||
| chr17:38506481 | A | C | 3 | a0004c0017t0004g0140 a0004c0017t0004g0141 a0004c0055t0004g0298 |
3 | HG02486.hp1 HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3448-3463A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38506481 | |||||||
| chr17:38506638 | C | G | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(86): Show |
92 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.3448-3306C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38506638 | |||||||
| chr17:38506655 | G | T | 1 | a0001c0001t0001g0293 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.3448-3289G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38506655 | |||||||
| chr17:38506656 | C | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(127): Show |
132 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.3448-3288C>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38506656 | |||||||
| chr17:38506694 | C | G | 265 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(262): Show |
270 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.3448-3250C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38506694 | |||||||
| chr17:38506989 | C | T | 29 | a0001c0001t0001g0269 a0001c0001t0003g0174 a0001c0004t0001g0056 others(26): Show |
29 | HG00544.hp1 HG00642.hp1 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.3448-2955C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38506989 | |||||||
| chr17:38506999 | A | G | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(269): Show |
277 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.3448-2945A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38506999 | |||||||
| chr17:38507067 | A | C | 1 | a0001c0001t0001g0220 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3448-2877A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38507067 | |||||||
| chr17:38507157 | C | G | 1 | a0001c0001t0001g0231 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3448-2787C>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38507157 | |||||||
| chr17:38507227 | T | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(90): Show |
95 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.3448-2717T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38507227 | |||||||
| chr17:38507276 | A | AAAT | 3 | a0001c0001t0001g0058 a0001c0003t0001g0193 a0001c0004t0001g0059 |
3 | HG02293.hp1 HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3448-2640_3448-263 others(7): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38507276 | ||||||
| chr17:38507276 | A | AAATAATA others(2): Show |
19 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0114 others(16): Show |
19 | HG00099.hp2 HG00280.hp1 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.3448-2646_3448-263 others(13): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38507276 | ||||||
| chr17:38507276 | A | AAATAATA others(5): Show |
99 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(96): Show |
101 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.3448-2649_3448-263 others(16): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38507276 | ||||||
| chr17:38507276 | A | AAATAATA others(8): Show |
68 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(65): Show |
70 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.3448-2652_3448-263 others(19): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38507276 | ||||||
| chr17:38507276 | A | AAATAATA others(11): Show |
49 | a0001c0001t0001g0002 a0001c0001t0001g0085 a0001c0001t0001g0091 others(46): Show |
50 | HG00323.hp1 HG00558.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.3448-2655_3448-263 others(22): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38507276 | ||||||
| chr17:38507276 | A | AAATAATA others(14): Show |
16 | a0001c0001t0001g0145 a0001c0001t0001g0268 a0001c0001t0001g0290 others(13): Show |
16 | HG01257.hp2 HG01258.hp2 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.3448-2658_3448-263 others(25): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38507276 | ||||||
| chr17:38507276 | A | AAATAATA others(13): Show |
1 | a0001c0006t0002g0088 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3448-2652_3448-265 others(24): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38507276 | ||||||
| chr17:38507276 | A | ATAATAAT others(12): Show |
1 | a0001c0001t0001g0084 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3448-2668_3448-266 others(23): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38507276 | |||||||
| chr17:38507300 | T | TAATAATA others(11): Show |
1 | a0001c0002t0002g0125 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.3448-2638_3448-263 others(22): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38507300 | ||||||
| chr17:38507300 | T | TAATAATA others(14): Show |
4 | a0001c0002t0002g0015 a0001c0002t0002g0251 a0001c0040t0002g0137 others(1): Show |
4 | HG00735.hp2 HG01169.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.3448-2638_3448-263 others(25): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38507300 | ||||||
| chr17:38507753 | T | C | 10 | a0001c0005t0001g0040 a0001c0005t0001g0050 a0001c0005t0001g0052 others(7): Show |
10 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.3448-2191T>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38507753 | |||||||
| chr17:38508184 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3448-1760G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38508184 | |||||||
| chr17:38508505 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3448-1439G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38508505 | |||||||
| chr17:38508823 | A | C | 1 | a0001c0011t0001g0069 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3448-1121A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38508823 | |||||||
| chr17:38508825 | A | G | 1 | a0001c0011t0001g0069 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3448-1119A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38508825 | |||||||
| chr17:38508898 | A | G | 2 | a0001c0012t0003g0045 a0001c0031t0003g0067 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.3448-1046A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38508898 | |||||||
| chr17:38508918 | G | A | 2 | a0001c0001t0001g0005 a0001c0001t0009g0005 |
2 | NA18952.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.3448-1026G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38508918 | |||||||
| chr17:38508967 | A | G | 2 | a0001c0002t0002g0226 a0001c0054t0002g0227 |
2 | HG02602.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.3448-977A>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38508967 | |||||||
| chr17:38508989 | C | T | 8 | a0001c0007t0003g0053 a0001c0018t0001g0042 a0001c0018t0001g0046 others(5): Show |
8 | HG01884.hp2 HG02145.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.3448-955C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38508989 | |||||||
| chr17:38509021 | TGGGGAAG others(3): Show |
T | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.3448-908_3448-899d others(12): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 38509021 | ||||||
| chr17:38509041 | A | C | 1 | a0002c0035t0001g0234 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3448-903A>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38509041 | |||||||
| chr17:38509058 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3448-886C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38509058 | |||||||
| chr17:38509381 | G | T | 3 | a0001c0001t0001g0058 a0001c0001t0001g0156 a0001c0004t0001g0059 |
3 | HG02451.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3448-563G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38509381 | |||||||
| chr17:38509596 | C | T | 1 | a0001c0027t0005g0146 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3448-348C>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38509596 | |||||||
| chr17:38509609 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0207 |
2 | HG00544.hp2 HG00597.hp1 |
intron_variant | MODIFIER | c.3448-335G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38509609 | |||||||
| chr17:38509755 | G | T | 1 | a0001c0001t0001g0263 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3448-189G>T | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38509755 | |||||||
| chr17:38509761 | G | C | 2 | a0001c0016t0003g0047 a0001c0016t0003g0297 |
2 | HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3448-183G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38509761 | |||||||
| chr17:38509810 | G | C | 6 | a0001c0001t0001g0079 a0001c0005t0001g0050 a0001c0005t0001g0052 others(3): Show |
6 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.3448-134G>C | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38509810 | |||||||
| chr17:38509876 | G | A | 1 | a0001c0020t0005g0011 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3448-68G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38509876 | |||||||
| chr17:38509888 | G | A | 2 | a0001c0016t0003g0047 a0001c0016t0003g0297 |
2 | HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3448-56G>A | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38509888 | |||||||
| chr17:38509932 | T | G | 1 | a0014c0056t0001g0013 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3448-12T>G | ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | chr17 | 38509932 |