Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 29127 |
| ensemblid | ENSG00000161800.13 |
| hgncid | 9804 |
| symbol | RACGAP1 |
| name | Rac GTPase activating protein 1 |
| refseq_nuc | NM_001319999.2 |
| refseq_prot | NP_001306928.1 |
| ensembl_nuc | ENST00000312377.10 |
| ensembl_prot | ENSP00000309871.5 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 49989162 |
| end | 50025494 |
| strand | - |
| ver | v1.2 |
| region | chr12:49989162-50025494 |
| region5000 | chr12:49984162-50030494 |
| regionname0 | RACGAP1_chr12_49989162_50025494 |
| regionname5000 | RACGAP1_chr12_49984162_50030494 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 632 | 319 | 90 | 68 | 127 | 4 | 28 | 101 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | MDTMM others(627): Show |
chr12 | 49984162 | 50030494 |
| a0002 | 0/0 | 632 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | MDTMM others(627): Show |
chr12 | 49984162 | 50030494 |
| a0003 | 0/0 | 632 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | MDTMM others(627): Show |
chr12 | 49984162 | 50030494 |
| a0004 | 0/0 | 632 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | MDTMM others(627): Show |
chr12 | 49984162 | 50030494 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1896 | 292 | 63 | 68 | 127 | 4 | 28 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | ATGGA others(1891): Show |
chr12 | 49984162 | 50030494 | ||
| a0001c0002 | 0/0 | 1896 | 26 | 26 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | ATGGA others(1891): Show |
chr12 | 49984162 | 50030494 | ||
| a0001c0004 | 0/0 | 1896 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | ATGGA others(1891): Show |
chr12 | 49984162 | 50030494 | ||
| a0002c0003 | 0/0 | 1896 | 3 | 3 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | ATGGA others(1891): Show |
chr12 | 49984162 | 50030494 | ||
| a0003c0006 | 0/0 | 1896 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | ATGGA others(1891): Show |
chr12 | 49984162 | 50030494 | ||
| a0004c0005 | 0/0 | 1896 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | ATGGA others(1891): Show |
chr12 | 49984162 | 50030494 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3106 | 282 | 58 | 66 | 125 | 4 | 28 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | GTTTT others(3101): Show |
chr12 | 49984162 | 50030494 |
| a0001c0001t0002 | 1/0 | 3106 | 4 | 2 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | GTTTT others(3101): Show |
chr12 | 49984162 | 50030494 |
| a0001c0001t0004 | 0/0 | 3106 | 2 | 2 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | GTTTT others(3101): Show |
chr12 | 49984162 | 50030494 |
| a0001c0001t0005 | 0/0 | 3106 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | GTTTT others(3101): Show |
chr12 | 49984162 | 50030494 |
| a0001c0001t0006 | 0/0 | 3106 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | GTTTT others(3101): Show |
chr12 | 49984162 | 50030494 |
| a0001c0001t0007 | 0/0 | 3106 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | GTTTT others(3101): Show |
chr12 | 49984162 | 50030494 |
| a0001c0001t0008 | 0/0 | 3106 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | GTTTT others(3101): Show |
chr12 | 49984162 | 50030494 |
| a0001c0002t0001 | 0/0 | 3106 | 23 | 23 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | GTTTT others(3101): Show |
chr12 | 49984162 | 50030494 |
| a0001c0002t0003 | 0/0 | 3106 | 3 | 3 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | GTTTT others(3101): Show |
chr12 | 49984162 | 50030494 |
| a0001c0004t0009 | 0/0 | 3106 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | GTTTT others(3101): Show |
chr12 | 49984162 | 50030494 |
| a0002c0003t0001 | 0/0 | 3106 | 3 | 3 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | GTTTT others(3101): Show |
chr12 | 49984162 | 50030494 |
| a0003c0006t0001 | 0/0 | 3106 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | GTTTT others(3101): Show |
chr12 | 49984162 | 50030494 |
| a0004c0005t0001 | 0/0 | 3106 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | GTTTT others(3101): Show |
chr12 | 49984162 | 50030494 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0006 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0252 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0002g0243 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0005g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0006g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0007g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0001t0008g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0002t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0002t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0002t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0002t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0002t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0002t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0002t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0001c0004t0009g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0002c0003t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0002c0003t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0002c0003t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0003c0006t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| a0004c0005t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0157 | EUR | GBR | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0185 | EUR | GBR | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG00544 | hp1 | a0001 | c0001 | t0007 | g0122 | EAS | CHS | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0240 | AMR | PUR | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | CLM | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01884 | hp2 | a0001 | c0002 | t0003 | g0042 | AFR | ACB | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | ACB | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02055 | hp1 | a0001 | c0002 | t0003 | g0043 | AFR | ACB | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0272 | AFR | ACB | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CDX | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0273 | AFR | ACB | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0032 | AFR | ACB | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0039 | AFR | ACB | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0249 | AFR | ACB | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0271 | AFR | GWD | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | GWD | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | GWD | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02630 | hp1 | a0002 | c0003 | t0001 | g0045 | AFR | GWD | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0035 | AFR | GWD | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02717 | hp1 | a0001 | c0004 | t0009 | g0287 | AFR | GWD | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0034 | AFR | GWD | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02809 | hp1 | a0003 | c0006 | t0001 | g0036 | AFR | GWD | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0255 | AFR | GWD | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0031 | AFR | GWD | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0033 | AFR | GWD | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0270 | AFR | ESN | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0040 | AFR | ESN | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ESN | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | ESN | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ESN | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | GWD | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ESN | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0285 | AFR | ESN | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ESN | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0238 | AFR | ESN | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | MSL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03453 | hp2 | a0002 | c0003 | t0001 | g0046 | AFR | MSL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | MSL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0037 | AFR | MSL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ESN | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03540 | hp2 | a0001 | c0002 | t0003 | g0041 | AFR | GWD | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0248 | AFR | MSL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | MSL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | STU | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | STU | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | BEB | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | STU | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | STU | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | STU | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | STU | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | STU | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | STU | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | STU | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | STU | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | YRI | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CHB | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHB | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHB | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHB | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18906 | hp1 | a0002 | c0003 | t0001 | g0047 | AFR | YRI | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | YRI | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18948 | hp1 | a0001 | c0001 | t0008 | g0281 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | LWK | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | LWK | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | LWK | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0038 | AFR | LWK | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19090 | hp1 | a0004 | c0005 | t0001 | g0193 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | YRI | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0044 | AFR | YRI | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ASW | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0239 | AFR | ASW | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0098 | EUR | TSI | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0082 | EUR | TSI | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG01123 | hp2 | a0001 | c0001 | t0006 | g0179 | AMR | CLM | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0027 | AFR | ACB | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0029 | AFR | ACB | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0030 | AFR | ACB | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | MSL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0028 | AFR | MSL | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | USA | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | USA | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | USA | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | USA | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | LWK | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | LWK | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0252 | REF | REF | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0243 | REF | REF | RACGAP1_chr12_49984162_50030494 | RACGAP1 | chr12 | 49984162 | 50030494 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:49992037 | A | C | 1 | a0002 | 3 | HG02630.hp1 HG03453.hp2 NA18906.hp1 |
missense_variant | MODERATE | c.1675T>G | p.Ser559Ala | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/17 | 1776/3106 | 1675/1899 | 559/632 | chr12 | 49992037 | |||
| chr12:49999623 | C | A | 1 | a0004 | 1 | NA19090.hp1 | missense_variant | MODERATE | c.741G>T | p.Arg247Ser | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 8/17 | 842/3106 | 741/1899 | 247/632 | chr12 | 49999623 | |||
| chr12:50005295 | T | C | 1 | a0003 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.386A>G | p.Asn129Ser | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 4/17 | 487/3106 | 386/1899 | 129/632 | chr12 | 50005295 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:49990686 | A | G | 3 | a0001c0002 a0001c0004 a0003c0006 |
28 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(25): Show |
splice_region_variant&synonymous_variant | LOW | c.1821T>C | p.Pro607Pro | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 16/17 | 1922/3106 | 1821/1899 | 607/632 | chr12 | 49990686 | |||
| chr12:49992056 | G | A | 1 | a0001c0004 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.1656C>T | p.Pro552Pro | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/17 | 1757/3106 | 1656/1899 | 552/632 | chr12 | 49992056 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:49989260 | A | G | 1 | a0001c0001t0007 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1008T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 17/17 | 1008 | chr12 | 49989260 | ||||||
| chr12:49989365 | A | G | 1 | a0001c0001t0006 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*903T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 17/17 | 903 | chr12 | 49989365 | ||||||
| chr12:49989392 | C | T | 1 | a0001c0001t0004 | 2 | HG02280.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*876G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 17/17 | 876 | chr12 | 49989392 | ||||||
| chr12:49989503 | G | T | 1 | a0001c0001t0005 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*765C>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 17/17 | 765 | chr12 | 49989503 | ||||||
| chr12:49989504 | T | A | 1 | a0001c0001t0008 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*764A>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 17/17 | 764 | chr12 | 49989504 | ||||||
| chr12:49989586 | A | G | 12 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(9): Show |
319 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(316): Show |
3_prime_UTR_variant | MODIFIER | c.*682T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 17/17 | 682 | chr12 | 49989586 | ||||||
| chr12:49989855 | C | A | 1 | a0001c0002t0003 | 3 | HG01884.hp2 HG02055.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*413G>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 17/17 | 413 | chr12 | 49989855 | ||||||
| chr12:50025437 | G | A | 1 | a0001c0004t0009 | 1 | HG02717.hp1 | 5_prime_UTR_variant | MODIFIER | c.-44C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/17 | 8722 | chr12 | 50025437 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:49990388 | T | C | 35 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(32): Show |
45 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.1824-45A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 16/16 | chr12 | 49990388 | |||||||
| chr12:49990477 | T | C | 4 | a0001c0001t0001g0049 a0001c0001t0001g0055 a0001c0001t0001g0056 others(1): Show |
4 | HG01192.hp1 HG02735.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.1824-134A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 16/16 | chr12 | 49990477 | |||||||
| chr12:49990566 | T | C | 27 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(24): Show |
30 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1823+118A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 16/16 | chr12 | 49990566 | |||||||
| chr12:49990594 | A | G | 3 | a0001c0001t0002g0238 a0001c0001t0002g0239 a0001c0001t0002g0240 |
3 | HG01167.hp2 HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1823+90T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 16/16 | chr12 | 49990594 | |||||||
| chr12:49991015 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1715-223T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991015 | |||||||
| chr12:49991150 | T | C | 35 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(32): Show |
45 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.1715-358A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991150 | |||||||
| chr12:49991237 | C | T | 26 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0029 others(23): Show |
28 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.1715-445G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991237 | |||||||
| chr12:49991301 | T | C | 29 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0027 others(26): Show |
31 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.1715-509A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991301 | |||||||
| chr12:49991454 | C | CATATATA others(4): Show |
1 | a0001c0001t0001g0128 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1714+543_1714+544i others(13): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991454 | |||||||
| chr12:49991457 | T | TATATATA others(16): Show |
1 | a0001c0001t0001g0082 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1714+540_1714+541i others(25): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991457 | |||||||
| chr12:49991457 | T | TTATATAT others(1): Show |
8 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0095 others(5): Show |
8 | HG01123.hp1 HG02572.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.1714+533_1714+540d others(10): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991457 | |||||||
| chr12:49991457 | T | TTATATAT others(3): Show |
8 | a0001c0001t0001g0023 a0001c0001t0001g0087 a0001c0001t0001g0090 others(5): Show |
9 | HG00438.hp1 HG01175.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1714+531_1714+540d others(12): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991457 | |||||||
| chr12:49991457 | T | TTATATAT others(5): Show |
5 | a0001c0001t0001g0102 a0001c0001t0001g0114 a0001c0001t0001g0129 others(2): Show |
5 | HG01192.hp2 HG01928.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.1714+529_1714+540d others(14): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991457 | |||||||
| chr12:49991457 | T | TTATATAT others(7): Show |
12 | a0001c0001t0001g0021 a0001c0001t0001g0085 a0001c0001t0001g0115 others(9): Show |
13 | HG00099.hp1 HG01261.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.1714+527_1714+540d others(16): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991457 | |||||||
| chr12:49991457 | T | TTATATAT others(9): Show |
18 | a0001c0001t0001g0015 a0001c0001t0001g0083 a0001c0001t0001g0111 others(15): Show |
19 | HG00673.hp2 HG01071.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.1714+525_1714+540d others(18): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991457 | |||||||
| chr12:49991457 | T | TTATATAT others(11): Show |
11 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0093 others(8): Show |
11 | HG00733.hp1 HG00735.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1714+523_1714+540d others(20): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991457 | |||||||
| chr12:49991457 | T | TTATATAT others(13): Show |
4 | a0001c0001t0001g0143 a0001c0001t0001g0172 a0001c0001t0001g0211 others(1): Show |
4 | HG00597.hp2 HG03490.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.1714+521_1714+540d others(22): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991457 | |||||||
| chr12:49991457 | T | TTATATAT others(15): Show |
8 | a0001c0001t0001g0079 a0001c0001t0001g0118 a0001c0001t0001g0130 others(5): Show |
8 | HG00438.hp2 HG01070.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.1714+519_1714+540d others(24): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991457 | |||||||
| chr12:49991457 | T | TTATATAT others(17): Show |
2 | a0001c0001t0001g0131 a0001c0001t0001g0136 |
2 | HG03490.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1714+540_1714+541i others(26): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991457 | |||||||
| chr12:49991457 | T | TTATATAT others(19): Show |
4 | a0001c0001t0001g0138 a0001c0001t0001g0200 a0001c0001t0006g0179 others(1): Show |
4 | HG00544.hp2 HG01123.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1714+540_1714+541i others(28): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991457 | |||||||
| chr12:49991457 | T | TTATATAT others(21): Show |
1 | a0001c0001t0001g0149 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1714+540_1714+541i others(30): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991457 | |||||||
| chr12:49991457 | T | TTATATAT others(23): Show |
1 | a0001c0001t0001g0183 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1714+540_1714+541i others(32): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991457 | |||||||
| chr12:49991457 | T | TTATATAT others(27): Show |
1 | a0001c0001t0001g0140 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1714+540_1714+541i others(36): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991457 | |||||||
| chr12:49991457 | TTA | T | 4 | a0001c0001t0001g0263 a0001c0001t0001g0267 a0001c0001t0001g0275 others(1): Show |
4 | HG02572.hp2 HG03516.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.1714+539_1714+540d others(4): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991457 | |||||||
| chr12:49991458 | T | TATATATA others(5): Show |
1 | a0001c0004t0009g0287 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1714+539_1714+540i others(14): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991458 | |||||||
| chr12:49991459 | A | T | 1 | a0001c0001t0001g0257 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1714+539T>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991459 | |||||||
| chr12:49991475 | ATATATTT others(3): Show |
A | 1 | a0001c0001t0001g0063 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1714+513_1714+522d others(12): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991475 | |||||||
| chr12:49991477 | A | AT | 4 | a0001c0001t0001g0003 a0001c0001t0001g0235 a0001c0001t0001g0237 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1714+520dupA | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991477 | |||||||
| chr12:49991477 | A | T | 1 | a0001c0001t0001g0003 | 2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1714+521T>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991477 | |||||||
| chr12:49991477 | ATAT | A | 16 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0258 others(13): Show |
16 | HG01884.hp1 HG02109.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.1714+518_1714+520d others(5): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991477 | |||||||
| chr12:49991477 | ATATTTTT others(2): Show |
A | 11 | a0001c0001t0001g0011 a0001c0001t0001g0049 a0001c0001t0001g0053 others(8): Show |
11 | HG01192.hp1 HG02630.hp2 HG02735.hp1 others(8): Show |
intron_variant | MODIFIER | c.1714+512_1714+520d others(11): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991477 | |||||||
| chr12:49991477 | ATATTTTT others(3): Show |
A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0052 a0001c0001t0001g0074 |
4 | HG01433.hp2 HG01496.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.1714+511_1714+520d others(12): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991477 | |||||||
| chr12:49991477 | ATATTTTT others(4): Show |
A | 1 | a0001c0001t0001g0057 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1714+510_1714+520d others(13): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991477 | |||||||
| chr12:49991479 | A | ATATATAT others(4): Show |
3 | a0001c0001t0001g0230 a0001c0001t0001g0244 a0001c0001t0001g0247 |
3 | HG02145.hp2 HG02976.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1714+518_1714+519i others(13): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(8): Show |
2 | a0001c0001t0001g0019 a0001c0001t0001g0132 |
2 | HG02155.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1714+518_1714+519i others(17): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(10): Show |
5 | a0001c0001t0001g0020 a0001c0001t0001g0124 a0001c0001t0001g0148 others(2): Show |
6 | NA18944.hp2 NA18964.hp1 NA19003.hp1 others(3): Show |
intron_variant | MODIFIER | c.1714+518_1714+519i others(19): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(12): Show |
3 | a0001c0001t0001g0002 a0001c0001t0001g0196 a0001c0002t0001g0009 |
3 | HG01952.hp2 HG02273.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1714+518_1714+519i others(21): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0007 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1714+518_1714+519i others(23): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0184 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1714+518_1714+519i others(25): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(18): Show |
1 | a0001c0001t0001g0018 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1714+518_1714+519i others(27): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(20): Show |
1 | a0001c0001t0001g0213 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1714+518_1714+519i others(29): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(17): Show |
3 | a0001c0001t0001g0007 a0001c0001t0001g0175 a0001c0001t0001g0207 |
3 | HG00733.hp2 HG00735.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.1714+518_1714+519i others(26): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(26): Show |
1 | a0001c0001t0007g0122 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1714+518_1714+519i others(35): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0208 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1714+518_1714+519i others(24): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(16): Show |
2 | a0001c0001t0001g0016 a0001c0001t0001g0224 |
2 | HG01168.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.1714+518_1714+519i others(25): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(23): Show |
1 | a0002c0003t0001g0046 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1714+518_1714+519i others(32): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0007 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1714+518_1714+519i others(22): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(15): Show |
2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | NA18950.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1714+518_1714+519i others(24): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0174 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1714+518_1714+519i others(25): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(17): Show |
1 | a0001c0002t0001g0008 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1714+518_1714+519i others(26): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(19): Show |
1 | a0002c0003t0001g0045 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1714+518_1714+519i others(28): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(23): Show |
1 | a0002c0003t0001g0047 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1714+518_1714+519i others(32): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(11): Show |
3 | a0001c0001t0001g0125 a0001c0001t0001g0165 a0001c0002t0001g0009 |
3 | HG01496.hp2 HG03471.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1714+518_1714+519i others(20): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(12): Show |
4 | a0001c0001t0001g0080 a0001c0001t0001g0167 a0001c0001t0001g0168 others(1): Show |
4 | HG02145.hp1 NA18952.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.1714+518_1714+519i others(21): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0164 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1714+518_1714+519i others(22): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(14): Show |
4 | a0001c0001t0001g0014 a0001c0001t0001g0154 a0001c0002t0001g0040 others(1): Show |
4 | HG02922.hp1 HG02922.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.1714+518_1714+519i others(23): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(15): Show |
1 | a0001c0002t0001g0039 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1714+518_1714+519i others(24): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(16): Show |
1 | a0001c0002t0001g0032 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1714+518_1714+519i others(25): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(9): Show |
12 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0105 others(9): Show |
14 | HG00642.hp2 HG01978.hp2 HG03927.hp1 others(11): Show |
intron_variant | MODIFIER | c.1714+518_1714+519i others(18): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0016 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1714+518_1714+519i others(19): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(11): Show |
2 | a0001c0001t0001g0186 a0001c0001t0001g0286 |
2 | HG00642.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1714+518_1714+519i others(20): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0126 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1714+518_1714+519i others(21): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(13): Show |
3 | a0001c0001t0001g0014 a0001c0002t0001g0271 a0001c0002t0003g0043 |
3 | HG02055.hp1 HG02615.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.1714+518_1714+519i others(22): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(14): Show |
3 | a0001c0002t0001g0031 a0001c0002t0001g0033 a0001c0002t0001g0273 |
3 | HG02257.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1714+518_1714+519i others(23): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(15): Show |
2 | a0001c0002t0001g0255 a0001c0002t0001g0272 |
2 | HG02055.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1714+518_1714+519i others(24): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(19): Show |
1 | a0001c0002t0001g0034 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1714+518_1714+519i others(28): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(7): Show |
3 | a0001c0001t0001g0006 a0001c0001t0001g0145 a0001c0001t0001g0209 |
3 | HG02027.hp1 HG02300.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.1714+518_1714+519i others(16): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(8): Show |
4 | a0001c0001t0001g0017 a0001c0001t0001g0120 a0001c0001t0001g0158 others(1): Show |
4 | HG02040.hp1 HG02074.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1714+518_1714+519i others(17): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(9): Show |
4 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0180 others(1): Show |
4 | HG00099.hp2 HG01361.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.1714+518_1714+519i others(18): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(10): Show |
2 | a0001c0001t0001g0142 a0001c0002t0003g0041 |
2 | HG02148.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1714+518_1714+519i others(19): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(12): Show |
2 | a0001c0002t0001g0008 a0001c0002t0001g0038 |
2 | HG02622.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1714+518_1714+519i others(21): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(14): Show |
1 | a0001c0002t0003g0042 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1714+518_1714+519i others(23): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(15): Show |
2 | a0001c0001t0001g0191 a0003c0006t0001g0036 |
2 | HG02809.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1714+518_1714+519i others(24): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(5): Show |
7 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0097 others(4): Show |
7 | HG01433.hp1 HG01928.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.1714+518_1714+519i others(14): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(6): Show |
2 | a0001c0001t0001g0013 a0001c0001t0001g0108 |
2 | HG01358.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1714+518_1714+519i others(15): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(7): Show |
2 | a0001c0001t0001g0155 a0001c0001t0001g0163 |
2 | NA19003.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1714+518_1714+519i others(16): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(11): Show |
1 | a0001c0002t0001g0035 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1714+518_1714+519i others(20): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(12): Show |
1 | a0001c0002t0001g0037 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1714+518_1714+519i others(21): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0089 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1714+518_1714+519i others(12): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(4): Show |
1 | a0001c0002t0001g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1714+518_1714+519i others(13): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0257 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1714+518_1714+519i others(16): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0094 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1714+518_1714+519i others(12): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | A | T | 10 | a0001c0001t0001g0003 a0001c0001t0001g0234 a0001c0001t0001g0235 others(7): Show |
13 | HG01361.hp2 HG02257.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1714+519T>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991479 | ATTTTTTT others(2): Show |
A | 18 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(15): Show |
26 | HG01081.hp1 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.1714+510_1714+518d others(11): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991479 | |||||||
| chr12:49991480 | T | TATATATA others(2): Show |
3 | a0001c0001t0001g0099 a0001c0001t0001g0198 a0001c0001t0001g0218 |
3 | HG03710.hp1 NA18948.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1714+517_1714+518i others(11): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991480 | |||||||
| chr12:49991480 | T | TATATATA others(4): Show |
4 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0151 others(1): Show |
4 | HG01074.hp1 HG02040.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.1714+517_1714+518i others(13): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991480 | |||||||
| chr12:49991480 | T | TATATATA others(6): Show |
1 | a0001c0001t0001g0223 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1714+517_1714+518i others(15): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991480 | |||||||
| chr12:49991480 | T | TATATATA others(8): Show |
1 | a0001c0001t0001g0152 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1714+517_1714+518i others(17): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991480 | |||||||
| chr12:49991480 | T | TATATATA others(10): Show |
5 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0176 others(2): Show |
5 | HG01070.hp2 HG02027.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.1714+517_1714+518i others(19): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991480 | |||||||
| chr12:49991480 | T | TATATATA others(16): Show |
3 | a0001c0001t0001g0018 a0001c0001t0001g0177 a0001c0001t0001g0178 |
3 | HG00673.hp1 NA18747.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.1714+517_1714+518i others(25): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991480 | |||||||
| chr12:49991481 | T | A | 26 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0079 others(23): Show |
28 | HG00099.hp1 HG01070.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.1714+517A>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991481 | |||||||
| chr12:49991482 | T | A | 9 | a0001c0001t0001g0022 a0001c0001t0001g0177 a0001c0001t0001g0178 others(6): Show |
9 | HG00673.hp1 HG02015.hp1 HG02273.hp1 others(6): Show |
intron_variant | MODIFIER | c.1714+516A>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991482 | |||||||
| chr12:49991483 | T | A | 3 | a0001c0001t0001g0021 a0001c0001t0001g0115 a0001c0001t0001g0147 |
3 | HG01071.hp2 HG01358.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.1714+515A>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991483 | |||||||
| chr12:49991484 | T | A | 1 | a0001c0002t0001g0030 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1714+514A>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991484 | |||||||
| chr12:49991486 | T | A | 2 | a0001c0001t0001g0068 a0001c0002t0001g0030 |
2 | HG00738.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1714+512A>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991486 | |||||||
| chr12:49991488 | T | A | 2 | a0001c0001t0001g0068 a0001c0002t0001g0030 |
2 | HG00738.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1714+510A>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991488 | |||||||
| chr12:49991489 | T | A | 1 | a0001c0001t0001g0061 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1714+509A>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991489 | |||||||
| chr12:49991490 | T | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(4): Show |
9 | HG00738.hp2 HG01081.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.1714+508A>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991490 | |||||||
| chr12:49991492 | T | A | 1 | a0001c0002t0001g0030 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1714+506A>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991492 | |||||||
| chr12:49991494 | T | A | 1 | a0001c0002t0001g0030 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1714+504A>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991494 | |||||||
| chr12:49991496 | T | A | 1 | a0001c0002t0001g0030 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1714+502A>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991496 | |||||||
| chr12:49991498 | T | A | 1 | a0001c0002t0001g0030 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1714+500A>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991498 | |||||||
| chr12:49991507 | T | A | 2 | a0001c0002t0001g0027 a0001c0002t0001g0028 |
2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1714+491A>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991507 | |||||||
| chr12:49991615 | G | C | 1 | a0001c0001t0001g0139 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1714+383C>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991615 | |||||||
| chr12:49991853 | CA | C | 4 | a0001c0001t0001g0020 a0001c0001t0001g0084 a0001c0001t0001g0134 others(1): Show |
5 | NA18612.hp1 NA18949.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.1714+144delT | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991853 | |||||||
| chr12:49991873 | A | G | 1 | a0001c0001t0001g0083 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1714+125T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991873 | |||||||
| chr12:49991880 | T | C | 32 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(29): Show |
38 | HG00099.hp1 HG00673.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.1714+118A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991880 | |||||||
| chr12:49991898 | G | A | 1 | a0001c0001t0001g0214 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1714+100C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 15/16 | chr12 | 49991898 | |||||||
| chr12:49992147 | A | C | 1 | a0001c0001t0001g0181 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1579-14T>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 14/16 | chr12 | 49992147 | |||||||
| chr12:49992224 | C | A | 2 | a0001c0001t0001g0186 a0001c0001t0001g0191 |
2 | NA19058.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1578+21G>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 14/16 | chr12 | 49992224 | |||||||
| chr12:49992232 | C | T | 177 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(174): Show |
196 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(193): Show |
intron_variant | MODIFIER | c.1578+13G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 14/16 | chr12 | 49992232 | |||||||
| chr12:49992480 | C | A | 1 | a0001c0001t0001g0227 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1445+70G>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 13/16 | chr12 | 49992480 | |||||||
| chr12:49992505 | G | GA | 27 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(24): Show |
30 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1445+44dupT | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 13/16 | chr12 | 49992505 | |||||||
| chr12:49992804 | C | A | 1 | a0001c0001t0001g0024 | 2 | NA19079.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1340-149G>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 12/16 | chr12 | 49992804 | |||||||
| chr12:49992850 | T | A | 1 | a0001c0001t0001g0174 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1340-195A>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 12/16 | chr12 | 49992850 | |||||||
| chr12:49992907 | C | G | 3 | a0001c0001t0001g0085 a0001c0001t0001g0092 a0001c0001t0001g0093 |
3 | HG02976.hp1 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1340-252G>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 12/16 | chr12 | 49992907 | |||||||
| chr12:49992997 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1340-342A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 12/16 | chr12 | 49992997 | |||||||
| chr12:49992998 | G | A | 2 | a0001c0002t0001g0027 a0001c0002t0001g0028 |
2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1340-343C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 12/16 | chr12 | 49992998 | |||||||
| chr12:49993318 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1340-663A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 12/16 | chr12 | 49993318 | |||||||
| chr12:49993381 | G | A | 1 | a0001c0001t0001g0133 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1340-726C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 12/16 | chr12 | 49993381 | |||||||
| chr12:49993470 | T | C | 27 | a0001c0001t0001g0244 a0001c0002t0001g0008 a0001c0002t0001g0009 others(24): Show |
29 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.1339+661A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 12/16 | chr12 | 49993470 | |||||||
| chr12:49993618 | TA | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(58): Show |
73 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(70): Show |
intron_variant | MODIFIER | c.1339+512delT | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 12/16 | chr12 | 49993618 | |||||||
| chr12:49993704 | G | A | 34 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(31): Show |
44 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.1339+427C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 12/16 | chr12 | 49993704 | |||||||
| chr12:49993746 | T | TA | 201 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(198): Show |
222 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(219): Show |
intron_variant | MODIFIER | c.1339+384dupT | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 12/16 | chr12 | 49993746 | |||||||
| chr12:49993813 | G | A | 1 | a0001c0002t0001g0035 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1339+318C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 12/16 | chr12 | 49993813 | |||||||
| chr12:49993818 | A | G | 61 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(58): Show |
73 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(70): Show |
intron_variant | MODIFIER | c.1339+313T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 12/16 | chr12 | 49993818 | |||||||
| chr12:49993841 | C | T | 1 | a0001c0001t0001g0264 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1339+290G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 12/16 | chr12 | 49993841 | |||||||
| chr12:49993978 | G | T | 1 | a0001c0001t0001g0053 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1339+153C>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 12/16 | chr12 | 49993978 | |||||||
| chr12:49994087 | C | T | 26 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0027 others(23): Show |
28 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.1339+44G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 12/16 | chr12 | 49994087 | |||||||
| chr12:49994514 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG02300.hp1 | splice_region_variant&intron_variant | LOW | c.1045-5T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49994514 | |||||||
| chr12:49994913 | C | T | 26 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0027 others(23): Show |
28 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.1045-404G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49994913 | |||||||
| chr12:49994938 | T | C | 21 | a0001c0001t0001g0020 a0001c0001t0001g0084 a0001c0001t0001g0134 others(18): Show |
22 | HG00438.hp2 HG00544.hp2 HG01952.hp2 others(19): Show |
intron_variant | MODIFIER | c.1045-429A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49994938 | |||||||
| chr12:49995015 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1045-506G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49995015 | |||||||
| chr12:49995262 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1045-753G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49995262 | |||||||
| chr12:49995288 | T | C | 27 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(24): Show |
30 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1045-779A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49995288 | |||||||
| chr12:49995349 | A | AAAAAC | 30 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(27): Show |
33 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.1045-845_1045-841d others(7): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49995349 | |||||||
| chr12:49995349 | A | AAAAACAA others(3): Show |
2 | a0001c0001t0001g0151 a0001c0001t0001g0153 |
2 | HG01074.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1045-850_1045-841d others(12): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49995349 | |||||||
| chr12:49995349 | AAAAAC | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(58): Show |
73 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(70): Show |
intron_variant | MODIFIER | c.1045-845_1045-841d others(7): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49995349 | |||||||
| chr12:49995494 | T | C | 9 | a0001c0001t0001g0020 a0001c0001t0001g0084 a0001c0001t0001g0134 others(6): Show |
10 | HG01952.hp2 HG02027.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.1045-985A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49995494 | |||||||
| chr12:49995561 | C | T | 34 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(31): Show |
44 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.1045-1052G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49995561 | |||||||
| chr12:49995787 | A | G | 63 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(60): Show |
75 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(72): Show |
intron_variant | MODIFIER | c.1044+1253T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49995787 | |||||||
| chr12:49995929 | A | C | 1 | a0001c0002t0001g0034 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1044+1111T>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49995929 | |||||||
| chr12:49996019 | A | G | 29 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0027 others(26): Show |
31 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.1044+1021T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996019 | |||||||
| chr12:49996060 | C | T | 27 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(24): Show |
36 | HG00738.hp2 HG01081.hp1 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.1044+980G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996060 | |||||||
| chr12:49996164 | A | G | 27 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(24): Show |
30 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1044+876T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996164 | |||||||
| chr12:49996233 | G | C | 1 | a0003c0006t0001g0036 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1044+807C>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996233 | |||||||
| chr12:49996320 | G | A | 90 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(87): Show |
105 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(102): Show |
intron_variant | MODIFIER | c.1044+720C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996320 | |||||||
| chr12:49996555 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1044+485C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996555 | |||||||
| chr12:49996613 | C | T | 4 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0057 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1044+427G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996613 | |||||||
| chr12:49996628 | T | TA | 12 | a0001c0001t0001g0002 a0001c0001t0001g0117 a0001c0001t0001g0118 others(9): Show |
13 | HG00733.hp2 HG00735.hp1 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.1044+411dupT | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996628 | |||||||
| chr12:49996628 | T | TAA | 16 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0081 others(13): Show |
18 | HG00733.hp1 HG00738.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.1044+410_1044+411d others(4): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996628 | |||||||
| chr12:49996628 | T | TAAA | 22 | a0001c0001t0001g0017 a0001c0001t0001g0084 a0001c0001t0001g0110 others(19): Show |
22 | HG01168.hp2 HG01169.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.1044+409_1044+411d others(5): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996628 | |||||||
| chr12:49996628 | T | TAAAA | 19 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(16): Show |
20 | HG00099.hp2 HG00544.hp2 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.1044+408_1044+411d others(6): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996628 | |||||||
| chr12:49996628 | T | TAAAAA | 8 | a0001c0001t0001g0007 a0001c0001t0001g0136 a0001c0001t0001g0176 others(5): Show |
8 | HG00438.hp2 HG00597.hp2 HG03927.hp2 others(5): Show |
intron_variant | MODIFIER | c.1044+407_1044+411d others(7): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996628 | |||||||
| chr12:49996628 | T | TAAAAAAA | 9 | a0001c0001t0001g0015 a0001c0001t0001g0123 a0001c0001t0001g0137 others(6): Show |
9 | HG00673.hp1 HG01256.hp1 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.1044+405_1044+411d others(9): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996628 | |||||||
| chr12:49996628 | T | TAAAAAAA others(2): Show |
9 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0127 others(6): Show |
9 | HG02027.hp1 HG02155.hp1 HG02273.hp1 others(6): Show |
intron_variant | MODIFIER | c.1044+403_1044+411d others(11): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996628 | |||||||
| chr12:49996628 | T | TAAAAAAA others(3): Show |
10 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0021 others(7): Show |
10 | HG01081.hp2 HG01175.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.1044+402_1044+411d others(12): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996628 | |||||||
| chr12:49996628 | T | TAAAAAAA others(4): Show |
4 | a0001c0001t0001g0018 a0001c0001t0001g0199 a0001c0001t0001g0200 others(1): Show |
4 | HG00544.hp1 HG02074.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1044+401_1044+411d others(13): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996628 | |||||||
| chr12:49996628 | T | TAAAAAAA others(5): Show |
5 | a0001c0001t0001g0092 a0001c0001t0001g0100 a0001c0001t0001g0124 others(2): Show |
5 | HG03209.hp1 HG03516.hp1 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.1044+400_1044+411d others(14): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996628 | |||||||
| chr12:49996628 | T | TAAAAAAA others(6): Show |
1 | a0001c0001t0001g0216 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1044+399_1044+411d others(15): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996628 | |||||||
| chr12:49996628 | T | TAAAAAAA others(7): Show |
2 | a0001c0001t0001g0016 a0001c0001t0001g0220 |
2 | HG00597.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1044+398_1044+411d others(16): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996628 | |||||||
| chr12:49996628 | T | TAAAAAAA others(9): Show |
6 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0085 others(3): Show |
6 | HG02976.hp1 HG03130.hp2 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.1044+396_1044+411d others(18): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996628 | |||||||
| chr12:49996628 | T | TAAAAAAA others(12): Show |
1 | a0001c0002t0001g0034 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1044+393_1044+411d others(21): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996628 | |||||||
| chr12:49996628 | TAA | T | 9 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0223 others(6): Show |
10 | HG01361.hp2 HG02015.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1044+410_1044+411d others(4): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996628 | |||||||
| chr12:49996628 | TAAA | T | 11 | a0001c0001t0001g0012 a0001c0001t0001g0096 a0001c0001t0001g0101 others(8): Show |
11 | HG00735.hp2 HG02015.hp2 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.1044+409_1044+411d others(5): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996628 | |||||||
| chr12:49996628 | TAAAA | T | 14 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(11): Show |
15 | HG00642.hp1 HG00642.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.1044+408_1044+411d others(6): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996628 | |||||||
| chr12:49996628 | TAAAAA | T | 10 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0023 others(7): Show |
10 | HG00438.hp1 HG01358.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.1044+407_1044+411d others(7): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996628 | |||||||
| chr12:49996628 | TAAAAAAA others(2): Show |
T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0048 others(7): Show |
11 | HG01192.hp1 HG01981.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.1044+403_1044+411d others(11): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996628 | |||||||
| chr12:49996628 | TAAAAAAA others(3): Show |
T | 25 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(22): Show |
32 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.1044+402_1044+411d others(12): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996628 | |||||||
| chr12:49996628 | TAAAAAAA others(4): Show |
T | 3 | a0001c0001t0001g0061 a0001c0001t0001g0115 a0001c0001t0001g0116 |
3 | HG01123.hp1 HG01358.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1044+401_1044+411d others(13): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996628 | |||||||
| chr12:49996628 | TAAAAAAA others(5): Show |
T | 6 | a0001c0001t0001g0006 a0001c0001t0001g0113 a0001c0001t0001g0114 others(3): Show |
7 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1044+400_1044+411d others(14): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996628 | |||||||
| chr12:49996628 | TAAAAAAA others(8): Show |
T | 3 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 |
3 | NA18747.hp1 NA18946.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.1044+397_1044+411d others(17): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996628 | |||||||
| chr12:49996628 | TAAAAAAA others(9): Show |
T | 6 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(3): Show |
6 | HG02723.hp1 HG02809.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.1044+396_1044+411d others(18): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996628 | |||||||
| chr12:49996628 | TAAAAAAA others(10): Show |
T | 1 | a0001c0001t0001g0094 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1044+395_1044+411d others(19): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996628 | |||||||
| chr12:49996628 | TAAAAAAA others(11): Show |
T | 1 | a0001c0001t0001g0257 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1044+394_1044+411d others(20): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996628 | |||||||
| chr12:49996628 | TAAAAAAA others(12): Show |
T | 1 | a0001c0001t0001g0259 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1044+393_1044+411d others(21): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996628 | |||||||
| chr12:49996628 | TAAAAAAA others(14): Show |
T | 1 | a0001c0001t0001g0275 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1044+391_1044+411d others(23): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996628 | |||||||
| chr12:49996628 | TAAAAAAA others(15): Show |
T | 1 | a0001c0001t0001g0172 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1044+390_1044+411d others(24): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996628 | |||||||
| chr12:49996631 | A | T | 1 | a0001c0001t0001g0235 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1044+409T>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996631 | |||||||
| chr12:49996650 | AAAAAAAA others(12): Show |
A | 1 | a0001c0002t0001g0038 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1044+371_1044+389d others(21): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996650 | |||||||
| chr12:49996651 | AAAAAAAA others(11): Show |
A | 2 | a0001c0002t0001g0008 a0001c0002t0001g0039 |
2 | HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1044+371_1044+388d others(20): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996651 | |||||||
| chr12:49996655 | AAAAAAAA others(7): Show |
A | 3 | a0001c0002t0001g0032 a0001c0002t0001g0040 a0001c0002t0001g0270 |
3 | HG02258.hp1 HG02922.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1044+371_1044+384d others(16): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996655 | |||||||
| chr12:49996657 | AAAAAAAA others(5): Show |
A | 3 | a0001c0002t0001g0271 a0001c0002t0001g0272 a0001c0002t0001g0273 |
3 | HG02055.hp2 HG02257.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1044+371_1044+382d others(14): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996657 | |||||||
| chr12:49996668 | A | AAT | 9 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0263 others(6): Show |
10 | HG02970.hp1 HG03486.hp1 HG03516.hp2 others(7): Show |
intron_variant | MODIFIER | c.1044+371_1044+372i others(4): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996668 | |||||||
| chr12:49996668 | A | AT | 6 | a0001c0001t0001g0024 a0001c0001t0001g0262 a0001c0001t0001g0264 others(3): Show |
6 | HG03130.hp1 NA18954.hp1 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.1044+371dupA | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996668 | |||||||
| chr12:49996668 | A | T | 7 | a0001c0001t0001g0259 a0001c0001t0001g0274 a0001c0001t0001g0275 others(4): Show |
7 | HG02109.hp1 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1044+372T>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996668 | |||||||
| chr12:49996668 | AT | A | 6 | a0001c0002t0001g0028 a0001c0002t0003g0041 a0001c0002t0003g0042 others(3): Show |
6 | HG01884.hp2 HG02630.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1044+371delA | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996668 | |||||||
| chr12:49996669 | T | A | 11 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0027 others(8): Show |
12 | HG02109.hp2 HG02559.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1044+371A>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996669 | |||||||
| chr12:49996908 | C | T | 1 | a0001c0001t0001g0021 | 2 | HG02083.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.1044+132G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 10/16 | chr12 | 49996908 | |||||||
| chr12:49997252 | T | C | 6 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0186 others(3): Show |
6 | NA18950.hp1 NA18955.hp2 NA19058.hp1 others(3): Show |
intron_variant | MODIFIER | c.880-48A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 9/16 | chr12 | 49997252 | |||||||
| chr12:49997272 | C | CT | 11 | a0001c0001t0001g0109 a0001c0001t0001g0120 a0001c0001t0001g0124 others(8): Show |
11 | HG00673.hp1 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.880-69dupA | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 9/16 | chr12 | 49997272 | |||||||
| chr12:49997272 | CT | C | 40 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(37): Show |
50 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.880-69delA | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 9/16 | chr12 | 49997272 | |||||||
| chr12:49997272 | CTT | C | 54 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(51): Show |
59 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(56): Show |
intron_variant | MODIFIER | c.880-70_880-69delAA | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 9/16 | chr12 | 49997272 | |||||||
| chr12:49997314 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.880-110C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 9/16 | chr12 | 49997314 | |||||||
| chr12:49997398 | C | T | 29 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0027 others(26): Show |
31 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.880-194G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 9/16 | chr12 | 49997398 | |||||||
| chr12:49997427 | A | G | 2 | a0001c0002t0001g0027 a0001c0002t0001g0028 |
2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.880-223T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 9/16 | chr12 | 49997427 | |||||||
| chr12:49997535 | A | G | 1 | a0001c0001t0001g0153 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.880-331T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 9/16 | chr12 | 49997535 | |||||||
| chr12:49997681 | G | A | 2 | a0001c0002t0001g0032 a0001c0002t0001g0037 |
2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.880-477C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 9/16 | chr12 | 49997681 | |||||||
| chr12:49997726 | C | T | 1 | a0001c0001t0001g0010 | 2 | HG01433.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.880-522G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 9/16 | chr12 | 49997726 | |||||||
| chr12:49997738 | C | A | 1 | a0001c0001t0001g0224 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.880-534G>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 9/16 | chr12 | 49997738 | |||||||
| chr12:49997805 | C | T | 9 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0124 others(6): Show |
11 | HG00597.hp1 HG02074.hp1 NA18946.hp2 others(8): Show |
intron_variant | MODIFIER | c.880-601G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 9/16 | chr12 | 49997805 | |||||||
| chr12:49997885 | A | T | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.880-681T>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 9/16 | chr12 | 49997885 | |||||||
| chr12:49997973 | A | T | 26 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0029 others(23): Show |
28 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.880-769T>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 9/16 | chr12 | 49997973 | |||||||
| chr12:49998061 | A | C | 34 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(31): Show |
44 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.880-857T>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 9/16 | chr12 | 49998061 | |||||||
| chr12:49998140 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.880-936G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 9/16 | chr12 | 49998140 | |||||||
| chr12:49998334 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.879+807C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 9/16 | chr12 | 49998334 | |||||||
| chr12:49998505 | G | A | 1 | a0001c0002t0001g0035 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.879+636C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 9/16 | chr12 | 49998505 | |||||||
| chr12:49998635 | C | T | 5 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(2): Show |
5 | HG02109.hp1 HG02572.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.879+506G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 9/16 | chr12 | 49998635 | |||||||
| chr12:49998760 | G | T | 26 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0027 others(23): Show |
28 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.879+381C>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 9/16 | chr12 | 49998760 | |||||||
| chr12:49998890 | T | G | 2 | a0001c0001t0001g0123 a0001c0001t0001g0127 |
2 | NA18939.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.879+251A>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 9/16 | chr12 | 49998890 | |||||||
| chr12:49999582 | T | C | 5 | a0001c0001t0001g0083 a0001c0001t0001g0132 a0001c0001t0001g0133 others(2): Show |
5 | NA18966.hp1 NA19000.hp1 NA19065.hp2 others(2): Show |
intron_variant | MODIFIER | c.748+34A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 8/16 | chr12 | 49999582 | |||||||
| chr12:49999589 | G | T | 177 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(174): Show |
196 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(193): Show |
intron_variant | MODIFIER | c.748+27C>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 8/16 | chr12 | 49999589 | |||||||
| chr12:49999613 | G | A | 1 | a0001c0004t0009g0287 | 1 | HG02717.hp1 | splice_region_variant&intron_variant | LOW | c.748+3C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 8/16 | chr12 | 49999613 | |||||||
| chr12:49999801 | T | C | 2 | a0001c0001t0001g0143 a0001c0001t0001g0217 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.631-68A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 7/16 | chr12 | 49999801 | |||||||
| chr12:49999828 | T | C | 1 | a0001c0001t0001g0257 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.631-95A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 7/16 | chr12 | 49999828 | |||||||
| chr12:49999852 | C | A | 3 | a0001c0001t0001g0083 a0001c0001t0001g0133 a0001c0001t0001g0137 |
3 | NA18966.hp1 NA19000.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.631-119G>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 7/16 | chr12 | 49999852 | |||||||
| chr12:49999898 | C | G | 3 | a0002c0003t0001g0045 a0002c0003t0001g0046 a0002c0003t0001g0047 |
3 | HG02630.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.631-165G>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 7/16 | chr12 | 49999898 | |||||||
| chr12:49999932 | A | C | 1 | a0001c0001t0001g0177 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.631-199T>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 7/16 | chr12 | 49999932 | |||||||
| chr12:50000018 | A | ATGTTTTT others(7): Show |
2 | a0001c0001t0001g0056 a0001c0001t0001g0062 |
2 | HG02735.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.631-286_631-285ins others(14): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 7/16 | chr12 | 50000018 | |||||||
| chr12:50000018 | A | ATGTTTTT others(8): Show |
1 | a0001c0001t0001g0055 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.631-286_631-285ins others(15): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 7/16 | chr12 | 50000018 | |||||||
| chr12:50000018 | A | ATGTTTTT others(9): Show |
26 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(23): Show |
36 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.631-286_631-285ins others(16): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 7/16 | chr12 | 50000018 | |||||||
| chr12:50000018 | A | ATGTTTTT others(10): Show |
5 | a0001c0001t0001g0049 a0001c0001t0001g0053 a0001c0001t0001g0060 others(2): Show |
5 | HG02630.hp2 HG03098.hp2 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.631-286_631-285ins others(17): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 7/16 | chr12 | 50000018 | |||||||
| chr12:50000018 | A | ATT | 24 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0029 others(21): Show |
26 | HG02055.hp1 HG02055.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.631-287_631-286dup others(2): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 7/16 | chr12 | 50000018 | |||||||
| chr12:50000018 | A | ATTTTTTT others(3): Show |
1 | a0001c0001t0002g0240 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.631-295_631-286dup others(10): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 7/16 | chr12 | 50000018 | |||||||
| chr12:50000018 | A | ATTTTTTT others(4): Show |
25 | a0001c0001t0001g0003 a0001c0001t0001g0098 a0001c0001t0001g0101 others(22): Show |
28 | HG01074.hp1 HG01109.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.631-296_631-286dup others(11): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 7/16 | chr12 | 50000018 | |||||||
| chr12:50000018 | A | ATTTTTTT others(6): Show |
33 | a0001c0001t0001g0013 a0001c0001t0001g0077 a0001c0001t0001g0080 others(30): Show |
34 | HG01346.hp2 HG01358.hp2 HG01934.hp2 others(31): Show |
intron_variant | MODIFIER | c.631-298_631-286dup others(13): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 7/16 | chr12 | 50000018 | |||||||
| chr12:50000018 | A | ATTTTTTT others(7): Show |
4 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0002t0001g0027 others(1): Show |
4 | HG02109.hp2 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.631-286_631-285ins others(14): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 7/16 | chr12 | 50000018 | |||||||
| chr12:50000036 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.631-303G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 7/16 | chr12 | 50000036 | |||||||
| chr12:50000045 | G | A | 2 | a0001c0002t0001g0027 a0001c0002t0001g0028 |
2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.631-312C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 7/16 | chr12 | 50000045 | |||||||
| chr12:50000058 | C | T | 29 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0027 others(26): Show |
31 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.631-325G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 7/16 | chr12 | 50000058 | |||||||
| chr12:50000099 | C | T | 5 | a0001c0001t0001g0088 a0001c0001t0001g0091 a0001c0001t0001g0094 others(2): Show |
5 | HG03491.hp1 HG03492.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.631-366G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 7/16 | chr12 | 50000099 | |||||||
| chr12:50000205 | G | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(3): Show |
8 | HG00738.hp2 HG01081.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.631-472C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 7/16 | chr12 | 50000205 | |||||||
| chr12:50000293 | G | A | 1 | a0001c0001t0001g0236 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.631-560C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 7/16 | chr12 | 50000293 | |||||||
| chr12:50000349 | G | A | 26 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0027 others(23): Show |
28 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.631-616C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 7/16 | chr12 | 50000349 | |||||||
| chr12:50000434 | C | T | 29 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0027 others(26): Show |
31 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.631-701G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 7/16 | chr12 | 50000434 | |||||||
| chr12:50000446 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.631-713G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 7/16 | chr12 | 50000446 | |||||||
| chr12:50000574 | C | G | 29 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0027 others(26): Show |
31 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.630+598G>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 7/16 | chr12 | 50000574 | |||||||
| chr12:50000635 | C | T | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(265): Show |
302 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(299): Show |
intron_variant | MODIFIER | c.630+537G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 7/16 | chr12 | 50000635 | |||||||
| chr12:50000661 | G | T | 1 | a0001c0001t0001g0236 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.630+511C>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 7/16 | chr12 | 50000661 | |||||||
| chr12:50000733 | T | C | 7 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0057 others(4): Show |
7 | HG01167.hp1 HG01169.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.630+439A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 7/16 | chr12 | 50000733 | |||||||
| chr12:50001009 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.630+163A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 7/16 | chr12 | 50001009 | |||||||
| chr12:50001378 | A | G | 1 | a0001c0001t0001g0069 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.550-126T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 6/16 | chr12 | 50001378 | |||||||
| chr12:50001419 | A | C | 1 | a0001c0001t0001g0158 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.550-167T>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 6/16 | chr12 | 50001419 | |||||||
| chr12:50001478 | A | G | 1 | a0001c0001t0001g0218 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.550-226T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 6/16 | chr12 | 50001478 | |||||||
| chr12:50001626 | A | G | 3 | a0002c0003t0001g0045 a0002c0003t0001g0046 a0002c0003t0001g0047 |
3 | HG02630.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.550-374T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 6/16 | chr12 | 50001626 | |||||||
| chr12:50001804 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.549+443C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 6/16 | chr12 | 50001804 | |||||||
| chr12:50001937 | G | T | 1 | a0001c0002t0001g0255 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.549+310C>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 6/16 | chr12 | 50001937 | |||||||
| chr12:50002072 | G | GA | 11 | a0001c0001t0001g0098 a0001c0001t0001g0204 a0001c0001t0001g0205 others(8): Show |
11 | HG01167.hp2 HG01361.hp2 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.549+174dupT | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 6/16 | chr12 | 50002072 | |||||||
| chr12:50002072 | GA | G | 35 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(32): Show |
45 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.549+174delT | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 6/16 | chr12 | 50002072 | |||||||
| chr12:50002103 | T | C | 4 | a0001c0001t0001g0020 a0001c0001t0001g0084 a0001c0001t0001g0134 others(1): Show |
5 | NA18612.hp1 NA18949.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.549+144A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 6/16 | chr12 | 50002103 | |||||||
| chr12:50002153 | G | A | 1 | a0001c0001t0001g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.549+94C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 6/16 | chr12 | 50002153 | |||||||
| chr12:50002203 | A | G | 4 | a0001c0001t0001g0236 a0002c0003t0001g0045 a0002c0003t0001g0046 others(1): Show |
4 | HG02630.hp1 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.549+44T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 6/16 | chr12 | 50002203 | |||||||
| chr12:50002218 | T | A | 26 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0027 others(23): Show |
28 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.549+29A>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 6/16 | chr12 | 50002218 | |||||||
| chr12:50002605 | T | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0278 |
3 | NA18939.hp2 NA19002.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.496-305A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 5/16 | chr12 | 50002605 | |||||||
| chr12:50002609 | T | C | 26 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0029 others(23): Show |
28 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.496-309A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 5/16 | chr12 | 50002609 | |||||||
| chr12:50002718 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.496-418A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 5/16 | chr12 | 50002718 | |||||||
| chr12:50002781 | A | G | 1 | a0001c0002t0001g0029 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.496-481T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 5/16 | chr12 | 50002781 | |||||||
| chr12:50002814 | T | G | 63 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(60): Show |
75 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(72): Show |
intron_variant | MODIFIER | c.496-514A>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 5/16 | chr12 | 50002814 | |||||||
| chr12:50002818 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.496-518C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 5/16 | chr12 | 50002818 | |||||||
| chr12:50002837 | C | A | 32 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(29): Show |
38 | HG00099.hp1 HG00673.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.496-537G>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 5/16 | chr12 | 50002837 | |||||||
| chr12:50002885 | G | A | 34 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(31): Show |
44 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.496-585C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 5/16 | chr12 | 50002885 | |||||||
| chr12:50002949 | G | A | 34 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(31): Show |
44 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.496-649C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 5/16 | chr12 | 50002949 | |||||||
| chr12:50002993 | T | C | 63 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(60): Show |
75 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(72): Show |
intron_variant | MODIFIER | c.496-693A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 5/16 | chr12 | 50002993 | |||||||
| chr12:50003023 | C | CA | 20 | a0001c0001t0001g0048 a0001c0001t0001g0059 a0001c0001t0001g0069 others(17): Show |
20 | HG00733.hp1 HG01109.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.496-724dupT | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 5/16 | chr12 | 50003023 | |||||||
| chr12:50003023 | CA | C | 29 | a0001c0001t0001g0099 a0001c0001t0001g0113 a0001c0001t0001g0144 others(26): Show |
31 | HG01256.hp2 HG01884.hp2 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.496-724delT | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 5/16 | chr12 | 50003023 | |||||||
| chr12:50003052 | A | G | 29 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0027 others(26): Show |
31 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.496-752T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 5/16 | chr12 | 50003052 | |||||||
| chr12:50003125 | A | G | 1 | a0001c0001t0001g0216 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.496-825T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 5/16 | chr12 | 50003125 | |||||||
| chr12:50003477 | C | G | 1 | a0001c0001t0001g0253 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.495+758G>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 5/16 | chr12 | 50003477 | |||||||
| chr12:50003773 | C | T | 6 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0186 others(3): Show |
6 | NA18950.hp1 NA18955.hp2 NA19058.hp1 others(3): Show |
intron_variant | MODIFIER | c.495+462G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 5/16 | chr12 | 50003773 | |||||||
| chr12:50003992 | C | T | 1 | a0001c0001t0001g0236 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.495+243G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 5/16 | chr12 | 50003992 | |||||||
| chr12:50004529 | A | G | 2 | a0001c0001t0001g0160 a0001c0001t0001g0164 |
2 | HG01109.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.426-225T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 4/16 | chr12 | 50004529 | |||||||
| chr12:50005057 | A | T | 1 | a0001c0001t0001g0256 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.425+199T>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 4/16 | chr12 | 50005057 | |||||||
| chr12:50005121 | A | T | 1 | a0001c0001t0001g0188 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.425+135T>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 4/16 | chr12 | 50005121 | |||||||
| chr12:50005130 | A | G | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(265): Show |
302 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(299): Show |
intron_variant | MODIFIER | c.425+126T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 4/16 | chr12 | 50005130 | |||||||
| chr12:50005161 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.425+95T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 4/16 | chr12 | 50005161 | |||||||
| chr12:50005471 | C | T | 23 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0022 others(20): Show |
27 | HG00438.hp1 HG00642.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.289-79G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 3/16 | chr12 | 50005471 | |||||||
| chr12:50005605 | C | T | 2 | a0001c0001t0001g0089 a0001c0001t0001g0090 |
2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.289-213G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 3/16 | chr12 | 50005605 | |||||||
| chr12:50005692 | T | C | 7 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 others(4): Show |
7 | HG01891.hp1 HG02886.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.289-300A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 3/16 | chr12 | 50005692 | |||||||
| chr12:50005767 | A | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
102 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(99): Show |
intron_variant | MODIFIER | c.289-375T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 3/16 | chr12 | 50005767 | |||||||
| chr12:50006081 | C | T | 1 | a0001c0001t0001g0123 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.288+353G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 3/16 | chr12 | 50006081 | |||||||
| chr12:50006304 | T | C | 4 | a0001c0001t0001g0236 a0002c0003t0001g0045 a0002c0003t0001g0046 others(1): Show |
4 | HG02630.hp1 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.288+130A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 3/16 | chr12 | 50006304 | |||||||
| chr12:50006750 | A | G | 1 | a0001c0002t0001g0032 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.86-114T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50006750 | |||||||
| chr12:50006987 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.86-351A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50006987 | |||||||
| chr12:50007353 | A | G | 1 | a0001c0004t0009g0287 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.86-717T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50007353 | |||||||
| chr12:50007426 | A | G | 1 | a0001c0001t0001g0186 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.86-790T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50007426 | |||||||
| chr12:50007468 | G | A | 2 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
2 | HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.86-832C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50007468 | |||||||
| chr12:50007613 | T | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0199 a0001c0001t0001g0200 |
4 | HG02074.hp1 NA18953.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.86-977A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50007613 | |||||||
| chr12:50007622 | T | G | 1 | a0001c0001t0001g0148 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.86-986A>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50007622 | |||||||
| chr12:50007905 | G | GT | 30 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(27): Show |
33 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.86-1270dupA | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50007905 | |||||||
| chr12:50008033 | T | C | 1 | a0001c0001t0001g0236 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.86-1397A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50008033 | |||||||
| chr12:50008169 | G | GA | 72 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0019 others(69): Show |
78 | HG00544.hp1 HG00642.hp1 HG01070.hp1 others(75): Show |
intron_variant | MODIFIER | c.86-1534dupT | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50008169 | |||||||
| chr12:50008169 | G | GAA | 11 | a0001c0001t0001g0111 a0001c0001t0001g0135 a0001c0001t0001g0136 others(8): Show |
11 | HG00438.hp2 HG01169.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.86-1535_86-1534dup others(2): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50008169 | |||||||
| chr12:50008169 | G | GAAA | 17 | a0001c0002t0001g0008 a0001c0002t0001g0027 a0001c0002t0001g0031 others(14): Show |
18 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.86-1536_86-1534dup others(3): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50008169 | |||||||
| chr12:50008169 | G | GAAAA | 8 | a0001c0002t0001g0009 a0001c0002t0001g0028 a0001c0002t0001g0029 others(5): Show |
9 | HG02055.hp1 HG02055.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.86-1537_86-1534dup others(4): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50008169 | |||||||
| chr12:50008169 | GA | G | 25 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0052 others(22): Show |
28 | HG00099.hp1 HG00673.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.86-1534delT | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50008169 | |||||||
| chr12:50008169 | GAAAAAAA others(1): Show |
G | 21 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(18): Show |
30 | HG00738.hp2 HG01081.hp1 HG01261.hp2 others(27): Show |
intron_variant | MODIFIER | c.86-1541_86-1534del others(8): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50008169 | |||||||
| chr12:50008202 | C | CT | 30 | a0001c0001t0001g0108 a0001c0002t0001g0008 a0001c0002t0001g0009 others(27): Show |
32 | HG01884.hp2 HG01981.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.86-1567dupA | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50008202 | |||||||
| chr12:50008322 | C | T | 4 | a0001c0002t0001g0030 a0001c0002t0001g0034 a0001c0002t0001g0035 others(1): Show |
4 | HG02559.hp2 HG02647.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.86-1686G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50008322 | |||||||
| chr12:50008504 | T | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0076 |
2 | NA18949.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.86-1868A>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50008504 | |||||||
| chr12:50008784 | T | C | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(265): Show |
302 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(299): Show |
intron_variant | MODIFIER | c.86-2148A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50008784 | |||||||
| chr12:50009071 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.86-2435C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50009071 | |||||||
| chr12:50009147 | G | A | 29 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0027 others(26): Show |
31 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.86-2511C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50009147 | |||||||
| chr12:50009242 | C | CA | 15 | a0001c0001t0001g0108 a0001c0001t0001g0138 a0001c0001t0001g0140 others(12): Show |
16 | HG00544.hp2 HG01884.hp2 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.86-2607dupT | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50009242 | |||||||
| chr12:50009242 | C | CAA | 12 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(9): Show |
12 | HG02258.hp1 HG02559.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.86-2608_86-2607dup others(2): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50009242 | |||||||
| chr12:50009242 | C | CAAA | 5 | a0001c0002t0001g0008 a0001c0002t0001g0038 a0001c0002t0001g0039 others(2): Show |
6 | HG02258.hp2 HG02622.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.86-2609_86-2607dup others(3): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50009242 | |||||||
| chr12:50009242 | CA | C | 41 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(38): Show |
51 | HG00099.hp1 HG00738.hp2 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.86-2607delT | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50009242 | |||||||
| chr12:50009306 | C | T | 6 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 others(3): Show |
6 | HG01891.hp1 HG02886.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-2670G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50009306 | |||||||
| chr12:50009353 | A | T | 1 | a0001c0001t0005g0285 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.86-2717T>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50009353 | |||||||
| chr12:50009466 | A | AT | 176 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(173): Show |
195 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(192): Show |
intron_variant | MODIFIER | c.86-2831dupA | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50009466 | |||||||
| chr12:50009606 | C | G | 1 | a0001c0001t0001g0156 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.86-2970G>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50009606 | |||||||
| chr12:50009616 | A | G | 29 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0027 others(26): Show |
31 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.86-2980T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50009616 | |||||||
| chr12:50009753 | A | T | 3 | a0001c0001t0001g0085 a0001c0001t0001g0092 a0001c0001t0001g0093 |
3 | HG02976.hp1 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.86-3117T>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50009753 | |||||||
| chr12:50009891 | T | C | 1 | a0001c0001t0001g0257 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.86-3255A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50009891 | |||||||
| chr12:50009902 | C | G | 2 | a0001c0002t0001g0027 a0001c0002t0001g0028 |
2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.86-3266G>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50009902 | |||||||
| chr12:50010158 | A | T | 1 | a0001c0002t0001g0029 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.86-3522T>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50010158 | |||||||
| chr12:50010164 | C | T | 29 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0027 others(26): Show |
31 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.86-3528G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50010164 | |||||||
| chr12:50010167 | A | G | 3 | a0001c0002t0003g0041 a0001c0002t0003g0042 a0001c0002t0003g0043 |
3 | HG01884.hp2 HG02055.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.86-3531T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50010167 | |||||||
| chr12:50010213 | C | T | 2 | a0001c0001t0001g0175 a0001c0001t0001g0207 |
2 | HG00733.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.86-3577G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50010213 | |||||||
| chr12:50010270 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.86-3634G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50010270 | |||||||
| chr12:50010317 | A | AT | 4 | a0001c0002t0001g0031 a0001c0002t0001g0032 a0001c0002t0001g0033 others(1): Show |
4 | HG02258.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.86-3682_86-3681ins others(1): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50010317 | |||||||
| chr12:50010318 | C | CTT | 37 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(34): Show |
47 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(44): Show |
intron_variant | MODIFIER | c.86-3684_86-3683dup others(2): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50010318 | |||||||
| chr12:50010318 | C | CTTT | 21 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0029 others(18): Show |
23 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.86-3685_86-3683dup others(3): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50010318 | |||||||
| chr12:50010318 | C | T | 4 | a0001c0002t0001g0031 a0001c0002t0001g0032 a0001c0002t0001g0033 others(1): Show |
4 | HG02258.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.86-3682G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50010318 | |||||||
| chr12:50010361 | T | G | 26 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0029 others(23): Show |
28 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.86-3725A>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50010361 | |||||||
| chr12:50010427 | A | G | 63 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(60): Show |
75 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(72): Show |
intron_variant | MODIFIER | c.86-3791T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50010427 | |||||||
| chr12:50010481 | G | A | 34 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(31): Show |
44 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.86-3845C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50010481 | |||||||
| chr12:50010795 | G | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0048 |
4 | HG03139.hp2 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.86-4159C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50010795 | |||||||
| chr12:50010824 | C | T | 2 | a0001c0001t0001g0244 a0001c0001t0001g0247 |
2 | HG02145.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.86-4188G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50010824 | |||||||
| chr12:50010873 | A | G | 90 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(87): Show |
105 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(102): Show |
intron_variant | MODIFIER | c.86-4237T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50010873 | |||||||
| chr12:50010935 | C | CA | 282 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(279): Show |
319 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(316): Show |
intron_variant | MODIFIER | c.86-4300dupT | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50010935 | |||||||
| chr12:50010968 | G | A | 2 | a0001c0001t0001g0231 a0001c0001t0001g0232 |
2 | NA18981.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.86-4332C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50010968 | |||||||
| chr12:50011331 | C | CAA | 6 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(3): Show |
6 | HG01928.hp2 HG01975.hp1 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-4697_86-4696dup others(2): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50011331 | |||||||
| chr12:50011331 | CA | C | 63 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(60): Show |
76 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(73): Show |
intron_variant | MODIFIER | c.86-4696delT | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50011331 | |||||||
| chr12:50011455 | G | A | 7 | a0001c0002t0001g0008 a0001c0002t0001g0038 a0001c0002t0001g0039 others(4): Show |
8 | HG02258.hp2 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.86-4819C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50011455 | |||||||
| chr12:50011629 | T | C | 29 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0027 others(26): Show |
31 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.86-4993A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50011629 | |||||||
| chr12:50011640 | A | G | 2 | a0001c0001t0004g0248 a0001c0001t0004g0249 |
2 | HG02280.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.85+4991T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50011640 | |||||||
| chr12:50011771 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.85+4860G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50011771 | |||||||
| chr12:50011772 | G | A | 2 | a0001c0001t0001g0155 a0001c0001t0001g0163 |
2 | NA19003.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.85+4859C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50011772 | |||||||
| chr12:50011799 | C | A | 1 | a0001c0002t0001g0034 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.85+4832G>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50011799 | |||||||
| chr12:50011815 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.85+4816C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50011815 | |||||||
| chr12:50011886 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.85+4745C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50011886 | |||||||
| chr12:50011918 | T | C | 63 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(60): Show |
75 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(72): Show |
intron_variant | MODIFIER | c.85+4713A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50011918 | |||||||
| chr12:50011928 | T | C | 6 | a0001c0001t0001g0148 a0001c0001t0001g0204 a0001c0001t0001g0205 others(3): Show |
6 | HG00597.hp2 HG01928.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.85+4703A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50011928 | |||||||
| chr12:50011941 | G | A | 2 | a0001c0001t0001g0242 a0001c0001t0001g0251 |
2 | HG01361.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.85+4690C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50011941 | |||||||
| chr12:50011953 | C | CA | 40 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0087 others(37): Show |
44 | HG00438.hp1 HG00597.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.85+4677dupT | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50011953 | |||||||
| chr12:50011953 | CA | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(34): Show |
47 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(44): Show |
intron_variant | MODIFIER | c.85+4677delT | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50011953 | |||||||
| chr12:50011954 | A | C | 1 | a0001c0001t0001g0265 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.85+4677T>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50011954 | |||||||
| chr12:50012041 | T | C | 29 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0027 others(26): Show |
31 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.85+4590A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50012041 | |||||||
| chr12:50012118 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.85+4513T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50012118 | |||||||
| chr12:50012242 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.85+4389G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50012242 | |||||||
| chr12:50012243 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.85+4388C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50012243 | |||||||
| chr12:50012253 | C | T | 1 | a0001c0001t0007g0122 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.85+4378G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50012253 | |||||||
| chr12:50012411 | A | G | 1 | a0001c0001t0001g0067 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.85+4220T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50012411 | |||||||
| chr12:50012460 | C | A | 1 | a0001c0001t0001g0247 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.85+4171G>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50012460 | |||||||
| chr12:50012502 | G | A | 1 | a0001c0001t0001g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.85+4129C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50012502 | |||||||
| chr12:50012511 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.85+4120G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50012511 | |||||||
| chr12:50012570 | A | T | 27 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(24): Show |
30 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.85+4061T>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50012570 | |||||||
| chr12:50012574 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.85+4057T>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50012574 | |||||||
| chr12:50012578 | T | A | 4 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(1): Show |
4 | HG01074.hp2 NA18953.hp1 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+4053A>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50012578 | |||||||
| chr12:50012713 | C | T | 34 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(31): Show |
44 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.85+3918G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50012713 | |||||||
| chr12:50012853 | C | T | 1 | a0001c0001t0001g0048 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.85+3778G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50012853 | |||||||
| chr12:50012893 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.85+3738C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50012893 | |||||||
| chr12:50013028 | A | G | 27 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(24): Show |
30 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.85+3603T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50013028 | |||||||
| chr12:50013057 | CTT | C | 25 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0022 others(22): Show |
29 | HG00438.hp1 HG00642.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.85+3572_85+3573del others(2): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50013057 | |||||||
| chr12:50013235 | T | C | 1 | a0001c0002t0001g0037 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.85+3396A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50013235 | |||||||
| chr12:50013293 | A | G | 1 | a0001c0001t0005g0285 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.85+3338T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50013293 | |||||||
| chr12:50013316 | G | C | 7 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(4): Show |
7 | HG02723.hp1 HG02809.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.85+3315C>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50013316 | |||||||
| chr12:50013503 | T | C | 63 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(60): Show |
75 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(72): Show |
intron_variant | MODIFIER | c.85+3128A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50013503 | |||||||
| chr12:50014070 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.85+2561A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50014070 | |||||||
| chr12:50014282 | G | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(34): Show |
47 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(44): Show |
intron_variant | MODIFIER | c.85+2349C>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50014282 | |||||||
| chr12:50014293 | T | G | 38 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(35): Show |
48 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(45): Show |
intron_variant | MODIFIER | c.85+2338A>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50014293 | |||||||
| chr12:50014303 | T | C | 1 | a0001c0004t0009g0287 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.85+2328A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50014303 | |||||||
| chr12:50014375 | T | G | 1 | a0001c0001t0001g0257 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.85+2256A>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50014375 | |||||||
| chr12:50014436 | A | C | 1 | a0001c0001t0001g0169 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.85+2195T>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50014436 | |||||||
| chr12:50014495 | A | G | 1 | a0001c0001t0001g0015 | 2 | NA18950.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.85+2136T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50014495 | |||||||
| chr12:50014614 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.85+2017C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50014614 | |||||||
| chr12:50014991 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.85+1640G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50014991 | |||||||
| chr12:50015028 | G | A | 27 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(24): Show |
30 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.85+1603C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50015028 | |||||||
| chr12:50015042 | C | CA | 200 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(197): Show |
221 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(218): Show |
intron_variant | MODIFIER | c.85+1588dupT | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50015042 | |||||||
| chr12:50015167 | A | T | 1 | a0001c0001t0001g0171 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.85+1464T>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50015167 | |||||||
| chr12:50015217 | A | G | 34 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(31): Show |
44 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.85+1414T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50015217 | |||||||
| chr12:50015278 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.85+1353T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50015278 | |||||||
| chr12:50015398 | G | C | 1 | a0001c0001t0001g0014 | 2 | NA18944.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.85+1233C>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50015398 | |||||||
| chr12:50015671 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(88): Show |
106 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(103): Show |
intron_variant | MODIFIER | c.85+960C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50015671 | |||||||
| chr12:50015674 | C | T | 34 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(31): Show |
44 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.85+957G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50015674 | |||||||
| chr12:50015829 | T | A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(59): Show |
74 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(71): Show |
intron_variant | MODIFIER | c.85+802A>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50015829 | |||||||
| chr12:50015838 | A | T | 1 | a0001c0002t0001g0030 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.85+793T>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50015838 | |||||||
| chr12:50015838 | AT | A | 27 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(24): Show |
30 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.85+792delA | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50015838 | |||||||
| chr12:50015839 | T | A | 1 | a0001c0001t0001g0053 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.85+792A>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50015839 | |||||||
| chr12:50015842 | T | A | 1 | a0001c0001t0001g0165 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.85+789A>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50015842 | |||||||
| chr12:50016040 | C | T | 3 | a0002c0003t0001g0045 a0002c0003t0001g0046 a0002c0003t0001g0047 |
3 | HG02630.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.85+591G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50016040 | |||||||
| chr12:50016077 | A | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.85+554T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50016077 | |||||||
| chr12:50016088 | T | C | 2 | a0001c0001t0001g0143 a0001c0001t0001g0217 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.85+543A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50016088 | |||||||
| chr12:50016155 | G | A | 2 | a0001c0001t0004g0248 a0001c0001t0004g0249 |
2 | HG02280.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.85+476C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50016155 | |||||||
| chr12:50016244 | G | A | 27 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(24): Show |
30 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.85+387C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50016244 | |||||||
| chr12:50016290 | A | G | 3 | a0001c0001t0001g0024 a0001c0001t0001g0265 a0001c0001t0001g0266 |
4 | NA18962.hp2 NA18998.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+341T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50016290 | |||||||
| chr12:50016356 | T | A | 29 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0027 others(26): Show |
31 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.85+275A>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50016356 | |||||||
| chr12:50016442 | T | C | 1 | a0001c0001t0001g0218 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.85+189A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50016442 | |||||||
| chr12:50016496 | G | A | 7 | a0001c0001t0001g0013 a0001c0001t0001g0097 a0001c0001t0001g0104 others(4): Show |
8 | HG00642.hp2 HG00735.hp2 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.85+135C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 2/16 | chr12 | 50016496 | |||||||
| chr12:50016738 | T | C | 26 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0029 others(23): Show |
28 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.-4-19A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50016738 | |||||||
| chr12:50016750 | C | T | 34 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(31): Show |
44 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.-4-31G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50016750 | |||||||
| chr12:50016802 | C | A | 1 | a0001c0001t0001g0250 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-4-83G>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50016802 | |||||||
| chr12:50017048 | T | C | 29 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0027 others(26): Show |
31 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.-4-329A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50017048 | |||||||
| chr12:50017058 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-4-339A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50017058 | |||||||
| chr12:50017113 | T | A | 1 | a0001c0001t0001g0219 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-4-394A>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50017113 | |||||||
| chr12:50017224 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-4-505G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50017224 | |||||||
| chr12:50017409 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-4-690G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50017409 | |||||||
| chr12:50017669 | T | A | 6 | a0001c0001t0001g0021 a0001c0001t0001g0220 a0001c0001t0001g0221 others(3): Show |
7 | HG02015.hp1 HG02027.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.-4-950A>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50017669 | |||||||
| chr12:50017920 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-4-1201C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50017920 | |||||||
| chr12:50018003 | C | G | 2 | a0001c0001t0001g0001 a0001c0001t0001g0064 |
6 | HG02155.hp2 NA18957.hp2 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.-4-1284G>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50018003 | |||||||
| chr12:50018157 | C | CA | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(166): Show |
194 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(191): Show |
intron_variant | MODIFIER | c.-4-1439dupT | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50018157 | |||||||
| chr12:50018157 | CA | C | 8 | a0001c0001t0001g0088 a0001c0001t0001g0235 a0001c0001t0001g0258 others(5): Show |
8 | HG02559.hp1 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-4-1439delT | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50018157 | |||||||
| chr12:50018328 | C | A | 1 | a0001c0002t0001g0273 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-4-1609G>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50018328 | |||||||
| chr12:50018476 | G | A | 2 | a0001c0001t0001g0225 a0001c0001t0001g0226 |
2 | NA18946.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-4-1757C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50018476 | |||||||
| chr12:50018496 | T | C | 1 | a0001c0004t0009g0287 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-4-1777A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50018496 | |||||||
| chr12:50018680 | A | G | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | NA18955.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.-4-1961T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50018680 | |||||||
| chr12:50018699 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-4-1980G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50018699 | |||||||
| chr12:50018821 | A | T | 1 | a0001c0001t0001g0257 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-4-2102T>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50018821 | |||||||
| chr12:50018838 | A | AT | 30 | a0001c0001t0001g0096 a0001c0001t0001g0166 a0001c0002t0001g0008 others(27): Show |
32 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.-4-2120dupA | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50018838 | |||||||
| chr12:50018852 | A | T | 34 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(31): Show |
44 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.-4-2133T>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50018852 | |||||||
| chr12:50019065 | T | G | 2 | a0001c0002t0001g0035 a0003c0006t0001g0036 |
2 | HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-4-2346A>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50019065 | |||||||
| chr12:50019128 | C | A | 168 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(165): Show |
187 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(184): Show |
intron_variant | MODIFIER | c.-4-2409G>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50019128 | |||||||
| chr12:50019186 | C | G | 32 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(29): Show |
38 | HG00099.hp1 HG00673.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.-4-2467G>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50019186 | |||||||
| chr12:50019204 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-4-2485C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50019204 | |||||||
| chr12:50019232 | T | G | 282 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(279): Show |
319 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(316): Show |
intron_variant | MODIFIER | c.-4-2513A>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50019232 | |||||||
| chr12:50019251 | C | A | 16 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(13): Show |
23 | HG00738.hp2 HG01081.hp1 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.-4-2532G>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50019251 | |||||||
| chr12:50019276 | T | C | 3 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 |
3 | NA18747.hp1 NA18946.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.-4-2557A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50019276 | |||||||
| chr12:50019366 | T | C | 1 | a0001c0001t0001g0227 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-4-2647A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50019366 | |||||||
| chr12:50019596 | C | G | 3 | a0001c0001t0001g0085 a0001c0001t0001g0092 a0001c0001t0001g0093 |
3 | HG02976.hp1 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-4-2877G>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50019596 | |||||||
| chr12:50019597 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-4-2878C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50019597 | |||||||
| chr12:50019695 | A | AAAAT | 21 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0027 others(18): Show |
23 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-4-2980_-4-2977dup others(4): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50019695 | |||||||
| chr12:50019695 | A | AAAATAAA others(1): Show |
9 | a0001c0001t0001g0080 a0001c0001t0001g0150 a0001c0001t0001g0151 others(6): Show |
9 | HG01074.hp1 HG02145.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.-4-2984_-4-2977dup others(8): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50019695 | |||||||
| chr12:50019695 | A | AAAATAAA others(5): Show |
17 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0088 others(14): Show |
17 | HG01071.hp2 HG01109.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.-4-2988_-4-2977dup others(12): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50019695 | |||||||
| chr12:50019695 | A | AAAATAAA others(13): Show |
43 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(40): Show |
52 | HG00544.hp1 HG00544.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.-4-2996_-4-2977dup others(20): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50019695 | |||||||
| chr12:50019695 | A | AAAATAAA others(17): Show |
3 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 |
3 | HG01168.hp2 HG01169.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.-4-3000_-4-2977dup others(24): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50019695 | |||||||
| chr12:50019695 | AAAAT | A | 34 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(31): Show |
44 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.-4-2980_-4-2977del others(4): Show |
RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50019695 | |||||||
| chr12:50019897 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-4-3178T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50019897 | |||||||
| chr12:50019956 | G | C | 1 | a0001c0002t0001g0037 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-4-3237C>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50019956 | |||||||
| chr12:50020055 | A | T | 31 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(28): Show |
34 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.-4-3336T>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50020055 | |||||||
| chr12:50020071 | A | T | 59 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(56): Show |
71 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(68): Show |
intron_variant | MODIFIER | c.-4-3352T>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50020071 | |||||||
| chr12:50020194 | C | T | 59 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(56): Show |
71 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(68): Show |
intron_variant | MODIFIER | c.-4-3475G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50020194 | |||||||
| chr12:50020263 | C | CA | 177 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(174): Show |
196 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(193): Show |
intron_variant | MODIFIER | c.-4-3545dupT | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50020263 | |||||||
| chr12:50020326 | C | G | 1 | a0001c0001t0001g0237 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-4-3607G>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50020326 | |||||||
| chr12:50020344 | A | AT | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(265): Show |
302 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(299): Show |
intron_variant | MODIFIER | c.-4-3626dupA | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50020344 | |||||||
| chr12:50020404 | G | A | 138 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(135): Show |
153 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-4-3685C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50020404 | |||||||
| chr12:50020516 | A | G | 1 | a0001c0001t0001g0235 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-4-3797T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50020516 | |||||||
| chr12:50020926 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-4-4207C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50020926 | |||||||
| chr12:50020990 | A | G | 5 | a0001c0001t0005g0285 a0001c0002t0001g0270 a0001c0002t0001g0271 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4-4271T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50020990 | |||||||
| chr12:50021128 | A | G | 25 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0027 others(22): Show |
27 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.-5+4270T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50021128 | |||||||
| chr12:50021150 | A | AT | 25 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0027 others(22): Show |
27 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.-5+4247dupA | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50021150 | |||||||
| chr12:50021255 | A | G | 2 | a0001c0002t0001g0027 a0001c0002t0001g0028 |
2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-5+4143T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50021255 | |||||||
| chr12:50021650 | T | C | 7 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0228 others(4): Show |
9 | HG00438.hp1 NA18966.hp2 NA18975.hp2 others(6): Show |
intron_variant | MODIFIER | c.-5+3748A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50021650 | |||||||
| chr12:50021918 | C | T | 15 | a0001c0001t0001g0084 a0001c0002t0001g0009 a0001c0002t0001g0029 others(12): Show |
16 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-5+3480G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50021918 | |||||||
| chr12:50021931 | T | C | 22 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0029 others(19): Show |
24 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.-5+3467A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50021931 | |||||||
| chr12:50021941 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-5+3457C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50021941 | |||||||
| chr12:50022241 | C | G | 1 | a0001c0001t0001g0083 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-5+3157G>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50022241 | |||||||
| chr12:50022242 | A | G | 4 | a0001c0002t0001g0008 a0001c0002t0001g0038 a0001c0002t0001g0039 others(1): Show |
5 | HG02258.hp2 HG02622.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5+3156T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50022242 | |||||||
| chr12:50022302 | G | A | 25 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0027 others(22): Show |
27 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.-5+3096C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50022302 | |||||||
| chr12:50022372 | C | T | 176 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(173): Show |
195 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(192): Show |
intron_variant | MODIFIER | c.-5+3026G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50022372 | |||||||
| chr12:50022438 | C | T | 2 | a0001c0001t0001g0081 a0001c0001t0001g0082 |
2 | HG01891.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-5+2960G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50022438 | |||||||
| chr12:50022447 | C | T | 1 | a0001c0004t0009g0287 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-5+2951G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50022447 | |||||||
| chr12:50022475 | A | G | 59 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(56): Show |
71 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(68): Show |
intron_variant | MODIFIER | c.-5+2923T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50022475 | |||||||
| chr12:50022496 | C | T | 25 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0027 others(22): Show |
27 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.-5+2902G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50022496 | |||||||
| chr12:50022512 | G | T | 1 | a0001c0001t0001g0234 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-5+2886C>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50022512 | |||||||
| chr12:50022532 | A | G | 4 | a0001c0001t0001g0025 a0001c0001t0001g0267 a0001c0001t0001g0268 others(1): Show |
5 | HG01884.hp1 HG02970.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5+2866T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50022532 | |||||||
| chr12:50022557 | G | T | 175 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(172): Show |
194 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.-5+2841C>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50022557 | |||||||
| chr12:50022598 | G | A | 59 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(56): Show |
71 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(68): Show |
intron_variant | MODIFIER | c.-5+2800C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50022598 | |||||||
| chr12:50022787 | A | G | 59 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(56): Show |
71 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(68): Show |
intron_variant | MODIFIER | c.-5+2611T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50022787 | |||||||
| chr12:50023170 | A | G | 2 | a0001c0001t0001g0004 a0001c0001t0001g0048 |
4 | HG03139.hp2 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+2228T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50023170 | |||||||
| chr12:50023401 | C | A | 2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | HG01261.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-5+1997G>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50023401 | |||||||
| chr12:50023452 | G | C | 1 | a0001c0001t0005g0285 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-5+1946C>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50023452 | |||||||
| chr12:50023650 | T | C | 25 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0027 others(22): Show |
27 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.-5+1748A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50023650 | |||||||
| chr12:50023665 | A | G | 31 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(28): Show |
34 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.-5+1733T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50023665 | |||||||
| chr12:50023687 | C | T | 9 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(6): Show |
9 | HG02258.hp1 HG02559.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-5+1711G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50023687 | |||||||
| chr12:50023899 | T | C | 1 | a0001c0001t0001g0256 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-5+1499A>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50023899 | |||||||
| chr12:50023958 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-5+1440T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50023958 | |||||||
| chr12:50024058 | G | A | 28 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0258 others(25): Show |
30 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.-5+1340C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50024058 | |||||||
| chr12:50024155 | C | T | 7 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 others(4): Show |
7 | HG01891.hp1 HG02886.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.-5+1243G>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50024155 | |||||||
| chr12:50024192 | G | T | 1 | a0001c0001t0001g0079 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-5+1206C>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50024192 | |||||||
| chr12:50024194 | C | A | 1 | a0001c0001t0001g0257 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-5+1204G>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50024194 | |||||||
| chr12:50024319 | A | C | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | HG02572.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-5+1079T>G | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50024319 | |||||||
| chr12:50024605 | G | A | 31 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(28): Show |
34 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.-5+793C>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50024605 | |||||||
| chr12:50024652 | T | A | 1 | a0001c0001t0001g0286 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-5+746A>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50024652 | |||||||
| chr12:50024660 | T | A | 24 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0027 others(21): Show |
26 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.-5+738A>T | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50024660 | |||||||
| chr12:50024790 | T | TA | 21 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0029 others(18): Show |
23 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.-5+607dupT | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50024790 | |||||||
| chr12:50024791 | A | G | 34 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(31): Show |
44 | HG00738.hp2 HG01081.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.-5+607T>C | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50024791 | |||||||
| chr12:50024833 | G | T | 24 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0027 others(21): Show |
26 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.-5+565C>A | RACGAP1 | ENSG00000161800.13 | transcript | ENST00000312377.10 | protein_coding | 1/16 | chr12 | 50024833 |