Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10411 |
| ensemblid | ENSG00000079337.16 |
| hgncid | 16629 |
| symbol | RAPGEF3 |
| name | Rap guanine nucleotide exchange factor 3 |
| refseq_nuc | NM_001098531.4 |
| refseq_prot | NP_001092001.2 |
| ensembl_nuc | ENST00000449771.7 |
| ensembl_prot | ENSP00000395708.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 47734363 |
| end | 47758880 |
| strand | - |
| ver | v1.2 |
| region | chr12:47734363-47758880 |
| region5000 | chr12:47729363-47763880 |
| regionname0 | RAPGEF3_chr12_47734363_47758880 |
| regionname5000 | RAPGEF3_chr12_47729363_47763880 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 923 | 279 | 48 | 48 | 139 | 11 | 32 | 110 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | MKVGW others(918): Show |
chr12 | 47729363 | 47763880 |
| a0002 | 0/0 | 923 | 83 | 17 | 15 | 34 | 5 | 12 | 30 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | MKVGW others(918): Show |
chr12 | 47729363 | 47763880 |
| a0003 | 0/0 | 923 | 35 | 12 | 10 | 7 | 2 | 4 | 6 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | MKVGW others(918): Show |
chr12 | 47729363 | 47763880 |
| a0004 | 0/0 | 923 | 8 | 7 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | MKVGW others(918): Show |
chr12 | 47729363 | 47763880 |
| a0005 | 0/0 | 923 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | MKVGW others(918): Show |
chr12 | 47729363 | 47763880 |
| a0006 | 0/0 | 925 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | MKVGW others(920): Show |
chr12 | 47729363 | 47763880 |
| a0007 | 0/0 | 923 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | MKVGW others(918): Show |
chr12 | 47729363 | 47763880 |
| a0008 | 0/0 | 923 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | MKVGW others(918): Show |
chr12 | 47729363 | 47763880 |
| a0009 | 0/0 | 923 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | MKVGW others(918): Show |
chr12 | 47729363 | 47763880 |
| a0010 | 0/0 | 923 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | MKVGW others(918): Show |
chr12 | 47729363 | 47763880 |
| a0011 | 0/0 | 923 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | MKVGW others(918): Show |
chr12 | 47729363 | 47763880 |
| a0012 | 0/0 | 923 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | MKVGW others(918): Show |
chr12 | 47729363 | 47763880 |
| a0013 | 0/0 | 923 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | MKVGW others(918): Show |
chr12 | 47729363 | 47763880 |
| a0014 | 0/0 | 923 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | MKVGW others(918): Show |
chr12 | 47729363 | 47763880 |
| a0015 | 0/0 | 923 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | MKVGW others(918): Show |
chr12 | 47729363 | 47763880 |
| a0016 | 0/0 | 923 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | MKVGW others(918): Show |
chr12 | 47729363 | 47763880 |
| a0017 | 0/0 | 923 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | MKVGW others(918): Show |
chr12 | 47729363 | 47763880 |
| a0018 | 0/0 | 923 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | MKVGW others(918): Show |
chr12 | 47729363 | 47763880 |
| a0019 | 0/0 | 923 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | MKVGW others(918): Show |
chr12 | 47729363 | 47763880 |
| a0020 | 0/1 | 923 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | MKVGW others(918): Show |
chr12 | 47729363 | 47763880 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2769 | 278 | 47 | 48 | 139 | 11 | 32 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | ATGAA others(2764): Show |
chr12 | 47729363 | 47763880 | ||
| a0001c0020 | 0/0 | 2769 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | ATGAA others(2764): Show |
chr12 | 47729363 | 47763880 | ||
| a0002c0002 | 0/0 | 2769 | 80 | 15 | 15 | 33 | 5 | 12 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | ATGAA others(2764): Show |
chr12 | 47729363 | 47763880 | ||
| a0002c0011 | 0/0 | 2769 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | ATGAA others(2764): Show |
chr12 | 47729363 | 47763880 | ||
| a0002c0015 | 0/0 | 2769 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | ATGAA others(2764): Show |
chr12 | 47729363 | 47763880 | ||
| a0002c0016 | 0/0 | 2769 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | ATGAA others(2764): Show |
chr12 | 47729363 | 47763880 | ||
| a0003c0003 | 0/0 | 2769 | 34 | 12 | 10 | 6 | 2 | 4 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | ATGAA others(2764): Show |
chr12 | 47729363 | 47763880 | ||
| a0003c0014 | 0/0 | 2769 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | ATGAA others(2764): Show |
chr12 | 47729363 | 47763880 | ||
| a0004c0004 | 0/0 | 2769 | 8 | 7 | 1 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | ATGAA others(2764): Show |
chr12 | 47729363 | 47763880 | ||
| a0005c0005 | 0/0 | 2769 | 4 | 0 | 0 | 4 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | ATGAA others(2764): Show |
chr12 | 47729363 | 47763880 | ||
| a0006c0006 | 0/0 | 2775 | 3 | 3 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | ATGAA others(2770): Show |
chr12 | 47729363 | 47763880 | ||
| a0007c0007 | 0/0 | 2769 | 2 | 0 | 0 | 2 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | ATGAA others(2764): Show |
chr12 | 47729363 | 47763880 | ||
| a0008c0008 | 0/0 | 2769 | 2 | 0 | 0 | 2 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | ATGAA others(2764): Show |
chr12 | 47729363 | 47763880 | ||
| a0009c0010 | 0/0 | 2769 | 2 | 2 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | ATGAA others(2764): Show |
chr12 | 47729363 | 47763880 | ||
| a0010c0009 | 0/0 | 2769 | 2 | 2 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | ATGAA others(2764): Show |
chr12 | 47729363 | 47763880 | ||
| a0011c0025 | 0/0 | 2769 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | ATGAA others(2764): Show |
chr12 | 47729363 | 47763880 | ||
| a0012c0022 | 0/0 | 2769 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | ATGAA others(2764): Show |
chr12 | 47729363 | 47763880 | ||
| a0013c0024 | 0/0 | 2769 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | ATGAA others(2764): Show |
chr12 | 47729363 | 47763880 | ||
| a0014c0023 | 0/0 | 2769 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | ATGAA others(2764): Show |
chr12 | 47729363 | 47763880 | ||
| a0015c0013 | 0/0 | 2769 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | ATGAA others(2764): Show |
chr12 | 47729363 | 47763880 | ||
| a0016c0012 | 0/0 | 2769 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | ATGAA others(2764): Show |
chr12 | 47729363 | 47763880 | ||
| a0017c0019 | 0/0 | 2769 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | ATGAA others(2764): Show |
chr12 | 47729363 | 47763880 | ||
| a0018c0017 | 0/0 | 2769 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | ATGAA others(2764): Show |
chr12 | 47729363 | 47763880 | ||
| a0019c0021 | 0/0 | 2769 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | ATGAA others(2764): Show |
chr12 | 47729363 | 47763880 | ||
| a0020c0018 | 0/1 | 2769 | 1 | 0 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | ATGAA others(2764): Show |
chr12 | 47729363 | 47763880 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6300 | 65 | 0 | 2 | 48 | 4 | 11 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0001c0001t0002 | 0/0 | 6300 | 48 | 4 | 12 | 25 | 4 | 3 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0001c0001t0003 | 0/0 | 6300 | 7 | 0 | 4 | 2 | 0 | 1 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0001c0001t0004 | 0/0 | 6300 | 62 | 11 | 20 | 23 | 1 | 7 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0001c0001t0005 | 0/0 | 6300 | 21 | 0 | 1 | 20 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0001c0001t0006 | 1/0 | 6300 | 19 | 1 | 2 | 9 | 0 | 6 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0001c0001t0007 | 0/0 | 6300 | 15 | 11 | 3 | 0 | 0 | 1 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0001c0001t0010 | 0/0 | 6300 | 5 | 3 | 0 | 2 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0001c0001t0011 | 0/0 | 6300 | 4 | 0 | 0 | 4 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0001c0001t0012 | 0/0 | 6300 | 4 | 4 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0001c0001t0013 | 0/0 | 6300 | 4 | 4 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0001c0001t0014 | 0/0 | 6300 | 2 | 1 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0001c0001t0016 | 0/0 | 6300 | 2 | 2 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0001c0001t0017 | 0/0 | 6300 | 2 | 2 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0001c0001t0018 | 0/0 | 6300 | 2 | 0 | 2 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0001c0001t0019 | 0/0 | 6300 | 2 | 0 | 0 | 0 | 0 | 2 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0001c0001t0020 | 0/0 | 6300 | 2 | 0 | 0 | 2 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0001c0001t0022 | 0/0 | 6300 | 2 | 0 | 1 | 0 | 1 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0001c0001t0023 | 0/0 | 6300 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0001c0001t0027 | 0/0 | 6300 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0001c0001t0028 | 0/0 | 6300 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0001c0001t0029 | 0/0 | 6300 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0001c0001t0030 | 0/0 | 6300 | 1 | 0 | 0 | 0 | 1 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0001c0001t0032 | 0/0 | 6286 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6281): Show |
chr12 | 47729363 | 47763880 |
| a0001c0001t0037 | 0/0 | 6300 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0001c0001t0038 | 0/0 | 6300 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0001c0001t0040 | 0/0 | 6300 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0001c0001t0041 | 0/0 | 6300 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0001c0020t0003 | 0/0 | 6300 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0002c0002t0001 | 0/0 | 6300 | 4 | 4 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0002c0002t0002 | 0/0 | 6300 | 22 | 0 | 3 | 12 | 0 | 7 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0002c0002t0003 | 0/0 | 6300 | 23 | 2 | 1 | 17 | 0 | 3 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0002c0002t0004 | 0/0 | 6300 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0002c0002t0005 | 0/0 | 6300 | 6 | 1 | 1 | 2 | 2 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0002c0002t0007 | 0/0 | 6300 | 3 | 3 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0002c0002t0008 | 0/0 | 6300 | 11 | 1 | 7 | 0 | 2 | 1 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0002c0002t0014 | 0/0 | 6300 | 2 | 0 | 1 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0002c0002t0016 | 0/0 | 6300 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0002c0002t0017 | 0/0 | 6300 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0002c0002t0021 | 0/0 | 6300 | 2 | 0 | 2 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0002c0002t0025 | 0/0 | 6300 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0002c0002t0034 | 0/0 | 6300 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0002c0002t0035 | 0/0 | 6300 | 1 | 0 | 0 | 0 | 1 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0002c0002t0039 | 0/0 | 6300 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0002c0011t0001 | 0/0 | 6300 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0002c0015t0033 | 0/0 | 6300 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0002c0016t0003 | 0/0 | 6300 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0003c0003t0003 | 0/0 | 6300 | 30 | 12 | 7 | 5 | 2 | 4 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0003c0003t0006 | 0/0 | 6300 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0003c0003t0011 | 0/0 | 6300 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0003c0003t0026 | 0/0 | 6300 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0003c0003t0036 | 0/0 | 6300 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0003c0014t0003 | 0/0 | 6300 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0004c0004t0009 | 0/0 | 6300 | 8 | 7 | 1 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0005c0005t0006 | 0/0 | 6300 | 4 | 0 | 0 | 4 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0006c0006t0015 | 0/0 | 6306 | 3 | 3 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6301): Show |
chr12 | 47729363 | 47763880 |
| a0007c0007t0003 | 0/0 | 6300 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0007c0007t0031 | 0/0 | 6300 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0008c0008t0004 | 0/0 | 6300 | 2 | 0 | 0 | 2 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0009c0010t0010 | 0/0 | 6300 | 2 | 2 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0010c0009t0009 | 0/0 | 6300 | 2 | 2 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0011c0025t0001 | 0/0 | 6300 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0012c0022t0003 | 0/0 | 6300 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0013c0024t0002 | 0/0 | 6300 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0014c0023t0006 | 0/0 | 6300 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0015c0013t0001 | 0/0 | 6300 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0016c0012t0024 | 0/0 | 6300 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0017c0019t0012 | 0/0 | 6300 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0018c0017t0003 | 0/0 | 6300 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0019c0021t0001 | 0/0 | 6300 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| a0020c0018t0005 | 0/1 | 6300 | 1 | 0 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | AGCGC others(6295): Show |
chr12 | 47729363 | 47763880 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 33 | 0 | 2 | 22 | 0 | 9 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0001g0010 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0002g0001 | 0/0 | 38 | 4 | 9 | 19 | 3 | 3 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0002g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0002g0058 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0003g0017 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0003g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0004g0003 | 0/0 | 31 | 0 | 5 | 20 | 0 | 6 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0004g0005 | 0/0 | 12 | 0 | 11 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0004g0020 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0004g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0004g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0004g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0005g0008 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0005g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0005g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0005g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0005g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0005g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0005g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0005g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0005g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0006g0015 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0006g0016 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0006g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0006g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0006g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0006g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0006g0127 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0006g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0006g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0006g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0007g0012 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0007g0054 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0007g0055 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0007g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0007g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0007g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0007g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0010g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0010g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0010g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0011g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0011g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0011g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0012g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0012g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0013g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0013g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0014g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0014g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0016g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0016g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0017g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0018g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0019g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0019g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0020g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0022g0053 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0023g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0027g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0028g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0029g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0030g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0032g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0037g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0038g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0040g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0001t0041g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0001c0020t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0002c0002t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0002c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0002c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0002c0002t0002g0006 | 0/0 | 12 | 0 | 2 | 8 | 0 | 2 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0002c0002t0002g0048 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0002c0002t0002g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0002c0002t0002g0050 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0002c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0002c0002t0003g0007 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0002c0002t0003g0009 | 0/0 | 7 | 1 | 1 | 4 | 0 | 1 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0002c0002t0003g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0002c0002t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0002c0002t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0002c0002t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0002c0002t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0002c0002t0005g0018 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0002c0002t0005g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0002c0002t0005g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0002c0002t0007g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0002c0002t0008g0011 | 0/0 | 6 | 1 | 2 | 0 | 2 | 1 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0002c0002t0008g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0002c0002t0008g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0002c0002t0008g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0002c0002t0008g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0002c0002t0008g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0002c0002t0014g0047 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0002c0002t0016g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0002c0002t0017g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0002c0002t0021g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0002c0002t0025g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0002c0002t0034g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0002c0002t0035g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0002c0002t0039g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0002c0011t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0002c0015t0033g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0002c0016t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0003c0003t0003g0004 | 0/0 | 16 | 9 | 6 | 0 | 0 | 1 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0003c0003t0003g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0003c0003t0003g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0003c0003t0003g0034 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0003c0003t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0003c0003t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0003c0003t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0003c0003t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0003c0003t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0003c0003t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0003c0003t0006g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0003c0003t0011g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0003c0003t0026g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0003c0003t0036g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0003c0014t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0004c0004t0009g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0004c0004t0009g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0004c0004t0009g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0005c0005t0006g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0005c0005t0006g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0006c0006t0015g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0007c0007t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0007c0007t0031g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0008c0008t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0008c0008t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0009c0010t0010g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0009c0010t0010g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0010c0009t0009g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0010c0009t0009g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0011c0025t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0012c0022t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0013c0024t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0014c0023t0006g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0015c0013t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0016c0012t0024g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0017c0019t0012g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0018c0017t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0019c0021t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| a0020c0018t0005g0085 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG00099 | hp2 | a0002 | c0002 | t0005 | g0068 | EUR | GBR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0111 | EUR | GBR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG00140 | hp2 | a0002 | c0002 | t0035 | g0154 | EUR | GBR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG00280 | hp1 | a0001 | c0001 | t0022 | g0053 | EUR | FIN | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | FIN | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0182 | EUR | FIN | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG00408 | hp1 | a0001 | c0001 | t0005 | g0118 | EAS | CHS | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG00408 | hp2 | a0001 | c0001 | t0041 | g0178 | EAS | CHS | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG00544 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | CHS | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | CHS | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG00558 | hp2 | a0001 | c0001 | t0029 | g0143 | EAS | CHS | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG00597 | hp1 | a0011 | c0025 | t0001 | g0125 | EAS | CHS | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG00639 | hp2 | a0002 | c0002 | t0003 | g0009 | AMR | PUR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG00673 | hp2 | a0002 | c0002 | t0003 | g0007 | EAS | CHS | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG00733 | hp1 | a0001 | c0001 | t0023 | g0114 | AMR | PUR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG00738 | hp1 | a0001 | c0001 | t0007 | g0181 | AMR | PUR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG00738 | hp2 | a0003 | c0003 | t0006 | g0082 | AMR | PUR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG00741 | hp1 | a0002 | c0002 | t0008 | g0155 | AMR | PUR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01069 | hp1 | a0002 | c0002 | t0008 | g0152 | AMR | PUR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0005 | AMR | PUR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01070 | hp1 | a0002 | c0002 | t0021 | g0046 | AMR | PUR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | PUR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01071 | hp2 | a0002 | c0002 | t0021 | g0046 | AMR | PUR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01099 | hp1 | a0001 | c0001 | t0006 | g0130 | AMR | PUR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01099 | hp2 | a0003 | c0003 | t0003 | g0004 | AMR | PUR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0160 | AMR | PUR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0112 | AMR | PUR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | PUR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01109 | hp2 | a0003 | c0003 | t0003 | g0004 | AMR | PUR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01167 | hp1 | a0001 | c0001 | t0018 | g0035 | AMR | PUR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01167 | hp2 | a0004 | c0004 | t0009 | g0087 | AMR | PUR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01168 | hp1 | a0002 | c0002 | t0002 | g0048 | AMR | PUR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0037 | AMR | PUR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01169 | hp1 | a0001 | c0001 | t0018 | g0035 | AMR | PUR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0037 | AMR | PUR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01175 | hp1 | a0002 | c0002 | t0008 | g0158 | AMR | PUR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01175 | hp2 | a0001 | c0001 | t0022 | g0053 | AMR | PUR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01192 | hp1 | a0001 | c0001 | t0007 | g0055 | AMR | PUR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01192 | hp2 | a0003 | c0003 | t0036 | g0159 | AMR | PUR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | PUR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01243 | hp2 | a0002 | c0002 | t0008 | g0011 | AMR | PUR | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01255 | hp1 | a0002 | c0002 | t0005 | g0018 | AMR | CLM | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0020 | AMR | CLM | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01256 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | CLM | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01256 | hp2 | a0003 | c0003 | t0003 | g0004 | AMR | CLM | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0017 | AMR | CLM | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01257 | hp2 | a0003 | c0003 | t0026 | g0081 | AMR | CLM | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01258 | hp1 | a0003 | c0003 | t0003 | g0004 | AMR | CLM | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0017 | AMR | CLM | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01261 | hp1 | a0003 | c0003 | t0003 | g0004 | AMR | CLM | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0059 | AMR | CLM | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01346 | hp1 | a0001 | c0001 | t0007 | g0054 | AMR | CLM | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01346 | hp2 | a0001 | c0001 | t0006 | g0016 | AMR | CLM | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01358 | hp1 | a0002 | c0002 | t0014 | g0047 | AMR | CLM | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01358 | hp2 | a0003 | c0003 | t0003 | g0004 | AMR | CLM | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | CLM | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01361 | hp2 | a0002 | c0002 | t0008 | g0157 | AMR | CLM | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01433 | hp2 | a0002 | c0002 | t0008 | g0153 | AMR | CLM | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | CLM | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01515 | hp2 | a0002 | c0002 | t0008 | g0011 | EUR | IBS | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01516 | hp1 | a0002 | c0002 | t0005 | g0018 | EUR | IBS | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01517 | hp1 | a0002 | c0002 | t0008 | g0011 | EUR | IBS | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01884 | hp1 | a0002 | c0002 | t0007 | g0027 | AFR | ACB | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01884 | hp2 | a0006 | c0006 | t0015 | g0023 | AFR | ACB | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01891 | hp1 | a0003 | c0003 | t0003 | g0004 | AFR | ACB | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PEL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01943 | hp2 | a0001 | c0001 | t0004 | g0005 | AMR | PEL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PEL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0005 | AMR | PEL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | PEL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01978 | hp2 | a0002 | c0002 | t0008 | g0011 | AMR | PEL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01993 | hp1 | a0001 | c0001 | t0005 | g0151 | AMR | PEL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0005 | AMR | PEL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02004 | hp1 | a0001 | c0001 | t0004 | g0113 | AMR | PEL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02004 | hp2 | a0001 | c0001 | t0004 | g0003 | AMR | PEL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02015 | hp2 | a0007 | c0007 | t0003 | g0132 | EAS | KHV | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02040 | hp2 | a0008 | c0008 | t0004 | g0092 | EAS | KHV | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02055 | hp1 | a0001 | c0001 | t0010 | g0057 | AFR | ACB | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02055 | hp2 | a0001 | c0001 | t0016 | g0100 | AFR | ACB | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02056 | hp1 | a0012 | c0022 | t0003 | g0089 | EAS | KHV | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | KHV | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02080 | hp1 | a0007 | c0007 | t0031 | g0133 | EAS | KHV | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02129 | hp2 | a0003 | c0003 | t0011 | g0079 | EAS | KHV | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02132 | hp1 | a0001 | c0001 | t0005 | g0022 | EAS | KHV | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | KHV | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02135 | hp1 | a0002 | c0002 | t0003 | g0064 | EAS | KHV | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02145 | hp1 | a0001 | c0001 | t0010 | g0057 | AFR | ACB | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02145 | hp2 | a0002 | c0002 | t0007 | g0027 | AFR | ACB | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PEL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0005 | AMR | PEL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02155 | hp2 | a0013 | c0024 | t0002 | g0179 | EAS | CDX | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02165 | hp2 | a0002 | c0002 | t0014 | g0047 | EAS | CDX | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02257 | hp1 | a0001 | c0001 | t0012 | g0028 | AFR | ACB | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02257 | hp2 | a0002 | c0002 | t0016 | g0071 | AFR | ACB | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02258 | hp1 | a0001 | c0001 | t0007 | g0054 | AFR | ACB | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02258 | hp2 | a0014 | c0023 | t0006 | g0088 | AFR | ACB | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02280 | hp2 | a0003 | c0003 | t0003 | g0004 | AFR | ACB | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | PEL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | PEL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02451 | hp1 | a0015 | c0013 | t0001 | g0077 | AFR | ACB | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02451 | hp2 | a0003 | c0003 | t0003 | g0004 | AFR | ACB | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02523 | hp1 | a0002 | c0002 | t0003 | g0007 | EAS | KHV | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | KHV | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02572 | hp1 | a0003 | c0003 | t0003 | g0004 | AFR | GWD | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02572 | hp2 | a0001 | c0001 | t0007 | g0056 | AFR | GWD | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02602 | hp2 | a0001 | c0001 | t0004 | g0003 | SAS | PJL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02615 | hp1 | a0001 | c0001 | t0006 | g0090 | AFR | GWD | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02615 | hp2 | a0002 | c0002 | t0034 | g0156 | AFR | GWD | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0020 | AFR | GWD | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02622 | hp2 | a0003 | c0003 | t0003 | g0078 | AFR | GWD | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0039 | AFR | GWD | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02630 | hp2 | a0001 | c0001 | t0037 | g0166 | AFR | GWD | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02647 | hp1 | a0016 | c0012 | t0024 | g0075 | AFR | GWD | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | GWD | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02683 | hp1 | a0001 | c0001 | t0006 | g0128 | SAS | PJL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02683 | hp2 | a0002 | c0002 | t0003 | g0031 | SAS | PJL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02698 | hp1 | a0003 | c0003 | t0003 | g0004 | SAS | PJL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02698 | hp2 | a0002 | c0002 | t0008 | g0011 | SAS | PJL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02717 | hp1 | a0001 | c0001 | t0040 | g0170 | AFR | GWD | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0012 | AFR | GWD | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0066 | AFR | GWD | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02723 | hp2 | a0010 | c0009 | t0009 | g0116 | AFR | GWD | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02735 | hp1 | a0003 | c0003 | t0003 | g0030 | SAS | PJL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02809 | hp1 | a0001 | c0001 | t0007 | g0055 | AFR | GWD | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0099 | AFR | GWD | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02886 | hp1 | a0001 | c0001 | t0016 | g0094 | AFR | GWD | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02886 | hp2 | a0006 | c0006 | t0015 | g0023 | AFR | GWD | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02895 | hp1 | a0001 | c0001 | t0017 | g0045 | AFR | GWD | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0110 | AFR | GWD | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0012 | AFR | GWD | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02897 | hp2 | a0001 | c0001 | t0017 | g0045 | AFR | GWD | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0033 | AFR | ESN | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02922 | hp2 | a0004 | c0004 | t0009 | g0013 | AFR | ESN | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02965 | hp1 | a0004 | c0004 | t0009 | g0013 | AFR | ESN | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02965 | hp2 | a0017 | c0019 | t0012 | g0174 | AFR | ESN | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02970 | hp1 | a0001 | c0001 | t0007 | g0012 | AFR | ESN | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02970 | hp2 | a0010 | c0009 | t0009 | g0119 | AFR | ESN | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0033 | AFR | ESN | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02976 | hp2 | a0004 | c0004 | t0009 | g0036 | AFR | ESN | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03017 | hp2 | a0001 | c0001 | t0028 | g0106 | SAS | PJL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03041 | hp1 | a0001 | c0001 | t0014 | g0176 | AFR | GWD | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03041 | hp2 | a0001 | c0001 | t0007 | g0012 | AFR | GWD | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0097 | AFR | MSL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0056 | AFR | MSL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03130 | hp1 | a0001 | c0001 | t0027 | g0109 | AFR | ESN | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03130 | hp2 | a0004 | c0004 | t0009 | g0036 | AFR | ESN | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03139 | hp1 | a0003 | c0003 | t0003 | g0004 | AFR | ESN | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03139 | hp2 | a0001 | c0001 | t0013 | g0029 | AFR | ESN | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03195 | hp1 | a0003 | c0003 | t0003 | g0004 | AFR | ESN | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0117 | AFR | ESN | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0039 | AFR | MSL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03209 | hp2 | a0001 | c0001 | t0013 | g0029 | AFR | MSL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03225 | hp1 | a0001 | c0001 | t0012 | g0180 | AFR | MSL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | MSL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0020 | SAS | PJL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03239 | hp2 | a0002 | c0002 | t0003 | g0009 | SAS | PJL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03453 | hp1 | a0001 | c0001 | t0007 | g0012 | AFR | MSL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03453 | hp2 | a0018 | c0017 | t0003 | g0084 | AFR | MSL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0098 | AFR | MSL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03486 | hp2 | a0004 | c0004 | t0009 | g0013 | AFR | MSL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03490 | hp1 | a0001 | c0001 | t0006 | g0016 | SAS | PJL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03490 | hp2 | a0001 | c0001 | t0006 | g0015 | SAS | PJL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03491 | hp1 | a0002 | c0002 | t0002 | g0048 | SAS | PJL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03491 | hp2 | a0002 | c0002 | t0002 | g0050 | SAS | PJL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03492 | hp1 | a0001 | c0001 | t0006 | g0015 | SAS | PJL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03492 | hp2 | a0002 | c0002 | t0002 | g0050 | SAS | PJL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03516 | hp1 | a0002 | c0002 | t0007 | g0027 | AFR | ESN | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03516 | hp2 | a0001 | c0020 | t0003 | g0115 | AFR | ESN | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03540 | hp1 | a0003 | c0003 | t0003 | g0073 | AFR | GWD | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | GWD | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03579 | hp1 | a0004 | c0004 | t0009 | g0013 | AFR | MSL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03579 | hp2 | a0003 | c0003 | t0003 | g0004 | AFR | MSL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0003 | SAS | PJL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0163 | SAS | PJL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03669 | hp1 | a0002 | c0002 | t0002 | g0006 | SAS | PJL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0017 | SAS | PJL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03688 | hp2 | a0002 | c0002 | t0003 | g0031 | SAS | STU | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03704 | hp2 | a0002 | c0002 | t0002 | g0006 | SAS | PJL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0003 | SAS | PJL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03831 | hp2 | a0003 | c0003 | t0003 | g0034 | SAS | BEB | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0165 | SAS | BEB | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03927 | hp1 | a0001 | c0001 | t0006 | g0015 | SAS | BEB | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03942 | hp1 | a0003 | c0003 | t0003 | g0076 | SAS | BEB | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG04115 | hp1 | a0001 | c0001 | t0019 | g0104 | SAS | STU | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | STU | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG04199 | hp2 | a0001 | c0001 | t0019 | g0145 | SAS | STU | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0003 | SAS | STU | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG04204 | hp2 | a0001 | c0001 | t0007 | g0185 | SAS | STU | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG04228 | hp1 | a0001 | c0001 | t0006 | g0015 | SAS | STU | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0003 | SAS | STU | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18522 | hp1 | a0003 | c0003 | t0003 | g0086 | AFR | YRI | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18522 | hp2 | a0001 | c0001 | t0013 | g0171 | AFR | YRI | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18747 | hp1 | a0001 | c0001 | t0005 | g0022 | EAS | CHB | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18906 | hp1 | a0001 | c0001 | t0013 | g0029 | AFR | YRI | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18906 | hp2 | a0009 | c0010 | t0010 | g0184 | AFR | YRI | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18941 | hp1 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18942 | hp1 | a0002 | c0002 | t0003 | g0009 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18942 | hp2 | a0001 | c0001 | t0005 | g0095 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18944 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18945 | hp1 | a0003 | c0003 | t0003 | g0014 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18945 | hp2 | a0001 | c0001 | t0004 | g0138 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18946 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18947 | hp1 | a0001 | c0001 | t0006 | g0121 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18950 | hp1 | a0001 | c0001 | t0006 | g0016 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18951 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18953 | hp2 | a0001 | c0001 | t0020 | g0042 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18954 | hp2 | a0001 | c0001 | t0005 | g0038 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18957 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18957 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18959 | hp2 | a0001 | c0001 | t0020 | g0042 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18960 | hp2 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18962 | hp1 | a0002 | c0016 | t0003 | g0062 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18962 | hp2 | a0001 | c0001 | t0011 | g0043 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18963 | hp2 | a0001 | c0001 | t0006 | g0025 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18966 | hp1 | a0005 | c0005 | t0006 | g0024 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18966 | hp2 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18968 | hp1 | a0001 | c0001 | t0006 | g0040 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18969 | hp2 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18970 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18971 | hp1 | a0001 | c0001 | t0014 | g0168 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18971 | hp2 | a0005 | c0005 | t0006 | g0024 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18975 | hp2 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18977 | hp1 | a0002 | c0002 | t0002 | g0164 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18978 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18979 | hp1 | a0005 | c0005 | t0006 | g0024 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18980 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18980 | hp2 | a0002 | c0002 | t0005 | g0032 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18981 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18983 | hp2 | a0001 | c0001 | t0005 | g0126 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18984 | hp1 | a0002 | c0002 | t0003 | g0065 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18984 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18988 | hp1 | a0001 | c0001 | t0005 | g0108 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18989 | hp2 | a0001 | c0001 | t0006 | g0025 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18991 | hp1 | a0001 | c0001 | t0032 | g0107 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18991 | hp2 | a0001 | c0001 | t0005 | g0146 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18992 | hp2 | a0001 | c0001 | t0004 | g0091 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18993 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18993 | hp2 | a0001 | c0001 | t0011 | g0043 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18994 | hp1 | a0001 | c0001 | t0011 | g0142 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18994 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19000 | hp1 | a0001 | c0001 | t0010 | g0052 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19000 | hp2 | a0003 | c0014 | t0003 | g0080 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19001 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19002 | hp1 | a0001 | c0001 | t0005 | g0022 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19003 | hp1 | a0003 | c0003 | t0003 | g0014 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19004 | hp2 | a0002 | c0002 | t0003 | g0009 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19005 | hp1 | a0008 | c0008 | t0004 | g0093 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19006 | hp2 | a0001 | c0001 | t0006 | g0149 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19009 | hp1 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19009 | hp2 | a0001 | c0001 | t0006 | g0016 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19011 | hp1 | a0002 | c0002 | t0002 | g0161 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19012 | hp2 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19030 | hp1 | a0002 | c0011 | t0001 | g0061 | AFR | LWK | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19030 | hp2 | a0001 | c0001 | t0010 | g0183 | AFR | LWK | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19043 | hp1 | a0001 | c0001 | t0007 | g0012 | AFR | LWK | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19043 | hp2 | a0002 | c0015 | t0033 | g0074 | AFR | LWK | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19054 | hp2 | a0001 | c0001 | t0011 | g0102 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19056 | hp1 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19057 | hp1 | a0002 | c0002 | t0003 | g0009 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19062 | hp2 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19063 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19064 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19064 | hp2 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19066 | hp1 | a0003 | c0003 | t0003 | g0014 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19066 | hp2 | a0002 | c0002 | t0025 | g0072 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19067 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19068 | hp1 | a0002 | c0002 | t0005 | g0032 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19075 | hp1 | a0003 | c0003 | t0003 | g0014 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19075 | hp2 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19077 | hp2 | a0001 | c0001 | t0005 | g0124 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19078 | hp1 | a0001 | c0001 | t0006 | g0025 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19079 | hp1 | a0001 | c0001 | t0006 | g0040 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19079 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19080 | hp1 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19080 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19081 | hp1 | a0001 | c0001 | t0005 | g0038 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19082 | hp1 | a0002 | c0002 | t0003 | g0009 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19083 | hp1 | a0005 | c0005 | t0006 | g0120 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19083 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19085 | hp2 | a0019 | c0021 | t0001 | g0134 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19088 | hp1 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19088 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19089 | hp2 | a0003 | c0003 | t0003 | g0060 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19090 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19090 | hp2 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19240 | hp1 | a0004 | c0004 | t0009 | g0013 | AFR | YRI | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA19240 | hp2 | a0006 | c0006 | t0015 | g0023 | AFR | YRI | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA20129 | hp1 | a0001 | c0001 | t0012 | g0028 | AFR | ASW | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA20129 | hp2 | a0001 | c0001 | t0007 | g0172 | AFR | ASW | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA20752 | hp1 | a0001 | c0001 | t0030 | g0129 | EUR | TSI | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA20752 | hp2 | a0003 | c0003 | t0003 | g0034 | EUR | TSI | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0150 | EUR | TSI | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA20805 | hp2 | a0003 | c0003 | t0003 | g0083 | EUR | TSI | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0003 | SAS | GIH | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA20905 | hp2 | a0002 | c0002 | t0039 | g0162 | SAS | GIH | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01123 | hp1 | a0003 | c0003 | t0003 | g0030 | AMR | CLM | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02109 | hp1 | a0003 | c0003 | t0003 | g0004 | AFR | ACB | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02486 | hp2 | a0001 | c0001 | t0012 | g0028 | AFR | ACB | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02559 | hp1 | a0001 | c0001 | t0038 | g0173 | AFR | ACB | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG02559 | hp2 | a0009 | c0010 | t0010 | g0186 | AFR | ACB | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03471 | hp1 | a0002 | c0002 | t0004 | g0069 | AFR | MSL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG03471 | hp2 | a0002 | c0002 | t0003 | g0070 | AFR | MSL | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG06807 | hp1 | a0003 | c0003 | t0003 | g0004 | AFR | USA | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| HG06807 | hp2 | a0002 | c0002 | t0017 | g0063 | AFR | USA | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA18955 | hp2 | a0001 | c0001 | t0010 | g0052 | EAS | JPT | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA20300 | hp1 | a0002 | c0002 | t0005 | g0018 | AFR | USA | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA20300 | hp2 | a0002 | c0002 | t0003 | g0009 | AFR | USA | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA21309 | hp1 | a0002 | c0002 | t0008 | g0011 | AFR | LWK | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0067 | AFR | LWK | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| homoSapiens | chm13v2 | a0020 | c0018 | t0005 | g0085 | REF | REF | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0006 | g0127 | REF | REF | RAPGEF3_chr12_47729363_47763880 | RAPGEF3 | chr12 | 47729363 | 47763880 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:47737682 | G | A | 1 | a0013 | 1 | HG02155.hp2 | missense_variant | MODERATE | c.2657C>T | p.Ser886Leu | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 2981/6300 | 2657/2772 | 886/923 | chr12 | 47737682 | |||
| chr12:47740781 | C | T | 2 | a0009 a0015 |
3 | HG02451.hp1 HG02559.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.2092G>A | p.Asp698Asn | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 21/28 | 2416/6300 | 2092/2772 | 698/923 | chr12 | 47740781 | |||
| chr12:47740985 | A | T | 2 | a0004 a0010 |
10 | HG01167.hp2 HG02723.hp2 HG02922.hp2 others(7): Show |
missense_variant | MODERATE | c.1979T>A | p.Leu660Gln | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 20/28 | 2303/6300 | 1979/2772 | 660/923 | chr12 | 47740985 | |||
| chr12:47747550 | C | T | 2 | a0004 a0014 |
9 | HG01167.hp2 HG02258.hp2 HG02922.hp2 others(6): Show |
missense_variant | MODERATE | c.1550G>A | p.Cys517Tyr | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 15/28 | 1874/6300 | 1550/2772 | 517/923 | chr12 | 47747550 | |||
| chr12:47748102 | C | T | 1 | a0012 | 1 | HG02056.hp1 | missense_variant | MODERATE | c.1294G>A | p.Ala432Thr | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 13/28 | 1618/6300 | 1294/2772 | 432/923 | chr12 | 47748102 | |||
| chr12:47748470 | A | C | 1 | a0019 | 1 | NA19085.hp2 | missense_variant | MODERATE | c.1227T>G | p.Ser409Arg | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 12/28 | 1551/6300 | 1227/2772 | 409/923 | chr12 | 47748470 | |||
| chr12:47748514 | T | C | 1 | a0005 | 4 | NA18966.hp1 NA18971.hp2 NA18979.hp1 others(1): Show |
missense_variant | MODERATE | c.1183A>G | p.Lys395Glu | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 12/28 | 1507/6300 | 1183/2772 | 395/923 | chr12 | 47748514 | |||
| chr12:47748829 | C | G | 1 | a0008 | 2 | HG02040.hp2 NA19005.hp1 |
missense_variant | MODERATE | c.1144G>C | p.Gly382Arg | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 11/28 | 1468/6300 | 1144/2772 | 382/923 | chr12 | 47748829 | |||
| chr12:47748853 | C | T | 4 | a0003 a0007 a0015 others(1): Show |
39 | HG00738.hp2 HG01099.hp2 HG01109.hp2 others(36): Show |
missense_variant | MODERATE | c.1120G>A | p.Gly374Ser | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 11/28 | 1444/6300 | 1120/2772 | 374/923 | chr12 | 47748853 | |||
| chr12:47749936 | T | A | 1 | a0011 | 1 | HG00597.hp1 | missense_variant | MODERATE | c.811A>T | p.Thr271Ser | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 8/28 | 1135/6300 | 811/2772 | 271/923 | chr12 | 47749936 | |||
| chr12:47751067 | T | C | 1 | a0018 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.652A>G | p.Thr218Ala | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 6/28 | 976/6300 | 652/2772 | 218/923 | chr12 | 47751067 | |||
| chr12:47751144 | A | ACGGGCT | 1 | a0006 | 3 | HG01884.hp2 HG02886.hp2 NA19240.hp2 |
conservative_inframe_insertion | MODERATE | c.569_574dupAGCCCG | p.Glu190_Pro191dup | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 6/28 | 898/6300 | 574/2772 | 192/923 | chr12 | 47751144 | |||
| chr12:47751201 | G | T | 1 | a0016 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.518C>A | p.Ala173Asp | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 6/28 | 842/6300 | 518/2772 | 173/923 | chr12 | 47751201 | |||
| chr12:47751503 | C | T | 1 | a0017 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.398G>A | p.Arg133Gln | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 5/28 | 722/6300 | 398/2772 | 133/923 | chr12 | 47751503 | |||
| chr12:47758039 | C | G | 5 | a0002 a0003 a0015 others(2): Show |
121 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(118): Show |
missense_variant | MODERATE | c.46G>C | p.Ala16Pro | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/28 | 370/6300 | 46/2772 | 16/923 | chr12 | 47758039 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:47738053 | G | A | 1 | a0003c0014 | 1 | NA19000.hp2 | synonymous_variant | LOW | c.2622C>T | p.His874His | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 27/28 | 2946/6300 | 2622/2772 | 874/923 | chr12 | 47738053 | |||
| chr12:47740692 | C | A | 1 | a0002c0016 | 1 | NA18962.hp1 | synonymous_variant | LOW | c.2181G>T | p.Val727Val | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 21/28 | 2505/6300 | 2181/2772 | 727/923 | chr12 | 47740692 | |||
| chr12:47740710 | C | T | 1 | a0002c0015 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.2163G>A | p.Glu721Glu | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 21/28 | 2487/6300 | 2163/2772 | 721/923 | chr12 | 47740710 | |||
| chr12:47748100 | G | A | 1 | a0002c0011 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.1296C>T | p.Ala432Ala | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 13/28 | 1620/6300 | 1296/2772 | 432/923 | chr12 | 47748100 | |||
| chr12:47749937 | C | A | 1 | a0011c0025 | 1 | HG00597.hp1 | synonymous_variant | LOW | c.810G>T | p.Gly270Gly | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 8/28 | 1134/6300 | 810/2772 | 270/923 | chr12 | 47749937 | |||
| chr12:47750416 | C | T | 1 | a0001c0020 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.681G>A | p.Gln227Gln | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 7/28 | 1005/6300 | 681/2772 | 227/923 | chr12 | 47750416 | |||
| chr12:47757977 | C | T | 1 | a0002c0011 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.108G>A | p.Pro36Pro | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/28 | 432/6300 | 108/2772 | 36/923 | chr12 | 47757977 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:47734403 | C | A | 3 | a0001c0001t0013 a0001c0001t0016 a0002c0002t0016 |
7 | HG02055.hp2 HG02257.hp2 HG02886.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3164G>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 3164 | chr12 | 47734403 | ||||||
| chr12:47734500 | C | G | 16 | a0001c0001t0003 a0001c0001t0007 a0001c0020t0003 others(13): Show |
91 | HG00639.hp2 HG00673.hp2 HG00738.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*3067G>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 3067 | chr12 | 47734500 | ||||||
| chr12:47734521 | C | T | 1 | a0001c0001t0027 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3046G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 3046 | chr12 | 47734521 | ||||||
| chr12:47734627 | G | A | 18 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0037 others(15): Show |
101 | HG00639.hp2 HG00673.hp2 HG00738.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*2940C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 2940 | chr12 | 47734627 | ||||||
| chr12:47734721 | G | T | 7 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0041 others(4): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*2846C>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 2846 | chr12 | 47734721 | ||||||
| chr12:47734723 | G | T | 1 | a0001c0001t0029 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2844C>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 2844 | chr12 | 47734723 | ||||||
| chr12:47734732 | G | A | 1 | a0002c0002t0039 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2835C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 2835 | chr12 | 47734732 | ||||||
| chr12:47734761 | C | A | 3 | a0001c0001t0037 a0004c0004t0009 a0010c0009t0009 |
11 | HG01167.hp2 HG02630.hp2 HG02723.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2806G>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 2806 | chr12 | 47734761 | ||||||
| chr12:47734905 | C | T | 1 | a0001c0001t0030 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2662G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 2662 | chr12 | 47734905 | ||||||
| chr12:47734906 | G | A | 3 | a0001c0001t0037 a0004c0004t0009 a0010c0009t0009 |
11 | HG01167.hp2 HG02630.hp2 HG02723.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2661C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 2661 | chr12 | 47734906 | ||||||
| chr12:47734924 | G | C | 1 | a0016c0012t0024 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2643C>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 2643 | chr12 | 47734924 | ||||||
| chr12:47734939 | A | G | 10 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0013 others(7): Show |
107 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*2628T>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 2628 | chr12 | 47734939 | ||||||
| chr12:47734955 | C | T | 1 | a0016c0012t0024 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2612G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 2612 | chr12 | 47734955 | ||||||
| chr12:47734956 | G | A | 1 | a0001c0001t0018 | 2 | HG01167.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2611C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 2611 | chr12 | 47734956 | ||||||
| chr12:47734985 | G | A | 11 | a0001c0001t0004 a0001c0001t0014 a0001c0001t0023 others(8): Show |
75 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*2582C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 2582 | chr12 | 47734985 | ||||||
| chr12:47735113 | C | T | 4 | a0001c0001t0037 a0002c0015t0033 a0004c0004t0009 others(1): Show |
12 | HG01167.hp2 HG02630.hp2 HG02723.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2454G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 2454 | chr12 | 47735113 | ||||||
| chr12:47735127 | C | T | 3 | a0001c0001t0037 a0004c0004t0009 a0010c0009t0009 |
11 | HG01167.hp2 HG02630.hp2 HG02723.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2440G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 2440 | chr12 | 47735127 | ||||||
| chr12:47735416 | C | G | 4 | a0001c0001t0037 a0002c0015t0033 a0004c0004t0009 others(1): Show |
12 | HG01167.hp2 HG02630.hp2 HG02723.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2151G>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 2151 | chr12 | 47735416 | ||||||
| chr12:47735426 | C | A | 4 | a0001c0001t0037 a0002c0015t0033 a0004c0004t0009 others(1): Show |
12 | HG01167.hp2 HG02630.hp2 HG02723.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2141G>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 2141 | chr12 | 47735426 | ||||||
| chr12:47735471 | G | A | 8 | a0001c0001t0019 a0001c0001t0022 a0001c0001t0037 others(5): Show |
28 | HG00280.hp1 HG00741.hp1 HG01069.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2096C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 2096 | chr12 | 47735471 | ||||||
| chr12:47735536 | G | A | 1 | a0001c0001t0028 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2031C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 2031 | chr12 | 47735536 | ||||||
| chr12:47735561 | A | G | 11 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0037 others(8): Show |
112 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*2006T>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 2006 | chr12 | 47735561 | ||||||
| chr12:47735601 | G | A | 3 | a0001c0001t0037 a0004c0004t0009 a0010c0009t0009 |
11 | HG01167.hp2 HG02630.hp2 HG02723.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1966C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 1966 | chr12 | 47735601 | ||||||
| chr12:47735711 | G | A | 3 | a0001c0001t0037 a0004c0004t0009 a0010c0009t0009 |
11 | HG01167.hp2 HG02630.hp2 HG02723.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1856C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 1856 | chr12 | 47735711 | ||||||
| chr12:47735779 | A | G | 14 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0013 others(11): Show |
119 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*1788T>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 1788 | chr12 | 47735779 | ||||||
| chr12:47735896 | A | G | 14 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0013 others(11): Show |
119 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*1671T>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 1671 | chr12 | 47735896 | ||||||
| chr12:47735948 | G | C | 3 | a0001c0001t0037 a0004c0004t0009 a0010c0009t0009 |
11 | HG01167.hp2 HG02630.hp2 HG02723.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1619C>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 1619 | chr12 | 47735948 | ||||||
| chr12:47735995 | A | C | 14 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0013 others(11): Show |
119 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*1572T>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 1572 | chr12 | 47735995 | ||||||
| chr12:47736169 | C | A | 1 | a0001c0001t0040 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1398G>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 1398 | chr12 | 47736169 | ||||||
| chr12:47736220 | C | T | 1 | a0002c0002t0025 | 1 | NA19066.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1347G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 1347 | chr12 | 47736220 | ||||||
| chr12:47736257 | G | A | 3 | a0001c0001t0037 a0004c0004t0009 a0010c0009t0009 |
11 | HG01167.hp2 HG02630.hp2 HG02723.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1310C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 1310 | chr12 | 47736257 | ||||||
| chr12:47736318 | G | A | 3 | a0001c0001t0011 a0001c0001t0029 a0003c0003t0011 |
6 | HG00558.hp2 HG02129.hp2 NA18962.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1249C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 1249 | chr12 | 47736318 | ||||||
| chr12:47736373 | T | G | 3 | a0001c0001t0037 a0004c0004t0009 a0010c0009t0009 |
11 | HG01167.hp2 HG02630.hp2 HG02723.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1194A>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 1194 | chr12 | 47736373 | ||||||
| chr12:47736623 | C | T | 1 | a0001c0001t0038 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*944G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 944 | chr12 | 47736623 | ||||||
| chr12:47736627 | G | T | 3 | a0001c0001t0037 a0004c0004t0009 a0010c0009t0009 |
11 | HG01167.hp2 HG02630.hp2 HG02723.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*940C>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 940 | chr12 | 47736627 | ||||||
| chr12:47736660 | T | G | 1 | a0001c0001t0041 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*907A>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 907 | chr12 | 47736660 | ||||||
| chr12:47736707 | G | A | 1 | a0002c0015t0033 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*860C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 860 | chr12 | 47736707 | ||||||
| chr12:47736776 | A | G | 1 | a0016c0012t0024 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*791T>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 791 | chr12 | 47736776 | ||||||
| chr12:47736795 | C | T | 61 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(58): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
3_prime_UTR_variant | MODIFIER | c.*772G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 772 | chr12 | 47736795 | ||||||
| chr12:47736851 | G | A | 2 | a0001c0001t0017 a0002c0002t0017 |
3 | HG02895.hp1 HG02897.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*716C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 716 | chr12 | 47736851 | ||||||
| chr12:47736919 | C | G | 1 | a0001c0001t0023 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*648G>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 648 | chr12 | 47736919 | ||||||
| chr12:47736985 | C | T | 3 | a0001c0001t0013 a0001c0001t0016 a0002c0002t0016 |
7 | HG02055.hp2 HG02257.hp2 HG02886.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*582G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 582 | chr12 | 47736985 | ||||||
| chr12:47736990 | A | C | 3 | a0001c0001t0037 a0004c0004t0009 a0010c0009t0009 |
11 | HG01167.hp2 HG02630.hp2 HG02723.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*577T>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 577 | chr12 | 47736990 | ||||||
| chr12:47737236 | CACAGAAT others(7): Show |
C | 1 | a0001c0001t0032 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*317_*330delCTTCCA others(8): Show |
RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 317 | chr12 | 47737236 | ||||||
| chr12:47737260 | G | A | 3 | a0001c0001t0037 a0004c0004t0009 a0010c0009t0009 |
11 | HG01167.hp2 HG02630.hp2 HG02723.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*307C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 307 | chr12 | 47737260 | ||||||
| chr12:47737294 | G | A | 4 | a0001c0001t0019 a0001c0001t0022 a0002c0002t0008 others(1): Show |
16 | HG00280.hp1 HG00741.hp1 HG01069.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*273C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 273 | chr12 | 47737294 | ||||||
| chr12:47737328 | T | G | 3 | a0001c0001t0037 a0004c0004t0009 a0010c0009t0009 |
11 | HG01167.hp2 HG02630.hp2 HG02723.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*239A>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 239 | chr12 | 47737328 | ||||||
| chr12:47737340 | C | A | 1 | a0001c0001t0020 | 2 | NA18953.hp2 NA18959.hp2 |
3_prime_UTR_variant | MODIFIER | c.*227G>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 227 | chr12 | 47737340 | ||||||
| chr12:47737372 | G | A | 3 | a0001c0001t0037 a0004c0004t0009 a0010c0009t0009 |
11 | HG01167.hp2 HG02630.hp2 HG02723.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*195C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 195 | chr12 | 47737372 | ||||||
| chr12:47737383 | G | A | 1 | a0002c0015t0033 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*184C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 184 | chr12 | 47737383 | ||||||
| chr12:47737406 | A | G | 1 | a0006c0006t0015 | 3 | HG01884.hp2 HG02886.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*161T>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 161 | chr12 | 47737406 | ||||||
| chr12:47737453 | T | A | 3 | a0001c0001t0037 a0004c0004t0009 a0010c0009t0009 |
11 | HG01167.hp2 HG02630.hp2 HG02723.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*114A>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 114 | chr12 | 47737453 | ||||||
| chr12:47737454 | C | T | 3 | a0001c0001t0037 a0004c0004t0009 a0010c0009t0009 |
11 | HG01167.hp2 HG02630.hp2 HG02723.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*113G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 28/28 | 113 | chr12 | 47737454 | ||||||
| chr12:47758649 | G | A | 4 | a0002c0002t0008 a0002c0002t0021 a0002c0002t0034 others(1): Show |
15 | HG00140.hp2 HG00741.hp1 HG01069.hp1 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-93C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 1/28 | 93 | chr12 | 47758649 | ||||||
| chr12:47758764 | G | A | 1 | a0003c0003t0036 | 1 | HG01192.hp2 | 5_prime_UTR_variant | MODIFIER | c.-208C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 1/28 | 208 | chr12 | 47758764 | ||||||
| chr12:47758822 | G | C | 18 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0010 others(15): Show |
116 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(113): Show |
5_prime_UTR_variant | MODIFIER | c.-266C>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 1/28 | 266 | chr12 | 47758822 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:47737797 | C | T | 1 | a0016c0012t0024g0075 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2654-112G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 27/27 | chr12 | 47737797 | |||||||
| chr12:47737895 | T | C | 1 | a0001c0001t0005g0126 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2653+127A>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 27/27 | chr12 | 47737895 | |||||||
| chr12:47737927 | G | A | 3 | a0009c0010t0010g0184 a0009c0010t0010g0186 a0015c0013t0001g0077 |
3 | HG02451.hp1 HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2653+95C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 27/27 | chr12 | 47737927 | |||||||
| chr12:47737945 | G | A | 38 | a0001c0001t0002g0001 a0001c0001t0002g0051 a0001c0001t0002g0058 others(35): Show |
107 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.2653+77C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 27/27 | chr12 | 47737945 | |||||||
| chr12:47738098 | G | T | 1 | a0002c0002t0003g0031 | 2 | HG02683.hp2 HG03688.hp2 |
splice_region_variant&intron_variant | LOW | c.2582-5C>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 26/27 | chr12 | 47738098 | |||||||
| chr12:47738130 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2582-37G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 26/27 | chr12 | 47738130 | |||||||
| chr12:47738376 | A | T | 44 | a0001c0001t0002g0001 a0001c0001t0002g0051 a0001c0001t0002g0058 others(41): Show |
118 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.2527-129T>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 25/27 | chr12 | 47738376 | |||||||
| chr12:47738393 | T | C | 44 | a0001c0001t0002g0001 a0001c0001t0002g0051 a0001c0001t0002g0058 others(41): Show |
118 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.2527-146A>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 25/27 | chr12 | 47738393 | |||||||
| chr12:47738439 | C | G | 1 | a0001c0001t0007g0181 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2527-192G>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 25/27 | chr12 | 47738439 | |||||||
| chr12:47738495 | T | C | 1 | a0016c0012t0024g0075 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2526+195A>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 25/27 | chr12 | 47738495 | |||||||
| chr12:47738668 | T | C | 167 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0019 others(164): Show |
397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.2526+22A>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 25/27 | chr12 | 47738668 | |||||||
| chr12:47738931 | G | A | 37 | a0001c0001t0002g0001 a0001c0001t0002g0051 a0001c0001t0002g0058 others(34): Show |
106 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.2462-177C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 24/27 | chr12 | 47738931 | |||||||
| chr12:47738986 | C | T | 1 | a0007c0007t0003g0132 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2461+157G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 24/27 | chr12 | 47738986 | |||||||
| chr12:47739106 | G | A | 41 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0019 others(38): Show |
91 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.2461+37C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 24/27 | chr12 | 47739106 | |||||||
| chr12:47739394 | C | T | 1 | a0008c0008t0004g0093 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2374-164G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 23/27 | chr12 | 47739394 | |||||||
| chr12:47739573 | C | T | 1 | a0001c0001t0002g0177 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2374-343G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 23/27 | chr12 | 47739573 | |||||||
| chr12:47739750 | C | G | 1 | a0001c0001t0007g0054 | 2 | HG01346.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.2373+391G>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 23/27 | chr12 | 47739750 | |||||||
| chr12:47739768 | C | T | 2 | a0001c0001t0001g0122 a0001c0001t0001g0141 |
2 | NA19011.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.2373+373G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 23/27 | chr12 | 47739768 | |||||||
| chr12:47739780 | A | G | 93 | a0001c0001t0002g0001 a0001c0001t0002g0051 a0001c0001t0002g0058 others(90): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.2373+361T>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 23/27 | chr12 | 47739780 | |||||||
| chr12:47739919 | G | A | 165 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0019 others(162): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.2373+222C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 23/27 | chr12 | 47739919 | |||||||
| chr12:47739927 | G | A | 1 | a0001c0001t0040g0170 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2373+214C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 23/27 | chr12 | 47739927 | |||||||
| chr12:47740120 | C | T | 2 | a0002c0002t0001g0033 a0002c0011t0001g0061 |
3 | HG02922.hp1 HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2373+21G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 23/27 | chr12 | 47740120 | |||||||
| chr12:47740233 | C | T | 6 | a0001c0001t0003g0105 a0001c0001t0003g0148 a0002c0002t0003g0007 others(3): Show |
16 | HG00673.hp2 HG02135.hp1 HG02523.hp1 others(13): Show |
intron_variant | MODIFIER | c.2323-42G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 22/27 | chr12 | 47740233 | |||||||
| chr12:47740277 | AG | A | 2 | a0003c0003t0003g0014 a0003c0003t0003g0060 |
5 | NA18945.hp1 NA19003.hp1 NA19066.hp1 others(2): Show |
intron_variant | MODIFIER | c.2322+27delC | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 22/27 | chr12 | 47740277 | |||||||
| chr12:47740431 | G | C | 38 | a0001c0001t0002g0001 a0001c0001t0002g0051 a0001c0001t0002g0058 others(35): Show |
107 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.2232-36C>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 21/27 | chr12 | 47740431 | |||||||
| chr12:47740453 | C | T | 1 | a0001c0001t0018g0035 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2232-58G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 21/27 | chr12 | 47740453 | |||||||
| chr12:47740517 | G | A | 53 | a0001c0001t0003g0017 a0001c0001t0003g0037 a0001c0001t0003g0105 others(50): Show |
116 | HG00280.hp1 HG00639.hp2 HG00673.hp2 others(113): Show |
intron_variant | MODIFIER | c.2232-122C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 21/27 | chr12 | 47740517 | |||||||
| chr12:47740577 | G | T | 38 | a0001c0001t0002g0001 a0001c0001t0002g0051 a0001c0001t0002g0058 others(35): Show |
107 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.2231+65C>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 21/27 | chr12 | 47740577 | |||||||
| chr12:47740598 | CG | C | 93 | a0001c0001t0002g0001 a0001c0001t0002g0051 a0001c0001t0002g0058 others(90): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.2231+43delC | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 21/27 | chr12 | 47740598 | |||||||
| chr12:47740604 | G | A | 2 | a0001c0001t0002g0167 a0001c0001t0005g0108 |
2 | NA18988.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.2231+38C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 21/27 | chr12 | 47740604 | |||||||
| chr12:47740616 | G | A | 1 | a0002c0015t0033g0074 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2231+26C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 21/27 | chr12 | 47740616 | |||||||
| chr12:47740851 | C | T | 47 | a0001c0001t0003g0017 a0001c0001t0003g0037 a0001c0001t0003g0105 others(44): Show |
105 | HG00280.hp1 HG00639.hp2 HG00673.hp2 others(102): Show |
intron_variant | MODIFIER | c.2050-28G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 20/27 | chr12 | 47740851 | |||||||
| chr12:47740912 | T | C | 94 | a0001c0001t0002g0001 a0001c0001t0002g0051 a0001c0001t0002g0058 others(91): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
splice_region_variant&intron_variant | LOW | c.2049+3A>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 20/27 | chr12 | 47740912 | |||||||
| chr12:47741043 | G | A | 1 | a0002c0002t0002g0048 | 2 | HG01168.hp1 HG03491.hp1 |
splice_region_variant&intron_variant | LOW | c.1924-3C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 19/27 | chr12 | 47741043 | |||||||
| chr12:47741130 | C | T | 1 | a0007c0007t0003g0132 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1924-90G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 19/27 | chr12 | 47741130 | |||||||
| chr12:47741176 | G | T | 1 | a0001c0001t0004g0099 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1924-136C>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 19/27 | chr12 | 47741176 | |||||||
| chr12:47741198 | G | A | 1 | a0001c0001t0029g0143 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1924-158C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 19/27 | chr12 | 47741198 | |||||||
| chr12:47741202 | G | A | 1 | a0002c0002t0008g0155 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1924-162C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 19/27 | chr12 | 47741202 | |||||||
| chr12:47741420 | T | C | 1 | a0002c0015t0033g0074 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1923+85A>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 19/27 | chr12 | 47741420 | |||||||
| chr12:47741639 | G | A | 2 | a0001c0001t0005g0008 a0001c0001t0005g0124 |
10 | HG00544.hp1 NA18970.hp1 NA18975.hp2 others(7): Show |
intron_variant | MODIFIER | c.1826-37C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 18/27 | chr12 | 47741639 | |||||||
| chr12:47741679 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1826-77C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 18/27 | chr12 | 47741679 | |||||||
| chr12:47741729 | C | G | 1 | a0001c0001t0023g0114 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1826-127G>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 18/27 | chr12 | 47741729 | |||||||
| chr12:47741807 | G | A | 60 | a0001c0001t0001g0139 a0001c0001t0001g0144 a0001c0001t0003g0105 others(57): Show |
122 | HG00280.hp1 HG00438.hp2 HG00639.hp2 others(119): Show |
intron_variant | MODIFIER | c.1826-205C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 18/27 | chr12 | 47741807 | |||||||
| chr12:47741813 | T | C | 2 | a0001c0001t0004g0111 a0001c0001t0004g0112 |
2 | HG00140.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1826-211A>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 18/27 | chr12 | 47741813 | |||||||
| chr12:47741823 | G | A | 1 | a0016c0012t0024g0075 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1826-221C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 18/27 | chr12 | 47741823 | |||||||
| chr12:47741824 | T | C | 10 | a0001c0001t0019g0104 a0001c0001t0019g0145 a0001c0001t0022g0053 others(7): Show |
16 | HG00280.hp1 HG00741.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.1826-222A>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 18/27 | chr12 | 47741824 | |||||||
| chr12:47742107 | C | G | 3 | a0009c0010t0010g0184 a0009c0010t0010g0186 a0015c0013t0001g0077 |
3 | HG02451.hp1 HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1826-505G>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 18/27 | chr12 | 47742107 | |||||||
| chr12:47742199 | C | T | 46 | a0001c0001t0003g0105 a0001c0001t0003g0148 a0001c0001t0007g0012 others(43): Show |
101 | HG00280.hp1 HG00639.hp2 HG00673.hp2 others(98): Show |
intron_variant | MODIFIER | c.1826-597G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 18/27 | chr12 | 47742199 | |||||||
| chr12:47742205 | TATG | T | 45 | a0001c0001t0003g0105 a0001c0001t0003g0148 a0001c0001t0007g0012 others(42): Show |
100 | HG00280.hp1 HG00639.hp2 HG00673.hp2 others(97): Show |
intron_variant | MODIFIER | c.1826-606_1826-604d others(5): Show |
RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 18/27 | chr12 | 47742205 | |||||||
| chr12:47742270 | G | A | 1 | a0002c0015t0033g0074 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1826-668C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 18/27 | chr12 | 47742270 | |||||||
| chr12:47742304 | C | T | 1 | a0002c0002t0007g0027 | 3 | HG01884.hp1 HG02145.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1826-702G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 18/27 | chr12 | 47742304 | |||||||
| chr12:47742364 | A | G | 1 | a0001c0001t0038g0173 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1826-762T>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 18/27 | chr12 | 47742364 | |||||||
| chr12:47742459 | T | C | 1 | a0002c0002t0002g0049 | 2 | NA18941.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.1826-857A>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 18/27 | chr12 | 47742459 | |||||||
| chr12:47742771 | C | T | 11 | a0001c0001t0013g0029 a0001c0001t0013g0171 a0001c0001t0016g0094 others(8): Show |
18 | HG01167.hp2 HG02055.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1825+759G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 18/27 | chr12 | 47742771 | |||||||
| chr12:47742939 | A | G | 1 | a0001c0001t0010g0183 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1825+591T>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 18/27 | chr12 | 47742939 | |||||||
| chr12:47743058 | T | C | 1 | a0001c0001t0006g0130 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1825+472A>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 18/27 | chr12 | 47743058 | |||||||
| chr12:47743207 | A | G | 1 | a0001c0001t0005g0151 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1825+323T>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 18/27 | chr12 | 47743207 | |||||||
| chr12:47743425 | G | A | 1 | a0001c0001t0038g0173 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1825+105C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 18/27 | chr12 | 47743425 | |||||||
| chr12:47743958 | G | C | 1 | a0002c0002t0004g0069 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1678+29C>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 17/27 | chr12 | 47743958 | |||||||
| chr12:47744086 | G | A | 1 | a0001c0001t0012g0180 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1597-18C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47744086 | |||||||
| chr12:47744097 | G | T | 1 | a0001c0001t0001g0140 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1597-29C>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47744097 | |||||||
| chr12:47744162 | C | T | 1 | a0002c0011t0001g0061 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1597-94G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47744162 | |||||||
| chr12:47744167 | G | A | 11 | a0001c0001t0013g0029 a0001c0001t0013g0171 a0001c0001t0016g0094 others(8): Show |
18 | HG01167.hp2 HG02055.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1597-99C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47744167 | |||||||
| chr12:47744188 | C | T | 1 | a0001c0001t0006g0128 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1597-120G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47744188 | |||||||
| chr12:47744238 | A | G | 1 | a0001c0001t0040g0170 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1597-170T>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47744238 | |||||||
| chr12:47744239 | C | A | 6 | a0001c0001t0037g0166 a0004c0004t0009g0013 a0004c0004t0009g0036 others(3): Show |
11 | HG01167.hp2 HG02630.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.1597-171G>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47744239 | |||||||
| chr12:47744340 | TCTAATA | T | 5 | a0001c0001t0013g0029 a0001c0001t0013g0171 a0001c0001t0016g0094 others(2): Show |
7 | HG02055.hp2 HG02257.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1597-278_1597-273d others(8): Show |
RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47744340 | |||||||
| chr12:47744500 | G | T | 10 | a0001c0001t0019g0104 a0001c0001t0019g0145 a0001c0001t0022g0053 others(7): Show |
16 | HG00280.hp1 HG00741.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.1597-432C>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47744500 | |||||||
| chr12:47744511 | A | C | 1 | a0001c0001t0004g0113 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1597-443T>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47744511 | |||||||
| chr12:47744566 | C | T | 1 | a0005c0005t0006g0120 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1597-498G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47744566 | |||||||
| chr12:47744583 | C | T | 31 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0019 others(28): Show |
76 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.1597-515G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47744583 | |||||||
| chr12:47744679 | G | A | 1 | a0001c0001t0010g0057 | 2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.1597-611C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47744679 | |||||||
| chr12:47744855 | A | G | 1 | a0002c0002t0001g0033 | 2 | HG02922.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1597-787T>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47744855 | |||||||
| chr12:47744895 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1597-827G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47744895 | |||||||
| chr12:47744931 | C | G | 1 | a0001c0001t0038g0173 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1597-863G>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47744931 | |||||||
| chr12:47744943 | CT | C | 6 | a0001c0001t0013g0029 a0001c0001t0013g0171 a0001c0001t0016g0094 others(3): Show |
8 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1597-876delA | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47744943 | |||||||
| chr12:47745070 | G | A | 6 | a0001c0001t0037g0166 a0004c0004t0009g0013 a0004c0004t0009g0036 others(3): Show |
11 | HG01167.hp2 HG02630.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.1597-1002C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47745070 | |||||||
| chr12:47745103 | T | C | 2 | a0001c0001t0007g0055 a0001c0001t0007g0181 |
3 | HG00738.hp1 HG01192.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1597-1035A>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47745103 | |||||||
| chr12:47745111 | G | T | 1 | a0001c0001t0004g0039 | 2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1597-1043C>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47745111 | |||||||
| chr12:47745324 | G | A | 1 | a0001c0001t0018g0035 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1597-1256C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47745324 | |||||||
| chr12:47745568 | C | T | 45 | a0001c0001t0001g0139 a0001c0001t0003g0017 a0001c0001t0003g0037 others(42): Show |
95 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1596+1292G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47745568 | |||||||
| chr12:47745595 | G | A | 2 | a0001c0001t0007g0056 a0017c0019t0012g0174 |
3 | HG02572.hp2 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1596+1265C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47745595 | |||||||
| chr12:47745681 | G | T | 3 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0004g0138 |
3 | NA18945.hp2 NA19001.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1596+1179C>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47745681 | |||||||
| chr12:47745793 | C | T | 1 | a0010c0009t0009g0116 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1596+1067G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47745793 | |||||||
| chr12:47745819 | G | A | 26 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0041 others(23): Show |
67 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1596+1041C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47745819 | |||||||
| chr12:47745854 | G | A | 1 | a0003c0003t0003g0083 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1596+1006C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47745854 | |||||||
| chr12:47745892 | C | T | 1 | a0001c0001t0002g0175 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1596+968G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47745892 | |||||||
| chr12:47745993 | G | T | 2 | a0002c0002t0002g0163 a0002c0002t0002g0165 |
2 | HG03654.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1596+867C>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47745993 | |||||||
| chr12:47746027 | A | C | 15 | a0002c0002t0008g0011 a0002c0002t0008g0152 a0002c0002t0008g0153 others(12): Show |
26 | HG00140.hp2 HG00741.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.1596+833T>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47746027 | |||||||
| chr12:47746062 | C | T | 1 | a0002c0002t0025g0072 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1596+798G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47746062 | |||||||
| chr12:47746150 | A | G | 56 | a0001c0001t0001g0026 a0001c0001t0001g0096 a0001c0001t0001g0101 others(53): Show |
138 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.1596+710T>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47746150 | |||||||
| chr12:47746315 | A | C | 1 | a0002c0002t0008g0157 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1596+545T>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47746315 | |||||||
| chr12:47746470 | A | G | 1 | a0002c0002t0001g0033 | 2 | HG02922.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1596+390T>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47746470 | |||||||
| chr12:47746482 | G | C | 1 | a0002c0002t0002g0050 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1596+378C>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47746482 | |||||||
| chr12:47746598 | T | C | 30 | a0001c0001t0001g0026 a0001c0001t0001g0096 a0001c0001t0001g0101 others(27): Show |
87 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.1596+262A>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47746598 | |||||||
| chr12:47746645 | G | A | 3 | a0001c0001t0004g0039 a0001c0001t0004g0117 a0010c0009t0009g0116 |
4 | HG02630.hp1 HG02723.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596+215C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47746645 | |||||||
| chr12:47746718 | C | T | 1 | a0002c0011t0001g0061 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1596+142G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47746718 | |||||||
| chr12:47746788 | A | C | 1 | a0001c0001t0010g0057 | 2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.1596+72T>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47746788 | |||||||
| chr12:47746799 | G | T | 1 | a0001c0001t0004g0097 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1596+61C>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47746799 | |||||||
| chr12:47746800 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1596+60G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 16/27 | chr12 | 47746800 | |||||||
| chr12:47746907 | C | G | 1 | a0001c0001t0037g0166 | 1 | HG02630.hp2 | splice_region_variant&intron_variant | LOW | c.1557-8G>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 15/27 | chr12 | 47746907 | |||||||
| chr12:47746986 | G | A | 1 | a0008c0008t0004g0093 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1557-87C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 15/27 | chr12 | 47746986 | |||||||
| chr12:47747015 | C | T | 17 | a0002c0002t0003g0070 a0002c0002t0008g0011 a0002c0002t0008g0152 others(14): Show |
28 | HG00140.hp2 HG00741.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.1557-116G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 15/27 | chr12 | 47747015 | |||||||
| chr12:47747032 | C | T | 1 | a0001c0001t0011g0043 | 2 | NA18962.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.1557-133G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 15/27 | chr12 | 47747032 | |||||||
| chr12:47747044 | A | C | 30 | a0001c0001t0003g0148 a0001c0001t0038g0173 a0002c0002t0001g0066 others(27): Show |
58 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.1557-145T>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 15/27 | chr12 | 47747044 | |||||||
| chr12:47747111 | G | C | 1 | a0001c0001t0002g0182 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1557-212C>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 15/27 | chr12 | 47747111 | |||||||
| chr12:47747180 | A | T | 17 | a0002c0002t0003g0070 a0002c0002t0008g0011 a0002c0002t0008g0152 others(14): Show |
28 | HG00140.hp2 HG00741.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.1557-281T>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 15/27 | chr12 | 47747180 | |||||||
| chr12:47747374 | G | T | 14 | a0001c0001t0003g0148 a0001c0001t0038g0173 a0002c0002t0001g0066 others(11): Show |
31 | HG00099.hp2 HG00639.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.1556+170C>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 15/27 | chr12 | 47747374 | |||||||
| chr12:47747673 | C | T | 3 | a0001c0001t0005g0095 a0008c0008t0004g0092 a0008c0008t0004g0093 |
3 | HG02040.hp2 NA18942.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1473+39G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 14/27 | chr12 | 47747673 | |||||||
| chr12:47747689 | C | T | 17 | a0002c0002t0003g0070 a0002c0002t0008g0011 a0002c0002t0008g0152 others(14): Show |
28 | HG00140.hp2 HG00741.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.1473+23G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 14/27 | chr12 | 47747689 | |||||||
| chr12:47747692 | T | C | 17 | a0002c0002t0003g0070 a0002c0002t0008g0011 a0002c0002t0008g0152 others(14): Show |
28 | HG00140.hp2 HG00741.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.1473+20A>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 14/27 | chr12 | 47747692 | |||||||
| chr12:47747908 | A | C | 1 | a0001c0001t0016g0094 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1323-46T>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 13/27 | chr12 | 47747908 | |||||||
| chr12:47747968 | G | C | 2 | a0002c0002t0002g0163 a0002c0002t0002g0165 |
2 | HG03654.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1322+106C>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 13/27 | chr12 | 47747968 | |||||||
| chr12:47748015 | T | C | 30 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0019 others(27): Show |
79 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.1322+59A>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 13/27 | chr12 | 47748015 | |||||||
| chr12:47748243 | C | A | 11 | a0001c0001t0001g0123 a0001c0001t0005g0124 a0001c0001t0006g0016 others(8): Show |
19 | HG01099.hp1 HG01346.hp2 HG02895.hp1 others(16): Show |
intron_variant | MODIFIER | c.1244-91G>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 12/27 | chr12 | 47748243 | |||||||
| chr12:47748368 | G | A | 17 | a0002c0002t0003g0070 a0002c0002t0008g0011 a0002c0002t0008g0152 others(14): Show |
28 | HG00140.hp2 HG00741.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.1243+86C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 12/27 | chr12 | 47748368 | |||||||
| chr12:47748560 | T | C | 19 | a0003c0003t0003g0004 a0003c0003t0003g0014 a0003c0003t0003g0030 others(16): Show |
39 | HG00738.hp2 HG01099.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.1155-18A>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 11/27 | chr12 | 47748560 | |||||||
| chr12:47748635 | C | G | 151 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0019 others(148): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.1155-93G>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 11/27 | chr12 | 47748635 | |||||||
| chr12:47748731 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1154+88C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 11/27 | chr12 | 47748731 | |||||||
| chr12:47749114 | C | T | 4 | a0001c0001t0003g0017 a0001c0001t0003g0037 a0001c0001t0004g0020 others(1): Show |
9 | HG01168.hp2 HG01169.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.1042-183G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 10/27 | chr12 | 47749114 | |||||||
| chr12:47749312 | G | GCTCTGGT | 92 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0019 others(89): Show |
223 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.1041+71_1041+77dup others(7): Show |
RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 10/27 | chr12 | 47749312 | |||||||
| chr12:47749577 | T | C | 150 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0019 others(147): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.895-41A>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 9/27 | chr12 | 47749577 | |||||||
| chr12:47749832 | C | G | 1 | a0001c0001t0007g0185 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.818-15G>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 8/27 | chr12 | 47749832 | |||||||
| chr12:47749840 | C | T | 1 | a0006c0006t0015g0023 | 3 | HG01884.hp2 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.818-23G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 8/27 | chr12 | 47749840 | |||||||
| chr12:47749901 | C | T | 1 | a0003c0003t0003g0034 | 2 | HG03831.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.817+29G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 8/27 | chr12 | 47749901 | |||||||
| chr12:47750119 | T | C | 1 | a0001c0001t0037g0166 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.757-129A>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 7/27 | chr12 | 47750119 | |||||||
| chr12:47750195 | C | T | 18 | a0001c0001t0010g0057 a0003c0003t0003g0004 a0003c0003t0003g0014 others(15): Show |
39 | HG00738.hp2 HG01099.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.756+146G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 7/27 | chr12 | 47750195 | |||||||
| chr12:47750460 | A | C | 150 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0019 others(147): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.672-35T>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 6/27 | chr12 | 47750460 | |||||||
| chr12:47750585 | G | A | 2 | a0002c0002t0003g0070 a0002c0002t0016g0071 |
2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.672-160C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 6/27 | chr12 | 47750585 | |||||||
| chr12:47750661 | C | G | 1 | a0002c0002t0003g0065 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.672-236G>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 6/27 | chr12 | 47750661 | |||||||
| chr12:47750737 | G | C | 42 | a0001c0001t0001g0123 a0001c0001t0002g0001 a0001c0001t0002g0051 others(39): Show |
104 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.671+311C>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 6/27 | chr12 | 47750737 | |||||||
| chr12:47750851 | T | TG | 17 | a0003c0003t0003g0004 a0003c0003t0003g0014 a0003c0003t0003g0030 others(14): Show |
37 | HG00738.hp2 HG01099.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.671+196dupC | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 6/27 | chr12 | 47750851 | |||||||
| chr12:47750898 | G | A | 2 | a0001c0001t0004g0110 a0001c0001t0027g0109 |
2 | HG02895.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.671+150C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 6/27 | chr12 | 47750898 | |||||||
| chr12:47750934 | G | A | 1 | a0012c0022t0003g0089 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.671+114C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 6/27 | chr12 | 47750934 | |||||||
| chr12:47750989 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.671+59G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 6/27 | chr12 | 47750989 | |||||||
| chr12:47751321 | G | A | 74 | a0001c0001t0001g0096 a0001c0001t0001g0101 a0001c0001t0001g0103 others(71): Show |
173 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.502+78C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 5/27 | chr12 | 47751321 | |||||||
| chr12:47751370 | G | A | 74 | a0001c0001t0001g0096 a0001c0001t0001g0101 a0001c0001t0001g0103 others(71): Show |
173 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.502+29C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 5/27 | chr12 | 47751370 | |||||||
| chr12:47751388 | C | T | 74 | a0001c0001t0001g0096 a0001c0001t0001g0101 a0001c0001t0001g0103 others(71): Show |
173 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.502+11G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 5/27 | chr12 | 47751388 | |||||||
| chr12:47751585 | A | G | 27 | a0001c0001t0002g0001 a0001c0001t0002g0051 a0001c0001t0002g0058 others(24): Show |
80 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.381-65T>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 4/27 | chr12 | 47751585 | |||||||
| chr12:47751621 | G | A | 1 | a0001c0001t0005g0038 | 2 | NA18954.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.381-101C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 4/27 | chr12 | 47751621 | |||||||
| chr12:47751673 | G | A | 13 | a0002c0002t0002g0006 a0002c0002t0002g0048 a0002c0002t0002g0049 others(10): Show |
33 | HG01168.hp1 HG01243.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.380+50C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 4/27 | chr12 | 47751673 | |||||||
| chr12:47752072 | C | A | 1 | a0003c0003t0003g0086 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.220-103G>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47752072 | |||||||
| chr12:47752186 | T | C | 74 | a0001c0001t0001g0096 a0001c0001t0001g0101 a0001c0001t0001g0103 others(71): Show |
173 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.220-217A>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47752186 | |||||||
| chr12:47752258 | T | C | 75 | a0001c0001t0001g0096 a0001c0001t0001g0101 a0001c0001t0001g0103 others(72): Show |
174 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.220-289A>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47752258 | |||||||
| chr12:47752259 | G | A | 1 | a0002c0011t0001g0061 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.220-290C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47752259 | |||||||
| chr12:47752319 | G | A | 1 | a0002c0011t0001g0061 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.220-350C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47752319 | |||||||
| chr12:47752388 | G | A | 1 | a0001c0001t0018g0035 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.220-419C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47752388 | |||||||
| chr12:47752399 | G | A | 33 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0019 others(30): Show |
82 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.220-430C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47752399 | |||||||
| chr12:47752480 | G | A | 9 | a0002c0002t0008g0011 a0002c0002t0008g0152 a0002c0002t0008g0153 others(6): Show |
15 | HG00140.hp2 HG00741.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.220-511C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47752480 | |||||||
| chr12:47752652 | G | C | 2 | a0001c0001t0004g0111 a0001c0001t0004g0112 |
2 | HG00140.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.220-683C>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47752652 | |||||||
| chr12:47752807 | T | C | 90 | a0001c0001t0001g0096 a0001c0001t0001g0101 a0001c0001t0001g0103 others(87): Show |
200 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.220-838A>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47752807 | |||||||
| chr12:47752817 | G | A | 1 | a0002c0002t0002g0163 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.220-848C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47752817 | |||||||
| chr12:47752942 | C | T | 12 | a0001c0001t0038g0173 a0002c0002t0001g0066 a0002c0002t0001g0067 others(9): Show |
29 | HG00099.hp2 HG00639.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.220-973G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47752942 | |||||||
| chr12:47752967 | C | T | 1 | a0012c0022t0003g0089 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.220-998G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47752967 | |||||||
| chr12:47753086 | C | T | 1 | a0001c0001t0007g0172 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.220-1117G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47753086 | |||||||
| chr12:47753264 | A | G | 1 | a0002c0002t0002g0161 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.220-1295T>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47753264 | |||||||
| chr12:47753532 | C | T | 1 | a0002c0002t0005g0032 | 2 | NA18980.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.220-1563G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47753532 | |||||||
| chr12:47753775 | T | C | 1 | a0002c0002t0017g0063 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.220-1806A>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47753775 | |||||||
| chr12:47753904 | G | C | 3 | a0001c0001t0004g0005 a0001c0001t0004g0113 a0001c0001t0023g0114 |
14 | HG00733.hp1 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.220-1935C>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47753904 | |||||||
| chr12:47754026 | A | C | 1 | a0001c0001t0013g0171 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.220-2057T>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47754026 | |||||||
| chr12:47754233 | A | C | 1 | a0016c0012t0024g0075 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.220-2264T>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47754233 | |||||||
| chr12:47754397 | C | G | 74 | a0001c0001t0001g0096 a0001c0001t0001g0101 a0001c0001t0001g0103 others(71): Show |
173 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.220-2428G>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47754397 | |||||||
| chr12:47754499 | C | T | 1 | a0001c0001t0002g0169 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.220-2530G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47754499 | |||||||
| chr12:47754524 | G | A | 9 | a0002c0002t0008g0011 a0002c0002t0008g0152 a0002c0002t0008g0153 others(6): Show |
15 | HG00140.hp2 HG00741.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.220-2555C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47754524 | |||||||
| chr12:47754871 | G | A | 1 | a0001c0001t0001g0044 | 2 | NA18970.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.220-2902C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47754871 | |||||||
| chr12:47754917 | C | T | 2 | a0001c0001t0001g0041 a0011c0025t0001g0125 |
3 | HG00423.hp1 HG00597.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.220-2948G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47754917 | |||||||
| chr12:47755075 | G | A | 4 | a0001c0001t0004g0039 a0001c0001t0004g0117 a0001c0020t0003g0115 others(1): Show |
5 | HG02630.hp1 HG02723.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.219+2791C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47755075 | |||||||
| chr12:47755137 | T | C | 9 | a0002c0002t0008g0011 a0002c0002t0008g0152 a0002c0002t0008g0153 others(6): Show |
15 | HG00140.hp2 HG00741.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.219+2729A>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47755137 | |||||||
| chr12:47755150 | A | G | 1 | a0002c0002t0003g0065 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.219+2716T>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47755150 | |||||||
| chr12:47755418 | G | A | 1 | a0002c0002t0002g0164 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.219+2448C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47755418 | |||||||
| chr12:47755513 | T | C | 1 | a0001c0001t0002g0058 | 2 | HG01943.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.219+2353A>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47755513 | |||||||
| chr12:47755537 | C | T | 1 | a0002c0011t0001g0061 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.219+2329G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47755537 | |||||||
| chr12:47755688 | T | G | 1 | a0002c0002t0002g0165 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.219+2178A>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47755688 | |||||||
| chr12:47755703 | T | C | 2 | a0004c0004t0009g0036 a0014c0023t0006g0088 |
3 | HG02258.hp2 HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.219+2163A>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47755703 | |||||||
| chr12:47755844 | C | T | 1 | a0001c0001t0018g0035 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.219+2022G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47755844 | |||||||
| chr12:47755969 | T | G | 44 | a0001c0001t0001g0096 a0001c0001t0001g0101 a0001c0001t0001g0103 others(41): Show |
106 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.219+1897A>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47755969 | |||||||
| chr12:47755977 | C | G | 1 | a0005c0005t0006g0120 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.219+1889G>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47755977 | |||||||
| chr12:47755978 | C | A | 1 | a0005c0005t0006g0120 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.219+1888G>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47755978 | |||||||
| chr12:47755979 | C | G | 1 | a0005c0005t0006g0120 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.219+1887G>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47755979 | |||||||
| chr12:47755980 | C | A | 1 | a0005c0005t0006g0120 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.219+1886G>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47755980 | |||||||
| chr12:47755982 | C | G | 1 | a0005c0005t0006g0120 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.219+1884G>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47755982 | |||||||
| chr12:47755984 | C | A | 1 | a0005c0005t0006g0120 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.219+1882G>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47755984 | |||||||
| chr12:47755985 | C | G | 1 | a0005c0005t0006g0120 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.219+1881G>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47755985 | |||||||
| chr12:47755988 | T | A | 1 | a0005c0005t0006g0120 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.219+1878A>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47755988 | |||||||
| chr12:47755989 | C | A | 1 | a0005c0005t0006g0120 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.219+1877G>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47755989 | |||||||
| chr12:47755989 | C | T | 1 | a0002c0015t0033g0074 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.219+1877G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47755989 | |||||||
| chr12:47755991 | C | G | 1 | a0005c0005t0006g0120 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.219+1875G>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47755991 | |||||||
| chr12:47755992 | C | A | 1 | a0005c0005t0006g0120 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.219+1874G>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47755992 | |||||||
| chr12:47755993 | A | G | 1 | a0001c0001t0014g0168 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.219+1873T>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47755993 | |||||||
| chr12:47755994 | A | G | 1 | a0005c0005t0006g0120 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.219+1872T>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47755994 | |||||||
| chr12:47755997 | T | A | 1 | a0005c0005t0006g0120 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.219+1869A>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47755997 | |||||||
| chr12:47755998 | T | G | 1 | a0005c0005t0006g0120 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.219+1868A>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47755998 | |||||||
| chr12:47755999 | G | A | 1 | a0005c0005t0006g0120 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.219+1867C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47755999 | |||||||
| chr12:47756001 | T | A | 1 | a0005c0005t0006g0120 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.219+1865A>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47756001 | |||||||
| chr12:47756002 | C | T | 1 | a0005c0005t0006g0120 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.219+1864G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47756002 | |||||||
| chr12:47756013 | G | C | 1 | a0001c0001t0006g0149 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.219+1853C>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47756013 | |||||||
| chr12:47756022 | G | A | 1 | a0002c0002t0025g0072 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.219+1844C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47756022 | |||||||
| chr12:47756067 | C | T | 6 | a0001c0001t0001g0123 a0001c0001t0005g0124 a0001c0001t0006g0040 others(3): Show |
9 | NA18947.hp1 NA18966.hp1 NA18968.hp1 others(6): Show |
intron_variant | MODIFIER | c.219+1799G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47756067 | |||||||
| chr12:47756080 | C | T | 1 | a0006c0006t0015g0023 | 3 | HG01884.hp2 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.219+1786G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47756080 | |||||||
| chr12:47756117 | C | T | 1 | a0002c0002t0003g0064 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.219+1749G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47756117 | |||||||
| chr12:47756276 | A | C | 1 | a0003c0003t0003g0078 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.219+1590T>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47756276 | |||||||
| chr12:47756454 | G | A | 1 | a0009c0010t0010g0186 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.219+1412C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47756454 | |||||||
| chr12:47756520 | T | G | 17 | a0003c0003t0003g0004 a0003c0003t0003g0014 a0003c0003t0003g0030 others(14): Show |
37 | HG00738.hp2 HG01099.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.219+1346A>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47756520 | |||||||
| chr12:47756602 | A | T | 1 | a0002c0002t0017g0063 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.219+1264T>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47756602 | |||||||
| chr12:47756626 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.219+1240C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47756626 | |||||||
| chr12:47756686 | C | T | 1 | a0015c0013t0001g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.219+1180G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47756686 | |||||||
| chr12:47756753 | G | A | 16 | a0003c0003t0003g0004 a0003c0003t0003g0014 a0003c0003t0003g0030 others(13): Show |
36 | HG00738.hp2 HG01099.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.219+1113C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47756753 | |||||||
| chr12:47756851 | C | T | 1 | a0001c0001t0037g0166 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.219+1015G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47756851 | |||||||
| chr12:47756966 | TA | T | 6 | a0001c0001t0001g0122 a0001c0001t0002g0051 a0001c0001t0006g0121 others(3): Show |
7 | HG01069.hp1 NA18946.hp1 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.219+899delT | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47756966 | |||||||
| chr12:47756994 | A | G | 5 | a0004c0004t0009g0013 a0004c0004t0009g0036 a0004c0004t0009g0087 others(2): Show |
10 | HG01167.hp2 HG02258.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.219+872T>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47756994 | |||||||
| chr12:47757011 | C | T | 42 | a0001c0001t0001g0096 a0001c0001t0001g0101 a0001c0001t0001g0103 others(39): Show |
103 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.219+855G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47757011 | |||||||
| chr12:47757019 | C | T | 1 | a0003c0003t0003g0073 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.219+847G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47757019 | |||||||
| chr12:47757094 | G | A | 1 | a0002c0002t0007g0027 | 3 | HG01884.hp1 HG02145.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.219+772C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47757094 | |||||||
| chr12:47757168 | A | G | 79 | a0001c0001t0001g0096 a0001c0001t0001g0101 a0001c0001t0001g0103 others(76): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.219+698T>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47757168 | |||||||
| chr12:47757208 | G | C | 2 | a0002c0002t0008g0157 a0002c0002t0008g0158 |
2 | HG01175.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.219+658C>G | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47757208 | |||||||
| chr12:47757222 | A | G | 1 | a0001c0001t0001g0019 | 3 | HG00323.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.219+644T>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47757222 | |||||||
| chr12:47757241 | A | G | 4 | a0004c0004t0009g0013 a0004c0004t0009g0036 a0004c0004t0009g0087 others(1): Show |
9 | HG01167.hp2 HG02258.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.219+625T>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47757241 | |||||||
| chr12:47757371 | C | T | 1 | a0001c0001t0037g0166 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.219+495G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47757371 | |||||||
| chr12:47757511 | C | T | 1 | a0001c0001t0018g0035 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.219+355G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47757511 | |||||||
| chr12:47757579 | A | G | 1 | a0003c0003t0003g0030 | 2 | HG01123.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.219+287T>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47757579 | |||||||
| chr12:47757633 | A | G | 1 | a0002c0011t0001g0061 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.219+233T>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47757633 | |||||||
| chr12:47757792 | T | A | 1 | a0001c0001t0017g0045 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.219+74A>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 2/27 | chr12 | 47757792 | |||||||
| chr12:47758125 | C | G | 1 | a0003c0003t0003g0060 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.7-47G>C | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 1/27 | chr12 | 47758125 | |||||||
| chr12:47758127 | G | T | 1 | a0003c0003t0003g0060 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.7-49C>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 1/27 | chr12 | 47758127 | |||||||
| chr12:47758255 | C | T | 1 | a0001c0001t0002g0160 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.7-177G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 1/27 | chr12 | 47758255 | |||||||
| chr12:47758263 | C | T | 1 | a0001c0001t0003g0017 | 3 | HG01257.hp1 HG01258.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.7-185G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 1/27 | chr12 | 47758263 | |||||||
| chr12:47758264 | G | A | 1 | a0001c0001t0005g0151 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.7-186C>T | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 1/27 | chr12 | 47758264 | |||||||
| chr12:47758363 | C | T | 1 | a0001c0001t0004g0059 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6+188G>A | RAPGEF3 | ENSG00000079337.16 | transcript | ENST00000449771.7 | protein_coding | 1/27 | chr12 | 47758363 |