Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 65059 |
| ensemblid | ENSG00000173166.18 |
| hgncid | 14436 |
| symbol | RAPH1 |
| name | Ras association (RalGDS/AF-6) and pleckstrin homology domains 1 |
| refseq_nuc | NM_213589.3 |
| refseq_prot | NP_998754.1 |
| ensembl_nuc | ENST00000319170.10 |
| ensembl_prot | ENSP00000316543.5 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 203433682 |
| end | 203535301 |
| strand | - |
| ver | v1.2 |
| region | chr2:203433682-203535301 |
| region5000 | chr2:203428682-203540301 |
| regionname0 | RAPH1_chr2_203433682_203535301 |
| regionname5000 | RAPH1_chr2_203428682_203540301 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1250 | 244 | 67 | 46 | 97 | 11 | 21 | 75 | RAPH1_chr2_203428682_203540301 | RAPH1 | MEQLS others(1245): Show |
chr2 | 203428682 | 203540301 |
| a0002 | 0/0 | 684 | 35 | 9 | 4 | 18 | 1 | 3 | 9 | RAPH1_chr2_203428682_203540301 | RAPH1 | MEQLS others(679): Show |
chr2 | 203428682 | 203540301 |
| a0003 | 0/0 | 921 | 4 | 1 | 1 | 2 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | MEQLS others(916): Show |
chr2 | 203428682 | 203540301 |
| a0004 | 0/0 | 1250 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | RAPH1_chr2_203428682_203540301 | RAPH1 | MEQLS others(1245): Show |
chr2 | 203428682 | 203540301 |
| a0005 | 0/0 | 1250 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | MEQLS others(1245): Show |
chr2 | 203428682 | 203540301 |
| a0006 | 0/0 | 684 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | MEQLS others(679): Show |
chr2 | 203428682 | 203540301 |
| a0007 | 0/0 | 1250 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | MEQLS others(1245): Show |
chr2 | 203428682 | 203540301 |
| a0008 | 0/0 | 1250 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | MEQLS others(1245): Show |
chr2 | 203428682 | 203540301 |
| a0009 | 0/0 | 1250 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | MEQLS others(1245): Show |
chr2 | 203428682 | 203540301 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3750 | 100 | 21 | 17 | 46 | 5 | 10 | RAPH1_chr2_203428682_203540301 | RAPH1 | ATGGA others(3745): Show |
chr2 | 203428682 | 203540301 | ||
| a0001c0002 | 0/1 | 3750 | 73 | 5 | 17 | 33 | 6 | 11 | RAPH1_chr2_203428682_203540301 | RAPH1 | ATGGA others(3745): Show |
chr2 | 203428682 | 203540301 | ||
| a0001c0003 | 0/0 | 3750 | 28 | 16 | 2 | 10 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | ATGGA others(3745): Show |
chr2 | 203428682 | 203540301 | ||
| a0001c0004 | 0/0 | 3750 | 16 | 13 | 3 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | ATGGA others(3745): Show |
chr2 | 203428682 | 203540301 | ||
| a0001c0007 | 0/0 | 3750 | 9 | 8 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | ATGGA others(3745): Show |
chr2 | 203428682 | 203540301 | ||
| a0001c0008 | 0/0 | 3750 | 4 | 0 | 0 | 4 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | ATGGA others(3745): Show |
chr2 | 203428682 | 203540301 | ||
| a0001c0010 | 0/0 | 3750 | 3 | 0 | 3 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | ATGGA others(3745): Show |
chr2 | 203428682 | 203540301 | ||
| a0001c0011 | 0/0 | 3750 | 3 | 0 | 1 | 2 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | ATGGA others(3745): Show |
chr2 | 203428682 | 203540301 | ||
| a0001c0015 | 0/0 | 3750 | 2 | 0 | 2 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | ATGGA others(3745): Show |
chr2 | 203428682 | 203540301 | ||
| a0001c0020 | 0/0 | 3750 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | ATGGA others(3745): Show |
chr2 | 203428682 | 203540301 | ||
| a0001c0021 | 0/0 | 3750 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | ATGGA others(3745): Show |
chr2 | 203428682 | 203540301 | ||
| a0001c0026 | 0/0 | 3750 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | ATGGA others(3745): Show |
chr2 | 203428682 | 203540301 | ||
| a0001c0027 | 0/0 | 3750 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | ATGGA others(3745): Show |
chr2 | 203428682 | 203540301 | ||
| a0001c0029 | 0/0 | 3750 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | ATGGA others(3745): Show |
chr2 | 203428682 | 203540301 | ||
| a0001c0033 | 0/0 | 3750 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | ATGGA others(3745): Show |
chr2 | 203428682 | 203540301 | ||
| a0002c0005 | 0/0 | 3751 | 11 | 3 | 1 | 5 | 0 | 2 | RAPH1_chr2_203428682_203540301 | RAPH1 | ATGGA others(3746): Show |
chr2 | 203428682 | 203540301 | ||
| a0002c0006 | 0/0 | 3751 | 10 | 1 | 2 | 6 | 1 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | ATGGA others(3746): Show |
chr2 | 203428682 | 203540301 | ||
| a0002c0012 | 0/0 | 3751 | 3 | 1 | 0 | 1 | 0 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | ATGGA others(3746): Show |
chr2 | 203428682 | 203540301 | ||
| a0002c0013 | 0/0 | 3752 | 2 | 0 | 1 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | ATGGA others(3747): Show |
chr2 | 203428682 | 203540301 | ||
| a0002c0016 | 0/0 | 3752 | 2 | 0 | 0 | 2 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | ATGGA others(3747): Show |
chr2 | 203428682 | 203540301 | ||
| a0002c0017 | 0/0 | 3751 | 2 | 2 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | ATGGA others(3746): Show |
chr2 | 203428682 | 203540301 | ||
| a0002c0018 | 0/0 | 3751 | 2 | 2 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | ATGGA others(3746): Show |
chr2 | 203428682 | 203540301 | ||
| a0002c0022 | 0/0 | 3752 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | ATGGA others(3747): Show |
chr2 | 203428682 | 203540301 | ||
| a0002c0023 | 0/0 | 3751 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | ATGGA others(3746): Show |
chr2 | 203428682 | 203540301 | ||
| a0002c0031 | 0/0 | 3751 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | ATGGA others(3746): Show |
chr2 | 203428682 | 203540301 | ||
| a0003c0009 | 0/0 | 3751 | 3 | 1 | 0 | 2 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | ATGGA others(3746): Show |
chr2 | 203428682 | 203540301 | ||
| a0003c0028 | 0/0 | 3751 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | ATGGA others(3746): Show |
chr2 | 203428682 | 203540301 | ||
| a0004c0014 | 0/0 | 3750 | 2 | 0 | 0 | 2 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | ATGGA others(3745): Show |
chr2 | 203428682 | 203540301 | ||
| a0005c0024 | 0/0 | 3750 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | ATGGA others(3745): Show |
chr2 | 203428682 | 203540301 | ||
| a0006c0025 | 0/0 | 3752 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | ATGGA others(3747): Show |
chr2 | 203428682 | 203540301 | ||
| a0007c0030 | 0/0 | 3750 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | ATGGA others(3745): Show |
chr2 | 203428682 | 203540301 | ||
| a0008c0019 | 0/0 | 3750 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | ATGGA others(3745): Show |
chr2 | 203428682 | 203540301 | ||
| a0009c0032 | 0/0 | 3750 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | ATGGA others(3745): Show |
chr2 | 203428682 | 203540301 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 9696 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9691): Show |
chr2 | 203428682 | 203540301 |
| a0001c0001t0002 | 1/0 | 9699 | 22 | 4 | 1 | 13 | 2 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9694): Show |
chr2 | 203428682 | 203540301 |
| a0001c0001t0003 | 0/0 | 9702 | 9 | 0 | 4 | 3 | 0 | 2 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9697): Show |
chr2 | 203428682 | 203540301 |
| a0001c0001t0008 | 0/0 | 9699 | 6 | 0 | 0 | 6 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9694): Show |
chr2 | 203428682 | 203540301 |
| a0001c0001t0009 | 0/0 | 9702 | 5 | 0 | 4 | 0 | 0 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9697): Show |
chr2 | 203428682 | 203540301 |
| a0001c0001t0010 | 0/0 | 9699 | 5 | 5 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9694): Show |
chr2 | 203428682 | 203540301 |
| a0001c0001t0011 | 0/0 | 9695 | 4 | 0 | 0 | 4 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9690): Show |
chr2 | 203428682 | 203540301 |
| a0001c0001t0012 | 0/0 | 9699 | 4 | 0 | 0 | 2 | 0 | 2 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9694): Show |
chr2 | 203428682 | 203540301 |
| a0001c0001t0013 | 0/0 | 9701 | 4 | 1 | 0 | 3 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9696): Show |
chr2 | 203428682 | 203540301 |
| a0001c0001t0016 | 0/0 | 9698 | 3 | 3 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9693): Show |
chr2 | 203428682 | 203540301 |
| a0001c0001t0017 | 0/0 | 9703 | 4 | 4 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9698): Show |
chr2 | 203428682 | 203540301 |
| a0001c0001t0019 | 0/0 | 9695 | 3 | 0 | 1 | 0 | 1 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9690): Show |
chr2 | 203428682 | 203540301 |
| a0001c0001t0022 | 0/0 | 9697 | 2 | 0 | 2 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9692): Show |
chr2 | 203428682 | 203540301 |
| a0001c0001t0023 | 0/0 | 9700 | 3 | 0 | 0 | 3 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9695): Show |
chr2 | 203428682 | 203540301 |
| a0001c0001t0028 | 0/0 | 9694 | 2 | 2 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9689): Show |
chr2 | 203428682 | 203540301 |
| a0001c0001t0031 | 0/0 | 9699 | 2 | 0 | 0 | 2 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9694): Show |
chr2 | 203428682 | 203540301 |
| a0001c0001t0032 | 0/0 | 9697 | 2 | 0 | 1 | 0 | 1 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9692): Show |
chr2 | 203428682 | 203540301 |
| a0001c0001t0037 | 0/0 | 9703 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9698): Show |
chr2 | 203428682 | 203540301 |
| a0001c0001t0045 | 0/0 | 9695 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9690): Show |
chr2 | 203428682 | 203540301 |
| a0001c0001t0046 | 0/0 | 9696 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9691): Show |
chr2 | 203428682 | 203540301 |
| a0001c0001t0052 | 0/0 | 9701 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9696): Show |
chr2 | 203428682 | 203540301 |
| a0001c0001t0053 | 0/0 | 9703 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9698): Show |
chr2 | 203428682 | 203540301 |
| a0001c0001t0055 | 0/0 | 9697 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9692): Show |
chr2 | 203428682 | 203540301 |
| a0001c0001t0056 | 0/0 | 9697 | 1 | 0 | 0 | 0 | 1 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9692): Show |
chr2 | 203428682 | 203540301 |
| a0001c0001t0059 | 0/0 | 9701 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9696): Show |
chr2 | 203428682 | 203540301 |
| a0001c0001t0060 | 0/0 | 9703 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9698): Show |
chr2 | 203428682 | 203540301 |
| a0001c0001t0061 | 0/0 | 9703 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9698): Show |
chr2 | 203428682 | 203540301 |
| a0001c0001t0063 | 0/0 | 9715 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9710): Show |
chr2 | 203428682 | 203540301 |
| a0001c0001t0064 | 0/0 | 9699 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9694): Show |
chr2 | 203428682 | 203540301 |
| a0001c0001t0065 | 0/0 | 9699 | 1 | 0 | 0 | 0 | 0 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9694): Show |
chr2 | 203428682 | 203540301 |
| a0001c0001t0081 | 0/0 | 9703 | 1 | 0 | 0 | 0 | 0 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9698): Show |
chr2 | 203428682 | 203540301 |
| a0001c0001t0084 | 0/0 | 9706 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9701): Show |
chr2 | 203428682 | 203540301 |
| a0001c0001t0085 | 0/0 | 9704 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9699): Show |
chr2 | 203428682 | 203540301 |
| a0001c0001t0086 | 0/0 | 9704 | 1 | 0 | 0 | 0 | 0 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9699): Show |
chr2 | 203428682 | 203540301 |
| a0001c0001t0088 | 0/0 | 9703 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9698): Show |
chr2 | 203428682 | 203540301 |
| a0001c0001t0089 | 0/0 | 9703 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9698): Show |
chr2 | 203428682 | 203540301 |
| a0001c0002t0001 | 0/0 | 9696 | 38 | 0 | 8 | 25 | 1 | 4 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9691): Show |
chr2 | 203428682 | 203540301 |
| a0001c0002t0004 | 0/1 | 9702 | 9 | 1 | 4 | 1 | 2 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9697): Show |
chr2 | 203428682 | 203540301 |
| a0001c0002t0007 | 0/0 | 9698 | 6 | 0 | 2 | 1 | 0 | 3 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9693): Show |
chr2 | 203428682 | 203540301 |
| a0001c0002t0020 | 0/0 | 9696 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9691): Show |
chr2 | 203428682 | 203540301 |
| a0001c0002t0024 | 0/0 | 9700 | 3 | 0 | 0 | 3 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9695): Show |
chr2 | 203428682 | 203540301 |
| a0001c0002t0033 | 0/0 | 9704 | 2 | 1 | 0 | 0 | 0 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9699): Show |
chr2 | 203428682 | 203540301 |
| a0001c0002t0035 | 0/0 | 9702 | 2 | 1 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9697): Show |
chr2 | 203428682 | 203540301 |
| a0001c0002t0038 | 0/0 | 9706 | 2 | 2 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9701): Show |
chr2 | 203428682 | 203540301 |
| a0001c0002t0042 | 0/0 | 9692 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9687): Show |
chr2 | 203428682 | 203540301 |
| a0001c0002t0043 | 0/0 | 9693 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9688): Show |
chr2 | 203428682 | 203540301 |
| a0001c0002t0047 | 0/0 | 9697 | 1 | 0 | 0 | 0 | 0 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9692): Show |
chr2 | 203428682 | 203540301 |
| a0001c0002t0049 | 0/0 | 9698 | 1 | 0 | 0 | 0 | 0 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9693): Show |
chr2 | 203428682 | 203540301 |
| a0001c0002t0067 | 0/0 | 9702 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9697): Show |
chr2 | 203428682 | 203540301 |
| a0001c0002t0071 | 0/0 | 9706 | 1 | 0 | 0 | 0 | 1 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9701): Show |
chr2 | 203428682 | 203540301 |
| a0001c0002t0072 | 0/0 | 9706 | 1 | 0 | 0 | 0 | 0 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9701): Show |
chr2 | 203428682 | 203540301 |
| a0001c0002t0073 | 0/0 | 9706 | 1 | 0 | 0 | 0 | 1 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9701): Show |
chr2 | 203428682 | 203540301 |
| a0001c0002t0079 | 0/0 | 9702 | 1 | 0 | 0 | 0 | 1 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9697): Show |
chr2 | 203428682 | 203540301 |
| a0001c0002t0090 | 0/0 | 9706 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9701): Show |
chr2 | 203428682 | 203540301 |
| a0001c0003t0006 | 0/0 | 9716 | 6 | 6 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9711): Show |
chr2 | 203428682 | 203540301 |
| a0001c0003t0025 | 0/0 | 9720 | 3 | 0 | 0 | 3 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9715): Show |
chr2 | 203428682 | 203540301 |
| a0001c0003t0036 | 0/0 | 9712 | 2 | 2 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9707): Show |
chr2 | 203428682 | 203540301 |
| a0001c0003t0039 | 0/0 | 9716 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9711): Show |
chr2 | 203428682 | 203540301 |
| a0001c0003t0069 | 0/0 | 9713 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9708): Show |
chr2 | 203428682 | 203540301 |
| a0001c0003t0070 | 0/0 | 9703 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9698): Show |
chr2 | 203428682 | 203540301 |
| a0001c0003t0076 | 0/0 | 9700 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9695): Show |
chr2 | 203428682 | 203540301 |
| a0001c0003t0078 | 0/0 | 9712 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9707): Show |
chr2 | 203428682 | 203540301 |
| a0001c0003t0092 | 0/0 | 9724 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9719): Show |
chr2 | 203428682 | 203540301 |
| a0001c0003t0093 | 0/0 | 9718 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9713): Show |
chr2 | 203428682 | 203540301 |
| a0001c0003t0094 | 0/0 | 9714 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9709): Show |
chr2 | 203428682 | 203540301 |
| a0001c0003t0095 | 0/0 | 9728 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9723): Show |
chr2 | 203428682 | 203540301 |
| a0001c0003t0096 | 0/0 | 9724 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9719): Show |
chr2 | 203428682 | 203540301 |
| a0001c0003t0097 | 0/0 | 9724 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9719): Show |
chr2 | 203428682 | 203540301 |
| a0001c0003t0098 | 0/0 | 9720 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9715): Show |
chr2 | 203428682 | 203540301 |
| a0001c0003t0101 | 0/0 | 9720 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9715): Show |
chr2 | 203428682 | 203540301 |
| a0001c0003t0102 | 0/0 | 9716 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9711): Show |
chr2 | 203428682 | 203540301 |
| a0001c0003t0103 | 0/0 | 9720 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9715): Show |
chr2 | 203428682 | 203540301 |
| a0001c0003t0104 | 0/0 | 9718 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9713): Show |
chr2 | 203428682 | 203540301 |
| a0001c0003t0106 | 0/0 | 9725 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9720): Show |
chr2 | 203428682 | 203540301 |
| a0001c0004t0005 | 0/0 | 9698 | 7 | 4 | 3 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9693): Show |
chr2 | 203428682 | 203540301 |
| a0001c0004t0015 | 0/0 | 9698 | 3 | 3 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9693): Show |
chr2 | 203428682 | 203540301 |
| a0001c0004t0018 | 0/0 | 9702 | 3 | 3 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9697): Show |
chr2 | 203428682 | 203540301 |
| a0001c0004t0034 | 0/0 | 9706 | 2 | 2 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9701): Show |
chr2 | 203428682 | 203540301 |
| a0001c0004t0051 | 0/0 | 9704 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9699): Show |
chr2 | 203428682 | 203540301 |
| a0001c0007t0001 | 0/0 | 9696 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9691): Show |
chr2 | 203428682 | 203540301 |
| a0001c0007t0021 | 0/0 | 9704 | 2 | 2 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9699): Show |
chr2 | 203428682 | 203540301 |
| a0001c0007t0026 | 0/0 | 9701 | 2 | 2 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9696): Show |
chr2 | 203428682 | 203540301 |
| a0001c0007t0057 | 0/0 | 9719 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9714): Show |
chr2 | 203428682 | 203540301 |
| a0001c0007t0068 | 0/0 | 9705 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9700): Show |
chr2 | 203428682 | 203540301 |
| a0001c0007t0075 | 0/0 | 9707 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9702): Show |
chr2 | 203428682 | 203540301 |
| a0001c0007t0082 | 0/0 | 9706 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9701): Show |
chr2 | 203428682 | 203540301 |
| a0001c0008t0014 | 0/0 | 9698 | 4 | 0 | 0 | 4 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9693): Show |
chr2 | 203428682 | 203540301 |
| a0001c0010t0002 | 0/0 | 9699 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9694): Show |
chr2 | 203428682 | 203540301 |
| a0001c0010t0040 | 0/0 | 9699 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9694): Show |
chr2 | 203428682 | 203540301 |
| a0001c0010t0062 | 0/0 | 9699 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9694): Show |
chr2 | 203428682 | 203540301 |
| a0001c0011t0002 | 0/0 | 9699 | 2 | 0 | 1 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9694): Show |
chr2 | 203428682 | 203540301 |
| a0001c0011t0003 | 0/0 | 9702 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9697): Show |
chr2 | 203428682 | 203540301 |
| a0001c0015t0001 | 0/0 | 9696 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9691): Show |
chr2 | 203428682 | 203540301 |
| a0001c0015t0044 | 0/0 | 9704 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9699): Show |
chr2 | 203428682 | 203540301 |
| a0001c0020t0058 | 0/0 | 9708 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9703): Show |
chr2 | 203428682 | 203540301 |
| a0001c0021t0002 | 0/0 | 9699 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9694): Show |
chr2 | 203428682 | 203540301 |
| a0001c0026t0077 | 0/0 | 9700 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9695): Show |
chr2 | 203428682 | 203540301 |
| a0001c0027t0020 | 0/0 | 9696 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9691): Show |
chr2 | 203428682 | 203540301 |
| a0001c0029t0066 | 0/0 | 9702 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9697): Show |
chr2 | 203428682 | 203540301 |
| a0001c0033t0050 | 0/0 | 9705 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9700): Show |
chr2 | 203428682 | 203540301 |
| a0002c0005t0002 | 0/0 | 9700 | 2 | 1 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9695): Show |
chr2 | 203428682 | 203540301 |
| a0002c0005t0003 | 0/0 | 9703 | 1 | 0 | 0 | 0 | 0 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9698): Show |
chr2 | 203428682 | 203540301 |
| a0002c0005t0011 | 0/0 | 9696 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9691): Show |
chr2 | 203428682 | 203540301 |
| a0002c0005t0012 | 0/0 | 9700 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9695): Show |
chr2 | 203428682 | 203540301 |
| a0002c0005t0013 | 0/0 | 9702 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9697): Show |
chr2 | 203428682 | 203540301 |
| a0002c0005t0022 | 0/0 | 9698 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9693): Show |
chr2 | 203428682 | 203540301 |
| a0002c0005t0029 | 0/0 | 9694 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9689): Show |
chr2 | 203428682 | 203540301 |
| a0002c0005t0080 | 0/0 | 9700 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9695): Show |
chr2 | 203428682 | 203540301 |
| a0002c0005t0087 | 0/0 | 9704 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9699): Show |
chr2 | 203428682 | 203540301 |
| a0002c0005t0107 | 0/0 | 9711 | 1 | 0 | 0 | 0 | 0 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9706): Show |
chr2 | 203428682 | 203540301 |
| a0002c0006t0001 | 0/0 | 9697 | 4 | 0 | 0 | 4 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9692): Show |
chr2 | 203428682 | 203540301 |
| a0002c0006t0004 | 0/0 | 9703 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9698): Show |
chr2 | 203428682 | 203540301 |
| a0002c0006t0027 | 0/0 | 9697 | 2 | 0 | 2 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9692): Show |
chr2 | 203428682 | 203540301 |
| a0002c0006t0030 | 0/0 | 9698 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9693): Show |
chr2 | 203428682 | 203540301 |
| a0002c0006t0048 | 0/0 | 9699 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9694): Show |
chr2 | 203428682 | 203540301 |
| a0002c0006t0074 | 0/0 | 9709 | 1 | 0 | 0 | 0 | 1 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9704): Show |
chr2 | 203428682 | 203540301 |
| a0002c0012t0039 | 0/0 | 9717 | 1 | 0 | 0 | 0 | 0 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9712): Show |
chr2 | 203428682 | 203540301 |
| a0002c0012t0091 | 0/0 | 9717 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9712): Show |
chr2 | 203428682 | 203540301 |
| a0002c0012t0099 | 0/0 | 9721 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9716): Show |
chr2 | 203428682 | 203540301 |
| a0002c0013t0002 | 0/0 | 9701 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9696): Show |
chr2 | 203428682 | 203540301 |
| a0002c0013t0009 | 0/0 | 9704 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9699): Show |
chr2 | 203428682 | 203540301 |
| a0002c0016t0001 | 0/0 | 9698 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9693): Show |
chr2 | 203428682 | 203540301 |
| a0002c0016t0020 | 0/0 | 9698 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9693): Show |
chr2 | 203428682 | 203540301 |
| a0002c0017t0015 | 0/0 | 9699 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9694): Show |
chr2 | 203428682 | 203540301 |
| a0002c0017t0018 | 0/0 | 9703 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9698): Show |
chr2 | 203428682 | 203540301 |
| a0002c0018t0021 | 0/0 | 9705 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9700): Show |
chr2 | 203428682 | 203540301 |
| a0002c0018t0083 | 0/0 | 9710 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9705): Show |
chr2 | 203428682 | 203540301 |
| a0002c0022t0054 | 0/0 | 9703 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9698): Show |
chr2 | 203428682 | 203540301 |
| a0002c0023t0003 | 0/0 | 9703 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9698): Show |
chr2 | 203428682 | 203540301 |
| a0002c0031t0105 | 0/0 | 9720 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9715): Show |
chr2 | 203428682 | 203540301 |
| a0003c0009t0016 | 0/0 | 9699 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9694): Show |
chr2 | 203428682 | 203540301 |
| a0003c0009t0037 | 0/0 | 9704 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9699): Show |
chr2 | 203428682 | 203540301 |
| a0003c0009t0041 | 0/0 | 9692 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9687): Show |
chr2 | 203428682 | 203540301 |
| a0003c0028t0005 | 0/0 | 9699 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9694): Show |
chr2 | 203428682 | 203540301 |
| a0004c0014t0100 | 0/0 | 9710 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9705): Show |
chr2 | 203428682 | 203540301 |
| a0004c0014t0108 | 0/0 | 9728 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9723): Show |
chr2 | 203428682 | 203540301 |
| a0005c0024t0002 | 0/0 | 9699 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9694): Show |
chr2 | 203428682 | 203540301 |
| a0006c0025t0030 | 0/0 | 9699 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9694): Show |
chr2 | 203428682 | 203540301 |
| a0007c0030t0006 | 0/0 | 9716 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9711): Show |
chr2 | 203428682 | 203540301 |
| a0008c0019t0029 | 0/0 | 9693 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9688): Show |
chr2 | 203428682 | 203540301 |
| a0009c0032t0001 | 0/0 | 9696 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | CCAGT others(9691): Show |
chr2 | 203428682 | 203540301 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0002g0176 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0008g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0008g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0008g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0008g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0008g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0008g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0009g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0009g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0009g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0009g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0009g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0010g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0010g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0010g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0010g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0010g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0011g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0011g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0011g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0011g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0012g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0012g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0012g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0012g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0013g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0013g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0013g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0013g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0016g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0016g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0016g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0017g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0017g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0017g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0017g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0019g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0019g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0019g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0022g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0022g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0023g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0023g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0023g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0028g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0028g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0031g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0031g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0032g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0032g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0037g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0045g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0046g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0052g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0053g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0055g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0056g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0059g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0060g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0061g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0063g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0064g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0065g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0081g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0084g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0085g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0086g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0088g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0001t0089g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0004g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0004g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0004g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0004g0110 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0004g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0004g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0004g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0007g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0007g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0007g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0007g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0007g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0007g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0020g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0024g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0024g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0024g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0033g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0033g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0035g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0035g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0038g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0038g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0042g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0043g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0047g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0049g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0067g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0071g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0072g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0073g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0079g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0002t0090g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0003t0006g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0003t0006g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0003t0006g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0003t0006g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0003t0006g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0003t0006g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0003t0025g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0003t0025g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0003t0025g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0003t0036g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0003t0036g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0003t0039g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0003t0069g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0003t0070g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0003t0076g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0003t0078g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0003t0092g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0003t0093g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0003t0094g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0003t0095g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0003t0096g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0003t0097g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0003t0098g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0003t0101g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0003t0102g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0003t0103g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0003t0104g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0003t0106g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0004t0005g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0004t0005g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0004t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0004t0005g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0004t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0004t0005g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0004t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0004t0015g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0004t0015g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0004t0015g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0004t0018g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0004t0018g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0004t0018g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0004t0034g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0004t0034g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0004t0051g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0007t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0007t0021g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0007t0021g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0007t0026g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0007t0026g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0007t0057g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0007t0068g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0007t0075g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0007t0082g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0008t0014g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0008t0014g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0008t0014g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0008t0014g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0010t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0010t0040g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0010t0062g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0011t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0011t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0011t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0015t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0015t0044g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0020t0058g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0021t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0026t0077g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0027t0020g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0029t0066g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0001c0033t0050g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0002c0005t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0002c0005t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0002c0005t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0002c0005t0011g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0002c0005t0012g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0002c0005t0013g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0002c0005t0022g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0002c0005t0029g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0002c0005t0080g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0002c0005t0087g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0002c0005t0107g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0002c0006t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0002c0006t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0002c0006t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0002c0006t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0002c0006t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0002c0006t0027g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0002c0006t0027g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0002c0006t0030g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0002c0006t0048g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0002c0006t0074g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0002c0012t0039g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0002c0012t0091g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0002c0012t0099g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0002c0013t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0002c0013t0009g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0002c0016t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0002c0016t0020g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0002c0017t0015g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0002c0017t0018g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0002c0018t0021g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0002c0018t0083g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0002c0022t0054g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0002c0023t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0002c0031t0105g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0003c0009t0016g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0003c0009t0037g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0003c0009t0041g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0003c0028t0005g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0004c0014t0100g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0004c0014t0108g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0005c0024t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0006c0025t0030g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0007c0030t0006g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0008c0019t0029g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| a0009c0032t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0079 | g0159 | EUR | GBR | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG00140 | hp2 | a0001 | c0002 | t0004 | g0107 | EUR | GBR | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG00280 | hp1 | a0001 | c0002 | t0071 | g0113 | EUR | FIN | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0145 | EUR | FIN | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG00323 | hp1 | a0001 | c0001 | t0019 | g0032 | EUR | FIN | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0077 | EUR | FIN | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG00408 | hp1 | a0001 | c0011 | t0003 | g0116 | EAS | CHS | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | CHS | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | CHS | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG00423 | hp2 | a0005 | c0024 | t0002 | g0189 | EAS | CHS | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG00438 | hp1 | a0002 | c0005 | t0029 | g0035 | EAS | CHS | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG00438 | hp2 | a0002 | c0006 | t0030 | g0048 | EAS | CHS | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG00544 | hp1 | a0001 | c0002 | t0004 | g0130 | EAS | CHS | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | CHS | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0044 | EAS | CHS | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG00597 | hp2 | a0003 | c0009 | t0037 | g0259 | EAS | CHS | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | CHS | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | CHS | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG00621 | hp1 | a0002 | c0005 | t0013 | g0170 | EAS | CHS | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG00621 | hp2 | a0002 | c0022 | t0054 | g0166 | EAS | CHS | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG00642 | hp1 | a0001 | c0001 | t0009 | g0249 | AMR | PUR | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG00642 | hp2 | a0001 | c0001 | t0022 | g0168 | AMR | PUR | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG00673 | hp1 | a0002 | c0006 | t0001 | g0054 | EAS | CHS | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG00673 | hp2 | a0002 | c0013 | t0002 | g0216 | EAS | CHS | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG00733 | hp1 | a0001 | c0002 | t0035 | g0115 | AMR | PUR | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG00733 | hp2 | a0001 | c0004 | t0005 | g0093 | AMR | PUR | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG00735 | hp1 | a0001 | c0010 | t0002 | g0120 | AMR | PUR | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG00735 | hp2 | a0001 | c0002 | t0004 | g0106 | AMR | PUR | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG00738 | hp1 | a0002 | c0005 | t0022 | g0117 | AMR | PUR | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG00738 | hp2 | a0001 | c0003 | t0039 | g0269 | AMR | PUR | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG00741 | hp1 | a0001 | c0001 | t0064 | g0215 | AMR | PUR | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG00741 | hp2 | a0001 | c0002 | t0004 | g0109 | AMR | PUR | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01071 | hp1 | a0001 | c0002 | t0007 | g0025 | AMR | PUR | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0105 | AMR | PUR | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01081 | hp1 | a0001 | c0002 | t0004 | g0132 | AMR | PUR | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01081 | hp2 | a0001 | c0001 | t0061 | g0223 | AMR | PUR | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0075 | AMR | PUR | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01099 | hp2 | a0001 | c0010 | t0040 | g0001 | AMR | PUR | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01109 | hp1 | a0001 | c0002 | t0042 | g0003 | AMR | PUR | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01109 | hp2 | a0003 | c0028 | t0005 | g0096 | AMR | PUR | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01167 | hp1 | a0002 | c0006 | t0027 | g0019 | AMR | PUR | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01167 | hp2 | a0001 | c0001 | t0032 | g0142 | AMR | PUR | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01168 | hp1 | a0001 | c0004 | t0005 | g0100 | AMR | PUR | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01168 | hp2 | a0001 | c0001 | t0019 | g0081 | AMR | PUR | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01169 | hp1 | a0002 | c0006 | t0027 | g0024 | AMR | PUR | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01169 | hp2 | a0001 | c0004 | t0005 | g0095 | AMR | PUR | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01175 | hp1 | a0001 | c0001 | t0045 | g0060 | AMR | PUR | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01175 | hp2 | a0006 | c0025 | t0030 | g0026 | AMR | PUR | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01255 | hp1 | a0001 | c0001 | t0009 | g0247 | AMR | CLM | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0083 | AMR | CLM | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01257 | hp1 | a0001 | c0007 | t0001 | g0089 | AMR | CLM | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0137 | AMR | CLM | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0136 | AMR | CLM | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01258 | hp2 | a0001 | c0002 | t0004 | g0133 | AMR | CLM | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01358 | hp1 | a0001 | c0015 | t0001 | g0021 | AMR | CLM | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01358 | hp2 | a0001 | c0001 | t0009 | g0255 | AMR | CLM | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0092 | AMR | CLM | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0221 | AMR | CLM | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01433 | hp1 | a0001 | c0001 | t0022 | g0180 | AMR | CLM | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0037 | AMR | CLM | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01496 | hp1 | a0001 | c0010 | t0062 | g0140 | AMR | CLM | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01496 | hp2 | a0001 | c0002 | t0007 | g0029 | AMR | CLM | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01515 | hp1 | a0001 | c0001 | t0056 | g0134 | EUR | IBS | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01515 | hp2 | a0001 | c0002 | t0073 | g0165 | EUR | IBS | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01517 | hp1 | a0002 | c0006 | t0074 | g0164 | EUR | IBS | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01517 | hp2 | a0001 | c0001 | t0032 | g0118 | EUR | IBS | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01884 | hp1 | a0001 | c0033 | t0050 | g0231 | AFR | ACB | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01884 | hp2 | a0001 | c0004 | t0018 | g0233 | AFR | ACB | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01943 | hp1 | a0001 | c0011 | t0002 | g0158 | AMR | PEL | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01943 | hp2 | a0001 | c0003 | t0094 | g0267 | AMR | PEL | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01952 | hp1 | a0002 | c0013 | t0009 | g0256 | AMR | PEL | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0023 | AMR | PEL | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01981 | hp1 | a0001 | c0002 | t0067 | g0201 | AMR | PEL | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG01981 | hp2 | a0001 | c0001 | t0085 | g0248 | AMR | PEL | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02027 | hp1 | a0001 | c0002 | t0007 | g0039 | EAS | KHV | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02027 | hp2 | a0001 | c0001 | t0012 | g0186 | EAS | KHV | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02055 | hp1 | a0002 | c0005 | t0002 | g0174 | AFR | ACB | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02055 | hp2 | a0002 | c0018 | t0083 | g0253 | AFR | ACB | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02080 | hp1 | a0002 | c0005 | t0002 | g0149 | EAS | KHV | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02080 | hp2 | a0002 | c0006 | t0001 | g0073 | EAS | KHV | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | KHV | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02129 | hp2 | a0001 | c0003 | t0097 | g0287 | EAS | KHV | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02132 | hp1 | a0001 | c0003 | t0095 | g0271 | EAS | KHV | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | KHV | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02135 | hp1 | a0002 | c0023 | t0003 | g0169 | EAS | KHV | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02135 | hp2 | a0001 | c0001 | t0012 | g0153 | EAS | KHV | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02145 | hp1 | a0002 | c0012 | t0091 | g0262 | AFR | ACB | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02145 | hp2 | a0001 | c0001 | t0017 | g0126 | AFR | ACB | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02155 | hp1 | a0001 | c0008 | t0014 | g0013 | EAS | CDX | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02155 | hp2 | a0001 | c0021 | t0002 | g0210 | EAS | CDX | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | CDX | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02165 | hp2 | a0001 | c0001 | t0023 | g0224 | EAS | CDX | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02258 | hp1 | a0001 | c0020 | t0058 | g0171 | AFR | ACB | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02258 | hp2 | a0001 | c0004 | t0005 | g0098 | AFR | ACB | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0070 | AMR | PEL | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02273 | hp2 | a0001 | c0001 | t0009 | g0257 | AMR | PEL | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | ACB | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02280 | hp2 | a0001 | c0004 | t0034 | g0235 | AFR | ACB | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0139 | AMR | PEL | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02293 | hp2 | a0001 | c0015 | t0044 | g0007 | AMR | PEL | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0086 | AMR | PEL | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0152 | AMR | PEL | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02451 | hp1 | a0001 | c0003 | t0076 | g0228 | AFR | ACB | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02451 | hp2 | a0001 | c0007 | t0082 | g0260 | AFR | ACB | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02523 | hp1 | a0001 | c0003 | t0103 | g0264 | EAS | KHV | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02523 | hp2 | a0003 | c0009 | t0041 | g0002 | EAS | KHV | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02572 | hp1 | a0001 | c0004 | t0015 | g0099 | AFR | GWD | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02572 | hp2 | a0003 | c0009 | t0016 | g0178 | AFR | GWD | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02622 | hp1 | a0001 | c0003 | t0106 | g0273 | AFR | GWD | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02622 | hp2 | a0001 | c0002 | t0038 | g0245 | AFR | GWD | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02630 | hp1 | a0001 | c0003 | t0006 | g0274 | AFR | GWD | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02630 | hp2 | a0001 | c0001 | t0010 | g0063 | AFR | GWD | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02698 | hp1 | a0001 | c0002 | t0047 | g0022 | SAS | PJL | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02698 | hp2 | a0001 | c0001 | t0009 | g0246 | SAS | PJL | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02717 | hp1 | a0001 | c0003 | t0036 | g0230 | AFR | GWD | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02717 | hp2 | a0001 | c0001 | t0055 | g0157 | AFR | GWD | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02723 | hp1 | a0001 | c0003 | t0006 | g0263 | AFR | GWD | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02723 | hp2 | a0001 | c0001 | t0016 | g0141 | AFR | GWD | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0150 | SAS | PJL | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02735 | hp2 | a0001 | c0002 | t0007 | g0018 | SAS | PJL | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02809 | hp1 | a0001 | c0001 | t0017 | g0217 | AFR | GWD | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02809 | hp2 | a0002 | c0018 | t0021 | g0161 | AFR | GWD | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02818 | hp1 | a0001 | c0001 | t0010 | g0064 | AFR | GWD | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02818 | hp2 | a0001 | c0004 | t0005 | g0103 | AFR | GWD | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02886 | hp1 | a0001 | c0001 | t0016 | g0205 | AFR | GWD | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02886 | hp2 | a0001 | c0003 | t0006 | g0288 | AFR | GWD | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02895 | hp1 | a0001 | c0003 | t0036 | g0229 | AFR | GWD | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02895 | hp2 | a0001 | c0004 | t0005 | g0101 | AFR | GWD | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02896 | hp1 | a0001 | c0004 | t0015 | g0094 | AFR | GWD | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02896 | hp2 | a0001 | c0001 | t0028 | g0065 | AFR | GWD | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02897 | hp1 | a0001 | c0001 | t0028 | g0085 | AFR | GWD | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02897 | hp2 | a0001 | c0004 | t0005 | g0102 | AFR | GWD | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0195 | AFR | ESN | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02965 | hp2 | a0001 | c0001 | t0017 | g0194 | AFR | ESN | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02970 | hp1 | a0007 | c0030 | t0006 | g0285 | AFR | ESN | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02970 | hp2 | a0001 | c0003 | t0070 | g0225 | AFR | ESN | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02976 | hp1 | a0001 | c0007 | t0068 | g0218 | AFR | ESN | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02976 | hp2 | a0001 | c0001 | t0016 | g0172 | AFR | ESN | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG03098 | hp1 | a0002 | c0017 | t0015 | g0097 | AFR | MSL | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG03098 | hp2 | a0001 | c0026 | t0077 | g0238 | AFR | MSL | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG03130 | hp1 | a0001 | c0004 | t0018 | g0234 | AFR | ESN | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG03130 | hp2 | a0001 | c0003 | t0101 | g0277 | AFR | ESN | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG03139 | hp1 | a0001 | c0002 | t0004 | g0200 | AFR | ESN | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG03139 | hp2 | a0001 | c0007 | t0021 | g0220 | AFR | ESN | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG03195 | hp1 | a0001 | c0029 | t0066 | g0219 | AFR | ESN | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG03195 | hp2 | a0001 | c0003 | t0102 | g0268 | AFR | ESN | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG03209 | hp1 | a0001 | c0001 | t0010 | g0062 | AFR | MSL | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG03209 | hp2 | a0001 | c0003 | t0006 | g0276 | AFR | MSL | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG03225 | hp1 | a0001 | c0004 | t0034 | g0240 | AFR | MSL | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG03225 | hp2 | a0001 | c0007 | t0026 | g0005 | AFR | MSL | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG03453 | hp1 | a0001 | c0002 | t0033 | g0202 | AFR | MSL | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG03453 | hp2 | a0001 | c0007 | t0026 | g0006 | AFR | MSL | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG03490 | hp1 | a0001 | c0002 | t0049 | g0049 | SAS | PJL | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG03490 | hp2 | a0001 | c0001 | t0019 | g0082 | SAS | PJL | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG03491 | hp1 | a0001 | c0002 | t0072 | g0108 | SAS | PJL | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG03491 | hp2 | a0001 | c0001 | t0065 | g0124 | SAS | PJL | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG03516 | hp1 | a0002 | c0017 | t0018 | g0232 | AFR | ESN | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG03516 | hp2 | a0001 | c0001 | t0013 | g0214 | AFR | ESN | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG03540 | hp1 | a0001 | c0004 | t0015 | g0104 | AFR | GWD | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG03540 | hp2 | a0001 | c0003 | t0104 | g0275 | AFR | GWD | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | MSL | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG03579 | hp2 | a0002 | c0005 | t0012 | g0206 | AFR | MSL | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG03669 | hp1 | a0001 | c0001 | t0012 | g0122 | SAS | PJL | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0079 | SAS | PJL | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0016 | SAS | PJL | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG03704 | hp2 | a0001 | c0002 | t0033 | g0131 | SAS | PJL | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG03710 | hp1 | a0002 | c0005 | t0107 | g0289 | SAS | PJL | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG03710 | hp2 | a0002 | c0012 | t0039 | g0270 | SAS | PJL | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG03831 | hp1 | a0002 | c0005 | t0003 | g0135 | SAS | BEB | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG03831 | hp2 | a0001 | c0002 | t0007 | g0011 | SAS | BEB | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0182 | SAS | BEB | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG03834 | hp2 | a0001 | c0002 | t0007 | g0033 | SAS | BEB | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG04115 | hp1 | a0001 | c0001 | t0086 | g0243 | SAS | STU | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0050 | SAS | STU | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG04204 | hp1 | a0001 | c0001 | t0012 | g0185 | SAS | STU | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0179 | SAS | STU | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG04228 | hp1 | a0001 | c0001 | t0081 | g0241 | SAS | STU | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0028 | SAS | STU | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18522 | hp1 | a0001 | c0001 | t0017 | g0193 | AFR | YRI | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0175 | AFR | YRI | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18747 | hp1 | a0001 | c0008 | t0014 | g0014 | EAS | CHB | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18747 | hp2 | a0001 | c0003 | t0096 | g0279 | EAS | CHB | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18906 | hp1 | a0001 | c0001 | t0010 | g0059 | AFR | YRI | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18906 | hp2 | a0001 | c0003 | t0093 | g0286 | AFR | YRI | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18945 | hp1 | a0001 | c0001 | t0011 | g0067 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18945 | hp2 | a0001 | c0002 | t0090 | g0258 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18948 | hp2 | a0004 | c0014 | t0100 | g0278 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18949 | hp1 | a0001 | c0002 | t0043 | g0004 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18949 | hp2 | a0001 | c0001 | t0011 | g0020 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18951 | hp2 | a0001 | c0001 | t0008 | g0212 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18962 | hp1 | a0001 | c0001 | t0052 | g0138 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18962 | hp2 | a0001 | c0001 | t0011 | g0030 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18965 | hp1 | a0001 | c0008 | t0014 | g0047 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18965 | hp2 | a0002 | c0006 | t0001 | g0008 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18966 | hp1 | a0001 | c0003 | t0092 | g0272 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18966 | hp2 | a0008 | c0019 | t0029 | g0031 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18968 | hp1 | a0001 | c0003 | t0025 | g0283 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18968 | hp2 | a0001 | c0001 | t0008 | g0204 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18969 | hp1 | a0001 | c0001 | t0088 | g0261 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18969 | hp2 | a0001 | c0003 | t0025 | g0280 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18970 | hp1 | a0001 | c0001 | t0013 | g0211 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18977 | hp2 | a0002 | c0005 | t0011 | g0015 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18982 | hp1 | a0009 | c0032 | t0001 | g0069 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18982 | hp2 | a0001 | c0001 | t0013 | g0173 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18983 | hp2 | a0001 | c0001 | t0013 | g0184 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18984 | hp1 | a0001 | c0011 | t0002 | g0208 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18987 | hp1 | a0002 | c0012 | t0099 | g0265 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18988 | hp2 | a0002 | c0031 | t0105 | g0266 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18992 | hp1 | a0001 | c0001 | t0037 | g0250 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18994 | hp1 | a0002 | c0006 | t0001 | g0055 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18994 | hp2 | a0001 | c0001 | t0023 | g0207 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18995 | hp2 | a0001 | c0008 | t0014 | g0071 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18998 | hp1 | a0001 | c0002 | t0024 | g0160 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18998 | hp2 | a0001 | c0001 | t0053 | g0144 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18999 | hp1 | a0001 | c0001 | t0031 | g0198 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19001 | hp1 | a0002 | c0006 | t0048 | g0084 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19001 | hp2 | a0001 | c0001 | t0023 | g0197 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19004 | hp1 | a0001 | c0001 | t0011 | g0066 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19004 | hp2 | a0001 | c0002 | t0024 | g0209 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19009 | hp1 | a0001 | c0001 | t0059 | g0222 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19010 | hp1 | a0002 | c0016 | t0020 | g0074 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19010 | hp2 | a0001 | c0001 | t0008 | g0181 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19030 | hp1 | a0002 | c0006 | t0004 | g0143 | AFR | LWK | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19030 | hp2 | a0002 | c0005 | t0087 | g0254 | AFR | LWK | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19043 | hp1 | a0001 | c0002 | t0038 | g0244 | AFR | LWK | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19043 | hp2 | a0001 | c0004 | t0051 | g0236 | AFR | LWK | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19057 | hp1 | a0001 | c0001 | t0031 | g0199 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19060 | hp1 | a0001 | c0001 | t0089 | g0251 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19060 | hp2 | a0001 | c0001 | t0063 | g0121 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19062 | hp1 | a0001 | c0001 | t0008 | g0125 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19062 | hp2 | a0001 | c0002 | t0020 | g0080 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19064 | hp2 | a0001 | c0003 | t0098 | g0281 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19066 | hp1 | a0001 | c0001 | t0046 | g0072 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19066 | hp2 | a0001 | c0002 | t0024 | g0147 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19067 | hp1 | a0002 | c0016 | t0001 | g0010 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19067 | hp2 | a0001 | c0001 | t0008 | g0187 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19076 | hp1 | a0001 | c0027 | t0020 | g0017 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19077 | hp2 | a0001 | c0003 | t0078 | g0239 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19078 | hp1 | a0002 | c0005 | t0080 | g0127 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19078 | hp2 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19081 | hp1 | a0001 | c0001 | t0084 | g0242 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19081 | hp2 | a0001 | c0001 | t0008 | g0123 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19084 | hp2 | a0001 | c0003 | t0025 | g0282 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA19088 | hp2 | a0004 | c0014 | t0108 | g0290 | EAS | JPT | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0146 | EUR | TSI | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA20752 | hp2 | a0001 | c0002 | t0004 | g0114 | EUR | TSI | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02109 | hp1 | a0001 | c0007 | t0021 | g0162 | AFR | ACB | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02109 | hp2 | a0001 | c0007 | t0057 | g0237 | AFR | ACB | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02486 | hp1 | a0001 | c0003 | t0069 | g0163 | AFR | ACB | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02486 | hp2 | a0001 | c0001 | t0060 | g0192 | AFR | ACB | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02559 | hp1 | a0001 | c0003 | t0006 | g0284 | AFR | ACB | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG02559 | hp2 | a0001 | c0007 | t0075 | g0227 | AFR | ACB | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG06807 | hp1 | a0001 | c0004 | t0018 | g0226 | AFR | USA | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| HG06807 | hp2 | a0001 | c0001 | t0010 | g0061 | AFR | USA | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA21309 | hp1 | a0001 | c0002 | t0035 | g0128 | AFR | LWK | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| NA21309 | hp2 | a0001 | c0003 | t0006 | g0252 | AFR | LWK | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0004 | g0110 | REF | REF | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0176 | REF | REF | RAPH1_chr2_203428682_203540301 | RAPH1 | chr2 | 203428682 | 203540301 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:203439943 | G | A | 2 | a0002 a0004 |
3 | NA18948.hp2 NA18988.hp2 NA19088.hp2 |
missense_variant | MODERATE | c.3247C>T | p.Pro1083Ser | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 3438/9699 | 3247/3753 | 1083/1250 | chr2 | 203439943 | |||
| chr2:203440679 | C | CG | 3 | a0002 a0003 a0006 |
10 | HG00597.hp2 HG00621.hp2 HG00673.hp2 others(7): Show |
frameshift_variant | HIGH | c.2510dupC | p.Pro838fs | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 2701/9699 | 2510/3753 | 837/1250 | chr2 | 203440679 | |||
| chr2:203440970 | G | C | 1 | a0007 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.2220C>G | p.Phe740Leu | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 2411/9699 | 2220/3753 | 740/1250 | chr2 | 203440970 | |||
| chr2:203441175 | C | T | 1 | a0002 | 1 | HG00621.hp2 | missense_variant | MODERATE | c.2015G>A | p.Arg672Gln | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 2206/9699 | 2015/3753 | 672/1250 | chr2 | 203441175 | |||
| chr2:203441288 | T | TG | 2 | a0002 a0006 |
36 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(33): Show |
frameshift_variant | HIGH | c.1901dupC | p.Pro635fs | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 2092/9699 | 1901/3753 | 634/1250 | chr2 | 203441288 | |||
| chr2:203441358 | G | A | 1 | a0005 | 1 | HG00423.hp2 | missense_variant | MODERATE | c.1832C>T | p.Pro611Leu | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 2023/9699 | 1832/3753 | 611/1250 | chr2 | 203441358 | |||
| chr2:203448075 | C | T | 1 | a0006 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.1517G>A | p.Gly506Glu | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 12/14 | 1708/9699 | 1517/3753 | 506/1250 | chr2 | 203448075 | |||
| chr2:203448775 | G | A | 1 | a0009 | 1 | NA18982.hp1 | missense_variant | MODERATE | c.1475C>T | p.Thr492Ile | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 11/14 | 1666/9699 | 1475/3753 | 492/1250 | chr2 | 203448775 | |||
| chr2:203461300 | C | T | 1 | a0008 | 1 | NA18966.hp2 | missense_variant | MODERATE | c.919G>A | p.Gly307Ser | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 6/14 | 1110/9699 | 919/3753 | 307/1250 | chr2 | 203461300 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:203439491 | G | A | 9 | a0001c0003 a0001c0010 a0001c0015 others(6): Show |
42 | HG00735.hp1 HG00738.hp2 HG01099.hp2 others(39): Show |
synonymous_variant | LOW | c.3699C>T | p.Pro1233Pro | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 3890/9699 | 3699/3753 | 1233/1250 | chr2 | 203439491 | |||
| chr2:203439794 | G | A | 1 | a0001c0020 | 1 | HG02258.hp1 | synonymous_variant | LOW | c.3396C>T | p.Arg1132Arg | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 3587/9699 | 3396/3753 | 1132/1250 | chr2 | 203439794 | |||
| chr2:203440235 | A | G | 4 | a0001c0004 a0001c0029 a0002c0017 others(1): Show |
20 | HG00733.hp2 HG01109.hp2 HG01168.hp1 others(17): Show |
synonymous_variant | LOW | c.2955T>C | p.Ser985Ser | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 3146/9699 | 2955/3753 | 985/1250 | chr2 | 203440235 | |||
| chr2:203440370 | T | C | 10 | a0001c0002 a0001c0011 a0001c0015 others(7): Show |
94 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
synonymous_variant | LOW | c.2820A>G | p.Pro940Pro | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 3011/9699 | 2820/3753 | 940/1250 | chr2 | 203440370 | |||
| chr2:203440610 | C | T | 1 | a0001c0029 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.2580G>A | p.Ser860Ser | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 2771/9699 | 2580/3753 | 860/1250 | chr2 | 203440610 | |||
| chr2:203441105 | C | T | 1 | a0001c0027 | 1 | NA19076.hp1 | synonymous_variant | LOW | c.2085G>A | p.Gln695Gln | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 2276/9699 | 2085/3753 | 695/1250 | chr2 | 203441105 | |||
| chr2:203441258 | G | A | 1 | a0001c0021 | 1 | HG02155.hp2 | synonymous_variant | LOW | c.1932C>T | p.Pro644Pro | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 2123/9699 | 1932/3753 | 644/1250 | chr2 | 203441258 | |||
| chr2:203441297 | C | T | 1 | a0001c0033 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.1893G>A | p.Pro631Pro | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 2084/9699 | 1893/3753 | 631/1250 | chr2 | 203441297 | |||
| chr2:203441402 | C | T | 1 | a0001c0008 | 4 | HG02155.hp1 NA18747.hp1 NA18965.hp1 others(1): Show |
synonymous_variant | LOW | c.1788G>A | p.Glu596Glu | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 1979/9699 | 1788/3753 | 596/1250 | chr2 | 203441402 | |||
| chr2:203447984 | C | T | 1 | a0001c0026 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.1608G>A | p.Ser536Ser | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 12/14 | 1799/9699 | 1608/3753 | 536/1250 | chr2 | 203447984 | |||
| chr2:203457575 | T | C | 20 | a0001c0002 a0001c0003 a0001c0004 others(17): Show |
157 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
synonymous_variant | LOW | c.1113A>G | p.Lys371Lys | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 8/14 | 1304/9699 | 1113/3753 | 371/1250 | chr2 | 203457575 | |||
| chr2:203489662 | G | A | 1 | a0001c0033 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.654C>T | p.Ser218Ser | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/14 | 845/9699 | 654/3753 | 218/1250 | chr2 | 203489662 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:203433829 | A | G | 1 | a0001c0007t0026 | 2 | HG03225.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5608T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 5608 | chr2 | 203433829 | ||||||
| chr2:203433833 | AT | A | 7 | a0001c0001t0022 a0001c0001t0032 a0001c0001t0055 others(4): Show |
9 | HG00438.hp1 HG00642.hp2 HG00738.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5603delA | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 5603 | chr2 | 203433833 | ||||||
| chr2:203434040 | A | ATATATAT others(5): Show |
6 | a0001c0003t0006 a0001c0003t0036 a0001c0003t0102 others(3): Show |
12 | HG02145.hp1 HG02293.hp2 HG02559.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*5396_*5397insGATA others(8): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 5396 | chr2 | 203434040 | ||||||
| chr2:203434040 | A | ATATATAT others(9): Show |
5 | a0001c0003t0025 a0001c0003t0101 a0001c0003t0103 others(2): Show |
7 | HG02523.hp1 HG03130.hp2 NA18968.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5396_*5397insGATA others(12): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 5396 | chr2 | 203434040 | ||||||
| chr2:203434040 | A | ATATATAT others(13): Show |
2 | a0001c0003t0097 a0001c0003t0106 |
2 | HG02129.hp2 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5396_*5397insGATA others(16): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 5396 | chr2 | 203434040 | ||||||
| chr2:203434040 | A | ATATATAT others(17): Show |
1 | a0001c0003t0095 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5396_*5397insGATA others(20): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 5396 | chr2 | 203434040 | ||||||
| chr2:203434040 | A | ATATC | 4 | a0001c0001t0010 a0001c0001t0017 a0001c0001t0060 others(1): Show |
11 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5393_*5396dupGATA | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 5396 | chr2 | 203434040 | ||||||
| chr2:203434040 | A | ATATCTAT others(5): Show |
4 | a0001c0003t0039 a0001c0003t0078 a0001c0003t0104 others(1): Show |
4 | HG00738.hp2 HG03540.hp2 HG03710.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5385_*5396dupGATA others(8): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 5396 | chr2 | 203434040 | ||||||
| chr2:203434040 | A | ATATCTAT others(9): Show |
2 | a0001c0001t0063 a0001c0003t0098 |
2 | NA19060.hp2 NA19064.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5381_*5396dupGATA others(12): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 5396 | chr2 | 203434040 | ||||||
| chr2:203434040 | A | ATATCTAT others(13): Show |
2 | a0001c0003t0092 a0001c0003t0096 |
2 | NA18747.hp2 NA18966.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5396_*5397insGATA others(16): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 5396 | chr2 | 203434040 | ||||||
| chr2:203434040 | A | ATCTATCT others(7): Show |
1 | a0001c0007t0057 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5396_*5397insGATA others(10): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 5396 | chr2 | 203434040 | ||||||
| chr2:203434040 | A | C | 3 | a0001c0001t0019 a0001c0001t0045 a0001c0001t0089 |
5 | HG00323.hp1 HG01168.hp2 HG01175.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5397T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 5397 | chr2 | 203434040 | ||||||
| chr2:203434044 | C | A | 4 | a0001c0003t0093 a0001c0033t0050 a0002c0031t0105 others(1): Show |
4 | HG01884.hp1 NA18906.hp2 NA18948.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5393G>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 5393 | chr2 | 203434044 | ||||||
| chr2:203434056 | C | A | 4 | a0001c0001t0019 a0001c0001t0055 a0001c0007t0057 others(1): Show |
6 | HG00323.hp1 HG01168.hp2 HG01496.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5381G>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 5381 | chr2 | 203434056 | ||||||
| chr2:203434056 | C | CTA | 6 | a0001c0001t0013 a0001c0001t0059 a0001c0001t0086 others(3): Show |
9 | HG00621.hp1 HG02451.hp2 HG02976.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5379_*5380dupTA | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 5380 | chr2 | 203434056 | ||||||
| chr2:203434056 | C | CTATA | 3 | a0001c0001t0061 a0001c0001t0081 a0001c0002t0033 |
4 | HG01081.hp2 HG03453.hp1 HG03704.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5377_*5380dupTATA | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 5380 | chr2 | 203434056 | ||||||
| chr2:203434056 | C | CTATCTA | 3 | a0001c0002t0073 a0001c0007t0026 a0002c0006t0074 |
4 | HG01515.hp2 HG01517.hp1 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5380_*5381insTAGA others(2): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 5380 | chr2 | 203434056 | ||||||
| chr2:203434056 | C | CTATCTAT others(3): Show |
1 | a0001c0003t0069 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5380_*5381insTATA others(6): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 5380 | chr2 | 203434056 | ||||||
| chr2:203434056 | C | CTATCTAT others(3): Show |
1 | a0001c0020t0058 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5380_*5381insTAGA others(6): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 5380 | chr2 | 203434056 | ||||||
| chr2:203434058 | A | ATC | 30 | a0001c0001t0003 a0001c0001t0052 a0001c0001t0053 others(27): Show |
67 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*5378_*5379insGA | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 5378 | chr2 | 203434058 | ||||||
| chr2:203434058 | A | ATCTATC | 3 | a0001c0002t0071 a0001c0002t0072 a0004c0014t0100 |
3 | HG00280.hp1 HG03491.hp1 NA18948.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5378_*5379insGATA others(2): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 5378 | chr2 | 203434058 | ||||||
| chr2:203434058 | A | ATCTATCT others(3): Show |
1 | a0001c0003t0094 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5378_*5379insGATA others(6): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 5378 | chr2 | 203434058 | ||||||
| chr2:203434058 | A | ATCTATCT others(7): Show |
2 | a0001c0003t0093 a0002c0031t0105 |
2 | NA18906.hp2 NA18988.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5378_*5379insGATA others(10): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 5378 | chr2 | 203434058 | ||||||
| chr2:203434058 | A | C | 1 | a0001c0033t0050 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5379T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 5379 | chr2 | 203434058 | ||||||
| chr2:203434060 | A | C | 40 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0032 others(37): Show |
94 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*5377T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 5377 | chr2 | 203434060 | ||||||
| chr2:203434062 | A | C | 14 | a0001c0001t0003 a0001c0001t0052 a0001c0001t0053 others(11): Show |
26 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*5375T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 5375 | chr2 | 203434062 | ||||||
| chr2:203434064 | A | C | 7 | a0001c0002t0020 a0001c0002t0043 a0001c0003t0025 others(4): Show |
9 | HG01884.hp1 NA18949.hp1 NA18966.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5373T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 5373 | chr2 | 203434064 | ||||||
| chr2:203434077 | T | G | 1 | a0001c0003t0103 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5360A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 5360 | chr2 | 203434077 | ||||||
| chr2:203434079 | T | G | 27 | a0001c0001t0063 a0001c0001t0089 a0001c0003t0006 others(24): Show |
35 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*5358A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 5358 | chr2 | 203434079 | ||||||
| chr2:203434533 | C | T | 21 | a0001c0003t0006 a0001c0003t0025 a0001c0003t0039 others(18): Show |
28 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*4904G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 4904 | chr2 | 203434533 | ||||||
| chr2:203434566 | C | CA | 6 | a0001c0001t0023 a0001c0001t0046 a0001c0002t0047 others(3): Show |
8 | HG01517.hp1 HG02165.hp2 HG02698.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4870dupT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 4870 | chr2 | 203434566 | ||||||
| chr2:203434566 | C | CAAA | 6 | a0001c0001t0052 a0001c0003t0069 a0001c0003t0070 others(3): Show |
7 | HG02451.hp2 HG02486.hp1 HG02970.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4868_*4870dupTTT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 4870 | chr2 | 203434566 | ||||||
| chr2:203434566 | C | CAAAA | 11 | a0001c0001t0003 a0001c0004t0034 a0001c0004t0051 others(8): Show |
23 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*4867_*4870dupTTTT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 4870 | chr2 | 203434566 | ||||||
| chr2:203434566 | C | CAAAAA | 5 | a0001c0001t0053 a0001c0001t0084 a0001c0007t0021 others(2): Show |
6 | HG02109.hp1 HG02559.hp2 HG02809.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4866_*4870dupTTTT others(1): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 4870 | chr2 | 203434566 | ||||||
| chr2:203434566 | CAA | C | 26 | a0001c0003t0006 a0001c0003t0025 a0001c0003t0036 others(23): Show |
34 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*4869_*4870delTT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 4869 | chr2 | 203434566 | ||||||
| chr2:203434611 | C | T | 1 | a0001c0001t0017 | 4 | HG02145.hp2 HG02809.hp1 HG02965.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4826G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 4826 | chr2 | 203434611 | ||||||
| chr2:203434717 | C | T | 1 | a0001c0007t0057 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4720G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 4720 | chr2 | 203434717 | ||||||
| chr2:203434748 | T | C | 1 | a0001c0001t0064 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4689A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 4689 | chr2 | 203434748 | ||||||
| chr2:203434817 | A | G | 15 | a0001c0001t0003 a0001c0001t0052 a0001c0001t0053 others(12): Show |
27 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*4620T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 4620 | chr2 | 203434817 | ||||||
| chr2:203435048 | C | T | 1 | a0001c0001t0059 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4389G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 4389 | chr2 | 203435048 | ||||||
| chr2:203435213 | G | A | 9 | a0001c0004t0005 a0001c0004t0015 a0001c0004t0018 others(6): Show |
20 | HG00733.hp2 HG01109.hp2 HG01168.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*4224C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 4224 | chr2 | 203435213 | ||||||
| chr2:203435341 | G | C | 1 | a0001c0003t0078 | 1 | NA19077.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4096C>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 4096 | chr2 | 203435341 | ||||||
| chr2:203435369 | CA | C | 87 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0016 others(84): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*4067delT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 4067 | chr2 | 203435369 | ||||||
| chr2:203435380 | A | C | 1 | a0001c0001t0008 | 6 | NA18951.hp2 NA18968.hp2 NA19010.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4057T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 4057 | chr2 | 203435380 | ||||||
| chr2:203435383 | AAC | A | 9 | a0001c0001t0003 a0001c0001t0052 a0001c0001t0053 others(6): Show |
20 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*4052_*4053delGT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 4052 | chr2 | 203435383 | ||||||
| chr2:203435521 | T | TAA | 27 | a0001c0003t0006 a0001c0003t0025 a0001c0003t0036 others(24): Show |
35 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*3914_*3915dupTT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 3915 | chr2 | 203435521 | ||||||
| chr2:203435589 | C | T | 1 | a0001c0003t0069 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3848G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 3848 | chr2 | 203435589 | ||||||
| chr2:203435603 | C | A | 1 | a0001c0007t0057 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3834G>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 3834 | chr2 | 203435603 | ||||||
| chr2:203435755 | T | C | 1 | a0001c0001t0065 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3682A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 3682 | chr2 | 203435755 | ||||||
| chr2:203436227 | C | T | 1 | a0001c0007t0057 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3210G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 3210 | chr2 | 203436227 | ||||||
| chr2:203436398 | A | AG | 9 | a0001c0001t0003 a0001c0001t0052 a0001c0001t0053 others(6): Show |
20 | HG00408.hp1 HG00544.hp2 HG01257.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*3038dupC | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 3038 | chr2 | 203436398 | ||||||
| chr2:203436400 | G | C | 1 | a0001c0007t0075 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3037C>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 3037 | chr2 | 203436400 | ||||||
| chr2:203436400 | G | T | 3 | a0001c0004t0015 a0001c0007t0068 a0002c0017t0015 |
5 | HG02572.hp1 HG02896.hp1 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3037C>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 3037 | chr2 | 203436400 | ||||||
| chr2:203436468 | C | T | 1 | a0001c0001t0031 | 2 | NA18999.hp1 NA19057.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2969G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 2969 | chr2 | 203436468 | ||||||
| chr2:203436473 | A | T | 1 | a0001c0002t0067 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2964T>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 2964 | chr2 | 203436473 | ||||||
| chr2:203436573 | G | A | 88 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0052 others(85): Show |
178 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*2864C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 2864 | chr2 | 203436573 | ||||||
| chr2:203436732 | G | A | 1 | a0001c0002t0049 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2705C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 2705 | chr2 | 203436732 | ||||||
| chr2:203436882 | C | T | 1 | a0001c0029t0066 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2555G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 2555 | chr2 | 203436882 | ||||||
| chr2:203437027 | G | GAC | 88 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0052 others(85): Show |
178 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*2409_*2410insGT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 2409 | chr2 | 203437027 | ||||||
| chr2:203437049 | T | A | 1 | a0001c0033t0050 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2388A>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 2388 | chr2 | 203437049 | ||||||
| chr2:203437066 | T | TAGC | 2 | a0001c0007t0021 a0002c0018t0021 |
3 | HG02109.hp1 HG02809.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2370_*2371insGCT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 2370 | chr2 | 203437066 | ||||||
| chr2:203437069 | T | G | 2 | a0001c0007t0021 a0002c0018t0021 |
3 | HG02109.hp1 HG02809.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2368A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 2368 | chr2 | 203437069 | ||||||
| chr2:203437070 | G | C | 2 | a0001c0007t0021 a0002c0018t0021 |
3 | HG02109.hp1 HG02809.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2367C>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 2367 | chr2 | 203437070 | ||||||
| chr2:203437071 | T | A | 2 | a0001c0007t0021 a0002c0018t0021 |
3 | HG02109.hp1 HG02809.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2366A>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 2366 | chr2 | 203437071 | ||||||
| chr2:203437259 | C | T | 2 | a0001c0007t0057 a0001c0033t0050 |
2 | HG01884.hp1 HG02109.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2178G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 2178 | chr2 | 203437259 | ||||||
| chr2:203437358 | ACT | A | 2 | a0001c0007t0021 a0002c0018t0021 |
3 | HG02109.hp1 HG02809.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2077_*2078delAG | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 2077 | chr2 | 203437358 | ||||||
| chr2:203437437 | C | T | 1 | a0001c0001t0056 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2000G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 2000 | chr2 | 203437437 | ||||||
| chr2:203437579 | A | G | 1 | a0001c0033t0050 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1858T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 1858 | chr2 | 203437579 | ||||||
| chr2:203437593 | C | T | 3 | a0001c0003t0036 a0001c0003t0076 a0002c0012t0091 |
4 | HG02145.hp1 HG02451.hp1 HG02717.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1844G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 1844 | chr2 | 203437593 | ||||||
| chr2:203437664 | T | G | 1 | a0001c0002t0035 | 2 | HG00733.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1773A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 1773 | chr2 | 203437664 | ||||||
| chr2:203437673 | T | C | 27 | a0001c0003t0006 a0001c0003t0025 a0001c0003t0036 others(24): Show |
35 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1764A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 1764 | chr2 | 203437673 | ||||||
| chr2:203437749 | A | G | 1 | a0001c0001t0008 | 6 | NA18951.hp2 NA18968.hp2 NA19010.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1688T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 1688 | chr2 | 203437749 | ||||||
| chr2:203438032 | G | A | 1 | a0001c0002t0079 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1405C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 1405 | chr2 | 203438032 | ||||||
| chr2:203438043 | C | T | 1 | a0001c0001t0055 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1394G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 1394 | chr2 | 203438043 | ||||||
| chr2:203438073 | A | G | 2 | a0001c0007t0021 a0002c0018t0021 |
3 | HG02109.hp1 HG02809.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1364T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 1364 | chr2 | 203438073 | ||||||
| chr2:203438376 | TTTTG | T | 13 | a0001c0001t0003 a0001c0001t0052 a0001c0001t0053 others(10): Show |
25 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1057_*1060delCAAA | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 1057 | chr2 | 203438376 | ||||||
| chr2:203438418 | A | G | 1 | a0001c0004t0051 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1019T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 1019 | chr2 | 203438418 | ||||||
| chr2:203438558 | A | G | 1 | a0001c0033t0050 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*879T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 879 | chr2 | 203438558 | ||||||
| chr2:203438914 | A | G | 1 | a0002c0006t0027 | 2 | HG01167.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*523T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 523 | chr2 | 203438914 | ||||||
| chr2:203439216 | T | G | 1 | a0002c0005t0080 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*221A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 14/14 | 221 | chr2 | 203439216 | ||||||
| chr2:203535227 | G | A | 1 | a0001c0001t0081 | 1 | HG04228.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-117C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/14 | chr2 | 203535227 | |||||||
| chr2:203535258 | G | GTGAC | 35 | a0001c0001t0009 a0001c0001t0037 a0001c0001t0084 others(32): Show |
47 | HG00597.hp2 HG00642.hp1 HG00738.hp2 others(44): Show |
5_prime_UTR_variant | MODIFIER | c.-152_-149dupGTCA | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/14 | 39906 | chr2 | 203535258 | ||||||
| chr2:203535258 | G | GTGACTGA others(5): Show |
2 | a0002c0005t0107 a0004c0014t0108 |
2 | HG03710.hp1 NA19088.hp2 |
5_prime_UTR_variant | MODIFIER | c.-160_-149dupGTCAGT others(6): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/14 | 39906 | chr2 | 203535258 | ||||||
| chr2:203535258 | GTGAC | G | 31 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0011 others(28): Show |
98 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(95): Show |
5_prime_UTR_variant | MODIFIER | c.-152_-149delGTCA | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/14 | 39906 | chr2 | 203535258 | ||||||
| chr2:203535258 | GTGACTGA others(1): Show |
G | 5 | a0001c0002t0042 a0001c0002t0043 a0001c0007t0026 others(2): Show |
6 | HG01109.hp1 HG02293.hp2 HG02523.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-156_-149delGTCAGT others(2): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/14 | 39906 | chr2 | 203535258 | ||||||
| chr2:203535274 | C | T | 1 | a0001c0010t0040 | 1 | HG01099.hp2 | 5_prime_UTR_variant | MODIFIER | c.-164G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/14 | 39921 | chr2 | 203535274 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:203441438 | G | A | 1 | a0001c0002t0001g0083 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1777-25C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 13/13 | chr2 | 203441438 | |||||||
| chr2:203441522 | T | C | 1 | a0001c0007t0057g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1777-109A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 13/13 | chr2 | 203441522 | |||||||
| chr2:203441574 | G | A | 1 | a0001c0001t0063g0121 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1777-161C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 13/13 | chr2 | 203441574 | |||||||
| chr2:203441633 | A | G | 94 | a0001c0001t0003g0150 a0001c0001t0009g0247 a0001c0001t0022g0168 others(91): Show |
94 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.1777-220T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 13/13 | chr2 | 203441633 | |||||||
| chr2:203441703 | G | A | 4 | a0001c0001t0010g0062 a0001c0001t0010g0063 a0001c0001t0010g0064 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1777-290C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 13/13 | chr2 | 203441703 | |||||||
| chr2:203441710 | T | C | 61 | a0001c0001t0009g0247 a0001c0002t0038g0244 a0001c0002t0038g0245 others(58): Show |
61 | HG00733.hp2 HG00738.hp2 HG01109.hp2 others(58): Show |
intron_variant | MODIFIER | c.1777-297A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 13/13 | chr2 | 203441710 | |||||||
| chr2:203441729 | T | C | 92 | a0001c0001t0002g0148 a0001c0001t0011g0030 a0001c0002t0001g0009 others(89): Show |
92 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.1777-316A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 13/13 | chr2 | 203441729 | |||||||
| chr2:203441816 | A | G | 1 | a0001c0002t0001g0046 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1777-403T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 13/13 | chr2 | 203441816 | |||||||
| chr2:203442031 | A | G | 1 | a0001c0002t0001g0079 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1777-618T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 13/13 | chr2 | 203442031 | |||||||
| chr2:203442279 | C | T | 1 | a0002c0006t0001g0008 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1777-866G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 13/13 | chr2 | 203442279 | |||||||
| chr2:203442280 | G | A | 37 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(34): Show |
37 | HG00738.hp2 HG01884.hp1 HG01943.hp2 others(34): Show |
intron_variant | MODIFIER | c.1777-867C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 13/13 | chr2 | 203442280 | |||||||
| chr2:203442443 | G | T | 35 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(32): Show |
35 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(32): Show |
intron_variant | MODIFIER | c.1777-1030C>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 13/13 | chr2 | 203442443 | |||||||
| chr2:203442493 | C | T | 4 | a0001c0001t0017g0126 a0001c0001t0017g0193 a0001c0001t0017g0194 others(1): Show |
4 | HG02145.hp2 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1777-1080G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 13/13 | chr2 | 203442493 | |||||||
| chr2:203442728 | G | C | 2 | a0001c0001t0022g0168 a0001c0001t0022g0180 |
2 | HG00642.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.1777-1315C>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 13/13 | chr2 | 203442728 | |||||||
| chr2:203442815 | T | C | 1 | a0001c0001t0019g0081 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1777-1402A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 13/13 | chr2 | 203442815 | |||||||
| chr2:203442932 | C | T | 1 | a0001c0007t0057g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1777-1519G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 13/13 | chr2 | 203442932 | |||||||
| chr2:203443330 | T | G | 20 | a0001c0004t0005g0093 a0001c0004t0005g0095 a0001c0004t0005g0098 others(17): Show |
20 | HG00733.hp2 HG01109.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.1776+1538A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 13/13 | chr2 | 203443330 | |||||||
| chr2:203443446 | A | G | 1 | a0002c0013t0009g0256 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1776+1422T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 13/13 | chr2 | 203443446 | |||||||
| chr2:203443640 | T | TA | 35 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(32): Show |
35 | HG00738.hp2 HG01884.hp1 HG01943.hp2 others(32): Show |
intron_variant | MODIFIER | c.1776+1227dupT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 13/13 | chr2 | 203443640 | |||||||
| chr2:203444019 | G | A | 1 | a0001c0001t0002g0145 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1776+849C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 13/13 | chr2 | 203444019 | |||||||
| chr2:203444096 | AAGG | A | 34 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(31): Show |
34 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(31): Show |
intron_variant | MODIFIER | c.1776+769_1776+771d others(5): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 13/13 | chr2 | 203444096 | |||||||
| chr2:203444138 | AAAAG | A | 32 | a0001c0003t0006g0263 a0001c0003t0006g0274 a0001c0003t0006g0276 others(29): Show |
32 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(29): Show |
intron_variant | MODIFIER | c.1776+726_1776+729d others(6): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 13/13 | chr2 | 203444138 | |||||||
| chr2:203444138 | AAAAGAGA others(1): Show |
A | 3 | a0001c0003t0006g0252 a0001c0003t0006g0288 a0001c0015t0044g0007 |
3 | HG02293.hp2 HG02886.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1776+722_1776+729d others(10): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 13/13 | chr2 | 203444138 | |||||||
| chr2:203444214 | T | A | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1776+654A>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 13/13 | chr2 | 203444214 | |||||||
| chr2:203444293 | G | A | 2 | a0001c0001t0013g0211 a0001c0001t0059g0222 |
2 | NA18970.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1776+575C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 13/13 | chr2 | 203444293 | |||||||
| chr2:203444357 | G | A | 5 | a0001c0001t0010g0059 a0001c0001t0010g0062 a0001c0001t0010g0063 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1776+511C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 13/13 | chr2 | 203444357 | |||||||
| chr2:203444386 | C | G | 1 | a0001c0007t0026g0005 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1776+482G>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 13/13 | chr2 | 203444386 | |||||||
| chr2:203444428 | C | CA | 49 | a0001c0001t0001g0012 a0001c0001t0002g0119 a0001c0001t0002g0155 others(46): Show |
49 | HG00733.hp2 HG00738.hp2 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.1776+439dupT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 13/13 | chr2 | 203444428 | |||||||
| chr2:203444428 | C | CAA | 10 | a0001c0003t0025g0280 a0001c0003t0025g0282 a0001c0003t0025g0283 others(7): Show |
10 | HG02129.hp2 HG02132.hp1 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.1776+438_1776+439d others(4): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 13/13 | chr2 | 203444428 | |||||||
| chr2:203444428 | CA | C | 90 | a0001c0001t0003g0150 a0001c0001t0008g0125 a0001c0001t0010g0063 others(87): Show |
90 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.1776+439delT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 13/13 | chr2 | 203444428 | |||||||
| chr2:203444465 | G | A | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1776+403C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 13/13 | chr2 | 203444465 | |||||||
| chr2:203444532 | T | A | 1 | a0001c0002t0043g0004 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1776+336A>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 13/13 | chr2 | 203444532 | |||||||
| chr2:203444602 | G | A | 156 | a0001c0002t0001g0009 a0001c0002t0001g0016 a0001c0002t0001g0023 others(153): Show |
156 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.1776+266C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 13/13 | chr2 | 203444602 | |||||||
| chr2:203444611 | A | G | 20 | a0001c0004t0005g0093 a0001c0004t0005g0095 a0001c0004t0005g0098 others(17): Show |
20 | HG00733.hp2 HG01109.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.1776+257T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 13/13 | chr2 | 203444611 | |||||||
| chr2:203444620 | G | GT | 4 | a0001c0002t0035g0115 a0001c0002t0035g0128 a0001c0002t0071g0113 others(1): Show |
4 | HG00280.hp1 HG00733.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1776+247dupA | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 13/13 | chr2 | 203444620 | |||||||
| chr2:203444696 | C | A | 3 | a0001c0007t0021g0162 a0001c0007t0021g0220 a0002c0018t0021g0161 |
3 | HG02109.hp1 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1776+172G>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 13/13 | chr2 | 203444696 | |||||||
| chr2:203444741 | T | C | 4 | a0001c0002t0004g0106 a0001c0002t0004g0109 a0001c0002t0072g0108 others(1): Show |
4 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(1): Show |
intron_variant | MODIFIER | c.1776+127A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 13/13 | chr2 | 203444741 | |||||||
| chr2:203444754 | A | G | 2 | a0001c0003t0101g0277 a0001c0003t0102g0268 |
2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1776+114T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 13/13 | chr2 | 203444754 | |||||||
| chr2:203445347 | A | G | 18 | a0001c0001t0001g0012 a0001c0001t0002g0188 a0001c0001t0002g0191 others(15): Show |
18 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.1634-337T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 12/13 | chr2 | 203445347 | |||||||
| chr2:203445393 | T | C | 1 | a0001c0002t0072g0108 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1634-383A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 12/13 | chr2 | 203445393 | |||||||
| chr2:203445441 | C | T | 2 | a0001c0003t0069g0163 a0001c0003t0070g0225 |
2 | HG02486.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1634-431G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 12/13 | chr2 | 203445441 | |||||||
| chr2:203445551 | C | T | 1 | a0001c0001t0002g0221 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1634-541G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 12/13 | chr2 | 203445551 | |||||||
| chr2:203445609 | G | A | 1 | a0001c0001t0017g0194 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1634-599C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 12/13 | chr2 | 203445609 | |||||||
| chr2:203445961 | G | T | 1 | a0001c0002t0001g0083 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1634-951C>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 12/13 | chr2 | 203445961 | |||||||
| chr2:203445962 | G | A | 1 | a0001c0002t0001g0083 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1634-952C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 12/13 | chr2 | 203445962 | |||||||
| chr2:203445963 | G | A | 1 | a0001c0002t0001g0083 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1634-953C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 12/13 | chr2 | 203445963 | |||||||
| chr2:203445965 | A | G | 1 | a0001c0002t0001g0083 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1634-955T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 12/13 | chr2 | 203445965 | |||||||
| chr2:203445990 | C | T | 1 | a0001c0002t0001g0079 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1634-980G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 12/13 | chr2 | 203445990 | |||||||
| chr2:203446136 | C | T | 1 | a0001c0002t0001g0036 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1634-1126G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 12/13 | chr2 | 203446136 | |||||||
| chr2:203446401 | A | G | 1 | a0001c0002t0020g0080 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1634-1391T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 12/13 | chr2 | 203446401 | |||||||
| chr2:203446445 | G | A | 1 | a0001c0004t0034g0235 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1634-1435C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 12/13 | chr2 | 203446445 | |||||||
| chr2:203446773 | T | A | 2 | a0001c0007t0026g0005 a0001c0007t0026g0006 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1633+1186A>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 12/13 | chr2 | 203446773 | |||||||
| chr2:203446795 | G | T | 20 | a0001c0004t0005g0093 a0001c0004t0005g0095 a0001c0004t0005g0098 others(17): Show |
20 | HG00733.hp2 HG01109.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.1633+1164C>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 12/13 | chr2 | 203446795 | |||||||
| chr2:203446856 | G | T | 1 | a0002c0005t0003g0135 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1633+1103C>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 12/13 | chr2 | 203446856 | |||||||
| chr2:203446909 | T | TA | 7 | a0001c0001t0019g0032 a0001c0001t0019g0081 a0001c0001t0019g0082 others(4): Show |
7 | HG00323.hp1 HG01168.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1633+1049dupT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 12/13 | chr2 | 203446909 | |||||||
| chr2:203446909 | TA | T | 57 | a0001c0001t0016g0141 a0001c0001t0088g0261 a0001c0003t0006g0252 others(54): Show |
57 | HG00733.hp2 HG00738.hp2 HG01109.hp2 others(54): Show |
intron_variant | MODIFIER | c.1633+1049delT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 12/13 | chr2 | 203446909 | |||||||
| chr2:203446909 | TAAAAAA | T | 6 | a0001c0002t0001g0027 a0001c0002t0001g0040 a0001c0002t0001g0041 others(3): Show |
6 | HG00438.hp2 HG00609.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.1633+1044_1633+104 others(10): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 12/13 | chr2 | 203446909 | |||||||
| chr2:203446929 | A | T | 1 | a0001c0001t0017g0194 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1633+1030T>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 12/13 | chr2 | 203446929 | |||||||
| chr2:203446996 | T | C | 1 | a0001c0001t0023g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1633+963A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 12/13 | chr2 | 203446996 | |||||||
| chr2:203447128 | G | C | 19 | a0001c0001t0003g0112 a0001c0001t0003g0136 a0001c0001t0003g0137 others(16): Show |
19 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.1633+831C>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 12/13 | chr2 | 203447128 | |||||||
| chr2:203447178 | TTTC | T | 14 | a0001c0002t0001g0052 a0001c0002t0001g0053 a0001c0002t0001g0056 others(11): Show |
14 | HG01071.hp2 HG01361.hp1 HG02273.hp1 others(11): Show |
intron_variant | MODIFIER | c.1633+778_1633+780d others(5): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 12/13 | chr2 | 203447178 | |||||||
| chr2:203447181 | C | CT | 71 | a0001c0002t0001g0016 a0001c0002t0001g0023 a0001c0002t0001g0027 others(68): Show |
71 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.1633+777dupA | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 12/13 | chr2 | 203447181 | |||||||
| chr2:203447181 | C | CTT | 10 | a0001c0002t0001g0009 a0001c0002t0001g0043 a0001c0002t0001g0068 others(7): Show |
10 | HG00408.hp2 HG01255.hp2 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.1633+776_1633+777d others(4): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 12/13 | chr2 | 203447181 | |||||||
| chr2:203447181 | CT | C | 13 | a0001c0001t0028g0065 a0001c0003t0006g0252 a0001c0003t0006g0284 others(10): Show |
13 | HG00408.hp1 HG01943.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1633+777delA | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 12/13 | chr2 | 203447181 | |||||||
| chr2:203447185 | T | C | 1 | a0001c0001t0011g0067 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1633+774A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 12/13 | chr2 | 203447185 | |||||||
| chr2:203447199 | T | G | 35 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(32): Show |
35 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(32): Show |
intron_variant | MODIFIER | c.1633+760A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 12/13 | chr2 | 203447199 | |||||||
| chr2:203447432 | A | G | 4 | a0001c0003t0036g0229 a0001c0003t0036g0230 a0001c0003t0076g0228 others(1): Show |
4 | HG02145.hp1 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1633+527T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 12/13 | chr2 | 203447432 | |||||||
| chr2:203447525 | T | C | 2 | a0001c0007t0082g0260 a0002c0018t0083g0253 |
2 | HG02055.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1633+434A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 12/13 | chr2 | 203447525 | |||||||
| chr2:203447578 | T | G | 1 | a0008c0019t0029g0031 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1633+381A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 12/13 | chr2 | 203447578 | |||||||
| chr2:203447624 | G | A | 1 | a0001c0003t0070g0225 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1633+335C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 12/13 | chr2 | 203447624 | |||||||
| chr2:203448463 | G | A | 4 | a0001c0001t0010g0062 a0001c0001t0010g0063 a0001c0001t0010g0064 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1512+275C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 11/13 | chr2 | 203448463 | |||||||
| chr2:203448876 | G | A | 1 | a0001c0002t0004g0130 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1414-40C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203448876 | |||||||
| chr2:203449076 | C | T | 1 | a0001c0007t0068g0218 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1414-240G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203449076 | |||||||
| chr2:203449099 | G | A | 57 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(54): Show |
57 | HG00733.hp2 HG00738.hp2 HG01109.hp2 others(54): Show |
intron_variant | MODIFIER | c.1414-263C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203449099 | |||||||
| chr2:203449196 | A | C | 1 | a0007c0030t0006g0285 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1414-360T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203449196 | |||||||
| chr2:203449209 | C | T | 2 | a0001c0001t0002g0203 a0002c0005t0013g0170 |
2 | HG00621.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.1414-373G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203449209 | |||||||
| chr2:203449795 | C | T | 4 | a0001c0002t0001g0052 a0001c0002t0001g0053 a0001c0002t0001g0057 others(1): Show |
4 | NA18980.hp1 NA18999.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.1414-959G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203449795 | |||||||
| chr2:203449849 | C | T | 1 | a0002c0017t0015g0097 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1414-1013G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203449849 | |||||||
| chr2:203449995 | C | G | 4 | a0001c0003t0036g0229 a0001c0003t0036g0230 a0001c0003t0076g0228 others(1): Show |
4 | HG02145.hp1 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1414-1159G>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203449995 | |||||||
| chr2:203450018 | G | A | 1 | a0008c0019t0029g0031 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1414-1182C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203450018 | |||||||
| chr2:203450023 | C | CA | 6 | a0001c0002t0004g0132 a0001c0002t0004g0133 a0001c0002t0067g0201 others(3): Show |
6 | HG01081.hp1 HG01258.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1414-1188dupT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203450023 | |||||||
| chr2:203450175 | G | A | 4 | a0001c0001t0002g0148 a0001c0001t0002g0151 a0001c0001t0011g0030 others(1): Show |
4 | NA18962.hp2 NA18986.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.1414-1339C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203450175 | |||||||
| chr2:203450221 | C | G | 1 | a0001c0001t0037g0250 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1414-1385G>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203450221 | |||||||
| chr2:203450513 | G | A | 2 | a0001c0003t0069g0163 a0001c0003t0070g0225 |
2 | HG02486.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1414-1677C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203450513 | |||||||
| chr2:203450516 | T | C | 1 | a0001c0002t0001g0043 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1414-1680A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203450516 | |||||||
| chr2:203450671 | G | A | 88 | a0001c0002t0001g0009 a0001c0002t0001g0016 a0001c0002t0001g0023 others(85): Show |
88 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1414-1835C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203450671 | |||||||
| chr2:203450894 | A | AT | 6 | a0001c0002t0001g0009 a0001c0002t0001g0043 a0001c0002t0001g0058 others(3): Show |
6 | HG00323.hp2 HG01099.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.1414-2059_1414-205 others(5): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203450894 | |||||||
| chr2:203450895 | G | T | 82 | a0001c0002t0001g0016 a0001c0002t0001g0023 a0001c0002t0001g0027 others(79): Show |
82 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.1414-2059C>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203450895 | |||||||
| chr2:203450897 | G | GT | 25 | a0001c0001t0064g0215 a0001c0003t0006g0288 a0001c0003t0096g0279 others(22): Show |
25 | HG00733.hp2 HG00741.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1414-2062dupA | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203450897 | |||||||
| chr2:203450897 | G | T | 6 | a0001c0002t0001g0009 a0001c0002t0001g0043 a0001c0002t0001g0058 others(3): Show |
6 | HG00323.hp2 HG01099.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.1414-2061C>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203450897 | |||||||
| chr2:203450897 | GT | G | 6 | a0001c0001t0002g0190 a0001c0001t0003g0150 a0001c0001t0013g0173 others(3): Show |
6 | HG02280.hp1 HG02735.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1414-2062delA | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203450897 | |||||||
| chr2:203450900 | T | G | 1 | a0002c0005t0022g0117 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1414-2064A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203450900 | |||||||
| chr2:203451241 | A | G | 1 | a0001c0011t0003g0116 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1414-2405T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203451241 | |||||||
| chr2:203451276 | A | G | 1 | a0001c0029t0066g0219 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1414-2440T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203451276 | |||||||
| chr2:203451535 | T | A | 1 | a0001c0002t0067g0201 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1414-2699A>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203451535 | |||||||
| chr2:203451809 | C | T | 88 | a0001c0002t0001g0009 a0001c0002t0001g0016 a0001c0002t0001g0023 others(85): Show |
88 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1413+2621G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203451809 | |||||||
| chr2:203451910 | A | G | 35 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(32): Show |
35 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(32): Show |
intron_variant | MODIFIER | c.1413+2520T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203451910 | |||||||
| chr2:203451994 | T | C | 1 | a0001c0002t0035g0115 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1413+2436A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203451994 | |||||||
| chr2:203452505 | G | T | 1 | a0001c0001t0053g0144 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1413+1925C>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203452505 | |||||||
| chr2:203452555 | G | C | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1413+1875C>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203452555 | |||||||
| chr2:203452830 | C | T | 89 | a0001c0002t0001g0009 a0001c0002t0001g0016 a0001c0002t0001g0023 others(86): Show |
89 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.1413+1600G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203452830 | |||||||
| chr2:203453055 | G | A | 2 | a0001c0007t0082g0260 a0002c0018t0083g0253 |
2 | HG02055.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1413+1375C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203453055 | |||||||
| chr2:203453258 | C | T | 1 | a0001c0002t0004g0133 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1413+1172G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203453258 | |||||||
| chr2:203453391 | C | G | 3 | a0001c0002t0001g0088 a0001c0002t0001g0091 a0001c0002t0020g0080 |
3 | NA18946.hp1 NA18951.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.1413+1039G>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203453391 | |||||||
| chr2:203453461 | G | A | 1 | a0001c0003t0092g0272 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1413+969C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203453461 | |||||||
| chr2:203453543 | C | T | 1 | a0001c0007t0057g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1413+887G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203453543 | |||||||
| chr2:203453545 | C | CA | 21 | a0001c0001t0002g0146 a0001c0001t0002g0221 a0001c0001t0003g0139 others(18): Show |
21 | HG00438.hp1 HG01099.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.1413+884dupT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203453545 | |||||||
| chr2:203453545 | CA | C | 109 | a0001c0001t0001g0012 a0001c0001t0002g0154 a0001c0001t0002g0182 others(106): Show |
109 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.1413+884delT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203453545 | |||||||
| chr2:203453545 | CAA | C | 25 | a0001c0001t0064g0215 a0001c0002t0001g0051 a0001c0002t0001g0077 others(22): Show |
25 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.1413+883_1413+884d others(4): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203453545 | |||||||
| chr2:203453545 | CAAAAAAA | C | 17 | a0001c0004t0005g0093 a0001c0004t0005g0098 a0001c0004t0005g0100 others(14): Show |
17 | HG00733.hp2 HG01109.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.1413+878_1413+884d others(9): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203453545 | |||||||
| chr2:203453545 | CAAAAAAA others(4): Show |
C | 3 | a0001c0007t0026g0005 a0001c0007t0026g0006 a0001c0033t0050g0231 |
3 | HG01884.hp1 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1413+874_1413+884d others(13): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203453545 | |||||||
| chr2:203453545 | CAAAAAAA others(7): Show |
C | 1 | a0001c0007t0068g0218 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1413+871_1413+884d others(16): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203453545 | |||||||
| chr2:203453576 | G | A | 2 | a0001c0007t0021g0162 a0001c0007t0021g0220 |
2 | HG02109.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1413+854C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203453576 | |||||||
| chr2:203453645 | C | T | 1 | a0001c0007t0057g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1413+785G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203453645 | |||||||
| chr2:203454319 | G | A | 1 | a0001c0026t0077g0238 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1413+111C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 10/13 | chr2 | 203454319 | |||||||
| chr2:203454576 | T | C | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1303-36A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 9/13 | chr2 | 203454576 | |||||||
| chr2:203454673 | G | A | 1 | a0001c0001t0086g0243 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1303-133C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 9/13 | chr2 | 203454673 | |||||||
| chr2:203454735 | C | A | 1 | a0001c0001t0002g0155 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1303-195G>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 9/13 | chr2 | 203454735 | |||||||
| chr2:203455108 | T | G | 2 | a0001c0003t0101g0277 a0001c0003t0102g0268 |
2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1302+329A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 9/13 | chr2 | 203455108 | |||||||
| chr2:203455116 | C | G | 88 | a0001c0002t0001g0009 a0001c0002t0001g0016 a0001c0002t0001g0023 others(85): Show |
88 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1302+321G>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 9/13 | chr2 | 203455116 | |||||||
| chr2:203455846 | T | TA | 8 | a0001c0001t0010g0062 a0001c0001t0016g0141 a0001c0001t0016g0172 others(5): Show |
8 | HG01943.hp1 HG02572.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1159-267dupT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 8/13 | chr2 | 203455846 | |||||||
| chr2:203456008 | CAAAACA | C | 4 | a0001c0003t0069g0163 a0001c0003t0070g0225 a0001c0029t0066g0219 others(1): Show |
4 | HG01884.hp1 HG02486.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1159-434_1159-429d others(8): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 8/13 | chr2 | 203456008 | |||||||
| chr2:203456008 | CAAAACAA others(5): Show |
C | 88 | a0001c0002t0001g0009 a0001c0002t0001g0016 a0001c0002t0001g0023 others(85): Show |
88 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1159-440_1159-429d others(14): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 8/13 | chr2 | 203456008 | |||||||
| chr2:203456033 | AAAACAAA others(3): Show |
A | 16 | a0001c0004t0005g0093 a0001c0004t0005g0095 a0001c0004t0005g0098 others(13): Show |
16 | HG00733.hp2 HG01109.hp2 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.1159-463_1159-454d others(12): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 8/13 | chr2 | 203456033 | |||||||
| chr2:203456039 | AAAAC | A | 4 | a0001c0004t0034g0235 a0001c0004t0034g0240 a0001c0004t0051g0236 others(1): Show |
4 | HG02280.hp2 HG02559.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1159-463_1159-460d others(6): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 8/13 | chr2 | 203456039 | |||||||
| chr2:203456428 | A | C | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1159-848T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 8/13 | chr2 | 203456428 | |||||||
| chr2:203456592 | G | A | 3 | a0001c0007t0021g0162 a0001c0007t0021g0220 a0002c0018t0021g0161 |
3 | HG02109.hp1 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1158+938C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 8/13 | chr2 | 203456592 | |||||||
| chr2:203456640 | G | A | 1 | a0002c0005t0012g0206 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1158+890C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 8/13 | chr2 | 203456640 | |||||||
| chr2:203456763 | A | C | 1 | a0001c0002t0007g0011 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1158+767T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 8/13 | chr2 | 203456763 | |||||||
| chr2:203456807 | A | G | 35 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(32): Show |
35 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(32): Show |
intron_variant | MODIFIER | c.1158+723T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 8/13 | chr2 | 203456807 | |||||||
| chr2:203456920 | A | G | 35 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(32): Show |
35 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(32): Show |
intron_variant | MODIFIER | c.1158+610T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 8/13 | chr2 | 203456920 | |||||||
| chr2:203457180 | T | A | 2 | a0001c0001t0011g0020 a0003c0009t0041g0002 |
2 | HG02523.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.1158+350A>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 8/13 | chr2 | 203457180 | |||||||
| chr2:203457184 | T | A | 2 | a0001c0001t0011g0020 a0003c0009t0041g0002 |
2 | HG02523.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.1158+346A>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 8/13 | chr2 | 203457184 | |||||||
| chr2:203457185 | T | A | 2 | a0001c0001t0011g0020 a0003c0009t0041g0002 |
2 | HG02523.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.1158+345A>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 8/13 | chr2 | 203457185 | |||||||
| chr2:203457188 | T | A | 2 | a0001c0001t0011g0020 a0003c0009t0041g0002 |
2 | HG02523.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.1158+342A>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 8/13 | chr2 | 203457188 | |||||||
| chr2:203457189 | T | A | 2 | a0001c0001t0011g0020 a0003c0009t0041g0002 |
2 | HG02523.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.1158+341A>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 8/13 | chr2 | 203457189 | |||||||
| chr2:203457193 | TTATTTAT others(21): Show |
T | 2 | a0001c0001t0011g0020 a0003c0009t0041g0002 |
2 | HG02523.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.1158+309_1158+336d others(30): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 8/13 | chr2 | 203457193 | |||||||
| chr2:203457245 | T | C | 34 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(31): Show |
34 | HG00738.hp2 HG01943.hp2 HG02132.hp1 others(31): Show |
intron_variant | MODIFIER | c.1158+285A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 8/13 | chr2 | 203457245 | |||||||
| chr2:203457296 | C | T | 285 | a0001c0001t0001g0012 a0001c0001t0002g0111 a0001c0001t0002g0119 others(282): Show |
285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.1158+234G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 8/13 | chr2 | 203457296 | |||||||
| chr2:203457331 | C | T | 2 | a0001c0001t0002g0129 a0001c0001t0002g0196 |
2 | NA19056.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1158+199G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 8/13 | chr2 | 203457331 | |||||||
| chr2:203457394 | C | A | 1 | a0001c0011t0002g0208 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1158+136G>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 8/13 | chr2 | 203457394 | |||||||
| chr2:203457441 | C | T | 1 | a0002c0012t0039g0270 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1158+89G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 8/13 | chr2 | 203457441 | |||||||
| chr2:203457664 | C | T | 35 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(32): Show |
35 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(32): Show |
intron_variant | MODIFIER | c.1093-69G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 7/13 | chr2 | 203457664 | |||||||
| chr2:203457908 | C | A | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1093-313G>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 7/13 | chr2 | 203457908 | |||||||
| chr2:203457919 | C | G | 1 | a0001c0029t0066g0219 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1093-324G>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 7/13 | chr2 | 203457919 | |||||||
| chr2:203458239 | C | T | 1 | a0001c0007t0068g0218 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1093-644G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 7/13 | chr2 | 203458239 | |||||||
| chr2:203458259 | T | C | 157 | a0001c0002t0001g0009 a0001c0002t0001g0016 a0001c0002t0001g0023 others(154): Show |
157 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.1093-664A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 7/13 | chr2 | 203458259 | |||||||
| chr2:203458382 | A | G | 1 | a0001c0002t0035g0128 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1093-787T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 7/13 | chr2 | 203458382 | |||||||
| chr2:203458586 | T | C | 2 | a0001c0007t0082g0260 a0002c0018t0083g0253 |
2 | HG02055.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1093-991A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 7/13 | chr2 | 203458586 | |||||||
| chr2:203458770 | C | CT | 35 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(32): Show |
35 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(32): Show |
intron_variant | MODIFIER | c.1092+1136dupA | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 7/13 | chr2 | 203458770 | |||||||
| chr2:203458838 | G | C | 1 | a0001c0001t0002g0155 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1092+1069C>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 7/13 | chr2 | 203458838 | |||||||
| chr2:203458844 | G | A | 1 | a0002c0018t0083g0253 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1092+1063C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 7/13 | chr2 | 203458844 | |||||||
| chr2:203458912 | G | A | 1 | a0001c0002t0079g0159 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1092+995C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 7/13 | chr2 | 203458912 | |||||||
| chr2:203459060 | G | A | 1 | a0002c0013t0009g0256 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1092+847C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 7/13 | chr2 | 203459060 | |||||||
| chr2:203459091 | G | C | 4 | a0001c0001t0019g0032 a0001c0001t0019g0081 a0001c0001t0019g0082 others(1): Show |
4 | HG00323.hp1 HG01168.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1092+816C>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 7/13 | chr2 | 203459091 | |||||||
| chr2:203459252 | T | A | 2 | a0001c0001t0064g0215 a0001c0011t0002g0158 |
2 | HG00741.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.1092+655A>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 7/13 | chr2 | 203459252 | |||||||
| chr2:203459371 | A | C | 28 | a0001c0001t0003g0112 a0001c0001t0003g0136 a0001c0001t0003g0137 others(25): Show |
28 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.1092+536T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 7/13 | chr2 | 203459371 | |||||||
| chr2:203459461 | A | G | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1092+446T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 7/13 | chr2 | 203459461 | |||||||
| chr2:203460050 | G | A | 37 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(34): Show |
37 | HG00738.hp2 HG01884.hp1 HG01943.hp2 others(34): Show |
intron_variant | MODIFIER | c.971-22C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 6/13 | chr2 | 203460050 | |||||||
| chr2:203460843 | G | A | 3 | a0001c0007t0021g0162 a0001c0007t0021g0220 a0002c0018t0021g0161 |
3 | HG02109.hp1 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.970+406C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 6/13 | chr2 | 203460843 | |||||||
| chr2:203460942 | C | T | 4 | a0001c0002t0004g0106 a0001c0002t0004g0109 a0001c0002t0072g0108 others(1): Show |
4 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(1): Show |
intron_variant | MODIFIER | c.970+307G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 6/13 | chr2 | 203460942 | |||||||
| chr2:203461086 | A | G | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.970+163T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 6/13 | chr2 | 203461086 | |||||||
| chr2:203461532 | A | C | 1 | a0001c0007t0068g0218 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.811-124T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 5/13 | chr2 | 203461532 | |||||||
| chr2:203461560 | A | AATCAG | 90 | a0001c0001t0001g0012 a0001c0002t0001g0009 a0001c0002t0001g0016 others(87): Show |
90 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.811-157_811-153dup others(5): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 5/13 | chr2 | 203461560 | |||||||
| chr2:203461769 | T | C | 3 | a0001c0003t0006g0284 a0001c0003t0093g0286 a0007c0030t0006g0285 |
3 | HG02559.hp1 HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.810+79A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 5/13 | chr2 | 203461769 | |||||||
| chr2:203461817 | A | T | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.810+31T>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 5/13 | chr2 | 203461817 | |||||||
| chr2:203462332 | T | C | 39 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(36): Show |
39 | HG00738.hp2 HG01884.hp1 HG01943.hp2 others(36): Show |
intron_variant | MODIFIER | c.733-407A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203462332 | |||||||
| chr2:203462347 | G | A | 2 | a0001c0001t0011g0020 a0003c0009t0041g0002 |
2 | HG02523.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.733-422C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203462347 | |||||||
| chr2:203462488 | T | C | 90 | a0001c0001t0001g0012 a0001c0002t0001g0009 a0001c0002t0001g0016 others(87): Show |
90 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.733-563A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203462488 | |||||||
| chr2:203462544 | T | C | 2 | a0001c0004t0015g0099 a0001c0004t0015g0104 |
2 | HG02572.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.733-619A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203462544 | |||||||
| chr2:203462916 | T | C | 158 | a0001c0001t0001g0012 a0001c0002t0001g0009 a0001c0002t0001g0016 others(155): Show |
158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.733-991A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203462916 | |||||||
| chr2:203462991 | G | A | 1 | a0001c0003t0103g0264 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.733-1066C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203462991 | |||||||
| chr2:203463028 | C | T | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.733-1103G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203463028 | |||||||
| chr2:203463201 | CAA | C | 33 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(30): Show |
33 | HG00738.hp2 HG01884.hp1 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.733-1278_733-1277d others(4): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203463201 | |||||||
| chr2:203463225 | A | G | 35 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(32): Show |
35 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(32): Show |
intron_variant | MODIFIER | c.733-1300T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203463225 | |||||||
| chr2:203463235 | C | T | 6 | a0001c0001t0008g0123 a0001c0001t0008g0125 a0001c0001t0008g0181 others(3): Show |
6 | NA18951.hp2 NA18968.hp2 NA19010.hp2 others(3): Show |
intron_variant | MODIFIER | c.733-1310G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203463235 | |||||||
| chr2:203463443 | A | G | 35 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(32): Show |
35 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(32): Show |
intron_variant | MODIFIER | c.733-1518T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203463443 | |||||||
| chr2:203463639 | T | C | 4 | a0001c0001t0011g0067 a0001c0001t0037g0250 a0001c0001t0088g0261 others(1): Show |
4 | NA18945.hp1 NA18969.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.733-1714A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203463639 | |||||||
| chr2:203463751 | T | A | 16 | a0001c0002t0004g0106 a0001c0002t0004g0109 a0001c0002t0004g0114 others(13): Show |
16 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(13): Show |
intron_variant | MODIFIER | c.733-1826A>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203463751 | |||||||
| chr2:203463903 | A | G | 35 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(32): Show |
35 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(32): Show |
intron_variant | MODIFIER | c.733-1978T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203463903 | |||||||
| chr2:203464422 | C | A | 29 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(26): Show |
29 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(26): Show |
intron_variant | MODIFIER | c.733-2497G>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203464422 | |||||||
| chr2:203464775 | AG | A | 30 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(27): Show |
30 | HG00738.hp2 HG01943.hp2 HG02109.hp2 others(27): Show |
intron_variant | MODIFIER | c.733-2851delC | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203464775 | |||||||
| chr2:203464776 | G | A | 7 | a0001c0003t0036g0229 a0001c0003t0036g0230 a0001c0003t0076g0228 others(4): Show |
7 | HG01884.hp1 HG02145.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.733-2851C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203464776 | |||||||
| chr2:203464778 | G | A | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.733-2853C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203464778 | |||||||
| chr2:203464785 | A | C | 1 | a0001c0002t0001g0092 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.733-2860T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203464785 | |||||||
| chr2:203464951 | C | A | 8 | a0001c0003t0069g0163 a0001c0003t0070g0225 a0001c0007t0021g0162 others(5): Show |
8 | HG02055.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.733-3026G>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203464951 | |||||||
| chr2:203464999 | C | G | 1 | a0001c0003t0078g0239 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.733-3074G>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203464999 | |||||||
| chr2:203465500 | C | T | 1 | a0001c0001t0002g0213 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.733-3575G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203465500 | |||||||
| chr2:203465507 | C | T | 1 | a0001c0002t0001g0083 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.733-3582G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203465507 | |||||||
| chr2:203465528 | A | G | 1 | a0002c0005t0029g0035 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.733-3603T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203465528 | |||||||
| chr2:203465620 | G | A | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.733-3695C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203465620 | |||||||
| chr2:203465688 | C | T | 1 | a0001c0002t0004g0200 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.733-3763G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203465688 | |||||||
| chr2:203465805 | A | C | 37 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(34): Show |
37 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(34): Show |
intron_variant | MODIFIER | c.733-3880T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203465805 | |||||||
| chr2:203465873 | G | A | 3 | a0001c0007t0021g0162 a0001c0007t0021g0220 a0002c0018t0021g0161 |
3 | HG02109.hp1 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.733-3948C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203465873 | |||||||
| chr2:203465930 | G | A | 1 | a0001c0001t0008g0125 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.733-4005C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203465930 | |||||||
| chr2:203466039 | C | T | 1 | a0001c0011t0002g0158 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.733-4114G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203466039 | |||||||
| chr2:203466356 | A | C | 39 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(36): Show |
39 | HG00738.hp2 HG01884.hp1 HG01943.hp2 others(36): Show |
intron_variant | MODIFIER | c.733-4431T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203466356 | |||||||
| chr2:203466512 | A | T | 1 | a0002c0017t0015g0097 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.733-4587T>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203466512 | |||||||
| chr2:203466513 | A | T | 1 | a0002c0017t0015g0097 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.733-4588T>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203466513 | |||||||
| chr2:203466685 | T | C | 285 | a0001c0001t0001g0012 a0001c0001t0002g0111 a0001c0001t0002g0119 others(282): Show |
285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.733-4760A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203466685 | |||||||
| chr2:203467428 | TA | T | 37 | a0001c0001t0017g0126 a0001c0003t0006g0252 a0001c0003t0006g0263 others(34): Show |
37 | HG00738.hp2 HG01943.hp2 HG02109.hp2 others(34): Show |
intron_variant | MODIFIER | c.733-5504delT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203467428 | |||||||
| chr2:203467704 | T | C | 38 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(35): Show |
38 | HG00738.hp2 HG01884.hp1 HG01943.hp2 others(35): Show |
intron_variant | MODIFIER | c.733-5779A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203467704 | |||||||
| chr2:203467735 | A | C | 2 | a0001c0002t0001g0016 a0001c0002t0033g0131 |
2 | HG03704.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.733-5810T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203467735 | |||||||
| chr2:203468076 | A | T | 1 | a0001c0007t0068g0218 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.733-6151T>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203468076 | |||||||
| chr2:203468133 | T | C | 1 | a0001c0004t0018g0233 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.733-6208A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203468133 | |||||||
| chr2:203468351 | C | T | 1 | a0001c0004t0051g0236 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.733-6426G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203468351 | |||||||
| chr2:203468546 | C | T | 2 | a0001c0001t0013g0184 a0001c0001t0061g0223 |
2 | HG01081.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.733-6621G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203468546 | |||||||
| chr2:203468605 | T | TTA | 4 | a0001c0003t0036g0229 a0001c0003t0036g0230 a0001c0003t0076g0228 others(1): Show |
4 | HG02145.hp1 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.733-6682_733-6681d others(4): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203468605 | |||||||
| chr2:203468609 | T | C | 2 | a0001c0007t0026g0005 a0001c0007t0026g0006 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.733-6684A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203468609 | |||||||
| chr2:203469187 | T | A | 16 | a0001c0004t0005g0093 a0001c0004t0005g0095 a0001c0004t0005g0098 others(13): Show |
16 | HG00733.hp2 HG01109.hp2 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.733-7262A>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203469187 | |||||||
| chr2:203469552 | C | A | 1 | a0001c0002t0001g0050 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.733-7627G>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203469552 | |||||||
| chr2:203469785 | C | T | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.733-7860G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203469785 | |||||||
| chr2:203469951 | T | C | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.733-8026A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203469951 | |||||||
| chr2:203470751 | G | A | 2 | a0001c0002t0073g0165 a0002c0006t0074g0164 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.733-8826C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203470751 | |||||||
| chr2:203470834 | T | G | 34 | a0001c0001t0002g0145 a0001c0001t0002g0221 a0001c0002t0073g0165 others(31): Show |
34 | HG00280.hp2 HG00738.hp2 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.733-8909A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203470834 | |||||||
| chr2:203471313 | G | A | 1 | a0002c0005t0107g0289 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.733-9388C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203471313 | |||||||
| chr2:203471483 | G | C | 2 | a0001c0001t0028g0065 a0001c0001t0028g0085 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.733-9558C>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203471483 | |||||||
| chr2:203471497 | A | G | 1 | a0001c0011t0003g0116 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.733-9572T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203471497 | |||||||
| chr2:203471573 | T | C | 1 | a0001c0002t0049g0049 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.733-9648A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203471573 | |||||||
| chr2:203471596 | G | C | 4 | a0001c0003t0036g0229 a0001c0003t0036g0230 a0001c0003t0076g0228 others(1): Show |
4 | HG02145.hp1 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.733-9671C>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203471596 | |||||||
| chr2:203471630 | A | G | 1 | a0002c0005t0029g0035 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.733-9705T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203471630 | |||||||
| chr2:203471814 | T | A | 1 | a0001c0002t0001g0023 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.733-9889A>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203471814 | |||||||
| chr2:203471814 | T | C | 163 | a0001c0001t0001g0012 a0001c0001t0003g0137 a0001c0001t0003g0167 others(160): Show |
163 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.733-9889A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203471814 | |||||||
| chr2:203471817 | A | ATTT | 161 | a0001c0001t0001g0012 a0001c0001t0003g0167 a0001c0001t0011g0066 others(158): Show |
161 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.733-9893_733-9892i others(5): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203471817 | |||||||
| chr2:203471817 | A | T | 1 | a0001c0002t0001g0023 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.733-9892T>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203471817 | |||||||
| chr2:203471818 | A | T | 1 | a0009c0032t0001g0069 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.733-9893T>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203471818 | |||||||
| chr2:203471907 | A | G | 2 | a0001c0001t0012g0122 a0001c0001t0012g0185 |
2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.733-9982T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203471907 | |||||||
| chr2:203471977 | C | T | 35 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(32): Show |
35 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(32): Show |
intron_variant | MODIFIER | c.733-10052G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203471977 | |||||||
| chr2:203472143 | A | T | 3 | a0001c0003t0006g0284 a0001c0003t0093g0286 a0007c0030t0006g0285 |
3 | HG02559.hp1 HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.733-10218T>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203472143 | |||||||
| chr2:203472391 | C | T | 1 | a0001c0029t0066g0219 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.733-10466G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203472391 | |||||||
| chr2:203472412 | G | A | 1 | a0001c0007t0057g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.733-10487C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203472412 | |||||||
| chr2:203472600 | A | G | 2 | a0001c0001t0031g0198 a0001c0001t0031g0199 |
2 | NA18999.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.733-10675T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203472600 | |||||||
| chr2:203472666 | G | A | 3 | a0001c0001t0003g0112 a0001c0001t0084g0242 a0002c0022t0054g0166 |
3 | HG00621.hp2 NA18992.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.733-10741C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203472666 | |||||||
| chr2:203472895 | A | G | 1 | a0001c0029t0066g0219 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.733-10970T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203472895 | |||||||
| chr2:203473055 | A | G | 1 | a0001c0020t0058g0171 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.733-11130T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203473055 | |||||||
| chr2:203473113 | CAT | C | 4 | a0001c0003t0036g0229 a0001c0003t0036g0230 a0001c0003t0076g0228 others(1): Show |
4 | HG02145.hp1 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.733-11190_733-1118 others(6): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203473113 | |||||||
| chr2:203473215 | G | T | 1 | a0001c0002t0079g0159 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.733-11290C>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203473215 | |||||||
| chr2:203473267 | C | A | 1 | a0001c0007t0068g0218 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.733-11342G>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203473267 | |||||||
| chr2:203473627 | T | TA | 4 | a0001c0007t0021g0162 a0001c0007t0021g0220 a0002c0018t0021g0161 others(1): Show |
4 | HG02055.hp2 HG02109.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.733-11703dupT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203473627 | |||||||
| chr2:203473761 | C | T | 35 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(32): Show |
35 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(32): Show |
intron_variant | MODIFIER | c.733-11836G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203473761 | |||||||
| chr2:203474052 | G | A | 1 | a0002c0005t0003g0135 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.733-12127C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203474052 | |||||||
| chr2:203474936 | C | T | 2 | a0001c0001t0003g0150 a0002c0005t0003g0135 |
2 | HG02735.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.733-13011G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203474936 | |||||||
| chr2:203475008 | C | T | 5 | a0001c0002t0001g0027 a0001c0002t0001g0040 a0001c0002t0001g0041 others(2): Show |
5 | HG00438.hp2 HG00609.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.733-13083G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203475008 | |||||||
| chr2:203475073 | T | C | 1 | a0003c0009t0016g0178 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.733-13148A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203475073 | |||||||
| chr2:203475205 | A | G | 2 | a0001c0007t0026g0005 a0001c0007t0026g0006 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.733-13280T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203475205 | |||||||
| chr2:203475271 | G | A | 2 | a0001c0003t0069g0163 a0001c0003t0070g0225 |
2 | HG02486.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.733-13346C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203475271 | |||||||
| chr2:203475337 | G | A | 1 | a0001c0007t0057g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.733-13412C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203475337 | |||||||
| chr2:203475364 | G | A | 1 | a0001c0007t0068g0218 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.733-13439C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203475364 | |||||||
| chr2:203475402 | G | A | 1 | a0002c0006t0048g0084 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.733-13477C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203475402 | |||||||
| chr2:203475749 | TA | T | 32 | a0001c0003t0006g0252 a0001c0003t0006g0284 a0001c0003t0006g0288 others(29): Show |
32 | HG00738.hp2 HG01884.hp1 HG01943.hp2 others(29): Show |
intron_variant | MODIFIER | c.733-13825delT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203475749 | |||||||
| chr2:203475807 | T | C | 1 | a0001c0002t0007g0033 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.732+13777A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203475807 | |||||||
| chr2:203476148 | T | C | 1 | a0001c0029t0066g0219 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.732+13436A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203476148 | |||||||
| chr2:203476257 | G | A | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.732+13327C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203476257 | |||||||
| chr2:203476320 | G | A | 1 | a0001c0001t0002g0196 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.732+13264C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203476320 | |||||||
| chr2:203476324 | C | T | 1 | a0001c0001t0053g0144 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.732+13260G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203476324 | |||||||
| chr2:203476431 | A | C | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.732+13153T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203476431 | |||||||
| chr2:203476441 | G | A | 5 | a0001c0002t0001g0052 a0001c0002t0001g0053 a0001c0002t0001g0056 others(2): Show |
5 | NA18980.hp1 NA18999.hp2 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.732+13143C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203476441 | |||||||
| chr2:203476856 | A | G | 1 | a0004c0014t0108g0290 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.732+12728T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203476856 | |||||||
| chr2:203476929 | T | C | 1 | a0005c0024t0002g0189 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.732+12655A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203476929 | |||||||
| chr2:203476988 | A | C | 1 | a0001c0003t0096g0279 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.732+12596T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203476988 | |||||||
| chr2:203477205 | G | A | 1 | a0001c0007t0082g0260 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.732+12379C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203477205 | |||||||
| chr2:203477491 | G | A | 1 | a0001c0001t0002g0221 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.732+12093C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203477491 | |||||||
| chr2:203477876 | C | T | 4 | a0001c0004t0015g0094 a0001c0004t0015g0099 a0001c0004t0015g0104 others(1): Show |
4 | HG02572.hp1 HG02896.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.732+11708G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203477876 | |||||||
| chr2:203478036 | GT | G | 37 | a0001c0001t0055g0157 a0001c0003t0006g0252 a0001c0003t0006g0263 others(34): Show |
37 | HG00738.hp2 HG01884.hp1 HG01943.hp2 others(34): Show |
intron_variant | MODIFIER | c.732+11547delA | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203478036 | |||||||
| chr2:203478244 | T | C | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.732+11340A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203478244 | |||||||
| chr2:203478330 | G | A | 8 | a0001c0003t0069g0163 a0001c0003t0070g0225 a0001c0007t0021g0162 others(5): Show |
8 | HG02055.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.732+11254C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203478330 | |||||||
| chr2:203478467 | A | T | 1 | a0001c0004t0015g0094 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.732+11117T>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203478467 | |||||||
| chr2:203478485 | G | GT | 5 | a0001c0001t0055g0157 a0001c0003t0036g0229 a0001c0003t0036g0230 others(2): Show |
5 | HG02145.hp1 HG02451.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.732+11098dupA | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203478485 | |||||||
| chr2:203478709 | G | C | 1 | a0001c0015t0044g0007 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.732+10875C>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203478709 | |||||||
| chr2:203478818 | C | T | 1 | a0001c0002t0001g0079 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.732+10766G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203478818 | |||||||
| chr2:203478934 | C | T | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.732+10650G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203478934 | |||||||
| chr2:203479047 | C | T | 7 | a0001c0003t0069g0163 a0001c0003t0070g0225 a0001c0007t0021g0162 others(4): Show |
7 | HG02055.hp2 HG02109.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.732+10537G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203479047 | |||||||
| chr2:203479369 | T | A | 1 | a0001c0001t0064g0215 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.732+10215A>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203479369 | |||||||
| chr2:203479466 | T | C | 1 | a0001c0026t0077g0238 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.732+10118A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203479466 | |||||||
| chr2:203479605 | C | CA | 15 | a0001c0001t0003g0139 a0001c0002t0001g0036 a0001c0002t0004g0109 others(12): Show |
15 | HG00741.hp2 HG01175.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.732+9978dupT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203479605 | |||||||
| chr2:203479623 | A | G | 1 | a0001c0002t0007g0039 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.732+9961T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203479623 | |||||||
| chr2:203479667 | T | C | 1 | a0001c0003t0070g0225 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.732+9917A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203479667 | |||||||
| chr2:203479747 | C | T | 1 | a0001c0002t0047g0022 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.732+9837G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203479747 | |||||||
| chr2:203479989 | GA | G | 37 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(34): Show |
37 | HG00738.hp2 HG01884.hp1 HG01943.hp2 others(34): Show |
intron_variant | MODIFIER | c.732+9594delT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203479989 | |||||||
| chr2:203480072 | C | T | 6 | a0001c0001t0008g0123 a0001c0001t0008g0125 a0001c0001t0008g0181 others(3): Show |
6 | NA18951.hp2 NA18968.hp2 NA19010.hp2 others(3): Show |
intron_variant | MODIFIER | c.732+9512G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203480072 | |||||||
| chr2:203480726 | G | C | 1 | a0001c0002t0004g0107 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.732+8858C>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203480726 | |||||||
| chr2:203480832 | C | T | 1 | a0001c0026t0077g0238 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.732+8752G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203480832 | |||||||
| chr2:203480930 | G | A | 1 | a0001c0003t0078g0239 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.732+8654C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203480930 | |||||||
| chr2:203481159 | A | G | 1 | a0001c0007t0057g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.732+8425T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203481159 | |||||||
| chr2:203481296 | C | G | 1 | a0001c0007t0026g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.732+8288G>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203481296 | |||||||
| chr2:203481426 | C | G | 2 | a0001c0003t0039g0269 a0001c0003t0094g0267 |
2 | HG00738.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.732+8158G>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203481426 | |||||||
| chr2:203481568 | A | AAT | 12 | a0001c0001t0002g0129 a0001c0001t0002g0155 a0001c0001t0008g0181 others(9): Show |
12 | HG01167.hp1 HG01167.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.732+8014_732+8015d others(4): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203481568 | |||||||
| chr2:203481568 | A | AATAT | 11 | a0001c0001t0002g0188 a0001c0001t0008g0123 a0001c0001t0017g0126 others(8): Show |
11 | HG00423.hp2 HG00609.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.732+8012_732+8015d others(6): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203481568 | |||||||
| chr2:203481568 | A | AATATATA others(3): Show |
1 | a0001c0001t0002g0111 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.732+8006_732+8015d others(12): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203481568 | |||||||
| chr2:203481568 | A | AATATATA others(9): Show |
2 | a0001c0007t0021g0162 a0002c0018t0021g0161 |
2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.732+8000_732+8015d others(18): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203481568 | |||||||
| chr2:203481568 | A | AATATATA others(15): Show |
1 | a0001c0007t0021g0220 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.732+7994_732+8015d others(24): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203481568 | |||||||
| chr2:203481568 | A | AATATATA others(31): Show |
1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.732+8015_732+8016i others(40): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203481568 | |||||||
| chr2:203481568 | AAT | A | 75 | a0001c0001t0001g0012 a0001c0001t0002g0119 a0001c0001t0002g0203 others(72): Show |
75 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.732+8014_732+8015d others(4): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203481568 | |||||||
| chr2:203481568 | AATAT | A | 81 | a0001c0001t0002g0151 a0001c0001t0003g0136 a0001c0001t0003g0167 others(78): Show |
81 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.732+8012_732+8015d others(6): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203481568 | |||||||
| chr2:203481568 | AATATAT | A | 7 | a0001c0003t0036g0229 a0001c0003t0036g0230 a0001c0003t0076g0228 others(4): Show |
7 | HG02145.hp1 HG02451.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.732+8010_732+8015d others(8): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203481568 | |||||||
| chr2:203481568 | AATATATA others(1): Show |
A | 16 | a0001c0003t0025g0280 a0001c0003t0025g0282 a0001c0003t0025g0283 others(13): Show |
16 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(13): Show |
intron_variant | MODIFIER | c.732+8008_732+8015d others(10): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203481568 | |||||||
| chr2:203481594 | T | C | 31 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(28): Show |
31 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(28): Show |
intron_variant | MODIFIER | c.732+7990A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203481594 | |||||||
| chr2:203481650 | G | A | 2 | a0001c0001t0010g0063 a0001c0001t0010g0064 |
2 | HG02630.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.732+7934C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203481650 | |||||||
| chr2:203481717 | G | A | 1 | a0001c0001t0002g0213 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.732+7867C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203481717 | |||||||
| chr2:203481740 | T | C | 2 | a0001c0003t0069g0163 a0001c0003t0070g0225 |
2 | HG02486.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.732+7844A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203481740 | |||||||
| chr2:203481758 | A | AT | 23 | a0001c0001t0002g0221 a0001c0001t0009g0255 a0001c0001t0013g0214 others(20): Show |
23 | HG00733.hp2 HG01109.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.732+7825dupA | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203481758 | |||||||
| chr2:203481839 | C | T | 286 | a0001c0001t0001g0012 a0001c0001t0002g0111 a0001c0001t0002g0119 others(283): Show |
286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.732+7745G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203481839 | |||||||
| chr2:203481991 | T | C | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.732+7593A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203481991 | |||||||
| chr2:203482008 | G | GA | 79 | a0001c0001t0002g0111 a0001c0001t0002g0151 a0001c0001t0002g0203 others(76): Show |
79 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.732+7575dupT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203482008 | |||||||
| chr2:203482017 | A | C | 9 | a0001c0001t0016g0141 a0001c0001t0016g0172 a0001c0001t0016g0205 others(6): Show |
9 | HG00323.hp1 HG01168.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.732+7567T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203482017 | |||||||
| chr2:203482019 | C | A | 37 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(34): Show |
37 | HG00738.hp2 HG01884.hp1 HG01943.hp2 others(34): Show |
intron_variant | MODIFIER | c.732+7565G>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203482019 | |||||||
| chr2:203482020 | A | C | 1 | a0001c0003t0078g0239 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.732+7564T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203482020 | |||||||
| chr2:203482453 | C | T | 2 | a0001c0007t0082g0260 a0002c0018t0083g0253 |
2 | HG02055.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.732+7131G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203482453 | |||||||
| chr2:203482798 | G | A | 1 | a0002c0005t0011g0015 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.732+6786C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203482798 | |||||||
| chr2:203482806 | A | C | 35 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(32): Show |
35 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(32): Show |
intron_variant | MODIFIER | c.732+6778T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203482806 | |||||||
| chr2:203482831 | CA | C | 59 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(56): Show |
59 | HG00733.hp2 HG00738.hp2 HG01109.hp2 others(56): Show |
intron_variant | MODIFIER | c.732+6752delT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203482831 | |||||||
| chr2:203482877 | A | C | 10 | a0001c0001t0010g0059 a0001c0001t0010g0061 a0001c0001t0010g0062 others(7): Show |
10 | HG02145.hp2 HG02486.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.732+6707T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203482877 | |||||||
| chr2:203482896 | C | T | 1 | a0001c0003t0103g0264 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.732+6688G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203482896 | |||||||
| chr2:203483393 | T | G | 35 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(32): Show |
35 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(32): Show |
intron_variant | MODIFIER | c.732+6191A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203483393 | |||||||
| chr2:203483400 | G | T | 4 | a0001c0002t0001g0052 a0001c0002t0001g0053 a0001c0002t0001g0057 others(1): Show |
4 | NA18980.hp1 NA18999.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.732+6184C>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203483400 | |||||||
| chr2:203483454 | T | C | 1 | a0001c0003t0078g0239 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.732+6130A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203483454 | |||||||
| chr2:203483556 | C | G | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.732+6028G>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203483556 | |||||||
| chr2:203484001 | A | G | 1 | a0001c0001t0002g0190 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.732+5583T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203484001 | |||||||
| chr2:203484363 | C | T | 1 | a0001c0007t0057g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.732+5221G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203484363 | |||||||
| chr2:203484561 | T | G | 37 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(34): Show |
37 | HG00738.hp2 HG01884.hp1 HG01943.hp2 others(34): Show |
intron_variant | MODIFIER | c.732+5023A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203484561 | |||||||
| chr2:203484584 | T | C | 29 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(26): Show |
29 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(26): Show |
intron_variant | MODIFIER | c.732+5000A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203484584 | |||||||
| chr2:203484815 | A | T | 1 | a0001c0002t0001g0040 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.732+4769T>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203484815 | |||||||
| chr2:203485169 | C | T | 1 | a0002c0006t0004g0143 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.732+4415G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203485169 | |||||||
| chr2:203485277 | G | A | 5 | a0001c0001t0008g0123 a0001c0001t0008g0181 a0001c0001t0008g0187 others(2): Show |
5 | NA18951.hp2 NA18968.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.732+4307C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203485277 | |||||||
| chr2:203485410 | CA | C | 113 | a0001c0001t0001g0012 a0001c0001t0002g0119 a0001c0001t0002g0151 others(110): Show |
113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.732+4173delT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203485410 | |||||||
| chr2:203485410 | CAA | C | 30 | a0001c0002t0033g0131 a0001c0003t0006g0252 a0001c0003t0006g0263 others(27): Show |
30 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(27): Show |
intron_variant | MODIFIER | c.732+4172_732+4173d others(4): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203485410 | |||||||
| chr2:203485450 | G | A | 1 | a0001c0001t0002g0190 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.732+4134C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203485450 | |||||||
| chr2:203485494 | T | C | 17 | a0001c0004t0005g0093 a0001c0004t0005g0095 a0001c0004t0005g0098 others(14): Show |
17 | HG00733.hp2 HG01109.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.732+4090A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203485494 | |||||||
| chr2:203485565 | A | G | 35 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(32): Show |
35 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(32): Show |
intron_variant | MODIFIER | c.732+4019T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203485565 | |||||||
| chr2:203485777 | G | A | 1 | a0001c0029t0066g0219 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.732+3807C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203485777 | |||||||
| chr2:203485873 | A | G | 35 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(32): Show |
35 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(32): Show |
intron_variant | MODIFIER | c.732+3711T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203485873 | |||||||
| chr2:203485930 | A | G | 1 | a0001c0002t0007g0025 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.732+3654T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203485930 | |||||||
| chr2:203486093 | C | CA | 97 | a0001c0001t0001g0012 a0001c0001t0002g0151 a0001c0001t0011g0020 others(94): Show |
97 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.732+3490dupT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203486093 | |||||||
| chr2:203486093 | CA | C | 23 | a0001c0004t0005g0093 a0001c0004t0005g0095 a0001c0004t0005g0098 others(20): Show |
23 | HG00733.hp2 HG01109.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.732+3490delT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203486093 | |||||||
| chr2:203486173 | CAG | C | 20 | a0001c0001t0001g0012 a0001c0001t0002g0119 a0001c0001t0003g0112 others(17): Show |
20 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.732+3409_732+3410d others(4): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203486173 | |||||||
| chr2:203486250 | C | T | 1 | a0001c0001t0086g0243 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.732+3334G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203486250 | |||||||
| chr2:203486494 | C | T | 2 | a0001c0007t0026g0005 a0001c0007t0026g0006 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.732+3090G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203486494 | |||||||
| chr2:203486640 | G | A | 3 | a0001c0001t0028g0065 a0001c0001t0028g0085 a0002c0006t0004g0143 |
3 | HG02896.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.732+2944C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203486640 | |||||||
| chr2:203486709 | A | C | 1 | a0001c0002t0001g0016 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.732+2875T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203486709 | |||||||
| chr2:203486937 | T | C | 2 | a0001c0002t0038g0244 a0001c0002t0038g0245 |
2 | HG02622.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.732+2647A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203486937 | |||||||
| chr2:203487034 | G | A | 5 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0139 others(2): Show |
5 | HG01257.hp2 HG01258.hp1 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.732+2550C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203487034 | |||||||
| chr2:203487529 | C | T | 4 | a0001c0001t0002g0146 a0001c0010t0002g0120 a0001c0010t0040g0001 others(1): Show |
4 | HG00735.hp1 HG01099.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.732+2055G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203487529 | |||||||
| chr2:203487530 | G | A | 1 | a0001c0007t0057g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.732+2054C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203487530 | |||||||
| chr2:203487770 | T | TGATA | 5 | a0001c0001t0002g0111 a0001c0001t0063g0121 a0001c0002t0043g0004 others(2): Show |
5 | HG02523.hp2 NA18949.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.732+1810_732+1813d others(6): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203487770 | |||||||
| chr2:203487772 | A | G | 2 | a0001c0007t0026g0005 a0001c0007t0026g0006 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.732+1812T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203487772 | |||||||
| chr2:203487866 | C | T | 2 | a0001c0002t0001g0075 a0001c0002t0001g0077 |
2 | HG00323.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.732+1718G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203487866 | |||||||
| chr2:203487934 | A | G | 1 | a0001c0026t0077g0238 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.732+1650T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203487934 | |||||||
| chr2:203488067 | T | G | 1 | a0003c0009t0016g0178 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.732+1517A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203488067 | |||||||
| chr2:203488186 | G | A | 1 | a0001c0007t0068g0218 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.732+1398C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203488186 | |||||||
| chr2:203488403 | G | A | 156 | a0001c0001t0011g0020 a0001c0001t0011g0066 a0001c0001t0011g0067 others(153): Show |
156 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.732+1181C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203488403 | |||||||
| chr2:203488472 | C | A | 1 | a0001c0007t0068g0218 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.732+1112G>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203488472 | |||||||
| chr2:203488494 | C | T | 88 | a0001c0001t0011g0020 a0001c0001t0011g0066 a0001c0001t0011g0067 others(85): Show |
88 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.732+1090G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203488494 | |||||||
| chr2:203488549 | T | G | 2 | a0001c0002t0001g0036 a0009c0032t0001g0069 |
2 | NA18982.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.732+1035A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203488549 | |||||||
| chr2:203488588 | T | TA | 136 | a0001c0001t0001g0012 a0001c0001t0002g0111 a0001c0001t0002g0129 others(133): Show |
136 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.732+995dupT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203488588 | |||||||
| chr2:203488588 | T | TAA | 44 | a0001c0001t0002g0119 a0001c0001t0002g0155 a0001c0001t0002g0183 others(41): Show |
44 | HG00408.hp1 HG00423.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.732+994_732+995dup others(2): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203488588 | |||||||
| chr2:203488588 | T | TAAA | 7 | a0001c0001t0009g0255 a0001c0001t0022g0180 a0001c0001t0064g0215 others(4): Show |
7 | HG00741.hp1 HG01358.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.732+993_732+995dup others(3): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203488588 | |||||||
| chr2:203488609 | A | C | 2 | a0001c0007t0026g0005 a0001c0007t0026g0006 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.732+975T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203488609 | |||||||
| chr2:203488708 | A | G | 1 | a0001c0007t0075g0227 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.732+876T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203488708 | |||||||
| chr2:203488804 | C | T | 1 | a0001c0002t0033g0131 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.732+780G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203488804 | |||||||
| chr2:203488857 | C | T | 1 | a0001c0021t0002g0210 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.732+727G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203488857 | |||||||
| chr2:203488978 | G | A | 1 | a0001c0001t0081g0241 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.732+606C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203488978 | |||||||
| chr2:203489011 | C | G | 1 | a0001c0001t0023g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.732+573G>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203489011 | |||||||
| chr2:203489022 | A | T | 1 | a0002c0005t0002g0149 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.732+562T>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203489022 | |||||||
| chr2:203489082 | C | T | 1 | a0001c0002t0001g0036 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.732+502G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203489082 | |||||||
| chr2:203489139 | GA | G | 156 | a0001c0001t0011g0020 a0001c0001t0011g0066 a0001c0001t0011g0067 others(153): Show |
156 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.732+444delT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203489139 | |||||||
| chr2:203489259 | C | T | 1 | a0001c0003t0076g0228 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.732+325G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203489259 | |||||||
| chr2:203489484 | T | C | 1 | a0001c0001t0089g0251 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.732+100A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 4/13 | chr2 | 203489484 | |||||||
| chr2:203490100 | C | T | 30 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(27): Show |
30 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(27): Show |
intron_variant | MODIFIER | c.227-11G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 3/13 | chr2 | 203490100 | |||||||
| chr2:203490800 | T | C | 89 | a0001c0001t0011g0020 a0001c0001t0011g0066 a0001c0001t0011g0067 others(86): Show |
89 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.226+414A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 3/13 | chr2 | 203490800 | |||||||
| chr2:203490853 | G | A | 1 | a0001c0001t0002g0175 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.226+361C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 3/13 | chr2 | 203490853 | |||||||
| chr2:203490958 | C | T | 1 | a0001c0007t0057g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.226+256G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 3/13 | chr2 | 203490958 | |||||||
| chr2:203490968 | T | C | 40 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(37): Show |
40 | HG00738.hp2 HG01884.hp1 HG01943.hp2 others(37): Show |
intron_variant | MODIFIER | c.226+246A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 3/13 | chr2 | 203490968 | |||||||
| chr2:203491039 | T | C | 1 | a0001c0029t0066g0219 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.226+175A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 3/13 | chr2 | 203491039 | |||||||
| chr2:203491044 | C | CA | 9 | a0001c0001t0008g0123 a0001c0001t0008g0125 a0001c0001t0008g0181 others(6): Show |
9 | HG02109.hp2 NA18951.hp2 NA18968.hp2 others(6): Show |
intron_variant | MODIFIER | c.226+169dupT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 3/13 | chr2 | 203491044 | |||||||
| chr2:203491099 | G | A | 157 | a0001c0001t0011g0020 a0001c0001t0011g0066 a0001c0001t0011g0067 others(154): Show |
157 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.226+115C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 3/13 | chr2 | 203491099 | |||||||
| chr2:203491124 | G | A | 1 | a0001c0004t0034g0240 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.226+90C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 3/13 | chr2 | 203491124 | |||||||
| chr2:203491341 | T | C | 1 | a0001c0029t0066g0219 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.121-22A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 2/13 | chr2 | 203491341 | |||||||
| chr2:203491369 | T | C | 5 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0139 others(2): Show |
5 | HG01257.hp2 HG01258.hp1 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.121-50A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 2/13 | chr2 | 203491369 | |||||||
| chr2:203491570 | A | G | 2 | a0001c0001t0032g0118 a0001c0001t0032g0142 |
2 | HG01167.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.121-251T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 2/13 | chr2 | 203491570 | |||||||
| chr2:203491576 | C | T | 1 | a0002c0006t0001g0073 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.121-257G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 2/13 | chr2 | 203491576 | |||||||
| chr2:203491613 | C | T | 1 | a0001c0001t0009g0255 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.121-294G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 2/13 | chr2 | 203491613 | |||||||
| chr2:203491788 | G | A | 39 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(36): Show |
39 | HG00738.hp2 HG01943.hp2 HG02109.hp1 others(36): Show |
intron_variant | MODIFIER | c.121-469C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 2/13 | chr2 | 203491788 | |||||||
| chr2:203491841 | T | C | 1 | a0001c0007t0057g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.121-522A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 2/13 | chr2 | 203491841 | |||||||
| chr2:203492049 | C | T | 3 | a0001c0001t0023g0197 a0001c0001t0023g0207 a0001c0001t0023g0224 |
3 | HG02165.hp2 NA18994.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.121-730G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 2/13 | chr2 | 203492049 | |||||||
| chr2:203492102 | C | T | 38 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(35): Show |
38 | HG00738.hp2 HG01943.hp2 HG02109.hp1 others(35): Show |
intron_variant | MODIFIER | c.121-783G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 2/13 | chr2 | 203492102 | |||||||
| chr2:203492182 | C | T | 1 | a0001c0002t0001g0068 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.121-863G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 2/13 | chr2 | 203492182 | |||||||
| chr2:203492233 | C | CA | 147 | a0001c0001t0011g0020 a0001c0001t0011g0066 a0001c0001t0011g0067 others(144): Show |
147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.121-915dupT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 2/13 | chr2 | 203492233 | |||||||
| chr2:203492233 | C | CAA | 11 | a0001c0002t0038g0244 a0001c0002t0038g0245 a0001c0002t0067g0201 others(8): Show |
11 | HG01175.hp2 HG01981.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.121-916_121-915dup others(2): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 2/13 | chr2 | 203492233 | |||||||
| chr2:203492380 | C | T | 1 | a0001c0007t0057g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.121-1061G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 2/13 | chr2 | 203492380 | |||||||
| chr2:203492456 | T | C | 2 | a0001c0001t0011g0067 a0001c0002t0007g0039 |
2 | HG02027.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.121-1137A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 2/13 | chr2 | 203492456 | |||||||
| chr2:203492532 | G | A | 38 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(35): Show |
38 | HG00738.hp2 HG01943.hp2 HG02109.hp1 others(35): Show |
intron_variant | MODIFIER | c.121-1213C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 2/13 | chr2 | 203492532 | |||||||
| chr2:203492774 | C | CT | 9 | a0001c0001t0008g0123 a0001c0001t0008g0181 a0001c0001t0008g0187 others(6): Show |
9 | HG02055.hp2 HG03225.hp2 HG03453.hp2 others(6): Show |
intron_variant | MODIFIER | c.121-1456dupA | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 2/13 | chr2 | 203492774 | |||||||
| chr2:203492774 | CT | C | 157 | a0001c0001t0002g0203 a0001c0001t0009g0246 a0001c0001t0009g0249 others(154): Show |
157 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.121-1456delA | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 2/13 | chr2 | 203492774 | |||||||
| chr2:203492912 | A | T | 1 | a0001c0007t0057g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.121-1593T>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 2/13 | chr2 | 203492912 | |||||||
| chr2:203492924 | A | G | 1 | a0001c0001t0003g0179 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.121-1605T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 2/13 | chr2 | 203492924 | |||||||
| chr2:203493418 | C | T | 1 | a0001c0001t0002g0190 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.120+1816G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 2/13 | chr2 | 203493418 | |||||||
| chr2:203493902 | C | T | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.120+1332G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 2/13 | chr2 | 203493902 | |||||||
| chr2:203493971 | C | CA | 42 | a0001c0001t0002g0111 a0001c0001t0002g0154 a0001c0001t0003g0150 others(39): Show |
42 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.120+1262dupT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 2/13 | chr2 | 203493971 | |||||||
| chr2:203493971 | C | CAA | 6 | a0001c0001t0012g0186 a0001c0002t0001g0023 a0001c0002t0001g0038 others(3): Show |
6 | HG00673.hp1 HG01952.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.120+1261_120+1262d others(4): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 2/13 | chr2 | 203493971 | |||||||
| chr2:203493971 | CA | C | 15 | a0001c0001t0002g0175 a0001c0001t0003g0136 a0001c0001t0003g0137 others(12): Show |
15 | HG01099.hp2 HG01257.hp2 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.120+1262delT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 2/13 | chr2 | 203493971 | |||||||
| chr2:203493971 | CAA | C | 19 | a0001c0004t0005g0093 a0001c0004t0005g0095 a0001c0004t0005g0098 others(16): Show |
19 | HG00733.hp2 HG01109.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.120+1261_120+1262d others(4): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 2/13 | chr2 | 203493971 | |||||||
| chr2:203493992 | A | G | 2 | a0002c0031t0105g0266 a0004c0014t0108g0290 |
2 | NA18988.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.120+1242T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 2/13 | chr2 | 203493992 | |||||||
| chr2:203494017 | A | T | 282 | a0001c0001t0001g0012 a0001c0001t0002g0111 a0001c0001t0002g0119 others(279): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.120+1217T>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 2/13 | chr2 | 203494017 | |||||||
| chr2:203494547 | G | T | 1 | a0002c0013t0009g0256 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.120+687C>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 2/13 | chr2 | 203494547 | |||||||
| chr2:203494585 | G | T | 1 | a0001c0026t0077g0238 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.120+649C>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 2/13 | chr2 | 203494585 | |||||||
| chr2:203494702 | G | A | 30 | a0001c0001t0001g0012 a0001c0001t0002g0119 a0001c0001t0003g0112 others(27): Show |
30 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.120+532C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 2/13 | chr2 | 203494702 | |||||||
| chr2:203494735 | G | A | 2 | a0001c0007t0026g0005 a0001c0007t0026g0006 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.120+499C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 2/13 | chr2 | 203494735 | |||||||
| chr2:203494824 | G | A | 1 | a0002c0005t0080g0127 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.120+410C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 2/13 | chr2 | 203494824 | |||||||
| chr2:203494842 | C | A | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.120+392G>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 2/13 | chr2 | 203494842 | |||||||
| chr2:203495478 | A | G | 86 | a0001c0001t0011g0020 a0001c0001t0011g0066 a0001c0001t0011g0067 others(83): Show |
86 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.1-125T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203495478 | |||||||
| chr2:203495808 | G | C | 1 | a0001c0029t0066g0219 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1-455C>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203495808 | |||||||
| chr2:203495884 | C | T | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1-531G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203495884 | |||||||
| chr2:203496369 | T | TAAATA | 158 | a0001c0001t0011g0020 a0001c0001t0011g0066 a0001c0001t0011g0067 others(155): Show |
158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.1-1021_1-1017dupTA others(3): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203496369 | |||||||
| chr2:203496461 | C | T | 1 | a0001c0003t0006g0252 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1-1108G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203496461 | |||||||
| chr2:203496480 | T | G | 1 | a0001c0001t0002g0145 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1-1127A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203496480 | |||||||
| chr2:203496524 | A | G | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1-1171T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203496524 | |||||||
| chr2:203496620 | T | C | 2 | a0001c0002t0001g0009 a0002c0016t0001g0010 |
2 | NA19065.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1-1267A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203496620 | |||||||
| chr2:203496901 | C | T | 1 | a0009c0032t0001g0069 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1-1548G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203496901 | |||||||
| chr2:203496961 | G | C | 1 | a0001c0001t0055g0157 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1-1608C>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203496961 | |||||||
| chr2:203496965 | T | C | 4 | a0001c0001t0003g0112 a0001c0001t0037g0250 a0001c0001t0084g0242 others(1): Show |
4 | HG00621.hp2 NA18992.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.1-1612A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203496965 | |||||||
| chr2:203497015 | C | T | 1 | a0001c0002t0033g0131 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1-1662G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203497015 | |||||||
| chr2:203497077 | T | C | 2 | a0001c0007t0026g0005 a0001c0007t0026g0006 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1-1724A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203497077 | |||||||
| chr2:203497174 | T | C | 4 | a0001c0001t0011g0066 a0001c0002t0001g0078 a0001c0002t0001g0087 others(1): Show |
4 | NA18939.hp1 NA18974.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.1-1821A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203497174 | |||||||
| chr2:203497577 | G | T | 1 | a0001c0002t0001g0056 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1-2224C>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203497577 | |||||||
| chr2:203498346 | C | T | 1 | a0006c0025t0030g0026 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1-2993G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203498346 | |||||||
| chr2:203498433 | T | C | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1-3080A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203498433 | |||||||
| chr2:203498529 | C | T | 6 | a0001c0001t0008g0123 a0001c0001t0008g0125 a0001c0001t0008g0181 others(3): Show |
6 | NA18951.hp2 NA18968.hp2 NA19010.hp2 others(3): Show |
intron_variant | MODIFIER | c.1-3176G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203498529 | |||||||
| chr2:203498582 | C | T | 1 | a0001c0002t0042g0003 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1-3229G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203498582 | |||||||
| chr2:203498750 | G | A | 1 | a0001c0029t0066g0219 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1-3397C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203498750 | |||||||
| chr2:203499337 | T | C | 1 | a0001c0001t0002g0151 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1-3984A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203499337 | |||||||
| chr2:203499385 | A | T | 2 | a0001c0007t0082g0260 a0002c0018t0083g0253 |
2 | HG02055.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1-4032T>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203499385 | |||||||
| chr2:203499412 | G | C | 1 | a0001c0002t0001g0068 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1-4059C>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203499412 | |||||||
| chr2:203499427 | A | C | 35 | a0001c0001t0001g0012 a0001c0001t0002g0119 a0001c0001t0003g0112 others(32): Show |
35 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.1-4074T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203499427 | |||||||
| chr2:203499490 | G | A | 1 | a0001c0002t0001g0016 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1-4137C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203499490 | |||||||
| chr2:203499525 | T | C | 4 | a0001c0003t0036g0229 a0001c0003t0036g0230 a0001c0003t0076g0228 others(1): Show |
4 | HG02145.hp1 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1-4172A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203499525 | |||||||
| chr2:203499539 | T | C | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1-4186A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203499539 | |||||||
| chr2:203499674 | T | C | 1 | a0001c0002t0042g0003 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1-4321A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203499674 | |||||||
| chr2:203499834 | G | A | 1 | a0001c0007t0068g0218 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1-4481C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203499834 | |||||||
| chr2:203499857 | A | G | 4 | a0001c0001t0011g0066 a0001c0002t0001g0078 a0001c0002t0001g0087 others(1): Show |
4 | NA18939.hp1 NA18974.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.1-4504T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203499857 | |||||||
| chr2:203499865 | T | C | 1 | a0001c0001t0003g0167 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1-4512A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203499865 | |||||||
| chr2:203499998 | C | T | 156 | a0001c0001t0011g0020 a0001c0001t0011g0066 a0001c0001t0011g0067 others(153): Show |
156 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.1-4645G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203499998 | |||||||
| chr2:203500443 | G | A | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1-5090C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203500443 | |||||||
| chr2:203500602 | C | A | 1 | a0001c0007t0068g0218 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1-5249G>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203500602 | |||||||
| chr2:203500653 | C | T | 2 | a0001c0004t0005g0101 a0001c0004t0005g0102 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1-5300G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203500653 | |||||||
| chr2:203500697 | C | T | 2 | a0001c0001t0003g0136 a0001c0001t0003g0137 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1-5344G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203500697 | |||||||
| chr2:203500722 | T | C | 5 | a0001c0001t0008g0123 a0001c0001t0008g0181 a0001c0001t0008g0187 others(2): Show |
5 | NA18951.hp2 NA18968.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.1-5369A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203500722 | |||||||
| chr2:203501513 | T | C | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1-6160A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203501513 | |||||||
| chr2:203501538 | C | T | 2 | a0001c0007t0026g0005 a0001c0007t0026g0006 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1-6185G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203501538 | |||||||
| chr2:203501571 | C | G | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1-6218G>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203501571 | |||||||
| chr2:203501730 | A | G | 89 | a0001c0001t0011g0020 a0001c0001t0011g0066 a0001c0001t0011g0067 others(86): Show |
89 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.1-6377T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203501730 | |||||||
| chr2:203501815 | G | GA | 27 | a0001c0001t0002g0177 a0001c0001t0008g0187 a0001c0001t0009g0255 others(24): Show |
27 | HG00738.hp2 HG01358.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.1-6463dupT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203501815 | |||||||
| chr2:203501815 | G | GAA | 18 | a0001c0003t0093g0286 a0001c0004t0005g0093 a0001c0004t0005g0095 others(15): Show |
18 | HG00733.hp2 HG01109.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.1-6464_1-6463dupTT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203501815 | |||||||
| chr2:203501815 | GA | G | 88 | a0001c0001t0002g0190 a0001c0001t0011g0066 a0001c0001t0011g0067 others(85): Show |
88 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1-6463delT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203501815 | |||||||
| chr2:203501815 | GAA | G | 6 | a0001c0002t0001g0040 a0001c0007t0026g0005 a0001c0007t0026g0006 others(3): Show |
6 | HG00609.hp1 HG01517.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1-6464_1-6463delTT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203501815 | |||||||
| chr2:203501816 | A | G | 1 | a0001c0003t0076g0228 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1-6463T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203501816 | |||||||
| chr2:203501858 | G | C | 89 | a0001c0001t0011g0020 a0001c0001t0011g0066 a0001c0001t0011g0067 others(86): Show |
89 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.1-6505C>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203501858 | |||||||
| chr2:203502053 | G | A | 68 | a0001c0001t0002g0111 a0001c0001t0002g0129 a0001c0001t0002g0145 others(65): Show |
68 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.1-6700C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203502053 | |||||||
| chr2:203502058 | A | G | 37 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(34): Show |
37 | HG00738.hp2 HG01884.hp1 HG01943.hp2 others(34): Show |
intron_variant | MODIFIER | c.1-6705T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203502058 | |||||||
| chr2:203502588 | G | A | 3 | a0001c0001t0032g0118 a0001c0001t0032g0142 a0001c0001t0056g0134 |
3 | HG01167.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1-7235C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203502588 | |||||||
| chr2:203502650 | C | G | 2 | a0001c0007t0082g0260 a0002c0018t0083g0253 |
2 | HG02055.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1-7297G>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203502650 | |||||||
| chr2:203502676 | C | T | 1 | a0001c0001t0002g0221 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1-7323G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203502676 | |||||||
| chr2:203502995 | C | T | 5 | a0001c0001t0016g0141 a0001c0001t0016g0172 a0001c0001t0016g0205 others(2): Show |
5 | HG02572.hp2 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1-7642G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203502995 | |||||||
| chr2:203503081 | T | C | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1-7728A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203503081 | |||||||
| chr2:203503093 | A | G | 1 | a0001c0003t0069g0163 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1-7740T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203503093 | |||||||
| chr2:203503105 | T | C | 1 | a0001c0020t0058g0171 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1-7752A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203503105 | |||||||
| chr2:203503108 | C | T | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1-7755G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203503108 | |||||||
| chr2:203503419 | A | G | 2 | a0001c0003t0069g0163 a0001c0003t0070g0225 |
2 | HG02486.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1-8066T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203503419 | |||||||
| chr2:203503429 | C | A | 6 | a0001c0003t0006g0252 a0001c0003t0006g0284 a0001c0003t0006g0288 others(3): Show |
6 | HG02293.hp2 HG02559.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1-8076G>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203503429 | |||||||
| chr2:203503730 | A | G | 1 | a0001c0003t0078g0239 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1-8377T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203503730 | |||||||
| chr2:203504129 | T | C | 1 | a0001c0001t0017g0126 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1-8776A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203504129 | |||||||
| chr2:203504307 | C | T | 5 | a0001c0003t0006g0263 a0001c0003t0006g0274 a0001c0003t0006g0276 others(2): Show |
5 | HG02622.hp1 HG02630.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1-8954G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203504307 | |||||||
| chr2:203504362 | A | G | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1-9009T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203504362 | |||||||
| chr2:203504601 | T | C | 158 | a0001c0001t0011g0020 a0001c0001t0011g0066 a0001c0001t0011g0067 others(155): Show |
158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.1-9248A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203504601 | |||||||
| chr2:203504624 | C | T | 1 | a0001c0007t0068g0218 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1-9271G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203504624 | |||||||
| chr2:203504670 | T | TA | 17 | a0001c0001t0019g0032 a0001c0001t0019g0081 a0001c0001t0019g0082 others(14): Show |
17 | HG00323.hp1 HG00323.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.1-9318dupT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203504670 | |||||||
| chr2:203504670 | T | TAA | 35 | a0001c0002t0049g0049 a0001c0003t0006g0252 a0001c0003t0006g0263 others(32): Show |
35 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(32): Show |
intron_variant | MODIFIER | c.1-9319_1-9318dupTT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203504670 | |||||||
| chr2:203504670 | TA | T | 23 | a0001c0001t0002g0195 a0001c0001t0009g0249 a0001c0001t0056g0134 others(20): Show |
23 | HG00642.hp1 HG00733.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1-9318delT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203504670 | |||||||
| chr2:203504675 | A | C | 1 | a0002c0005t0012g0206 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1-9322T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203504675 | |||||||
| chr2:203504886 | G | A | 1 | a0001c0001t0002g0221 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1-9533C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203504886 | |||||||
| chr2:203505195 | C | T | 4 | a0001c0001t0017g0126 a0001c0001t0017g0193 a0001c0001t0017g0194 others(1): Show |
4 | HG02145.hp2 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1-9842G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203505195 | |||||||
| chr2:203505219 | G | A | 1 | a0001c0007t0068g0218 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1-9866C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203505219 | |||||||
| chr2:203505272 | G | A | 1 | a0002c0012t0099g0265 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1-9919C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203505272 | |||||||
| chr2:203505287 | T | C | 6 | a0001c0001t0002g0155 a0001c0001t0002g0196 a0001c0001t0037g0250 others(3): Show |
6 | NA18945.hp2 NA18969.hp1 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.1-9934A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203505287 | |||||||
| chr2:203505306 | C | T | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1-9953G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203505306 | |||||||
| chr2:203505344 | G | C | 1 | a0001c0026t0077g0238 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1-9991C>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203505344 | |||||||
| chr2:203505414 | A | G | 2 | a0001c0007t0082g0260 a0002c0018t0083g0253 |
2 | HG02055.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1-10061T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203505414 | |||||||
| chr2:203505441 | A | AC | 106 | a0001c0001t0002g0146 a0001c0001t0002g0154 a0001c0001t0003g0150 others(103): Show |
106 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.1-10089dupG | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203505441 | |||||||
| chr2:203505441 | A | ACC | 15 | a0001c0001t0011g0066 a0001c0002t0001g0038 a0001c0002t0001g0078 others(12): Show |
15 | HG02129.hp2 HG02132.hp1 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.1-10090_1-10089dup others(2): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203505441 | |||||||
| chr2:203505480 | A | G | 158 | a0001c0001t0011g0020 a0001c0001t0011g0066 a0001c0001t0011g0067 others(155): Show |
158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.1-10127T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203505480 | |||||||
| chr2:203505560 | A | G | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1-10207T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203505560 | |||||||
| chr2:203505658 | CCA | C | 3 | a0001c0007t0021g0162 a0001c0007t0021g0220 a0002c0018t0021g0161 |
3 | HG02109.hp1 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1-10307_1-10306del others(2): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203505658 | |||||||
| chr2:203505676 | A | C | 2 | a0001c0007t0082g0260 a0002c0018t0083g0253 |
2 | HG02055.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1-10323T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203505676 | |||||||
| chr2:203505702 | AATTG | A | 4 | a0001c0003t0036g0229 a0001c0003t0036g0230 a0001c0003t0076g0228 others(1): Show |
4 | HG02145.hp1 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1-10353_1-10350del others(4): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203505702 | |||||||
| chr2:203505757 | A | G | 1 | a0001c0002t0049g0049 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1-10404T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203505757 | |||||||
| chr2:203505841 | G | A | 1 | a0001c0002t0001g0092 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1-10488C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203505841 | |||||||
| chr2:203505849 | G | A | 2 | a0001c0003t0095g0271 a0001c0003t0103g0264 |
2 | HG02132.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.1-10496C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203505849 | |||||||
| chr2:203505862 | C | T | 1 | a0001c0001t0086g0243 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1-10509G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203505862 | |||||||
| chr2:203505971 | G | A | 1 | a0001c0026t0077g0238 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1-10618C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203505971 | |||||||
| chr2:203506042 | G | T | 1 | a0001c0003t0069g0163 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1-10689C>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506042 | |||||||
| chr2:203506144 | A | AG | 7 | a0001c0002t0001g0075 a0002c0006t0001g0008 a0002c0006t0001g0073 others(4): Show |
7 | HG00673.hp2 HG01099.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1-10792dupC | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506144 | |||||||
| chr2:203506346 | G | A | 1 | a0009c0032t0001g0069 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1-10993C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506346 | |||||||
| chr2:203506728 | ATATAGAT others(23): Show |
A | 1 | a0002c0012t0091g0262 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1-11405_1-11376del others(30): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506728 | |||||||
| chr2:203506731 | TAG | T | 34 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(31): Show |
34 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(31): Show |
intron_variant | MODIFIER | c.1-11380_1-11379del others(2): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506731 | |||||||
| chr2:203506733 | G | T | 2 | a0001c0007t0057g0237 a0001c0033t0050g0231 |
2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1-11380C>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506733 | |||||||
| chr2:203506733 | GATATATA others(21): Show |
G | 1 | a0001c0007t0075g0227 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1-11408_1-11381del others(28): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506733 | |||||||
| chr2:203506735 | T | TATATATA others(51): Show |
2 | a0001c0007t0021g0162 a0001c0007t0021g0220 |
2 | HG02109.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1-11383_1-11382ins others(58): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506735 | |||||||
| chr2:203506742 | C | A | 3 | a0001c0007t0021g0162 a0001c0007t0021g0220 a0001c0033t0050g0231 |
3 | HG01884.hp1 HG02109.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1-11389G>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506742 | |||||||
| chr2:203506742 | CTA | C | 21 | a0001c0001t0063g0121 a0001c0004t0005g0093 a0001c0004t0005g0095 others(18): Show |
21 | HG00733.hp2 HG01109.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.1-11391_1-11390del others(2): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506742 | |||||||
| chr2:203506742 | CTATATA | C | 3 | a0001c0003t0036g0229 a0001c0003t0078g0239 a0001c0026t0077g0238 |
3 | HG02895.hp1 HG03098.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1-11395_1-11390del others(6): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506742 | |||||||
| chr2:203506742 | CTATATAT others(35): Show |
C | 2 | a0001c0003t0036g0230 a0001c0003t0076g0228 |
2 | HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1-11431_1-11390del others(42): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506742 | |||||||
| chr2:203506744 | ATATATAT others(19): Show |
A | 1 | a0001c0003t0096g0279 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1-11417_1-11392del others(26): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506744 | |||||||
| chr2:203506745 | T | G | 31 | a0001c0001t0001g0012 a0001c0001t0002g0119 a0001c0001t0003g0112 others(28): Show |
31 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.1-11392A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506745 | |||||||
| chr2:203506746 | A | ATATATAT others(5): Show |
1 | a0001c0029t0066g0219 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1-11405_1-11394dup others(12): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506746 | |||||||
| chr2:203506746 | A | ATATATAT others(3): Show |
1 | a0001c0007t0082g0260 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1-11394_1-11393ins others(10): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506746 | |||||||
| chr2:203506746 | A | C | 91 | a0001c0001t0011g0020 a0001c0001t0011g0066 a0001c0001t0011g0067 others(88): Show |
91 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1-11393T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506746 | |||||||
| chr2:203506747 | T | G | 1 | a0002c0017t0015g0097 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1-11394A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506747 | |||||||
| chr2:203506751 | T | G | 5 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0139 others(2): Show |
5 | HG01257.hp2 HG01258.hp1 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.1-11398A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506751 | |||||||
| chr2:203506752 | A | ATATCTAT others(45): Show |
1 | a0002c0018t0083g0253 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1-11400_1-11399ins others(52): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506752 | |||||||
| chr2:203506753 | T | G | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1-11400A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506753 | |||||||
| chr2:203506754 | A | ATCTATAT others(7): Show |
1 | a0001c0007t0057g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1-11402_1-11401ins others(14): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506754 | |||||||
| chr2:203506754 | A | C | 28 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(25): Show |
28 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(25): Show |
intron_variant | MODIFIER | c.1-11401T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506754 | |||||||
| chr2:203506756 | ATC | A | 3 | a0001c0003t0006g0263 a0001c0003t0006g0276 a0002c0012t0099g0265 |
3 | HG02723.hp1 HG03209.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.1-11405_1-11404del others(2): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506756 | |||||||
| chr2:203506758 | C | A | 27 | a0001c0003t0006g0252 a0001c0003t0006g0274 a0001c0003t0006g0284 others(24): Show |
27 | HG00738.hp2 HG01943.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.1-11405G>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506758 | |||||||
| chr2:203506761 | T | G | 6 | a0001c0001t0003g0112 a0001c0001t0032g0118 a0001c0001t0032g0142 others(3): Show |
6 | HG00621.hp2 HG01167.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.1-11408A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506761 | |||||||
| chr2:203506764 | A | C | 2 | a0001c0001t0010g0061 a0002c0018t0083g0253 |
2 | HG02055.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1-11411T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506764 | |||||||
| chr2:203506768 | A | C | 24 | a0001c0003t0006g0252 a0001c0003t0006g0274 a0001c0003t0006g0284 others(21): Show |
24 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(21): Show |
intron_variant | MODIFIER | c.1-11415T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506768 | |||||||
| chr2:203506770 | C | A | 25 | a0001c0001t0010g0061 a0001c0003t0006g0252 a0001c0003t0006g0274 others(22): Show |
25 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(22): Show |
intron_variant | MODIFIER | c.1-11417G>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506770 | |||||||
| chr2:203506776 | A | ATATATCT others(41): Show |
2 | a0001c0007t0026g0005 a0001c0007t0026g0006 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1-11424_1-11423ins others(48): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506776 | |||||||
| chr2:203506776 | A | C | 2 | a0001c0002t0004g0130 a0001c0033t0050g0231 |
2 | HG00544.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.1-11423T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506776 | |||||||
| chr2:203506778 | ATCTAGAT others(47): Show |
A | 1 | a0001c0003t0036g0229 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1-11479_1-11426del others(54): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506778 | |||||||
| chr2:203506779 | T | A | 6 | a0001c0001t0016g0141 a0001c0001t0016g0172 a0001c0001t0016g0205 others(3): Show |
6 | HG02572.hp2 HG02723.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1-11426A>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506779 | |||||||
| chr2:203506780 | C | A | 7 | a0001c0003t0006g0263 a0001c0003t0006g0276 a0001c0003t0069g0163 others(4): Show |
7 | HG00738.hp1 HG02486.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1-11427G>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506780 | |||||||
| chr2:203506780 | CTAGA | C | 5 | a0001c0003t0025g0280 a0001c0003t0025g0282 a0001c0003t0025g0283 others(2): Show |
5 | HG01943.hp2 NA18968.hp1 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.1-11431_1-11428del others(4): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506780 | |||||||
| chr2:203506782 | A | C | 5 | a0001c0003t0006g0263 a0001c0003t0006g0276 a0001c0003t0069g0163 others(2): Show |
5 | HG00738.hp1 HG02486.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1-11429T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506782 | |||||||
| chr2:203506783 | G | T | 30 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(27): Show |
30 | HG00738.hp1 HG00738.hp2 HG02109.hp2 others(27): Show |
intron_variant | MODIFIER | c.1-11430C>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506783 | |||||||
| chr2:203506784 | A | C | 2 | a0001c0003t0078g0239 a0001c0026t0077g0238 |
2 | HG03098.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1-11431T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506784 | |||||||
| chr2:203506788 | A | C | 1 | a0001c0007t0057g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1-11435T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506788 | |||||||
| chr2:203506792 | A | C | 2 | a0001c0003t0069g0163 a0001c0003t0070g0225 |
2 | HG02486.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1-11439T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506792 | |||||||
| chr2:203506794 | C | A | 4 | a0001c0003t0069g0163 a0001c0003t0070g0225 a0001c0003t0078g0239 others(1): Show |
4 | HG02486.hp1 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1-11441G>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506794 | |||||||
| chr2:203506795 | T | G | 2 | a0001c0003t0069g0163 a0001c0003t0070g0225 |
2 | HG02486.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1-11442A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506795 | |||||||
| chr2:203506796 | A | C | 4 | a0001c0001t0011g0020 a0001c0003t0078g0239 a0001c0008t0014g0071 others(1): Show |
4 | HG03098.hp2 NA18949.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.1-11443T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506796 | |||||||
| chr2:203506797 | T | G | 20 | a0001c0004t0005g0093 a0001c0004t0005g0095 a0001c0004t0005g0098 others(17): Show |
20 | HG00733.hp2 HG01109.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.1-11444A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506797 | |||||||
| chr2:203506798 | A | ATATATCT others(31): Show |
1 | a0001c0001t0012g0185 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1-11446_1-11445ins others(38): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506798 | |||||||
| chr2:203506800 | A | C | 4 | a0001c0001t0002g0119 a0001c0001t0055g0157 a0001c0002t0004g0133 others(1): Show |
4 | HG00738.hp1 HG01258.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1-11447T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506800 | |||||||
| chr2:203506806 | C | A | 4 | a0001c0001t0055g0157 a0001c0002t0004g0133 a0002c0005t0022g0117 others(1): Show |
4 | HG00738.hp1 HG01258.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1-11453G>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506806 | |||||||
| chr2:203506808 | A | C | 3 | a0001c0001t0055g0157 a0001c0002t0004g0133 a0002c0005t0022g0117 |
3 | HG00738.hp1 HG01258.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1-11455T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506808 | |||||||
| chr2:203506808 | ATATC | A | 21 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(18): Show |
21 | HG00738.hp2 HG02129.hp2 HG02132.hp1 others(18): Show |
intron_variant | MODIFIER | c.1-11459_1-11456del others(4): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506808 | |||||||
| chr2:203506809 | T | G | 5 | a0001c0001t0011g0020 a0001c0007t0057g0237 a0001c0008t0014g0071 others(2): Show |
5 | HG02109.hp2 HG03098.hp2 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.1-11456A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506809 | |||||||
| chr2:203506812 | C | A | 15 | a0001c0001t0011g0020 a0001c0001t0055g0157 a0001c0002t0004g0133 others(12): Show |
15 | HG00738.hp1 HG01258.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1-11459G>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506812 | |||||||
| chr2:203506812 | C | CTATATAT others(9): Show |
1 | a0001c0007t0082g0260 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1-11460_1-11459ins others(16): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506812 | |||||||
| chr2:203506812 | C | CTATATAT others(5): Show |
107 | a0001c0001t0001g0012 a0001c0001t0002g0111 a0001c0001t0002g0129 others(104): Show |
107 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.1-11471_1-11460dup others(12): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506812 | |||||||
| chr2:203506814 | A | C | 5 | a0001c0003t0006g0252 a0001c0003t0006g0284 a0001c0003t0006g0288 others(2): Show |
5 | HG02559.hp1 HG02886.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1-11461T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506814 | |||||||
| chr2:203506816 | ATATCTAT others(23): Show |
A | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1-11493_1-11464del others(30): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506816 | |||||||
| chr2:203506818 | A | C | 2 | a0001c0003t0069g0163 a0001c0003t0070g0225 |
2 | HG02486.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1-11465T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506818 | |||||||
| chr2:203506820 | C | A | 9 | a0001c0003t0025g0280 a0001c0003t0025g0282 a0001c0003t0025g0283 others(6): Show |
9 | HG01943.hp2 HG02486.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1-11467G>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506820 | |||||||
| chr2:203506820 | C | CTATATAT others(7): Show |
4 | a0001c0001t0016g0205 a0002c0005t0087g0254 a0002c0006t0004g0143 others(1): Show |
4 | HG02572.hp2 HG02886.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1-11481_1-11468dup others(14): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506820 | |||||||
| chr2:203506822 | A | ATATATAT others(3): Show |
1 | a0001c0001t0013g0173 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1-11479_1-11470dup others(10): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506822 | |||||||
| chr2:203506823 | T | G | 1 | a0001c0029t0066g0219 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1-11470A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506823 | |||||||
| chr2:203506824 | A | C | 2 | a0001c0003t0069g0163 a0001c0003t0070g0225 |
2 | HG02486.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1-11471T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506824 | |||||||
| chr2:203506826 | A | C | 2 | a0001c0003t0092g0272 a0002c0012t0039g0270 |
2 | HG03710.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1-11473T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506826 | |||||||
| chr2:203506826 | ATATATCT others(23): Show |
A | 1 | a0002c0012t0099g0265 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1-11503_1-11474del others(30): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506826 | |||||||
| chr2:203506827 | T | G | 4 | a0001c0003t0025g0280 a0001c0003t0025g0282 a0001c0003t0025g0283 others(1): Show |
4 | NA18968.hp1 NA18969.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.1-11474A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506827 | |||||||
| chr2:203506828 | A | C | 2 | a0001c0003t0036g0230 a0001c0003t0076g0228 |
2 | HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1-11475T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506828 | |||||||
| chr2:203506828 | ATATCTAT others(11): Show |
A | 1 | a0001c0003t0094g0267 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1-11493_1-11476del others(18): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506828 | |||||||
| chr2:203506830 | A | C | 1 | a0001c0002t0001g0083 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1-11477T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506830 | |||||||
| chr2:203506832 | C | A | 8 | a0001c0002t0001g0083 a0001c0003t0025g0280 a0001c0003t0025g0282 others(5): Show |
8 | HG01255.hp2 HG02451.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1-11479G>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506832 | |||||||
| chr2:203506835 | T | G | 2 | a0001c0003t0096g0279 a0002c0012t0091g0262 |
2 | HG02145.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.1-11482A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506835 | |||||||
| chr2:203506836 | ATC | A | 20 | a0001c0004t0005g0093 a0001c0004t0005g0095 a0001c0004t0005g0098 others(17): Show |
20 | HG00733.hp2 HG01109.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.1-11485_1-11484del others(2): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506836 | |||||||
| chr2:203506836 | ATCTATAT others(7): Show |
A | 2 | a0001c0003t0025g0282 a0001c0003t0098g0281 |
2 | NA19064.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1-11497_1-11484del others(14): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506836 | |||||||
| chr2:203506838 | C | A | 99 | a0001c0001t0011g0066 a0001c0001t0011g0067 a0001c0001t0046g0072 others(96): Show |
99 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1-11485G>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506838 | |||||||
| chr2:203506842 | A | ATC | 3 | a0001c0003t0069g0163 a0001c0003t0070g0225 a0009c0032t0001g0069 |
3 | HG02486.hp1 HG02970.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.1-11490_1-11489ins others(2): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506842 | |||||||
| chr2:203506842 | A | ATCTATAT others(1): Show |
6 | a0001c0007t0021g0162 a0001c0007t0021g0220 a0001c0007t0026g0005 others(3): Show |
6 | HG02109.hp1 HG02809.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1-11490_1-11489ins others(8): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506842 | |||||||
| chr2:203506844 | A | C | 87 | a0001c0001t0011g0066 a0001c0001t0011g0067 a0001c0001t0046g0072 others(84): Show |
87 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.1-11491T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506844 | |||||||
| chr2:203506844 | ATCTATCT others(5): Show |
A | 2 | a0001c0003t0025g0280 a0001c0003t0025g0283 |
2 | NA18968.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.1-11503_1-11492del others(12): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506844 | |||||||
| chr2:203506846 | C | A | 124 | a0001c0001t0011g0066 a0001c0001t0011g0067 a0001c0001t0046g0072 others(121): Show |
124 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.1-11493G>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506846 | |||||||
| chr2:203506846 | C | CTA | 3 | a0001c0001t0011g0020 a0001c0007t0082g0260 a0001c0008t0014g0071 |
3 | HG02451.hp2 NA18949.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1-11495_1-11494dup others(2): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506846 | |||||||
| chr2:203506847 | T | G | 3 | a0001c0003t0006g0263 a0001c0003t0006g0276 a0001c0003t0092g0272 |
3 | HG02723.hp1 HG03209.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1-11494A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506847 | |||||||
| chr2:203506848 | ATC | A | 19 | a0001c0004t0005g0093 a0001c0004t0005g0095 a0001c0004t0005g0098 others(16): Show |
19 | HG00733.hp2 HG01109.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.1-11497_1-11496del others(2): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506848 | |||||||
| chr2:203506850 | C | A | 30 | a0001c0001t0011g0020 a0001c0002t0004g0133 a0001c0003t0006g0252 others(27): Show |
30 | HG00738.hp2 HG01258.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.1-11497G>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506850 | |||||||
| chr2:203506850 | C | CTA | 85 | a0001c0001t0002g0146 a0001c0001t0011g0066 a0001c0001t0046g0072 others(82): Show |
85 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.1-11499_1-11498dup others(2): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506850 | |||||||
| chr2:203506852 | A | ATATATAT others(29): Show |
1 | a0001c0002t0001g0016 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1-11500_1-11499ins others(36): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506852 | |||||||
| chr2:203506852 | A | ATATATCT others(51): Show |
2 | a0001c0001t0011g0067 a0001c0002t0007g0039 |
2 | HG02027.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.1-11500_1-11499ins others(58): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506852 | |||||||
| chr2:203506853 | T | G | 19 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(16): Show |
19 | HG02129.hp2 HG02132.hp1 HG02523.hp1 others(16): Show |
intron_variant | MODIFIER | c.1-11500A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506853 | |||||||
| chr2:203506856 | C | A | 63 | a0001c0001t0002g0146 a0001c0001t0011g0067 a0001c0002t0001g0016 others(60): Show |
63 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.1-11503G>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506856 | |||||||
| chr2:203506856 | C | CTA | 29 | a0001c0001t0002g0119 a0001c0001t0002g0196 a0001c0001t0003g0136 others(26): Show |
29 | HG00642.hp2 HG00738.hp1 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.1-11505_1-11504dup others(2): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506856 | |||||||
| chr2:203506856 | C | CTATA | 16 | a0001c0001t0001g0012 a0001c0001t0003g0150 a0001c0001t0011g0030 others(13): Show |
16 | HG00408.hp1 HG00438.hp1 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.1-11507_1-11504dup others(4): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506856 | |||||||
| chr2:203506856 | C | CTATATAT others(9): Show |
1 | a0001c0001t0003g0112 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1-11519_1-11504dup others(16): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506856 | |||||||
| chr2:203506856 | CTATATAT others(19): Show |
C | 1 | a0001c0001t0010g0059 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1-11529_1-11504del others(26): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506856 | |||||||
| chr2:203506857 | T | G | 3 | a0001c0003t0025g0280 a0001c0003t0025g0283 a0001c0003t0096g0279 |
3 | NA18747.hp2 NA18968.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.1-11504A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506857 | |||||||
| chr2:203506859 | T | G | 5 | a0001c0003t0025g0282 a0001c0003t0078g0239 a0001c0003t0101g0277 others(2): Show |
5 | HG03098.hp2 HG03130.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1-11506A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506859 | |||||||
| chr2:203506860 | A | C | 3 | a0001c0001t0008g0125 a0001c0002t0004g0133 a0001c0007t0075g0227 |
3 | HG01258.hp2 HG02559.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1-11507T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506860 | |||||||
| chr2:203506862 | A | C | 22 | a0001c0001t0023g0197 a0001c0001t0023g0207 a0001c0001t0023g0224 others(19): Show |
22 | HG00733.hp2 HG01109.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.1-11509T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506862 | |||||||
| chr2:203506864 | A | C | 8 | a0001c0003t0069g0163 a0001c0003t0070g0225 a0001c0007t0021g0162 others(5): Show |
8 | HG02109.hp1 HG02486.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1-11511T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506864 | |||||||
| chr2:203506865 | T | G | 1 | a0001c0007t0075g0227 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1-11512A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506865 | |||||||
| chr2:203506866 | A | ATATC | 72 | a0001c0001t0011g0066 a0001c0001t0046g0072 a0001c0002t0001g0009 others(69): Show |
72 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.1-11514_1-11513ins others(4): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506866 | |||||||
| chr2:203506866 | A | ATCTATAT others(35): Show |
4 | a0001c0002t0001g0023 a0001c0002t0001g0046 a0001c0002t0001g0079 others(1): Show |
4 | HG00423.hp1 HG01257.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.1-11514_1-11513ins others(42): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506866 | |||||||
| chr2:203506866 | A | ATCTATAT others(23): Show |
3 | a0001c0001t0011g0020 a0001c0007t0082g0260 a0001c0008t0014g0071 |
3 | HG02451.hp2 NA18949.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1-11514_1-11513ins others(30): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506866 | |||||||
| chr2:203506866 | A | ATCTC | 6 | a0001c0002t0007g0018 a0001c0002t0007g0025 a0001c0015t0001g0021 others(3): Show |
6 | HG01071.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1-11514_1-11513ins others(4): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506866 | |||||||
| chr2:203506866 | A | C | 5 | a0001c0001t0011g0067 a0001c0002t0001g0016 a0001c0002t0007g0033 others(2): Show |
5 | HG02027.hp1 HG02080.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.1-11513T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506866 | |||||||
| chr2:203506867 | T | G | 20 | a0001c0004t0005g0093 a0001c0004t0005g0095 a0001c0004t0005g0098 others(17): Show |
20 | HG00733.hp2 HG01109.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.1-11514A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506867 | |||||||
| chr2:203506868 | A | C | 2 | a0001c0003t0036g0229 a0001c0033t0050g0231 |
2 | HG01884.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1-11515T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506868 | |||||||
| chr2:203506871 | T | G | 1 | a0001c0015t0044g0007 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1-11518A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506871 | |||||||
| chr2:203506872 | A | C | 3 | a0001c0003t0006g0284 a0001c0007t0057g0237 a0007c0030t0006g0285 |
3 | HG02109.hp2 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1-11519T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506872 | |||||||
| chr2:203506872 | A | T | 1 | a0001c0003t0096g0279 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1-11519T>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506872 | |||||||
| chr2:203506874 | A | C | 4 | a0001c0003t0093g0286 a0001c0003t0095g0271 a0001c0003t0103g0264 others(1): Show |
4 | HG02132.hp1 HG02523.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.1-11521T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506874 | |||||||
| chr2:203506874 | A | T | 1 | a0001c0003t0096g0279 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1-11521T>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506874 | |||||||
| chr2:203506875 | T | G | 2 | a0001c0002t0004g0133 a0001c0003t0097g0287 |
2 | HG01258.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.1-11522A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506875 | |||||||
| chr2:203506876 | A | T | 3 | a0001c0003t0025g0280 a0001c0003t0025g0283 a0002c0012t0099g0265 |
3 | NA18968.hp1 NA18969.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.1-11523T>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506876 | |||||||
| chr2:203506877 | T | G | 3 | a0001c0001t0002g0221 a0001c0007t0075g0227 a0001c0026t0077g0238 |
3 | HG01361.hp2 HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1-11524A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506877 | |||||||
| chr2:203506878 | A | C | 1 | a0001c0007t0057g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1-11525T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506878 | |||||||
| chr2:203506878 | A | T | 5 | a0001c0003t0025g0280 a0001c0003t0025g0282 a0001c0003t0025g0283 others(2): Show |
5 | HG01943.hp2 NA18968.hp1 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.1-11525T>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506878 | |||||||
| chr2:203506879 | T | G | 18 | a0001c0004t0005g0093 a0001c0004t0005g0095 a0001c0004t0005g0098 others(15): Show |
18 | HG00733.hp2 HG01109.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.1-11526A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506879 | |||||||
| chr2:203506879 | TAGA | T | 3 | a0001c0003t0025g0280 a0001c0003t0025g0283 a0002c0012t0099g0265 |
3 | NA18968.hp1 NA18969.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.1-11529_1-11527del others(3): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506879 | |||||||
| chr2:203506880 | A | C | 1 | a0001c0003t0103g0264 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1-11527T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506880 | |||||||
| chr2:203506880 | A | T | 3 | a0001c0003t0025g0282 a0001c0003t0094g0267 a0001c0003t0098g0281 |
3 | HG01943.hp2 NA19064.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1-11527T>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506880 | |||||||
| chr2:203506881 | G | GAT | 20 | a0001c0001t0002g0155 a0001c0001t0002g0190 a0001c0001t0088g0261 others(17): Show |
20 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(17): Show |
intron_variant | MODIFIER | c.1-11530_1-11529dup others(2): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506881 | |||||||
| chr2:203506881 | G | T | 55 | a0001c0001t0011g0067 a0001c0002t0004g0133 a0001c0003t0006g0252 others(52): Show |
55 | HG00597.hp2 HG00733.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.1-11528C>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506881 | |||||||
| chr2:203506882 | A | C | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1-11529T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506882 | |||||||
| chr2:203506882 | A | T | 4 | a0001c0003t0025g0282 a0001c0003t0092g0272 a0001c0003t0094g0267 others(1): Show |
4 | HG01943.hp2 NA18966.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.1-11529T>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506882 | |||||||
| chr2:203506883 | T | G | 1 | a0001c0007t0057g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1-11530A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506883 | |||||||
| chr2:203506884 | A | T | 9 | a0001c0003t0025g0280 a0001c0003t0025g0282 a0001c0003t0025g0283 others(6): Show |
9 | HG01943.hp2 HG02145.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.1-11531T>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506884 | |||||||
| chr2:203506885 | T | G | 1 | a0003c0009t0037g0259 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1-11532A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506885 | |||||||
| chr2:203506886 | A | T | 10 | a0001c0003t0025g0280 a0001c0003t0025g0282 a0001c0003t0025g0283 others(7): Show |
10 | HG00738.hp2 HG01943.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1-11533T>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506886 | |||||||
| chr2:203506888 | A | ATTTTTTT others(3): Show |
1 | a0001c0003t0006g0274 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1-11536_1-11535ins others(10): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506888 | |||||||
| chr2:203506888 | A | ATTTTTTT others(4): Show |
1 | a0001c0003t0106g0273 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1-11536_1-11535ins others(11): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506888 | |||||||
| chr2:203506888 | A | ATTTTTTT others(5): Show |
1 | a0001c0003t0097g0287 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1-11536_1-11535ins others(12): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506888 | |||||||
| chr2:203506888 | A | ATTTTTTT others(6): Show |
1 | a0001c0003t0006g0288 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1-11536_1-11535ins others(13): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506888 | |||||||
| chr2:203506888 | A | T | 13 | a0001c0003t0025g0280 a0001c0003t0025g0282 a0001c0003t0025g0283 others(10): Show |
13 | HG00738.hp2 HG01943.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1-11535T>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506888 | |||||||
| chr2:203506889 | T | G | 1 | a0001c0001t0002g0221 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1-11536A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506889 | |||||||
| chr2:203506890 | A | ATTTTTTT others(3): Show |
2 | a0001c0003t0006g0263 a0001c0003t0006g0276 |
2 | HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1-11538_1-11537ins others(10): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506890 | |||||||
| chr2:203506890 | A | ATTTTTTT others(4): Show |
1 | a0007c0030t0006g0285 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1-11538_1-11537ins others(11): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506890 | |||||||
| chr2:203506890 | A | ATTTTTTT others(6): Show |
1 | a0001c0003t0006g0252 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1-11538_1-11537ins others(13): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506890 | |||||||
| chr2:203506890 | A | T | 19 | a0001c0003t0006g0274 a0001c0003t0006g0288 a0001c0003t0025g0280 others(16): Show |
19 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(16): Show |
intron_variant | MODIFIER | c.1-11537T>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506890 | |||||||
| chr2:203506891 | T | G | 3 | a0001c0001t0001g0012 a0001c0001t0053g0144 a0001c0002t0033g0131 |
3 | HG03704.hp2 NA18995.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1-11538A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506891 | |||||||
| chr2:203506892 | A | ATTTTTTT others(5): Show |
1 | a0004c0014t0108g0290 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1-11540_1-11539ins others(12): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506892 | |||||||
| chr2:203506892 | A | T | 25 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(22): Show |
25 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(22): Show |
intron_variant | MODIFIER | c.1-11539T>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506892 | |||||||
| chr2:203506893 | T | G | 2 | a0001c0001t0002g0148 a0001c0002t0007g0033 |
2 | HG03834.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.1-11540A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506893 | |||||||
| chr2:203506894 | A | ATTTTTTT others(4): Show |
1 | a0002c0031t0105g0266 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1-11542_1-11541ins others(11): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506894 | |||||||
| chr2:203506894 | A | ATTTTTTT others(5): Show |
4 | a0001c0003t0006g0284 a0001c0003t0095g0271 a0001c0003t0103g0264 others(1): Show |
4 | HG02132.hp1 HG02523.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1-11542_1-11541ins others(12): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506894 | |||||||
| chr2:203506894 | A | ATTTTTTT others(8): Show |
1 | a0001c0003t0093g0286 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1-11542_1-11541ins others(15): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506894 | |||||||
| chr2:203506894 | A | T | 29 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(26): Show |
29 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(26): Show |
intron_variant | MODIFIER | c.1-11541T>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506894 | |||||||
| chr2:203506896 | A | T | 49 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(46): Show |
49 | HG00733.hp2 HG00738.hp2 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.1-11543T>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506896 | |||||||
| chr2:203506898 | A | AT | 6 | a0001c0001t0002g0111 a0001c0001t0081g0241 a0001c0002t0035g0115 others(3): Show |
6 | HG00733.hp1 HG02523.hp2 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.1-11546dupA | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506898 | |||||||
| chr2:203506898 | A | ATATATTT others(21): Show |
1 | a0001c0015t0044g0007 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1-11546_1-11545ins others(28): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506898 | |||||||
| chr2:203506898 | A | ATTTTTTT others(5): Show |
1 | a0001c0003t0092g0272 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1-11557_1-11546dup others(12): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506898 | |||||||
| chr2:203506898 | A | ATTTTTTT others(11): Show |
1 | a0002c0012t0039g0270 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1-11546_1-11545ins others(18): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506898 | |||||||
| chr2:203506898 | A | T | 74 | a0001c0001t0002g0183 a0001c0001t0003g0112 a0001c0001t0003g0136 others(71): Show |
74 | HG00621.hp2 HG00733.hp2 HG00738.hp2 others(71): Show |
intron_variant | MODIFIER | c.1-11545T>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506898 | |||||||
| chr2:203506898 | AT | A | 9 | a0001c0001t0002g0129 a0001c0001t0002g0148 a0001c0001t0002g0151 others(6): Show |
9 | HG02080.hp1 HG02109.hp1 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.1-11546delA | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506898 | |||||||
| chr2:203506899 | T | TA | 3 | a0001c0002t0001g0042 a0001c0002t0043g0004 a0002c0023t0003g0169 |
3 | HG02132.hp2 HG02135.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.1-11547_1-11546ins others(1): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506899 | |||||||
| chr2:203506900 | T | A | 74 | a0001c0001t0002g0145 a0001c0001t0002g0190 a0001c0001t0002g0221 others(71): Show |
74 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.1-11547A>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506900 | |||||||
| chr2:203506901 | T | A | 1 | a0001c0007t0021g0162 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1-11548A>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506901 | |||||||
| chr2:203506902 | T | A | 12 | a0001c0001t0011g0020 a0001c0002t0004g0106 a0001c0002t0007g0018 others(9): Show |
12 | HG00735.hp2 HG01071.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.1-11549A>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506902 | |||||||
| chr2:203506981 | C | T | 1 | a0001c0001t0003g0167 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1-11628G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203506981 | |||||||
| chr2:203507149 | G | A | 3 | a0001c0001t0012g0122 a0001c0001t0012g0185 a0001c0001t0065g0124 |
3 | HG03491.hp2 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1-11796C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203507149 | |||||||
| chr2:203507349 | G | A | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1-11996C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203507349 | |||||||
| chr2:203507614 | A | C | 87 | a0001c0001t0011g0020 a0001c0001t0011g0066 a0001c0001t0011g0067 others(84): Show |
87 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.1-12261T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203507614 | |||||||
| chr2:203507739 | A | G | 3 | a0001c0002t0001g0038 a0001c0008t0014g0047 a0002c0006t0001g0054 |
3 | HG00673.hp1 NA18965.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.1-12386T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203507739 | |||||||
| chr2:203507749 | C | G | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1-12396G>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203507749 | |||||||
| chr2:203507814 | T | C | 1 | a0009c0032t0001g0069 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1-12461A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203507814 | |||||||
| chr2:203508002 | G | C | 7 | a0001c0003t0069g0163 a0001c0003t0070g0225 a0001c0007t0021g0162 others(4): Show |
7 | HG02055.hp2 HG02109.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1-12649C>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203508002 | |||||||
| chr2:203508004 | AG | A | 4 | a0001c0002t0001g0070 a0001c0002t0001g0086 a0001c0002t0001g0092 others(1): Show |
4 | HG01071.hp2 HG01361.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.1-12652delC | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203508004 | |||||||
| chr2:203508092 | T | G | 9 | a0001c0001t0009g0246 a0001c0001t0009g0249 a0001c0001t0009g0255 others(6): Show |
9 | HG00642.hp1 HG01358.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.1-12739A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203508092 | |||||||
| chr2:203508145 | G | A | 1 | a0001c0001t0002g0196 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1-12792C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203508145 | |||||||
| chr2:203508168 | G | A | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1-12815C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203508168 | |||||||
| chr2:203508221 | C | CA | 34 | a0001c0001t0001g0012 a0001c0001t0002g0119 a0001c0001t0002g0145 others(31): Show |
34 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.1-12869dupT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203508221 | |||||||
| chr2:203508221 | CA | C | 6 | a0001c0001t0002g0175 a0001c0001t0002g0183 a0001c0001t0009g0246 others(3): Show |
6 | HG02698.hp2 HG03098.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1-12869delT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203508221 | |||||||
| chr2:203508221 | CAA | C | 34 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(31): Show |
34 | HG00738.hp2 HG01884.hp1 HG01943.hp2 others(31): Show |
intron_variant | MODIFIER | c.1-12870_1-12869del others(2): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203508221 | |||||||
| chr2:203508239 | A | G | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1-12886T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203508239 | |||||||
| chr2:203508244 | G | A | 37 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(34): Show |
37 | HG00738.hp2 HG01884.hp1 HG01943.hp2 others(34): Show |
intron_variant | MODIFIER | c.1-12891C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203508244 | |||||||
| chr2:203508259 | T | G | 4 | a0001c0001t0019g0032 a0001c0001t0019g0081 a0001c0001t0019g0082 others(1): Show |
4 | HG00323.hp1 HG01168.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1-12906A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203508259 | |||||||
| chr2:203508507 | C | T | 1 | a0001c0002t0001g0075 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1-13154G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203508507 | |||||||
| chr2:203508527 | T | TATACCCA others(4): Show |
1 | a0001c0001t0003g0152 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1-13185_1-13175dup others(11): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203508527 | |||||||
| chr2:203508643 | G | T | 3 | a0001c0002t0001g0045 a0001c0002t0001g0051 a0001c0002t0024g0160 |
3 | NA18998.hp1 NA19057.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1-13290C>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203508643 | |||||||
| chr2:203508845 | T | C | 3 | a0001c0001t0009g0249 a0001c0001t0009g0255 a0001c0001t0085g0248 |
3 | HG00642.hp1 HG01358.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1-13492A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203508845 | |||||||
| chr2:203509066 | A | AT | 9 | a0001c0001t0002g0221 a0001c0001t0003g0139 a0001c0001t0009g0249 others(6): Show |
9 | HG00597.hp2 HG00621.hp1 HG00642.hp1 others(6): Show |
intron_variant | MODIFIER | c.1-13714dupA | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203509066 | |||||||
| chr2:203509066 | AT | A | 91 | a0001c0001t0002g0154 a0001c0001t0002g0183 a0001c0001t0010g0061 others(88): Show |
91 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1-13714delA | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203509066 | |||||||
| chr2:203509066 | ATT | A | 56 | a0001c0002t0001g0027 a0001c0002t0001g0077 a0001c0002t0001g0091 others(53): Show |
56 | HG00323.hp2 HG00733.hp2 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.1-13715_1-13714del others(2): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203509066 | |||||||
| chr2:203509256 | G | C | 2 | a0001c0007t0026g0005 a0001c0007t0026g0006 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1-13903C>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203509256 | |||||||
| chr2:203509382 | T | A | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1-14029A>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203509382 | |||||||
| chr2:203509421 | T | C | 1 | a0002c0013t0009g0256 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1-14068A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203509421 | |||||||
| chr2:203509856 | G | A | 2 | a0001c0001t0002g0154 a0001c0001t0012g0186 |
2 | HG02027.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.1-14503C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203509856 | |||||||
| chr2:203509933 | T | C | 1 | a0001c0007t0068g0218 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1-14580A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203509933 | |||||||
| chr2:203510012 | C | G | 1 | a0008c0019t0029g0031 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1-14659G>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203510012 | |||||||
| chr2:203510041 | A | C | 158 | a0001c0001t0011g0020 a0001c0001t0011g0066 a0001c0001t0011g0067 others(155): Show |
158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.1-14688T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203510041 | |||||||
| chr2:203510048 | C | T | 1 | a0001c0001t0055g0157 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1-14695G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203510048 | |||||||
| chr2:203510205 | G | A | 1 | a0001c0001t0012g0186 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1-14852C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203510205 | |||||||
| chr2:203510239 | C | T | 17 | a0001c0004t0005g0093 a0001c0004t0005g0095 a0001c0004t0005g0098 others(14): Show |
17 | HG00733.hp2 HG01109.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.1-14886G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203510239 | |||||||
| chr2:203510277 | A | G | 1 | a0001c0002t0004g0106 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1-14924T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203510277 | |||||||
| chr2:203510335 | C | CA | 116 | a0001c0001t0001g0012 a0001c0001t0003g0167 a0001c0001t0008g0125 others(113): Show |
116 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.1-14983dupT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203510335 | |||||||
| chr2:203510335 | C | CAA | 36 | a0001c0001t0011g0020 a0001c0001t0011g0066 a0001c0002t0001g0058 others(33): Show |
36 | HG00738.hp2 HG01109.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.1-14984_1-14983dup others(2): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203510335 | |||||||
| chr2:203510335 | C | CAAA | 9 | a0001c0002t0001g0050 a0001c0003t0036g0229 a0001c0003t0036g0230 others(6): Show |
9 | HG02451.hp1 HG02717.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.1-14985_1-14983dup others(3): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203510335 | |||||||
| chr2:203510335 | CA | C | 11 | a0001c0001t0002g0111 a0001c0001t0002g0183 a0001c0001t0002g0191 others(8): Show |
11 | HG01517.hp2 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1-14983delT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203510335 | |||||||
| chr2:203510412 | G | A | 4 | a0001c0003t0036g0229 a0001c0003t0036g0230 a0001c0003t0076g0228 others(1): Show |
4 | HG02145.hp1 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1-15059C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203510412 | |||||||
| chr2:203510420 | G | C | 1 | a0002c0013t0009g0256 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1-15067C>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203510420 | |||||||
| chr2:203510517 | T | C | 3 | a0002c0031t0105g0266 a0004c0014t0100g0278 a0004c0014t0108g0290 |
3 | NA18948.hp2 NA18988.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1-15164A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203510517 | |||||||
| chr2:203510876 | T | C | 4 | a0001c0001t0013g0184 a0001c0001t0013g0211 a0001c0001t0059g0222 others(1): Show |
4 | HG01081.hp2 NA18970.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.1-15523A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203510876 | |||||||
| chr2:203510879 | C | T | 29 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(26): Show |
29 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(26): Show |
intron_variant | MODIFIER | c.1-15526G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203510879 | |||||||
| chr2:203511249 | A | G | 1 | a0001c0007t0057g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1-15896T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203511249 | |||||||
| chr2:203511266 | C | CT | 4 | a0001c0003t0036g0229 a0001c0003t0036g0230 a0001c0003t0076g0228 others(1): Show |
4 | HG02145.hp1 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1-15914dupA | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203511266 | |||||||
| chr2:203511269 | TA | T | 10 | a0001c0001t0002g0183 a0001c0001t0016g0172 a0001c0001t0019g0081 others(7): Show |
10 | HG01167.hp2 HG01168.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1-15917delT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203511269 | |||||||
| chr2:203511270 | A | T | 30 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(27): Show |
30 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(27): Show |
intron_variant | MODIFIER | c.1-15917T>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203511270 | |||||||
| chr2:203511271 | A | T | 1 | a0001c0003t0103g0264 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1-15918T>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203511271 | |||||||
| chr2:203511495 | T | C | 1 | a0002c0013t0009g0256 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1-16142A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203511495 | |||||||
| chr2:203511595 | C | T | 10 | a0001c0001t0010g0059 a0001c0001t0010g0061 a0001c0001t0010g0062 others(7): Show |
10 | HG02145.hp2 HG02486.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1-16242G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203511595 | |||||||
| chr2:203511665 | A | G | 1 | a0001c0002t0035g0128 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1-16312T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203511665 | |||||||
| chr2:203511807 | C | T | 2 | a0001c0007t0026g0005 a0001c0007t0026g0006 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1-16454G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203511807 | |||||||
| chr2:203511829 | C | T | 1 | a0001c0001t0060g0192 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1-16476G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203511829 | |||||||
| chr2:203512146 | C | T | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1-16793G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203512146 | |||||||
| chr2:203512243 | A | G | 1 | a0001c0015t0044g0007 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1-16890T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203512243 | |||||||
| chr2:203512355 | C | CA | 96 | a0001c0001t0002g0111 a0001c0001t0003g0152 a0001c0001t0003g0167 others(93): Show |
96 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1-17003dupT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203512355 | |||||||
| chr2:203512355 | C | CAA | 18 | a0001c0001t0056g0134 a0001c0002t0004g0109 a0001c0002t0033g0202 others(15): Show |
18 | HG00280.hp1 HG00733.hp2 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.1-17004_1-17003dup others(2): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203512355 | |||||||
| chr2:203512440 | A | C | 2 | a0001c0002t0001g0083 a0001c0002t0007g0033 |
2 | HG01255.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1-17087T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203512440 | |||||||
| chr2:203512621 | C | CT | 43 | a0001c0001t0002g0111 a0001c0001t0002g0129 a0001c0001t0002g0213 others(40): Show |
43 | HG00544.hp2 HG00642.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.1-17269dupA | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203512621 | |||||||
| chr2:203512621 | C | CTT | 25 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(22): Show |
25 | HG01943.hp2 HG02129.hp2 HG02132.hp1 others(22): Show |
intron_variant | MODIFIER | c.1-17270_1-17269dup others(2): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203512621 | |||||||
| chr2:203512621 | CT | C | 10 | a0001c0001t0010g0059 a0001c0001t0010g0061 a0001c0001t0010g0062 others(7): Show |
10 | HG02109.hp2 HG02145.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1-17269delA | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203512621 | |||||||
| chr2:203512761 | T | G | 1 | a0001c0020t0058g0171 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1-17408A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203512761 | |||||||
| chr2:203512969 | A | G | 1 | a0002c0006t0004g0143 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1-17616T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203512969 | |||||||
| chr2:203513109 | G | C | 2 | a0001c0001t0002g0154 a0001c0001t0012g0186 |
2 | HG02027.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.1-17756C>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203513109 | |||||||
| chr2:203513148 | C | G | 89 | a0001c0001t0011g0020 a0001c0001t0011g0066 a0001c0001t0011g0067 others(86): Show |
89 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.1-17795G>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203513148 | |||||||
| chr2:203513209 | T | TG | 37 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(34): Show |
37 | HG00738.hp2 HG01943.hp2 HG02109.hp2 others(34): Show |
intron_variant | MODIFIER | c.1-17857dupC | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203513209 | |||||||
| chr2:203513264 | C | A | 1 | a0001c0002t0001g0083 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1-17911G>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203513264 | |||||||
| chr2:203513270 | T | C | 1 | a0001c0007t0057g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1-17917A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203513270 | |||||||
| chr2:203513346 | T | TC | 37 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(34): Show |
37 | HG00738.hp2 HG01884.hp1 HG01943.hp2 others(34): Show |
intron_variant | MODIFIER | c.1-17994dupG | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203513346 | |||||||
| chr2:203513351 | C | CT | 11 | a0001c0001t0002g0111 a0001c0001t0003g0179 a0001c0001t0011g0030 others(8): Show |
11 | HG01433.hp1 HG02135.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.1-17999dupA | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203513351 | |||||||
| chr2:203513351 | C | CTT | 35 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(32): Show |
35 | HG00738.hp2 HG01884.hp1 HG01943.hp2 others(32): Show |
intron_variant | MODIFIER | c.1-18000_1-17999dup others(2): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203513351 | |||||||
| chr2:203513351 | C | CTTT | 25 | a0001c0003t0069g0163 a0001c0003t0070g0225 a0001c0004t0005g0093 others(22): Show |
25 | HG00733.hp2 HG01109.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.1-18001_1-17999dup others(3): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203513351 | |||||||
| chr2:203513351 | CT | C | 93 | a0001c0001t0008g0123 a0001c0001t0009g0257 a0001c0001t0011g0020 others(90): Show |
93 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.1-17999delA | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203513351 | |||||||
| chr2:203513379 | GAGTCTCG others(11): Show |
G | 1 | a0001c0029t0066g0219 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1-18044_1-18027del others(18): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203513379 | |||||||
| chr2:203513503 | C | T | 16 | a0001c0002t0004g0106 a0001c0002t0004g0107 a0001c0002t0004g0109 others(13): Show |
16 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(13): Show |
intron_variant | MODIFIER | c.1-18150G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203513503 | |||||||
| chr2:203513532 | C | CA | 47 | a0001c0001t0002g0154 a0001c0001t0008g0212 a0001c0001t0010g0062 others(44): Show |
47 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.1-18180dupT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203513532 | |||||||
| chr2:203513532 | CA | C | 29 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(26): Show |
29 | HG01943.hp2 HG02129.hp2 HG02132.hp1 others(26): Show |
intron_variant | MODIFIER | c.1-18180delT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203513532 | |||||||
| chr2:203513564 | G | A | 30 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(27): Show |
30 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(27): Show |
intron_variant | MODIFIER | c.1-18211C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203513564 | |||||||
| chr2:203513609 | G | A | 1 | a0001c0007t0057g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1-18256C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203513609 | |||||||
| chr2:203513686 | T | C | 10 | a0001c0003t0025g0280 a0001c0003t0025g0282 a0001c0003t0025g0283 others(7): Show |
10 | HG02129.hp2 HG02132.hp1 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.1-18333A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203513686 | |||||||
| chr2:203513837 | G | GA | 10 | a0001c0001t0002g0146 a0001c0001t0003g0167 a0001c0002t0001g0038 others(7): Show |
10 | HG00544.hp2 HG00735.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.1-18485dupT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203513837 | |||||||
| chr2:203513894 | G | A | 3 | a0001c0007t0021g0162 a0001c0007t0021g0220 a0002c0018t0021g0161 |
3 | HG02109.hp1 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1-18541C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203513894 | |||||||
| chr2:203514161 | C | T | 2 | a0001c0007t0026g0005 a0001c0007t0026g0006 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1-18808G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203514161 | |||||||
| chr2:203514380 | C | T | 2 | a0001c0001t0028g0065 a0001c0001t0028g0085 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1-19027G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203514380 | |||||||
| chr2:203514594 | G | A | 1 | a0001c0007t0068g0218 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1-19241C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203514594 | |||||||
| chr2:203514647 | C | T | 1 | a0001c0001t0085g0248 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1-19294G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203514647 | |||||||
| chr2:203514676 | T | A | 1 | a0001c0008t0014g0047 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1-19323A>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203514676 | |||||||
| chr2:203514692 | T | C | 1 | a0002c0005t0022g0117 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1-19339A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203514692 | |||||||
| chr2:203514720 | A | G | 1 | a0001c0026t0077g0238 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1-19367T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203514720 | |||||||
| chr2:203515005 | C | A | 1 | a0002c0005t0107g0289 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1-19652G>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203515005 | |||||||
| chr2:203515049 | A | G | 4 | a0001c0003t0036g0229 a0001c0003t0036g0230 a0001c0003t0076g0228 others(1): Show |
4 | HG02145.hp1 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1-19696T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203515049 | |||||||
| chr2:203515070 | G | C | 1 | a0002c0005t0029g0035 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1-19717C>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203515070 | |||||||
| chr2:203515184 | GCTA | G | 28 | a0001c0003t0006g0263 a0001c0003t0006g0274 a0001c0003t0006g0276 others(25): Show |
28 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(25): Show |
intron_variant | MODIFIER | c.1-19834_1-19832del others(3): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203515184 | |||||||
| chr2:203515212 | C | T | 1 | a0001c0002t0001g0038 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1-19859G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203515212 | |||||||
| chr2:203515251 | T | C | 1 | a0001c0002t0007g0029 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-1+19860A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203515251 | |||||||
| chr2:203515768 | G | C | 34 | a0001c0003t0006g0263 a0001c0003t0006g0274 a0001c0003t0006g0276 others(31): Show |
34 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(31): Show |
intron_variant | MODIFIER | c.-1+19343C>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203515768 | |||||||
| chr2:203515985 | T | C | 1 | a0001c0001t0002g0183 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-1+19126A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203515985 | |||||||
| chr2:203515991 | A | G | 3 | a0001c0007t0021g0162 a0001c0007t0021g0220 a0002c0018t0021g0161 |
3 | HG02109.hp1 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-1+19120T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203515991 | |||||||
| chr2:203516485 | C | T | 1 | a0001c0002t0004g0107 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-1+18626G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203516485 | |||||||
| chr2:203516487 | C | T | 1 | a0001c0004t0034g0240 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1+18624G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203516487 | |||||||
| chr2:203516558 | G | A | 2 | a0001c0003t0069g0163 a0001c0003t0070g0225 |
2 | HG02486.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-1+18553C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203516558 | |||||||
| chr2:203516577 | C | T | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-1+18534G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203516577 | |||||||
| chr2:203516685 | T | C | 4 | a0001c0001t0028g0065 a0001c0001t0028g0085 a0002c0005t0012g0206 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1+18426A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203516685 | |||||||
| chr2:203516792 | G | C | 1 | a0001c0001t0065g0124 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-1+18319C>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203516792 | |||||||
| chr2:203516845 | A | G | 1 | a0001c0003t0006g0284 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-1+18266T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203516845 | |||||||
| chr2:203517046 | A | T | 35 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(32): Show |
35 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(32): Show |
intron_variant | MODIFIER | c.-1+18065T>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203517046 | |||||||
| chr2:203517048 | TAAAG | T | 12 | a0001c0001t0009g0246 a0001c0001t0009g0249 a0001c0001t0009g0255 others(9): Show |
12 | HG00642.hp1 HG01358.hp2 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.-1+18059_-1+18062d others(6): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203517048 | |||||||
| chr2:203517049 | A | T | 35 | a0001c0003t0006g0252 a0001c0003t0006g0263 a0001c0003t0006g0274 others(32): Show |
35 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(32): Show |
intron_variant | MODIFIER | c.-1+18062T>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203517049 | |||||||
| chr2:203517282 | A | G | 2 | a0001c0002t0001g0023 a0001c0007t0001g0089 |
2 | HG01257.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.-1+17829T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203517282 | |||||||
| chr2:203517354 | A | C | 285 | a0001c0001t0001g0012 a0001c0001t0002g0111 a0001c0001t0002g0119 others(282): Show |
285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.-1+17757T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203517354 | |||||||
| chr2:203517359 | C | CA | 56 | a0001c0001t0002g0119 a0001c0001t0002g0154 a0001c0001t0002g0213 others(53): Show |
56 | HG00438.hp1 HG00621.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.-1+17751dupT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203517359 | |||||||
| chr2:203517359 | C | CAA | 7 | a0001c0003t0069g0163 a0001c0003t0070g0225 a0001c0007t0021g0162 others(4): Show |
7 | HG02055.hp2 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1+17750_-1+17751d others(4): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203517359 | |||||||
| chr2:203517617 | T | C | 2 | a0001c0003t0069g0163 a0001c0003t0070g0225 |
2 | HG02486.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-1+17494A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203517617 | |||||||
| chr2:203517648 | A | G | 1 | a0001c0007t0057g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-1+17463T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203517648 | |||||||
| chr2:203517987 | A | G | 1 | a0001c0002t0079g0159 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-1+17124T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203517987 | |||||||
| chr2:203518466 | C | T | 2 | a0001c0001t0003g0150 a0002c0005t0003g0135 |
2 | HG02735.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.-1+16645G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203518466 | |||||||
| chr2:203518539 | C | CA | 166 | a0001c0001t0002g0111 a0001c0001t0002g0129 a0001c0001t0002g0148 others(163): Show |
166 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.-1+16571dupT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203518539 | |||||||
| chr2:203518616 | C | T | 19 | a0001c0004t0005g0093 a0001c0004t0005g0095 a0001c0004t0005g0098 others(16): Show |
19 | HG00733.hp2 HG01109.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.-1+16495G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203518616 | |||||||
| chr2:203518707 | G | C | 19 | a0001c0004t0005g0093 a0001c0004t0005g0095 a0001c0004t0005g0098 others(16): Show |
19 | HG00733.hp2 HG01109.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.-1+16404C>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203518707 | |||||||
| chr2:203518709 | A | T | 19 | a0001c0004t0005g0093 a0001c0004t0005g0095 a0001c0004t0005g0098 others(16): Show |
19 | HG00733.hp2 HG01109.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.-1+16402T>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203518709 | |||||||
| chr2:203518796 | G | A | 1 | a0001c0001t0002g0213 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-1+16315C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203518796 | |||||||
| chr2:203518960 | T | C | 2 | a0001c0004t0034g0240 a0001c0029t0066g0219 |
2 | HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-1+16151A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203518960 | |||||||
| chr2:203519193 | GGAAAA | G | 34 | a0001c0003t0006g0263 a0001c0003t0006g0274 a0001c0003t0006g0276 others(31): Show |
34 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(31): Show |
intron_variant | MODIFIER | c.-1+15913_-1+15917d others(7): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203519193 | |||||||
| chr2:203519389 | T | A | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-1+15722A>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203519389 | |||||||
| chr2:203519501 | T | C | 1 | a0001c0001t0031g0199 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-1+15610A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203519501 | |||||||
| chr2:203519638 | T | C | 29 | a0001c0001t0001g0012 a0001c0001t0002g0119 a0001c0001t0003g0112 others(26): Show |
29 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.-1+15473A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203519638 | |||||||
| chr2:203519696 | T | C | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-1+15415A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203519696 | |||||||
| chr2:203519831 | G | A | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-1+15280C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203519831 | |||||||
| chr2:203519868 | A | G | 1 | a0002c0005t0003g0135 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-1+15243T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203519868 | |||||||
| chr2:203519960 | C | G | 1 | a0001c0007t0057g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-1+15151G>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203519960 | |||||||
| chr2:203520070 | G | C | 3 | a0001c0007t0021g0162 a0001c0007t0021g0220 a0002c0018t0021g0161 |
3 | HG02109.hp1 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-1+15041C>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203520070 | |||||||
| chr2:203520331 | C | CA | 130 | a0001c0001t0003g0139 a0001c0001t0008g0187 a0001c0001t0011g0020 others(127): Show |
130 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.-1+14779dupT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203520331 | |||||||
| chr2:203520331 | C | CAA | 17 | a0001c0003t0025g0280 a0001c0003t0025g0282 a0001c0003t0025g0283 others(14): Show |
17 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(14): Show |
intron_variant | MODIFIER | c.-1+14778_-1+14779d others(4): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203520331 | |||||||
| chr2:203520399 | G | A | 2 | a0001c0001t0032g0118 a0001c0001t0032g0142 |
2 | HG01167.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-1+14712C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203520399 | |||||||
| chr2:203520652 | G | C | 1 | a0001c0015t0044g0007 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-1+14459C>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203520652 | |||||||
| chr2:203520669 | T | C | 1 | a0002c0005t0012g0206 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-1+14442A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203520669 | |||||||
| chr2:203520715 | C | A | 19 | a0001c0004t0005g0093 a0001c0004t0005g0095 a0001c0004t0005g0098 others(16): Show |
19 | HG00733.hp2 HG01109.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.-1+14396G>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203520715 | |||||||
| chr2:203520743 | A | G | 1 | a0001c0004t0005g0103 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-1+14368T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203520743 | |||||||
| chr2:203520772 | T | C | 1 | a0001c0001t0013g0184 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-1+14339A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203520772 | |||||||
| chr2:203520793 | T | C | 2 | a0001c0001t0028g0065 a0001c0001t0028g0085 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-1+14318A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203520793 | |||||||
| chr2:203521086 | C | T | 3 | a0001c0002t0001g0028 a0001c0002t0001g0037 a0001c0002t0079g0159 |
3 | HG00140.hp1 HG01433.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-1+14025G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203521086 | |||||||
| chr2:203521636 | AAAC | A | 5 | a0001c0003t0006g0284 a0001c0003t0006g0288 a0001c0003t0093g0286 others(2): Show |
5 | HG02293.hp2 HG02559.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1+13472_-1+13474d others(5): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203521636 | |||||||
| chr2:203521732 | C | T | 1 | a0001c0001t0053g0144 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-1+13379G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203521732 | |||||||
| chr2:203521745 | A | G | 1 | a0001c0002t0033g0131 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-1+13366T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203521745 | |||||||
| chr2:203521803 | G | A | 1 | a0001c0002t0033g0202 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-1+13308C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203521803 | |||||||
| chr2:203521871 | G | C | 1 | a0001c0003t0097g0287 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-1+13240C>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203521871 | |||||||
| chr2:203521940 | T | C | 5 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0139 others(2): Show |
5 | HG01257.hp2 HG01258.hp1 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1+13171A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203521940 | |||||||
| chr2:203521983 | G | T | 1 | a0001c0001t0023g0207 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-1+13128C>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203521983 | |||||||
| chr2:203522072 | T | C | 2 | a0001c0004t0034g0240 a0001c0029t0066g0219 |
2 | HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-1+13039A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203522072 | |||||||
| chr2:203522107 | C | A | 1 | a0001c0007t0057g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-1+13004G>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203522107 | |||||||
| chr2:203522364 | T | C | 2 | a0001c0001t0046g0072 a0002c0006t0048g0084 |
2 | NA19001.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-1+12747A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203522364 | |||||||
| chr2:203522568 | A | C | 1 | a0001c0003t0092g0272 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-1+12543T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203522568 | |||||||
| chr2:203522652 | A | G | 2 | a0001c0007t0082g0260 a0002c0018t0083g0253 |
2 | HG02055.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.-1+12459T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203522652 | |||||||
| chr2:203522658 | T | C | 1 | a0001c0001t0012g0185 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-1+12453A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203522658 | |||||||
| chr2:203522759 | G | A | 89 | a0001c0001t0011g0020 a0001c0001t0011g0066 a0001c0001t0011g0067 others(86): Show |
89 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.-1+12352C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203522759 | |||||||
| chr2:203522771 | G | A | 2 | a0001c0002t0001g0009 a0002c0016t0001g0010 |
2 | NA19065.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.-1+12340C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203522771 | |||||||
| chr2:203522895 | C | CA | 6 | a0001c0001t0003g0139 a0001c0001t0008g0187 a0001c0001t0010g0064 others(3): Show |
6 | HG00597.hp2 HG02293.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1+12215dupT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203522895 | |||||||
| chr2:203522895 | CA | C | 33 | a0001c0001t0010g0061 a0001c0001t0028g0085 a0001c0001t0056g0134 others(30): Show |
33 | HG00733.hp2 HG01081.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.-1+12215delT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203522895 | |||||||
| chr2:203522895 | CAA | C | 119 | a0001c0001t0011g0020 a0001c0001t0011g0066 a0001c0001t0011g0067 others(116): Show |
119 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.-1+12214_-1+12215d others(4): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203522895 | |||||||
| chr2:203522912 | A | G | 1 | a0001c0002t0001g0088 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-1+12199T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203522912 | |||||||
| chr2:203522954 | T | C | 36 | a0001c0003t0006g0263 a0001c0003t0006g0274 a0001c0003t0006g0276 others(33): Show |
36 | HG00738.hp2 HG01884.hp1 HG01943.hp2 others(33): Show |
intron_variant | MODIFIER | c.-1+12157A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203522954 | |||||||
| chr2:203523286 | G | A | 1 | a0001c0002t0004g0200 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-1+11825C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203523286 | |||||||
| chr2:203523368 | G | T | 1 | a0001c0003t0095g0271 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-1+11743C>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203523368 | |||||||
| chr2:203523369 | G | A | 34 | a0001c0003t0006g0263 a0001c0003t0006g0274 a0001c0003t0006g0276 others(31): Show |
34 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(31): Show |
intron_variant | MODIFIER | c.-1+11742C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203523369 | |||||||
| chr2:203523392 | C | CA | 68 | a0001c0001t0002g0111 a0001c0001t0002g0129 a0001c0001t0002g0145 others(65): Show |
68 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.-1+11718dupT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203523392 | |||||||
| chr2:203523392 | C | CAA | 6 | a0001c0001t0008g0125 a0001c0001t0008g0187 a0001c0001t0012g0186 others(3): Show |
6 | HG00741.hp1 HG02027.hp2 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1+11717_-1+11718d others(4): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203523392 | |||||||
| chr2:203523407 | A | C | 1 | a0001c0002t0079g0159 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-1+11704T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203523407 | |||||||
| chr2:203523495 | A | G | 3 | a0001c0007t0021g0162 a0001c0007t0021g0220 a0002c0018t0021g0161 |
3 | HG02109.hp1 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-1+11616T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203523495 | |||||||
| chr2:203523772 | C | T | 34 | a0001c0003t0006g0263 a0001c0003t0006g0274 a0001c0003t0006g0276 others(31): Show |
34 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(31): Show |
intron_variant | MODIFIER | c.-1+11339G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203523772 | |||||||
| chr2:203523943 | G | A | 1 | a0001c0015t0044g0007 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-1+11168C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203523943 | |||||||
| chr2:203524168 | A | C | 1 | a0001c0002t0001g0083 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-1+10943T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203524168 | |||||||
| chr2:203524231 | C | T | 1 | a0001c0011t0003g0116 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-1+10880G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203524231 | |||||||
| chr2:203524357 | T | G | 2 | a0001c0007t0026g0005 a0001c0007t0026g0006 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-1+10754A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203524357 | |||||||
| chr2:203524455 | T | A | 56 | a0001c0001t0017g0126 a0001c0003t0006g0263 a0001c0003t0006g0274 others(53): Show |
56 | HG00733.hp2 HG00738.hp2 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.-1+10656A>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203524455 | |||||||
| chr2:203524497 | G | A | 1 | a0001c0002t0001g0056 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-1+10614C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203524497 | |||||||
| chr2:203524682 | C | T | 35 | a0001c0003t0006g0263 a0001c0003t0006g0274 a0001c0003t0006g0276 others(32): Show |
35 | HG00738.hp2 HG01884.hp1 HG01943.hp2 others(32): Show |
intron_variant | MODIFIER | c.-1+10429G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203524682 | |||||||
| chr2:203525144 | C | T | 1 | a0001c0029t0066g0219 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-1+9967G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203525144 | |||||||
| chr2:203525186 | C | G | 7 | a0001c0003t0069g0163 a0001c0003t0070g0225 a0001c0007t0021g0162 others(4): Show |
7 | HG02055.hp2 HG02109.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1+9925G>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203525186 | |||||||
| chr2:203525193 | T | A | 2 | a0001c0001t0002g0190 a0001c0001t0013g0214 |
2 | HG02280.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-1+9918A>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203525193 | |||||||
| chr2:203525331 | G | A | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-1+9780C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203525331 | |||||||
| chr2:203525428 | C | G | 1 | a0001c0002t0001g0051 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-1+9683G>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203525428 | |||||||
| chr2:203525491 | A | G | 1 | a0002c0012t0039g0270 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-1+9620T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203525491 | |||||||
| chr2:203525594 | C | T | 4 | a0001c0003t0036g0229 a0001c0003t0036g0230 a0001c0003t0076g0228 others(1): Show |
4 | HG02145.hp1 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+9517G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203525594 | |||||||
| chr2:203525823 | G | A | 2 | a0001c0001t0003g0150 a0002c0005t0003g0135 |
2 | HG02735.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.-1+9288C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203525823 | |||||||
| chr2:203525882 | G | A | 29 | a0001c0003t0006g0263 a0001c0003t0006g0274 a0001c0003t0006g0276 others(26): Show |
29 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(26): Show |
intron_variant | MODIFIER | c.-1+9229C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203525882 | |||||||
| chr2:203526018 | GAA | G | 34 | a0001c0003t0006g0263 a0001c0003t0006g0274 a0001c0003t0006g0276 others(31): Show |
34 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(31): Show |
intron_variant | MODIFIER | c.-1+9091_-1+9092del others(2): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203526018 | |||||||
| chr2:203526351 | C | G | 2 | a0001c0004t0005g0101 a0001c0004t0005g0102 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-1+8760G>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203526351 | |||||||
| chr2:203526405 | G | A | 2 | a0001c0007t0082g0260 a0002c0018t0083g0253 |
2 | HG02055.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.-1+8706C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203526405 | |||||||
| chr2:203526461 | A | G | 1 | a0001c0002t0004g0200 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-1+8650T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203526461 | |||||||
| chr2:203526595 | G | A | 1 | a0001c0002t0047g0022 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-1+8516C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203526595 | |||||||
| chr2:203526693 | C | T | 34 | a0001c0003t0006g0263 a0001c0003t0006g0274 a0001c0003t0006g0276 others(31): Show |
34 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(31): Show |
intron_variant | MODIFIER | c.-1+8418G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203526693 | |||||||
| chr2:203526706 | C | CA | 25 | a0001c0001t0002g0151 a0001c0001t0002g0191 a0001c0001t0002g0196 others(22): Show |
25 | HG00438.hp1 HG00642.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.-1+8404dupT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203526706 | |||||||
| chr2:203526706 | CA | C | 105 | a0001c0001t0002g0154 a0001c0001t0011g0020 a0001c0001t0011g0066 others(102): Show |
105 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.-1+8404delT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203526706 | |||||||
| chr2:203526706 | CAA | C | 6 | a0001c0007t0026g0005 a0001c0007t0026g0006 a0001c0007t0057g0237 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1+8403_-1+8404del others(2): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203526706 | |||||||
| chr2:203526742 | G | T | 1 | a0001c0001t0013g0173 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-1+8369C>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203526742 | |||||||
| chr2:203526790 | C | CT | 33 | a0001c0003t0006g0263 a0001c0003t0006g0274 a0001c0003t0006g0276 others(30): Show |
33 | HG00738.hp2 HG01943.hp2 HG02129.hp2 others(30): Show |
intron_variant | MODIFIER | c.-1+8320dupA | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203526790 | |||||||
| chr2:203526819 | C | G | 1 | a0001c0007t0068g0218 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-1+8292G>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203526819 | |||||||
| chr2:203526943 | C | T | 4 | a0001c0003t0036g0229 a0001c0003t0036g0230 a0001c0003t0076g0228 others(1): Show |
4 | HG02145.hp1 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+8168G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203526943 | |||||||
| chr2:203526972 | C | T | 1 | a0001c0007t0057g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-1+8139G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203526972 | |||||||
| chr2:203527035 | T | C | 1 | a0001c0007t0068g0218 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-1+8076A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203527035 | |||||||
| chr2:203527036 | G | A | 1 | a0001c0007t0068g0218 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-1+8075C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203527036 | |||||||
| chr2:203527049 | G | A | 1 | a0001c0007t0057g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-1+8062C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203527049 | |||||||
| chr2:203527113 | G | A | 1 | a0001c0001t0002g0196 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-1+7998C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203527113 | |||||||
| chr2:203527127 | T | C | 1 | a0001c0007t0057g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-1+7984A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203527127 | |||||||
| chr2:203527287 | C | T | 1 | a0001c0001t0009g0255 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-1+7824G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203527287 | |||||||
| chr2:203527351 | T | C | 1 | a0001c0002t0001g0027 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-1+7760A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203527351 | |||||||
| chr2:203527713 | T | C | 5 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0139 others(2): Show |
5 | HG01257.hp2 HG01258.hp1 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1+7398A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203527713 | |||||||
| chr2:203527727 | G | A | 2 | a0001c0004t0034g0235 a0001c0004t0051g0236 |
2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-1+7384C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203527727 | |||||||
| chr2:203527746 | G | C | 5 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0139 others(2): Show |
5 | HG01257.hp2 HG01258.hp1 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1+7365C>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203527746 | |||||||
| chr2:203527767 | T | C | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-1+7344A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203527767 | |||||||
| chr2:203527800 | C | CA | 30 | a0001c0001t0010g0063 a0001c0001t0012g0153 a0001c0001t0031g0199 others(27): Show |
30 | HG00673.hp2 HG00733.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.-1+7310dupT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203527800 | |||||||
| chr2:203527800 | CA | C | 8 | a0001c0001t0002g0203 a0001c0001t0008g0204 a0001c0001t0011g0066 others(5): Show |
8 | HG02451.hp2 HG02976.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1+7310delT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203527800 | |||||||
| chr2:203527800 | CAA | C | 33 | a0001c0003t0006g0263 a0001c0003t0006g0274 a0001c0003t0006g0276 others(30): Show |
33 | HG00738.hp2 HG01884.hp1 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.-1+7309_-1+7310del others(2): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203527800 | |||||||
| chr2:203527852 | C | T | 1 | a0001c0007t0057g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-1+7259G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203527852 | |||||||
| chr2:203528119 | A | G | 2 | a0001c0002t0001g0009 a0002c0016t0001g0010 |
2 | NA19065.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.-1+6992T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203528119 | |||||||
| chr2:203528294 | A | G | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-1+6817T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203528294 | |||||||
| chr2:203528907 | T | A | 1 | a0001c0007t0075g0227 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-1+6204A>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203528907 | |||||||
| chr2:203528979 | C | CTA | 6 | a0001c0001t0002g0154 a0001c0001t0010g0061 a0001c0001t0010g0062 others(3): Show |
6 | HG01081.hp1 HG02486.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1+6130_-1+6131dup others(2): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203528979 | |||||||
| chr2:203528979 | C | CTATA | 3 | a0001c0001t0017g0126 a0001c0001t0017g0193 a0001c0001t0017g0217 |
3 | HG02145.hp2 HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-1+6128_-1+6131dup others(4): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203528979 | |||||||
| chr2:203528979 | C | CTATATAT others(11): Show |
1 | a0001c0007t0026g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-1+6114_-1+6131dup others(18): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203528979 | |||||||
| chr2:203528979 | CTA | C | 45 | a0001c0001t0002g0203 a0001c0001t0003g0139 a0001c0001t0011g0020 others(42): Show |
45 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.-1+6130_-1+6131del others(2): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203528979 | |||||||
| chr2:203528979 | CTATA | C | 15 | a0001c0001t0001g0012 a0001c0001t0003g0112 a0001c0001t0003g0136 others(12): Show |
15 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.-1+6128_-1+6131del others(4): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203528979 | |||||||
| chr2:203528998 | TATATATA | T | 3 | a0001c0007t0021g0162 a0001c0007t0021g0220 a0002c0018t0021g0161 |
3 | HG02109.hp1 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-1+6106_-1+6112del others(7): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203528998 | |||||||
| chr2:203528999 | ATATATAT others(4): Show |
A | 2 | a0001c0004t0015g0094 a0002c0017t0015g0097 |
2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-1+6101_-1+6111del others(11): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203528999 | |||||||
| chr2:203529000 | TA | T | 3 | a0001c0001t0002g0182 a0001c0001t0053g0144 a0002c0006t0001g0054 |
3 | HG00673.hp1 HG03834.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-1+6110delT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529000 | |||||||
| chr2:203529001 | A | T | 1 | a0001c0001t0012g0153 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-1+6110T>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529001 | |||||||
| chr2:203529001 | ATATATTT others(3): Show |
A | 12 | a0001c0004t0005g0093 a0001c0004t0005g0095 a0001c0004t0005g0100 others(9): Show |
12 | HG00733.hp2 HG01109.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.-1+6100_-1+6109del others(10): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529001 | |||||||
| chr2:203529001 | ATATATTT others(4): Show |
A | 1 | a0001c0004t0005g0098 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-1+6099_-1+6109del others(11): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529001 | |||||||
| chr2:203529002 | TA | T | 3 | a0001c0001t0028g0085 a0001c0002t0001g0079 a0001c0002t0042g0003 |
3 | HG01109.hp1 HG02897.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.-1+6108delT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529002 | |||||||
| chr2:203529002 | TATA | T | 3 | a0001c0002t0001g0034 a0001c0002t0001g0076 a0002c0016t0020g0074 |
3 | NA18983.hp1 NA19010.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-1+6106_-1+6108del others(3): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529002 | |||||||
| chr2:203529003 | A | AT | 7 | a0001c0001t0002g0196 a0001c0001t0013g0184 a0001c0001t0013g0211 others(4): Show |
7 | HG00735.hp1 HG01175.hp1 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1+6107dupA | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529003 | |||||||
| chr2:203529003 | A | T | 18 | a0001c0001t0002g0182 a0001c0001t0008g0125 a0001c0001t0009g0247 others(15): Show |
18 | HG00597.hp2 HG00621.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.-1+6108T>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529003 | |||||||
| chr2:203529003 | ATAT | A | 7 | a0001c0001t0003g0179 a0001c0002t0001g0078 a0001c0002t0001g0087 others(4): Show |
7 | HG01169.hp1 HG02155.hp2 HG04204.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1+6105_-1+6107del others(3): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529003 | |||||||
| chr2:203529004 | TA | T | 10 | a0001c0001t0002g0148 a0001c0001t0002g0221 a0001c0001t0019g0081 others(7): Show |
10 | HG01071.hp1 HG01071.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.-1+6106delT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529004 | |||||||
| chr2:203529005 | A | AT | 6 | a0001c0001t0002g0151 a0001c0001t0008g0123 a0001c0001t0009g0257 others(3): Show |
6 | HG00323.hp1 HG02273.hp2 NA18906.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1+6105dupA | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529005 | |||||||
| chr2:203529005 | A | ATATATAT others(4): Show |
1 | a0001c0007t0026g0005 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-1+6105_-1+6106ins others(11): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529005 | |||||||
| chr2:203529005 | A | ATATATAT others(15): Show |
1 | a0001c0003t0006g0284 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-1+6105_-1+6106ins others(22): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529005 | |||||||
| chr2:203529005 | A | ATATATAT others(16): Show |
1 | a0007c0030t0006g0285 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-1+6105_-1+6106ins others(23): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529005 | |||||||
| chr2:203529005 | A | ATATATAT others(17): Show |
1 | a0001c0003t0094g0267 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-1+6105_-1+6106ins others(24): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529005 | |||||||
| chr2:203529005 | A | ATATATAT others(11): Show |
1 | a0002c0012t0039g0270 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-1+6105_-1+6106ins others(18): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529005 | |||||||
| chr2:203529005 | A | ATATATAT others(17): Show |
1 | a0001c0003t0006g0288 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-1+6105_-1+6106ins others(24): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529005 | |||||||
| chr2:203529005 | A | ATATATAT others(7): Show |
1 | a0001c0003t0093g0286 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-1+6105_-1+6106ins others(14): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529005 | |||||||
| chr2:203529005 | A | ATATATAT others(9): Show |
1 | a0001c0003t0039g0269 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-1+6105_-1+6106ins others(16): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529005 | |||||||
| chr2:203529005 | A | ATATATAT others(4): Show |
2 | a0001c0003t0103g0264 a0001c0007t0057g0237 |
2 | HG02109.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.-1+6105_-1+6106ins others(11): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529005 | |||||||
| chr2:203529005 | A | ATATATAT others(5): Show |
1 | a0001c0003t0092g0272 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-1+6105_-1+6106ins others(12): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529005 | |||||||
| chr2:203529005 | A | ATATATAT others(9): Show |
2 | a0001c0003t0078g0239 a0001c0003t0101g0277 |
2 | HG03130.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.-1+6105_-1+6106ins others(16): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529005 | |||||||
| chr2:203529005 | A | ATATATTT others(4): Show |
1 | a0001c0003t0025g0282 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-1+6105_-1+6106ins others(11): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529005 | |||||||
| chr2:203529005 | A | ATATATTT others(8): Show |
1 | a0001c0003t0006g0274 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-1+6105_-1+6106ins others(15): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529005 | |||||||
| chr2:203529005 | A | ATATATTT others(16): Show |
1 | a0001c0015t0044g0007 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-1+6105_-1+6106ins others(23): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529005 | |||||||
| chr2:203529005 | A | ATATTTTT others(4): Show |
5 | a0001c0003t0025g0280 a0001c0003t0025g0283 a0001c0003t0096g0279 others(2): Show |
5 | HG02129.hp2 NA18747.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1+6105_-1+6106ins others(11): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529005 | |||||||
| chr2:203529005 | A | ATATTTTT others(5): Show |
1 | a0002c0012t0099g0265 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-1+6105_-1+6106ins others(12): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529005 | |||||||
| chr2:203529005 | A | ATATTTTT others(7): Show |
1 | a0001c0003t0006g0276 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-1+6105_-1+6106ins others(14): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529005 | |||||||
| chr2:203529005 | A | ATATTTTT others(8): Show |
3 | a0001c0003t0006g0263 a0001c0003t0104g0275 a0004c0014t0108g0290 |
3 | HG02723.hp1 HG03540.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-1+6105_-1+6106ins others(15): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529005 | |||||||
| chr2:203529005 | A | ATATTTTT others(10): Show |
1 | a0002c0031t0105g0266 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-1+6105_-1+6106ins others(17): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529005 | |||||||
| chr2:203529005 | A | ATT | 10 | a0001c0001t0002g0111 a0001c0001t0008g0181 a0001c0001t0008g0187 others(7): Show |
10 | HG01081.hp2 HG02523.hp2 NA18945.hp2 others(7): Show |
intron_variant | MODIFIER | c.-1+6104_-1+6105dup others(2): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529005 | |||||||
| chr2:203529005 | A | ATTTTTTT others(4): Show |
1 | a0001c0003t0095g0271 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-1+6095_-1+6105dup others(11): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529005 | |||||||
| chr2:203529005 | A | ATTTTTTT others(9): Show |
1 | a0004c0014t0100g0278 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-1+6090_-1+6105dup others(16): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529005 | |||||||
| chr2:203529005 | A | ATTTTTTT others(10): Show |
1 | a0001c0003t0102g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-1+6089_-1+6105dup others(17): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529005 | |||||||
| chr2:203529005 | A | T | 67 | a0001c0001t0002g0129 a0001c0001t0002g0145 a0001c0001t0002g0146 others(64): Show |
67 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.-1+6106T>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529005 | |||||||
| chr2:203529005 | AT | A | 12 | a0001c0001t0012g0185 a0001c0001t0013g0173 a0001c0001t0065g0124 others(9): Show |
12 | HG01515.hp2 HG02622.hp2 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.-1+6105delA | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529005 | |||||||
| chr2:203529006 | T | TA | 5 | a0001c0001t0010g0064 a0001c0002t0004g0130 a0001c0002t0067g0201 others(2): Show |
5 | HG00280.hp1 HG00544.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1+6104_-1+6105ins others(1): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529006 | |||||||
| chr2:203529007 | T | A | 17 | a0001c0001t0002g0188 a0001c0001t0002g0190 a0001c0001t0002g0191 others(14): Show |
17 | HG00423.hp2 HG00609.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.-1+6104A>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529007 | |||||||
| chr2:203529008 | T | A | 7 | a0001c0001t0002g0195 a0001c0001t0010g0064 a0001c0001t0017g0194 others(4): Show |
7 | HG01515.hp2 HG01981.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1+6103A>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529008 | |||||||
| chr2:203529009 | T | A | 5 | a0001c0002t0004g0114 a0001c0002t0004g0132 a0001c0002t0004g0133 others(2): Show |
5 | HG01081.hp1 HG01258.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1+6102A>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529009 | |||||||
| chr2:203529010 | T | A | 3 | a0001c0002t0035g0115 a0001c0002t0035g0128 a0001c0002t0073g0165 |
3 | HG00733.hp1 HG01515.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-1+6101A>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529010 | |||||||
| chr2:203529011 | T | A | 2 | a0001c0002t0004g0132 a0001c0002t0004g0133 |
2 | HG01081.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-1+6100A>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529011 | |||||||
| chr2:203529013 | T | A | 1 | a0001c0002t0004g0133 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-1+6098A>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529013 | |||||||
| chr2:203529053 | T | C | 36 | a0001c0003t0006g0263 a0001c0003t0006g0274 a0001c0003t0006g0276 others(33): Show |
36 | HG00738.hp2 HG01884.hp1 HG01943.hp2 others(33): Show |
intron_variant | MODIFIER | c.-1+6058A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529053 | |||||||
| chr2:203529087 | C | T | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-1+6024G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529087 | |||||||
| chr2:203529089 | C | T | 1 | a0002c0005t0087g0254 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-1+6022G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529089 | |||||||
| chr2:203529104 | G | A | 6 | a0001c0001t0002g0155 a0001c0001t0002g0196 a0001c0001t0037g0250 others(3): Show |
6 | NA18945.hp2 NA18969.hp1 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1+6007C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529104 | |||||||
| chr2:203529274 | T | A | 1 | a0001c0007t0057g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-1+5837A>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529274 | |||||||
| chr2:203529295 | T | C | 1 | a0003c0009t0037g0259 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-1+5816A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529295 | |||||||
| chr2:203529513 | C | T | 156 | a0001c0001t0011g0020 a0001c0001t0011g0066 a0001c0001t0011g0067 others(153): Show |
156 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.-1+5598G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529513 | |||||||
| chr2:203529523 | G | C | 1 | a0001c0002t0007g0033 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-1+5588C>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529523 | |||||||
| chr2:203529689 | G | T | 1 | a0001c0001t0002g0129 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-1+5422C>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203529689 | |||||||
| chr2:203530207 | C | T | 2 | a0001c0004t0034g0240 a0001c0029t0066g0219 |
2 | HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-1+4904G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203530207 | |||||||
| chr2:203530391 | T | C | 1 | a0001c0001t0003g0156 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-1+4720A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203530391 | |||||||
| chr2:203530540 | A | T | 2 | a0001c0001t0028g0065 a0001c0001t0028g0085 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-1+4571T>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203530540 | |||||||
| chr2:203530563 | G | A | 1 | a0001c0001t0055g0157 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-1+4548C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203530563 | |||||||
| chr2:203530601 | A | G | 1 | a0001c0029t0066g0219 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-1+4510T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203530601 | |||||||
| chr2:203530733 | A | G | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-1+4378T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203530733 | |||||||
| chr2:203530875 | G | C | 1 | a0001c0004t0034g0235 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-1+4236C>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203530875 | |||||||
| chr2:203530891 | C | CA | 6 | a0001c0001t0086g0243 a0001c0002t0001g0083 a0001c0007t0057g0237 others(3): Show |
6 | HG01255.hp2 HG01884.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1+4219dupT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203530891 | |||||||
| chr2:203530891 | CA | C | 21 | a0001c0001t0003g0112 a0001c0004t0005g0093 a0001c0004t0005g0095 others(18): Show |
21 | HG00733.hp2 HG01109.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.-1+4219delT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203530891 | |||||||
| chr2:203531261 | G | C | 1 | a0001c0002t0004g0106 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-1+3850C>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203531261 | |||||||
| chr2:203531310 | C | T | 1 | a0001c0011t0002g0158 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-1+3801G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203531310 | |||||||
| chr2:203531401 | TA | T | 54 | a0001c0003t0006g0263 a0001c0003t0006g0274 a0001c0003t0006g0276 others(51): Show |
54 | HG00733.hp2 HG00738.hp2 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.-1+3709delT | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203531401 | |||||||
| chr2:203531890 | G | A | 1 | a0001c0004t0051g0236 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-1+3221C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203531890 | |||||||
| chr2:203532068 | C | T | 1 | a0001c0002t0035g0128 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-1+3043G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203532068 | |||||||
| chr2:203532478 | A | G | 1 | a0001c0002t0001g0036 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-1+2633T>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203532478 | |||||||
| chr2:203532559 | T | C | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-1+2552A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203532559 | |||||||
| chr2:203532660 | A | T | 1 | a0001c0001t0023g0197 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-1+2451T>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203532660 | |||||||
| chr2:203532892 | G | C | 1 | a0001c0003t0006g0252 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-1+2219C>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203532892 | |||||||
| chr2:203533044 | G | A | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-1+2067C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203533044 | |||||||
| chr2:203533167 | A | C | 1 | a0001c0001t0023g0197 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-1+1944T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203533167 | |||||||
| chr2:203533168 | C | A | 1 | a0001c0001t0023g0197 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-1+1943G>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203533168 | |||||||
| chr2:203533246 | C | T | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-1+1865G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203533246 | |||||||
| chr2:203533504 | C | T | 1 | a0002c0005t0029g0035 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-1+1607G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203533504 | |||||||
| chr2:203533592 | G | C | 1 | a0001c0026t0077g0238 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-1+1519C>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203533592 | |||||||
| chr2:203533658 | G | T | 1 | a0001c0033t0050g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-1+1453C>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203533658 | |||||||
| chr2:203533756 | C | T | 1 | a0001c0002t0001g0034 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-1+1355G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203533756 | |||||||
| chr2:203533927 | C | T | 1 | a0001c0026t0077g0238 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-1+1184G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203533927 | |||||||
| chr2:203533976 | A | C | 1 | a0001c0026t0077g0238 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-1+1135T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203533976 | |||||||
| chr2:203534367 | C | T | 1 | a0001c0007t0057g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-1+744G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203534367 | |||||||
| chr2:203534460 | T | C | 2 | a0001c0001t0031g0198 a0001c0001t0031g0199 |
2 | NA18999.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.-1+651A>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203534460 | |||||||
| chr2:203534508 | A | AC | 62 | a0001c0001t0002g0129 a0001c0001t0002g0145 a0001c0001t0002g0146 others(59): Show |
62 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.-1+602dupG | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203534508 | |||||||
| chr2:203534508 | A | ACC | 28 | a0001c0001t0001g0012 a0001c0001t0002g0119 a0001c0001t0003g0112 others(25): Show |
28 | HG00280.hp1 HG00408.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.-1+601_-1+602dupGG | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203534508 | |||||||
| chr2:203534508 | AC | A | 48 | a0001c0001t0002g0203 a0001c0001t0002g0213 a0001c0001t0008g0204 others(45): Show |
48 | HG00323.hp2 HG00408.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.-1+602delG | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203534508 | |||||||
| chr2:203534508 | ACC | A | 26 | a0001c0001t0002g0221 a0001c0001t0023g0224 a0001c0001t0028g0085 others(23): Show |
26 | HG00738.hp2 HG01081.hp2 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.-1+601_-1+602delGG | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203534508 | |||||||
| chr2:203534508 | ACCCC | A | 26 | a0001c0003t0006g0274 a0001c0003t0006g0276 a0001c0003t0006g0284 others(23): Show |
26 | HG02109.hp2 HG02129.hp2 HG02132.hp1 others(23): Show |
intron_variant | MODIFIER | c.-1+599_-1+602delGG others(2): Show |
RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203534508 | |||||||
| chr2:203534516 | C | A | 1 | a0001c0004t0034g0240 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1+595G>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203534516 | |||||||
| chr2:203534525 | A | C | 1 | a0001c0001t0002g0111 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-1+586T>G | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203534525 | |||||||
| chr2:203534593 | G | A | 1 | a0001c0003t0006g0288 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-1+518C>T | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203534593 | |||||||
| chr2:203534612 | T | G | 56 | a0001c0003t0006g0263 a0001c0003t0006g0274 a0001c0003t0006g0276 others(53): Show |
56 | HG00733.hp2 HG00738.hp2 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.-1+499A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203534612 | |||||||
| chr2:203534711 | C | T | 4 | a0001c0002t0004g0106 a0001c0002t0004g0107 a0001c0002t0004g0109 others(1): Show |
4 | HG00140.hp2 HG00735.hp2 HG00741.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1+400G>A | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203534711 | |||||||
| chr2:203535075 | T | G | 1 | a0001c0002t0001g0105 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-1+36A>C | RAPH1 | ENSG00000173166.18 | transcript | ENST00000319170.10 | protein_coding | 1/13 | chr2 | 203535075 |