Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5911 |
| ensemblid | ENSG00000125249.7 |
| hgncid | 9861 |
| symbol | RAP2A |
| name | RAP2A, member of RAS oncogene family |
| refseq_nuc | NM_021033.7 |
| refseq_prot | NP_066361.1 |
| ensembl_nuc | ENST00000245304.5 |
| ensembl_prot | ENSP00000245304.3 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 97434169 |
| end | 97469128 |
| strand | + |
| ver | v1.2 |
| region | chr13:97434169-97469128 |
| region5000 | chr13:97429169-97474128 |
| regionname0 | RAP2A_chr13_97434169_97469128 |
| regionname5000 | RAP2A_chr13_97429169_97474128 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 549 | 342 | 84 | 60 | 150 | 10 | 36 | RAP2A_chr13_97429169_97474128 | RAP2A | ATGCG others(544): Show |
chr13 | 97429169 | 97474128 | ||
| a0001c0002 | 0/0 | 549 | 2 | 0 | 0 | 2 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | ATGCG others(544): Show |
chr13 | 97429169 | 97474128 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5540 | 86 | 12 | 12 | 50 | 4 | 7 | RAP2A_chr13_97429169_97474128 | RAP2A | ACTGC others(5535): Show |
chr13 | 97429169 | 97474128 |
| a0001c0001t0002 | 0/0 | 5541 | 79 | 10 | 14 | 39 | 3 | 13 | RAP2A_chr13_97429169_97474128 | RAP2A | ACTGC others(5536): Show |
chr13 | 97429169 | 97474128 |
| a0001c0001t0003 | 0/1 | 5541 | 71 | 5 | 16 | 35 | 3 | 11 | RAP2A_chr13_97429169_97474128 | RAP2A | ACTGC others(5536): Show |
chr13 | 97429169 | 97474128 |
| a0001c0001t0004 | 0/0 | 5541 | 53 | 30 | 3 | 16 | 0 | 4 | RAP2A_chr13_97429169_97474128 | RAP2A | ACTGC others(5536): Show |
chr13 | 97429169 | 97474128 |
| a0001c0001t0005 | 0/0 | 5540 | 10 | 5 | 1 | 4 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | ACTGC others(5535): Show |
chr13 | 97429169 | 97474128 |
| a0001c0001t0006 | 0/0 | 5539 | 5 | 1 | 3 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | ACTGC others(5534): Show |
chr13 | 97429169 | 97474128 |
| a0001c0001t0007 | 0/0 | 5540 | 4 | 3 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | ACTGC others(5535): Show |
chr13 | 97429169 | 97474128 |
| a0001c0001t0008 | 0/0 | 5541 | 4 | 3 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | ACTGC others(5536): Show |
chr13 | 97429169 | 97474128 |
| a0001c0001t0009 | 0/0 | 5541 | 4 | 0 | 4 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | ACTGC others(5536): Show |
chr13 | 97429169 | 97474128 |
| a0001c0001t0010 | 0/0 | 5541 | 3 | 3 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | ACTGC others(5536): Show |
chr13 | 97429169 | 97474128 |
| a0001c0001t0011 | 0/0 | 5541 | 3 | 2 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | ACTGC others(5536): Show |
chr13 | 97429169 | 97474128 |
| a0001c0001t0012 | 0/0 | 5541 | 3 | 3 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | ACTGC others(5536): Show |
chr13 | 97429169 | 97474128 |
| a0001c0001t0013 | 0/0 | 5541 | 2 | 0 | 0 | 2 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | ACTGC others(5536): Show |
chr13 | 97429169 | 97474128 |
| a0001c0001t0014 | 0/0 | 5541 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | ACTGC others(5536): Show |
chr13 | 97429169 | 97474128 |
| a0001c0001t0015 | 0/0 | 5540 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | ACTGC others(5535): Show |
chr13 | 97429169 | 97474128 |
| a0001c0001t0016 | 0/0 | 5541 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | ACTGC others(5536): Show |
chr13 | 97429169 | 97474128 |
| a0001c0001t0017 | 0/0 | 5541 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | ACTGC others(5536): Show |
chr13 | 97429169 | 97474128 |
| a0001c0001t0018 | 0/0 | 5541 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | ACTGC others(5536): Show |
chr13 | 97429169 | 97474128 |
| a0001c0001t0019 | 0/0 | 5540 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | ACTGC others(5535): Show |
chr13 | 97429169 | 97474128 |
| a0001c0001t0020 | 0/0 | 5540 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | ACTGC others(5535): Show |
chr13 | 97429169 | 97474128 |
| a0001c0001t0021 | 0/0 | 5541 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | ACTGC others(5536): Show |
chr13 | 97429169 | 97474128 |
| a0001c0001t0022 | 0/0 | 5541 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | ACTGC others(5536): Show |
chr13 | 97429169 | 97474128 |
| a0001c0001t0023 | 0/0 | 5541 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | ACTGC others(5536): Show |
chr13 | 97429169 | 97474128 |
| a0001c0001t0024 | 0/0 | 5541 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | ACTGC others(5536): Show |
chr13 | 97429169 | 97474128 |
| a0001c0001t0025 | 0/0 | 5541 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | ACTGC others(5536): Show |
chr13 | 97429169 | 97474128 |
| a0001c0001t0026 | 0/0 | 5540 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | ACTGC others(5535): Show |
chr13 | 97429169 | 97474128 |
| a0001c0001t0027 | 0/0 | 5541 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | ACTGC others(5536): Show |
chr13 | 97429169 | 97474128 |
| a0001c0001t0028 | 0/0 | 5540 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | ACTGC others(5535): Show |
chr13 | 97429169 | 97474128 |
| a0001c0002t0003 | 0/0 | 5541 | 2 | 0 | 0 | 2 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | ACTGC others(5536): Show |
chr13 | 97429169 | 97474128 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 14 | 1 | 5 | 5 | 2 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0004 | 1/0 | 12 | 0 | 0 | 10 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0005 | 0/0 | 11 | 3 | 1 | 6 | 1 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0025 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0003 | 0/0 | 13 | 1 | 5 | 4 | 2 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0006 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0011 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0019 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0020 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0003g0001 | 0/0 | 26 | 1 | 7 | 16 | 0 | 2 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0003g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0003g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0003g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0003g0023 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0003g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0003g0033 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0003g0034 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0003g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0003g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0004g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0004g0007 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0004g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0004g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0004g0014 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0004g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0004g0024 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0004g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0004g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0004g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0004g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0004g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0005g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0005g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0005g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0005g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0005g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0005g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0006g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0006g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0006g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0006g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0006g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0007g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0007g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0007g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0008g0041 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0008g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0009g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0009g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0010g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0010g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0010g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0011g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0011g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0011g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0012g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0012g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0012g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0013g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0013g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0014g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0015g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0016g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0017g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0018g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0019g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0020g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0021g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0022g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0023g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0024g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0025g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0026g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0027g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0001t0028g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| a0001c0002t0003g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0091 | EUR | GBR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | FIN | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | CHS | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0123 | EAS | CHS | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | CHS | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | CHS | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | CHS | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG00438 | hp2 | a0001 | c0001 | t0013 | g0001 | EAS | CHS | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG00544 | hp2 | a0001 | c0001 | t0005 | g0013 | EAS | CHS | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | CHS | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0129 | EAS | CHS | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | CHS | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG00639 | hp2 | a0001 | c0001 | t0026 | g0105 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG00642 | hp1 | a0001 | c0001 | t0006 | g0014 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | CHS | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG00735 | hp2 | a0001 | c0001 | t0006 | g0139 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0023 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG00741 | hp2 | a0001 | c0001 | t0006 | g0120 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0066 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0023 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0023 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0136 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01106 | hp2 | a0001 | c0001 | t0025 | g0114 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0039 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0024 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01192 | hp1 | a0001 | c0001 | t0007 | g0154 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01192 | hp2 | a0001 | c0001 | t0008 | g0041 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0095 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01243 | hp2 | a0001 | c0001 | t0011 | g0144 | AMR | PUR | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | CLM | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0032 | AMR | CLM | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0106 | AMR | CLM | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01361 | hp2 | a0001 | c0001 | t0020 | g0005 | AMR | CLM | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0045 | EUR | IBS | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0033 | EUR | IBS | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0135 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01884 | hp2 | a0001 | c0001 | t0027 | g0137 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0039 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01891 | hp2 | a0001 | c0001 | t0010 | g0160 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01928 | hp1 | a0001 | c0001 | t0009 | g0021 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01943 | hp1 | a0001 | c0001 | t0009 | g0118 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01975 | hp2 | a0001 | c0001 | t0028 | g0017 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01981 | hp1 | a0001 | c0001 | t0004 | g0087 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02027 | hp1 | a0001 | c0001 | t0014 | g0003 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02027 | hp2 | a0001 | c0001 | t0023 | g0134 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0031 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0085 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0037 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0132 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02083 | hp1 | a0001 | c0001 | t0024 | g0109 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0111 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0110 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CDX | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CDX | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02257 | hp1 | a0001 | c0001 | t0011 | g0057 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0058 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02273 | hp2 | a0001 | c0001 | t0009 | g0021 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02280 | hp1 | a0001 | c0001 | t0011 | g0141 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0138 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02293 | hp2 | a0001 | c0001 | t0009 | g0021 | AMR | PEL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02622 | hp1 | a0001 | c0001 | t0010 | g0099 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0090 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02630 | hp1 | a0001 | c0001 | t0012 | g0163 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0147 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0042 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0098 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02723 | hp1 | a0001 | c0001 | t0012 | g0162 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0042 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0130 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0034 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0112 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0088 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0086 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0150 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0159 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0038 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0038 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0036 | AFR | ESN | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0153 | AFR | ESN | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0140 | AFR | ESN | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | ESN | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02976 | hp1 | a0001 | c0001 | t0022 | g0149 | AFR | ESN | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02976 | hp2 | a0001 | c0001 | t0008 | g0043 | AFR | ESN | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0032 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | MSL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03098 | hp2 | a0001 | c0001 | t0018 | g0161 | AFR | MSL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0158 | AFR | ESN | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03130 | hp2 | a0001 | c0001 | t0010 | g0100 | AFR | ESN | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | ESN | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03139 | hp2 | a0001 | c0001 | t0017 | g0148 | AFR | ESN | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03195 | hp1 | a0001 | c0001 | t0019 | g0165 | AFR | ESN | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03195 | hp2 | a0001 | c0001 | t0015 | g0097 | AFR | ESN | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0055 | AFR | MSL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0093 | AFR | MSL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0101 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | MSL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | MSL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0155 | AFR | MSL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0035 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0035 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0024 | AFR | ESN | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0089 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0152 | AFR | MSL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0077 | AFR | MSL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0081 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | STU | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0092 | SAS | STU | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0013 | SAS | BEB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0018 | SAS | BEB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0103 | SAS | BEB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0007 | SAS | BEB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | BEB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0133 | SAS | BEB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0051 | SAS | STU | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG04115 | hp2 | a0001 | c0001 | t0021 | g0083 | SAS | STU | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | BEB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0052 | SAS | BEB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0033 | SAS | STU | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0076 | SAS | STU | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0030 | AFR | YRI | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | YRI | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | CHB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | CHB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0127 | EAS | CHB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | CHB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18906 | hp1 | a0001 | c0001 | t0008 | g0043 | AFR | YRI | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0017 | AFR | YRI | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18944 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18959 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18963 | hp1 | a0001 | c0001 | t0004 | g0121 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18977 | hp1 | a0001 | c0001 | t0013 | g0107 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18998 | hp2 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19003 | hp1 | a0001 | c0001 | t0005 | g0125 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | LWK | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19043 | hp2 | a0001 | c0001 | t0016 | g0008 | AFR | LWK | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19056 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0128 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19058 | hp1 | a0001 | c0001 | t0005 | g0044 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19060 | hp2 | a0001 | c0001 | t0004 | g0126 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19062 | hp1 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19072 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19074 | hp1 | a0001 | c0001 | t0006 | g0026 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19075 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ASW | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA20129 | hp2 | a0001 | c0001 | t0012 | g0164 | AFR | ASW | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0115 | EUR | TSI | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0102 | EUR | TSI | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | TSI | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0071 | SAS | GIH | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0117 | SAS | GIH | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0017 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0096 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | ACB | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0031 | AFR | MSL | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0119 | AFR | USA | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0030 | AFR | USA | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA20300 | hp1 | a0001 | c0001 | t0008 | g0041 | AFR | USA | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | USA | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0108 | AFR | LWK | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | LWK | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0034 | REF | REF | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0004 | REF | REF | RAP2A_chr13_97429169_97474128 | RAP2A | chr13 | 97429169 | 97474128 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:97434740 | C | T | 1 | a0001c0002 | 2 | NA18944.hp2 NA19072.hp2 |
synonymous_variant | LOW | c.270C>T | p.Phe90Phe | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/2 | 572/5540 | 270/552 | 90/183 | chr13 | 97434740 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:97434249 | G | A | 1 | a0001c0001t0014 | 1 | HG02027.hp1 | 5_prime_UTR_variant | MODIFIER | c.-222G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/2 | 222 | chr13 | 97434249 | ||||||
| chr13:97464501 | C | T | 1 | a0001c0001t0012 | 3 | HG02630.hp1 HG02723.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*59C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 59 | chr13 | 97464501 | ||||||
| chr13:97464506 | A | C | 1 | a0001c0001t0028 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*64A>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 64 | chr13 | 97464506 | ||||||
| chr13:97464683 | C | G | 1 | a0001c0001t0027 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*241C>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 241 | chr13 | 97464683 | ||||||
| chr13:97464910 | A | G | 9 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0009 others(6): Show |
161 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*468A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 468 | chr13 | 97464910 | ||||||
| chr13:97465535 | G | A | 1 | a0001c0001t0010 | 3 | HG01891.hp2 HG02622.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1093G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1093 | chr13 | 97465535 | ||||||
| chr13:97465680 | C | G | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1238C>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1238 | chr13 | 97465680 | ||||||
| chr13:97465698 | T | C | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1256T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1256 | chr13 | 97465698 | ||||||
| chr13:97465704 | A | G | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1262A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1262 | chr13 | 97465704 | ||||||
| chr13:97465709 | G | A | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1267G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1267 | chr13 | 97465709 | ||||||
| chr13:97465710 | C | G | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1268C>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1268 | chr13 | 97465710 | ||||||
| chr13:97465712 | C | G | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1270C>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1270 | chr13 | 97465712 | ||||||
| chr13:97465716 | C | G | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1274C>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1274 | chr13 | 97465716 | ||||||
| chr13:97465718 | C | T | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1276C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1276 | chr13 | 97465718 | ||||||
| chr13:97465726 | T | A | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1284T>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1284 | chr13 | 97465726 | ||||||
| chr13:97465727 | T | G | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1285T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1285 | chr13 | 97465727 | ||||||
| chr13:97465732 | T | A | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1290T>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1290 | chr13 | 97465732 | ||||||
| chr13:97465733 | T | G | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1291T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1291 | chr13 | 97465733 | ||||||
| chr13:97465734 | T | G | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1292T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1292 | chr13 | 97465734 | ||||||
| chr13:97465735 | C | T | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1293C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1293 | chr13 | 97465735 | ||||||
| chr13:97465736 | A | C | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1294A>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1294 | chr13 | 97465736 | ||||||
| chr13:97465745 | A | C | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1303A>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1303 | chr13 | 97465745 | ||||||
| chr13:97465752 | T | C | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1310T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1310 | chr13 | 97465752 | ||||||
| chr13:97465753 | A | C | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1311A>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1311 | chr13 | 97465753 | ||||||
| chr13:97465756 | A | T | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1314A>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1314 | chr13 | 97465756 | ||||||
| chr13:97465757 | T | A | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1315T>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1315 | chr13 | 97465757 | ||||||
| chr13:97465780 | A | C | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1338A>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1338 | chr13 | 97465780 | ||||||
| chr13:97465784 | C | T | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1342C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1342 | chr13 | 97465784 | ||||||
| chr13:97465791 | A | T | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1349A>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1349 | chr13 | 97465791 | ||||||
| chr13:97465798 | T | G | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1356T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1356 | chr13 | 97465798 | ||||||
| chr13:97465822 | T | A | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1380T>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1380 | chr13 | 97465822 | ||||||
| chr13:97465830 | C | A | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1388C>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1388 | chr13 | 97465830 | ||||||
| chr13:97465836 | T | C | 1 | a0001c0001t0023 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1394T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1394 | chr13 | 97465836 | ||||||
| chr13:97465853 | A | G | 1 | a0001c0001t0013 | 2 | HG00438.hp2 NA18977.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1411A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1411 | chr13 | 97465853 | ||||||
| chr13:97465900 | C | A | 1 | a0001c0001t0015 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1458C>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1458 | chr13 | 97465900 | ||||||
| chr13:97466086 | A | G | 1 | a0001c0001t0022 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1644A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1644 | chr13 | 97466086 | ||||||
| chr13:97466209 | GA | G | 4 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0015 others(1): Show |
17 | HG00544.hp2 HG00639.hp2 HG00642.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1781delA | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1781 | INFO_REALIGN_3_PRIME | chr13 | 97466209 | |||||
| chr13:97466290 | C | T | 1 | a0001c0001t0027 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1848C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 1848 | chr13 | 97466290 | ||||||
| chr13:97466451 | T | C | 1 | a0001c0001t0016 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2009T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 2009 | chr13 | 97466451 | ||||||
| chr13:97466675 | T | C | 2 | a0001c0001t0017 a0001c0001t0022 |
2 | HG02976.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2233T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 2233 | chr13 | 97466675 | ||||||
| chr13:97466974 | G | A | 1 | a0001c0001t0018 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2532G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 2532 | chr13 | 97466974 | ||||||
| chr13:97467270 | T | C | 3 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0014 |
84 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*2828T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 2828 | chr13 | 97467270 | ||||||
| chr13:97467588 | AT | A | 3 | a0001c0001t0007 a0001c0001t0019 a0001c0001t0028 |
6 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3153delT | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 3153 | INFO_REALIGN_3_PRIME | chr13 | 97467588 | |||||
| chr13:97467677 | C | CT | 26 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(23): Show |
251 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(248): Show |
3_prime_UTR_variant | MODIFIER | c.*3246dupT | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 3247 | INFO_REALIGN_3_PRIME | chr13 | 97467677 | |||||
| chr13:97467678 | T | C | 1 | a0001c0001t0020 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3236T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 3236 | chr13 | 97467678 | ||||||
| chr13:97467767 | T | C | 1 | a0001c0001t0024 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3325T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 3325 | chr13 | 97467767 | ||||||
| chr13:97467986 | A | C | 1 | a0001c0001t0009 | 4 | HG01928.hp1 HG01943.hp1 HG02273.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3544A>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 3544 | chr13 | 97467986 | ||||||
| chr13:97468059 | T | C | 1 | a0001c0001t0021 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3617T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 3617 | chr13 | 97468059 | ||||||
| chr13:97468391 | C | T | 2 | a0001c0001t0011 a0001c0001t0027 |
4 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3949C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 3949 | chr13 | 97468391 | ||||||
| chr13:97468394 | A | T | 1 | a0001c0001t0008 | 4 | HG01192.hp2 HG02976.hp2 NA18906.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3952A>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 3952 | chr13 | 97468394 | ||||||
| chr13:97468461 | A | T | 3 | a0001c0001t0007 a0001c0001t0019 a0001c0001t0028 |
6 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4019A>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 4019 | chr13 | 97468461 | ||||||
| chr13:97468551 | G | A | 1 | a0001c0001t0025 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4109G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 4109 | chr13 | 97468551 | ||||||
| chr13:97468962 | C | T | 1 | a0001c0001t0019 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4520C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 4520 | chr13 | 97468962 | ||||||
| chr13:97468993 | G | A | 1 | a0001c0001t0019 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4551G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 4551 | chr13 | 97468993 | ||||||
| chr13:97469117 | T | G | 1 | a0001c0001t0018 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4675T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 2/2 | 4675 | chr13 | 97469117 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:97434801 | G | A | 1 | a0001c0001t0003g0049 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.314+17G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97434801 | |||||||
| chr13:97434842 | T | C | 168 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(165): Show |
279 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.314+58T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97434842 | |||||||
| chr13:97434844 | G | T | 1 | a0001c0001t0019g0165 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.314+60G>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97434844 | |||||||
| chr13:97434911 | A | G | 3 | a0001c0001t0012g0162 a0001c0001t0012g0163 a0001c0001t0012g0164 |
3 | HG02630.hp1 HG02723.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.314+127A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97434911 | |||||||
| chr13:97435183 | A | C | 1 | a0001c0001t0018g0161 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.314+399A>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97435183 | |||||||
| chr13:97435465 | C | CA | 57 | a0001c0001t0001g0025 a0001c0001t0001g0045 a0001c0001t0001g0046 others(54): Show |
107 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.314+703dupA | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97435465 | ||||||
| chr13:97435465 | C | CAA | 9 | a0001c0001t0002g0050 a0001c0001t0002g0051 a0001c0001t0002g0052 others(6): Show |
10 | HG00558.hp1 HG00621.hp2 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.314+702_314+703dup others(2): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97435465 | ||||||
| chr13:97435465 | CA | C | 9 | a0001c0001t0001g0016 a0001c0001t0001g0181 a0001c0001t0001g0182 others(6): Show |
12 | HG01943.hp2 HG02148.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.314+703delA | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97435465 | ||||||
| chr13:97435465 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0010g0160 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.314+692_314+703del others(12): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97435465 | ||||||
| chr13:97435540 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.314+756A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97435540 | |||||||
| chr13:97435641 | G | A | 1 | a0001c0001t0003g0092 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.314+857G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97435641 | |||||||
| chr13:97435724 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.314+940A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97435724 | |||||||
| chr13:97436268 | T | TA | 6 | a0001c0001t0001g0094 a0001c0001t0004g0008 a0001c0001t0004g0058 others(3): Show |
9 | HG02257.hp1 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.314+1487dupA | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97436268 | ||||||
| chr13:97436454 | A | G | 1 | a0001c0001t0002g0056 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.314+1670A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97436454 | |||||||
| chr13:97436507 | C | G | 6 | a0001c0001t0007g0017 a0001c0001t0007g0154 a0001c0001t0007g0155 others(3): Show |
7 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.314+1723C>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97436507 | |||||||
| chr13:97436517 | G | T | 1 | a0001c0001t0019g0165 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.314+1733G>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97436517 | |||||||
| chr13:97436790 | C | T | 1 | a0001c0001t0004g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.314+2006C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97436790 | |||||||
| chr13:97436881 | C | T | 1 | a0001c0001t0002g0091 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.314+2097C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97436881 | |||||||
| chr13:97436962 | A | G | 6 | a0001c0001t0007g0017 a0001c0001t0007g0154 a0001c0001t0007g0155 others(3): Show |
7 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.314+2178A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97436962 | |||||||
| chr13:97436990 | C | T | 4 | a0001c0001t0002g0089 a0001c0001t0002g0090 a0001c0001t0004g0088 others(1): Show |
4 | HG02622.hp2 HG02809.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+2206C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97436990 | |||||||
| chr13:97436994 | C | G | 1 | a0001c0001t0007g0155 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.314+2210C>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97436994 | |||||||
| chr13:97437155 | T | C | 1 | a0001c0001t0004g0093 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.314+2371T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97437155 | |||||||
| chr13:97437171 | A | G | 2 | a0001c0001t0001g0048 a0001c0001t0001g0179 |
3 | HG02132.hp1 NA18993.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.314+2387A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97437171 | |||||||
| chr13:97437383 | ATGCT | A | 6 | a0001c0001t0004g0096 a0001c0001t0005g0030 a0001c0001t0005g0031 others(3): Show |
8 | HG01243.hp1 HG02055.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.314+2605_314+2608d others(6): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97437383 | ||||||
| chr13:97437561 | GT | G | 3 | a0001c0001t0010g0099 a0001c0001t0010g0100 a0001c0001t0010g0160 |
3 | HG01891.hp2 HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.314+2778delT | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97437561 | |||||||
| chr13:97438510 | AGACCTTA others(5): Show |
A | 2 | a0001c0001t0004g0044 a0001c0001t0005g0044 |
2 | NA18947.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.314+3733_314+3744d others(14): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97438510 | ||||||
| chr13:97438695 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.314+3911C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97438695 | |||||||
| chr13:97438754 | T | C | 81 | a0001c0001t0001g0082 a0001c0001t0002g0003 a0001c0001t0002g0006 others(78): Show |
155 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.314+3970T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97438754 | |||||||
| chr13:97438858 | A | T | 1 | a0001c0001t0008g0043 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.314+4074A>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97438858 | |||||||
| chr13:97439074 | A | C | 1 | a0001c0001t0002g0091 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.314+4290A>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97439074 | |||||||
| chr13:97439214 | T | G | 1 | a0001c0001t0001g0179 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.314+4430T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97439214 | |||||||
| chr13:97439224 | T | A | 3 | a0001c0001t0001g0166 a0001c0001t0001g0169 a0001c0001t0001g0170 |
3 | HG00673.hp1 NA18969.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.314+4440T>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97439224 | |||||||
| chr13:97439364 | G | A | 1 | a0001c0001t0002g0059 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.314+4580G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97439364 | |||||||
| chr13:97439425 | G | GGAATGTT others(5): Show |
6 | a0001c0001t0007g0017 a0001c0001t0007g0154 a0001c0001t0007g0155 others(3): Show |
7 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.314+4647_314+4658d others(14): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97439425 | ||||||
| chr13:97439531 | A | T | 1 | a0001c0001t0004g0042 | 2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.314+4747A>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97439531 | |||||||
| chr13:97439671 | G | C | 1 | a0001c0001t0002g0060 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.314+4887G>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97439671 | |||||||
| chr13:97439780 | G | T | 3 | a0001c0001t0001g0047 a0001c0001t0001g0177 a0001c0001t0001g0178 |
4 | HG02258.hp2 HG02615.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+4996G>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97439780 | |||||||
| chr13:97440129 | CT | C | 17 | a0001c0001t0001g0013 a0001c0001t0001g0131 a0001c0001t0004g0007 others(14): Show |
23 | HG00544.hp2 HG00609.hp2 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.314+5346delT | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97440129 | |||||||
| chr13:97440209 | G | A | 2 | a0001c0001t0003g0032 a0001c0001t0003g0101 |
3 | HG01346.hp2 HG03017.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.314+5425G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97440209 | |||||||
| chr13:97440408 | C | G | 1 | a0001c0001t0005g0098 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.314+5624C>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97440408 | |||||||
| chr13:97440499 | T | G | 4 | a0001c0001t0007g0017 a0001c0001t0007g0154 a0001c0001t0007g0155 others(1): Show |
5 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.314+5715T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97440499 | |||||||
| chr13:97440502 | T | C | 1 | a0001c0001t0001g0084 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.314+5718T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97440502 | |||||||
| chr13:97440615 | G | A | 6 | a0001c0001t0007g0017 a0001c0001t0007g0154 a0001c0001t0007g0155 others(3): Show |
7 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.314+5831G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97440615 | |||||||
| chr13:97440629 | CT | C | 4 | a0001c0001t0007g0017 a0001c0001t0007g0154 a0001c0001t0007g0155 others(1): Show |
5 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.314+5852delT | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97440629 | ||||||
| chr13:97440696 | T | C | 1 | a0001c0001t0004g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.314+5912T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97440696 | |||||||
| chr13:97440778 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.314+5994A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97440778 | |||||||
| chr13:97440806 | CCATT | C | 2 | a0001c0001t0008g0041 a0001c0001t0008g0043 |
4 | HG01192.hp2 HG02976.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+6043_314+6046d others(6): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97440806 | ||||||
| chr13:97441172 | G | A | 1 | a0001c0001t0019g0165 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.314+6388G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97441172 | |||||||
| chr13:97441172 | G | C | 1 | a0001c0001t0002g0050 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.314+6388G>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97441172 | |||||||
| chr13:97441618 | T | G | 1 | a0001c0001t0001g0169 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.314+6834T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97441618 | |||||||
| chr13:97441752 | C | T | 1 | a0001c0001t0019g0165 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.314+6968C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97441752 | |||||||
| chr13:97441767 | G | A | 1 | a0001c0001t0005g0125 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.314+6983G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97441767 | |||||||
| chr13:97441832 | G | A | 1 | a0001c0001t0003g0102 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.314+7048G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97441832 | |||||||
| chr13:97442314 | T | C | 1 | a0001c0001t0004g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.314+7530T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97442314 | |||||||
| chr13:97442348 | C | A | 1 | a0001c0001t0006g0135 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.314+7564C>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97442348 | |||||||
| chr13:97442392 | A | G | 1 | a0001c0001t0003g0124 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.314+7608A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97442392 | |||||||
| chr13:97442414 | A | G | 1 | a0001c0001t0012g0164 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.314+7630A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97442414 | |||||||
| chr13:97442669 | C | G | 1 | a0001c0001t0003g0035 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.314+7885C>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97442669 | |||||||
| chr13:97442675 | A | G | 1 | a0001c0001t0004g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.314+7891A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97442675 | |||||||
| chr13:97442710 | A | G | 2 | a0001c0001t0002g0011 a0001c0001t0002g0081 |
5 | HG00642.hp2 HG01070.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+7926A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97442710 | |||||||
| chr13:97443439 | G | A | 17 | a0001c0001t0001g0013 a0001c0001t0001g0131 a0001c0001t0004g0007 others(14): Show |
23 | HG00544.hp2 HG00609.hp2 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.314+8655G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97443439 | |||||||
| chr13:97443445 | C | T | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | NA18985.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.314+8661C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97443445 | |||||||
| chr13:97443448 | C | T | 3 | a0001c0001t0004g0015 a0001c0001t0004g0150 a0001c0001t0004g0153 |
6 | HG02895.hp2 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.314+8664C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97443448 | |||||||
| chr13:97443511 | C | G | 1 | a0001c0001t0023g0134 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.314+8727C>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97443511 | |||||||
| chr13:97443575 | A | G | 1 | a0001c0001t0003g0123 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.314+8791A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97443575 | |||||||
| chr13:97443727 | T | C | 1 | a0001c0001t0002g0009 | 4 | NA18964.hp2 NA18965.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+8943T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97443727 | |||||||
| chr13:97443872 | T | G | 1 | a0001c0001t0002g0061 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.314+9088T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97443872 | |||||||
| chr13:97443937 | G | A | 1 | a0001c0001t0018g0161 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.314+9153G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97443937 | |||||||
| chr13:97444014 | A | T | 1 | a0001c0001t0022g0149 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.314+9230A>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97444014 | |||||||
| chr13:97444166 | C | T | 1 | a0001c0001t0001g0178 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.314+9382C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97444166 | |||||||
| chr13:97444167 | G | A | 3 | a0001c0001t0003g0036 a0001c0001t0003g0085 a0001c0001t0003g0136 |
4 | HG01106.hp1 HG02055.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+9383G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97444167 | |||||||
| chr13:97444197 | G | A | 1 | a0001c0001t0002g0062 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.314+9413G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97444197 | |||||||
| chr13:97444234 | A | G | 1 | a0001c0001t0019g0165 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.314+9450A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97444234 | |||||||
| chr13:97444348 | TTTG | T | 38 | a0001c0001t0002g0018 a0001c0001t0002g0027 a0001c0001t0003g0001 others(35): Show |
74 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.314+9567_314+9569d others(5): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97444348 | ||||||
| chr13:97444628 | G | A | 39 | a0001c0001t0001g0082 a0001c0001t0002g0003 a0001c0001t0002g0006 others(36): Show |
77 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.314+9844G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97444628 | |||||||
| chr13:97444633 | A | C | 7 | a0001c0001t0002g0006 a0001c0001t0002g0022 a0001c0001t0002g0050 others(4): Show |
17 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(14): Show |
intron_variant | MODIFIER | c.314+9849A>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97444633 | |||||||
| chr13:97444770 | G | T | 102 | a0001c0001t0001g0082 a0001c0001t0002g0003 a0001c0001t0002g0006 others(99): Show |
183 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.314+9986G>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97444770 | |||||||
| chr13:97444830 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.314+10046A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97444830 | |||||||
| chr13:97444874 | A | C | 8 | a0001c0001t0001g0146 a0001c0001t0004g0096 a0001c0001t0004g0158 others(5): Show |
10 | HG01243.hp1 HG02055.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.314+10090A>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97444874 | |||||||
| chr13:97445026 | A | G | 6 | a0001c0001t0007g0017 a0001c0001t0007g0154 a0001c0001t0007g0155 others(3): Show |
7 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.314+10242A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97445026 | |||||||
| chr13:97445134 | A | G | 1 | a0001c0001t0001g0145 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.314+10350A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97445134 | |||||||
| chr13:97445138 | C | A | 1 | a0001c0001t0003g0103 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.314+10354C>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97445138 | |||||||
| chr13:97445142 | G | A | 3 | a0001c0001t0003g0012 a0001c0001t0003g0063 a0001c0001t0003g0157 |
6 | NA18946.hp2 NA18960.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.314+10358G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97445142 | |||||||
| chr13:97445464 | T | C | 1 | a0001c0001t0004g0037 | 2 | HG02074.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.314+10680T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97445464 | |||||||
| chr13:97445724 | C | T | 1 | a0001c0001t0018g0161 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.314+10940C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97445724 | |||||||
| chr13:97445898 | C | T | 2 | a0001c0001t0002g0053 a0001c0001t0002g0078 |
2 | NA18947.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.314+11114C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97445898 | |||||||
| chr13:97445930 | A | C | 1 | a0001c0001t0011g0144 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.314+11146A>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97445930 | |||||||
| chr13:97446114 | C | G | 1 | a0001c0001t0008g0043 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.314+11330C>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97446114 | |||||||
| chr13:97446270 | T | C | 23 | a0001c0001t0001g0013 a0001c0001t0001g0131 a0001c0001t0004g0007 others(20): Show |
29 | HG00544.hp2 HG00609.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.314+11486T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97446270 | |||||||
| chr13:97446684 | T | C | 1 | a0001c0001t0004g0086 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.314+11900T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97446684 | |||||||
| chr13:97446703 | G | A | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | NA18985.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.314+11919G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97446703 | |||||||
| chr13:97446728 | G | A | 19 | a0001c0001t0001g0013 a0001c0001t0001g0131 a0001c0001t0004g0007 others(16): Show |
25 | HG00544.hp2 HG00609.hp2 HG02027.hp2 others(22): Show |
intron_variant | MODIFIER | c.314+11944G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97446728 | |||||||
| chr13:97446992 | C | T | 1 | a0001c0001t0008g0041 | 2 | HG01192.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.314+12208C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97446992 | |||||||
| chr13:97447044 | T | C | 1 | a0001c0001t0002g0068 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.314+12260T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97447044 | |||||||
| chr13:97447249 | A | G | 1 | a0001c0001t0002g0081 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.314+12465A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97447249 | |||||||
| chr13:97447510 | A | G | 1 | a0001c0001t0002g0117 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.314+12726A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97447510 | |||||||
| chr13:97447585 | C | T | 2 | a0001c0001t0001g0173 a0001c0001t0001g0183 |
2 | HG03492.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.314+12801C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97447585 | |||||||
| chr13:97447667 | C | T | 1 | a0001c0001t0003g0116 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.314+12883C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97447667 | |||||||
| chr13:97447668 | G | A | 1 | a0001c0001t0004g0126 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.314+12884G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97447668 | |||||||
| chr13:97447845 | G | T | 1 | a0001c0001t0002g0061 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.314+13061G>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97447845 | |||||||
| chr13:97447846 | C | T | 1 | a0001c0001t0002g0061 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.314+13062C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97447846 | |||||||
| chr13:97447971 | GT | G | 5 | a0001c0001t0001g0045 a0001c0001t0007g0017 a0001c0001t0007g0154 others(2): Show |
7 | HG01192.hp1 HG01516.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.314+13201delT | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97447971 | ||||||
| chr13:97448019 | A | G | 2 | a0001c0001t0002g0077 a0001c0001t0002g0119 |
2 | HG03579.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.314+13235A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97448019 | |||||||
| chr13:97448529 | A | G | 1 | a0001c0001t0006g0135 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.314+13745A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97448529 | |||||||
| chr13:97448798 | A | C | 3 | a0001c0001t0010g0099 a0001c0001t0010g0100 a0001c0001t0010g0160 |
3 | HG01891.hp2 HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.314+14014A>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97448798 | |||||||
| chr13:97449017 | A | G | 1 | a0001c0001t0019g0165 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.314+14233A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97449017 | |||||||
| chr13:97449103 | G | C | 2 | a0001c0001t0002g0077 a0001c0001t0002g0119 |
2 | HG03579.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.314+14319G>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97449103 | |||||||
| chr13:97449168 | T | A | 8 | a0001c0001t0001g0146 a0001c0001t0004g0096 a0001c0001t0004g0158 others(5): Show |
10 | HG01243.hp1 HG02055.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.314+14384T>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97449168 | |||||||
| chr13:97449375 | G | A | 2 | a0001c0001t0004g0055 a0001c0001t0004g0086 |
2 | HG02809.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.314+14591G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97449375 | |||||||
| chr13:97449489 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.314+14705G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97449489 | |||||||
| chr13:97449636 | C | T | 4 | a0001c0001t0007g0017 a0001c0001t0007g0154 a0001c0001t0007g0155 others(1): Show |
5 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.315-14569C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97449636 | |||||||
| chr13:97449726 | A | AT | 54 | a0001c0001t0001g0146 a0001c0001t0001g0176 a0001c0001t0002g0018 others(51): Show |
97 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.315-14469dupT | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97449726 | ||||||
| chr13:97449792 | C | T | 1 | a0001c0001t0002g0075 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.315-14413C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97449792 | |||||||
| chr13:97449964 | G | A | 3 | a0001c0001t0001g0166 a0001c0001t0001g0169 a0001c0001t0001g0170 |
3 | HG00673.hp1 NA18969.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.315-14241G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97449964 | |||||||
| chr13:97449965 | G | GT | 8 | a0001c0001t0001g0146 a0001c0001t0004g0096 a0001c0001t0005g0030 others(5): Show |
10 | HG01243.hp1 HG02055.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.315-14228dupT | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97449965 | ||||||
| chr13:97449965 | GT | G | 5 | a0001c0001t0004g0024 a0001c0001t0004g0055 a0001c0001t0004g0086 others(2): Show |
7 | HG01109.hp2 HG01981.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.315-14228delT | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97449965 | ||||||
| chr13:97450163 | G | A | 1 | a0001c0001t0004g0127 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.315-14042G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97450163 | |||||||
| chr13:97450259 | T | G | 1 | a0001c0001t0003g0104 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.315-13946T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97450259 | |||||||
| chr13:97450474 | T | C | 4 | a0001c0001t0007g0017 a0001c0001t0007g0154 a0001c0001t0007g0155 others(1): Show |
5 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.315-13731T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97450474 | |||||||
| chr13:97450551 | G | A | 1 | a0001c0001t0026g0105 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.315-13654G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97450551 | |||||||
| chr13:97450658 | T | TA | 5 | a0001c0001t0002g0069 a0001c0001t0004g0008 a0001c0001t0004g0058 others(2): Show |
8 | HG02257.hp2 HG02886.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.315-13535dupA | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97450658 | ||||||
| chr13:97450695 | G | GT | 6 | a0001c0001t0001g0146 a0001c0001t0005g0030 a0001c0001t0005g0031 others(3): Show |
8 | HG01243.hp1 HG02055.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.315-13504dupT | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97450695 | ||||||
| chr13:97450809 | A | C | 1 | a0001c0001t0002g0029 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.315-13396A>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97450809 | |||||||
| chr13:97450944 | G | A | 1 | a0001c0001t0008g0043 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.315-13261G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97450944 | |||||||
| chr13:97451001 | T | G | 1 | a0001c0001t0002g0060 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.315-13204T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97451001 | |||||||
| chr13:97451256 | G | A | 1 | a0001c0001t0003g0106 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.315-12949G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97451256 | |||||||
| chr13:97451663 | T | C | 1 | a0001c0001t0004g0128 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.315-12542T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97451663 | |||||||
| chr13:97451664 | GTATACTT | G | 33 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0002g0003 others(30): Show |
67 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.315-12539_315-1253 others(11): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97451664 | ||||||
| chr13:97451672 | T | C | 1 | a0001c0001t0004g0121 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.315-12533T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97451672 | |||||||
| chr13:97451687 | T | C | 6 | a0001c0001t0002g0029 a0001c0001t0004g0024 a0001c0001t0004g0055 others(3): Show |
9 | HG01109.hp2 HG01981.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.315-12518T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97451687 | |||||||
| chr13:97451816 | A | C | 6 | a0001c0001t0002g0029 a0001c0001t0004g0024 a0001c0001t0004g0055 others(3): Show |
9 | HG01109.hp2 HG01981.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.315-12389A>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97451816 | |||||||
| chr13:97451881 | T | C | 1 | a0001c0001t0004g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.315-12324T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97451881 | |||||||
| chr13:97452058 | T | C | 2 | a0001c0001t0002g0077 a0001c0001t0002g0119 |
2 | HG03579.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.315-12147T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97452058 | |||||||
| chr13:97452517 | C | T | 1 | a0001c0001t0003g0067 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.315-11688C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97452517 | |||||||
| chr13:97452616 | T | C | 1 | a0001c0001t0019g0165 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.315-11589T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97452616 | |||||||
| chr13:97452648 | A | G | 1 | a0001c0001t0008g0041 | 2 | HG01192.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.315-11557A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97452648 | |||||||
| chr13:97452650 | G | GCA | 54 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0094 others(51): Show |
96 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.315-11536_315-1153 others(6): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97452650 | ||||||
| chr13:97452650 | G | GCACA | 32 | a0001c0001t0002g0018 a0001c0001t0002g0022 a0001c0001t0002g0027 others(29): Show |
68 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.315-11538_315-1153 others(8): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97452650 | ||||||
| chr13:97452650 | G | GCACACAC others(1): Show |
5 | a0001c0001t0003g0033 a0001c0001t0003g0034 a0001c0001t0003g0066 others(2): Show |
6 | HG01069.hp1 HG01106.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.315-11542_315-1153 others(12): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97452650 | ||||||
| chr13:97452650 | GCA | G | 8 | a0001c0001t0004g0126 a0001c0001t0004g0158 a0001c0001t0005g0030 others(5): Show |
10 | HG01243.hp1 HG02055.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.315-11536_315-1153 others(6): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97452650 | ||||||
| chr13:97452750 | A | G | 1 | a0001c0001t0003g0065 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.315-11455A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97452750 | |||||||
| chr13:97452764 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.315-11441A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97452764 | |||||||
| chr13:97453091 | A | G | 6 | a0001c0001t0004g0096 a0001c0001t0005g0030 a0001c0001t0005g0031 others(3): Show |
8 | HG01243.hp1 HG02055.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.315-11114A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97453091 | |||||||
| chr13:97453238 | T | C | 1 | a0001c0001t0003g0067 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.315-10967T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97453238 | |||||||
| chr13:97453402 | C | G | 1 | a0001c0001t0005g0098 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.315-10803C>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97453402 | |||||||
| chr13:97453578 | G | A | 39 | a0001c0001t0002g0018 a0001c0001t0003g0001 a0001c0001t0003g0012 others(36): Show |
75 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.315-10627G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97453578 | |||||||
| chr13:97453745 | G | C | 1 | a0001c0001t0002g0071 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.315-10460G>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97453745 | |||||||
| chr13:97453842 | C | T | 1 | a0001c0001t0004g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.315-10363C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97453842 | |||||||
| chr13:97453989 | G | T | 4 | a0001c0001t0007g0017 a0001c0001t0007g0154 a0001c0001t0007g0155 others(1): Show |
5 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.315-10216G>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97453989 | |||||||
| chr13:97454030 | A | G | 2 | a0001c0001t0001g0040 a0001c0001t0001g0151 |
3 | HG02015.hp2 NA18950.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.315-10175A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97454030 | |||||||
| chr13:97454057 | C | T | 1 | a0001c0001t0004g0133 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.315-10148C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97454057 | |||||||
| chr13:97454166 | T | C | 2 | a0001c0001t0017g0148 a0001c0001t0022g0149 |
2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.315-10039T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97454166 | |||||||
| chr13:97454240 | T | C | 1 | a0001c0001t0018g0161 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.315-9965T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97454240 | |||||||
| chr13:97454268 | G | A | 1 | a0001c0001t0005g0098 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.315-9937G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97454268 | |||||||
| chr13:97454429 | A | G | 4 | a0001c0001t0007g0017 a0001c0001t0007g0154 a0001c0001t0007g0155 others(1): Show |
5 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.315-9776A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97454429 | |||||||
| chr13:97454794 | C | T | 6 | a0001c0001t0007g0017 a0001c0001t0007g0154 a0001c0001t0007g0155 others(3): Show |
7 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.315-9411C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97454794 | |||||||
| chr13:97454800 | A | G | 1 | a0001c0001t0019g0165 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.315-9405A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97454800 | |||||||
| chr13:97454997 | T | TCTC | 6 | a0001c0001t0007g0017 a0001c0001t0007g0154 a0001c0001t0007g0155 others(3): Show |
7 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.315-9206_315-9205i others(5): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97454997 | ||||||
| chr13:97455052 | T | C | 1 | a0001c0001t0022g0149 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.315-9153T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97455052 | |||||||
| chr13:97455304 | T | C | 1 | a0001c0001t0019g0165 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.315-8901T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97455304 | |||||||
| chr13:97455434 | T | G | 1 | a0001c0001t0006g0139 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.315-8771T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97455434 | |||||||
| chr13:97455592 | G | A | 1 | a0001c0001t0004g0128 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.315-8613G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97455592 | |||||||
| chr13:97455680 | T | C | 2 | a0001c0001t0002g0061 a0001c0001t0002g0075 |
2 | HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.315-8525T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97455680 | |||||||
| chr13:97455911 | A | G | 1 | a0001c0001t0019g0165 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.315-8294A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97455911 | |||||||
| chr13:97455949 | G | C | 3 | a0001c0001t0012g0162 a0001c0001t0012g0163 a0001c0001t0012g0164 |
3 | HG02630.hp1 HG02723.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.315-8256G>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97455949 | |||||||
| chr13:97455967 | G | A | 2 | a0001c0001t0004g0140 a0001c0001t0022g0149 |
2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.315-8238G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97455967 | |||||||
| chr13:97455992 | T | C | 6 | a0001c0001t0007g0017 a0001c0001t0007g0154 a0001c0001t0007g0155 others(3): Show |
7 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.315-8213T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97455992 | |||||||
| chr13:97456397 | T | G | 1 | a0001c0001t0024g0109 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.315-7808T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97456397 | |||||||
| chr13:97456438 | T | C | 1 | a0001c0001t0004g0129 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.315-7767T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97456438 | |||||||
| chr13:97456513 | A | G | 3 | a0001c0001t0001g0166 a0001c0001t0001g0169 a0001c0001t0001g0170 |
3 | HG00673.hp1 NA18969.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.315-7692A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97456513 | |||||||
| chr13:97456781 | C | T | 6 | a0001c0001t0002g0029 a0001c0001t0004g0024 a0001c0001t0004g0055 others(3): Show |
9 | HG01109.hp2 HG01981.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.315-7424C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97456781 | |||||||
| chr13:97456953 | T | C | 1 | a0001c0001t0018g0161 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.315-7252T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97456953 | |||||||
| chr13:97456977 | G | A | 1 | a0001c0001t0003g0101 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.315-7228G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97456977 | |||||||
| chr13:97456999 | T | C | 1 | a0001c0001t0004g0129 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.315-7206T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97456999 | |||||||
| chr13:97457141 | C | T | 5 | a0001c0001t0007g0017 a0001c0001t0007g0154 a0001c0001t0007g0155 others(2): Show |
6 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.315-7064C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97457141 | |||||||
| chr13:97457182 | A | T | 5 | a0001c0001t0007g0017 a0001c0001t0007g0154 a0001c0001t0007g0155 others(2): Show |
6 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.315-7023A>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97457182 | |||||||
| chr13:97457240 | C | T | 5 | a0001c0001t0005g0030 a0001c0001t0005g0031 a0001c0001t0005g0095 others(2): Show |
7 | HG01243.hp1 HG02055.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.315-6965C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97457240 | |||||||
| chr13:97457249 | T | G | 5 | a0001c0001t0001g0094 a0001c0001t0004g0008 a0001c0001t0004g0058 others(2): Show |
8 | HG02257.hp2 HG02451.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.315-6956T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97457249 | |||||||
| chr13:97457449 | C | T | 1 | a0001c0001t0019g0165 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.315-6756C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97457449 | |||||||
| chr13:97457455 | A | G | 1 | a0001c0001t0002g0071 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.315-6750A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97457455 | |||||||
| chr13:97457529 | G | A | 1 | a0001c0001t0018g0161 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.315-6676G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97457529 | |||||||
| chr13:97457614 | T | C | 4 | a0001c0001t0004g0159 a0001c0001t0012g0162 a0001c0001t0012g0163 others(1): Show |
4 | HG02630.hp1 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-6591T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97457614 | |||||||
| chr13:97457827 | T | C | 2 | a0001c0001t0002g0019 a0001c0001t0002g0076 |
4 | HG02602.hp2 HG03017.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-6378T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97457827 | |||||||
| chr13:97457889 | A | AT | 6 | a0001c0001t0007g0017 a0001c0001t0007g0154 a0001c0001t0007g0155 others(3): Show |
7 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.315-6315dupT | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97457889 | ||||||
| chr13:97458005 | G | C | 6 | a0001c0001t0007g0017 a0001c0001t0007g0154 a0001c0001t0007g0155 others(3): Show |
7 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.315-6200G>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97458005 | |||||||
| chr13:97458091 | C | G | 1 | a0001c0001t0019g0165 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.315-6114C>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97458091 | |||||||
| chr13:97458131 | A | G | 7 | a0001c0001t0004g0096 a0001c0001t0004g0158 a0001c0001t0005g0030 others(4): Show |
9 | HG01243.hp1 HG02055.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.315-6074A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97458131 | |||||||
| chr13:97458193 | A | C | 1 | a0001c0001t0003g0113 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.315-6012A>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97458193 | |||||||
| chr13:97458346 | G | A | 2 | a0001c0001t0010g0099 a0001c0001t0010g0100 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.315-5859G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97458346 | |||||||
| chr13:97458439 | T | G | 1 | a0001c0001t0018g0161 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.315-5766T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97458439 | |||||||
| chr13:97458456 | G | A | 1 | a0001c0001t0025g0114 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.315-5749G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97458456 | |||||||
| chr13:97458579 | C | T | 1 | a0001c0001t0003g0123 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.315-5626C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97458579 | |||||||
| chr13:97458720 | A | G | 5 | a0001c0001t0007g0017 a0001c0001t0007g0154 a0001c0001t0007g0155 others(2): Show |
6 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.315-5485A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97458720 | |||||||
| chr13:97458736 | G | A | 1 | a0001c0001t0002g0072 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.315-5469G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97458736 | |||||||
| chr13:97458827 | A | G | 2 | a0001c0001t0005g0031 a0001c0001t0005g0095 |
3 | HG01243.hp1 HG02055.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.315-5378A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97458827 | |||||||
| chr13:97458860 | T | G | 3 | a0001c0001t0012g0162 a0001c0001t0012g0163 a0001c0001t0012g0164 |
3 | HG02630.hp1 HG02723.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.315-5345T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97458860 | |||||||
| chr13:97458914 | G | A | 1 | a0001c0001t0004g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.315-5291G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97458914 | |||||||
| chr13:97459187 | G | A | 5 | a0001c0001t0001g0094 a0001c0001t0004g0008 a0001c0001t0004g0058 others(2): Show |
8 | HG02257.hp2 HG02451.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.315-5018G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97459187 | |||||||
| chr13:97459245 | CAAATGAT others(18): Show |
C | 1 | a0001c0001t0002g0073 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.315-4942_315-4918d others(27): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97459245 | ||||||
| chr13:97459269 | AGAAATGA others(10): Show |
A | 1 | a0001c0001t0022g0149 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.315-4914_315-4898d others(19): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97459269 | ||||||
| chr13:97459283 | G | T | 1 | a0001c0001t0001g0177 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.315-4922G>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97459283 | |||||||
| chr13:97459303 | G | T | 1 | a0001c0001t0004g0147 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.315-4902G>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97459303 | |||||||
| chr13:97459345 | C | T | 4 | a0001c0001t0007g0017 a0001c0001t0007g0154 a0001c0001t0007g0155 others(1): Show |
5 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.315-4860C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97459345 | |||||||
| chr13:97459352 | GTAAC | G | 2 | a0001c0001t0001g0026 a0001c0001t0006g0026 |
3 | NA18950.hp1 NA19010.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.315-4851_315-4848d others(6): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97459352 | ||||||
| chr13:97459398 | CAG | C | 4 | a0001c0001t0002g0020 a0001c0001t0002g0028 a0001c0001t0002g0052 others(1): Show |
7 | HG01069.hp2 HG01071.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.315-4804_315-4803d others(4): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97459398 | ||||||
| chr13:97459467 | G | A | 1 | a0001c0001t0019g0165 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.315-4738G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97459467 | |||||||
| chr13:97459577 | G | A | 1 | a0001c0001t0002g0081 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.315-4628G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97459577 | |||||||
| chr13:97459982 | T | C | 4 | a0001c0001t0004g0159 a0001c0001t0012g0162 a0001c0001t0012g0163 others(1): Show |
4 | HG02630.hp1 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-4223T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97459982 | |||||||
| chr13:97460131 | A | G | 1 | a0001c0001t0002g0075 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.315-4074A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97460131 | |||||||
| chr13:97460382 | A | G | 6 | a0001c0001t0004g0096 a0001c0001t0005g0030 a0001c0001t0005g0031 others(3): Show |
8 | HG01243.hp1 HG02055.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.315-3823A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97460382 | |||||||
| chr13:97460520 | T | C | 1 | a0001c0001t0004g0150 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.315-3685T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97460520 | |||||||
| chr13:97460754 | C | T | 1 | a0001c0001t0004g0132 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.315-3451C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97460754 | |||||||
| chr13:97460847 | G | T | 1 | a0001c0001t0019g0165 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.315-3358G>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97460847 | |||||||
| chr13:97460956 | T | C | 1 | a0001c0001t0003g0023 | 3 | HG00741.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.315-3249T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97460956 | |||||||
| chr13:97461114 | G | A | 1 | a0001c0001t0004g0132 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.315-3091G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97461114 | |||||||
| chr13:97461256 | A | T | 1 | a0001c0001t0018g0161 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.315-2949A>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97461256 | |||||||
| chr13:97461269 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.315-2936A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97461269 | |||||||
| chr13:97461398 | C | CAATT | 15 | a0001c0001t0001g0146 a0001c0001t0003g0112 a0001c0001t0004g0096 others(12): Show |
18 | HG01192.hp1 HG01243.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.315-2805_315-2804i others(6): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97461398 | ||||||
| chr13:97461451 | C | T | 1 | a0001c0001t0015g0097 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.315-2754C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97461451 | |||||||
| chr13:97461680 | C | T | 7 | a0001c0001t0003g0112 a0001c0001t0007g0017 a0001c0001t0007g0154 others(4): Show |
8 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.315-2525C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97461680 | |||||||
| chr13:97461715 | G | A | 3 | a0001c0001t0003g0023 a0001c0001t0003g0108 a0001c0001t0003g0110 |
5 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.315-2490G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97461715 | |||||||
| chr13:97461778 | A | G | 3 | a0001c0001t0007g0017 a0001c0001t0007g0154 a0001c0001t0028g0017 |
4 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.315-2427A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97461778 | |||||||
| chr13:97461941 | A | C | 7 | a0001c0001t0003g0112 a0001c0001t0007g0017 a0001c0001t0007g0154 others(4): Show |
8 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.315-2264A>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97461941 | |||||||
| chr13:97461962 | CA | C | 5 | a0001c0001t0001g0172 a0001c0001t0007g0017 a0001c0001t0007g0154 others(2): Show |
6 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.315-2233delA | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97461962 | ||||||
| chr13:97461969 | A | AAT | 15 | a0001c0001t0001g0013 a0001c0001t0003g0122 a0001c0001t0004g0007 others(12): Show |
22 | HG00544.hp2 HG00609.hp2 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.315-2235_315-2234i others(4): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97461969 | ||||||
| chr13:97461969 | A | T | 3 | a0001c0001t0001g0131 a0001c0001t0003g0112 a0001c0001t0004g0133 |
3 | HG02738.hp1 HG03942.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.315-2236A>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97461969 | |||||||
| chr13:97461971 | A | AAAATATA others(15): Show |
1 | a0001c0001t0019g0165 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.315-2233_315-2232i others(24): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97461971 | ||||||
| chr13:97461971 | A | AAT | 16 | a0001c0001t0001g0094 a0001c0001t0002g0069 a0001c0001t0004g0008 others(13): Show |
19 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.315-2217_315-2216d others(4): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97461971 | ||||||
| chr13:97461971 | A | T | 26 | a0001c0001t0001g0013 a0001c0001t0001g0131 a0001c0001t0002g0020 others(23): Show |
37 | HG00544.hp2 HG00609.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.315-2234A>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97461971 | |||||||
| chr13:97461973 | T | A | 42 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(39): Show |
79 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.315-2232T>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97461973 | |||||||
| chr13:97461975 | T | A | 1 | a0001c0001t0001g0168 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.315-2230T>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97461975 | |||||||
| chr13:97461980 | A | ATATATAT others(45): Show |
1 | a0001c0001t0001g0171 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.315-2207_315-2156d others(54): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97461980 | ||||||
| chr13:97461990 | T | A | 1 | a0001c0001t0019g0165 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.315-2215T>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97461990 | |||||||
| chr13:97462004 | T | A | 1 | a0001c0001t0019g0165 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.315-2201T>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97462004 | |||||||
| chr13:97462005 | T | G | 1 | a0001c0001t0019g0165 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.315-2200T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97462005 | |||||||
| chr13:97462024 | TTATATAT others(3): Show |
T | 3 | a0001c0001t0010g0099 a0001c0001t0010g0100 a0001c0001t0010g0160 |
3 | HG01891.hp2 HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.315-2163_315-2154d others(12): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97462024 | ||||||
| chr13:97462032 | T | TTATATAT others(5): Show |
1 | a0001c0001t0004g0159 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.315-2143_315-2132d others(14): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97462032 | ||||||
| chr13:97462032 | TTATATAT others(5): Show |
T | 6 | a0001c0001t0001g0004 a0001c0001t0002g0062 a0001c0001t0003g0112 others(3): Show |
6 | HG00423.hp2 HG02071.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.315-2143_315-2132d others(14): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97462032 | ||||||
| chr13:97462033 | T | G | 1 | a0001c0001t0002g0079 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.315-2172T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97462033 | |||||||
| chr13:97462056 | A | T | 2 | a0001c0001t0004g0088 a0001c0001t0004g0152 |
2 | HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.315-2149A>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97462056 | |||||||
| chr13:97462061 | T | G | 1 | a0001c0001t0018g0161 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.315-2144T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97462061 | |||||||
| chr13:97462065 | T | G | 4 | a0001c0001t0007g0017 a0001c0001t0007g0154 a0001c0001t0007g0155 others(1): Show |
5 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.315-2140T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97462065 | |||||||
| chr13:97462074 | T | C | 1 | a0001c0001t0026g0105 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.315-2131T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97462074 | |||||||
| chr13:97462155 | A | T | 5 | a0001c0001t0004g0024 a0001c0001t0004g0055 a0001c0001t0004g0086 others(2): Show |
7 | HG01109.hp2 HG01981.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.315-2050A>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97462155 | |||||||
| chr13:97462160 | TAGAC | T | 2 | a0001c0001t0008g0041 a0001c0001t0008g0043 |
4 | HG01192.hp2 HG02976.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-2040_315-2037d others(6): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97462160 | ||||||
| chr13:97462244 | A | G | 12 | a0001c0001t0001g0005 a0001c0001t0001g0040 a0001c0001t0001g0082 others(9): Show |
24 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.315-1961A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97462244 | |||||||
| chr13:97462299 | T | C | 1 | a0001c0001t0010g0099 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.315-1906T>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97462299 | |||||||
| chr13:97462395 | A | G | 1 | a0001c0001t0004g0055 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.315-1810A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97462395 | |||||||
| chr13:97462429 | TG | T | 2 | a0001c0001t0008g0041 a0001c0001t0008g0043 |
4 | HG01192.hp2 HG02976.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-1774delG | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97462429 | ||||||
| chr13:97462633 | T | G | 1 | a0001c0001t0004g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.315-1572T>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97462633 | |||||||
| chr13:97462738 | A | T | 3 | a0001c0001t0010g0099 a0001c0001t0010g0100 a0001c0001t0010g0160 |
3 | HG01891.hp2 HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.315-1467A>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97462738 | |||||||
| chr13:97462911 | G | A | 6 | a0001c0001t0004g0096 a0001c0001t0005g0030 a0001c0001t0005g0031 others(3): Show |
8 | HG01243.hp1 HG02055.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.315-1294G>A | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97462911 | |||||||
| chr13:97462938 | G | C | 79 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0009 others(76): Show |
153 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.315-1267G>C | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97462938 | |||||||
| chr13:97463014 | AT | A | 102 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0009 others(99): Show |
183 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.315-1188delT | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97463014 | ||||||
| chr13:97463119 | AAC | A | 35 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0009 others(32): Show |
67 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.315-1072_315-1071d others(4): Show |
RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr13 | 97463119 | ||||||
| chr13:97463258 | C | G | 1 | a0001c0001t0005g0098 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.315-947C>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97463258 | |||||||
| chr13:97463663 | C | T | 77 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0009 others(74): Show |
151 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.315-542C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97463663 | |||||||
| chr13:97463680 | C | T | 4 | a0001c0001t0007g0017 a0001c0001t0007g0154 a0001c0001t0007g0155 others(1): Show |
5 | HG01192.hp1 HG01975.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.315-525C>T | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97463680 | |||||||
| chr13:97463790 | A | G | 3 | a0001c0001t0002g0011 a0001c0001t0002g0081 a0001c0001t0002g0117 |
6 | HG00642.hp2 HG01070.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.315-415A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97463790 | |||||||
| chr13:97463815 | A | G | 5 | a0001c0001t0004g0159 a0001c0001t0012g0162 a0001c0001t0012g0163 others(2): Show |
5 | HG01106.hp2 HG02630.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.315-390A>G | RAP2A | ENSG00000125249.7 | transcript | ENST00000245304.5 | protein_coding | 1/1 | chr13 | 97463815 |