Item | Value |
---|---|
geneid | 5908 |
ensemblid | ENSG00000127314.18 |
hgncid | 9857 |
symbol | RAP1B |
name | RAP1B, member of RAS oncogene family |
refseq_nuc | NM_001010942.3 |
refseq_prot | NP_001010942.1 |
ensembl_nuc | ENST00000250559.14 |
ensembl_prot | ENSP00000250559.9 |
mane_status | MANE Select |
chr | chr12 |
start | 68610899 |
end | 68671901 |
strand | + |
ver | v1.2 |
region | chr12:68610899-68671901 |
region5000 | chr12:68605899-68676901 |
regionname0 | RAP1B_chr12_68610899_68671901 |
regionname5000 | RAP1B_chr12_68605899_68676901 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 552 | 387 | 82 | 65 | 184 | 12 | 42 | RAP1B_chr12_68605899_68676901 | RAP1B | ATGCG others(547): Show |
chr12 | 68605899 | 68676901 | ||
a0001c0002 | 0/0 | 552 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | ATGCG others(547): Show |
chr12 | 68605899 | 68676901 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 13380 | 60 | 7 | 14 | 32 | 1 | 5 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13375): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0002 | 0/0 | 13378 | 43 | 5 | 11 | 21 | 2 | 4 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13373): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0003 | 0/0 | 13377 | 31 | 1 | 0 | 21 | 1 | 8 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13372): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0004 | 0/0 | 13379 | 16 | 0 | 0 | 16 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13374): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0005 | 0/0 | 13378 | 16 | 2 | 2 | 9 | 1 | 2 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13373): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0006 | 0/0 | 13377 | 14 | 13 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13372): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0007 | 0/0 | 13379 | 12 | 0 | 1 | 11 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13374): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0008 | 0/0 | 13377 | 9 | 0 | 1 | 8 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13372): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0009 | 0/0 | 13382 | 8 | 8 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13377): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0010 | 0/0 | 13382 | 5 | 1 | 1 | 2 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13377): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0011 | 0/0 | 13384 | 4 | 0 | 4 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13379): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0012 | 0/0 | 13381 | 4 | 1 | 1 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13376): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0013 | 0/0 | 13377 | 4 | 1 | 2 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13372): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0014 | 0/0 | 13378 | 4 | 0 | 1 | 2 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13373): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0015 | 0/0 | 13374 | 4 | 0 | 4 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13369): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0016 | 0/0 | 13380 | 3 | 0 | 0 | 3 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13375): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0017 | 0/0 | 13382 | 3 | 0 | 2 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13377): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0018 | 0/0 | 13379 | 3 | 0 | 1 | 0 | 0 | 2 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13374): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0019 | 0/0 | 13380 | 3 | 0 | 0 | 3 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13375): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0020 | 0/0 | 13379 | 3 | 0 | 0 | 3 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13374): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0021 | 0/0 | 13377 | 3 | 0 | 0 | 3 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13372): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0022 | 0/0 | 13377 | 3 | 0 | 1 | 0 | 0 | 2 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13372): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0023 | 0/0 | 13378 | 2 | 0 | 0 | 0 | 0 | 2 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13373): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0024 | 0/0 | 13377 | 3 | 3 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13372): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0025 | 0/0 | 13407 | 2 | 0 | 0 | 0 | 2 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13402): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0026 | 0/0 | 13384 | 2 | 0 | 0 | 0 | 1 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13379): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0027 | 0/0 | 13384 | 2 | 0 | 2 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13379): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0028 | 0/0 | 13382 | 2 | 2 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13377): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0029 | 0/0 | 13378 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13373): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0030 | 0/0 | 13379 | 2 | 0 | 1 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13374): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0031 | 0/0 | 13381 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13376): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0032 | 0/0 | 13381 | 2 | 0 | 1 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13376): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0033 | 0/0 | 13372 | 2 | 2 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13367): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0034 | 0/0 | 13380 | 2 | 2 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13375): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0035 | 0/0 | 13381 | 2 | 1 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13376): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0036 | 0/0 | 13378 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13373): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0037 | 0/0 | 13379 | 2 | 0 | 1 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13374): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0038 | 0/0 | 13379 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13374): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0039 | 0/0 | 13377 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13372): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0040 | 0/0 | 13376 | 2 | 0 | 0 | 0 | 0 | 2 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13371): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0041 | 0/0 | 13377 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13372): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0042 | 0/0 | 13379 | 2 | 2 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13374): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0043 | 0/0 | 13378 | 2 | 0 | 0 | 0 | 1 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13373): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0044 | 0/0 | 13377 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13372): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0045 | 0/0 | 13380 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13375): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0046 | 0/0 | 13405 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13400): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0047 | 0/0 | 13366 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13361): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0048 | 0/0 | 13379 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13374): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0049 | 0/0 | 13386 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13381): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0050 | 0/0 | 13386 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13381): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0051 | 0/0 | 13387 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13382): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0052 | 0/0 | 13384 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13379): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0053 | 0/0 | 13385 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13380): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0054 | 0/0 | 13384 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13379): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0055 | 0/0 | 13384 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13379): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0056 | 0/0 | 13384 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13379): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0057 | 0/0 | 13382 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13377): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0058 | 0/0 | 13381 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13376): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0059 | 0/0 | 13382 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13377): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0060 | 0/0 | 13382 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13377): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0061 | 0/0 | 13382 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13377): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0062 | 0/0 | 13382 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13377): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0063 | 0/0 | 13381 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13376): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0064 | 0/0 | 13381 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13376): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0065 | 0/0 | 13382 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13377): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0066 | 0/0 | 13381 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13376): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0067 | 0/0 | 13380 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13375): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0068 | 0/0 | 13380 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13375): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0069 | 0/0 | 13380 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13375): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0070 | 1/0 | 13378 | 1 | 0 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13373): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0071 | 0/0 | 13380 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13375): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0072 | 0/0 | 13380 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13375): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0073 | 0/0 | 13380 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13375): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0074 | 0/0 | 13380 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13375): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0075 | 0/0 | 13379 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13374): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0076 | 0/0 | 13380 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13375): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0077 | 0/0 | 13382 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13377): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0078 | 0/0 | 13380 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13375): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0079 | 0/0 | 13372 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13367): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0080 | 0/0 | 13378 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13373): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0081 | 0/0 | 13378 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13373): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0082 | 0/0 | 13377 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13372): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0083 | 0/0 | 13378 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13373): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0084 | 0/0 | 13379 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13374): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0085 | 0/0 | 13380 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13375): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0086 | 0/0 | 13378 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13373): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0087 | 0/0 | 13379 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13374): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0088 | 0/0 | 13381 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13376): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0089 | 0/0 | 13379 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13374): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0090 | 0/0 | 13381 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13376): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0091 | 0/0 | 13379 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13374): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0092 | 0/0 | 13380 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13375): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0093 | 0/0 | 13378 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13373): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0094 | 0/0 | 13379 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13374): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0095 | 0/0 | 13377 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13372): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0096 | 0/0 | 13377 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13372): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0097 | 0/0 | 13378 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13373): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0098 | 0/0 | 13377 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13372): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0099 | 0/0 | 13377 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13372): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0100 | 0/0 | 13378 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13373): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0101 | 0/0 | 13378 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13373): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0102 | 0/0 | 13377 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13372): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0103 | 0/0 | 13377 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13372): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0104 | 0/0 | 13378 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13373): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0105 | 0/0 | 13376 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13371): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0106 | 0/0 | 13377 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13372): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0107 | 0/0 | 13379 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13374): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0108 | 0/0 | 13377 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13372): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0109 | 0/0 | 13378 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13373): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0110 | 0/0 | 13377 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13372): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0111 | 0/0 | 13376 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13371): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0112 | 0/0 | 13378 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13373): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0113 | 0/0 | 13375 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13370): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0114 | 0/0 | 13376 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13371): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0115 | 0/0 | 13379 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13374): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0116 | 0/0 | 13376 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13371): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0117 | 0/0 | 13377 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13372): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0118 | 0/0 | 13378 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13373): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0119 | 0/0 | 13373 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13368): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0120 | 0/0 | 13378 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13373): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0121 | 0/0 | 13381 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13376): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0122 | 0/0 | 13379 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13374): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0123 | 0/0 | 13381 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13376): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0124 | 0/0 | 13378 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13373): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0125 | 0/0 | 13377 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13372): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0126 | 0/0 | 13393 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13388): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0127 | 0/0 | 13382 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13377): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0128 | 0/0 | 13377 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13372): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0129 | 0/0 | 13381 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13376): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0130 | 0/0 | 13380 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13375): Show |
chr12 | 68605899 | 68676901 |
a0001c0001t0131 | 0/0 | 13377 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GAGAT others(13372): Show |
chr12 | 68605899 | 68676901 |
a0001c0002t0023 | 0/0 | 13378 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | GACAT others(13373): Show |
chr12 | 68605899 | 68676901 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 12 | 0 | 1 | 10 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0149 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0004g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0004g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0005g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0005g0005 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0005g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0005g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0005g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0005g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0005g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0005g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0005g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0005g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0005g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0006g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0006g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0006g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0006g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0006g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0006g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0006g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0006g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0006g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0006g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0006g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0007g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0007g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0007g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0007g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0007g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0007g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0007g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0007g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0007g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0007g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0007g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0007g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0008g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0008g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0008g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0008g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0008g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0008g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0008g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0008g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0008g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0009g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0009g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0009g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0009g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0009g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0009g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0009g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0009g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0010g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0010g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0010g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0010g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0010g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0011g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0011g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0011g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0011g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0012g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0012g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0012g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0012g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0013g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0013g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0013g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0013g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0014g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0014g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0014g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0014g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0015g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0015g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0015g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0015g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0016g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0016g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0016g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0017g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0017g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0017g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0018g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0018g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0018g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0019g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0019g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0019g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0020g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0020g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0020g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0021g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0021g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0022g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0022g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0022g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0023g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0023g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0024g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0024g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0024g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0025g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0026g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0026g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0027g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0027g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0028g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0028g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0029g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0029g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0030g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0030g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0031g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0031g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0032g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0032g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0033g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0033g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0034g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0034g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0035g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0035g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0036g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0036g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0037g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0037g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0038g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0038g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0039g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0039g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0040g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0040g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0041g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0041g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0042g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0042g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0043g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0043g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0044g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0044g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0045g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0046g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0047g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0048g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0049g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0050g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0051g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0052g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0053g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0054g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0055g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0056g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0057g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0058g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0059g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0060g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0061g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0062g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0063g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0064g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0065g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0066g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0067g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0068g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0069g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0070g0264 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0071g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0072g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0073g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0074g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0075g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0076g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0077g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0078g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0079g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0080g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0081g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0082g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0083g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0084g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0085g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0086g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0087g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0088g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0089g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0090g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0091g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0092g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0093g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0094g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0095g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0096g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0097g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0098g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0099g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0100g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0101g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0102g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0103g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0104g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0105g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0106g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0107g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0108g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0109g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0110g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0111g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0112g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0113g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0114g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0115g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0116g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0117g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0118g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0119g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0120g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0121g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0122g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0123g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0124g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0125g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0126g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0127g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0128g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0129g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0130g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0001t0131g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
a0001c0002t0023g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0088 | EUR | GBR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG00099 | hp2 | a0001 | c0001 | t0026 | g0138 | EUR | GBR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG00280 | hp1 | a0001 | c0001 | t0043 | g0094 | EUR | FIN | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0273 | EUR | FIN | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0012 | EUR | FIN | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG00323 | hp2 | a0001 | c0001 | t0076 | g0016 | EUR | FIN | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG00408 | hp2 | a0001 | c0001 | t0036 | g0010 | EAS | CHS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG00423 | hp1 | a0001 | c0001 | t0004 | g0059 | EAS | CHS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0305 | EAS | CHS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG00438 | hp1 | a0001 | c0001 | t0014 | g0309 | EAS | CHS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG00544 | hp1 | a0001 | c0001 | t0091 | g0043 | EAS | CHS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG00558 | hp1 | a0001 | c0001 | t0029 | g0186 | EAS | CHS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG00558 | hp2 | a0001 | c0001 | t0005 | g0052 | EAS | CHS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG00597 | hp1 | a0001 | c0001 | t0004 | g0067 | EAS | CHS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG00621 | hp1 | a0001 | c0001 | t0007 | g0035 | EAS | CHS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG00621 | hp2 | a0001 | c0001 | t0031 | g0192 | EAS | CHS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG00639 | hp1 | a0001 | c0001 | t0071 | g0012 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG00639 | hp2 | a0001 | c0001 | t0078 | g0025 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG00642 | hp1 | a0001 | c0001 | t0027 | g0255 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG00642 | hp2 | a0001 | c0001 | t0014 | g0301 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG00673 | hp1 | a0001 | c0001 | t0004 | g0058 | EAS | CHS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG00673 | hp2 | a0001 | c0001 | t0010 | g0182 | EAS | CHS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG00735 | hp1 | a0001 | c0001 | t0037 | g0031 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG00738 | hp1 | a0001 | c0001 | t0022 | g0223 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG00738 | hp2 | a0001 | c0001 | t0098 | g0283 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01069 | hp1 | a0001 | c0001 | t0013 | g0005 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01069 | hp2 | a0001 | c0001 | t0006 | g0332 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01070 | hp1 | a0001 | c0001 | t0030 | g0024 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01071 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0318 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01074 | hp2 | a0001 | c0001 | t0013 | g0061 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01081 | hp1 | a0001 | c0001 | t0010 | g0326 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01081 | hp2 | a0001 | c0001 | t0105 | g0083 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01106 | hp1 | a0001 | c0001 | t0050 | g0090 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01106 | hp2 | a0001 | c0001 | t0052 | g0325 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01109 | hp1 | a0001 | c0001 | t0011 | g0316 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01109 | hp2 | a0001 | c0001 | t0127 | g0340 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01168 | hp2 | a0001 | c0001 | t0017 | g0014 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01175 | hp1 | a0001 | c0001 | t0117 | g0306 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0132 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01192 | hp1 | a0001 | c0001 | t0017 | g0113 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01192 | hp2 | a0001 | c0001 | t0032 | g0178 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01255 | hp1 | a0001 | c0001 | t0015 | g0201 | AMR | CLM | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01255 | hp2 | a0001 | c0001 | t0027 | g0259 | AMR | CLM | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01256 | hp1 | a0001 | c0001 | t0119 | g0208 | AMR | CLM | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01256 | hp2 | a0001 | c0001 | t0018 | g0300 | AMR | CLM | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01257 | hp1 | a0001 | c0001 | t0005 | g0029 | AMR | CLM | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0093 | AMR | CLM | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0106 | AMR | CLM | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01258 | hp2 | a0001 | c0001 | t0015 | g0209 | AMR | CLM | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01261 | hp2 | a0001 | c0001 | t0012 | g0016 | AMR | CLM | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01358 | hp1 | a0001 | c0001 | t0015 | g0115 | AMR | CLM | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01358 | hp2 | a0001 | c0001 | t0051 | g0085 | AMR | CLM | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01361 | hp1 | a0001 | c0001 | t0035 | g0220 | AMR | CLM | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01433 | hp1 | a0001 | c0001 | t0011 | g0080 | AMR | CLM | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01433 | hp2 | a0001 | c0001 | t0007 | g0030 | AMR | CLM | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0087 | AMR | CLM | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01516 | hp1 | a0001 | c0001 | t0053 | g0084 | EUR | IBS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01516 | hp2 | a0001 | c0001 | t0025 | g0023 | EUR | IBS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01517 | hp1 | a0001 | c0001 | t0005 | g0064 | EUR | IBS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01517 | hp2 | a0001 | c0001 | t0025 | g0023 | EUR | IBS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01884 | hp1 | a0001 | c0001 | t0061 | g0253 | AFR | ACB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01884 | hp2 | a0001 | c0001 | t0005 | g0062 | AFR | ACB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01891 | hp1 | a0001 | c0001 | t0054 | g0144 | AFR | ACB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01891 | hp2 | a0001 | c0001 | t0006 | g0328 | AFR | ACB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | PEL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01978 | hp1 | a0001 | c0001 | t0095 | g0341 | AMR | PEL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01993 | hp1 | a0001 | c0001 | t0015 | g0159 | AMR | PEL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02004 | hp1 | a0001 | c0001 | t0011 | g0320 | AMR | PEL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02004 | hp2 | a0001 | c0001 | t0011 | g0019 | AMR | PEL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02040 | hp2 | a0001 | c0001 | t0007 | g0044 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02055 | hp1 | a0001 | c0001 | t0079 | g0222 | AFR | ACB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02055 | hp2 | a0001 | c0001 | t0010 | g0191 | AFR | ACB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02056 | hp1 | a0001 | c0001 | t0019 | g0070 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02056 | hp2 | a0001 | c0001 | t0129 | g0295 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0294 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0242 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02074 | hp2 | a0001 | c0001 | t0016 | g0164 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0275 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02083 | hp1 | a0001 | c0001 | t0088 | g0046 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02083 | hp2 | a0001 | c0001 | t0008 | g0298 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02132 | hp1 | a0001 | c0001 | t0120 | g0013 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02132 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02135 | hp1 | a0001 | c0001 | t0104 | g0014 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02135 | hp2 | a0001 | c0001 | t0077 | g0197 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02145 | hp1 | a0001 | c0001 | t0009 | g0226 | AFR | ACB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02145 | hp2 | a0001 | c0001 | t0126 | g0339 | AFR | ACB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0107 | AMR | PEL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02148 | hp2 | a0001 | c0001 | t0008 | g0311 | AMR | PEL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | CDX | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02155 | hp2 | a0001 | c0001 | t0045 | g0162 | EAS | CDX | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02165 | hp1 | a0001 | c0001 | t0007 | g0045 | EAS | CDX | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CDX | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02257 | hp1 | a0001 | c0001 | t0024 | g0336 | AFR | ACB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02257 | hp2 | a0001 | c0001 | t0012 | g0151 | AFR | ACB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02258 | hp1 | a0001 | c0001 | t0059 | g0251 | AFR | ACB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0105 | AFR | ACB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02293 | hp1 | a0001 | c0002 | t0023 | g0127 | AMR | PEL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02300 | hp1 | a0001 | c0001 | t0067 | g0218 | AMR | PEL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02451 | hp1 | a0001 | c0001 | t0060 | g0252 | AFR | ACB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02451 | hp2 | a0001 | c0001 | t0028 | g0319 | AFR | ACB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02572 | hp1 | a0001 | c0001 | t0034 | g0199 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02572 | hp2 | a0001 | c0001 | t0006 | g0333 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02602 | hp1 | a0001 | c0001 | t0094 | g0282 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02602 | hp2 | a0001 | c0001 | t0124 | g0246 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02615 | hp1 | a0001 | c0001 | t0085 | g0017 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02615 | hp2 | a0001 | c0001 | t0063 | g0010 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02622 | hp1 | a0001 | c0001 | t0024 | g0337 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02622 | hp2 | a0001 | c0001 | t0006 | g0008 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02630 | hp1 | a0001 | c0001 | t0082 | g0069 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02630 | hp2 | a0001 | c0001 | t0072 | g0321 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02647 | hp1 | a0001 | c0001 | t0033 | g0247 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02647 | hp2 | a0001 | c0001 | t0005 | g0075 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02683 | hp1 | a0001 | c0001 | t0005 | g0005 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02698 | hp1 | a0001 | c0001 | t0022 | g0227 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02698 | hp2 | a0001 | c0001 | t0043 | g0092 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02717 | hp1 | a0001 | c0001 | t0042 | g0214 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02735 | hp1 | a0001 | c0001 | t0018 | g0284 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02735 | hp2 | a0001 | c0001 | t0018 | g0243 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02738 | hp1 | a0001 | c0001 | t0107 | g0116 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02738 | hp2 | a0001 | c0001 | t0128 | g0292 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02809 | hp1 | a0001 | c0001 | t0009 | g0256 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02809 | hp2 | a0001 | c0001 | t0073 | g0025 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02818 | hp1 | a0001 | c0001 | t0006 | g0026 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02818 | hp2 | a0001 | c0001 | t0114 | g0141 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02886 | hp1 | a0001 | c0001 | t0035 | g0215 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02886 | hp2 | a0001 | c0001 | t0006 | g0331 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02895 | hp1 | a0001 | c0001 | t0006 | g0327 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02895 | hp2 | a0001 | c0001 | t0081 | g0032 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0082 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02896 | hp2 | a0001 | c0001 | t0006 | g0335 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02897 | hp2 | a0001 | c0001 | t0006 | g0026 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02922 | hp1 | a0001 | c0001 | t0013 | g0060 | AFR | ESN | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02922 | hp2 | a0001 | c0001 | t0047 | g0123 | AFR | ESN | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02970 | hp1 | a0001 | c0001 | t0006 | g0329 | AFR | ESN | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02970 | hp2 | a0001 | c0001 | t0123 | g0140 | AFR | ESN | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02976 | hp1 | a0001 | c0001 | t0058 | g0213 | AFR | ESN | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02976 | hp2 | a0001 | c0001 | t0009 | g0261 | AFR | ESN | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03041 | hp1 | a0001 | c0001 | t0102 | g0143 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03041 | hp2 | a0001 | c0001 | t0009 | g0257 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03098 | hp1 | a0001 | c0001 | t0056 | g0322 | AFR | MSL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03098 | hp2 | a0001 | c0001 | t0009 | g0258 | AFR | MSL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03130 | hp1 | a0001 | c0001 | t0115 | g0135 | AFR | ESN | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03130 | hp2 | a0001 | c0001 | t0057 | g0134 | AFR | ESN | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03195 | hp1 | a0001 | c0001 | t0006 | g0334 | AFR | ESN | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03195 | hp2 | a0001 | c0001 | t0009 | g0254 | AFR | ESN | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03209 | hp1 | a0001 | c0001 | t0122 | g0211 | AFR | MSL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03209 | hp2 | a0001 | c0001 | t0006 | g0008 | AFR | MSL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03239 | hp1 | a0001 | c0001 | t0040 | g0304 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03239 | hp2 | a0001 | c0001 | t0030 | g0027 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03453 | hp1 | a0001 | c0001 | t0042 | g0216 | AFR | MSL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03453 | hp2 | a0001 | c0001 | t0009 | g0260 | AFR | MSL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03486 | hp1 | a0001 | c0001 | t0112 | g0104 | AFR | MSL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03486 | hp2 | a0001 | c0001 | t0009 | g0249 | AFR | MSL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0317 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03491 | hp1 | a0001 | c0001 | t0017 | g0095 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03491 | hp2 | a0001 | c0001 | t0066 | g0231 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03516 | hp1 | a0001 | c0001 | t0028 | g0323 | AFR | ESN | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03579 | hp1 | a0001 | c0001 | t0055 | g0133 | AFR | MSL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0244 | AFR | MSL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03654 | hp2 | a0001 | c0001 | t0022 | g0245 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03669 | hp1 | a0001 | c0001 | t0026 | g0142 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03669 | hp2 | a0001 | c0001 | t0005 | g0054 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0109 | SAS | STU | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03688 | hp2 | a0001 | c0001 | t0118 | g0235 | SAS | STU | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03704 | hp1 | a0001 | c0001 | t0023 | g0126 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0285 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03710 | hp1 | a0001 | c0001 | t0040 | g0307 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0291 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0314 | SAS | BEB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03834 | hp2 | a0001 | c0001 | t0023 | g0125 | SAS | BEB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03927 | hp1 | a0001 | c0001 | t0065 | g0157 | SAS | BEB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0310 | SAS | BEB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | BEB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0299 | SAS | BEB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG04115 | hp1 | a0001 | c0001 | t0064 | g0228 | SAS | STU | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0303 | SAS | STU | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG04184 | hp2 | a0001 | c0001 | t0014 | g0293 | SAS | BEB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0280 | SAS | STU | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0286 | SAS | STU | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0278 | SAS | STU | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG04204 | hp2 | a0001 | c0001 | t0010 | g0079 | SAS | STU | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG04228 | hp1 | a0001 | c0001 | t0111 | g0007 | SAS | STU | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0091 | SAS | STU | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18522 | hp1 | a0001 | c0001 | t0024 | g0338 | AFR | YRI | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18522 | hp2 | a0001 | c0001 | t0034 | g0017 | AFR | YRI | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18612 | hp2 | a0001 | c0001 | t0110 | g0204 | EAS | CHB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18747 | hp1 | a0001 | c0001 | t0100 | g0265 | EAS | CHB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18747 | hp2 | a0001 | c0001 | t0004 | g0065 | EAS | CHB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18906 | hp1 | a0001 | c0001 | t0033 | g0248 | AFR | YRI | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18906 | hp2 | a0001 | c0001 | t0049 | g0137 | AFR | YRI | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18939 | hp2 | a0001 | c0001 | t0044 | g0271 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18940 | hp1 | a0001 | c0001 | t0090 | g0124 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18940 | hp2 | a0001 | c0001 | t0007 | g0047 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18944 | hp1 | a0001 | c0001 | t0032 | g0174 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18944 | hp2 | a0001 | c0001 | t0008 | g0274 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18946 | hp1 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18948 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18948 | hp2 | a0001 | c0001 | t0130 | g0001 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18949 | hp1 | a0001 | c0001 | t0007 | g0034 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18949 | hp2 | a0001 | c0001 | t0068 | g0181 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18950 | hp1 | a0001 | c0001 | t0099 | g0312 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18951 | hp1 | a0001 | c0001 | t0021 | g0290 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18952 | hp2 | a0001 | c0001 | t0008 | g0279 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18953 | hp1 | a0001 | c0001 | t0014 | g0276 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18953 | hp2 | a0001 | c0001 | t0004 | g0053 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18954 | hp2 | a0001 | c0001 | t0007 | g0050 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18957 | hp2 | a0001 | c0001 | t0096 | g0236 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18961 | hp1 | a0001 | c0001 | t0005 | g0042 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18961 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18962 | hp2 | a0001 | c0001 | t0005 | g0073 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18963 | hp1 | a0001 | c0001 | t0038 | g0108 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18964 | hp2 | a0001 | c0001 | t0108 | g0111 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18965 | hp1 | a0001 | c0001 | t0004 | g0072 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18966 | hp1 | a0001 | c0001 | t0019 | g0004 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18966 | hp2 | a0001 | c0001 | t0016 | g0001 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18969 | hp1 | a0001 | c0001 | t0004 | g0056 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0313 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18971 | hp2 | a0001 | c0001 | t0097 | g0272 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18972 | hp1 | a0001 | c0001 | t0012 | g0168 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18972 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18973 | hp1 | a0001 | c0001 | t0008 | g0287 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18973 | hp2 | a0001 | c0001 | t0007 | g0051 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18974 | hp1 | a0001 | c0001 | t0005 | g0028 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18974 | hp2 | a0001 | c0001 | t0075 | g0262 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18975 | hp1 | a0001 | c0001 | t0004 | g0068 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18975 | hp2 | a0001 | c0001 | t0016 | g0206 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18978 | hp1 | a0001 | c0001 | t0020 | g0098 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18978 | hp2 | a0001 | c0001 | t0092 | g0071 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18980 | hp2 | a0001 | c0001 | t0131 | g0232 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18982 | hp1 | a0001 | c0001 | t0074 | g0170 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18982 | hp2 | a0001 | c0001 | t0086 | g0066 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18983 | hp1 | a0001 | c0001 | t0012 | g0183 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18983 | hp2 | a0001 | c0001 | t0008 | g0302 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18986 | hp2 | a0001 | c0001 | t0084 | g0281 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18989 | hp1 | a0001 | c0001 | t0041 | g0296 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18992 | hp2 | a0001 | c0001 | t0013 | g0038 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18993 | hp1 | a0001 | c0001 | t0089 | g0049 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18994 | hp2 | a0001 | c0001 | t0036 | g0037 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18998 | hp1 | a0001 | c0001 | t0007 | g0076 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18999 | hp2 | a0001 | c0001 | t0004 | g0057 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19002 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19004 | hp2 | a0001 | c0001 | t0039 | g0233 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19005 | hp2 | a0001 | c0001 | t0007 | g0004 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19010 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19011 | hp1 | a0001 | c0001 | t0007 | g0048 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0297 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19043 | hp1 | a0001 | c0001 | t0121 | g0210 | AFR | LWK | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | LWK | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19054 | hp1 | a0001 | c0001 | t0069 | g0184 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19054 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19056 | hp1 | a0001 | c0001 | t0020 | g0128 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19057 | hp1 | a0001 | c0001 | t0005 | g0041 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19057 | hp2 | a0001 | c0001 | t0125 | g0267 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19060 | hp1 | a0001 | c0001 | t0010 | g0171 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19062 | hp1 | a0001 | c0001 | t0116 | g0234 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19064 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19064 | hp2 | a0001 | c0001 | t0021 | g0022 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19066 | hp1 | a0001 | c0001 | t0101 | g0114 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19068 | hp1 | a0001 | c0001 | t0038 | g0003 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19068 | hp2 | a0001 | c0001 | t0008 | g0308 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19072 | hp1 | a0001 | c0001 | t0008 | g0289 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19072 | hp2 | a0001 | c0001 | t0005 | g0033 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19074 | hp1 | a0001 | c0001 | t0029 | g0156 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19077 | hp1 | a0001 | c0001 | t0008 | g0288 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19077 | hp2 | a0001 | c0001 | t0005 | g0039 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19078 | hp1 | a0001 | c0001 | t0031 | g0176 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19078 | hp2 | a0001 | c0001 | t0005 | g0036 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19080 | hp1 | a0001 | c0001 | t0004 | g0078 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19081 | hp2 | a0001 | c0001 | t0007 | g0077 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19082 | hp1 | a0001 | c0001 | t0044 | g0270 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19082 | hp2 | a0001 | c0001 | t0039 | g0266 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19084 | hp1 | a0001 | c0001 | t0021 | g0022 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19085 | hp1 | a0001 | c0001 | t0103 | g0277 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19085 | hp2 | a0001 | c0001 | t0109 | g0006 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19087 | hp2 | a0001 | c0001 | t0037 | g0040 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19089 | hp1 | a0001 | c0001 | t0080 | g0002 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19089 | hp2 | a0001 | c0001 | t0020 | g0167 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19091 | hp1 | a0001 | c0001 | t0019 | g0009 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19091 | hp2 | a0001 | c0001 | t0106 | g0006 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19240 | hp1 | a0001 | c0001 | t0006 | g0008 | AFR | YRI | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA19240 | hp2 | a0001 | c0001 | t0113 | g0136 | AFR | YRI | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ASW | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ASW | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA20805 | hp1 | a0001 | c0001 | t0046 | g0315 | EUR | TSI | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0263 | EUR | TSI | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02109 | hp1 | a0001 | c0001 | t0087 | g0225 | AFR | ACB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02109 | hp2 | a0001 | c0001 | t0006 | g0330 | AFR | ACB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02486 | hp1 | a0001 | c0001 | t0083 | g0074 | AFR | ACB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG02486 | hp2 | a0001 | c0001 | t0048 | g0324 | AFR | ACB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | USA | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | USA | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18955 | hp1 | a0001 | c0001 | t0041 | g0269 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA18955 | hp2 | a0001 | c0001 | t0004 | g0055 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | USA | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | USA | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA21309 | hp1 | a0001 | c0001 | t0062 | g0250 | AFR | LWK | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
NA21309 | hp2 | a0001 | c0001 | t0093 | g0130 | AFR | LWK | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0149 | REF | REF | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
homoSapiens | grch38p0 | a0001 | c0001 | t0070 | g0264 | REF | REF | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:68654177 | C | T | 1 | a0001c0002 | 1 | HG02293.hp1 | synonymous_variant | LOW | c.249C>T | p.Ser83Ser | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/8 | 420/13378 | 249/555 | 83/184 | chr12 | 68654177 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:68610901 | C | G | 1 | a0001c0001t0131 | 1 | NA18980.hp2 | 5_prime_UTR_variant | MODIFIER | c.-169C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/8 | 37824 | chr12 | 68610901 | ||||||
chr12:68610914 | C | T | 1 | a0001c0001t0130 | 1 | NA18948.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-156C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/8 | chr12 | 68610914 | |||||||
chr12:68610915 | G | C | 1 | a0001c0001t0045 | 1 | HG02155.hp2 | 5_prime_UTR_variant | MODIFIER | c.-155G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/8 | 37810 | chr12 | 68610915 | ||||||
chr12:68610963 | G | C | 2 | a0001c0001t0025 a0001c0001t0046 |
3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
5_prime_UTR_variant | MODIFIER | c.-107G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/8 | 37762 | chr12 | 68610963 | ||||||
chr12:68610996 | G | A | 1 | a0001c0001t0016 | 3 | HG02074.hp2 NA18966.hp2 NA18975.hp2 |
5_prime_UTR_variant | MODIFIER | c.-74G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/8 | 37729 | chr12 | 68610996 | ||||||
chr12:68611003 | GGGGCGAC others(3): Show |
G | 1 | a0001c0001t0047 | 1 | HG02922.hp2 | 5_prime_UTR_variant | MODIFIER | c.-64_-55delGCGACGCT others(2): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/8 | 37710 | INFO_REALIGN_3_PRIME | chr12 | 68611003 | |||||
chr12:68648715 | A | G | 2 | a0001c0001t0008 a0001c0001t0129 |
10 | HG02056.hp2 HG02083.hp2 HG02148.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-10A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 2/8 | 10 | chr12 | 68648715 | ||||||
chr12:68659457 | A | C | 1 | a0001c0001t0128 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*208A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 2270 | chr12 | 68659457 | ||||||
chr12:68659838 | C | T | 6 | a0001c0001t0006 a0001c0001t0024 a0001c0001t0025 others(3): Show |
22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*589C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 2651 | chr12 | 68659838 | ||||||
chr12:68660165 | A | G | 2 | a0001c0001t0044 a0001c0001t0125 |
3 | NA18939.hp2 NA19057.hp2 NA19082.hp1 |
3_prime_UTR_variant | MODIFIER | c.*916A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 2978 | chr12 | 68660165 | ||||||
chr12:68660580 | C | T | 1 | a0001c0001t0124 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1331C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 3393 | chr12 | 68660580 | ||||||
chr12:68660777 | C | T | 6 | a0001c0001t0006 a0001c0001t0024 a0001c0001t0025 others(3): Show |
22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1528C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 3590 | chr12 | 68660777 | ||||||
chr12:68660847 | A | C | 1 | a0001c0001t0123 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1598A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 3660 | chr12 | 68660847 | ||||||
chr12:68660954 | A | G | 1 | a0001c0001t0043 | 2 | HG00280.hp1 HG02698.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1705A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 3767 | chr12 | 68660954 | ||||||
chr12:68661190 | C | G | 5 | a0001c0001t0023 a0001c0001t0047 a0001c0001t0121 others(2): Show |
6 | HG02293.hp1 HG02922.hp2 HG03209.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1941C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4003 | chr12 | 68661190 | ||||||
chr12:68661327 | G | A | 1 | a0001c0001t0048 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2078G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4140 | chr12 | 68661327 | ||||||
chr12:68661345 | C | T | 1 | a0001c0001t0120 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2096C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4158 | chr12 | 68661345 | ||||||
chr12:68661569 | A | G | 3 | a0001c0001t0006 a0001c0001t0024 a0001c0001t0127 |
18 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2320A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4382 | chr12 | 68661569 | ||||||
chr12:68662008 | C | CTA | 15 | a0001c0001t0009 a0001c0001t0010 a0001c0001t0017 others(12): Show |
29 | HG00673.hp2 HG01081.hp1 HG01109.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2783_*2784dupAT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4847 | INFO_REALIGN_3_PRIME | chr12 | 68662008 | |||||
chr12:68662008 | C | CTATA | 8 | a0001c0001t0011 a0001c0001t0026 a0001c0001t0027 others(5): Show |
13 | HG00099.hp2 HG00642.hp1 HG01106.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2781_*2784dupATAT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4847 | INFO_REALIGN_3_PRIME | chr12 | 68662008 | |||||
chr12:68662008 | C | CTATATA | 3 | a0001c0001t0049 a0001c0001t0050 a0001c0001t0051 |
3 | HG01106.hp1 HG01358.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2779_*2784dupATAT others(2): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4847 | INFO_REALIGN_3_PRIME | chr12 | 68662008 | |||||
chr12:68662008 | C | CTATATAT others(7): Show |
1 | a0001c0001t0126 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2771_*2784dupATAT others(10): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4847 | INFO_REALIGN_3_PRIME | chr12 | 68662008 | |||||
chr12:68662008 | C | CTATATAT others(17): Show |
1 | a0001c0001t0046 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2761_*2784dupATAT others(20): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4847 | INFO_REALIGN_3_PRIME | chr12 | 68662008 | |||||
chr12:68662008 | C | CTATATAT others(19): Show |
1 | a0001c0001t0025 | 2 | HG01516.hp2 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2784_*2785insATAT others(22): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4847 | INFO_REALIGN_3_PRIME | chr12 | 68662008 | |||||
chr12:68662008 | CTA | C | 45 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0008 others(42): Show |
141 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*2783_*2784delAT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4845 | INFO_REALIGN_3_PRIME | chr12 | 68662008 | |||||
chr12:68662008 | CTATATA | C | 2 | a0001c0001t0015 a0001c0001t0119 |
5 | HG01255.hp1 HG01256.hp1 HG01258.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2779_*2784delATAT others(2): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4841 | INFO_REALIGN_3_PRIME | chr12 | 68662008 | |||||
chr12:68662032 | ATT | A | 3 | a0001c0001t0023 a0001c0001t0047 a0001c0002t0023 |
4 | HG02293.hp1 HG02922.hp2 HG03704.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2784_*2785delTT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4846 | chr12 | 68662032 | ||||||
chr12:68662033 | T | TA | 1 | a0001c0001t0019 | 3 | HG02056.hp1 NA18966.hp1 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2784_*2785insA | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4847 | chr12 | 68662033 | ||||||
chr12:68662033 | T | TATA | 2 | a0001c0001t0004 a0001c0001t0087 |
11 | HG00423.hp1 HG00597.hp1 HG00673.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2784_*2785insATA | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4847 | chr12 | 68662033 | ||||||
chr12:68662033 | T | TATATA | 1 | a0001c0001t0004 | 4 | NA18946.hp1 NA18953.hp2 NA19010.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2784_*2785insATAT others(1): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4847 | chr12 | 68662033 | ||||||
chr12:68662033 | T | TATATATA | 2 | a0001c0001t0004 a0001c0001t0086 |
3 | NA18955.hp2 NA18982.hp2 NA19002.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2784_*2785insATAT others(3): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4847 | chr12 | 68662033 | ||||||
chr12:68662034 | T | A | 10 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0013 others(7): Show |
41 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*2785T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4847 | chr12 | 68662034 | ||||||
chr12:68662035 | A | AT | 4 | a0001c0001t0004 a0001c0001t0019 a0001c0001t0086 others(1): Show |
21 | HG00423.hp1 HG00597.hp1 HG00673.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2787dupT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4850 | INFO_REALIGN_3_PRIME | chr12 | 68662035 | |||||
chr12:68662035 | A | T | 10 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0013 others(7): Show |
41 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*2786A>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4848 | chr12 | 68662035 | ||||||
chr12:68662059 | G | GTA | 3 | a0001c0001t0025 a0001c0001t0046 a0001c0001t0065 |
4 | HG01516.hp2 HG01517.hp2 HG03927.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2822_*2823dupAT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4886 | INFO_REALIGN_3_PRIME | chr12 | 68662059 | |||||
chr12:68662103 | A | G | 1 | a0001c0001t0024 | 3 | HG02257.hp1 HG02622.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2854A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4916 | chr12 | 68662103 | ||||||
chr12:68662113 | T | C | 1 | a0001c0001t0093 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2864T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4926 | chr12 | 68662113 | ||||||
chr12:68662206 | A | G | 3 | a0001c0001t0022 a0001c0001t0064 a0001c0001t0118 |
5 | HG00738.hp1 HG02698.hp1 HG03654.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2957A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 5019 | chr12 | 68662206 | ||||||
chr12:68662413 | C | T | 1 | a0001c0001t0087 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3164C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 5226 | chr12 | 68662413 | ||||||
chr12:68662454 | G | T | 2 | a0001c0001t0028 a0001c0001t0056 |
3 | HG02451.hp2 HG03098.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3205G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 5267 | chr12 | 68662454 | ||||||
chr12:68662492 | C | T | 1 | a0001c0001t0117 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3243C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 5305 | chr12 | 68662492 | ||||||
chr12:68662504 | T | A | 3 | a0001c0001t0006 a0001c0001t0024 a0001c0001t0127 |
18 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3255T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 5317 | chr12 | 68662504 | ||||||
chr12:68662837 | A | T | 1 | a0001c0001t0055 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3588A>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 5650 | chr12 | 68662837 | ||||||
chr12:68662945 | C | T | 2 | a0001c0001t0035 a0001c0001t0042 |
4 | HG01361.hp1 HG02717.hp1 HG02886.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3696C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 5758 | chr12 | 68662945 | ||||||
chr12:68662947 | C | T | 2 | a0001c0001t0034 a0001c0001t0085 |
3 | HG02572.hp1 HG02615.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3698C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 5760 | chr12 | 68662947 | ||||||
chr12:68663115 | G | A | 1 | a0001c0001t0065 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3866G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 5928 | chr12 | 68663115 | ||||||
chr12:68663561 | A | G | 1 | a0001c0001t0116 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4312A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 6374 | chr12 | 68663561 | ||||||
chr12:68664075 | C | T | 3 | a0001c0001t0021 a0001c0001t0041 a0001c0001t0084 |
6 | NA18951.hp1 NA18955.hp1 NA18986.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4826C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 6888 | chr12 | 68664075 | ||||||
chr12:68664099 | C | T | 24 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0007 others(21): Show |
80 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*4850C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 6912 | chr12 | 68664099 | ||||||
chr12:68664261 | G | A | 5 | a0001c0001t0023 a0001c0001t0047 a0001c0001t0121 others(2): Show |
6 | HG02293.hp1 HG02922.hp2 HG03209.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5012G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 7074 | chr12 | 68664261 | ||||||
chr12:68664570 | A | G | 1 | a0001c0001t0054 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5321A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 7383 | chr12 | 68664570 | ||||||
chr12:68664584 | C | T | 2 | a0001c0001t0025 a0001c0001t0046 |
3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5335C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 7397 | chr12 | 68664584 | ||||||
chr12:68664639 | G | A | 1 | a0001c0001t0041 | 2 | NA18955.hp1 NA18989.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5390G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 7452 | chr12 | 68664639 | ||||||
chr12:68664641 | C | T | 5 | a0001c0001t0035 a0001c0001t0042 a0001c0001t0113 others(2): Show |
7 | HG01361.hp1 HG02717.hp1 HG02818.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5392C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 7454 | chr12 | 68664641 | ||||||
chr12:68664703 | C | CA | 29 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0014 others(26): Show |
81 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*5462dupA | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 7525 | INFO_REALIGN_3_PRIME | chr12 | 68664703 | |||||
chr12:68664718 | G | T | 2 | a0001c0001t0033 a0001c0001t0079 |
3 | HG02055.hp1 HG02647.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5469G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 7531 | chr12 | 68664718 | ||||||
chr12:68664875 | T | C | 1 | a0001c0001t0045 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5626T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 7688 | chr12 | 68664875 | ||||||
chr12:68664895 | G | A | 2 | a0001c0001t0036 a0001c0001t0080 |
3 | HG00408.hp2 NA18994.hp2 NA19089.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5646G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 7708 | chr12 | 68664895 | ||||||
chr12:68664904 | A | G | 1 | a0001c0001t0099 | 1 | NA18950.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5655A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 7717 | chr12 | 68664904 | ||||||
chr12:68664923 | C | G | 1 | a0001c0001t0054 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5674C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 7736 | chr12 | 68664923 | ||||||
chr12:68664925 | G | A | 5 | a0001c0001t0006 a0001c0001t0024 a0001c0001t0025 others(2): Show |
21 | HG01069.hp2 HG01516.hp2 HG01517.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*5676G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 7738 | chr12 | 68664925 | ||||||
chr12:68665088 | G | C | 1 | a0001c0001t0059 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5839G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 7901 | chr12 | 68665088 | ||||||
chr12:68665269 | G | C | 1 | a0001c0001t0067 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6020G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 8082 | chr12 | 68665269 | ||||||
chr12:68665296 | T | TAG | 2 | a0001c0001t0025 a0001c0001t0046 |
3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6050_*6051dupAG | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 8114 | INFO_REALIGN_3_PRIME | chr12 | 68665296 | |||||
chr12:68665326 | A | G | 1 | a0001c0001t0126 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6077A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 8139 | chr12 | 68665326 | ||||||
chr12:68665858 | C | CT | 7 | a0001c0001t0024 a0001c0001t0032 a0001c0001t0051 others(4): Show |
10 | HG00639.hp2 HG01192.hp2 HG01358.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*6624dupT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 8687 | INFO_REALIGN_3_PRIME | chr12 | 68665858 | |||||
chr12:68665872 | T | G | 3 | a0001c0001t0025 a0001c0001t0046 a0001c0001t0052 |
4 | HG01106.hp2 HG01516.hp2 HG01517.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6623T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 8685 | chr12 | 68665872 | ||||||
chr12:68665872 | T | TG | 2 | a0001c0001t0006 a0001c0001t0113 |
15 | HG01069.hp2 HG01891.hp2 HG02109.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*6623_*6624insG | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 8686 | chr12 | 68665872 | ||||||
chr12:68665873 | T | A | 5 | a0001c0001t0006 a0001c0001t0025 a0001c0001t0046 others(2): Show |
19 | HG01069.hp2 HG01106.hp2 HG01516.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*6624T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 8686 | chr12 | 68665873 | ||||||
chr12:68665873 | T | TGA | 7 | a0001c0001t0009 a0001c0001t0027 a0001c0001t0059 others(4): Show |
15 | HG00642.hp1 HG01255.hp2 HG01884.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*6630_*6631dupAG | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 8694 | INFO_REALIGN_3_PRIME | chr12 | 68665873 | |||||
chr12:68665920 | C | T | 1 | a0001c0001t0112 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6671C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 8733 | chr12 | 68665920 | ||||||
chr12:68665940 | G | A | 1 | a0001c0001t0100 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6691G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 8753 | chr12 | 68665940 | ||||||
chr12:68666073 | G | A | 1 | a0001c0001t0068 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6824G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 8886 | chr12 | 68666073 | ||||||
chr12:68666147 | G | T | 1 | a0001c0001t0126 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6898G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 8960 | chr12 | 68666147 | ||||||
chr12:68666206 | A | C | 1 | a0001c0001t0041 | 2 | NA18955.hp1 NA18989.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6957A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 9019 | chr12 | 68666206 | ||||||
chr12:68666286 | T | C | 4 | a0001c0001t0006 a0001c0001t0024 a0001c0001t0113 others(1): Show |
19 | HG01069.hp2 HG01891.hp2 HG02109.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*7037T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 9099 | chr12 | 68666286 | ||||||
chr12:68666299 | T | G | 1 | a0001c0001t0101 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7050T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 9112 | chr12 | 68666299 | ||||||
chr12:68666336 | G | A | 1 | a0001c0001t0055 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7087G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 9149 | chr12 | 68666336 | ||||||
chr12:68666422 | TA | T | 27 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0014 others(24): Show |
78 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*7174delA | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 9236 | chr12 | 68666422 | ||||||
chr12:68666423 | A | T | 1 | a0001c0001t0103 | 1 | NA19085.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7174A>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 9236 | chr12 | 68666423 | ||||||
chr12:68666424 | C | T | 27 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0014 others(24): Show |
78 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*7175C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 9237 | chr12 | 68666424 | ||||||
chr12:68666425 | T | G | 28 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0014 others(25): Show |
79 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*7176T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 9238 | chr12 | 68666425 | ||||||
chr12:68666993 | G | C | 1 | a0001c0001t0126 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7744G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 9806 | chr12 | 68666993 | ||||||
chr12:68667214 | A | G | 4 | a0001c0001t0006 a0001c0001t0024 a0001c0001t0113 others(1): Show |
19 | HG01069.hp2 HG01891.hp2 HG02109.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*7965A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 10027 | chr12 | 68667214 | ||||||
chr12:68667451 | G | A | 1 | a0001c0001t0125 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8202G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 10264 | chr12 | 68667451 | ||||||
chr12:68667451 | G | C | 1 | a0001c0001t0089 | 1 | NA18993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8202G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 10264 | chr12 | 68667451 | ||||||
chr12:68667459 | G | A | 1 | a0001c0001t0059 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8210G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 10272 | chr12 | 68667459 | ||||||
chr12:68667744 | G | A | 1 | a0001c0001t0095 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8495G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 10557 | chr12 | 68667744 | ||||||
chr12:68667953 | T | C | 1 | a0001c0001t0060 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8704T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 10766 | chr12 | 68667953 | ||||||
chr12:68668076 | T | C | 2 | a0001c0001t0090 a0001c0001t0096 |
2 | NA18940.hp1 NA18957.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8827T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 10889 | chr12 | 68668076 | ||||||
chr12:68668078 | C | A | 1 | a0001c0001t0090 | 1 | NA18940.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8829C>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 10891 | chr12 | 68668078 | ||||||
chr12:68668083 | G | A | 1 | a0001c0001t0090 | 1 | NA18940.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8834G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 10896 | chr12 | 68668083 | ||||||
chr12:68668086 | C | G | 1 | a0001c0001t0090 | 1 | NA18940.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8837C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 10899 | chr12 | 68668086 | ||||||
chr12:68668089 | G | T | 1 | a0001c0001t0090 | 1 | NA18940.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8840G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 10902 | chr12 | 68668089 | ||||||
chr12:68668091 | C | T | 1 | a0001c0001t0090 | 1 | NA18940.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8842C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 10904 | chr12 | 68668091 | ||||||
chr12:68668092 | A | T | 1 | a0001c0001t0090 | 1 | NA18940.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8843A>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 10905 | chr12 | 68668092 | ||||||
chr12:68668160 | C | G | 1 | a0001c0001t0034 | 2 | HG02572.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8911C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 10973 | chr12 | 68668160 | ||||||
chr12:68668279 | A | T | 1 | a0001c0001t0089 | 1 | NA18993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9030A>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 11092 | chr12 | 68668279 | ||||||
chr12:68668386 | A | T | 1 | a0001c0001t0098 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9137A>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 11199 | chr12 | 68668386 | ||||||
chr12:68668511 | A | G | 1 | a0001c0001t0059 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9262A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 11324 | chr12 | 68668511 | ||||||
chr12:68668655 | T | C | 1 | a0001c0001t0102 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9406T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 11468 | chr12 | 68668655 | ||||||
chr12:68668924 | C | T | 2 | a0001c0001t0025 a0001c0001t0046 |
3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9675C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 11737 | chr12 | 68668924 | ||||||
chr12:68668951 | A | G | 15 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0007 others(12): Show |
63 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*9702A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 11764 | chr12 | 68668951 | ||||||
chr12:68669043 | T | C | 29 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0014 others(26): Show |
80 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*9794T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 11856 | chr12 | 68669043 | ||||||
chr12:68669088 | A | G | 34 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0011 others(31): Show |
113 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*9839A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 11901 | chr12 | 68669088 | ||||||
chr12:68669137 | CTTTATA | C | 2 | a0001c0001t0033 a0001c0001t0079 |
3 | HG02055.hp1 HG02647.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9895_*9900delTTTA others(2): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 11957 | INFO_REALIGN_3_PRIME | chr12 | 68669137 | |||||
chr12:68669304 | A | G | 1 | a0001c0001t0045 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10055A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 12117 | chr12 | 68669304 | ||||||
chr12:68669342 | A | T | 2 | a0001c0001t0025 a0001c0001t0046 |
3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10093A>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 12155 | chr12 | 68669342 | ||||||
chr12:68669395 | C | T | 1 | a0001c0001t0083 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10146C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 12208 | chr12 | 68669395 | ||||||
chr12:68669503 | T | C | 2 | a0001c0001t0025 a0001c0001t0046 |
3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10254T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 12316 | chr12 | 68669503 | ||||||
chr12:68669551 | C | T | 70 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0010 others(67): Show |
201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
3_prime_UTR_variant | MODIFIER | c.*10302C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 12364 | chr12 | 68669551 | ||||||
chr12:68669585 | G | A | 1 | a0001c0001t0104 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10336G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 12398 | chr12 | 68669585 | ||||||
chr12:68669603 | C | T | 1 | a0001c0001t0125 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10354C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 12416 | chr12 | 68669603 | ||||||
chr12:68669629 | C | T | 1 | a0001c0001t0079 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10380C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 12442 | chr12 | 68669629 | ||||||
chr12:68669765 | A | C | 2 | a0001c0001t0025 a0001c0001t0046 |
3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10516A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 12578 | chr12 | 68669765 | ||||||
chr12:68669767 | T | C | 1 | a0001c0001t0061 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10518T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 12580 | chr12 | 68669767 | ||||||
chr12:68669859 | T | C | 2 | a0001c0001t0073 a0001c0001t0078 |
2 | HG00639.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10610T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 12672 | chr12 | 68669859 | ||||||
chr12:68669881 | C | T | 2 | a0001c0001t0006 a0001c0001t0113 |
15 | HG01069.hp2 HG01891.hp2 HG02109.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*10632C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 12694 | chr12 | 68669881 | ||||||
chr12:68669935 | C | CT | 34 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0018 others(31): Show |
84 | HG00280.hp2 HG00423.hp2 HG00639.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*10706dupT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 12769 | INFO_REALIGN_3_PRIME | chr12 | 68669935 | |||||
chr12:68669935 | C | CTT | 54 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0010 others(51): Show |
179 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*10705_*10706dupTT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 12769 | INFO_REALIGN_3_PRIME | chr12 | 68669935 | |||||
chr12:68669935 | C | CTTT | 9 | a0001c0001t0012 a0001c0001t0020 a0001c0001t0035 others(6): Show |
16 | HG01261.hp2 HG01361.hp1 HG01516.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*10704_*10706dupTT others(1): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 12769 | INFO_REALIGN_3_PRIME | chr12 | 68669935 | |||||
chr12:68669935 | CTT | C | 3 | a0001c0001t0006 a0001c0001t0024 a0001c0001t0113 |
18 | HG01069.hp2 HG01891.hp2 HG02109.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*10705_*10706delTT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 12767 | INFO_REALIGN_3_PRIME | chr12 | 68669935 | |||||
chr12:68669947 | T | C | 1 | a0001c0001t0126 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10698T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 12760 | chr12 | 68669947 | ||||||
chr12:68670090 | C | A | 1 | a0001c0001t0062 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10841C>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 12903 | chr12 | 68670090 | ||||||
chr12:68670211 | C | A | 1 | a0001c0001t0074 | 1 | NA18982.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10962C>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 13024 | chr12 | 68670211 | ||||||
chr12:68670233 | G | T | 1 | a0001c0001t0076 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10984G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 13046 | chr12 | 68670233 | ||||||
chr12:68670819 | A | G | 1 | a0001c0001t0046 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11570A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 13632 | chr12 | 68670819 | ||||||
chr12:68670845 | G | A | 1 | a0001c0001t0102 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11596G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 13658 | chr12 | 68670845 | ||||||
chr12:68671016 | G | A | 2 | a0001c0001t0039 a0001c0001t0116 |
3 | NA19004.hp2 NA19062.hp1 NA19082.hp2 |
3_prime_UTR_variant | MODIFIER | c.*11767G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 13829 | chr12 | 68671016 | ||||||
chr12:68671027 | T | TA | 11 | a0001c0001t0007 a0001c0001t0019 a0001c0001t0031 others(8): Show |
25 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*11799dupA | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 13862 | INFO_REALIGN_3_PRIME | chr12 | 68671027 | |||||
chr12:68671027 | TA | T | 13 | a0001c0001t0013 a0001c0001t0025 a0001c0001t0040 others(10): Show |
18 | HG01069.hp1 HG01074.hp2 HG01256.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*11799delA | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 13861 | INFO_REALIGN_3_PRIME | chr12 | 68671027 | |||||
chr12:68671181 | C | T | 1 | a0001c0001t0091 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11932C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 13994 | chr12 | 68671181 | ||||||
chr12:68671198 | C | T | 19 | a0001c0001t0002 a0001c0001t0017 a0001c0001t0020 others(16): Show |
67 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*11949C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 14011 | chr12 | 68671198 | ||||||
chr12:68671415 | T | C | 2 | a0001c0001t0121 a0001c0001t0122 |
2 | HG03209.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*12166T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 14228 | chr12 | 68671415 | ||||||
chr12:68671551 | G | A | 1 | a0001c0001t0065 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12302G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 14364 | chr12 | 68671551 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:68611086 | GCGGCCGC others(14): Show |
G | 1 | a0001c0001t0095g0341 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-27+48_-27+68delCG others(19): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68611086 | ||||||
chr12:68611095 | CG | C | 17 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(14): Show |
20 | HG00639.hp2 HG01069.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-27+56delG | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68611095 | ||||||
chr12:68611170 | G | A | 1 | a0001c0001t0030g0027 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-27+127G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68611170 | |||||||
chr12:68611188 | G | A | 62 | a0001c0001t0004g0002 a0001c0001t0004g0009 a0001c0001t0004g0053 others(59): Show |
65 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.-27+145G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68611188 | |||||||
chr12:68611225 | C | G | 33 | a0001c0001t0001g0024 a0001c0001t0001g0317 a0001c0001t0001g0318 others(30): Show |
37 | HG00639.hp2 HG01069.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.-27+182C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68611225 | |||||||
chr12:68611291 | C | T | 1 | a0001c0001t0002g0314 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-27+248C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68611291 | |||||||
chr12:68611346 | A | T | 55 | a0001c0001t0003g0007 a0001c0001t0003g0021 a0001c0001t0003g0268 others(52): Show |
58 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.-27+303A>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68611346 | |||||||
chr12:68611697 | T | C | 358 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(355): Show |
385 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(382): Show |
intron_variant | MODIFIER | c.-27+654T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68611697 | |||||||
chr12:68611892 | C | T | 2 | a0001c0001t0007g0076 a0001c0001t0007g0077 |
2 | NA18998.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.-27+849C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68611892 | |||||||
chr12:68612081 | G | T | 1 | a0001c0001t0003g0313 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-27+1038G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68612081 | |||||||
chr12:68612164 | C | G | 1 | a0001c0001t0075g0262 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-27+1121C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68612164 | |||||||
chr12:68612198 | T | C | 2 | a0001c0001t0007g0076 a0001c0001t0007g0077 |
2 | NA18998.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.-27+1155T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68612198 | |||||||
chr12:68612208 | G | A | 2 | a0001c0001t0025g0023 a0001c0001t0046g0315 |
3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-27+1165G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68612208 | |||||||
chr12:68612263 | C | T | 174 | a0001c0001t0003g0007 a0001c0001t0003g0020 a0001c0001t0003g0021 others(171): Show |
185 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.-27+1220C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68612263 | |||||||
chr12:68612624 | T | G | 1 | a0001c0001t0010g0079 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-27+1581T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68612624 | |||||||
chr12:68612699 | T | C | 1 | a0001c0001t0011g0080 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-27+1656T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68612699 | |||||||
chr12:68612723 | T | C | 2 | a0001c0001t0006g0026 a0001c0001t0006g0327 |
3 | HG02818.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-27+1680T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68612723 | |||||||
chr12:68612734 | T | C | 1 | a0001c0001t0095g0341 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-27+1691T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68612734 | |||||||
chr12:68612755 | ATAGTCTT others(61): Show |
A | 1 | a0001c0001t0079g0222 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-27+1781_-27+1848d others(70): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68612755 | ||||||
chr12:68612905 | A | G | 1 | a0001c0001t0001g0221 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-27+1862A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68612905 | |||||||
chr12:68613030 | C | G | 1 | a0001c0001t0127g0340 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-27+1987C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68613030 | |||||||
chr12:68613088 | T | C | 18 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(15): Show |
22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.-27+2045T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68613088 | |||||||
chr12:68613294 | T | C | 2 | a0001c0001t0002g0081 a0001c0001t0002g0082 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-27+2251T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68613294 | |||||||
chr12:68613389 | T | TA | 129 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0012 others(126): Show |
138 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.-27+2365dupA | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68613389 | ||||||
chr12:68613389 | T | TAA | 17 | a0001c0001t0002g0011 a0001c0001t0002g0086 a0001c0001t0002g0087 others(14): Show |
19 | HG00099.hp1 HG00738.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.-27+2364_-27+2365d others(4): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68613389 | ||||||
chr12:68613389 | TA | T | 11 | a0001c0001t0001g0217 a0001c0001t0001g0219 a0001c0001t0005g0075 others(8): Show |
11 | HG01081.hp1 HG01361.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.-27+2365delA | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68613389 | ||||||
chr12:68613424 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-27+2381A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68613424 | |||||||
chr12:68613502 | T | C | 11 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(8): Show |
14 | HG01069.hp2 HG01891.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-27+2459T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68613502 | |||||||
chr12:68613684 | A | C | 2 | a0001c0001t0025g0023 a0001c0001t0046g0315 |
3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-27+2641A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68613684 | |||||||
chr12:68613798 | T | C | 18 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(15): Show |
22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.-27+2755T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68613798 | |||||||
chr12:68613842 | T | C | 2 | a0001c0001t0005g0029 a0001c0001t0007g0030 |
2 | HG01257.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.-27+2799T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68613842 | |||||||
chr12:68614172 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-27+3129C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68614172 | |||||||
chr12:68614284 | C | T | 2 | a0001c0001t0121g0210 a0001c0001t0122g0211 |
2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-27+3241C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68614284 | |||||||
chr12:68614291 | A | G | 1 | a0001c0001t0124g0246 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-27+3248A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68614291 | |||||||
chr12:68614299 | A | G | 1 | a0001c0001t0022g0245 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-27+3256A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68614299 | |||||||
chr12:68614492 | T | C | 1 | a0001c0001t0037g0031 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-27+3449T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68614492 | |||||||
chr12:68614621 | A | AG | 76 | a0001c0001t0003g0007 a0001c0001t0003g0020 a0001c0001t0003g0021 others(73): Show |
80 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-27+3580dupG | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68614621 | ||||||
chr12:68614862 | C | T | 1 | a0001c0001t0126g0339 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-27+3819C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68614862 | |||||||
chr12:68615186 | A | C | 2 | a0001c0001t0015g0209 a0001c0001t0119g0208 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-27+4143A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68615186 | |||||||
chr12:68615193 | A | AT | 8 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0119 others(5): Show |
8 | HG02015.hp2 HG02027.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.-27+4153dupT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68615193 | ||||||
chr12:68615332 | C | T | 1 | a0001c0001t0008g0311 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-27+4289C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68615332 | |||||||
chr12:68615875 | C | A | 1 | a0001c0001t0126g0339 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-27+4832C>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68615875 | |||||||
chr12:68615936 | C | A | 76 | a0001c0001t0003g0007 a0001c0001t0003g0020 a0001c0001t0003g0021 others(73): Show |
80 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-27+4893C>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68615936 | |||||||
chr12:68615967 | AT | A | 248 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0011 others(245): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.-27+4938delT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68615967 | ||||||
chr12:68615982 | G | A | 3 | a0001c0001t0022g0223 a0001c0001t0022g0227 a0001c0001t0064g0228 |
3 | HG00738.hp1 HG02698.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-27+4939G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68615982 | |||||||
chr12:68616027 | G | A | 1 | a0001c0001t0081g0032 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-27+4984G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68616027 | |||||||
chr12:68616242 | G | A | 1 | a0001c0001t0054g0144 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-27+5199G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68616242 | |||||||
chr12:68616251 | T | C | 16 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(13): Show |
19 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-27+5208T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68616251 | |||||||
chr12:68616273 | G | T | 1 | a0001c0001t0102g0143 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-27+5230G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68616273 | |||||||
chr12:68616330 | G | A | 1 | a0001c0001t0037g0031 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-27+5287G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68616330 | |||||||
chr12:68616438 | A | AT | 40 | a0001c0001t0001g0019 a0001c0001t0001g0196 a0001c0001t0001g0198 others(37): Show |
40 | HG00099.hp1 HG00099.hp2 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.-27+5421dupT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68616438 | ||||||
chr12:68616438 | AT | A | 62 | a0001c0001t0001g0145 a0001c0001t0001g0221 a0001c0001t0001g0317 others(59): Show |
69 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.-27+5421delT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68616438 | ||||||
chr12:68616438 | ATT | A | 45 | a0001c0001t0003g0007 a0001c0001t0003g0021 a0001c0001t0003g0242 others(42): Show |
48 | HG00280.hp2 HG00438.hp1 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.-27+5420_-27+5421d others(4): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68616438 | ||||||
chr12:68616438 | ATTT | A | 20 | a0001c0001t0003g0020 a0001c0001t0003g0224 a0001c0001t0003g0229 others(17): Show |
21 | HG00738.hp1 HG02602.hp2 HG02698.hp1 others(18): Show |
intron_variant | MODIFIER | c.-27+5419_-27+5421d others(5): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68616438 | ||||||
chr12:68616438 | ATTTTTTT others(3): Show |
A | 25 | a0001c0001t0005g0004 a0001c0001t0005g0036 a0001c0001t0005g0039 others(22): Show |
25 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.-27+5412_-27+5421d others(12): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68616438 | ||||||
chr12:68616438 | ATTTTTTT others(4): Show |
A | 2 | a0001c0001t0005g0033 a0001c0001t0007g0034 |
2 | NA18949.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.-27+5411_-27+5421d others(13): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68616438 | ||||||
chr12:68616577 | G | A | 4 | a0001c0001t0023g0125 a0001c0001t0023g0126 a0001c0001t0047g0123 others(1): Show |
4 | HG02293.hp1 HG02922.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.-27+5534G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68616577 | |||||||
chr12:68616583 | A | C | 2 | a0001c0001t0002g0110 a0001c0001t0108g0111 |
2 | NA18964.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-27+5540A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68616583 | |||||||
chr12:68616719 | C | T | 16 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(13): Show |
19 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-27+5676C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68616719 | |||||||
chr12:68616781 | A | G | 1 | a0001c0001t0086g0066 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-27+5738A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68616781 | |||||||
chr12:68616851 | C | T | 1 | a0001c0001t0004g0065 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-27+5808C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68616851 | |||||||
chr12:68617094 | C | T | 1 | a0001c0001t0005g0052 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-27+6051C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68617094 | |||||||
chr12:68617481 | A | G | 1 | a0001c0001t0039g0266 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-27+6438A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68617481 | |||||||
chr12:68617581 | A | G | 1 | a0001c0001t0049g0137 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-27+6538A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68617581 | |||||||
chr12:68617719 | A | G | 4 | a0001c0001t0009g0226 a0001c0001t0009g0256 a0001c0001t0009g0257 others(1): Show |
4 | HG02145.hp1 HG02809.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-27+6676A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68617719 | |||||||
chr12:68617735 | G | A | 18 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(15): Show |
22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.-27+6692G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68617735 | |||||||
chr12:68617747 | AACCATAA others(14): Show |
A | 4 | a0001c0001t0003g0238 a0001c0001t0003g0239 a0001c0001t0003g0240 others(1): Show |
4 | NA18951.hp2 NA18972.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.-27+6705_-27+6725d others(23): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68617747 | |||||||
chr12:68617774 | A | AT | 20 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(17): Show |
24 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(21): Show |
intron_variant | MODIFIER | c.-27+6742dupT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68617774 | ||||||
chr12:68617839 | C | T | 2 | a0001c0001t0009g0260 a0001c0001t0009g0261 |
2 | HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-27+6796C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68617839 | |||||||
chr12:68617910 | C | A | 1 | a0001c0001t0026g0138 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-27+6867C>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68617910 | |||||||
chr12:68618025 | A | G | 2 | a0001c0001t0026g0138 a0001c0001t0026g0142 |
2 | HG00099.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-27+6982A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68618025 | |||||||
chr12:68618082 | A | G | 1 | a0001c0001t0117g0306 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-27+7039A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68618082 | |||||||
chr12:68618086 | C | CT | 159 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(156): Show |
175 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.-27+7068dupT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68618086 | ||||||
chr12:68618086 | C | CTT | 23 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0205 others(20): Show |
23 | HG00621.hp2 HG00735.hp1 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.-27+7067_-27+7068d others(4): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68618086 | ||||||
chr12:68618086 | C | CTTT | 14 | a0001c0001t0001g0195 a0001c0001t0003g0021 a0001c0001t0003g0229 others(11): Show |
15 | HG01106.hp2 HG01109.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.-27+7066_-27+7068d others(5): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68618086 | ||||||
chr12:68618086 | C | CTTTT | 50 | a0001c0001t0003g0007 a0001c0001t0003g0020 a0001c0001t0003g0230 others(47): Show |
52 | HG00280.hp2 HG00438.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.-27+7065_-27+7068d others(6): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68618086 | ||||||
chr12:68618086 | C | CTTTTT | 19 | a0001c0001t0003g0224 a0001c0001t0003g0237 a0001c0001t0003g0238 others(16): Show |
20 | HG00423.hp2 HG01175.hp1 HG02056.hp2 others(17): Show |
intron_variant | MODIFIER | c.-27+7064_-27+7068d others(7): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68618086 | ||||||
chr12:68618086 | CTTTTTTT others(2): Show |
C | 15 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(12): Show |
18 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-27+7060_-27+7068d others(11): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68618086 | ||||||
chr12:68618150 | C | T | 2 | a0001c0001t0002g0105 a0001c0001t0107g0116 |
2 | HG02258.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.-27+7107C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68618150 | |||||||
chr12:68618174 | G | GC | 18 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(15): Show |
22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.-27+7132dupC | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68618174 | ||||||
chr12:68618204 | A | G | 1 | a0001c0001t0007g0034 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-27+7161A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68618204 | |||||||
chr12:68618280 | G | A | 2 | a0001c0001t0007g0076 a0001c0001t0007g0077 |
2 | NA18998.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.-27+7237G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68618280 | |||||||
chr12:68618310 | G | A | 1 | a0001c0001t0124g0246 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-27+7267G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68618310 | |||||||
chr12:68618315 | C | T | 1 | a0001c0001t0004g0078 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-27+7272C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68618315 | |||||||
chr12:68618683 | G | C | 1 | a0001c0001t0001g0147 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-27+7640G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68618683 | |||||||
chr12:68618698 | CTGTCCTA others(8): Show |
C | 2 | a0001c0001t0025g0023 a0001c0001t0046g0315 |
3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-27+7659_-27+7673d others(17): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68618698 | ||||||
chr12:68618740 | ATTT | A | 15 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(12): Show |
18 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-27+7704_-27+7706d others(5): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68618740 | ||||||
chr12:68619040 | C | T | 1 | a0001c0001t0017g0113 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-27+7997C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68619040 | |||||||
chr12:68619055 | G | A | 1 | a0001c0001t0126g0339 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-27+8012G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68619055 | |||||||
chr12:68619361 | G | A | 58 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0011 others(55): Show |
62 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.-27+8318G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68619361 | |||||||
chr12:68619466 | GAA | G | 7 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(4): Show |
7 | HG00558.hp1 HG02027.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-27+8425_-27+8426d others(4): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68619466 | ||||||
chr12:68619550 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-27+8507A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68619550 | |||||||
chr12:68619637 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-27+8594G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68619637 | |||||||
chr12:68619661 | T | C | 1 | a0001c0001t0099g0312 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-27+8618T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68619661 | |||||||
chr12:68619894 | A | G | 2 | a0001c0001t0069g0184 a0001c0001t0090g0124 |
2 | NA18940.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.-27+8851A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68619894 | |||||||
chr12:68619895 | T | C | 1 | a0001c0001t0097g0272 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-27+8852T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68619895 | |||||||
chr12:68619943 | C | T | 1 | a0001c0001t0002g0121 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-27+8900C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68619943 | |||||||
chr12:68620032 | T | C | 18 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(15): Show |
22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.-27+8989T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68620032 | |||||||
chr12:68620036 | T | C | 1 | a0001c0001t0125g0267 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-27+8993T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68620036 | |||||||
chr12:68620055 | A | G | 1 | a0001c0001t0126g0339 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-27+9012A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68620055 | |||||||
chr12:68620111 | G | C | 3 | a0001c0001t0005g0005 a0001c0001t0005g0054 a0001c0001t0013g0005 |
4 | HG01069.hp1 HG01071.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.-27+9068G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68620111 | |||||||
chr12:68620207 | T | A | 64 | a0001c0001t0004g0002 a0001c0001t0004g0009 a0001c0001t0004g0053 others(61): Show |
67 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.-27+9164T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68620207 | |||||||
chr12:68620450 | T | G | 23 | a0001c0001t0003g0020 a0001c0001t0003g0224 a0001c0001t0003g0229 others(20): Show |
24 | HG00738.hp1 HG02074.hp1 HG02602.hp2 others(21): Show |
intron_variant | MODIFIER | c.-27+9407T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68620450 | |||||||
chr12:68620502 | C | G | 1 | a0001c0001t0112g0104 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-27+9459C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68620502 | |||||||
chr12:68620606 | C | CT | 74 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0011 others(71): Show |
78 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.-27+9577dupT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68620606 | ||||||
chr12:68620825 | C | T | 1 | a0001c0001t0007g0077 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-27+9782C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68620825 | |||||||
chr12:68620878 | G | A | 1 | a0001c0001t0029g0186 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-27+9835G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68620878 | |||||||
chr12:68620951 | G | A | 18 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(15): Show |
22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.-27+9908G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68620951 | |||||||
chr12:68621105 | A | T | 1 | a0001c0001t0079g0222 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-27+10062A>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68621105 | |||||||
chr12:68621130 | A | C | 18 | a0001c0001t0005g0004 a0001c0001t0005g0073 a0001c0001t0007g0004 others(15): Show |
18 | HG00544.hp1 HG00621.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.-27+10087A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68621130 | |||||||
chr12:68621132 | G | A | 1 | a0001c0001t0124g0246 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-27+10089G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68621132 | |||||||
chr12:68621232 | C | T | 1 | a0001c0001t0012g0183 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-27+10189C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68621232 | |||||||
chr12:68621253 | ATAAT | A | 60 | a0001c0001t0004g0002 a0001c0001t0004g0009 a0001c0001t0004g0053 others(57): Show |
63 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.-27+10214_-27+1021 others(8): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68621253 | ||||||
chr12:68621280 | A | G | 1 | a0001c0001t0014g0293 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-27+10237A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68621280 | |||||||
chr12:68621349 | CACTGACT others(3): Show |
C | 1 | a0001c0001t0102g0143 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-27+10308_-27+1031 others(14): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68621349 | ||||||
chr12:68621558 | G | T | 16 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(13): Show |
19 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-27+10515G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68621558 | |||||||
chr12:68621875 | T | C | 18 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(15): Show |
22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.-27+10832T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68621875 | |||||||
chr12:68622139 | C | T | 15 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(12): Show |
18 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-27+11096C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68622139 | |||||||
chr12:68622227 | A | G | 18 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(15): Show |
22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.-27+11184A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68622227 | |||||||
chr12:68622294 | C | A | 1 | a0001c0001t0001g0148 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-27+11251C>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68622294 | |||||||
chr12:68622453 | C | A | 1 | a0001c0001t0003g0230 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-27+11410C>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68622453 | |||||||
chr12:68622584 | A | G | 1 | a0001c0001t0003g0224 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-27+11541A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68622584 | |||||||
chr12:68622622 | C | T | 4 | a0001c0001t0035g0215 a0001c0001t0035g0220 a0001c0001t0042g0214 others(1): Show |
4 | HG01361.hp1 HG02717.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-27+11579C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68622622 | |||||||
chr12:68622734 | A | T | 1 | a0001c0001t0126g0339 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-27+11691A>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68622734 | |||||||
chr12:68622736 | C | G | 1 | a0001c0001t0004g0065 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-27+11693C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68622736 | |||||||
chr12:68623016 | A | G | 1 | a0001c0001t0030g0027 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-27+11973A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68623016 | |||||||
chr12:68623030 | A | G | 2 | a0001c0001t0003g0291 a0001c0001t0128g0292 |
2 | HG02738.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-27+11987A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68623030 | |||||||
chr12:68623065 | C | T | 1 | a0001c0001t0010g0182 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-27+12022C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68623065 | |||||||
chr12:68623144 | A | C | 15 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(12): Show |
18 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-27+12101A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68623144 | |||||||
chr12:68623199 | T | G | 77 | a0001c0001t0004g0002 a0001c0001t0004g0009 a0001c0001t0004g0053 others(74): Show |
80 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.-27+12156T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68623199 | |||||||
chr12:68623266 | G | A | 1 | a0001c0001t0112g0104 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-27+12223G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68623266 | |||||||
chr12:68623361 | A | C | 1 | a0001c0001t0089g0049 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-27+12318A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68623361 | |||||||
chr12:68623497 | T | G | 1 | a0001c0001t0083g0074 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-27+12454T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68623497 | |||||||
chr12:68623629 | G | A | 180 | a0001c0001t0003g0007 a0001c0001t0003g0020 a0001c0001t0003g0021 others(177): Show |
191 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.-27+12586G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68623629 | |||||||
chr12:68623838 | C | T | 76 | a0001c0001t0003g0007 a0001c0001t0003g0020 a0001c0001t0003g0021 others(73): Show |
80 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-27+12795C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68623838 | |||||||
chr12:68623839 | G | A | 2 | a0001c0001t0025g0023 a0001c0001t0046g0315 |
3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-27+12796G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68623839 | |||||||
chr12:68623877 | C | T | 16 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(13): Show |
19 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-27+12834C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68623877 | |||||||
chr12:68623973 | A | G | 16 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(13): Show |
19 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-27+12930A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68623973 | |||||||
chr12:68623975 | T | C | 336 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0146 others(333): Show |
362 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(359): Show |
intron_variant | MODIFIER | c.-27+12932T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68623975 | |||||||
chr12:68624038 | A | AG | 2 | a0001c0001t0021g0022 a0001c0001t0021g0290 |
3 | NA18951.hp1 NA19064.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-27+12995_-27+1299 others(5): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68624038 | |||||||
chr12:68624445 | C | A | 1 | a0001c0001t0126g0339 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-27+13402C>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68624445 | |||||||
chr12:68624457 | A | G | 1 | a0001c0001t0095g0341 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-27+13414A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68624457 | |||||||
chr12:68624618 | C | G | 1 | a0001c0001t0002g0103 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-27+13575C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68624618 | |||||||
chr12:68624653 | T | TA | 2 | a0001c0001t0025g0023 a0001c0001t0046g0315 |
3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-27+13615dupA | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68624653 | ||||||
chr12:68624661 | T | C | 1 | a0001c0001t0002g0086 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-27+13618T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68624661 | |||||||
chr12:68624703 | C | G | 3 | a0001c0001t0010g0171 a0001c0001t0010g0182 a0001c0001t0110g0204 |
3 | HG00673.hp2 NA18612.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-27+13660C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68624703 | |||||||
chr12:68624721 | A | G | 1 | a0001c0001t0010g0079 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-27+13678A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68624721 | |||||||
chr12:68624746 | C | G | 1 | a0001c0001t0040g0304 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-27+13703C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68624746 | |||||||
chr12:68624856 | A | G | 16 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(13): Show |
19 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-27+13813A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68624856 | |||||||
chr12:68624943 | G | T | 18 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(15): Show |
22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.-27+13900G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68624943 | |||||||
chr12:68625014 | C | T | 1 | a0001c0001t0003g0303 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-27+13971C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68625014 | |||||||
chr12:68625158 | C | T | 3 | a0001c0001t0048g0324 a0001c0001t0073g0025 a0001c0001t0078g0025 |
3 | HG00639.hp2 HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-27+14115C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68625158 | |||||||
chr12:68625254 | G | T | 15 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(12): Show |
18 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-27+14211G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68625254 | |||||||
chr12:68625299 | C | G | 18 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(15): Show |
22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.-27+14256C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68625299 | |||||||
chr12:68625327 | T | A | 1 | a0001c0001t0002g0088 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-27+14284T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68625327 | |||||||
chr12:68625570 | A | G | 1 | a0001c0001t0008g0289 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-27+14527A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68625570 | |||||||
chr12:68625624 | T | A | 1 | a0001c0001t0004g0053 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-27+14581T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68625624 | |||||||
chr12:68625625 | T | A | 1 | a0001c0001t0004g0053 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-27+14582T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68625625 | |||||||
chr12:68625668 | C | G | 16 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(13): Show |
19 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-27+14625C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68625668 | |||||||
chr12:68625685 | C | T | 2 | a0001c0001t0008g0287 a0001c0001t0008g0288 |
2 | NA18973.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.-27+14642C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68625685 | |||||||
chr12:68625751 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-27+14708G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68625751 | |||||||
chr12:68625778 | C | T | 1 | a0001c0001t0074g0170 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-27+14735C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68625778 | |||||||
chr12:68625791 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-27+14748G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68625791 | |||||||
chr12:68625848 | G | A | 1 | a0001c0001t0125g0267 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-27+14805G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68625848 | |||||||
chr12:68625876 | C | T | 63 | a0001c0001t0004g0002 a0001c0001t0004g0009 a0001c0001t0004g0053 others(60): Show |
66 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.-27+14833C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68625876 | |||||||
chr12:68625899 | C | T | 2 | a0001c0001t0002g0011 a0001c0001t0002g0087 |
3 | HG01496.hp1 HG02300.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.-27+14856C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68625899 | |||||||
chr12:68625920 | CA | C | 19 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(16): Show |
22 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.-27+14892delA | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68625920 | ||||||
chr12:68626075 | A | G | 1 | a0001c0001t0113g0136 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-27+15032A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68626075 | |||||||
chr12:68626142 | A | C | 1 | a0001c0001t0127g0340 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-27+15099A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68626142 | |||||||
chr12:68626178 | C | T | 1 | a0001c0001t0007g0051 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-27+15135C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68626178 | |||||||
chr12:68626213 | A | G | 76 | a0001c0001t0003g0007 a0001c0001t0003g0020 a0001c0001t0003g0021 others(73): Show |
80 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-27+15170A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68626213 | |||||||
chr12:68626227 | G | C | 1 | a0001c0001t0057g0134 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-27+15184G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68626227 | |||||||
chr12:68626705 | C | T | 11 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(8): Show |
14 | HG01069.hp2 HG01891.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-27+15662C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68626705 | |||||||
chr12:68626723 | C | T | 3 | a0001c0001t0028g0319 a0001c0001t0028g0323 a0001c0001t0056g0322 |
3 | HG02451.hp2 HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-27+15680C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68626723 | |||||||
chr12:68626785 | GTTGT | G | 2 | a0001c0001t0025g0023 a0001c0001t0046g0315 |
3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-27+15761_-27+1576 others(8): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68626785 | ||||||
chr12:68626872 | A | T | 3 | a0001c0001t0015g0115 a0001c0001t0015g0209 a0001c0001t0119g0208 |
3 | HG01256.hp1 HG01258.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.-27+15829A>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68626872 | |||||||
chr12:68626929 | G | A | 2 | a0001c0001t0004g0055 a0001c0001t0004g0056 |
2 | NA18955.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.-27+15886G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68626929 | |||||||
chr12:68626963 | C | G | 15 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(12): Show |
18 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-27+15920C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68626963 | |||||||
chr12:68626971 | C | A | 2 | a0001c0001t0121g0210 a0001c0001t0122g0211 |
2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-27+15928C>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68626971 | |||||||
chr12:68627031 | G | C | 1 | a0001c0001t0003g0273 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-27+15988G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68627031 | |||||||
chr12:68627173 | G | C | 1 | a0001c0001t0091g0043 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-27+16130G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68627173 | |||||||
chr12:68627263 | CATACA | C | 18 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(15): Show |
22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.-27+16227_-27+1623 others(9): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68627263 | ||||||
chr12:68627467 | T | A | 2 | a0001c0001t0025g0023 a0001c0001t0046g0315 |
3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-27+16424T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68627467 | |||||||
chr12:68627479 | A | G | 3 | a0001c0001t0033g0247 a0001c0001t0033g0248 a0001c0001t0079g0222 |
3 | HG02055.hp1 HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-27+16436A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68627479 | |||||||
chr12:68627503 | G | A | 1 | a0001c0001t0005g0036 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-27+16460G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68627503 | |||||||
chr12:68627576 | T | C | 2 | a0001c0001t0121g0210 a0001c0001t0122g0211 |
2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-27+16533T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68627576 | |||||||
chr12:68627693 | G | A | 1 | a0001c0001t0105g0083 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-27+16650G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68627693 | |||||||
chr12:68627947 | A | T | 4 | a0001c0001t0018g0300 a0001c0001t0025g0023 a0001c0001t0040g0304 others(1): Show |
5 | HG01256.hp2 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27+16904A>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68627947 | |||||||
chr12:68627957 | A | G | 1 | a0001c0001t0012g0183 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-27+16914A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68627957 | |||||||
chr12:68627984 | A | G | 1 | a0001c0001t0081g0032 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-27+16941A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68627984 | |||||||
chr12:68628416 | C | G | 3 | a0001c0001t0002g0118 a0001c0001t0002g0120 a0001c0001t0002g0122 |
3 | HG02027.hp1 HG02080.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.-27+17373C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68628416 | |||||||
chr12:68628449 | G | T | 3 | a0001c0001t0049g0137 a0001c0001t0055g0133 a0001c0001t0058g0213 |
3 | HG02976.hp1 HG03579.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-27+17406G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68628449 | |||||||
chr12:68628516 | C | G | 66 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0011 others(63): Show |
70 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.-27+17473C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68628516 | |||||||
chr12:68628660 | T | A | 258 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0011 others(255): Show |
273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.-27+17617T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68628660 | |||||||
chr12:68628876 | A | G | 1 | a0001c0001t0007g0048 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-27+17833A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68628876 | |||||||
chr12:68628925 | A | G | 3 | a0001c0001t0004g0053 a0001c0001t0004g0063 a0001c0001t0004g0078 |
3 | NA18946.hp1 NA18953.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.-27+17882A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68628925 | |||||||
chr12:68628988 | C | G | 18 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(15): Show |
22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.-27+17945C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68628988 | |||||||
chr12:68629013 | A | ATCTG | 73 | a0001c0001t0003g0007 a0001c0001t0003g0020 a0001c0001t0003g0021 others(70): Show |
77 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.-27+17986_-27+1798 others(8): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68629013 | ||||||
chr12:68629013 | A | ATCTGTCT others(1): Show |
3 | a0001c0001t0039g0266 a0001c0001t0044g0270 a0001c0001t0044g0271 |
3 | NA18939.hp2 NA19082.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.-27+17982_-27+1798 others(12): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68629013 | ||||||
chr12:68629018 | T | G | 66 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0011 others(63): Show |
70 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.-27+17975T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68629018 | |||||||
chr12:68629039 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-27+17996A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68629039 | |||||||
chr12:68629247 | A | G | 2 | a0001c0001t0009g0254 a0001c0001t0061g0253 |
2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-27+18204A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68629247 | |||||||
chr12:68629269 | G | C | 1 | a0001c0001t0008g0289 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-27+18226G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68629269 | |||||||
chr12:68629319 | C | G | 1 | a0001c0001t0018g0243 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-27+18276C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68629319 | |||||||
chr12:68629494 | G | A | 1 | a0001c0001t0081g0032 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-27+18451G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68629494 | |||||||
chr12:68629680 | T | C | 1 | a0001c0001t0077g0197 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-27+18637T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68629680 | |||||||
chr12:68629682 | C | T | 2 | a0001c0001t0001g0169 a0001c0001t0001g0203 |
2 | HG03516.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-27+18639C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68629682 | |||||||
chr12:68630111 | C | G | 1 | a0001c0001t0127g0340 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-26-18588C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68630111 | |||||||
chr12:68630331 | C | T | 1 | a0001c0001t0024g0338 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-26-18368C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68630331 | |||||||
chr12:68630487 | T | C | 3 | a0001c0001t0003g0021 a0001c0001t0003g0268 a0001c0001t0014g0309 |
4 | HG00438.hp1 NA18961.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-18212T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68630487 | |||||||
chr12:68630608 | G | A | 1 | a0001c0001t0126g0339 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-26-18091G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68630608 | |||||||
chr12:68630746 | C | T | 2 | a0001c0001t0025g0023 a0001c0001t0046g0315 |
3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-26-17953C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68630746 | |||||||
chr12:68630764 | A | G | 1 | a0001c0001t0102g0143 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-26-17935A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68630764 | |||||||
chr12:68630778 | A | G | 4 | a0001c0001t0035g0215 a0001c0001t0035g0220 a0001c0001t0042g0214 others(1): Show |
4 | HG01361.hp1 HG02717.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-17921A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68630778 | |||||||
chr12:68630915 | G | A | 16 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(13): Show |
19 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-26-17784G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68630915 | |||||||
chr12:68630932 | G | GT | 10 | a0001c0001t0002g0003 a0001c0001t0002g0100 a0001c0001t0002g0101 others(7): Show |
12 | HG02486.hp2 HG02622.hp1 NA18968.hp2 others(9): Show |
intron_variant | MODIFIER | c.-26-17757dupT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68630932 | ||||||
chr12:68630932 | G | T | 1 | a0001c0001t0008g0302 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-26-17767G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68630932 | |||||||
chr12:68630936 | T | C | 1 | a0001c0001t0123g0140 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-26-17763T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68630936 | |||||||
chr12:68630962 | G | A | 1 | a0001c0001t0018g0243 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-26-17737G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68630962 | |||||||
chr12:68631045 | C | G | 2 | a0001c0001t0003g0285 a0001c0001t0003g0286 |
2 | HG03704.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-26-17654C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68631045 | |||||||
chr12:68631046 | C | T | 1 | a0001c0001t0005g0064 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-26-17653C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68631046 | |||||||
chr12:68631279 | T | C | 1 | a0001c0001t0117g0306 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-26-17420T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68631279 | |||||||
chr12:68631577 | C | T | 2 | a0001c0001t0121g0210 a0001c0001t0122g0211 |
2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-26-17122C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68631577 | |||||||
chr12:68631620 | A | C | 1 | a0001c0001t0002g0109 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-26-17079A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68631620 | |||||||
chr12:68631841 | G | T | 1 | a0001c0001t0007g0047 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-26-16858G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68631841 | |||||||
chr12:68632035 | A | G | 76 | a0001c0001t0003g0007 a0001c0001t0003g0020 a0001c0001t0003g0021 others(73): Show |
80 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-26-16664A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632035 | |||||||
chr12:68632050 | GT | G | 16 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(13): Show |
19 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-26-16639delT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68632050 | ||||||
chr12:68632086 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-26-16613A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632086 | |||||||
chr12:68632128 | T | G | 1 | a0001c0001t0126g0339 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-26-16571T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632128 | |||||||
chr12:68632129 | G | GT | 26 | a0001c0001t0001g0018 a0001c0001t0001g0163 a0001c0001t0001g0165 others(23): Show |
27 | HG00438.hp1 HG01361.hp1 HG01978.hp2 others(24): Show |
intron_variant | MODIFIER | c.-26-16554dupT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68632129 | ||||||
chr12:68632129 | G | T | 2 | a0001c0001t0041g0269 a0001c0001t0041g0296 |
2 | NA18955.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.-26-16570G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632129 | |||||||
chr12:68632129 | GT | G | 10 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0169 others(7): Show |
10 | HG02055.hp2 HG02257.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-26-16554delT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68632129 | ||||||
chr12:68632132 | T | G | 2 | a0001c0001t0025g0023 a0001c0001t0046g0315 |
3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-26-16567T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632132 | |||||||
chr12:68632137 | T | TTG | 6 | a0001c0001t0006g0026 a0001c0001t0006g0327 a0001c0001t0006g0330 others(3): Show |
7 | HG01109.hp2 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-26-16561_-26-1656 others(6): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68632137 | ||||||
chr12:68632138 | T | G | 2 | a0001c0001t0018g0243 a0001c0001t0043g0092 |
2 | HG02698.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.-26-16561T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632138 | |||||||
chr12:68632138 | T | TG | 8 | a0001c0001t0006g0008 a0001c0001t0006g0328 a0001c0001t0006g0329 others(5): Show |
10 | HG01069.hp2 HG01891.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-26-16561_-26-1656 others(5): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632138 | |||||||
chr12:68632140 | T | G | 8 | a0001c0001t0001g0185 a0001c0001t0023g0125 a0001c0001t0023g0126 others(5): Show |
8 | HG00639.hp2 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-26-16559T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632140 | |||||||
chr12:68632141 | T | G | 11 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0169 others(8): Show |
11 | HG00738.hp1 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-26-16558T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632141 | |||||||
chr12:68632142 | T | G | 80 | a0001c0001t0001g0187 a0001c0001t0001g0194 a0001c0001t0001g0205 others(77): Show |
84 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.-26-16557T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632142 | |||||||
chr12:68632143 | T | G | 2 | a0001c0001t0039g0266 a0001c0001t0044g0270 |
2 | NA19082.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.-26-16556T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632143 | |||||||
chr12:68632143 | TTTGTTTG | T | 64 | a0001c0001t0004g0002 a0001c0001t0004g0009 a0001c0001t0004g0053 others(61): Show |
67 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.-26-16553_-26-1654 others(11): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68632143 | ||||||
chr12:68632144 | TTGTTTG | T | 13 | a0001c0001t0004g0055 a0001c0001t0004g0057 a0001c0001t0004g0067 others(10): Show |
13 | HG00597.hp1 HG02040.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-26-16553_-26-1654 others(10): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68632144 | ||||||
chr12:68632145 | T | G | 9 | a0001c0001t0003g0238 a0001c0001t0010g0079 a0001c0001t0023g0125 others(6): Show |
9 | HG00639.hp2 HG02293.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-26-16554T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632145 | |||||||
chr12:68632146 | G | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(127): Show |
144 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.-26-16553G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632146 | |||||||
chr12:68632150 | G | T | 26 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0169 others(23): Show |
29 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.-26-16549G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632150 | |||||||
chr12:68632151 | T | G | 10 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0169 others(7): Show |
10 | HG02055.hp2 HG02257.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-26-16548T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632151 | |||||||
chr12:68632154 | T | G | 3 | a0001c0001t0002g0139 a0001c0001t0002g0207 a0001c0001t0053g0084 |
3 | HG01516.hp1 HG02040.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.-26-16545T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632154 | |||||||
chr12:68632155 | T | G | 5 | a0001c0001t0003g0244 a0001c0001t0023g0125 a0001c0001t0023g0126 others(2): Show |
5 | HG02293.hp1 HG02922.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.-26-16544T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632155 | |||||||
chr12:68632156 | T | G | 1 | a0001c0001t0001g0173 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-26-16543T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632156 | |||||||
chr12:68632160 | T | C | 77 | a0001c0001t0004g0002 a0001c0001t0004g0009 a0001c0001t0004g0053 others(74): Show |
80 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.-26-16539T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632160 | |||||||
chr12:68632505 | C | T | 1 | a0001c0001t0004g0053 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-26-16194C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632505 | |||||||
chr12:68632526 | A | G | 15 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(12): Show |
18 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-26-16173A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632526 | |||||||
chr12:68632577 | G | C | 16 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(13): Show |
19 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-26-16122G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632577 | |||||||
chr12:68632700 | A | G | 1 | a0001c0001t0003g0241 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-26-15999A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632700 | |||||||
chr12:68632934 | G | T | 1 | a0001c0001t0001g0148 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-26-15765G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632934 | |||||||
chr12:68632947 | T | C | 1 | a0001c0001t0026g0142 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-26-15752T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632947 | |||||||
chr12:68633029 | T | A | 1 | a0001c0001t0123g0140 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-26-15670T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68633029 | |||||||
chr12:68633050 | A | T | 1 | a0001c0001t0003g0224 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-26-15649A>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68633050 | |||||||
chr12:68633132 | G | A | 18 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(15): Show |
22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.-26-15567G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68633132 | |||||||
chr12:68633148 | A | G | 1 | a0001c0001t0003g0294 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-26-15551A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68633148 | |||||||
chr12:68633153 | A | T | 1 | a0001c0001t0037g0031 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-26-15546A>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68633153 | |||||||
chr12:68633173 | A | G | 16 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(13): Show |
19 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-26-15526A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68633173 | |||||||
chr12:68633389 | A | G | 5 | a0001c0001t0026g0138 a0001c0001t0026g0142 a0001c0001t0049g0137 others(2): Show |
5 | HG00099.hp2 HG02976.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-26-15310A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68633389 | |||||||
chr12:68633461 | G | A | 1 | a0001c0001t0003g0230 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-26-15238G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68633461 | |||||||
chr12:68633943 | G | A | 1 | a0001c0001t0032g0174 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-26-14756G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68633943 | |||||||
chr12:68634093 | C | T | 12 | a0001c0001t0001g0024 a0001c0001t0001g0317 a0001c0001t0001g0318 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.-26-14606C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68634093 | |||||||
chr12:68634309 | T | G | 3 | a0001c0001t0081g0032 a0001c0001t0082g0069 a0001c0001t0083g0074 |
3 | HG02486.hp1 HG02630.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-26-14390T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68634309 | |||||||
chr12:68634319 | A | G | 1 | a0001c0001t0010g0182 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-26-14380A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68634319 | |||||||
chr12:68634327 | A | G | 3 | a0001c0001t0005g0036 a0001c0001t0005g0042 a0001c0001t0092g0071 |
3 | NA18961.hp1 NA18978.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.-26-14372A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68634327 | |||||||
chr12:68634349 | C | T | 1 | a0001c0001t0103g0277 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-26-14350C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68634349 | |||||||
chr12:68634391 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-26-14308A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68634391 | |||||||
chr12:68634450 | C | T | 5 | a0001c0001t0026g0138 a0001c0001t0026g0142 a0001c0001t0049g0137 others(2): Show |
5 | HG00099.hp2 HG02976.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-26-14249C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68634450 | |||||||
chr12:68634582 | A | AT | 3 | a0001c0001t0006g0329 a0001c0001t0025g0023 a0001c0001t0046g0315 |
4 | HG01516.hp2 HG01517.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-14115dupT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68634582 | ||||||
chr12:68634585 | A | AT | 8 | a0001c0001t0001g0150 a0001c0001t0005g0042 a0001c0001t0010g0182 others(5): Show |
8 | HG00673.hp2 HG02145.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-26-14103dupT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68634585 | ||||||
chr12:68634585 | A | ATT | 59 | a0001c0001t0004g0002 a0001c0001t0004g0009 a0001c0001t0004g0053 others(56): Show |
61 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.-26-14104_-26-1410 others(6): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68634585 | ||||||
chr12:68634585 | A | T | 16 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(13): Show |
20 | HG01109.hp2 HG01516.hp2 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.-26-14114A>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68634585 | |||||||
chr12:68634629 | T | TA | 4 | a0001c0001t0023g0125 a0001c0001t0023g0126 a0001c0001t0047g0123 others(1): Show |
4 | HG02293.hp1 HG02922.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-14064dupA | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68634629 | ||||||
chr12:68634781 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-26-13918A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68634781 | |||||||
chr12:68634811 | C | T | 1 | a0001c0001t0030g0027 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-26-13888C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68634811 | |||||||
chr12:68634824 | A | G | 1 | a0001c0001t0126g0339 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-26-13875A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68634824 | |||||||
chr12:68634912 | G | C | 1 | a0001c0001t0003g0278 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-26-13787G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68634912 | |||||||
chr12:68635126 | A | G | 1 | a0001c0001t0005g0041 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-26-13573A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68635126 | |||||||
chr12:68635158 | A | C | 2 | a0001c0001t0025g0023 a0001c0001t0046g0315 |
3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-26-13541A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68635158 | |||||||
chr12:68635192 | G | A | 1 | a0001c0001t0024g0338 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-26-13507G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68635192 | |||||||
chr12:68635213 | G | A | 2 | a0001c0001t0003g0285 a0001c0001t0003g0286 |
2 | HG03704.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-26-13486G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68635213 | |||||||
chr12:68635555 | A | G | 1 | a0001c0001t0003g0240 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-26-13144A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68635555 | |||||||
chr12:68635622 | A | G | 76 | a0001c0001t0003g0007 a0001c0001t0003g0020 a0001c0001t0003g0021 others(73): Show |
80 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-26-13077A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68635622 | |||||||
chr12:68635643 | C | T | 76 | a0001c0001t0003g0007 a0001c0001t0003g0020 a0001c0001t0003g0021 others(73): Show |
80 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-26-13056C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68635643 | |||||||
chr12:68635657 | A | G | 1 | a0001c0001t0098g0283 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-26-13042A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68635657 | |||||||
chr12:68635682 | T | A | 1 | a0001c0001t0003g0285 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-26-13017T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68635682 | |||||||
chr12:68635882 | T | TGCA | 18 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(15): Show |
22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.-26-12816_-26-1281 others(7): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68635882 | ||||||
chr12:68635885 | A | AGAG | 163 | a0001c0001t0003g0007 a0001c0001t0003g0020 a0001c0001t0003g0021 others(160): Show |
170 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.-26-12814_-26-1281 others(7): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68635885 | |||||||
chr12:68635885 | A | G | 18 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(15): Show |
22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.-26-12814A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68635885 | |||||||
chr12:68635902 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-26-12797G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68635902 | |||||||
chr12:68635918 | G | A | 1 | a0001c0001t0117g0306 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-26-12781G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68635918 | |||||||
chr12:68636027 | C | T | 1 | a0001c0001t0102g0143 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-26-12672C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68636027 | |||||||
chr12:68636044 | A | AT | 7 | a0001c0001t0002g0081 a0001c0001t0002g0082 a0001c0001t0002g0131 others(4): Show |
8 | HG01516.hp2 HG01517.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-26-12643dupT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68636044 | ||||||
chr12:68636068 | A | G | 2 | a0001c0001t0005g0041 a0001c0001t0013g0038 |
2 | NA18992.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.-26-12631A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68636068 | |||||||
chr12:68636165 | A | G | 2 | a0001c0001t0005g0062 a0001c0001t0005g0075 |
2 | HG01884.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-26-12534A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68636165 | |||||||
chr12:68636356 | A | G | 3 | a0001c0001t0024g0336 a0001c0001t0024g0337 a0001c0001t0024g0338 |
3 | HG02257.hp1 HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-26-12343A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68636356 | |||||||
chr12:68636407 | A | C | 1 | a0001c0001t0094g0282 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-26-12292A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68636407 | |||||||
chr12:68636574 | T | C | 18 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(15): Show |
22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.-26-12125T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68636574 | |||||||
chr12:68636725 | G | GT | 77 | a0001c0001t0003g0007 a0001c0001t0003g0020 a0001c0001t0003g0021 others(74): Show |
81 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.-26-11965dupT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68636725 | ||||||
chr12:68636725 | G | GTT | 17 | a0001c0001t0003g0294 a0001c0001t0006g0008 a0001c0001t0006g0026 others(14): Show |
20 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-26-11966_-26-1196 others(6): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68636725 | ||||||
chr12:68636778 | G | T | 2 | a0001c0001t0114g0141 a0001c0001t0115g0135 |
2 | HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-26-11921G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68636778 | |||||||
chr12:68636816 | G | A | 1 | a0001c0001t0127g0340 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-26-11883G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68636816 | |||||||
chr12:68636915 | A | G | 2 | a0001c0001t0121g0210 a0001c0001t0122g0211 |
2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-26-11784A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68636915 | |||||||
chr12:68637490 | G | A | 2 | a0001c0001t0025g0023 a0001c0001t0046g0315 |
3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-26-11209G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68637490 | |||||||
chr12:68637577 | T | C | 283 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(280): Show |
307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.-26-11122T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68637577 | |||||||
chr12:68637599 | C | CA | 46 | a0001c0001t0001g0147 a0001c0001t0001g0154 a0001c0001t0001g0155 others(43): Show |
47 | HG00323.hp2 HG00408.hp2 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.-26-11071dupA | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68637599 | ||||||
chr12:68637599 | C | CAAAAAAA others(8): Show |
1 | a0001c0002t0023g0127 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-26-11085_-26-1107 others(19): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68637599 | ||||||
chr12:68637599 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0023g0126 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-26-11086_-26-1107 others(20): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68637599 | ||||||
chr12:68637599 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0023g0125 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-26-11087_-26-1107 others(21): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68637599 | ||||||
chr12:68637599 | CA | C | 61 | a0001c0001t0001g0146 a0001c0001t0001g0152 a0001c0001t0001g0153 others(58): Show |
61 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.-26-11071delA | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68637599 | ||||||
chr12:68637599 | CAA | C | 110 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0011 others(107): Show |
120 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.-26-11072_-26-1107 others(6): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68637599 | ||||||
chr12:68637599 | CAAA | C | 10 | a0001c0001t0002g0099 a0001c0001t0002g0101 a0001c0001t0018g0284 others(7): Show |
12 | HG01070.hp2 HG01516.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.-26-11073_-26-1107 others(7): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68637599 | ||||||
chr12:68637610 | A | C | 1 | a0001c0001t0001g0196 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-26-11089A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68637610 | |||||||
chr12:68637616 | A | C | 2 | a0001c0001t0025g0023 a0001c0001t0046g0315 |
3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-26-11083A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68637616 | |||||||
chr12:68637618 | A | C | 1 | a0001c0001t0060g0252 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-26-11081A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68637618 | |||||||
chr12:68637851 | C | T | 1 | a0001c0001t0018g0243 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-26-10848C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68637851 | |||||||
chr12:68638016 | T | C | 15 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(12): Show |
18 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-26-10683T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68638016 | |||||||
chr12:68638057 | G | T | 14 | a0001c0001t0009g0226 a0001c0001t0009g0249 a0001c0001t0009g0254 others(11): Show |
14 | HG00642.hp1 HG01255.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.-26-10642G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68638057 | |||||||
chr12:68638133 | G | A | 8 | a0001c0001t0002g0012 a0001c0001t0002g0015 a0001c0001t0002g0093 others(5): Show |
9 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(6): Show |
intron_variant | MODIFIER | c.-26-10566G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68638133 | |||||||
chr12:68638283 | CT | C | 16 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(13): Show |
19 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-26-10413delT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68638283 | ||||||
chr12:68638337 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-26-10362G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68638337 | |||||||
chr12:68638473 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-26-10226T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68638473 | |||||||
chr12:68638579 | T | G | 1 | a0001c0001t0048g0324 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-26-10120T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68638579 | |||||||
chr12:68638647 | A | G | 3 | a0001c0001t0010g0171 a0001c0001t0010g0182 a0001c0001t0110g0204 |
3 | HG00673.hp2 NA18612.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-26-10052A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68638647 | |||||||
chr12:68638683 | A | C | 1 | a0001c0001t0107g0116 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-26-10016A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68638683 | |||||||
chr12:68638696 | G | C | 1 | a0001c0001t0017g0095 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-26-10003G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68638696 | |||||||
chr12:68638722 | G | A | 1 | a0001c0001t0031g0176 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-26-9977G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68638722 | |||||||
chr12:68638771 | C | T | 19 | a0001c0001t0003g0020 a0001c0001t0003g0229 a0001c0001t0003g0230 others(16): Show |
20 | HG00738.hp1 HG02074.hp1 HG02602.hp2 others(17): Show |
intron_variant | MODIFIER | c.-26-9928C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68638771 | |||||||
chr12:68638818 | A | G | 258 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0011 others(255): Show |
273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.-26-9881A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68638818 | |||||||
chr12:68638955 | C | A | 1 | a0001c0001t0123g0140 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-26-9744C>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68638955 | |||||||
chr12:68639065 | A | C | 1 | a0001c0001t0066g0231 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-26-9634A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68639065 | |||||||
chr12:68639122 | T | A | 6 | a0001c0001t0035g0215 a0001c0001t0035g0220 a0001c0001t0042g0214 others(3): Show |
6 | HG01361.hp1 HG02717.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-26-9577T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68639122 | |||||||
chr12:68639206 | C | A | 1 | a0001c0001t0001g0173 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-26-9493C>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68639206 | |||||||
chr12:68639362 | A | C | 1 | a0001c0001t0002g0107 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-26-9337A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68639362 | |||||||
chr12:68639366 | A | G | 6 | a0001c0001t0023g0125 a0001c0001t0023g0126 a0001c0001t0047g0123 others(3): Show |
6 | HG02293.hp1 HG02922.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-26-9333A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68639366 | |||||||
chr12:68639457 | G | A | 2 | a0001c0001t0007g0076 a0001c0001t0007g0077 |
2 | NA18998.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.-26-9242G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68639457 | |||||||
chr12:68639843 | A | AT | 13 | a0001c0001t0001g0172 a0001c0001t0001g0205 a0001c0001t0003g0224 others(10): Show |
14 | HG01516.hp2 HG01517.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.-26-8841dupT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68639843 | ||||||
chr12:68639859 | G | T | 16 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(13): Show |
19 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-26-8840G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68639859 | |||||||
chr12:68640127 | C | A | 1 | a0001c0002t0023g0127 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-26-8572C>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68640127 | |||||||
chr12:68640201 | AAATTT | A | 2 | a0001c0001t0025g0023 a0001c0001t0046g0315 |
3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-26-8494_-26-8490d others(7): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68640201 | ||||||
chr12:68640310 | T | C | 1 | a0001c0001t0029g0156 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-26-8389T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68640310 | |||||||
chr12:68640392 | G | C | 2 | a0001c0001t0023g0125 a0001c0001t0023g0126 |
2 | HG03704.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.-26-8307G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68640392 | |||||||
chr12:68640672 | G | A | 3 | a0001c0001t0027g0255 a0001c0001t0027g0259 a0001c0001t0062g0250 |
3 | HG00642.hp1 HG01255.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-26-8027G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68640672 | |||||||
chr12:68640836 | A | C | 65 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0011 others(62): Show |
69 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.-26-7863A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68640836 | |||||||
chr12:68640936 | A | G | 1 | a0001c0001t0009g0249 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-26-7763A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68640936 | |||||||
chr12:68640955 | C | T | 3 | a0001c0001t0011g0316 a0001c0001t0025g0023 a0001c0001t0046g0315 |
4 | HG01109.hp1 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.-26-7744C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68640955 | |||||||
chr12:68640957 | G | T | 1 | a0001c0001t0100g0265 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-26-7742G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68640957 | |||||||
chr12:68641006 | A | G | 2 | a0001c0001t0002g0110 a0001c0001t0108g0111 |
2 | NA18964.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-26-7693A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68641006 | |||||||
chr12:68641020 | G | A | 15 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(12): Show |
18 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-26-7679G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68641020 | |||||||
chr12:68641110 | G | A | 76 | a0001c0001t0003g0007 a0001c0001t0003g0020 a0001c0001t0003g0021 others(73): Show |
80 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-26-7589G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68641110 | |||||||
chr12:68641171 | T | G | 10 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0100 others(7): Show |
12 | NA18612.hp1 NA18968.hp2 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.-26-7528T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68641171 | |||||||
chr12:68641220 | G | A | 283 | a0001c0001t0001g0024 a0001c0001t0001g0152 a0001c0001t0001g0153 others(280): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.-26-7479G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68641220 | |||||||
chr12:68641279 | G | T | 11 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(8): Show |
14 | HG01069.hp2 HG01891.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-26-7420G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68641279 | |||||||
chr12:68641310 | T | A | 1 | a0001c0001t0017g0095 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-26-7389T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68641310 | |||||||
chr12:68641501 | G | C | 1 | a0001c0001t0126g0339 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-26-7198G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68641501 | |||||||
chr12:68641604 | T | C | 3 | a0001c0001t0033g0247 a0001c0001t0033g0248 a0001c0001t0079g0222 |
3 | HG02055.hp1 HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-26-7095T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68641604 | |||||||
chr12:68641745 | T | C | 2 | a0001c0001t0073g0025 a0001c0001t0078g0025 |
2 | HG00639.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-26-6954T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68641745 | |||||||
chr12:68641792 | T | TA | 22 | a0001c0001t0003g0020 a0001c0001t0003g0229 a0001c0001t0003g0230 others(19): Show |
23 | HG00738.hp1 HG02074.hp1 HG02602.hp2 others(20): Show |
intron_variant | MODIFIER | c.-26-6895dupA | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68641792 | ||||||
chr12:68641792 | T | TAA | 53 | a0001c0001t0003g0007 a0001c0001t0003g0021 a0001c0001t0003g0224 others(50): Show |
56 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.-26-6896_-26-6895d others(4): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68641792 | ||||||
chr12:68641792 | TA | T | 17 | a0001c0001t0001g0147 a0001c0001t0006g0008 a0001c0001t0006g0026 others(14): Show |
21 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(18): Show |
intron_variant | MODIFIER | c.-26-6895delA | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68641792 | ||||||
chr12:68641807 | G | C | 1 | a0001c0001t0024g0336 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-26-6892G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68641807 | |||||||
chr12:68641986 | A | C | 1 | a0001c0001t0013g0061 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-26-6713A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68641986 | |||||||
chr12:68642062 | G | A | 1 | a0001c0001t0102g0143 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-26-6637G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68642062 | |||||||
chr12:68642086 | G | C | 26 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0013 others(23): Show |
28 | HG01099.hp2 HG01975.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-26-6613G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68642086 | |||||||
chr12:68642364 | A | G | 1 | a0001c0001t0059g0251 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-26-6335A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68642364 | |||||||
chr12:68642814 | G | A | 3 | a0001c0001t0033g0247 a0001c0001t0033g0248 a0001c0001t0079g0222 |
3 | HG02055.hp1 HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-26-5885G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68642814 | |||||||
chr12:68642831 | C | A | 76 | a0001c0001t0003g0007 a0001c0001t0003g0020 a0001c0001t0003g0021 others(73): Show |
80 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-26-5868C>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68642831 | |||||||
chr12:68642844 | C | T | 18 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(15): Show |
22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.-26-5855C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68642844 | |||||||
chr12:68642983 | C | T | 1 | a0001c0001t0045g0162 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-26-5716C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68642983 | |||||||
chr12:68643009 | C | T | 1 | a0001c0001t0005g0052 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-26-5690C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68643009 | |||||||
chr12:68643010 | G | A | 2 | a0001c0001t0121g0210 a0001c0001t0122g0211 |
2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-26-5689G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68643010 | |||||||
chr12:68643029 | C | G | 65 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0011 others(62): Show |
69 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.-26-5670C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68643029 | |||||||
chr12:68643066 | T | A | 3 | a0001c0001t0003g0021 a0001c0001t0003g0268 a0001c0001t0014g0309 |
4 | HG00438.hp1 NA18961.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-5633T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68643066 | |||||||
chr12:68643292 | G | A | 18 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(15): Show |
22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.-26-5407G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68643292 | |||||||
chr12:68643346 | C | G | 1 | a0001c0001t0018g0284 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-26-5353C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68643346 | |||||||
chr12:68643701 | G | A | 1 | a0001c0001t0009g0258 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-26-4998G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68643701 | |||||||
chr12:68643918 | T | C | 2 | a0001c0001t0026g0138 a0001c0001t0026g0142 |
2 | HG00099.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-26-4781T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68643918 | |||||||
chr12:68644039 | A | C | 1 | a0001c0001t0001g0169 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-26-4660A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68644039 | |||||||
chr12:68644099 | T | C | 1 | a0001c0001t0002g0086 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-26-4600T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68644099 | |||||||
chr12:68644121 | A | G | 1 | a0001c0001t0046g0315 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-26-4578A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68644121 | |||||||
chr12:68644292 | T | A | 76 | a0001c0001t0003g0007 a0001c0001t0003g0020 a0001c0001t0003g0021 others(73): Show |
80 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-26-4407T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68644292 | |||||||
chr12:68644667 | A | T | 17 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(14): Show |
20 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-26-4032A>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68644667 | |||||||
chr12:68644686 | C | CT | 74 | a0001c0001t0001g0196 a0001c0001t0002g0101 a0001c0001t0003g0007 others(71): Show |
80 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-26-3993dupT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68644686 | ||||||
chr12:68644686 | C | CTT | 11 | a0001c0001t0003g0280 a0001c0001t0003g0286 a0001c0001t0014g0301 others(8): Show |
12 | HG00642.hp2 HG01109.hp2 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.-26-3994_-26-3993d others(4): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68644686 | ||||||
chr12:68644686 | CT | C | 7 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(4): Show |
7 | HG00558.hp1 HG02486.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-26-3993delT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68644686 | ||||||
chr12:68644770 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-26-3929C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68644770 | |||||||
chr12:68644950 | C | T | 2 | a0001c0001t0005g0062 a0001c0001t0005g0075 |
2 | HG01884.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-26-3749C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68644950 | |||||||
chr12:68644979 | G | A | 76 | a0001c0001t0003g0007 a0001c0001t0003g0020 a0001c0001t0003g0021 others(73): Show |
80 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-26-3720G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68644979 | |||||||
chr12:68645514 | AC | A | 16 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(13): Show |
19 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-26-3184delC | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68645514 | |||||||
chr12:68645831 | T | G | 1 | a0001c0001t0014g0309 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-26-2868T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68645831 | |||||||
chr12:68645957 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-26-2742A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68645957 | |||||||
chr12:68645978 | G | A | 1 | a0001c0001t0088g0046 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-26-2721G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68645978 | |||||||
chr12:68646029 | A | G | 2 | a0001c0001t0069g0184 a0001c0001t0090g0124 |
2 | NA18940.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.-26-2670A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68646029 | |||||||
chr12:68646050 | T | A | 2 | a0001c0001t0114g0141 a0001c0001t0115g0135 |
2 | HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-26-2649T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68646050 | |||||||
chr12:68646072 | G | C | 1 | a0001c0001t0002g0086 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-26-2627G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68646072 | |||||||
chr12:68646225 | T | G | 6 | a0001c0001t0023g0125 a0001c0001t0023g0126 a0001c0001t0047g0123 others(3): Show |
6 | HG02293.hp1 HG02922.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-26-2474T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68646225 | |||||||
chr12:68646275 | G | A | 258 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0011 others(255): Show |
273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.-26-2424G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68646275 | |||||||
chr12:68646303 | T | G | 1 | a0001c0001t0117g0306 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-26-2396T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68646303 | |||||||
chr12:68646373 | G | A | 1 | a0001c0001t0008g0308 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-26-2326G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68646373 | |||||||
chr12:68646493 | A | G | 2 | a0001c0001t0005g0029 a0001c0001t0007g0030 |
2 | HG01257.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.-26-2206A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68646493 | |||||||
chr12:68646631 | T | C | 1 | a0001c0001t0126g0339 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-26-2068T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68646631 | |||||||
chr12:68646903 | T | C | 16 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(13): Show |
19 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-26-1796T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68646903 | |||||||
chr12:68647170 | G | A | 2 | a0001c0001t0005g0064 a0001c0001t0037g0031 |
2 | HG00735.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-26-1529G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68647170 | |||||||
chr12:68647299 | C | T | 1 | a0001c0001t0013g0060 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-26-1400C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68647299 | |||||||
chr12:68647313 | T | A | 4 | a0001c0001t0003g0238 a0001c0001t0003g0239 a0001c0001t0003g0240 others(1): Show |
4 | NA18951.hp2 NA18972.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.-26-1386T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68647313 | |||||||
chr12:68647335 | C | T | 3 | a0001c0001t0003g0280 a0001c0001t0003g0299 a0001c0001t0003g0303 |
3 | HG03942.hp2 HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-26-1364C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68647335 | |||||||
chr12:68647387 | G | GC | 39 | a0001c0001t0002g0011 a0001c0001t0002g0015 a0001c0001t0002g0102 others(36): Show |
40 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.-26-1295dupC | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68647387 | ||||||
chr12:68647387 | G | GCC | 21 | a0001c0001t0002g0086 a0001c0001t0002g0091 a0001c0001t0004g0067 others(18): Show |
21 | HG00597.hp1 HG01192.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.-26-1296_-26-1295d others(4): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68647387 | ||||||
chr12:68647387 | G | GCCCCCCC others(5): Show |
1 | a0001c0001t0122g0211 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-26-1306_-26-1295d others(14): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68647387 | ||||||
chr12:68647387 | GC | G | 47 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0013 others(44): Show |
47 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.-26-1295delC | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68647387 | ||||||
chr12:68647387 | GCC | G | 55 | a0001c0001t0001g0152 a0001c0001t0001g0198 a0001c0001t0002g0097 others(52): Show |
58 | HG00423.hp2 HG00438.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.-26-1296_-26-1295d others(4): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68647387 | ||||||
chr12:68647387 | GCCC | G | 72 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0154 others(69): Show |
81 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.-26-1297_-26-1295d others(5): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68647387 | ||||||
chr12:68647387 | GCCCC | G | 50 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0024 others(47): Show |
52 | HG00323.hp2 HG00673.hp2 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.-26-1298_-26-1295d others(6): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68647387 | ||||||
chr12:68647387 | GCCCCC | G | 14 | a0001c0001t0001g0018 a0001c0001t0001g0147 a0001c0001t0001g0200 others(11): Show |
18 | HG01069.hp2 HG01516.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.-26-1299_-26-1295d others(7): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68647387 | ||||||
chr12:68647389 | C | G | 1 | a0001c0001t0064g0228 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-26-1310C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68647389 | |||||||
chr12:68647396 | C | A | 1 | a0001c0001t0010g0182 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-26-1303C>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68647396 | |||||||
chr12:68647403 | C | A | 1 | a0001c0001t0128g0292 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-26-1296C>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68647403 | |||||||
chr12:68647403 | C | G | 4 | a0001c0001t0014g0301 a0001c0001t0018g0284 a0001c0001t0018g0300 others(1): Show |
4 | HG00642.hp2 HG01256.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-1296C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68647403 | |||||||
chr12:68647404 | C | A | 1 | a0001c0001t0006g0008 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-26-1295C>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68647404 | |||||||
chr12:68647405 | A | C | 1 | a0001c0001t0079g0222 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-26-1294A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68647405 | |||||||
chr12:68647621 | C | T | 1 | a0001c0001t0123g0140 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-26-1078C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68647621 | |||||||
chr12:68647659 | A | G | 1 | a0001c0001t0113g0136 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-26-1040A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68647659 | |||||||
chr12:68648265 | T | C | 7 | a0001c0001t0001g0019 a0001c0001t0001g0172 a0001c0001t0001g0173 others(4): Show |
7 | HG01192.hp2 HG01981.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.-26-434T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68648265 | |||||||
chr12:68648328 | A | G | 4 | a0001c0001t0002g0081 a0001c0001t0002g0082 a0001c0001t0002g0131 others(1): Show |
4 | HG02717.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-371A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68648328 | |||||||
chr12:68648409 | G | A | 15 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(12): Show |
18 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-26-290G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68648409 | |||||||
chr12:68648552 | A | G | 1 | a0001c0001t0066g0231 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-26-147A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68648552 | |||||||
chr12:68648614 | A | G | 1 | a0001c0002t0023g0127 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-26-85A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68648614 | |||||||
chr12:68648647 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-26-52C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68648647 | |||||||
chr12:68648910 | T | G | 63 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0011 others(60): Show |
67 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.57+129T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 2/7 | chr12 | 68648910 | |||||||
chr12:68649246 | A | G | 1 | a0001c0001t0126g0339 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.57+465A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 2/7 | chr12 | 68649246 | |||||||
chr12:68649373 | G | A | 1 | a0001c0001t0040g0307 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.57+592G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 2/7 | chr12 | 68649373 | |||||||
chr12:68649393 | T | C | 2 | a0001c0001t0005g0054 a0001c0001t0017g0095 |
2 | HG03491.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.57+612T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 2/7 | chr12 | 68649393 | |||||||
chr12:68649441 | T | C | 1 | a0001c0001t0013g0060 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.57+660T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 2/7 | chr12 | 68649441 | |||||||
chr12:68649693 | A | G | 3 | a0001c0001t0009g0254 a0001c0001t0060g0252 a0001c0001t0061g0253 |
3 | HG01884.hp1 HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.58-707A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 2/7 | chr12 | 68649693 | |||||||
chr12:68650389 | T | A | 1 | a0001c0001t0102g0143 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.58-11T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 2/7 | chr12 | 68650389 | |||||||
chr12:68650501 | G | T | 14 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(11): Show |
17 | HG01069.hp2 HG01891.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.126+33G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 3/7 | chr12 | 68650501 | |||||||
chr12:68650514 | ATACT | A | 3 | a0001c0001t0048g0324 a0001c0001t0073g0025 a0001c0001t0078g0025 |
3 | HG00639.hp2 HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.126+49_126+52delCT others(2): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 68650514 | ||||||
chr12:68650662 | T | A | 1 | a0001c0001t0003g0230 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.126+194T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 3/7 | chr12 | 68650662 | |||||||
chr12:68650696 | T | G | 15 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(12): Show |
18 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.126+228T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 3/7 | chr12 | 68650696 | |||||||
chr12:68650954 | A | G | 1 | a0001c0001t0048g0324 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.126+486A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 3/7 | chr12 | 68650954 | |||||||
chr12:68651126 | C | T | 76 | a0001c0001t0003g0007 a0001c0001t0003g0020 a0001c0001t0003g0021 others(73): Show |
80 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.126+658C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 3/7 | chr12 | 68651126 | |||||||
chr12:68651330 | G | A | 3 | a0001c0001t0033g0247 a0001c0001t0033g0248 a0001c0001t0079g0222 |
3 | HG02055.hp1 HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.127-665G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 3/7 | chr12 | 68651330 | |||||||
chr12:68651662 | G | A | 18 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(15): Show |
22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.127-333G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 3/7 | chr12 | 68651662 | |||||||
chr12:68651685 | T | G | 2 | a0001c0001t0025g0023 a0001c0001t0046g0315 |
3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.127-310T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 3/7 | chr12 | 68651685 | |||||||
chr12:68651780 | C | T | 1 | a0001c0001t0087g0225 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.127-215C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 3/7 | chr12 | 68651780 | |||||||
chr12:68652088 | T | G | 6 | a0001c0001t0026g0138 a0001c0001t0026g0142 a0001c0001t0049g0137 others(3): Show |
6 | HG00099.hp2 HG02976.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.183+37T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68652088 | |||||||
chr12:68652170 | T | A | 1 | a0001c0001t0003g0275 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.183+119T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68652170 | |||||||
chr12:68652330 | C | T | 2 | a0001c0001t0019g0070 a0001c0001t0089g0049 |
2 | HG02056.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.183+279C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68652330 | |||||||
chr12:68652536 | C | T | 1 | a0001c0001t0097g0272 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.183+485C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68652536 | |||||||
chr12:68652614 | A | G | 1 | a0001c0001t0113g0136 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.183+563A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68652614 | |||||||
chr12:68652668 | A | T | 1 | a0001c0001t0001g0153 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.183+617A>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68652668 | |||||||
chr12:68652675 | G | T | 5 | a0001c0001t0026g0138 a0001c0001t0026g0142 a0001c0001t0049g0137 others(2): Show |
5 | HG00099.hp2 HG02976.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.183+624G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68652675 | |||||||
chr12:68652677 | G | T | 1 | a0001c0001t0001g0263 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.183+626G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68652677 | |||||||
chr12:68652708 | C | G | 1 | a0001c0001t0037g0040 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.183+657C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68652708 | |||||||
chr12:68652814 | G | A | 1 | a0001c0001t0107g0116 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.183+763G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68652814 | |||||||
chr12:68652858 | A | G | 6 | a0001c0001t0006g0026 a0001c0001t0006g0327 a0001c0001t0006g0328 others(3): Show |
7 | HG01069.hp2 HG01891.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.183+807A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68652858 | |||||||
chr12:68652880 | A | G | 1 | a0001c0001t0048g0324 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.183+829A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68652880 | |||||||
chr12:68652926 | G | C | 1 | a0001c0001t0001g0212 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.183+875G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68652926 | |||||||
chr12:68653208 | C | G | 1 | a0001c0001t0095g0341 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.184-904C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68653208 | |||||||
chr12:68653251 | A | G | 2 | a0001c0001t0025g0023 a0001c0001t0046g0315 |
3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.184-861A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68653251 | |||||||
chr12:68653370 | G | GTTACCTT others(3): Show |
77 | a0001c0001t0004g0002 a0001c0001t0004g0009 a0001c0001t0004g0053 others(74): Show |
80 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.184-741_184-732dup others(10): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 68653370 | ||||||
chr12:68653397 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.184-715A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68653397 | |||||||
chr12:68653429 | C | G | 75 | a0001c0001t0003g0007 a0001c0001t0003g0020 a0001c0001t0003g0021 others(72): Show |
79 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.184-683C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68653429 | |||||||
chr12:68653495 | C | T | 77 | a0001c0001t0004g0002 a0001c0001t0004g0009 a0001c0001t0004g0053 others(74): Show |
80 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.184-617C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68653495 | |||||||
chr12:68653516 | A | G | 53 | a0001c0001t0003g0007 a0001c0001t0003g0021 a0001c0001t0003g0244 others(50): Show |
56 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.184-596A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68653516 | |||||||
chr12:68653556 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.184-556T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68653556 | |||||||
chr12:68653622 | G | A | 18 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(15): Show |
22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.184-490G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68653622 | |||||||
chr12:68653694 | C | T | 3 | a0001c0001t0003g0275 a0001c0001t0003g0294 a0001c0001t0014g0276 |
3 | HG02071.hp2 HG02080.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.184-418C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68653694 | |||||||
chr12:68653818 | C | T | 1 | a0001c0001t0001g0195 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.184-294C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68653818 | |||||||
chr12:68653883 | G | A | 93 | a0001c0001t0003g0007 a0001c0001t0003g0020 a0001c0001t0003g0021 others(90): Show |
101 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.184-229G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68653883 | |||||||
chr12:68653929 | C | CA | 7 | a0001c0001t0025g0023 a0001c0001t0026g0138 a0001c0001t0026g0142 others(4): Show |
8 | HG00099.hp2 HG01516.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.184-172dupA | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 68653929 | ||||||
chr12:68654351 | T | TG | 263 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(260): Show |
287 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.324+109dupG | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 68654351 | ||||||
chr12:68654351 | T | TGG | 41 | a0001c0001t0001g0154 a0001c0001t0001g0163 a0001c0001t0001g0188 others(38): Show |
41 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.324+108_324+109dup others(2): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 68654351 | ||||||
chr12:68654354 | G | GA | 4 | a0001c0001t0002g0129 a0001c0001t0002g0139 a0001c0001t0020g0098 others(1): Show |
4 | NA18963.hp1 NA18978.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+102_324+103ins others(1): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | chr12 | 68654354 | |||||||
chr12:68654358 | G | A | 16 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(13): Show |
19 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.324+106G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | chr12 | 68654358 | |||||||
chr12:68654359 | G | T | 1 | a0001c0001t0033g0248 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.324+107G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | chr12 | 68654359 | |||||||
chr12:68654543 | G | A | 16 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(13): Show |
19 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.324+291G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | chr12 | 68654543 | |||||||
chr12:68654603 | G | A | 1 | a0001c0001t0008g0311 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.324+351G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | chr12 | 68654603 | |||||||
chr12:68654719 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.324+467C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | chr12 | 68654719 | |||||||
chr12:68654752 | T | TAAAG | 18 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(15): Show |
22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.324+501_324+504dup others(4): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 68654752 | ||||||
chr12:68654831 | C | T | 3 | a0001c0001t0001g0200 a0001c0001t0012g0183 a0001c0001t0077g0197 |
3 | HG02135.hp2 NA18983.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.324+579C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | chr12 | 68654831 | |||||||
chr12:68655156 | T | A | 90 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0169 others(87): Show |
97 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.324+904T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | chr12 | 68655156 | |||||||
chr12:68655316 | C | G | 1 | a0001c0001t0014g0293 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.325-990C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | chr12 | 68655316 | |||||||
chr12:68655535 | C | CT | 78 | a0001c0001t0001g0160 a0001c0001t0001g0189 a0001c0001t0001g0194 others(75): Show |
82 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.325-753dupT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 68655535 | ||||||
chr12:68655535 | CT | C | 22 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(19): Show |
26 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(23): Show |
intron_variant | MODIFIER | c.325-753delT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 68655535 | ||||||
chr12:68655558 | C | T | 1 | a0001c0001t0088g0046 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.325-748C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | chr12 | 68655558 | |||||||
chr12:68655643 | C | G | 1 | a0001c0001t0092g0071 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.325-663C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | chr12 | 68655643 | |||||||
chr12:68655727 | G | C | 1 | a0001c0001t0001g0188 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.325-579G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | chr12 | 68655727 | |||||||
chr12:68655732 | C | T | 1 | a0001c0001t0072g0321 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.325-574C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | chr12 | 68655732 | |||||||
chr12:68655895 | C | T | 1 | a0001c0001t0002g0121 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.325-411C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | chr12 | 68655895 | |||||||
chr12:68655960 | T | TTTCTCAA others(3): Show |
1 | a0001c0001t0115g0135 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.325-343_325-334dup others(10): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 68655960 | ||||||
chr12:68656081 | A | T | 2 | a0001c0001t0025g0023 a0001c0001t0046g0315 |
3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.325-225A>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | chr12 | 68656081 | |||||||
chr12:68656455 | G | A | 2 | a0001c0001t0025g0023 a0001c0001t0046g0315 |
3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
splice_region_variant&intron_variant | LOW | c.468+6G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 6/7 | chr12 | 68656455 | |||||||
chr12:68656554 | TGATGTTA others(3): Show |
T | 1 | a0001c0001t0115g0135 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.468+107_468+116del others(10): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 68656554 | ||||||
chr12:68656566 | C | CA | 7 | a0001c0001t0002g0117 a0001c0001t0005g0028 a0001c0001t0007g0045 others(4): Show |
7 | HG01255.hp2 HG02015.hp2 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.468+129dupA | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 68656566 | ||||||
chr12:68656581 | C | T | 3 | a0001c0001t0002g0118 a0001c0001t0002g0120 a0001c0001t0002g0122 |
3 | HG02027.hp1 HG02080.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.468+132C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 6/7 | chr12 | 68656581 | |||||||
chr12:68656609 | TAAAC | T | 16 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(13): Show |
19 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.468+163_468+166del others(4): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 68656609 | ||||||
chr12:68656859 | A | G | 1 | a0001c0001t0029g0156 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.469-242A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 6/7 | chr12 | 68656859 | |||||||
chr12:68656949 | G | A | 3 | a0001c0001t0009g0254 a0001c0001t0060g0252 a0001c0001t0061g0253 |
3 | HG01884.hp1 HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.469-152G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 6/7 | chr12 | 68656949 | |||||||
chr12:68656981 | G | GC | 16 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(13): Show |
19 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.469-119dupC | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 68656981 | ||||||
chr12:68657231 | T | C | 1 | a0001c0001t0002g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.*30+14T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68657231 | |||||||
chr12:68657321 | A | G | 2 | a0001c0001t0025g0023 a0001c0001t0046g0315 |
3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.*30+104A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68657321 | |||||||
chr12:68657364 | C | G | 3 | a0001c0001t0034g0017 a0001c0001t0034g0199 a0001c0001t0085g0017 |
3 | HG02572.hp1 HG02615.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.*30+147C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68657364 | |||||||
chr12:68657447 | C | A | 2 | a0001c0001t0025g0023 a0001c0001t0046g0315 |
3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.*30+230C>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68657447 | |||||||
chr12:68657565 | C | T | 15 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(12): Show |
18 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.*30+348C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68657565 | |||||||
chr12:68657723 | AAAACACA others(5): Show |
A | 1 | a0001c0001t0040g0307 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.*30+508_*30+519del others(12): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657723 | ||||||
chr12:68657724 | AAACACAC others(4): Show |
A | 1 | a0001c0001t0008g0311 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.*30+509_*30+519del others(11): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657724 | ||||||
chr12:68657725 | A | AAC | 43 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(40): Show |
45 | HG00323.hp1 HG00408.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.*30+555_*30+556dup others(2): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657725 | ||||||
chr12:68657725 | A | AACAC | 18 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0148 others(15): Show |
19 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.*30+553_*30+556dup others(4): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657725 | ||||||
chr12:68657725 | A | AACACAC | 14 | a0001c0001t0001g0177 a0001c0001t0002g0081 a0001c0001t0002g0082 others(11): Show |
14 | HG01099.hp2 HG01975.hp2 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.*30+551_*30+556dup others(6): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657725 | ||||||
chr12:68657725 | A | AACACACA others(1): Show |
12 | a0001c0001t0002g0003 a0001c0001t0002g0089 a0001c0001t0002g0100 others(9): Show |
14 | HG02132.hp1 HG02135.hp1 HG03041.hp1 others(11): Show |
intron_variant | MODIFIER | c.*30+549_*30+556dup others(8): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657725 | ||||||
chr12:68657725 | A | AACACACA others(3): Show |
3 | a0001c0001t0020g0128 a0001c0001t0020g0167 a0001c0001t0107g0116 |
3 | HG02738.hp1 NA19056.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.*30+547_*30+556dup others(10): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657725 | ||||||
chr12:68657725 | A | AACACACA others(5): Show |
3 | a0001c0001t0002g0109 a0001c0001t0075g0262 a0001c0001t0112g0104 |
3 | HG03486.hp1 HG03688.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.*30+545_*30+556dup others(12): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657725 | ||||||
chr12:68657725 | A | AACACACA others(7): Show |
2 | a0001c0001t0002g0105 a0001c0001t0106g0006 |
2 | HG02258.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.*30+543_*30+556dup others(14): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657725 | ||||||
chr12:68657725 | A | ACAC | 3 | a0001c0001t0001g0196 a0001c0001t0002g0091 a0001c0001t0002g0121 |
3 | HG02027.hp2 HG04228.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.*30+508_*30+509ins others(3): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68657725 | |||||||
chr12:68657725 | A | ACACAC | 4 | a0001c0001t0001g0185 a0001c0001t0001g0187 a0001c0001t0032g0178 others(1): Show |
4 | HG01192.hp2 HG02647.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.*30+508_*30+509ins others(5): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68657725 | |||||||
chr12:68657725 | A | ACACACAC others(4): Show |
1 | a0001c0001t0109g0006 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.*30+508_*30+509ins others(11): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68657725 | |||||||
chr12:68657725 | A | ACACACAC others(6): Show |
1 | a0001c0001t0002g0117 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.*30+508_*30+509ins others(13): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68657725 | |||||||
chr12:68657725 | A | C | 3 | a0001c0001t0011g0019 a0001c0001t0011g0320 a0001c0001t0115g0135 |
3 | HG02004.hp1 HG02004.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.*30+508A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68657725 | |||||||
chr12:68657725 | AAC | A | 30 | a0001c0001t0001g0145 a0001c0001t0001g0160 a0001c0001t0001g0166 others(27): Show |
30 | HG00544.hp2 HG00673.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.*30+555_*30+556del others(2): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657725 | ||||||
chr12:68657725 | AACAC | A | 34 | a0001c0001t0001g0001 a0001c0001t0001g0152 a0001c0001t0001g0153 others(31): Show |
38 | HG00544.hp1 HG01069.hp1 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.*30+553_*30+556del others(4): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657725 | ||||||
chr12:68657725 | AACACAC | A | 52 | a0001c0001t0002g0086 a0001c0001t0003g0020 a0001c0001t0003g0224 others(49): Show |
54 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.*30+551_*30+556del others(6): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657725 | ||||||
chr12:68657725 | AACACACA others(1): Show |
A | 29 | a0001c0001t0002g0119 a0001c0001t0003g0020 a0001c0001t0003g0242 others(26): Show |
29 | HG00738.hp2 HG01081.hp2 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.*30+549_*30+556del others(8): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657725 | ||||||
chr12:68657725 | AACACACA others(3): Show |
A | 29 | a0001c0001t0001g0169 a0001c0001t0001g0198 a0001c0001t0001g0203 others(26): Show |
32 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.*30+547_*30+556del others(10): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657725 | ||||||
chr12:68657725 | AACACACA others(5): Show |
A | 20 | a0001c0001t0002g0011 a0001c0001t0002g0087 a0001c0001t0002g0132 others(17): Show |
22 | HG00438.hp1 HG01175.hp2 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.*30+545_*30+556del others(12): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657725 | ||||||
chr12:68657725 | AACACACA others(7): Show |
A | 4 | a0001c0001t0002g0088 a0001c0001t0004g0055 a0001c0001t0009g0258 others(1): Show |
4 | HG00099.hp1 HG02818.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.*30+543_*30+556del others(14): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657725 | ||||||
chr12:68657725 | AACACACA others(11): Show |
A | 15 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(12): Show |
18 | HG01069.hp2 HG01891.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.*30+539_*30+556del others(18): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657725 | ||||||
chr12:68657725 | AACACACA others(13): Show |
A | 6 | a0001c0001t0023g0125 a0001c0001t0023g0126 a0001c0001t0047g0123 others(3): Show |
6 | HG02293.hp1 HG02922.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.*30+537_*30+556del others(20): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657725 | ||||||
chr12:68657725 | AACACACA others(17): Show |
A | 1 | a0001c0001t0003g0291 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.*30+533_*30+556del others(24): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657725 | ||||||
chr12:68657725 | AACACACA others(19): Show |
A | 1 | a0001c0001t0128g0292 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.*30+531_*30+556del others(26): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657725 | ||||||
chr12:68657752 | ACACACAC others(19): Show |
A | 1 | a0001c0001t0127g0340 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.*30+537_*30+562del others(26): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657752 | ||||||
chr12:68657779 | C | T | 1 | a0001c0001t0003g0229 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.*30+562C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68657779 | |||||||
chr12:68657811 | C | CCT | 18 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(15): Show |
22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.*30+594_*30+595ins others(2): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68657811 | |||||||
chr12:68657825 | A | AAC | 9 | a0001c0001t0001g0185 a0001c0001t0004g0002 a0001c0001t0004g0055 others(6): Show |
11 | HG00597.hp1 HG03942.hp1 NA18747.hp2 others(8): Show |
intron_variant | MODIFIER | c.*30+627_*30+628dup others(2): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657825 | ||||||
chr12:68657825 | A | AACAC | 2 | a0001c0001t0025g0023 a0001c0001t0046g0315 |
3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.*30+625_*30+628dup others(4): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657825 | ||||||
chr12:68657906 | T | C | 1 | a0001c0001t0033g0248 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.*30+689T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68657906 | |||||||
chr12:68658018 | G | T | 1 | a0001c0001t0001g0212 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.*30+801G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68658018 | |||||||
chr12:68658044 | A | G | 1 | a0001c0001t0014g0301 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.*30+827A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68658044 | |||||||
chr12:68658063 | C | T | 271 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0169 others(268): Show |
286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.*30+846C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68658063 | |||||||
chr12:68658079 | A | G | 15 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(12): Show |
18 | HG01109.hp2 HG01891.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.*30+862A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68658079 | |||||||
chr12:68658466 | A | G | 18 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(15): Show |
22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.*31-814A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68658466 | |||||||
chr12:68658669 | TAATAG | T | 8 | a0001c0001t0002g0012 a0001c0001t0002g0015 a0001c0001t0002g0093 others(5): Show |
9 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(6): Show |
intron_variant | MODIFIER | c.*31-607_*31-603del others(5): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68658669 | ||||||
chr12:68659115 | A | C | 2 | a0001c0001t0043g0092 a0001c0001t0043g0094 |
2 | HG00280.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.*31-165A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68659115 | |||||||
chr12:68659214 | C | T | 15 | a0001c0001t0006g0008 a0001c0001t0006g0026 a0001c0001t0006g0327 others(12): Show |
18 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.*31-66C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68659214 |