Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 145226 |
| ensemblid | ENSG00000139988.10 |
| hgncid | 19977 |
| symbol | RDH12 |
| name | retinol dehydrogenase 12 |
| refseq_nuc | NM_152443.3 |
| refseq_prot | NP_689656.2 |
| ensembl_nuc | ENST00000551171.6 |
| ensembl_prot | ENSP00000449079.1 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 67701886 |
| end | 67734451 |
| strand | + |
| ver | v1.2 |
| region | chr14:67701886-67734451 |
| region5000 | chr14:67696886-67739451 |
| regionname0 | RDH12_chr14_67701886_67734451 |
| regionname5000 | RDH12_chr14_67696886_67739451 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 316 | 380 | 80 | 70 | 173 | 14 | 41 | 134 | RDH12_chr14_67696886_67739451 | RDH12 | MLVTL others(311): Show |
chr14 | 67696886 | 67739451 |
| a0002 | 0/0 | 316 | 52 | 9 | 11 | 27 | 2 | 3 | 20 | RDH12_chr14_67696886_67739451 | RDH12 | MLVTL others(311): Show |
chr14 | 67696886 | 67739451 |
| a0003 | 0/0 | 316 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | MLVTL others(311): Show |
chr14 | 67696886 | 67739451 |
| a0004 | 0/0 | 316 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | MLVTL others(311): Show |
chr14 | 67696886 | 67739451 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 948 | 374 | 80 | 70 | 167 | 14 | 41 | RDH12_chr14_67696886_67739451 | RDH12 | ATGCT others(943): Show |
chr14 | 67696886 | 67739451 | ||
| a0001c0003 | 0/0 | 948 | 5 | 0 | 0 | 5 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | ATGCT others(943): Show |
chr14 | 67696886 | 67739451 | ||
| a0001c0005 | 0/0 | 948 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | ATGCT others(943): Show |
chr14 | 67696886 | 67739451 | ||
| a0002c0002 | 0/0 | 948 | 52 | 9 | 11 | 27 | 2 | 3 | RDH12_chr14_67696886_67739451 | RDH12 | ATGCT others(943): Show |
chr14 | 67696886 | 67739451 | ||
| a0003c0004 | 0/0 | 948 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | ATGCT others(943): Show |
chr14 | 67696886 | 67739451 | ||
| a0004c0006 | 0/0 | 948 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | ATGCT others(943): Show |
chr14 | 67696886 | 67739451 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1878 | 341 | 75 | 69 | 142 | 13 | 40 | RDH12_chr14_67696886_67739451 | RDH12 | GGGCA others(1873): Show |
chr14 | 67696886 | 67739451 |
| a0001c0001t0002 | 0/0 | 1878 | 27 | 2 | 0 | 25 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | GGGCA others(1873): Show |
chr14 | 67696886 | 67739451 |
| a0001c0001t0003 | 0/0 | 1878 | 4 | 3 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | GGGCA others(1873): Show |
chr14 | 67696886 | 67739451 |
| a0001c0001t0004 | 0/0 | 1878 | 1 | 0 | 0 | 0 | 0 | 1 | RDH12_chr14_67696886_67739451 | RDH12 | GGGCA others(1873): Show |
chr14 | 67696886 | 67739451 |
| a0001c0001t0005 | 0/0 | 1878 | 1 | 0 | 0 | 0 | 1 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | GGGCA others(1873): Show |
chr14 | 67696886 | 67739451 |
| a0001c0003t0001 | 0/0 | 1878 | 5 | 0 | 0 | 5 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | GGGCA others(1873): Show |
chr14 | 67696886 | 67739451 |
| a0001c0005t0001 | 0/0 | 1878 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | GGGCA others(1873): Show |
chr14 | 67696886 | 67739451 |
| a0002c0002t0001 | 0/0 | 1878 | 52 | 9 | 11 | 27 | 2 | 3 | RDH12_chr14_67696886_67739451 | RDH12 | GGGCA others(1873): Show |
chr14 | 67696886 | 67739451 |
| a0003c0004t0001 | 0/0 | 1878 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | GGGCA others(1873): Show |
chr14 | 67696886 | 67739451 |
| a0004c0006t0001 | 0/0 | 1878 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | GGGCA others(1873): Show |
chr14 | 67696886 | 67739451 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 12 | 0 | 0 | 7 | 2 | 3 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0003 | 0/0 | 8 | 0 | 0 | 5 | 0 | 3 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0004 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0005 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0008 | 0/0 | 4 | 1 | 0 | 0 | 1 | 2 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0029 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0042 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0099 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0002g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0002g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0002g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0002g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0001t0005g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0003t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0003t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0003t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0003t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0001c0005t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0002c0002t0001g0002 | 0/0 | 9 | 0 | 2 | 5 | 2 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0002c0002t0001g0007 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0002c0002t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0002c0002t0001g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0002c0002t0001g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0002c0002t0001g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0002c0002t0001g0056 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0002c0002t0001g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0002c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0002c0002t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0002c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0002c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0002c0002t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0002c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0002c0002t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0002c0002t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0002c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0003c0004t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| a0004c0006t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0109 | EUR | GBR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0002 | EUR | GBR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0061 | EUR | GBR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | GBR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0189 | EUR | FIN | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0070 | EUR | FIN | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0249 | EUR | FIN | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG00323 | hp2 | a0001 | c0001 | t0005 | g0185 | EUR | FIN | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0308 | EAS | CHS | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG00408 | hp2 | a0001 | c0003 | t0001 | g0048 | EAS | CHS | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0291 | EAS | CHS | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0290 | EAS | CHS | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | CHS | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | CHS | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | CHS | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0294 | AMR | PUR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0319 | AMR | PUR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0299 | AMR | PUR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0204 | AMR | PUR | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01346 | hp2 | a0003 | c0004 | t0001 | g0285 | AMR | CLM | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0311 | AMR | CLM | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0296 | AFR | ACB | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0305 | AFR | ACB | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | PEL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0056 | AMR | PEL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0312 | EAS | KHV | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | KHV | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | KHV | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0060 | AFR | ACB | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0302 | EAS | KHV | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | KHV | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0293 | AMR | PEL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CDX | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CDX | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CDX | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0187 | EAS | CDX | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0284 | AFR | ACB | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | PEL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | PEL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0057 | AFR | ACB | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0286 | EAS | KHV | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | GWD | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0021 | AFR | GWD | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0313 | SAS | PJL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0274 | AFR | GWD | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | GWD | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | GWD | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02965 | hp2 | a0004 | c0006 | t0001 | g0112 | AFR | ESN | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | MSL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | MSL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | ESN | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0057 | AFR | ESN | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | MSL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | MSL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | MSL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0047 | SAS | PJL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0205 | AFR | ESN | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0207 | AFR | GWD | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0273 | AFR | MSL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0021 | AFR | MSL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | STU | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | STU | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | BEB | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0056 | SAS | BEB | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | BEB | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0300 | SAS | STU | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | STU | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | BEB | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | STU | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | STU | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | STU | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | STU | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | CHB | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHB | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | CHB | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHB | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | YRI | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | YRI | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18948 | hp2 | a0001 | c0003 | t0001 | g0048 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0306 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18956 | hp1 | a0001 | c0003 | t0001 | g0225 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0303 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0295 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0288 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18980 | hp1 | a0001 | c0005 | t0001 | g0139 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0292 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0301 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19003 | hp1 | a0001 | c0003 | t0001 | g0233 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19006 | hp2 | a0002 | c0002 | t0001 | g0289 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | LWK | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | LWK | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0304 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19081 | hp1 | a0001 | c0003 | t0001 | g0018 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0287 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | YRI | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | YRI | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ASW | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0002 | EUR | TSI | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | TSI | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | GIH | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0298 | SAS | GIH | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | CLM | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | ACB | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0021 | AFR | ACB | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | MSL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0206 | AFR | MSL | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | USA | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | USA | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | USA | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | USA | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | LWK | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | LWK | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0099 | REF | REF | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0042 | REF | REF | RDH12_chr14_67696886_67739451 | RDH12 | chr14 | 67696886 | 67739451 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:67725206 | C | A | 1 | a0003 | 1 | HG01346.hp2 | missense_variant | MODERATE | c.295C>A | p.Leu99Ile | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 5/9 | 619/1878 | 295/951 | 99/316 | chr14 | 67725206 | |||
| chr14:67727014 | G | A | 2 | a0002 a0003 |
53 | HG00099.hp2 HG00558.hp2 HG00597.hp2 others(50): Show |
missense_variant | MODERATE | c.482G>A | p.Arg161Gln | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 7/9 | 806/1878 | 482/951 | 161/316 | chr14 | 67727014 | |||
| chr14:67733766 | T | G | 1 | a0004 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.869T>G | p.Val290Gly | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 9/9 | 1193/1878 | 869/951 | 290/316 | chr14 | 67733766 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:67727102 | C | T | 1 | a0001c0003 | 5 | HG00408.hp2 NA18948.hp2 NA18956.hp1 others(2): Show |
synonymous_variant | LOW | c.570C>T | p.Ser190Ser | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 7/9 | 894/1878 | 570/951 | 190/316 | chr14 | 67727102 | |||
| chr14:67729330 | G | A | 1 | a0001c0005 | 1 | NA18980.hp1 | synonymous_variant | LOW | c.798G>A | p.Leu266Leu | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/9 | 1122/1878 | 798/951 | 266/316 | chr14 | 67729330 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:67722491 | A | G | 1 | a0001c0001t0002 | 27 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(24): Show |
5_prime_UTR_variant | MODIFIER | c.-152A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 3/9 | 152 | chr14 | 67722491 | ||||||
| chr14:67733902 | G | C | 1 | a0001c0001t0004 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*54G>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 9/9 | 54 | chr14 | 67733902 | ||||||
| chr14:67734233 | T | C | 1 | a0001c0001t0003 | 4 | HG01243.hp2 HG03471.hp2 HG03516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*385T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 9/9 | 385 | chr14 | 67734233 | ||||||
| chr14:67734276 | T | A | 1 | a0001c0001t0005 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*428T>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 9/9 | 428 | chr14 | 67734276 | ||||||
| chr14:67734394 | G | T | 1 | a0001c0001t0005 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*546G>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 9/9 | 546 | chr14 | 67734394 | ||||||
| chr14:67734432 | T | G | 1 | a0001c0001t0005 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*584T>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 9/9 | 584 | chr14 | 67734432 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:67701947 | C | T | 7 | a0001c0001t0001g0022 a0001c0001t0001g0314 a0001c0001t0001g0315 others(4): Show |
9 | HG01081.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-275+12C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67701947 | |||||||
| chr14:67702095 | T | G | 1 | a0001c0001t0001g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-275+160T>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67702095 | |||||||
| chr14:67702121 | T | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(72): Show |
103 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.-275+186T>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67702121 | |||||||
| chr14:67702156 | A | T | 1 | a0001c0001t0001g0313 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-275+221A>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67702156 | |||||||
| chr14:67702169 | A | T | 37 | a0001c0001t0001g0297 a0001c0001t0002g0307 a0001c0001t0002g0308 others(34): Show |
56 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.-275+234A>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67702169 | |||||||
| chr14:67702283 | T | A | 29 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0023 others(26): Show |
36 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.-275+348T>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67702283 | |||||||
| chr14:67702350 | A | G | 1 | a0001c0001t0001g0052 | 2 | HG03017.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-275+415A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67702350 | |||||||
| chr14:67702353 | G | C | 1 | a0001c0001t0001g0121 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-275+418G>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67702353 | |||||||
| chr14:67702437 | A | G | 2 | a0001c0001t0001g0282 a0001c0001t0001g0283 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-275+502A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67702437 | |||||||
| chr14:67702463 | G | A | 2 | a0002c0002t0001g0021 a0002c0002t0001g0284 |
4 | HG02257.hp1 HG02559.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-275+528G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67702463 | |||||||
| chr14:67702810 | T | C | 16 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0033 others(13): Show |
21 | HG00639.hp2 HG00735.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-275+875T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67702810 | |||||||
| chr14:67702827 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-275+892C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67702827 | |||||||
| chr14:67702990 | G | GT | 60 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0051 others(57): Show |
94 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.-275+1065dupT | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr14 | 67702990 | ||||||
| chr14:67703051 | C | T | 63 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0018 others(60): Show |
80 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.-275+1116C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67703051 | |||||||
| chr14:67703225 | G | A | 10 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0049 others(7): Show |
20 | HG00609.hp1 HG02080.hp1 NA18612.hp1 others(17): Show |
intron_variant | MODIFIER | c.-275+1290G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67703225 | |||||||
| chr14:67703550 | C | T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(72): Show |
103 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.-275+1615C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67703550 | |||||||
| chr14:67703926 | C | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(71): Show |
102 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.-275+1991C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67703926 | |||||||
| chr14:67704010 | T | C | 83 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(80): Show |
107 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.-275+2075T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67704010 | |||||||
| chr14:67704239 | C | T | 8 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0051 others(5): Show |
13 | HG01891.hp1 HG02622.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.-275+2304C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67704239 | |||||||
| chr14:67704552 | G | A | 83 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(80): Show |
107 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.-275+2617G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67704552 | |||||||
| chr14:67704577 | T | C | 1 | a0001c0001t0001g0084 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-275+2642T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67704577 | |||||||
| chr14:67704600 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-275+2665G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67704600 | |||||||
| chr14:67704623 | T | C | 83 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(80): Show |
107 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.-275+2688T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67704623 | |||||||
| chr14:67704715 | A | G | 3 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 |
3 | HG02145.hp1 HG02622.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-275+2780A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67704715 | |||||||
| chr14:67704916 | G | T | 4 | a0001c0001t0001g0033 a0001c0001t0001g0132 a0001c0001t0001g0133 others(1): Show |
5 | HG00735.hp1 HG01168.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.-275+2981G>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67704916 | |||||||
| chr14:67704939 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-275+3004A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67704939 | |||||||
| chr14:67705011 | C | A | 83 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(80): Show |
107 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.-275+3076C>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67705011 | |||||||
| chr14:67705151 | G | A | 2 | a0001c0001t0002g0273 a0001c0001t0002g0274 |
2 | HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-275+3216G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67705151 | |||||||
| chr14:67705173 | T | C | 63 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0018 others(60): Show |
80 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.-275+3238T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67705173 | |||||||
| chr14:67705312 | T | A | 2 | a0001c0001t0002g0273 a0001c0001t0002g0274 |
2 | HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-275+3377T>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67705312 | |||||||
| chr14:67705344 | C | T | 1 | a0002c0002t0001g0312 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-275+3409C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67705344 | |||||||
| chr14:67705381 | G | A | 1 | a0002c0002t0001g0286 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-275+3446G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67705381 | |||||||
| chr14:67705390 | T | C | 8 | a0002c0002t0001g0053 a0002c0002t0001g0054 a0002c0002t0001g0287 others(5): Show |
10 | HG00558.hp2 HG00597.hp2 NA18944.hp2 others(7): Show |
intron_variant | MODIFIER | c.-275+3455T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67705390 | |||||||
| chr14:67705530 | C | T | 2 | a0001c0001t0001g0040 a0001c0001t0001g0199 |
3 | NA18957.hp1 NA18970.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-275+3595C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67705530 | |||||||
| chr14:67705755 | A | T | 2 | a0001c0001t0001g0264 a0001c0001t0001g0265 |
2 | NA19007.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-275+3820A>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67705755 | |||||||
| chr14:67705770 | G | T | 1 | a0001c0001t0002g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-275+3835G>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67705770 | |||||||
| chr14:67705952 | A | C | 1 | a0002c0002t0001g0311 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-275+4017A>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67705952 | |||||||
| chr14:67706061 | G | C | 1 | a0001c0001t0002g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-275+4126G>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67706061 | |||||||
| chr14:67706083 | C | G | 2 | a0001c0001t0001g0025 a0001c0001t0001g0081 |
3 | HG01257.hp2 HG01258.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.-275+4148C>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67706083 | |||||||
| chr14:67706177 | C | T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(72): Show |
103 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.-275+4242C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67706177 | |||||||
| chr14:67706242 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-275+4307T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67706242 | |||||||
| chr14:67706246 | C | A | 2 | a0001c0001t0001g0022 a0001c0001t0001g0314 |
4 | HG02572.hp2 HG02965.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-275+4311C>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67706246 | |||||||
| chr14:67706279 | A | T | 1 | a0001c0001t0001g0263 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-275+4344A>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67706279 | |||||||
| chr14:67706428 | G | T | 1 | a0001c0001t0001g0120 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-275+4493G>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67706428 | |||||||
| chr14:67706502 | G | A | 33 | a0001c0001t0001g0297 a0002c0002t0001g0002 a0002c0002t0001g0007 others(30): Show |
52 | HG00099.hp2 HG00558.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.-275+4567G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67706502 | |||||||
| chr14:67706529 | C | G | 83 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(80): Show |
107 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.-275+4594C>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67706529 | |||||||
| chr14:67706630 | G | C | 1 | a0001c0001t0001g0135 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-275+4695G>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67706630 | |||||||
| chr14:67706718 | G | A | 50 | a0001c0001t0001g0058 a0001c0001t0001g0297 a0001c0001t0002g0006 others(47): Show |
79 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.-275+4783G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67706718 | |||||||
| chr14:67706738 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-275+4803C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67706738 | |||||||
| chr14:67706847 | G | A | 83 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(80): Show |
107 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.-275+4912G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67706847 | |||||||
| chr14:67706860 | G | A | 83 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(80): Show |
107 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.-275+4925G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67706860 | |||||||
| chr14:67706880 | T | C | 10 | a0001c0001t0001g0009 a0001c0001t0001g0034 a0001c0001t0001g0136 others(7): Show |
14 | NA18962.hp2 NA18964.hp1 NA18968.hp1 others(11): Show |
intron_variant | MODIFIER | c.-275+4945T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67706880 | |||||||
| chr14:67706930 | A | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(72): Show |
103 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.-275+4995A>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67706930 | |||||||
| chr14:67706936 | A | G | 1 | a0001c0001t0001g0262 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-275+5001A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67706936 | |||||||
| chr14:67707033 | T | A | 1 | a0001c0001t0001g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-275+5098T>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67707033 | |||||||
| chr14:67707049 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-275+5114C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67707049 | |||||||
| chr14:67707110 | A | G | 3 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0319 |
3 | HG01081.hp2 HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-275+5175A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67707110 | |||||||
| chr14:67707211 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-275+5276A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67707211 | |||||||
| chr14:67707284 | A | G | 1 | a0001c0001t0001g0261 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-275+5349A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67707284 | |||||||
| chr14:67707341 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-275+5406A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67707341 | |||||||
| chr14:67707385 | G | A | 49 | a0001c0001t0001g0297 a0001c0001t0002g0006 a0001c0001t0002g0010 others(46): Show |
78 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.-275+5450G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67707385 | |||||||
| chr14:67707498 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-275+5563A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67707498 | |||||||
| chr14:67707688 | T | C | 1 | a0001c0001t0001g0052 | 2 | HG03017.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-275+5753T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67707688 | |||||||
| chr14:67707716 | A | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0314 |
4 | HG02572.hp2 HG02965.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-275+5781A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67707716 | |||||||
| chr14:67707907 | A | G | 3 | a0001c0001t0001g0203 a0001c0001t0001g0213 a0001c0001t0001g0214 |
3 | HG01175.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-275+5972A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67707907 | |||||||
| chr14:67707969 | T | A | 83 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(80): Show |
107 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.-275+6034T>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67707969 | |||||||
| chr14:67708050 | C | T | 2 | a0001c0001t0002g0273 a0001c0001t0002g0274 |
2 | HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-275+6115C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67708050 | |||||||
| chr14:67708244 | G | A | 47 | a0001c0001t0001g0297 a0001c0001t0002g0006 a0001c0001t0002g0010 others(44): Show |
76 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.-275+6309G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67708244 | |||||||
| chr14:67708275 | A | T | 1 | a0001c0001t0001g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-275+6340A>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67708275 | |||||||
| chr14:67708308 | C | T | 8 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0051 others(5): Show |
13 | HG01891.hp1 HG02622.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.-275+6373C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67708308 | |||||||
| chr14:67708326 | G | A | 4 | a0001c0001t0003g0204 a0001c0001t0003g0205 a0001c0001t0003g0206 others(1): Show |
4 | HG01243.hp2 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-275+6391G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67708326 | |||||||
| chr14:67708767 | G | A | 47 | a0001c0001t0001g0297 a0001c0001t0002g0006 a0001c0001t0002g0010 others(44): Show |
76 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.-275+6832G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67708767 | |||||||
| chr14:67708776 | G | A | 83 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(80): Show |
107 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.-275+6841G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67708776 | |||||||
| chr14:67708789 | A | C | 4 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0278 others(1): Show |
4 | HG02622.hp2 HG02818.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-275+6854A>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67708789 | |||||||
| chr14:67708794 | C | CT | 46 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(43): Show |
67 | HG00099.hp1 HG00423.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.-275+6876dupT | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr14 | 67708794 | ||||||
| chr14:67708794 | CT | C | 6 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0144 others(3): Show |
6 | HG01070.hp2 HG01884.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.-275+6876delT | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr14 | 67708794 | ||||||
| chr14:67708794 | CTT | C | 49 | a0001c0001t0001g0297 a0001c0001t0002g0006 a0001c0001t0002g0010 others(46): Show |
78 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.-275+6875_-275+687 others(6): Show |
RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr14 | 67708794 | ||||||
| chr14:67708833 | G | A | 2 | a0001c0001t0002g0273 a0001c0001t0002g0274 |
2 | HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-275+6898G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67708833 | |||||||
| chr14:67708883 | C | T | 83 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(80): Show |
107 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.-275+6948C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67708883 | |||||||
| chr14:67708917 | C | T | 2 | a0001c0001t0001g0318 a0001c0001t0001g0319 |
2 | HG01081.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-275+6982C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67708917 | |||||||
| chr14:67708930 | C | T | 49 | a0001c0001t0001g0297 a0001c0001t0002g0006 a0001c0001t0002g0010 others(46): Show |
78 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.-275+6995C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67708930 | |||||||
| chr14:67708994 | C | T | 33 | a0001c0001t0001g0297 a0002c0002t0001g0002 a0002c0002t0001g0007 others(30): Show |
52 | HG00099.hp2 HG00558.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.-275+7059C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67708994 | |||||||
| chr14:67709146 | T | C | 15 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0049 others(12): Show |
25 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.-275+7211T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67709146 | |||||||
| chr14:67709229 | T | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(72): Show |
103 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.-275+7294T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67709229 | |||||||
| chr14:67709280 | C | T | 8 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0051 others(5): Show |
13 | HG01891.hp1 HG02622.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.-275+7345C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67709280 | |||||||
| chr14:67709314 | A | G | 1 | a0001c0001t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-275+7379A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67709314 | |||||||
| chr14:67709637 | G | A | 14 | a0002c0002t0001g0007 a0002c0002t0001g0053 a0002c0002t0001g0054 others(11): Show |
22 | HG00558.hp2 HG00597.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-275+7702G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67709637 | |||||||
| chr14:67709677 | C | G | 61 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0018 others(58): Show |
78 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.-275+7742C>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67709677 | |||||||
| chr14:67709678 | A | G | 50 | a0001c0001t0001g0297 a0001c0001t0002g0006 a0001c0001t0002g0010 others(47): Show |
79 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.-275+7743A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67709678 | |||||||
| chr14:67709874 | G | A | 50 | a0001c0001t0001g0297 a0001c0001t0002g0006 a0001c0001t0002g0010 others(47): Show |
79 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.-275+7939G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67709874 | |||||||
| chr14:67709912 | T | G | 1 | a0002c0002t0001g0294 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-275+7977T>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67709912 | |||||||
| chr14:67709966 | G | T | 4 | a0001c0001t0003g0204 a0001c0001t0003g0205 a0001c0001t0003g0206 others(1): Show |
4 | HG01243.hp2 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-275+8031G>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67709966 | |||||||
| chr14:67710177 | C | T | 48 | a0001c0001t0001g0297 a0001c0001t0002g0006 a0001c0001t0002g0010 others(45): Show |
77 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.-275+8242C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67710177 | |||||||
| chr14:67710201 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-275+8266C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67710201 | |||||||
| chr14:67710264 | G | A | 15 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(12): Show |
22 | HG01081.hp2 HG01891.hp1 HG02486.hp2 others(19): Show |
intron_variant | MODIFIER | c.-275+8329G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67710264 | |||||||
| chr14:67710313 | G | A | 51 | a0001c0001t0001g0058 a0001c0001t0001g0297 a0001c0001t0002g0006 others(48): Show |
80 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.-275+8378G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67710313 | |||||||
| chr14:67710352 | A | G | 1 | a0001c0001t0001g0039 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-275+8417A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67710352 | |||||||
| chr14:67710451 | T | G | 51 | a0001c0001t0001g0058 a0001c0001t0001g0297 a0001c0001t0002g0006 others(48): Show |
80 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.-275+8516T>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67710451 | |||||||
| chr14:67710467 | G | A | 4 | a0001c0001t0001g0044 a0001c0001t0001g0217 a0001c0001t0001g0218 others(1): Show |
5 | HG02071.hp2 HG02074.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.-275+8532G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67710467 | |||||||
| chr14:67710608 | T | G | 1 | a0001c0001t0001g0220 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-275+8673T>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67710608 | |||||||
| chr14:67710862 | T | G | 5 | a0001c0001t0001g0011 a0001c0001t0001g0061 a0001c0001t0001g0062 others(2): Show |
7 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.-275+8927T>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67710862 | |||||||
| chr14:67711103 | A | T | 33 | a0001c0001t0001g0297 a0002c0002t0001g0002 a0002c0002t0001g0007 others(30): Show |
52 | HG00099.hp2 HG00558.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.-275+9168A>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67711103 | |||||||
| chr14:67711184 | G | A | 128 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0018 others(125): Show |
181 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.-275+9249G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67711184 | |||||||
| chr14:67711213 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-275+9278A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67711213 | |||||||
| chr14:67711230 | G | A | 62 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0018 others(59): Show |
79 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.-275+9295G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67711230 | |||||||
| chr14:67711245 | G | C | 2 | a0001c0001t0002g0273 a0001c0001t0002g0274 |
2 | HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-275+9310G>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67711245 | |||||||
| chr14:67711272 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-275+9337A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67711272 | |||||||
| chr14:67711338 | C | T | 1 | a0002c0002t0001g0306 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-275+9403C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67711338 | |||||||
| chr14:67711625 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-274-9223G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67711625 | |||||||
| chr14:67711876 | A | G | 1 | a0001c0001t0001g0257 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-274-8972A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67711876 | |||||||
| chr14:67711911 | G | C | 1 | a0001c0001t0001g0091 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-274-8937G>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67711911 | |||||||
| chr14:67711936 | T | G | 1 | a0001c0001t0001g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-274-8912T>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67711936 | |||||||
| chr14:67711941 | C | T | 62 | a0001c0001t0001g0038 a0001c0001t0001g0135 a0001c0001t0001g0145 others(59): Show |
92 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.-274-8907C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67711941 | |||||||
| chr14:67711945 | G | A | 62 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0018 others(59): Show |
79 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.-274-8903G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67711945 | |||||||
| chr14:67711983 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-274-8865G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67711983 | |||||||
| chr14:67712067 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-274-8781G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67712067 | |||||||
| chr14:67712129 | A | C | 1 | a0001c0001t0001g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-274-8719A>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67712129 | |||||||
| chr14:67712199 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-274-8649C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67712199 | |||||||
| chr14:67712200 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-274-8648G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67712200 | |||||||
| chr14:67712215 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-274-8633C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67712215 | |||||||
| chr14:67712248 | CT | C | 33 | a0001c0001t0001g0297 a0002c0002t0001g0002 a0002c0002t0001g0007 others(30): Show |
52 | HG00099.hp2 HG00558.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.-274-8599delT | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67712248 | |||||||
| chr14:67712285 | T | A | 1 | a0001c0001t0001g0147 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-274-8563T>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67712285 | |||||||
| chr14:67712322 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-274-8526G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67712322 | |||||||
| chr14:67712351 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-274-8497G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67712351 | |||||||
| chr14:67712363 | T | G | 50 | a0001c0001t0001g0297 a0001c0001t0002g0006 a0001c0001t0002g0010 others(47): Show |
79 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.-274-8485T>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67712363 | |||||||
| chr14:67712387 | C | A | 1 | a0001c0001t0001g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-274-8461C>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67712387 | |||||||
| chr14:67712420 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-274-8428C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67712420 | |||||||
| chr14:67712493 | C | CA | 99 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(96): Show |
129 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.-274-8331dupA | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr14 | 67712493 | ||||||
| chr14:67712493 | C | CAA | 73 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(70): Show |
94 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.-274-8332_-274-833 others(6): Show |
RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr14 | 67712493 | ||||||
| chr14:67712493 | C | CAAA | 13 | a0001c0001t0001g0035 a0001c0001t0001g0136 a0001c0001t0001g0146 others(10): Show |
14 | HG02683.hp2 HG04184.hp1 HG04184.hp2 others(11): Show |
intron_variant | MODIFIER | c.-274-8333_-274-833 others(7): Show |
RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr14 | 67712493 | ||||||
| chr14:67712493 | CA | C | 24 | a0001c0001t0001g0119 a0001c0001t0001g0196 a0001c0001t0001g0203 others(21): Show |
34 | HG00558.hp2 HG00597.hp2 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.-274-8331delA | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr14 | 67712493 | ||||||
| chr14:67712493 | CAA | C | 13 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0050 others(10): Show |
24 | HG00408.hp1 HG00673.hp1 HG02027.hp2 others(21): Show |
intron_variant | MODIFIER | c.-274-8332_-274-833 others(6): Show |
RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr14 | 67712493 | ||||||
| chr14:67712493 | CAAAAAAA others(7): Show |
C | 4 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0278 others(1): Show |
4 | HG02622.hp2 HG02818.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-274-8344_-274-833 others(18): Show |
RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr14 | 67712493 | ||||||
| chr14:67712493 | CAAAAAAA others(8): Show |
C | 11 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(8): Show |
18 | HG01081.hp2 HG01891.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.-274-8345_-274-833 others(19): Show |
RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr14 | 67712493 | ||||||
| chr14:67712562 | C | T | 8 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0074 others(5): Show |
10 | HG00733.hp1 HG01070.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.-274-8286C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67712562 | |||||||
| chr14:67712670 | A | G | 1 | a0001c0001t0001g0251 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-274-8178A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67712670 | |||||||
| chr14:67712792 | C | T | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG01243.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-274-8056C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67712792 | |||||||
| chr14:67712816 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-274-8032T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67712816 | |||||||
| chr14:67712818 | C | CAGTTGGC others(16): Show |
1 | a0002c0002t0001g0287 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-274-8023_-274-802 others(27): Show |
RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr14 | 67712818 | ||||||
| chr14:67712826 | A | G | 51 | a0001c0001t0001g0058 a0001c0001t0001g0297 a0001c0001t0002g0006 others(48): Show |
80 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.-274-8022A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67712826 | |||||||
| chr14:67712836 | A | G | 83 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(80): Show |
107 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.-274-8012A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67712836 | |||||||
| chr14:67712916 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-274-7932C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67712916 | |||||||
| chr14:67713073 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-274-7775C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67713073 | |||||||
| chr14:67713265 | C | CA | 50 | a0001c0001t0001g0297 a0001c0001t0002g0006 a0001c0001t0002g0010 others(47): Show |
79 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.-274-7577dupA | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr14 | 67713265 | ||||||
| chr14:67713277 | C | CA | 17 | a0001c0001t0001g0083 a0001c0001t0001g0148 a0001c0001t0002g0006 others(14): Show |
27 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.-274-7562dupA | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr14 | 67713277 | ||||||
| chr14:67713286 | A | C | 35 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0297 others(32): Show |
54 | HG00099.hp2 HG00558.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.-274-7562A>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67713286 | |||||||
| chr14:67713397 | C | CA | 7 | a0001c0001t0001g0041 a0001c0001t0001g0159 a0001c0001t0001g0211 others(4): Show |
8 | HG01175.hp1 HG01243.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.-274-7424dupA | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr14 | 67713397 | ||||||
| chr14:67713397 | CA | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(157): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.-274-7424delA | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr14 | 67713397 | ||||||
| chr14:67713397 | CAA | C | 31 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0043 others(28): Show |
37 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.-274-7425_-274-742 others(6): Show |
RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr14 | 67713397 | ||||||
| chr14:67713397 | CAAA | C | 62 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(59): Show |
83 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.-274-7426_-274-742 others(7): Show |
RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr14 | 67713397 | ||||||
| chr14:67713397 | CAAAA | C | 16 | a0001c0001t0001g0044 a0001c0001t0001g0058 a0001c0001t0001g0131 others(13): Show |
17 | HG00323.hp1 HG00639.hp2 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.-274-7427_-274-742 others(8): Show |
RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr14 | 67713397 | ||||||
| chr14:67713699 | C | T | 83 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(80): Show |
107 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.-274-7149C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67713699 | |||||||
| chr14:67713719 | A | G | 15 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(12): Show |
22 | HG01081.hp2 HG01891.hp1 HG02486.hp2 others(19): Show |
intron_variant | MODIFIER | c.-274-7129A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67713719 | |||||||
| chr14:67713888 | A | C | 83 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(80): Show |
107 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.-274-6960A>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67713888 | |||||||
| chr14:67713961 | A | G | 51 | a0001c0001t0001g0058 a0001c0001t0001g0297 a0001c0001t0002g0006 others(48): Show |
80 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.-274-6887A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67713961 | |||||||
| chr14:67713972 | T | G | 51 | a0001c0001t0001g0058 a0001c0001t0001g0297 a0001c0001t0002g0006 others(48): Show |
80 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.-274-6876T>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67713972 | |||||||
| chr14:67714036 | T | C | 15 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0049 others(12): Show |
25 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.-274-6812T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67714036 | |||||||
| chr14:67714095 | A | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0090 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-274-6753A>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67714095 | |||||||
| chr14:67714172 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-274-6676G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67714172 | |||||||
| chr14:67714215 | A | C | 2 | a0001c0001t0002g0273 a0001c0001t0002g0274 |
2 | HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-274-6633A>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67714215 | |||||||
| chr14:67714319 | T | A | 2 | a0001c0001t0002g0273 a0001c0001t0002g0274 |
2 | HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-274-6529T>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67714319 | |||||||
| chr14:67714369 | T | A | 15 | a0001c0001t0001g0016 a0001c0001t0001g0039 a0001c0001t0001g0146 others(12): Show |
18 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(15): Show |
intron_variant | MODIFIER | c.-274-6479T>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67714369 | |||||||
| chr14:67714390 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-274-6458G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67714390 | |||||||
| chr14:67714716 | T | C | 51 | a0001c0001t0001g0058 a0001c0001t0001g0297 a0001c0001t0002g0006 others(48): Show |
80 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.-274-6132T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67714716 | |||||||
| chr14:67714722 | G | A | 1 | a0001c0001t0001g0297 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-274-6126G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67714722 | |||||||
| chr14:67714724 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-274-6124A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67714724 | |||||||
| chr14:67714751 | G | A | 308 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(305): Show |
419 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(416): Show |
intron_variant | MODIFIER | c.-274-6097G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67714751 | |||||||
| chr14:67714790 | A | T | 1 | a0001c0001t0001g0194 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-274-6058A>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67714790 | |||||||
| chr14:67714940 | C | G | 15 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0049 others(12): Show |
25 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.-274-5908C>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67714940 | |||||||
| chr14:67715038 | A | C | 1 | a0001c0001t0001g0126 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-274-5810A>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67715038 | |||||||
| chr14:67715138 | A | T | 2 | a0001c0001t0001g0318 a0001c0001t0001g0319 |
2 | HG01081.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-274-5710A>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67715138 | |||||||
| chr14:67715206 | A | C | 22 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0033 others(19): Show |
28 | HG00639.hp2 HG00735.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.-274-5642A>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67715206 | |||||||
| chr14:67715214 | T | TA | 23 | a0001c0001t0001g0058 a0001c0001t0001g0064 a0001c0001t0001g0114 others(20): Show |
33 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.-274-5628dupA | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr14 | 67715214 | ||||||
| chr14:67715214 | T | TAA | 272 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(269): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.-274-5629_-274-562 others(6): Show |
RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr14 | 67715214 | ||||||
| chr14:67715214 | T | TAAA | 10 | a0001c0001t0001g0038 a0001c0001t0001g0135 a0001c0001t0001g0192 others(7): Show |
11 | HG02145.hp1 HG02451.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-274-5630_-274-562 others(7): Show |
RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr14 | 67715214 | ||||||
| chr14:67715221 | T | A | 308 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(305): Show |
419 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(416): Show |
intron_variant | MODIFIER | c.-274-5627T>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67715221 | |||||||
| chr14:67715231 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-274-5617G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67715231 | |||||||
| chr14:67715233 | A | G | 1 | a0001c0001t0001g0316 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-274-5615A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67715233 | |||||||
| chr14:67715245 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-274-5603T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67715245 | |||||||
| chr14:67715394 | T | A | 1 | a0002c0002t0001g0298 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-274-5454T>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67715394 | |||||||
| chr14:67715472 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-274-5376G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67715472 | |||||||
| chr14:67715604 | T | C | 308 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(305): Show |
419 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(416): Show |
intron_variant | MODIFIER | c.-274-5244T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67715604 | |||||||
| chr14:67715674 | G | T | 1 | a0001c0001t0001g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-274-5174G>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67715674 | |||||||
| chr14:67715690 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-274-5158A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67715690 | |||||||
| chr14:67715827 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-274-5021A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67715827 | |||||||
| chr14:67715892 | A | G | 51 | a0001c0001t0001g0058 a0001c0001t0001g0297 a0001c0001t0002g0006 others(48): Show |
80 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.-274-4956A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67715892 | |||||||
| chr14:67715925 | G | A | 1 | a0001c0001t0002g0266 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-274-4923G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67715925 | |||||||
| chr14:67716025 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-274-4823C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67716025 | |||||||
| chr14:67716196 | C | CA | 117 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(114): Show |
160 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.-274-4638dupA | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr14 | 67716196 | ||||||
| chr14:67716458 | T | A | 1 | a0001c0001t0001g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-274-4390T>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67716458 | |||||||
| chr14:67716499 | A | G | 2 | a0002c0002t0001g0021 a0002c0002t0001g0284 |
4 | HG02257.hp1 HG02559.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-274-4349A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67716499 | |||||||
| chr14:67716579 | G | A | 51 | a0001c0001t0001g0058 a0001c0001t0001g0297 a0001c0001t0002g0006 others(48): Show |
80 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.-274-4269G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67716579 | |||||||
| chr14:67716682 | G | A | 50 | a0001c0001t0001g0297 a0001c0001t0002g0006 a0001c0001t0002g0010 others(47): Show |
79 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.-274-4166G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67716682 | |||||||
| chr14:67716833 | G | A | 11 | a0001c0001t0001g0038 a0001c0001t0001g0135 a0001c0001t0001g0145 others(8): Show |
12 | HG02145.hp1 HG02451.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-274-4015G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67716833 | |||||||
| chr14:67716841 | A | G | 51 | a0001c0001t0001g0058 a0001c0001t0001g0297 a0001c0001t0002g0006 others(48): Show |
80 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.-274-4007A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67716841 | |||||||
| chr14:67716880 | T | C | 14 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0049 others(11): Show |
24 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.-274-3968T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67716880 | |||||||
| chr14:67716881 | C | CA | 7 | a0001c0001t0001g0028 a0001c0001t0001g0034 a0001c0001t0001g0067 others(4): Show |
9 | HG01981.hp2 HG02055.hp2 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.-274-3951dupA | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr14 | 67716881 | ||||||
| chr14:67716881 | CA | C | 37 | a0001c0001t0001g0058 a0001c0001t0001g0113 a0001c0001t0001g0183 others(34): Show |
56 | HG00099.hp2 HG00558.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.-274-3951delA | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr14 | 67716881 | ||||||
| chr14:67716881 | CAA | C | 16 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0049 others(13): Show |
26 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.-274-3952_-274-395 others(6): Show |
RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr14 | 67716881 | ||||||
| chr14:67716882 | A | C | 1 | a0001c0001t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-274-3966A>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67716882 | |||||||
| chr14:67716977 | T | G | 2 | a0001c0001t0002g0273 a0001c0001t0002g0274 |
2 | HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-274-3871T>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67716977 | |||||||
| chr14:67717040 | A | G | 51 | a0001c0001t0001g0058 a0001c0001t0001g0297 a0001c0001t0002g0006 others(48): Show |
80 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.-274-3808A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67717040 | |||||||
| chr14:67717096 | G | GTA | 15 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(12): Show |
22 | HG01081.hp2 HG01891.hp1 HG02486.hp2 others(19): Show |
intron_variant | MODIFIER | c.-274-3744_-274-374 others(6): Show |
RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr14 | 67717096 | ||||||
| chr14:67717164 | G | A | 51 | a0001c0001t0001g0058 a0001c0001t0001g0297 a0001c0001t0002g0006 others(48): Show |
80 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.-274-3684G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67717164 | |||||||
| chr14:67717222 | A | G | 50 | a0001c0001t0001g0297 a0001c0001t0002g0006 a0001c0001t0002g0010 others(47): Show |
79 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.-274-3626A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67717222 | |||||||
| chr14:67717252 | T | C | 2 | a0001c0001t0002g0273 a0001c0001t0002g0274 |
2 | HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-274-3596T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67717252 | |||||||
| chr14:67717359 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-274-3489A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67717359 | |||||||
| chr14:67717398 | G | A | 33 | a0001c0001t0001g0297 a0002c0002t0001g0002 a0002c0002t0001g0007 others(30): Show |
52 | HG00099.hp2 HG00558.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.-274-3450G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67717398 | |||||||
| chr14:67717399 | A | T | 1 | a0001c0001t0001g0081 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-274-3449A>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67717399 | |||||||
| chr14:67717558 | G | T | 1 | a0001c0001t0001g0246 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-274-3290G>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67717558 | |||||||
| chr14:67717601 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-274-3247C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67717601 | |||||||
| chr14:67717619 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-274-3229A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67717619 | |||||||
| chr14:67717678 | C | G | 50 | a0001c0001t0001g0297 a0001c0001t0002g0006 a0001c0001t0002g0010 others(47): Show |
79 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.-274-3170C>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67717678 | |||||||
| chr14:67717717 | A | G | 74 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(71): Show |
102 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.-274-3131A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67717717 | |||||||
| chr14:67717821 | T | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0081 |
3 | HG01257.hp2 HG01258.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.-274-3027T>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67717821 | |||||||
| chr14:67717917 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-274-2931A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67717917 | |||||||
| chr14:67717933 | A | G | 308 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(305): Show |
419 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(416): Show |
intron_variant | MODIFIER | c.-274-2915A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67717933 | |||||||
| chr14:67718124 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-274-2724G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67718124 | |||||||
| chr14:67718264 | G | C | 1 | a0001c0001t0001g0081 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-274-2584G>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67718264 | |||||||
| chr14:67718282 | T | A | 1 | a0001c0001t0002g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-274-2566T>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67718282 | |||||||
| chr14:67718680 | C | T | 15 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0049 others(12): Show |
25 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.-274-2168C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67718680 | |||||||
| chr14:67718719 | T | C | 50 | a0001c0001t0001g0297 a0001c0001t0002g0006 a0001c0001t0002g0010 others(47): Show |
79 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.-274-2129T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67718719 | |||||||
| chr14:67718751 | G | A | 2 | a0001c0001t0002g0273 a0001c0001t0002g0274 |
2 | HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-274-2097G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67718751 | |||||||
| chr14:67718788 | T | G | 5 | a0001c0001t0001g0022 a0001c0001t0001g0314 a0001c0001t0001g0317 others(2): Show |
7 | HG01081.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-274-2060T>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67718788 | |||||||
| chr14:67718861 | CTTTA | C | 15 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(12): Show |
22 | HG01081.hp2 HG01891.hp1 HG02486.hp2 others(19): Show |
intron_variant | MODIFIER | c.-274-1983_-274-198 others(8): Show |
RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr14 | 67718861 | ||||||
| chr14:67719018 | C | T | 2 | a0001c0001t0001g0164 a0001c0001t0001g0169 |
2 | HG04115.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-274-1830C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67719018 | |||||||
| chr14:67719191 | T | C | 1 | a0001c0001t0001g0171 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-274-1657T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67719191 | |||||||
| chr14:67719253 | A | G | 1 | a0001c0001t0002g0258 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-274-1595A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67719253 | |||||||
| chr14:67719318 | T | C | 11 | a0001c0001t0001g0038 a0001c0001t0001g0135 a0001c0001t0001g0145 others(8): Show |
12 | HG02145.hp1 HG02451.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-274-1530T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67719318 | |||||||
| chr14:67719372 | T | C | 84 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(81): Show |
108 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.-274-1476T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67719372 | |||||||
| chr14:67719397 | C | T | 15 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0049 others(12): Show |
25 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.-274-1451C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67719397 | |||||||
| chr14:67719445 | G | C | 1 | a0001c0001t0001g0172 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-274-1403G>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67719445 | |||||||
| chr14:67719666 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-274-1182C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67719666 | |||||||
| chr14:67719667 | G | A | 1 | a0001c0001t0002g0273 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-274-1181G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67719667 | |||||||
| chr14:67719833 | A | T | 1 | a0002c0002t0001g0301 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-274-1015A>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67719833 | |||||||
| chr14:67720046 | C | A | 16 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0033 others(13): Show |
21 | HG00639.hp2 HG00735.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-274-802C>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67720046 | |||||||
| chr14:67720061 | C | A | 15 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0049 others(12): Show |
25 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.-274-787C>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67720061 | |||||||
| chr14:67720112 | T | C | 9 | a0001c0001t0001g0017 a0001c0001t0001g0150 a0001c0001t0001g0160 others(6): Show |
11 | HG00735.hp2 HG01070.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.-274-736T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67720112 | |||||||
| chr14:67720138 | G | C | 1 | a0001c0001t0002g0307 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-274-710G>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67720138 | |||||||
| chr14:67720290 | CTT | C | 16 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0033 others(13): Show |
21 | HG00639.hp2 HG00735.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-274-557_-274-556d others(4): Show |
RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67720290 | |||||||
| chr14:67720363 | G | T | 1 | a0001c0001t0001g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-274-485G>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67720363 | |||||||
| chr14:67720587 | C | T | 48 | a0001c0001t0001g0297 a0001c0001t0002g0006 a0001c0001t0002g0010 others(45): Show |
77 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.-274-261C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 1/8 | chr14 | 67720587 | |||||||
| chr14:67720966 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-220+64G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 2/8 | chr14 | 67720966 | |||||||
| chr14:67720983 | T | C | 64 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0018 others(61): Show |
81 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.-220+81T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 2/8 | chr14 | 67720983 | |||||||
| chr14:67721082 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-220+180G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 2/8 | chr14 | 67721082 | |||||||
| chr14:67721218 | A | T | 1 | a0001c0001t0001g0280 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-220+316A>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 2/8 | chr14 | 67721218 | |||||||
| chr14:67721378 | C | T | 1 | a0002c0002t0001g0294 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-220+476C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 2/8 | chr14 | 67721378 | |||||||
| chr14:67721437 | G | A | 15 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(12): Show |
22 | HG01081.hp2 HG01891.hp1 HG02486.hp2 others(19): Show |
intron_variant | MODIFIER | c.-220+535G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 2/8 | chr14 | 67721437 | |||||||
| chr14:67721634 | C | G | 80 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0018 others(77): Show |
107 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.-220+732C>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 2/8 | chr14 | 67721634 | |||||||
| chr14:67721738 | GAT | G | 7 | a0001c0001t0001g0203 a0001c0001t0001g0213 a0001c0001t0001g0214 others(4): Show |
7 | HG01175.hp1 HG01243.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.-219-661_-219-660d others(4): Show |
RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 67721738 | ||||||
| chr14:67721738 | GATAT | G | 5 | a0001c0001t0001g0046 a0001c0001t0001g0177 a0001c0001t0001g0230 others(2): Show |
6 | HG00621.hp1 HG01255.hp1 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.-219-663_-219-660d others(6): Show |
RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 67721738 | ||||||
| chr14:67721738 | GATATAT | G | 161 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
219 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.-219-665_-219-660d others(8): Show |
RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 67721738 | ||||||
| chr14:67721738 | GATATATA others(1): Show |
G | 125 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(122): Show |
170 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.-219-667_-219-660d others(10): Show |
RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 67721738 | ||||||
| chr14:67721738 | GATATATA others(3): Show |
G | 17 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(14): Show |
24 | HG01081.hp2 HG01891.hp1 HG02486.hp2 others(21): Show |
intron_variant | MODIFIER | c.-219-669_-219-660d others(12): Show |
RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr14 | 67721738 | ||||||
| chr14:67721790 | A | G | 2 | a0001c0001t0002g0273 a0001c0001t0002g0274 |
2 | HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-219-634A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 2/8 | chr14 | 67721790 | |||||||
| chr14:67722010 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-219-414A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 2/8 | chr14 | 67722010 | |||||||
| chr14:67722104 | C | T | 1 | a0001c0001t0001g0020 | 3 | HG02809.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-219-320C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 2/8 | chr14 | 67722104 | |||||||
| chr14:67722206 | A | G | 64 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0018 others(61): Show |
81 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.-219-218A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 2/8 | chr14 | 67722206 | |||||||
| chr14:67722261 | A | G | 2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | HG01081.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.-219-163A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 2/8 | chr14 | 67722261 | |||||||
| chr14:67722271 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-219-153A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 2/8 | chr14 | 67722271 | |||||||
| chr14:67722891 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.68+181C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 3/8 | chr14 | 67722891 | |||||||
| chr14:67722892 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.68+182G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 3/8 | chr14 | 67722892 | |||||||
| chr14:67722902 | A | C | 15 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(12): Show |
22 | HG01081.hp2 HG01891.hp1 HG02486.hp2 others(19): Show |
intron_variant | MODIFIER | c.68+192A>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 3/8 | chr14 | 67722902 | |||||||
| chr14:67722918 | T | G | 15 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(12): Show |
22 | HG01081.hp2 HG01891.hp1 HG02486.hp2 others(19): Show |
intron_variant | MODIFIER | c.68+208T>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 3/8 | chr14 | 67722918 | |||||||
| chr14:67723019 | G | T | 110 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0018 others(107): Show |
156 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.68+309G>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 3/8 | chr14 | 67723019 | |||||||
| chr14:67723217 | A | T | 215 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(212): Show |
292 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.68+507A>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 3/8 | chr14 | 67723217 | |||||||
| chr14:67723542 | T | C | 20 | a0001c0001t0001g0203 a0001c0001t0001g0213 a0001c0001t0001g0214 others(17): Show |
30 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.68+832T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 3/8 | chr14 | 67723542 | |||||||
| chr14:67723600 | C | G | 1 | a0001c0001t0002g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.69-873C>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 3/8 | chr14 | 67723600 | |||||||
| chr14:67723797 | G | A | 15 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0049 others(12): Show |
25 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.69-676G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 3/8 | chr14 | 67723797 | |||||||
| chr14:67723893 | G | A | 1 | a0002c0002t0001g0299 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.69-580G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 3/8 | chr14 | 67723893 | |||||||
| chr14:67723932 | G | A | 175 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(172): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.69-541G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 3/8 | chr14 | 67723932 | |||||||
| chr14:67724034 | C | A | 67 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(64): Show |
90 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.69-439C>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 3/8 | chr14 | 67724034 | |||||||
| chr14:67724041 | T | A | 1 | a0001c0001t0001g0132 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.69-432T>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 3/8 | chr14 | 67724041 | |||||||
| chr14:67724109 | G | GT | 67 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(64): Show |
90 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.69-360dupT | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 67724109 | ||||||
| chr14:67724114 | G | C | 15 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0049 others(12): Show |
25 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.69-359G>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 3/8 | chr14 | 67724114 | |||||||
| chr14:67724162 | G | A | 72 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(69): Show |
95 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.69-311G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 3/8 | chr14 | 67724162 | |||||||
| chr14:67724292 | C | A | 1 | a0001c0001t0003g0205 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.69-181C>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 3/8 | chr14 | 67724292 | |||||||
| chr14:67724292 | C | T | 15 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0033 others(12): Show |
20 | HG00639.hp2 HG00735.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.69-181C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 3/8 | chr14 | 67724292 | |||||||
| chr14:67724392 | GT | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(83): Show |
115 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.69-64delT | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 67724392 | ||||||
| chr14:67724392 | GTT | G | 105 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(102): Show |
135 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.69-65_69-64delTT | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 67724392 | ||||||
| chr14:67724392 | GTTT | G | 123 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(120): Show |
175 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.69-66_69-64delTTT | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr14 | 67724392 | ||||||
| chr14:67724398 | T | G | 87 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(84): Show |
120 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.69-75T>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 3/8 | chr14 | 67724398 | |||||||
| chr14:67724645 | A | T | 3 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0005g0185 |
3 | HG00323.hp2 HG01123.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.187+54A>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 4/8 | chr14 | 67724645 | |||||||
| chr14:67724651 | G | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(137): Show |
185 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.187+60G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 4/8 | chr14 | 67724651 | |||||||
| chr14:67724713 | G | C | 1 | a0001c0001t0003g0205 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.187+122G>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 4/8 | chr14 | 67724713 | |||||||
| chr14:67724770 | T | C | 3 | a0001c0001t0001g0074 a0001c0001t0001g0104 a0001c0001t0001g0105 |
3 | HG01952.hp1 HG02738.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.187+179T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 4/8 | chr14 | 67724770 | |||||||
| chr14:67724788 | T | C | 3 | a0001c0001t0001g0203 a0001c0001t0001g0213 a0001c0001t0001g0214 |
3 | HG01175.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.187+197T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 4/8 | chr14 | 67724788 | |||||||
| chr14:67724819 | C | A | 5 | a0001c0001t0001g0023 a0001c0001t0001g0064 a0001c0001t0001g0065 others(2): Show |
6 | HG00558.hp1 HG01192.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.187+228C>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 4/8 | chr14 | 67724819 | |||||||
| chr14:67724872 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.188-227A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 4/8 | chr14 | 67724872 | |||||||
| chr14:67725029 | A | G | 2 | a0001c0001t0001g0137 a0001c0001t0001g0141 |
2 | NA19004.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.188-70A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 4/8 | chr14 | 67725029 | |||||||
| chr14:67725041 | A | G | 3 | a0001c0001t0001g0014 a0001c0001t0001g0092 a0001c0001t0001g0103 |
5 | HG00597.hp1 HG02074.hp1 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.188-58A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 4/8 | chr14 | 67725041 | |||||||
| chr14:67725068 | A | G | 12 | a0001c0001t0001g0038 a0001c0001t0001g0135 a0001c0001t0001g0145 others(9): Show |
13 | HG02145.hp1 HG02451.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.188-31A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 4/8 | chr14 | 67725068 | |||||||
| chr14:67725078 | C | CT | 5 | a0001c0001t0001g0023 a0001c0001t0001g0064 a0001c0001t0001g0065 others(2): Show |
6 | HG00558.hp1 HG01192.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.188-14dupT | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr14 | 67725078 | ||||||
| chr14:67725471 | C | T | 2 | a0001c0001t0001g0067 a0001c0001t0001g0071 |
2 | HG01978.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.343+217C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 5/8 | chr14 | 67725471 | |||||||
| chr14:67725936 | G | C | 290 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(287): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.344-115G>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 5/8 | chr14 | 67725936 | |||||||
| chr14:67725955 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.344-96C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 5/8 | chr14 | 67725955 | |||||||
| chr14:67726584 | C | T | 16 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(13): Show |
23 | HG00733.hp1 HG01081.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.449-397C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 6/8 | chr14 | 67726584 | |||||||
| chr14:67726585 | A | G | 311 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(308): Show |
422 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(419): Show |
intron_variant | MODIFIER | c.449-396A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 6/8 | chr14 | 67726585 | |||||||
| chr14:67726776 | G | A | 6 | a0001c0001t0001g0043 a0001c0001t0001g0121 a0001c0001t0001g0209 others(3): Show |
7 | HG02145.hp2 HG02630.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.449-205G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 6/8 | chr14 | 67726776 | |||||||
| chr14:67727330 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.658+140A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 7/8 | chr14 | 67727330 | |||||||
| chr14:67727373 | AG | A | 16 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0033 others(13): Show |
21 | HG00639.hp2 HG00735.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.658+187delG | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr14 | 67727373 | ||||||
| chr14:67727376 | G | C | 16 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0033 others(13): Show |
21 | HG00639.hp2 HG00735.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.658+186G>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 7/8 | chr14 | 67727376 | |||||||
| chr14:67727476 | G | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(137): Show |
185 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.658+286G>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 7/8 | chr14 | 67727476 | |||||||
| chr14:67727479 | T | G | 3 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0106 |
3 | HG01261.hp2 HG01433.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.658+289T>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 7/8 | chr14 | 67727479 | |||||||
| chr14:67727480 | T | G | 2 | a0001c0001t0001g0182 a0001c0001t0001g0234 |
2 | NA18964.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.658+290T>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 7/8 | chr14 | 67727480 | |||||||
| chr14:67727481 | T | G | 5 | a0001c0001t0001g0025 a0001c0001t0001g0029 a0001c0001t0001g0126 others(2): Show |
7 | HG01192.hp2 HG01257.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.658+291T>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 7/8 | chr14 | 67727481 | |||||||
| chr14:67727485 | G | GT | 21 | a0001c0001t0001g0051 a0001c0001t0001g0078 a0001c0001t0001g0150 others(18): Show |
32 | HG00609.hp1 HG00673.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.658+308dupT | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr14 | 67727485 | ||||||
| chr14:67727489 | T | G | 1 | a0001c0001t0001g0236 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.658+299T>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 7/8 | chr14 | 67727489 | |||||||
| chr14:67727490 | T | G | 11 | a0001c0001t0001g0069 a0001c0001t0001g0079 a0001c0001t0001g0097 others(8): Show |
11 | HG01496.hp2 HG02698.hp2 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.658+300T>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 7/8 | chr14 | 67727490 | |||||||
| chr14:67727491 | T | G | 3 | a0001c0001t0001g0047 a0001c0001t0001g0083 a0001c0001t0004g0047 |
3 | HG00639.hp1 HG02258.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.658+301T>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 7/8 | chr14 | 67727491 | |||||||
| chr14:67727492 | T | G | 6 | a0001c0001t0001g0023 a0001c0001t0001g0064 a0001c0001t0001g0065 others(3): Show |
7 | HG00558.hp1 HG01192.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.658+302T>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 7/8 | chr14 | 67727492 | |||||||
| chr14:67727513 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.658+323G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 7/8 | chr14 | 67727513 | |||||||
| chr14:67727590 | C | T | 14 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0049 others(11): Show |
24 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.658+400C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 7/8 | chr14 | 67727590 | |||||||
| chr14:67727622 | A | G | 1 | a0001c0001t0001g0155 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.658+432A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 7/8 | chr14 | 67727622 | |||||||
| chr14:67727674 | C | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0119 |
2 | HG02040.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.658+484C>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 7/8 | chr14 | 67727674 | |||||||
| chr14:67727828 | A | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(258): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.658+638A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 7/8 | chr14 | 67727828 | |||||||
| chr14:67728297 | T | C | 4 | a0001c0001t0001g0145 a0001c0001t0001g0192 a0001c0001t0001g0194 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.659-894T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 7/8 | chr14 | 67728297 | |||||||
| chr14:67728667 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.659-524G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 7/8 | chr14 | 67728667 | |||||||
| chr14:67728685 | C | G | 311 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(308): Show |
422 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(419): Show |
intron_variant | MODIFIER | c.659-506C>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 7/8 | chr14 | 67728685 | |||||||
| chr14:67728703 | T | TG | 82 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(79): Show |
101 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.659-478dupG | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr14 | 67728703 | ||||||
| chr14:67728703 | T | TGG | 113 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(110): Show |
162 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.659-479_659-478dup others(2): Show |
RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr14 | 67728703 | ||||||
| chr14:67728703 | T | TGGG | 39 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0022 others(36): Show |
56 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.659-480_659-478dup others(3): Show |
RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr14 | 67728703 | ||||||
| chr14:67729179 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.659-12T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 7/8 | chr14 | 67729179 | |||||||
| chr14:67729547 | C | T | 2 | a0001c0001t0001g0066 a0001c0001t0001g0073 |
2 | HG00738.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.848+167C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67729547 | |||||||
| chr14:67729555 | T | C | 1 | a0001c0001t0001g0180 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.848+175T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67729555 | |||||||
| chr14:67729655 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.848+275G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67729655 | |||||||
| chr14:67729794 | C | T | 2 | a0001c0001t0002g0006 a0001c0001t0002g0267 |
7 | NA18953.hp2 NA18970.hp2 NA18982.hp2 others(4): Show |
intron_variant | MODIFIER | c.848+414C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67729794 | |||||||
| chr14:67729919 | C | T | 141 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(138): Show |
186 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.848+539C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67729919 | |||||||
| chr14:67729929 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.848+549C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67729929 | |||||||
| chr14:67729995 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.848+615T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67729995 | |||||||
| chr14:67730004 | C | T | 46 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0045 others(43): Show |
56 | HG00323.hp1 HG00408.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.848+624C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67730004 | |||||||
| chr14:67730098 | A | T | 4 | a0001c0001t0003g0204 a0001c0001t0003g0205 a0001c0001t0003g0206 others(1): Show |
4 | HG01243.hp2 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.848+718A>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67730098 | |||||||
| chr14:67730108 | G | A | 3 | a0001c0001t0001g0122 a0001c0001t0001g0127 a0001c0001t0001g0128 |
3 | HG01109.hp1 HG02055.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.848+728G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67730108 | |||||||
| chr14:67730156 | C | T | 14 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0049 others(11): Show |
24 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.848+776C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67730156 | |||||||
| chr14:67730295 | A | G | 16 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0033 others(13): Show |
21 | HG00639.hp2 HG00735.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.848+915A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67730295 | |||||||
| chr14:67730322 | T | C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0165 |
3 | HG01106.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.848+942T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67730322 | |||||||
| chr14:67730473 | T | C | 3 | a0001c0001t0001g0203 a0001c0001t0001g0213 a0001c0001t0001g0214 |
3 | HG01175.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.848+1093T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67730473 | |||||||
| chr14:67730633 | C | G | 15 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(12): Show |
22 | HG00733.hp1 HG01081.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.848+1253C>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67730633 | |||||||
| chr14:67730665 | T | A | 305 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(302): Show |
415 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(412): Show |
intron_variant | MODIFIER | c.848+1285T>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67730665 | |||||||
| chr14:67730707 | G | T | 1 | a0001c0001t0001g0279 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.848+1327G>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67730707 | |||||||
| chr14:67730713 | CCTGACTC others(26): Show |
C | 1 | a0001c0001t0001g0114 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.848+1334_848+1366d others(35): Show |
RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67730713 | |||||||
| chr14:67730861 | C | T | 11 | a0001c0001t0001g0005 a0001c0001t0001g0045 a0001c0001t0001g0221 others(8): Show |
18 | HG01167.hp2 HG01169.hp1 HG01993.hp1 others(15): Show |
intron_variant | MODIFIER | c.848+1481C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67730861 | |||||||
| chr14:67730875 | A | C | 8 | a0001c0001t0001g0075 a0001c0001t0001g0133 a0001c0001t0001g0134 others(5): Show |
8 | HG01168.hp1 HG01169.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.848+1495A>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67730875 | |||||||
| chr14:67730884 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.848+1504G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67730884 | |||||||
| chr14:67731207 | CT | C | 161 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
219 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.848+1851delT | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 67731207 | ||||||
| chr14:67731207 | CTT | C | 32 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0241 others(29): Show |
50 | HG00099.hp2 HG00558.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.848+1850_848+1851d others(4): Show |
RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 67731207 | ||||||
| chr14:67731208 | T | TC | 5 | a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0067 others(2): Show |
7 | HG01257.hp2 HG01258.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.848+1828_848+1829i others(3): Show |
RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67731208 | |||||||
| chr14:67731209 | T | C | 66 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(63): Show |
92 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.848+1829T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67731209 | |||||||
| chr14:67731210 | T | C | 2 | a0001c0001t0001g0070 a0001c0001t0001g0109 |
2 | HG00099.hp1 HG00280.hp2 |
intron_variant | MODIFIER | c.848+1830T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67731210 | |||||||
| chr14:67731211 | T | C | 1 | a0001c0001t0001g0193 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.848+1831T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67731211 | |||||||
| chr14:67731212 | T | C | 14 | a0001c0001t0001g0038 a0001c0001t0001g0135 a0001c0001t0001g0145 others(11): Show |
15 | HG02145.hp1 HG02451.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.848+1832T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67731212 | |||||||
| chr14:67731213 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.848+1833T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67731213 | |||||||
| chr14:67731260 | G | A | 1 | a0001c0001t0002g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.848+1880G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67731260 | |||||||
| chr14:67731340 | G | A | 1 | a0001c0001t0002g0273 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.848+1960G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67731340 | |||||||
| chr14:67731368 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.848+1988C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67731368 | |||||||
| chr14:67731458 | G | A | 3 | a0001c0001t0001g0083 a0001c0001t0001g0126 a0001c0001t0001g0216 |
3 | HG01192.hp2 HG02258.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.848+2078G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67731458 | |||||||
| chr14:67731636 | A | C | 14 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0049 others(11): Show |
24 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.849-2110A>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67731636 | |||||||
| chr14:67732047 | A | G | 4 | a0001c0001t0003g0204 a0001c0001t0003g0205 a0001c0001t0003g0206 others(1): Show |
4 | HG01243.hp2 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.849-1699A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67732047 | |||||||
| chr14:67732075 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.849-1671C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67732075 | |||||||
| chr14:67732113 | T | G | 13 | a0001c0001t0001g0038 a0001c0001t0001g0135 a0001c0001t0001g0145 others(10): Show |
14 | HG02145.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.849-1633T>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67732113 | |||||||
| chr14:67732126 | C | CA | 20 | a0001c0001t0001g0030 a0001c0001t0001g0080 a0001c0001t0001g0103 others(17): Show |
22 | HG00408.hp2 HG00597.hp1 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.849-1597dupA | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 67732126 | ||||||
| chr14:67732126 | CA | C | 85 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(82): Show |
119 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.849-1597delA | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 67732126 | ||||||
| chr14:67732126 | CAAAAAAA others(4): Show |
C | 16 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0033 others(13): Show |
21 | HG00639.hp2 HG00735.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.849-1607_849-1597d others(13): Show |
RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 67732126 | ||||||
| chr14:67732152 | T | G | 2 | a0002c0002t0001g0053 a0002c0002t0001g0287 |
3 | NA18969.hp2 NA18995.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.849-1594T>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67732152 | |||||||
| chr14:67732235 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.849-1511C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67732235 | |||||||
| chr14:67732264 | CCCATCTC others(4): Show |
C | 1 | a0001c0001t0001g0197 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.849-1481_849-1471d others(13): Show |
RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67732264 | |||||||
| chr14:67732404 | T | C | 1 | a0001c0001t0001g0223 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.849-1342T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67732404 | |||||||
| chr14:67732429 | CA | C | 291 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(288): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.849-1301delA | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 67732429 | ||||||
| chr14:67732515 | T | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(136): Show |
184 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.849-1231T>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67732515 | |||||||
| chr14:67732536 | C | CA | 131 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(128): Show |
176 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.849-1196dupA | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 67732536 | ||||||
| chr14:67732536 | C | CAA | 30 | a0001c0001t0001g0043 a0001c0001t0001g0070 a0001c0001t0001g0087 others(27): Show |
41 | HG00280.hp2 HG00408.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.849-1197_849-1196d others(4): Show |
RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 67732536 | ||||||
| chr14:67732536 | C | CAAAA | 64 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(61): Show |
87 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.849-1199_849-1196d others(6): Show |
RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 67732536 | ||||||
| chr14:67732607 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.849-1139G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67732607 | |||||||
| chr14:67732717 | C | T | 14 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0049 others(11): Show |
24 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.849-1029C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67732717 | |||||||
| chr14:67732738 | G | A | 13 | a0001c0001t0001g0038 a0001c0001t0001g0135 a0001c0001t0001g0145 others(10): Show |
14 | HG02145.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.849-1008G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67732738 | |||||||
| chr14:67732881 | G | A | 36 | a0001c0001t0001g0111 a0001c0001t0001g0115 a0002c0002t0001g0002 others(33): Show |
55 | HG00099.hp2 HG00558.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.849-865G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67732881 | |||||||
| chr14:67732889 | C | T | 8 | a0001c0001t0001g0009 a0001c0001t0001g0034 a0001c0001t0001g0136 others(5): Show |
12 | NA18962.hp2 NA18964.hp1 NA18968.hp1 others(9): Show |
intron_variant | MODIFIER | c.849-857C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67732889 | |||||||
| chr14:67732911 | G | C | 85 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(82): Show |
118 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.849-835G>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67732911 | |||||||
| chr14:67732943 | A | G | 36 | a0001c0001t0001g0111 a0001c0001t0001g0115 a0002c0002t0001g0002 others(33): Show |
55 | HG00099.hp2 HG00558.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.849-803A>G | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67732943 | |||||||
| chr14:67732978 | G | C | 3 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0005g0185 |
3 | HG00323.hp2 HG01123.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.849-768G>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67732978 | |||||||
| chr14:67733040 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0142 |
2 | NA18983.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.849-706G>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67733040 | |||||||
| chr14:67733133 | TA | T | 139 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(136): Show |
184 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.849-605delA | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr14 | 67733133 | ||||||
| chr14:67733134 | A | T | 1 | a0001c0001t0001g0190 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.849-612A>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67733134 | |||||||
| chr14:67733142 | C | A | 1 | a0001c0001t0001g0197 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.849-604C>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67733142 | |||||||
| chr14:67733331 | C | T | 12 | a0001c0001t0001g0038 a0001c0001t0001g0135 a0001c0001t0001g0145 others(9): Show |
13 | HG02145.hp1 HG02451.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.849-415C>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67733331 | |||||||
| chr14:67733486 | G | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(136): Show |
184 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.849-260G>C | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67733486 | |||||||
| chr14:67733538 | A | T | 1 | a0001c0001t0001g0129 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.849-208A>T | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67733538 | |||||||
| chr14:67733666 | C | A | 4 | a0001c0001t0001g0106 a0001c0001t0001g0109 a0001c0001t0001g0114 others(1): Show |
4 | HG00099.hp1 HG02257.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.849-80C>A | RDH12 | ENSG00000139988.10 | transcript | ENST00000551171.6 | protein_coding | 8/8 | chr14 | 67733666 |