Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 201475 |
| ensemblid | ENSG00000206418.5 |
| hgncid | 31332 |
| symbol | RAB12 |
| name | RAB12, member RAS oncogene family |
| refseq_nuc | NM_001025300.3 |
| refseq_prot | NP_001020471.3 |
| ensembl_nuc | ENST00000649141.2 |
| ensembl_prot | ENSP00000497886.1 |
| mane_status | MANE Select |
| chr | chr18 |
| start | 8609437 |
| end | 8639383 |
| strand | + |
| ver | v1.2 |
| region | chr18:8609437-8639383 |
| region5000 | chr18:8604437-8644383 |
| regionname0 | RAB12_chr18_8609437_8639383 |
| regionname5000 | RAB12_chr18_8604437_8644383 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 340 | 401 | 96 | 71 | 178 | 14 | 40 | 142 | RAB12_chr18_8604437_8644383 | RAB12 | MLLPL others(335): Show |
chr18 | 8604437 | 8644383 |
| a0002 | 0/0 | 340 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | MLLPL others(335): Show |
chr18 | 8604437 | 8644383 |
| a0003 | 0/0 | 340 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RAB12_chr18_8604437_8644383 | RAB12 | MLLPL others(335): Show |
chr18 | 8604437 | 8644383 |
| a0004 | 0/0 | 340 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RAB12_chr18_8604437_8644383 | RAB12 | MLLPL others(335): Show |
chr18 | 8604437 | 8644383 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1020 | 398 | 96 | 69 | 177 | 14 | 40 | RAB12_chr18_8604437_8644383 | RAB12 | ATGCT others(1015): Show |
chr18 | 8604437 | 8644383 | ||
| a0001c0002 | 0/0 | 1020 | 2 | 0 | 2 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | ATGCT others(1015): Show |
chr18 | 8604437 | 8644383 | ||
| a0001c0003 | 0/0 | 1020 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | ATGCT others(1015): Show |
chr18 | 8604437 | 8644383 | ||
| a0002c0005 | 0/0 | 1020 | 1 | 0 | 1 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | ATGCT others(1015): Show |
chr18 | 8604437 | 8644383 | ||
| a0003c0004 | 0/0 | 1020 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | ATGCT others(1015): Show |
chr18 | 8604437 | 8644383 | ||
| a0004c0006 | 0/0 | 1020 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | ATGCT others(1015): Show |
chr18 | 8604437 | 8644383 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2147 | 296 | 35 | 47 | 168 | 9 | 36 | RAB12_chr18_8604437_8644383 | RAB12 | GGGAT others(2142): Show |
chr18 | 8604437 | 8644383 |
| a0001c0001t0002 | 0/0 | 2147 | 66 | 44 | 15 | 0 | 3 | 4 | RAB12_chr18_8604437_8644383 | RAB12 | GGGAT others(2142): Show |
chr18 | 8604437 | 8644383 |
| a0001c0001t0003 | 0/0 | 2141 | 7 | 0 | 3 | 3 | 1 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | GGGAT others(2136): Show |
chr18 | 8604437 | 8644383 |
| a0001c0001t0004 | 0/0 | 2147 | 5 | 0 | 0 | 5 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | GGGAT others(2142): Show |
chr18 | 8604437 | 8644383 |
| a0001c0001t0005 | 0/0 | 2147 | 5 | 4 | 1 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | GGGAT others(2142): Show |
chr18 | 8604437 | 8644383 |
| a0001c0001t0006 | 0/0 | 2144 | 4 | 4 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | GGGAT others(2139): Show |
chr18 | 8604437 | 8644383 |
| a0001c0001t0007 | 0/0 | 2147 | 3 | 3 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | GGGAT others(2142): Show |
chr18 | 8604437 | 8644383 |
| a0001c0001t0008 | 0/0 | 2147 | 2 | 0 | 2 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | GGGAT others(2142): Show |
chr18 | 8604437 | 8644383 |
| a0001c0001t0009 | 0/0 | 2135 | 2 | 2 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | GGGAT others(2130): Show |
chr18 | 8604437 | 8644383 |
| a0001c0001t0010 | 0/0 | 2147 | 1 | 0 | 1 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | GGCAT others(2142): Show |
chr18 | 8604437 | 8644383 |
| a0001c0001t0011 | 0/0 | 2147 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | GGGAT others(2142): Show |
chr18 | 8604437 | 8644383 |
| a0001c0001t0012 | 0/0 | 2147 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | GGGAT others(2142): Show |
chr18 | 8604437 | 8644383 |
| a0001c0001t0013 | 0/0 | 2147 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | GGGAT others(2142): Show |
chr18 | 8604437 | 8644383 |
| a0001c0001t0014 | 0/1 | 2135 | 1 | 0 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | GGGAT others(2130): Show |
chr18 | 8604437 | 8644383 |
| a0001c0001t0015 | 0/0 | 2128 | 1 | 0 | 0 | 0 | 1 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | GGGAT others(2123): Show |
chr18 | 8604437 | 8644383 |
| a0001c0001t0016 | 0/0 | 2147 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | GGGAT others(2142): Show |
chr18 | 8604437 | 8644383 |
| a0001c0001t0017 | 0/0 | 2147 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | GGGAT others(2142): Show |
chr18 | 8604437 | 8644383 |
| a0001c0002t0001 | 0/0 | 2147 | 2 | 0 | 2 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | GGGAT others(2142): Show |
chr18 | 8604437 | 8644383 |
| a0001c0003t0001 | 0/0 | 2147 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | GGGAT others(2142): Show |
chr18 | 8604437 | 8644383 |
| a0002c0005t0001 | 0/0 | 2147 | 1 | 0 | 1 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | GGGAT others(2142): Show |
chr18 | 8604437 | 8644383 |
| a0003c0004t0001 | 0/0 | 2147 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | GGGAT others(2142): Show |
chr18 | 8604437 | 8644383 |
| a0004c0006t0001 | 0/0 | 2147 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | GGGAT others(2142): Show |
chr18 | 8604437 | 8644383 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 37 | 2 | 3 | 21 | 2 | 8 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0002 | 0/0 | 24 | 1 | 0 | 21 | 1 | 1 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0003 | 0/0 | 10 | 1 | 1 | 7 | 1 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0004 | 0/0 | 8 | 0 | 3 | 4 | 0 | 1 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0006 | 0/0 | 8 | 0 | 3 | 4 | 0 | 1 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0007 | 0/0 | 7 | 1 | 5 | 0 | 0 | 1 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0009 | 0/0 | 6 | 1 | 5 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0012 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0047 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0013 | 0/0 | 6 | 0 | 3 | 0 | 2 | 1 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0014 | 0/0 | 6 | 3 | 3 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0016 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0003g0005 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0004g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0005g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0005g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0005g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0006g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0006g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0006g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0007g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0007g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0008g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0009g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0010g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0011g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0012g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0013g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0014g0136 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0015g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0016g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0001t0017g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0001c0003t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0002c0005t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0003c0004t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| a0004c0006t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0016 | EUR | GBR | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0013 | EUR | GBR | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | FIN | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG00323 | hp2 | a0001 | c0001 | t0015 | g0089 | EUR | FIN | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0093 | EAS | CHS | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0124 | AMR | PUR | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01070 | hp1 | a0001 | c0001 | t0008 | g0037 | AMR | PUR | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01071 | hp1 | a0001 | c0001 | t0008 | g0037 | AMR | PUR | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01081 | hp1 | a0001 | c0001 | t0005 | g0068 | AMR | PUR | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0183 | AMR | PUR | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0167 | AMR | PUR | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0196 | AMR | PUR | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0130 | AMR | CLM | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01261 | hp2 | a0002 | c0005 | t0001 | g0001 | AMR | CLM | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0029 | EUR | IBS | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0092 | EUR | IBS | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0197 | AFR | ACB | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01891 | hp2 | a0001 | c0001 | t0007 | g0054 | AFR | ACB | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01934 | hp1 | a0001 | c0001 | t0010 | g0011 | AMR | PEL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0160 | AMR | PEL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0034 | EAS | KHV | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0034 | EAS | KHV | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0065 | AFR | ACB | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | ACB | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CDX | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CDX | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0212 | AFR | ACB | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0208 | AFR | ACB | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0143 | AFR | ACB | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02280 | hp2 | a0001 | c0001 | t0017 | g0198 | AFR | ACB | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | ACB | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | ACB | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0207 | AFR | GWD | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | GWD | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0205 | AFR | GWD | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0140 | AFR | GWD | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0023 | AFR | GWD | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | PJL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0138 | AFR | GWD | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | GWD | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0156 | AFR | GWD | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | GWD | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0211 | AFR | GWD | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | GWD | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0200 | AFR | GWD | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02896 | hp1 | a0001 | c0001 | t0009 | g0052 | AFR | GWD | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02897 | hp1 | a0001 | c0001 | t0009 | g0052 | AFR | GWD | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | GWD | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02922 | hp1 | a0001 | c0001 | t0013 | g0137 | AFR | ESN | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0191 | AFR | ESN | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ESN | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | ESN | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0190 | AFR | ESN | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | MSL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0023 | AFR | MSL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03130 | hp1 | a0001 | c0001 | t0007 | g0054 | AFR | ESN | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | ESN | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0055 | AFR | ESN | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | ESN | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03209 | hp2 | a0001 | c0001 | t0007 | g0209 | AFR | MSL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0170 | SAS | PJL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | MSL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0055 | AFR | MSL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03486 | hp1 | a0001 | c0001 | t0011 | g0066 | AFR | MSL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | MSL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | ESN | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0023 | AFR | ESN | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | GWD | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0216 | AFR | GWD | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | MSL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | MSL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | STU | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | STU | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | BEB | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0016 | SAS | BEB | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | BEB | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | STU | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | STU | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | STU | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0016 | SAS | STU | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | STU | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | YRI | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | YRI | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHB | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CHB | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | YRI | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | YRI | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18960 | hp2 | a0001 | c0001 | t0004 | g0102 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18971 | hp1 | a0003 | c0004 | t0001 | g0129 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18973 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18990 | hp1 | a0001 | c0001 | t0004 | g0115 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19030 | hp1 | a0001 | c0001 | t0006 | g0213 | AFR | LWK | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | LWK | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0144 | AFR | LWK | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | LWK | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19072 | hp2 | a0001 | c0001 | t0012 | g0101 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19079 | hp2 | a0004 | c0006 | t0001 | g0169 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19240 | hp1 | a0001 | c0001 | t0016 | g0201 | AFR | YRI | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | YRI | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ASW | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0174 | EUR | TSI | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0031 | EUR | TSI | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0013 | EUR | TSI | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | GIH | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0091 | AMR | CLM | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | ACB | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | ACB | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0142 | AFR | ACB | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0210 | AFR | ACB | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | MSL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0202 | AFR | MSL | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | USA | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | USA | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | USA | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | USA | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | LWK | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | LWK | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0014 | g0136 | REF | REF | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | RAB12_chr18_8604437_8644383 | RAB12 | chr18 | 8604437 | 8644383 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:8609680 | G | C | 1 | a0003 | 1 | NA18971.hp1 | missense_variant | MODERATE | c.241G>C | p.Gly81Arg | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/6 | 244/2147 | 241/1023 | 81/340 | chr18 | 8609680 | |||
| chr18:8609792 | C | T | 1 | a0004 | 1 | NA19079.hp2 | missense_variant | MODERATE | c.353C>T | p.Pro118Leu | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/6 | 356/2147 | 353/1023 | 118/340 | chr18 | 8609792 | |||
| chr18:8635588 | C | T | 1 | a0002 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.770C>T | p.Thr257Met | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 4/6 | 773/2147 | 770/1023 | 257/340 | chr18 | 8635588 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:8609601 | G | A | 1 | a0001c0003 | 1 | NA18973.hp1 | synonymous_variant | LOW | c.162G>A | p.Arg54Arg | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/6 | 165/2147 | 162/1023 | 54/340 | chr18 | 8609601 | |||
| chr18:8638190 | C | T | 1 | a0001c0002 | 2 | HG01168.hp2 HG01169.hp1 |
synonymous_variant | LOW | c.951C>T | p.Ile317Ile | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 954/2147 | 951/1023 | 317/340 | chr18 | 8638190 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:8609439 | G | C | 1 | a0001c0001t0010 | 1 | HG01934.hp1 | 5_prime_UTR_variant | MODIFIER | c.-1G>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/6 | 1 | chr18 | 8609439 | ||||||
| chr18:8638277 | G | C | 1 | a0001c0001t0011 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*15G>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 15 | chr18 | 8638277 | ||||||
| chr18:8638475 | C | T | 4 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0016 others(1): Show |
69 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*213C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 213 | chr18 | 8638475 | ||||||
| chr18:8638794 | G | T | 1 | a0001c0001t0006 | 4 | HG02257.hp1 HG03139.hp1 HG03453.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*532G>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 532 | chr18 | 8638794 | ||||||
| chr18:8638858 | T | C | 1 | a0001c0001t0004 | 5 | HG00558.hp2 HG02080.hp1 HG02129.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*596T>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 596 | chr18 | 8638858 | ||||||
| chr18:8638901 | T | G | 1 | a0001c0001t0012 | 1 | NA19072.hp2 | 3_prime_UTR_variant | MODIFIER | c.*639T>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 639 | chr18 | 8638901 | ||||||
| chr18:8639051 | A | G | 1 | a0001c0001t0007 | 3 | HG01891.hp2 HG03130.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*789A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 789 | chr18 | 8639051 | ||||||
| chr18:8639102 | CCTT | C | 1 | a0001c0001t0006 | 4 | HG02257.hp1 HG03139.hp1 HG03453.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*844_*846delCTT | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 844 | INFO_REALIGN_3_PRIME | chr18 | 8639102 | |||||
| chr18:8639112 | G | A | 1 | a0001c0001t0013 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*850G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 850 | chr18 | 8639112 | ||||||
| chr18:8639128 | A | G | 1 | a0001c0001t0017 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*866A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 866 | chr18 | 8639128 | ||||||
| chr18:8639144 | GTTCTTT | G | 1 | a0001c0001t0003 | 7 | HG01123.hp1 HG01258.hp2 HG01517.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*885_*890delCTTTTT | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 885 | INFO_REALIGN_3_PRIME | chr18 | 8639144 | |||||
| chr18:8639144 | GTTCTTTT others(5): Show |
G | 1 | a0001c0001t0009 | 2 | HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*885_*896delCTTTTT others(6): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 885 | INFO_REALIGN_3_PRIME | chr18 | 8639144 | |||||
| chr18:8639144 | GTTCTTTT others(12): Show |
G | 1 | a0001c0001t0015 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*885_*903delCTTTTT others(13): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 885 | INFO_REALIGN_3_PRIME | chr18 | 8639144 | |||||
| chr18:8639147 | C | CT | 3 | a0001c0001t0001 a0001c0001t0010 a0001c0002t0001 |
18 | HG01168.hp2 HG01169.hp1 HG01934.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*930dupT | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 931 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639147 | C | CTT | 3 | a0001c0001t0001 a0001c0001t0011 a0003c0004t0001 |
14 | HG00438.hp1 HG01255.hp2 HG01993.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*929_*930dupTT | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 931 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639147 | C | CTTT | 2 | a0001c0001t0001 a0002c0005t0001 |
7 | HG01261.hp2 HG02970.hp2 HG03139.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*928_*930dupTTT | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 931 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639147 | C | CTTTT | 2 | a0001c0001t0001 a0001c0001t0007 |
8 | HG01257.hp1 HG01515.hp2 HG03130.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*927_*930dupTTTT | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 931 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639147 | C | CTTTTT | 2 | a0001c0001t0001 a0004c0006t0001 |
9 | HG00099.hp1 HG00733.hp2 HG01167.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*926_*930dupTTTTT | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 931 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639147 | C | CTTTTTT | 2 | a0001c0001t0001 a0001c0001t0007 |
7 | HG01981.hp2 HG03209.hp2 NA18956.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*925_*930dupTTTTTT | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 931 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639147 | C | CTTTTTTT | 1 | a0001c0001t0001 | 8 | HG01106.hp2 HG01981.hp1 HG02735.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*924_*930dupTTTTTT others(1): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 931 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639147 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001 | 3 | HG03688.hp1 NA18961.hp2 NA19003.hp2 |
3_prime_UTR_variant | MODIFIER | c.*921_*930dupTTTTTT others(4): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 931 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639147 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*920_*930dupTTTTTT others(5): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 931 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639147 | C | CTTTTTTT others(5): Show |
2 | a0001c0001t0001 a0001c0001t0007 |
3 | HG00408.hp2 HG01891.hp2 NA19082.hp1 |
3_prime_UTR_variant | MODIFIER | c.*919_*930dupTTTTTT others(6): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 931 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639147 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0001 | 5 | HG02698.hp1 HG03491.hp2 NA18957.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*917_*930dupTTTTTT others(8): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 931 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639147 | C | CTTTTTTT others(8): Show |
1 | a0001c0001t0001 | 2 | HG01175.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*916_*930dupTTTTTT others(9): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 931 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639147 | C | CTTTTTTT others(11): Show |
1 | a0001c0001t0001 | 2 | HG02155.hp2 NA19067.hp1 |
3_prime_UTR_variant | MODIFIER | c.*913_*930dupTTTTTT others(12): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 931 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639147 | C | CTTTTTTT others(13): Show |
1 | a0001c0001t0001 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*911_*930dupTTTTTT others(14): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 931 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639147 | C | CTTTTTTT others(16): Show |
1 | a0001c0001t0001 | 2 | HG02148.hp1 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*908_*930dupTTTTTT others(17): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 931 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639147 | C | T | 1 | a0001c0001t0001 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*885C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 885 | chr18 | 8639147 | ||||||
| chr18:8639147 | CT | C | 2 | a0001c0001t0001 a0001c0001t0016 |
40 | HG00423.hp2 HG00642.hp2 HG01074.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*930delT | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 930 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639147 | CTT | C | 2 | a0001c0001t0001 a0001c0001t0002 |
27 | HG00323.hp1 HG00735.hp1 HG01069.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*929_*930delTT | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 929 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639147 | CTTT | C | 4 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(1): Show |
38 | HG00140.hp1 HG00558.hp2 HG01070.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*928_*930delTTT | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 928 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639147 | CTTTT | C | 4 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0017 others(1): Show |
32 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*927_*930delTTTT | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 927 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639147 | CTTTTT | C | 3 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0012 |
21 | HG00099.hp2 HG01261.hp1 HG01993.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*926_*930delTTTTT | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 926 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639147 | CTTTTTT | C | 2 | a0001c0001t0001 a0001c0001t0002 |
13 | HG00639.hp1 HG01123.hp2 HG02257.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*925_*930delTTTTTT | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 925 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639147 | CTTTTTTT | C | 1 | a0001c0001t0002 | 9 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*924_*930delTTTTTT others(1): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 924 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639147 | CTTTTTTT others(1): Show |
C | 2 | a0001c0001t0001 a0001c0001t0002 |
14 | HG00642.hp1 HG01074.hp2 HG01243.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*923_*930delTTTTTT others(2): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 923 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639147 | CTTTTTTT others(2): Show |
C | 2 | a0001c0001t0001 a0001c0001t0002 |
7 | HG01168.hp1 HG01256.hp1 HG01361.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*922_*930delTTTTTT others(3): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 922 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639147 | CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0001 a0001c0001t0002 |
6 | HG01258.hp1 HG02451.hp1 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*921_*930delTTTTTT others(4): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 921 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639147 | CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0013 |
7 | HG01070.hp2 HG02486.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*920_*930delTTTTTT others(5): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 920 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639147 | CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0001 a0001c0001t0002 |
8 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*919_*930delTTTTTT others(6): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 919 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639147 | CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0001 a0001c0001t0002 |
3 | HG02155.hp1 HG02559.hp2 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*918_*930delTTTTTT others(7): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 918 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639147 | CTTTTTTT others(7): Show |
C | 2 | a0001c0001t0001 a0001c0001t0006 |
2 | NA18954.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*917_*930delTTTTTT others(8): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 917 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639147 | CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0006 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*916_*930delTTTTTT others(9): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 916 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639147 | CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0006 | 2 | HG03139.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*915_*930delTTTTTT others(10): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 915 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639147 | CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0001 | 4 | HG02004.hp2 NA18943.hp2 NA18963.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*914_*930delTTTTTT others(11): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 914 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639147 | CTTTTTTT others(11): Show |
C | 1 | a0001c0001t0001 | 4 | HG02602.hp1 HG03942.hp2 NA18989.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*913_*930delTTTTTT others(12): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 913 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639147 | CTTTTTTT others(12): Show |
C | 1 | a0001c0001t0001 | 3 | HG04199.hp1 NA19067.hp2 NA19090.hp2 |
3_prime_UTR_variant | MODIFIER | c.*912_*930delTTTTTT others(13): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 912 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639147 | CTTTTTTT others(13): Show |
C | 1 | a0001c0001t0001 | 3 | HG00558.hp1 HG02040.hp1 NA19065.hp1 |
3_prime_UTR_variant | MODIFIER | c.*911_*930delTTTTTT others(14): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 911 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639147 | CTTTTTTT others(14): Show |
C | 1 | a0001c0001t0001 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*910_*930delTTTTTT others(15): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 910 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639147 | CTTTTTTT others(15): Show |
C | 2 | a0001c0001t0001 a0001c0001t0005 |
6 | HG01081.hp1 HG02647.hp2 HG02717.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*909_*930delTTTTTT others(16): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 909 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639147 | CTTTTTTT others(16): Show |
C | 1 | a0001c0001t0001 | 1 | NA19077.hp1 | 3_prime_UTR_variant | MODIFIER | c.*908_*930delTTTTTT others(17): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 908 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639147 | CTTTTTTT others(17): Show |
C | 2 | a0001c0001t0002 a0001c0001t0004 |
3 | HG01243.hp2 HG02129.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*907_*930delTTTTTT others(18): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 907 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639147 | CTTTTTTT others(20): Show |
C | 1 | a0001c0001t0002 | 2 | HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*904_*930delTTTTTT others(21): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 904 | INFO_REALIGN_3_PRIME | chr18 | 8639147 | |||||
| chr18:8639219 | A | G | 1 | a0001c0001t0005 | 5 | HG01081.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*957A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 957 | chr18 | 8639219 | ||||||
| chr18:8639242 | A | T | 1 | a0001c0001t0016 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*980A>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 980 | chr18 | 8639242 | ||||||
| chr18:8639249 | T | C | 1 | a0001c0001t0008 | 2 | HG01070.hp1 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*987T>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 6/6 | 987 | chr18 | 8639249 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:8610036 | G | C | 9 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0056 others(6): Show |
11 | HG01243.hp1 HG02451.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.514+83G>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8610036 | |||||||
| chr18:8610372 | G | A | 1 | a0001c0001t0001g0015 | 4 | HG02559.hp1 HG02630.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.514+419G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8610372 | |||||||
| chr18:8610456 | T | C | 1 | a0001c0001t0001g0063 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.514+503T>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8610456 | |||||||
| chr18:8610642 | T | C | 100 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(97): Show |
176 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.514+689T>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8610642 | |||||||
| chr18:8610728 | G | A | 1 | a0001c0001t0013g0137 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.514+775G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8610728 | |||||||
| chr18:8610828 | A | G | 1 | a0001c0001t0002g0216 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.514+875A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8610828 | |||||||
| chr18:8610913 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.514+960A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8610913 | |||||||
| chr18:8611053 | T | C | 1 | a0001c0001t0001g0017 | 4 | HG00408.hp2 HG02074.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.514+1100T>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8611053 | |||||||
| chr18:8611255 | A | C | 1 | a0001c0001t0001g0214 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.514+1302A>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8611255 | |||||||
| chr18:8611406 | C | G | 1 | a0001c0001t0001g0135 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.514+1453C>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8611406 | |||||||
| chr18:8611453 | A | T | 1 | a0001c0001t0001g0135 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.514+1500A>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8611453 | |||||||
| chr18:8611530 | C | T | 7 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0058 others(4): Show |
9 | HG01243.hp1 HG02451.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.514+1577C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8611530 | |||||||
| chr18:8611592 | G | A | 1 | a0001c0001t0013g0137 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.514+1639G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8611592 | |||||||
| chr18:8611671 | A | C | 1 | a0001c0001t0013g0137 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.514+1718A>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8611671 | |||||||
| chr18:8611766 | A | G | 2 | a0001c0001t0006g0212 a0001c0001t0006g0213 |
2 | HG02257.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.514+1813A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8611766 | |||||||
| chr18:8611778 | T | C | 1 | a0001c0001t0001g0064 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.514+1825T>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8611778 | |||||||
| chr18:8611826 | A | C | 1 | a0001c0001t0002g0134 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.514+1873A>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8611826 | |||||||
| chr18:8611840 | T | G | 2 | a0001c0001t0005g0023 a0001c0001t0005g0138 |
4 | HG02647.hp2 HG02717.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.514+1887T>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8611840 | |||||||
| chr18:8611919 | G | T | 3 | a0001c0001t0006g0055 a0001c0001t0006g0212 a0001c0001t0006g0213 |
4 | HG02257.hp1 HG03139.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.514+1966G>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8611919 | |||||||
| chr18:8612148 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.514+2195A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8612148 | |||||||
| chr18:8612153 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0132 |
2 | NA18949.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.514+2200C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8612153 | |||||||
| chr18:8612171 | C | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0041 |
6 | HG02258.hp1 HG02559.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.514+2218C>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8612171 | |||||||
| chr18:8612369 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.514+2416T>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8612369 | |||||||
| chr18:8612390 | A | G | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.514+2437A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8612390 | |||||||
| chr18:8612528 | C | G | 3 | a0001c0001t0002g0210 a0001c0001t0007g0054 a0001c0001t0007g0209 |
4 | HG01891.hp2 HG02559.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.514+2575C>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8612528 | |||||||
| chr18:8612865 | A | G | 6 | a0001c0001t0002g0014 a0001c0001t0002g0053 a0001c0001t0002g0205 others(3): Show |
12 | HG00639.hp1 HG01106.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.514+2912A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8612865 | |||||||
| chr18:8612951 | G | T | 65 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0015 others(62): Show |
118 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.514+2998G>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8612951 | |||||||
| chr18:8613139 | A | T | 1 | a0001c0001t0001g0204 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.514+3186A>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8613139 | |||||||
| chr18:8613147 | CAG | C | 4 | a0001c0001t0001g0203 a0001c0001t0002g0200 a0001c0001t0002g0202 others(1): Show |
4 | HG02895.hp2 HG03471.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.514+3197_514+3198d others(4): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 8613147 | ||||||
| chr18:8613155 | G | C | 1 | a0001c0001t0001g0092 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.514+3202G>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8613155 | |||||||
| chr18:8613335 | T | C | 9 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0056 others(6): Show |
11 | HG01243.hp1 HG02451.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.514+3382T>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8613335 | |||||||
| chr18:8613602 | A | C | 1 | a0001c0001t0001g0131 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.514+3649A>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8613602 | |||||||
| chr18:8613692 | G | A | 33 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(30): Show |
56 | HG00323.hp2 HG00733.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.514+3739G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8613692 | |||||||
| chr18:8613829 | A | AAGT | 72 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0020 others(69): Show |
128 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.514+3913_514+3915d others(5): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 8613829 | ||||||
| chr18:8613829 | A | AAGTAGT | 36 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(33): Show |
59 | HG01081.hp2 HG01123.hp1 HG01243.hp1 others(56): Show |
intron_variant | MODIFIER | c.514+3910_514+3915d others(8): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 8613829 | ||||||
| chr18:8613829 | A | AAGTAGTA others(2): Show |
4 | a0001c0001t0002g0056 a0001c0001t0002g0058 a0001c0001t0003g0141 others(1): Show |
4 | HG00558.hp2 HG02572.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.514+3907_514+3915d others(11): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 8613829 | ||||||
| chr18:8613829 | AAGT | A | 25 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(22): Show |
47 | HG00323.hp2 HG01069.hp1 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.514+3913_514+3915d others(5): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 8613829 | ||||||
| chr18:8613829 | AAGTAGT | A | 8 | a0001c0001t0002g0013 a0001c0001t0002g0091 a0001c0001t0002g0194 others(5): Show |
13 | HG00140.hp1 HG00642.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.514+3910_514+3915d others(8): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 8613829 | ||||||
| chr18:8613858 | G | C | 1 | a0001c0001t0002g0140 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.514+3905G>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8613858 | |||||||
| chr18:8613915 | A | G | 1 | a0001c0001t0002g0062 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.514+3962A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8613915 | |||||||
| chr18:8614033 | T | G | 34 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(31): Show |
57 | HG00323.hp2 HG00733.hp1 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.514+4080T>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8614033 | |||||||
| chr18:8614159 | A | G | 157 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.514+4206A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8614159 | |||||||
| chr18:8614245 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.514+4292G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8614245 | |||||||
| chr18:8614272 | CT | C | 33 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(30): Show |
56 | HG00323.hp2 HG00733.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.514+4323delT | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 8614272 | ||||||
| chr18:8614278 | A | G | 33 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(30): Show |
56 | HG00323.hp2 HG00733.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.514+4325A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8614278 | |||||||
| chr18:8614356 | A | G | 1 | a0001c0001t0002g0216 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.514+4403A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8614356 | |||||||
| chr18:8614480 | T | C | 33 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(30): Show |
56 | HG00323.hp2 HG00733.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.514+4527T>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8614480 | |||||||
| chr18:8614505 | T | G | 1 | a0001c0001t0005g0068 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.514+4552T>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8614505 | |||||||
| chr18:8614519 | G | A | 33 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(30): Show |
56 | HG00323.hp2 HG00733.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.514+4566G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8614519 | |||||||
| chr18:8614519 | G | GA | 11 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0146 others(8): Show |
19 | HG01123.hp1 HG01257.hp2 HG01258.hp2 others(16): Show |
intron_variant | MODIFIER | c.514+4576dupA | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 8614519 | ||||||
| chr18:8614519 | GA | G | 8 | a0001c0001t0001g0024 a0001c0001t0002g0013 a0001c0001t0002g0018 others(5): Show |
16 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.514+4576delA | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 8614519 | ||||||
| chr18:8614520 | A | AAG | 29 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(26): Show |
51 | HG00323.hp2 HG00733.hp1 HG01069.hp1 others(48): Show |
intron_variant | MODIFIER | c.514+4568_514+4569i others(4): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 8614520 | ||||||
| chr18:8614520 | A | AG | 4 | a0001c0001t0001g0028 a0001c0001t0001g0067 a0001c0001t0002g0065 others(1): Show |
5 | HG02145.hp1 HG02723.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.514+4567_514+4568i others(3): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8614520 | |||||||
| chr18:8614520 | A | G | 2 | a0001c0001t0001g0155 a0001c0001t0002g0199 |
2 | HG02895.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.514+4567A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8614520 | |||||||
| chr18:8614563 | A | G | 1 | a0001c0001t0001g0154 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.514+4610A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8614563 | |||||||
| chr18:8614615 | C | T | 32 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(29): Show |
55 | HG00323.hp2 HG00733.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.514+4662C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8614615 | |||||||
| chr18:8614648 | G | A | 2 | a0001c0001t0002g0065 a0001c0001t0011g0066 |
2 | HG02145.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.514+4695G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8614648 | |||||||
| chr18:8614742 | C | T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0146 others(7): Show |
18 | HG01123.hp1 HG01257.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.514+4789C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8614742 | |||||||
| chr18:8614743 | G | A | 16 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0070 others(13): Show |
30 | HG01069.hp2 HG01081.hp1 HG01192.hp2 others(27): Show |
intron_variant | MODIFIER | c.514+4790G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8614743 | |||||||
| chr18:8614840 | T | A | 32 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(29): Show |
55 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.514+4887T>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8614840 | |||||||
| chr18:8614881 | G | A | 7 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0056 others(4): Show |
9 | HG01243.hp1 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.514+4928G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8614881 | |||||||
| chr18:8615265 | G | A | 3 | a0001c0001t0002g0013 a0001c0001t0002g0091 a0001c0001t0002g0194 |
8 | HG00140.hp1 HG00642.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.514+5312G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8615265 | |||||||
| chr18:8615348 | C | T | 9 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0146 others(6): Show |
16 | HG01123.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.514+5395C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8615348 | |||||||
| chr18:8615710 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.514+5757G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8615710 | |||||||
| chr18:8615974 | G | C | 32 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(29): Show |
55 | HG00323.hp2 HG00733.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.514+6021G>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8615974 | |||||||
| chr18:8616025 | G | A | 4 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02615.hp2 HG02922.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.514+6072G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8616025 | |||||||
| chr18:8616038 | G | A | 32 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(29): Show |
55 | HG00323.hp2 HG00733.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.514+6085G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8616038 | |||||||
| chr18:8616076 | A | G | 3 | a0001c0001t0001g0028 a0001c0001t0001g0067 a0001c0001t0002g0065 |
4 | HG02145.hp1 HG02723.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.514+6123A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8616076 | |||||||
| chr18:8616152 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.514+6199G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8616152 | |||||||
| chr18:8616360 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.514+6407C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8616360 | |||||||
| chr18:8616379 | T | TA | 35 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0019 others(32): Show |
51 | HG00323.hp1 HG00323.hp2 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.514+6447dupA | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 8616379 | ||||||
| chr18:8616379 | T | TAA | 9 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0146 others(6): Show |
17 | HG01123.hp1 HG01257.hp2 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.514+6446_514+6447d others(4): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 8616379 | ||||||
| chr18:8616379 | TA | T | 13 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0081 others(10): Show |
15 | HG00639.hp2 HG01069.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.514+6447delA | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 8616379 | ||||||
| chr18:8616394 | A | C | 8 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0162 others(5): Show |
10 | HG01884.hp1 HG02622.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.514+6441A>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8616394 | |||||||
| chr18:8616652 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.514+6699C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8616652 | |||||||
| chr18:8616659 | C | G | 5 | a0001c0001t0002g0044 a0001c0001t0002g0142 a0001c0001t0002g0145 others(2): Show |
6 | HG02145.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.514+6706C>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8616659 | |||||||
| chr18:8616716 | A | G | 1 | a0001c0001t0002g0061 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.514+6763A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8616716 | |||||||
| chr18:8616757 | C | CA | 40 | a0001c0001t0001g0020 a0001c0001t0001g0031 a0001c0001t0001g0045 others(37): Show |
55 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.514+6819dupA | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 8616757 | ||||||
| chr18:8617126 | C | T | 3 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 |
3 | HG02615.hp2 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.514+7173C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8617126 | |||||||
| chr18:8617163 | G | A | 10 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0146 others(7): Show |
18 | HG01123.hp1 HG01257.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.514+7210G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8617163 | |||||||
| chr18:8617164 | T | G | 1 | a0001c0001t0001g0148 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.514+7211T>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8617164 | |||||||
| chr18:8617225 | T | C | 2 | a0001c0001t0007g0054 a0001c0001t0007g0209 |
3 | HG01891.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.514+7272T>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8617225 | |||||||
| chr18:8617449 | A | G | 1 | a0001c0001t0001g0121 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.515-7489A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8617449 | |||||||
| chr18:8617584 | A | G | 59 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0146 others(56): Show |
86 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.515-7354A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8617584 | |||||||
| chr18:8617591 | C | G | 3 | a0001c0001t0001g0028 a0001c0001t0001g0067 a0001c0001t0002g0065 |
4 | HG02145.hp1 HG02723.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.515-7347C>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8617591 | |||||||
| chr18:8618153 | G | A | 1 | a0001c0001t0002g0056 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.515-6785G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8618153 | |||||||
| chr18:8618226 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.515-6712G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8618226 | |||||||
| chr18:8618257 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.515-6681G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8618257 | |||||||
| chr18:8618511 | CT | C | 7 | a0001c0001t0001g0046 a0001c0001t0001g0094 a0001c0001t0001g0112 others(4): Show |
8 | HG01168.hp2 HG01169.hp1 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.515-6415delT | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 8618511 | ||||||
| chr18:8618571 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.515-6367G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8618571 | |||||||
| chr18:8618724 | G | A | 6 | a0001c0001t0002g0014 a0001c0001t0002g0053 a0001c0001t0002g0205 others(3): Show |
12 | HG00639.hp1 HG01106.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.515-6214G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8618724 | |||||||
| chr18:8618768 | T | G | 1 | a0001c0001t0013g0137 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.515-6170T>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8618768 | |||||||
| chr18:8618907 | G | A | 14 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0029 others(11): Show |
24 | HG00323.hp2 HG01123.hp1 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.515-6031G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8618907 | |||||||
| chr18:8619197 | A | G | 1 | a0001c0001t0001g0152 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.515-5741A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8619197 | |||||||
| chr18:8619203 | G | T | 1 | a0001c0001t0001g0087 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.515-5735G>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8619203 | |||||||
| chr18:8619238 | T | C | 2 | a0001c0001t0007g0054 a0001c0001t0007g0209 |
3 | HG01891.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.515-5700T>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8619238 | |||||||
| chr18:8619281 | G | T | 1 | a0001c0001t0001g0086 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.515-5657G>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8619281 | |||||||
| chr18:8619282 | G | T | 1 | a0001c0001t0001g0086 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.515-5656G>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8619282 | |||||||
| chr18:8619311 | G | C | 1 | a0001c0001t0001g0122 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.515-5627G>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8619311 | |||||||
| chr18:8619336 | C | T | 14 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0029 others(11): Show |
24 | HG00323.hp2 HG01123.hp1 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.515-5602C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8619336 | |||||||
| chr18:8619338 | G | A | 43 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0018 others(40): Show |
60 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.515-5600G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8619338 | |||||||
| chr18:8619355 | T | C | 1 | a0001c0001t0001g0032 | 2 | NA18948.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.515-5583T>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8619355 | |||||||
| chr18:8619404 | A | G | 2 | a0001c0001t0001g0025 a0001c0001t0001g0163 |
4 | NA18972.hp1 NA18989.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.515-5534A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8619404 | |||||||
| chr18:8619460 | C | G | 1 | a0001c0001t0002g0208 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.515-5478C>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8619460 | |||||||
| chr18:8619925 | G | A | 26 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
46 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.515-5013G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8619925 | |||||||
| chr18:8620017 | T | C | 26 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
46 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.515-4921T>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8620017 | |||||||
| chr18:8620130 | T | C | 28 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(25): Show |
48 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.515-4808T>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8620130 | |||||||
| chr18:8620132 | T | TC | 45 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0018 others(42): Show |
63 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.515-4805dupC | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 8620132 | ||||||
| chr18:8620139 | C | CT | 74 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0015 others(71): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.515-4778dupT | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 8620139 | ||||||
| chr18:8620139 | C | CTTTTTT | 19 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(16): Show |
39 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.515-4783_515-4778d others(8): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 8620139 | ||||||
| chr18:8620139 | CT | C | 23 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0029 others(20): Show |
33 | HG00323.hp2 HG01123.hp1 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.515-4778delT | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 8620139 | ||||||
| chr18:8620142 | T | C | 7 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0058 others(4): Show |
9 | HG01243.hp1 HG02451.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.515-4796T>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8620142 | |||||||
| chr18:8620165 | C | CA | 72 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0015 others(69): Show |
128 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.515-4760dupA | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 8620165 | ||||||
| chr18:8620165 | C | CAA | 75 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(72): Show |
119 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(116): Show |
intron_variant | MODIFIER | c.515-4761_515-4760d others(4): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 8620165 | ||||||
| chr18:8620165 | C | CAAA | 9 | a0001c0001t0002g0018 a0001c0001t0002g0027 a0001c0001t0002g0060 others(6): Show |
13 | HG02109.hp1 HG02258.hp2 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.515-4762_515-4760d others(5): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 8620165 | ||||||
| chr18:8620236 | C | T | 2 | a0001c0001t0002g0202 a0001c0001t0016g0201 |
2 | HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.515-4702C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8620236 | |||||||
| chr18:8620252 | A | G | 2 | a0001c0001t0007g0054 a0001c0001t0007g0209 |
3 | HG01891.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.515-4686A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8620252 | |||||||
| chr18:8620325 | C | A | 89 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(86): Show |
138 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(135): Show |
intron_variant | MODIFIER | c.515-4613C>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8620325 | |||||||
| chr18:8620507 | C | G | 89 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(86): Show |
138 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(135): Show |
intron_variant | MODIFIER | c.515-4431C>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8620507 | |||||||
| chr18:8620559 | C | CT | 28 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(25): Show |
48 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.515-4368dupT | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 8620559 | ||||||
| chr18:8620568 | T | C | 1 | a0001c0001t0002g0200 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.515-4370T>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8620568 | |||||||
| chr18:8620577 | T | C | 1 | a0001c0001t0005g0023 | 3 | HG02647.hp2 HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.515-4361T>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8620577 | |||||||
| chr18:8620585 | G | A | 2 | a0001c0001t0002g0195 a0001c0001t0002g0199 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.515-4353G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8620585 | |||||||
| chr18:8620745 | C | T | 2 | a0001c0001t0007g0054 a0001c0001t0007g0209 |
3 | HG01891.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.515-4193C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8620745 | |||||||
| chr18:8620885 | G | A | 2 | a0001c0001t0002g0202 a0001c0001t0016g0201 |
2 | HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.515-4053G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8620885 | |||||||
| chr18:8621050 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0015g0089 |
4 | HG00323.hp2 HG02683.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.515-3888G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8621050 | |||||||
| chr18:8621102 | G | A | 1 | a0001c0001t0004g0115 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.515-3836G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8621102 | |||||||
| chr18:8621124 | C | T | 26 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
46 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.515-3814C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8621124 | |||||||
| chr18:8621293 | A | G | 1 | a0001c0001t0002g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.515-3645A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8621293 | |||||||
| chr18:8621303 | A | G | 1 | a0001c0001t0001g0175 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.515-3635A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8621303 | |||||||
| chr18:8621319 | A | T | 11 | a0001c0001t0001g0009 a0001c0001t0001g0030 a0001c0001t0001g0069 others(8): Show |
17 | HG00733.hp1 HG01069.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.515-3619A>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8621319 | |||||||
| chr18:8621347 | A | G | 26 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
46 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.515-3591A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8621347 | |||||||
| chr18:8621357 | A | C | 16 | a0001c0001t0002g0044 a0001c0001t0002g0134 a0001c0001t0002g0140 others(13): Show |
18 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.515-3581A>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8621357 | |||||||
| chr18:8621422 | T | G | 26 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
46 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.515-3516T>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8621422 | |||||||
| chr18:8621432 | G | A | 157 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.515-3506G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8621432 | |||||||
| chr18:8621503 | G | A | 26 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
46 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.515-3435G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8621503 | |||||||
| chr18:8621561 | C | T | 26 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
46 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.515-3377C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8621561 | |||||||
| chr18:8621636 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.515-3302G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8621636 | |||||||
| chr18:8621638 | G | T | 26 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
46 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.515-3300G>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8621638 | |||||||
| chr18:8621658 | G | A | 26 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
46 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.515-3280G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8621658 | |||||||
| chr18:8621721 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.515-3217G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8621721 | |||||||
| chr18:8621729 | CATAGGAC others(3): Show |
C | 2 | a0001c0001t0002g0191 a0001c0001t0002g0211 |
2 | HG02886.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.515-3203_515-3194d others(12): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 8621729 | ||||||
| chr18:8621819 | C | CTA | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(91): Show |
169 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.515-3118_515-3117i others(4): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 8621819 | ||||||
| chr18:8621914 | T | A | 1 | a0001c0001t0002g0065 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.515-3024T>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8621914 | |||||||
| chr18:8622034 | G | A | 26 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
46 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.515-2904G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8622034 | |||||||
| chr18:8622155 | A | G | 1 | a0001c0001t0001g0161 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.515-2783A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8622155 | |||||||
| chr18:8622272 | T | G | 3 | a0001c0001t0002g0018 a0001c0001t0002g0143 a0001c0001t0002g0190 |
6 | HG02109.hp1 HG02258.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.515-2666T>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8622272 | |||||||
| chr18:8622302 | T | C | 1 | a0001c0001t0001g0116 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.515-2636T>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8622302 | |||||||
| chr18:8622433 | C | T | 1 | a0001c0001t0005g0068 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.515-2505C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8622433 | |||||||
| chr18:8622464 | A | G | 1 | a0001c0001t0001g0174 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.515-2474A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8622464 | |||||||
| chr18:8622669 | C | T | 6 | a0001c0001t0002g0014 a0001c0001t0002g0053 a0001c0001t0002g0205 others(3): Show |
12 | HG00639.hp1 HG01106.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.515-2269C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8622669 | |||||||
| chr18:8622694 | CGGTCTGA others(13): Show |
C | 1 | a0001c0001t0007g0054 | 2 | HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.515-2240_515-2221d others(22): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr18 | 8622694 | ||||||
| chr18:8622695 | G | A | 1 | a0001c0001t0002g0016 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.515-2243G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8622695 | |||||||
| chr18:8622727 | C | T | 1 | a0001c0001t0001g0030 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.515-2211C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8622727 | |||||||
| chr18:8622802 | G | A | 1 | a0001c0001t0002g0124 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.515-2136G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8622802 | |||||||
| chr18:8622809 | C | A | 2 | a0001c0001t0007g0054 a0001c0001t0007g0209 |
3 | HG01891.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.515-2129C>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8622809 | |||||||
| chr18:8622850 | G | A | 1 | a0001c0001t0002g0202 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.515-2088G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8622850 | |||||||
| chr18:8622971 | T | C | 2 | a0001c0001t0002g0191 a0001c0001t0002g0211 |
2 | HG02886.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.515-1967T>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8622971 | |||||||
| chr18:8623023 | A | G | 1 | a0001c0001t0002g0206 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.515-1915A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8623023 | |||||||
| chr18:8623052 | C | T | 1 | a0001c0001t0002g0140 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.515-1886C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8623052 | |||||||
| chr18:8623091 | A | G | 67 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0015 others(64): Show |
122 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.515-1847A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8623091 | |||||||
| chr18:8623119 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.515-1819C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8623119 | |||||||
| chr18:8623180 | G | A | 3 | a0001c0001t0002g0013 a0001c0001t0002g0091 a0001c0001t0002g0194 |
8 | HG00140.hp1 HG00642.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.515-1758G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8623180 | |||||||
| chr18:8623188 | T | A | 3 | a0001c0001t0002g0018 a0001c0001t0002g0143 a0001c0001t0002g0190 |
6 | HG02109.hp1 HG02258.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.515-1750T>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8623188 | |||||||
| chr18:8623472 | G | A | 1 | a0001c0001t0001g0050 | 2 | HG02723.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.515-1466G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8623472 | |||||||
| chr18:8623493 | A | C | 1 | a0001c0001t0002g0057 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.515-1445A>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8623493 | |||||||
| chr18:8623729 | C | G | 2 | a0001c0001t0007g0054 a0001c0001t0007g0209 |
3 | HG01891.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.515-1209C>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8623729 | |||||||
| chr18:8623999 | C | T | 25 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(22): Show |
45 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.515-939C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8623999 | |||||||
| chr18:8624000 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0112 a0001c0001t0001g0128 |
4 | HG02027.hp1 HG02071.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.515-938G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8624000 | |||||||
| chr18:8624044 | A | G | 28 | a0001c0001t0002g0013 a0001c0001t0002g0018 a0001c0001t0002g0044 others(25): Show |
38 | HG00140.hp1 HG00642.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.515-894A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8624044 | |||||||
| chr18:8624153 | A | G | 157 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.515-785A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8624153 | |||||||
| chr18:8624283 | G | C | 25 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(22): Show |
45 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.515-655G>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8624283 | |||||||
| chr18:8624863 | C | G | 1 | a0001c0001t0002g0091 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.515-75C>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8624863 | |||||||
| chr18:8624889 | A | G | 1 | a0001c0001t0001g0174 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.515-49A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8624889 | |||||||
| chr18:8624899 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.515-39T>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8624899 | |||||||
| chr18:8624935 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG01358.hp1 | splice_region_variant&intron_variant | LOW | c.515-3C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 1/5 | chr18 | 8624935 | |||||||
| chr18:8625249 | C | T | 3 | a0001c0001t0002g0016 a0001c0001t0002g0124 a0001c0001t0002g0130 |
6 | HG00099.hp2 HG00639.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.575+251C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8625249 | |||||||
| chr18:8625262 | A | G | 3 | a0001c0001t0002g0018 a0001c0001t0002g0143 a0001c0001t0002g0190 |
6 | HG02109.hp1 HG02258.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.575+264A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8625262 | |||||||
| chr18:8625314 | C | G | 1 | a0001c0001t0002g0057 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.575+316C>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8625314 | |||||||
| chr18:8625368 | A | G | 1 | a0001c0001t0003g0160 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.575+370A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8625368 | |||||||
| chr18:8625556 | A | G | 1 | a0001c0001t0016g0201 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.575+558A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8625556 | |||||||
| chr18:8625644 | G | A | 65 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0029 others(62): Show |
94 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.575+646G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8625644 | |||||||
| chr18:8625769 | G | A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0125 |
3 | HG00733.hp2 HG01106.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.575+771G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8625769 | |||||||
| chr18:8626000 | A | G | 2 | a0001c0001t0002g0195 a0001c0001t0002g0199 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.575+1002A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8626000 | |||||||
| chr18:8626016 | C | T | 2 | a0001c0001t0001g0154 a0001c0001t0001g0173 |
2 | NA19055.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.575+1018C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8626016 | |||||||
| chr18:8626038 | T | A | 25 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(22): Show |
45 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.575+1040T>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8626038 | |||||||
| chr18:8626067 | T | C | 25 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(22): Show |
45 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.575+1069T>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8626067 | |||||||
| chr18:8626081 | G | T | 1 | a0001c0001t0001g0123 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.575+1083G>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8626081 | |||||||
| chr18:8626140 | A | G | 62 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0020 others(59): Show |
112 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.575+1142A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8626140 | |||||||
| chr18:8626168 | T | C | 4 | a0001c0001t0001g0011 a0001c0001t0001g0155 a0001c0001t0001g0176 others(1): Show |
8 | HG00609.hp2 HG01934.hp1 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.575+1170T>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8626168 | |||||||
| chr18:8626459 | TAATG | T | 2 | a0001c0001t0007g0054 a0001c0001t0007g0209 |
3 | HG01891.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.575+1462_575+1465d others(6): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8626459 | |||||||
| chr18:8626596 | T | G | 90 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(87): Show |
139 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(136): Show |
intron_variant | MODIFIER | c.575+1598T>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8626596 | |||||||
| chr18:8626666 | T | C | 25 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(22): Show |
45 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.575+1668T>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8626666 | |||||||
| chr18:8626711 | A | G | 1 | a0001c0001t0005g0068 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.575+1713A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8626711 | |||||||
| chr18:8626830 | G | A | 1 | a0001c0001t0011g0066 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.575+1832G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8626830 | |||||||
| chr18:8626845 | G | A | 1 | a0001c0001t0001g0073 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.575+1847G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8626845 | |||||||
| chr18:8626963 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.575+1965A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8626963 | |||||||
| chr18:8627162 | A | G | 90 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(87): Show |
139 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(136): Show |
intron_variant | MODIFIER | c.575+2164A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8627162 | |||||||
| chr18:8627167 | C | G | 1 | a0001c0001t0013g0137 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.575+2169C>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8627167 | |||||||
| chr18:8627223 | C | T | 25 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(22): Show |
45 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.575+2225C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8627223 | |||||||
| chr18:8627458 | C | T | 25 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(22): Show |
45 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.575+2460C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8627458 | |||||||
| chr18:8627597 | A | G | 25 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(22): Show |
45 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.575+2599A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8627597 | |||||||
| chr18:8627639 | T | C | 11 | a0001c0001t0001g0009 a0001c0001t0001g0030 a0001c0001t0001g0069 others(8): Show |
17 | HG00733.hp1 HG01069.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.575+2641T>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8627639 | |||||||
| chr18:8627673 | G | A | 25 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(22): Show |
45 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.575+2675G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8627673 | |||||||
| chr18:8627745 | A | G | 2 | a0001c0001t0001g0166 a0001c0001t0001g0204 |
2 | HG01255.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.575+2747A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8627745 | |||||||
| chr18:8627881 | G | A | 25 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(22): Show |
45 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.575+2883G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8627881 | |||||||
| chr18:8627959 | C | T | 65 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0015 others(62): Show |
120 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.575+2961C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8627959 | |||||||
| chr18:8628047 | A | G | 1 | a0001c0001t0001g0168 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.575+3049A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8628047 | |||||||
| chr18:8628188 | G | A | 25 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(22): Show |
45 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.575+3190G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8628188 | |||||||
| chr18:8628270 | C | T | 25 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(22): Show |
45 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.575+3272C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8628270 | |||||||
| chr18:8628271 | G | A | 25 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(22): Show |
45 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.575+3273G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8628271 | |||||||
| chr18:8628336 | C | A | 25 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(22): Show |
45 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.575+3338C>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8628336 | |||||||
| chr18:8628419 | A | G | 1 | a0001c0001t0001g0120 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.575+3421A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8628419 | |||||||
| chr18:8628443 | A | C | 25 | a0001c0001t0002g0013 a0001c0001t0002g0018 a0001c0001t0002g0044 others(22): Show |
34 | HG00140.hp1 HG00642.hp1 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.575+3445A>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8628443 | |||||||
| chr18:8628558 | T | C | 1 | a0001c0001t0002g0056 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.575+3560T>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8628558 | |||||||
| chr18:8628595 | C | T | 2 | a0001c0001t0007g0054 a0001c0001t0007g0209 |
3 | HG01891.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.575+3597C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8628595 | |||||||
| chr18:8628871 | A | T | 90 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(87): Show |
139 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(136): Show |
intron_variant | MODIFIER | c.575+3873A>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8628871 | |||||||
| chr18:8629105 | G | A | 7 | a0001c0001t0001g0051 a0001c0001t0001g0162 a0001c0001t0001g0185 others(4): Show |
8 | HG01884.hp1 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.576-4084G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8629105 | |||||||
| chr18:8629170 | G | T | 89 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(86): Show |
138 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(135): Show |
intron_variant | MODIFIER | c.576-4019G>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8629170 | |||||||
| chr18:8629311 | C | T | 25 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(22): Show |
45 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.576-3878C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8629311 | |||||||
| chr18:8629436 | C | T | 25 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(22): Show |
45 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.576-3753C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8629436 | |||||||
| chr18:8629442 | G | A | 25 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(22): Show |
45 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.576-3747G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8629442 | |||||||
| chr18:8629641 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.576-3548G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8629641 | |||||||
| chr18:8629722 | T | A | 25 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(22): Show |
45 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.576-3467T>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8629722 | |||||||
| chr18:8629771 | G | T | 4 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0172 others(1): Show |
4 | HG02647.hp1 HG02970.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.576-3418G>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8629771 | |||||||
| chr18:8629848 | T | C | 25 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(22): Show |
45 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.576-3341T>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8629848 | |||||||
| chr18:8629976 | T | A | 2 | a0001c0001t0001g0084 a0001c0001t0001g0086 |
2 | HG02155.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.576-3213T>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8629976 | |||||||
| chr18:8630351 | GTTA | G | 4 | a0001c0001t0002g0140 a0001c0001t0002g0191 a0001c0001t0002g0192 others(1): Show |
4 | HG02630.hp2 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.576-2833_576-2831d others(5): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr18 | 8630351 | ||||||
| chr18:8630357 | A | G | 7 | a0001c0001t0001g0106 a0001c0001t0001g0121 a0001c0001t0004g0034 others(4): Show |
8 | HG00558.hp2 HG02080.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.576-2832A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8630357 | |||||||
| chr18:8630360 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.576-2829T>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8630360 | |||||||
| chr18:8630362 | T | A | 1 | a0001c0001t0001g0117 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.576-2827T>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8630362 | |||||||
| chr18:8630414 | C | T | 3 | a0001c0001t0002g0014 a0001c0001t0002g0207 a0001c0001t0002g0208 |
8 | HG00639.hp1 HG01106.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.576-2775C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8630414 | |||||||
| chr18:8630741 | C | T | 1 | a0001c0001t0002g0065 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.576-2448C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8630741 | |||||||
| chr18:8630876 | GTTTGTT | G | 14 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0029 others(11): Show |
24 | HG00323.hp2 HG01123.hp1 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.576-2291_576-2286d others(8): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr18 | 8630876 | ||||||
| chr18:8630876 | GTTTGTTT others(5): Show |
G | 1 | a0001c0001t0002g0065 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.576-2297_576-2286d others(14): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr18 | 8630876 | ||||||
| chr18:8630921 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.576-2268C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8630921 | |||||||
| chr18:8630952 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0164 a0001c0001t0001g0178 |
9 | HG00642.hp2 HG01167.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.576-2237G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8630952 | |||||||
| chr18:8630975 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.576-2214G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8630975 | |||||||
| chr18:8630983 | G | A | 25 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(22): Show |
45 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.576-2206G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8630983 | |||||||
| chr18:8630985 | C | T | 25 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(22): Show |
45 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.576-2204C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8630985 | |||||||
| chr18:8631109 | T | G | 1 | a0001c0001t0001g0118 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.576-2080T>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8631109 | |||||||
| chr18:8631232 | A | G | 1 | a0001c0001t0011g0066 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.576-1957A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8631232 | |||||||
| chr18:8631499 | C | A | 1 | a0001c0001t0001g0113 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.576-1690C>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8631499 | |||||||
| chr18:8631692 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.576-1497G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8631692 | |||||||
| chr18:8631714 | A | G | 1 | a0001c0001t0001g0150 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.576-1475A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8631714 | |||||||
| chr18:8631790 | G | A | 1 | a0001c0001t0002g0190 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.576-1399G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8631790 | |||||||
| chr18:8631906 | T | A | 61 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0029 others(58): Show |
89 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.576-1283T>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8631906 | |||||||
| chr18:8632001 | G | A | 14 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0029 others(11): Show |
24 | HG00323.hp2 HG01123.hp1 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.576-1188G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8632001 | |||||||
| chr18:8632146 | C | T | 2 | a0001c0001t0002g0197 a0001c0001t0017g0198 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.576-1043C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8632146 | |||||||
| chr18:8632202 | C | T | 9 | a0001c0001t0002g0013 a0001c0001t0002g0065 a0001c0001t0002g0091 others(6): Show |
14 | HG00140.hp1 HG00642.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.576-987C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8632202 | |||||||
| chr18:8632259 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.576-930G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8632259 | |||||||
| chr18:8632270 | A | T | 1 | a0001c0001t0001g0039 | 2 | NA18989.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.576-919A>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8632270 | |||||||
| chr18:8632281 | CCAAAAAA others(2): Show |
C | 14 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0029 others(11): Show |
24 | HG00323.hp2 HG01123.hp1 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.576-907_576-899del others(9): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8632281 | |||||||
| chr18:8632282 | C | CA | 8 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0033 others(5): Show |
13 | HG02717.hp2 HG03927.hp2 NA18941.hp1 others(10): Show |
intron_variant | MODIFIER | c.576-887dupA | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr18 | 8632282 | ||||||
| chr18:8632282 | CA | C | 17 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0033 others(14): Show |
20 | HG01069.hp1 HG01192.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.576-887delA | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr18 | 8632282 | ||||||
| chr18:8632284 | A | G | 1 | a0001c0001t0005g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.576-905A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8632284 | |||||||
| chr18:8632363 | C | G | 1 | a0001c0001t0001g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.576-826C>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8632363 | |||||||
| chr18:8632376 | C | T | 1 | a0001c0001t0016g0201 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.576-813C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8632376 | |||||||
| chr18:8632377 | TGTGCACG others(7): Show |
T | 1 | a0001c0001t0001g0133 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.576-806_576-793del others(14): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr18 | 8632377 | ||||||
| chr18:8632402 | G | A | 3 | a0001c0001t0002g0013 a0001c0001t0002g0091 a0001c0001t0002g0194 |
8 | HG00140.hp1 HG00642.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.576-787G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8632402 | |||||||
| chr18:8632469 | A | T | 1 | a0001c0001t0001g0113 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.576-720A>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8632469 | |||||||
| chr18:8632578 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0177 a0001c0001t0001g0179 |
8 | HG02015.hp1 HG02135.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.576-611G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8632578 | |||||||
| chr18:8632693 | G | T | 14 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0029 others(11): Show |
24 | HG00323.hp2 HG01123.hp1 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.576-496G>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8632693 | |||||||
| chr18:8632694 | G | A | 14 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0029 others(11): Show |
24 | HG00323.hp2 HG01123.hp1 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.576-495G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8632694 | |||||||
| chr18:8632697 | A | AAGTG | 14 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0029 others(11): Show |
24 | HG00323.hp2 HG01123.hp1 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.576-492_576-491ins others(4): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8632697 | |||||||
| chr18:8632700 | C | A | 1 | a0001c0001t0002g0192 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.576-489C>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8632700 | |||||||
| chr18:8632700 | C | T | 14 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0029 others(11): Show |
24 | HG00323.hp2 HG01123.hp1 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.576-489C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8632700 | |||||||
| chr18:8632795 | T | G | 1 | a0001c0001t0001g0081 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.576-394T>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8632795 | |||||||
| chr18:8632809 | C | T | 155 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.576-380C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8632809 | |||||||
| chr18:8632890 | T | C | 1 | a0004c0006t0001g0169 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.576-299T>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8632890 | |||||||
| chr18:8633150 | G | A | 3 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0210 |
3 | HG02559.hp2 HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.576-39G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 2/5 | chr18 | 8633150 | |||||||
| chr18:8633352 | A | G | 1 | a0001c0001t0002g0170 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.714+25A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 3/5 | chr18 | 8633352 | |||||||
| chr18:8633487 | T | G | 27 | a0001c0001t0001g0028 a0001c0001t0001g0067 a0001c0001t0002g0013 others(24): Show |
37 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.714+160T>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 3/5 | chr18 | 8633487 | |||||||
| chr18:8633536 | C | T | 2 | a0001c0001t0001g0029 a0001c0001t0003g0029 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.714+209C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 3/5 | chr18 | 8633536 | |||||||
| chr18:8633564 | C | T | 2 | a0001c0001t0007g0054 a0001c0001t0007g0209 |
3 | HG01891.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.714+237C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 3/5 | chr18 | 8633564 | |||||||
| chr18:8633587 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.714+260A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 3/5 | chr18 | 8633587 | |||||||
| chr18:8633731 | G | A | 1 | a0001c0001t0001g0036 | 2 | NA19000.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.714+404G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 3/5 | chr18 | 8633731 | |||||||
| chr18:8633750 | C | T | 3 | a0001c0001t0006g0055 a0001c0001t0006g0212 a0001c0001t0006g0213 |
4 | HG02257.hp1 HG03139.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+423C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 3/5 | chr18 | 8633750 | |||||||
| chr18:8633825 | G | A | 1 | a0001c0001t0002g0196 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.714+498G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 3/5 | chr18 | 8633825 | |||||||
| chr18:8634166 | ATGGTGAC others(106): Show |
A | 4 | a0001c0001t0001g0038 a0001c0001t0001g0067 a0001c0001t0001g0090 others(1): Show |
5 | HG00438.hp2 HG04228.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.714+841_714+953del | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr18 | 8634166 | ||||||
| chr18:8634166 | ATGGTGAC others(108): Show |
A | 60 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0015 others(57): Show |
111 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.714+841_714+955del | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr18 | 8634166 | ||||||
| chr18:8634167 | TGGTGACT others(109): Show |
T | 1 | a0001c0001t0012g0101 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.714+841_714+956del | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 3/5 | chr18 | 8634167 | |||||||
| chr18:8634199 | G | C | 1 | a0001c0001t0001g0003 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.714+872G>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 3/5 | chr18 | 8634199 | |||||||
| chr18:8634282 | TC | T | 4 | a0001c0001t0001g0038 a0001c0001t0001g0067 a0001c0001t0001g0090 others(1): Show |
5 | HG00438.hp2 HG04228.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.714+956delC | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 3/5 | chr18 | 8634282 | |||||||
| chr18:8634283 | C | CT | 16 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(13): Show |
26 | HG00639.hp1 HG01069.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.714+976dupT | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr18 | 8634283 | ||||||
| chr18:8634283 | CT | C | 38 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0019 others(35): Show |
56 | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.714+976delT | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr18 | 8634283 | ||||||
| chr18:8634283 | CTT | C | 19 | a0001c0001t0002g0027 a0001c0001t0002g0044 a0001c0001t0002g0058 others(16): Show |
22 | HG01243.hp1 HG02109.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.714+975_714+976del others(2): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr18 | 8634283 | ||||||
| chr18:8634284 | T | C | 1 | a0001c0001t0012g0101 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.714+957T>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 3/5 | chr18 | 8634284 | |||||||
| chr18:8634286 | T | C | 1 | a0001c0001t0002g0197 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.714+959T>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 3/5 | chr18 | 8634286 | |||||||
| chr18:8634449 | C | T | 93 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(90): Show |
145 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.715-1084C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 3/5 | chr18 | 8634449 | |||||||
| chr18:8634627 | C | T | 3 | a0001c0001t0006g0055 a0001c0001t0006g0212 a0001c0001t0006g0213 |
4 | HG02257.hp1 HG03139.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.715-906C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 3/5 | chr18 | 8634627 | |||||||
| chr18:8634683 | G | A | 1 | a0001c0001t0002g0197 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.715-850G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 3/5 | chr18 | 8634683 | |||||||
| chr18:8634763 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.715-770C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 3/5 | chr18 | 8634763 | |||||||
| chr18:8635177 | C | T | 1 | a0001c0001t0001g0049 | 2 | HG03688.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.715-356C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 3/5 | chr18 | 8635177 | |||||||
| chr18:8635394 | G | A | 1 | a0001c0001t0005g0068 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.715-139G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 3/5 | chr18 | 8635394 | |||||||
| chr18:8635403 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.715-130G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 3/5 | chr18 | 8635403 | |||||||
| chr18:8635429 | G | A | 1 | a0001c0001t0013g0137 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.715-104G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 3/5 | chr18 | 8635429 | |||||||
| chr18:8635448 | A | G | 3 | a0001c0001t0006g0055 a0001c0001t0006g0212 a0001c0001t0006g0213 |
4 | HG02257.hp1 HG03139.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.715-85A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 3/5 | chr18 | 8635448 | |||||||
| chr18:8635644 | G | A | 1 | a0001c0001t0001g0127 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.804+22G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 4/5 | chr18 | 8635644 | |||||||
| chr18:8635753 | C | T | 1 | a0001c0001t0002g0158 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.804+131C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 4/5 | chr18 | 8635753 | |||||||
| chr18:8635828 | A | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0147 |
3 | NA18971.hp2 NA18983.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.804+206A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 4/5 | chr18 | 8635828 | |||||||
| chr18:8636002 | T | C | 66 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0029 others(63): Show |
97 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.805-251T>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 4/5 | chr18 | 8636002 | |||||||
| chr18:8636089 | A | T | 2 | a0001c0001t0007g0054 a0001c0001t0007g0209 |
3 | HG01891.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.805-164A>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 4/5 | chr18 | 8636089 | |||||||
| chr18:8636387 | A | G | 3 | a0001c0001t0006g0055 a0001c0001t0006g0212 a0001c0001t0006g0213 |
4 | HG02257.hp1 HG03139.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.909+30A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 5/5 | chr18 | 8636387 | |||||||
| chr18:8636466 | T | C | 1 | a0001c0001t0001g0021 | 3 | NA18979.hp1 NA18999.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.909+109T>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 5/5 | chr18 | 8636466 | |||||||
| chr18:8636511 | C | T | 1 | a0001c0001t0002g0158 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.909+154C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 5/5 | chr18 | 8636511 | |||||||
| chr18:8636574 | G | A | 14 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0029 others(11): Show |
24 | HG00323.hp2 HG01123.hp1 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.909+217G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 5/5 | chr18 | 8636574 | |||||||
| chr18:8636599 | A | G | 3 | a0001c0001t0007g0054 a0001c0001t0007g0209 a0001c0001t0013g0137 |
4 | HG01891.hp2 HG02922.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.909+242A>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 5/5 | chr18 | 8636599 | |||||||
| chr18:8636811 | A | C | 14 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0029 others(11): Show |
24 | HG00323.hp2 HG01123.hp1 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.909+454A>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 5/5 | chr18 | 8636811 | |||||||
| chr18:8636868 | G | A | 2 | a0001c0001t0002g0202 a0001c0001t0016g0201 |
2 | HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.909+511G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 5/5 | chr18 | 8636868 | |||||||
| chr18:8636869 | G | T | 2 | a0001c0001t0001g0048 a0001c0001t0001g0168 |
3 | NA18948.hp2 NA18968.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.909+512G>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 5/5 | chr18 | 8636869 | |||||||
| chr18:8636936 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.909+579C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 5/5 | chr18 | 8636936 | |||||||
| chr18:8637231 | G | A | 24 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(21): Show |
44 | HG00733.hp1 HG01069.hp1 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.909+874G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 5/5 | chr18 | 8637231 | |||||||
| chr18:8637278 | T | TA | 88 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(85): Show |
140 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.910-855dupA | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr18 | 8637278 | ||||||
| chr18:8637351 | G | C | 1 | a0001c0001t0002g0191 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.910-798G>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 5/5 | chr18 | 8637351 | |||||||
| chr18:8637553 | G | A | 4 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02615.hp2 HG02922.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.910-596G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 5/5 | chr18 | 8637553 | |||||||
| chr18:8637627 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.910-522C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 5/5 | chr18 | 8637627 | |||||||
| chr18:8637731 | C | T | 14 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0029 others(11): Show |
24 | HG00323.hp2 HG01123.hp1 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.910-418C>T | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 5/5 | chr18 | 8637731 | |||||||
| chr18:8637880 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.910-269G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 5/5 | chr18 | 8637880 | |||||||
| chr18:8637928 | T | TGAG | 3 | a0001c0001t0007g0054 a0001c0001t0007g0209 a0001c0001t0011g0066 |
4 | HG01891.hp2 HG03130.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.910-201_910-199dup others(3): Show |
RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr18 | 8637928 | ||||||
| chr18:8637986 | G | A | 1 | a0001c0001t0002g0205 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.910-163G>A | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 5/5 | chr18 | 8637986 | |||||||
| chr18:8638031 | T | C | 3 | a0001c0001t0001g0047 a0001c0001t0001g0097 a0001c0001t0008g0037 |
5 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.910-118T>C | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 5/5 | chr18 | 8638031 | |||||||
| chr18:8638128 | T | G | 4 | a0001c0001t0001g0020 a0001c0001t0001g0107 a0001c0001t0001g0108 others(1): Show |
6 | HG01074.hp1 HG02293.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.910-21T>G | RAB12 | ENSG00000206418.5 | transcript | ENST00000649141.2 | protein_coding | 5/5 | chr18 | 8638128 |