Item | Value |
---|---|
geneid | 23011 |
ensemblid | ENSG00000080371.6 |
hgncid | 18263 |
symbol | RAB21 |
name | RAB21, member RAS oncogene family |
refseq_nuc | NM_014999.4 |
refseq_prot | NP_055814.1 |
ensembl_nuc | ENST00000261263.5 |
ensembl_prot | ENSP00000261263.3 |
mane_status | MANE Select |
chr | chr12 |
start | 71754863 |
end | 71800286 |
strand | + |
ver | v1.2 |
region | chr12:71754863-71800286 |
region5000 | chr12:71749863-71805286 |
regionname0 | RAB21_chr12_71754863_71800286 |
regionname5000 | RAB21_chr12_71749863_71805286 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 225 | 370 | 88 | 60 | 174 | 9 | 37 | 128 | RAB21_chr12_71749863_71805286 | RAB21 | MAAAG others(220): Show |
chr12 | 71749863 | 71805286 |
a0002 | 0/0 | 225 | 4 | 0 | 3 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | MAAAG others(220): Show |
chr12 | 71749863 | 71805286 |
a0003 | 0/0 | 225 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | MAAAG others(220): Show |
chr12 | 71749863 | 71805286 |
a0004 | 0/0 | 225 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | MAAAG others(220): Show |
chr12 | 71749863 | 71805286 |
a0005 | 0/0 | 225 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | MAAAG others(220): Show |
chr12 | 71749863 | 71805286 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 675 | 260 | 65 | 42 | 114 | 9 | 28 | RAB21_chr12_71749863_71805286 | RAB21 | ATGGC others(670): Show |
chr12 | 71749863 | 71805286 | ||
a0001c0002 | 0/0 | 675 | 93 | 6 | 18 | 60 | 0 | 9 | RAB21_chr12_71749863_71805286 | RAB21 | ATGGC others(670): Show |
chr12 | 71749863 | 71805286 | ||
a0001c0003 | 0/0 | 675 | 14 | 14 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | ATGGC others(670): Show |
chr12 | 71749863 | 71805286 | ||
a0001c0006 | 0/0 | 675 | 3 | 3 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | ATGGC others(670): Show |
chr12 | 71749863 | 71805286 | ||
a0002c0004 | 0/0 | 675 | 4 | 0 | 3 | 0 | 1 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | ATGGC others(670): Show |
chr12 | 71749863 | 71805286 | ||
a0003c0005 | 0/0 | 675 | 4 | 4 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | ATGGC others(670): Show |
chr12 | 71749863 | 71805286 | ||
a0004c0007 | 0/0 | 675 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | ATGGC others(670): Show |
chr12 | 71749863 | 71805286 | ||
a0005c0008 | 0/0 | 675 | 1 | 0 | 0 | 0 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | ATGGC others(670): Show |
chr12 | 71749863 | 71805286 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 15557 | 43 | 4 | 4 | 30 | 0 | 5 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15552): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0003 | 1/1 | 15558 | 20 | 1 | 4 | 4 | 3 | 6 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15553): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0004 | 0/0 | 15556 | 12 | 0 | 8 | 4 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15551): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0005 | 0/0 | 15551 | 13 | 12 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15546): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0006 | 0/0 | 14138 | 13 | 0 | 2 | 8 | 0 | 3 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14133): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0008 | 0/0 | 14137 | 9 | 9 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14132): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0009 | 0/0 | 15556 | 7 | 0 | 2 | 1 | 1 | 3 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15551): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0010 | 0/0 | 14136 | 7 | 0 | 0 | 6 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14131): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0011 | 0/0 | 15558 | 6 | 1 | 3 | 1 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15553): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0012 | 0/0 | 15557 | 6 | 6 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15552): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0013 | 0/0 | 15557 | 5 | 0 | 2 | 2 | 1 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15552): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0015 | 0/0 | 14132 | 4 | 4 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14127): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0016 | 0/0 | 15537 | 4 | 0 | 0 | 4 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15532): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0017 | 0/0 | 14136 | 4 | 0 | 1 | 3 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14131): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0020 | 0/0 | 15557 | 3 | 1 | 0 | 2 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15552): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0021 | 0/0 | 15556 | 3 | 0 | 0 | 3 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15551): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0022 | 0/0 | 14136 | 3 | 0 | 0 | 3 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14131): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0023 | 0/0 | 14137 | 3 | 3 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14132): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0025 | 0/0 | 14132 | 2 | 2 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14127): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0026 | 0/0 | 15558 | 2 | 0 | 2 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15553): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0027 | 0/0 | 15556 | 2 | 2 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15551): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0028 | 0/0 | 15557 | 2 | 0 | 0 | 2 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15552): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0029 | 0/0 | 15559 | 2 | 2 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15554): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0030 | 0/0 | 15557 | 2 | 1 | 0 | 0 | 1 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15552): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0031 | 0/0 | 15555 | 2 | 0 | 0 | 1 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15550): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0032 | 0/0 | 15556 | 2 | 0 | 0 | 2 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15551): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0033 | 0/0 | 14136 | 2 | 2 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14131): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0034 | 0/0 | 14136 | 2 | 0 | 0 | 2 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14131): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0035 | 0/0 | 14136 | 2 | 0 | 0 | 2 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14131): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0039 | 0/0 | 14137 | 2 | 2 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14132): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0040 | 0/0 | 15557 | 2 | 0 | 0 | 2 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15552): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0041 | 0/0 | 14132 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14127): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0042 | 0/0 | 14132 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14127): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0043 | 0/0 | 15557 | 1 | 0 | 0 | 0 | 1 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15552): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0044 | 0/0 | 15537 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15532): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0045 | 0/0 | 15537 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15532): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0046 | 0/0 | 14115 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14110): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0047 | 0/0 | 15557 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15552): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0048 | 0/0 | 15555 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15550): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0049 | 0/0 | 15557 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15552): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0050 | 0/0 | 15555 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15550): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0052 | 0/0 | 15558 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15553): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0053 | 0/0 | 15558 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15553): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0055 | 0/0 | 15558 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15553): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0056 | 0/0 | 15558 | 1 | 0 | 0 | 0 | 1 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15553): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0057 | 0/0 | 15556 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15551): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0058 | 0/0 | 15557 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15552): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0059 | 0/0 | 15558 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15553): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0060 | 0/0 | 15557 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15552): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0061 | 0/0 | 15557 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15552): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0062 | 0/0 | 15557 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15552): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0063 | 0/0 | 15557 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15552): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0064 | 0/0 | 15557 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15552): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0065 | 0/0 | 15557 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15552): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0066 | 0/0 | 15558 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15553): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0067 | 0/0 | 15557 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15552): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0068 | 0/0 | 15556 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15551): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0069 | 0/0 | 15558 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15553): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0070 | 0/0 | 15555 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15550): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0071 | 0/0 | 15557 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15552): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0072 | 0/0 | 15557 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15552): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0073 | 0/0 | 15557 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15552): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0074 | 0/0 | 15560 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15555): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0075 | 0/0 | 15558 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15553): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0076 | 0/0 | 15557 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15552): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0077 | 0/0 | 15556 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15551): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0078 | 0/0 | 15558 | 1 | 0 | 0 | 0 | 1 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15553): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0079 | 0/0 | 15557 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15552): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0080 | 0/0 | 15557 | 1 | 0 | 0 | 0 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15552): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0081 | 0/0 | 15558 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15553): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0082 | 0/0 | 15558 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15553): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0083 | 0/0 | 15559 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15554): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0084 | 0/0 | 15558 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15553): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0085 | 0/0 | 15558 | 1 | 0 | 0 | 0 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15553): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0086 | 0/0 | 15556 | 1 | 0 | 0 | 0 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15551): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0087 | 0/0 | 15557 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15552): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0091 | 0/0 | 14136 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14131): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0092 | 0/0 | 14136 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14131): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0093 | 0/0 | 14136 | 1 | 0 | 0 | 0 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14131): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0094 | 0/0 | 14136 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14131): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0095 | 0/0 | 14136 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14131): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0096 | 0/0 | 14136 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14131): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0097 | 0/0 | 14136 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14131): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0098 | 0/0 | 14136 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14131): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0099 | 0/0 | 14136 | 1 | 0 | 0 | 0 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14131): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0100 | 0/0 | 14136 | 1 | 0 | 0 | 0 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14131): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0101 | 0/0 | 14136 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14131): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0102 | 0/0 | 14138 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14133): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0103 | 0/0 | 14137 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14132): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0105 | 0/0 | 15558 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15553): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0106 | 0/0 | 14137 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14132): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0116 | 0/0 | 14139 | 1 | 0 | 0 | 0 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14134): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0117 | 0/0 | 14138 | 1 | 0 | 0 | 0 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14133): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0118 | 0/0 | 14138 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14133): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0119 | 0/0 | 14139 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14134): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0120 | 0/0 | 14137 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14132): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0121 | 0/0 | 14137 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14132): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0123 | 0/0 | 14138 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14133): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0125 | 0/0 | 15557 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15552): Show |
chr12 | 71749863 | 71805286 |
a0001c0001t0126 | 0/0 | 15557 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15552): Show |
chr12 | 71749863 | 71805286 |
a0001c0002t0001 | 0/0 | 14136 | 65 | 2 | 13 | 47 | 0 | 3 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14131): Show |
chr12 | 71749863 | 71805286 |
a0001c0002t0014 | 0/0 | 14137 | 5 | 0 | 1 | 3 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14132): Show |
chr12 | 71749863 | 71805286 |
a0001c0002t0019 | 0/0 | 14136 | 4 | 1 | 0 | 0 | 0 | 3 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14131): Show |
chr12 | 71749863 | 71805286 |
a0001c0002t0024 | 0/0 | 14136 | 3 | 0 | 0 | 3 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14131): Show |
chr12 | 71749863 | 71805286 |
a0001c0002t0037 | 0/0 | 14136 | 2 | 2 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14131): Show |
chr12 | 71749863 | 71805286 |
a0001c0002t0038 | 0/0 | 14136 | 2 | 0 | 0 | 2 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14131): Show |
chr12 | 71749863 | 71805286 |
a0001c0002t0104 | 0/0 | 14136 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14131): Show |
chr12 | 71749863 | 71805286 |
a0001c0002t0107 | 0/0 | 14137 | 1 | 0 | 0 | 0 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14132): Show |
chr12 | 71749863 | 71805286 |
a0001c0002t0108 | 0/0 | 14136 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14131): Show |
chr12 | 71749863 | 71805286 |
a0001c0002t0109 | 0/0 | 14124 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14119): Show |
chr12 | 71749863 | 71805286 |
a0001c0002t0110 | 0/0 | 14136 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14131): Show |
chr12 | 71749863 | 71805286 |
a0001c0002t0111 | 0/0 | 14136 | 1 | 0 | 0 | 0 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14131): Show |
chr12 | 71749863 | 71805286 |
a0001c0002t0112 | 0/0 | 14137 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14132): Show |
chr12 | 71749863 | 71805286 |
a0001c0002t0113 | 0/0 | 14136 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14131): Show |
chr12 | 71749863 | 71805286 |
a0001c0002t0114 | 0/0 | 14126 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14121): Show |
chr12 | 71749863 | 71805286 |
a0001c0002t0115 | 0/0 | 14136 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14131): Show |
chr12 | 71749863 | 71805286 |
a0001c0002t0122 | 0/0 | 14136 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14131): Show |
chr12 | 71749863 | 71805286 |
a0001c0002t0124 | 0/0 | 14136 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14131): Show |
chr12 | 71749863 | 71805286 |
a0001c0003t0007 | 0/0 | 15558 | 9 | 9 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15553): Show |
chr12 | 71749863 | 71805286 |
a0001c0003t0036 | 0/0 | 15557 | 2 | 2 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15552): Show |
chr12 | 71749863 | 71805286 |
a0001c0003t0088 | 0/0 | 15556 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15551): Show |
chr12 | 71749863 | 71805286 |
a0001c0003t0089 | 0/0 | 15557 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15552): Show |
chr12 | 71749863 | 71805286 |
a0001c0003t0090 | 0/0 | 15557 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15552): Show |
chr12 | 71749863 | 71805286 |
a0001c0006t0127 | 0/0 | 14138 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14133): Show |
chr12 | 71749863 | 71805286 |
a0001c0006t0128 | 0/0 | 14135 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14130): Show |
chr12 | 71749863 | 71805286 |
a0001c0006t0129 | 0/0 | 14126 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14121): Show |
chr12 | 71749863 | 71805286 |
a0002c0004t0004 | 0/0 | 15556 | 3 | 0 | 3 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15551): Show |
chr12 | 71749863 | 71805286 |
a0002c0004t0054 | 0/0 | 15558 | 1 | 0 | 0 | 0 | 1 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15553): Show |
chr12 | 71749863 | 71805286 |
a0003c0005t0018 | 0/0 | 14137 | 4 | 4 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(14132): Show |
chr12 | 71749863 | 71805286 |
a0004c0007t0009 | 0/0 | 15556 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15551): Show |
chr12 | 71749863 | 71805286 |
a0005c0008t0051 | 0/0 | 15558 | 1 | 0 | 0 | 0 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | GTAGG others(15553): Show |
chr12 | 71749863 | 71805286 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0003 | 0/0 | 13 | 4 | 0 | 8 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0002g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0002g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0002g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0003g0002 | 0/0 | 7 | 1 | 0 | 3 | 1 | 2 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0003g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0003g0037 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0003g0054 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0003g0136 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0004g0004 | 0/0 | 8 | 0 | 5 | 3 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0004g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0004g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0004g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0004g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0005g0005 | 0/0 | 10 | 9 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0006g0007 | 0/0 | 7 | 0 | 1 | 3 | 0 | 3 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0006g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0006g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0006g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0008g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0008g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0008g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0008g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0009g0002 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0009g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0009g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0009g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0009g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0010g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0010g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0010g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0010g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0011g0002 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0011g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0011g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0011g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0012g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0012g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0012g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0012g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0012g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0013g0002 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0013g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0013g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0015g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0015g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0015g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0015g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0016g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0016g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0016g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0017g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0017g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0017g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0020g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0020g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0021g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0021g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0022g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0022g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0022g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0023g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0023g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0025g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0026g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0026g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0027g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0027g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0028g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0028g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0029g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0029g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0030g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0030g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0031g0002 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0032g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0032g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0033g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0033g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0034g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0035g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0039g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0039g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0040g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0040g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0041g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0042g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0043g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0044g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0045g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0046g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0047g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0048g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0049g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0050g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0052g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0053g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0055g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0056g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0057g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0058g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0059g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0060g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0061g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0062g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0063g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0064g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0065g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0066g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0067g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0068g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0069g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0070g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0071g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0072g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0073g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0074g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0075g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0076g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0077g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0078g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0079g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0080g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0081g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0082g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0083g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0084g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0085g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0086g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0087g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0091g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0092g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0093g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0094g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0095g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0096g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0097g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0098g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0099g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0100g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0101g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0102g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0103g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0105g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0106g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0116g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0117g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0118g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0119g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0120g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0121g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0123g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0125g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0001t0126g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0001g0001 | 0/0 | 23 | 2 | 5 | 15 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0001g0009 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0014g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0014g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0014g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0014g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0014g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0019g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0019g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0019g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0024g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0024g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0037g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0037g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0038g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0038g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0104g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0107g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0108g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0109g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0110g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0111g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0112g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0113g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0114g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0115g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0122g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0002t0124g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0003t0007g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0003t0007g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0003t0007g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0003t0007g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0003t0036g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0003t0036g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0003t0088g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0003t0089g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0003t0090g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0006t0127g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0006t0128g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0001c0006t0129g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0002c0004t0004g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0002c0004t0004g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0002c0004t0054g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0003c0005t0018g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0004c0007t0009g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
a0005c0008t0051g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0078 | g0002 | EUR | GBR | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG00140 | hp2 | a0001 | c0001 | t0009 | g0024 | EUR | GBR | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG00408 | hp1 | a0001 | c0001 | t0052 | g0004 | EAS | CHS | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | CHS | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG00423 | hp1 | a0001 | c0002 | t0024 | g0079 | EAS | CHS | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG00423 | hp2 | a0001 | c0001 | t0063 | g0008 | EAS | CHS | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG00438 | hp1 | a0001 | c0002 | t0122 | g0001 | EAS | CHS | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG00438 | hp2 | a0001 | c0001 | t0028 | g0010 | EAS | CHS | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG00544 | hp1 | a0001 | c0001 | t0092 | g0006 | EAS | CHS | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG00544 | hp2 | a0001 | c0002 | t0038 | g0001 | EAS | CHS | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG00558 | hp1 | a0001 | c0001 | t0022 | g0173 | EAS | CHS | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | CHS | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG00597 | hp1 | a0001 | c0001 | t0034 | g0047 | EAS | CHS | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | CHS | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG00609 | hp2 | a0001 | c0001 | t0011 | g0002 | EAS | CHS | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG00621 | hp1 | a0001 | c0001 | t0034 | g0047 | EAS | CHS | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | CHS | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG00639 | hp1 | a0001 | c0001 | t0059 | g0063 | AMR | PUR | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG00639 | hp2 | a0001 | c0001 | t0011 | g0038 | AMR | PUR | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG00642 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG00642 | hp2 | a0001 | c0001 | t0006 | g0007 | AMR | PUR | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG00738 | hp2 | a0001 | c0001 | t0006 | g0060 | AMR | PUR | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG00741 | hp1 | a0001 | c0001 | t0118 | g0007 | AMR | PUR | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG00741 | hp2 | a0001 | c0001 | t0004 | g0038 | AMR | PUR | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01069 | hp1 | a0001 | c0001 | t0042 | g0017 | AMR | PUR | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01069 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01070 | hp1 | a0002 | c0004 | t0004 | g0039 | AMR | PUR | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01070 | hp2 | a0001 | c0001 | t0009 | g0040 | AMR | PUR | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01071 | hp2 | a0002 | c0004 | t0004 | g0039 | AMR | PUR | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01081 | hp1 | a0001 | c0001 | t0067 | g0151 | AMR | PUR | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01081 | hp2 | a0001 | c0001 | t0009 | g0139 | AMR | PUR | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01099 | hp2 | a0001 | c0001 | t0011 | g0004 | AMR | PUR | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01167 | hp2 | a0001 | c0001 | t0013 | g0023 | AMR | PUR | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01169 | hp1 | a0001 | c0001 | t0013 | g0023 | AMR | PUR | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0138 | AMR | PUR | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01243 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01256 | hp1 | a0001 | c0001 | t0048 | g0113 | AMR | CLM | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01256 | hp2 | a0001 | c0001 | t0047 | g0011 | AMR | CLM | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01257 | hp1 | a0001 | c0001 | t0004 | g0101 | AMR | CLM | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01257 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | CLM | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0023 | AMR | CLM | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01261 | hp2 | a0001 | c0002 | t0104 | g0033 | AMR | CLM | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01346 | hp1 | a0001 | c0001 | t0064 | g0003 | AMR | CLM | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01346 | hp2 | a0001 | c0001 | t0081 | g0123 | AMR | CLM | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0076 | AMR | CLM | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01358 | hp2 | a0001 | c0001 | t0084 | g0126 | AMR | CLM | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01361 | hp1 | a0001 | c0001 | t0079 | g0099 | AMR | CLM | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01361 | hp2 | a0001 | c0002 | t0114 | g0086 | AMR | CLM | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0040 | AMR | CLM | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01433 | hp2 | a0001 | c0001 | t0026 | g0128 | AMR | CLM | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | CLM | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01496 | hp2 | a0001 | c0002 | t0109 | g0088 | AMR | CLM | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01515 | hp1 | a0001 | c0001 | t0013 | g0002 | EUR | IBS | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01515 | hp2 | a0001 | c0001 | t0043 | g0122 | EUR | IBS | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01516 | hp1 | a0001 | c0001 | t0056 | g0002 | EUR | IBS | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0037 | EUR | IBS | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0037 | EUR | IBS | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0002 | EUR | IBS | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01884 | hp1 | a0001 | c0001 | t0015 | g0154 | AFR | ACB | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01884 | hp2 | a0001 | c0001 | t0008 | g0167 | AFR | ACB | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01891 | hp1 | a0003 | c0005 | t0018 | g0016 | AFR | ACB | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01891 | hp2 | a0001 | c0001 | t0020 | g0024 | AFR | ACB | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0108 | AMR | PEL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PEL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01934 | hp2 | a0001 | c0001 | t0011 | g0141 | AMR | PEL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01943 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | PEL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01943 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | PEL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01952 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PEL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01952 | hp2 | a0001 | c0001 | t0057 | g0132 | AMR | PEL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01975 | hp1 | a0001 | c0001 | t0017 | g0006 | AMR | PEL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01975 | hp2 | a0001 | c0001 | t0049 | g0004 | AMR | PEL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0134 | AMR | PEL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01978 | hp2 | a0001 | c0002 | t0014 | g0009 | AMR | PEL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01993 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | PEL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01993 | hp2 | a0001 | c0001 | t0055 | g0002 | AMR | PEL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02004 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PEL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02004 | hp2 | a0004 | c0007 | t0009 | g0002 | AMR | PEL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02027 | hp1 | a0001 | c0001 | t0103 | g0006 | EAS | KHV | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | KHV | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | KHV | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02040 | hp2 | a0001 | c0001 | t0028 | g0121 | EAS | KHV | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02055 | hp1 | a0001 | c0001 | t0091 | g0052 | AFR | ACB | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02056 | hp1 | a0001 | c0001 | t0046 | g0181 | EAS | KHV | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02071 | hp2 | a0001 | c0002 | t0108 | g0001 | EAS | KHV | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02074 | hp1 | a0001 | c0001 | t0020 | g0002 | EAS | KHV | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02080 | hp1 | a0001 | c0001 | t0016 | g0159 | EAS | KHV | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02080 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | KHV | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | KHV | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | KHV | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02129 | hp1 | a0001 | c0001 | t0006 | g0014 | EAS | KHV | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02129 | hp2 | a0001 | c0002 | t0115 | g0001 | EAS | KHV | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02132 | hp1 | a0001 | c0001 | t0119 | g0062 | EAS | KHV | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02132 | hp2 | a0001 | c0001 | t0016 | g0018 | EAS | KHV | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02135 | hp1 | a0001 | c0001 | t0006 | g0007 | EAS | KHV | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02135 | hp2 | a0001 | c0001 | t0083 | g0002 | EAS | KHV | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | ACB | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02145 | hp2 | a0001 | c0001 | t0015 | g0155 | AFR | ACB | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02155 | hp1 | a0001 | c0001 | t0022 | g0174 | EAS | CDX | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CDX | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | CDX | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02165 | hp2 | a0001 | c0001 | t0050 | g0002 | EAS | CDX | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02257 | hp1 | a0001 | c0001 | t0005 | g0053 | AFR | ACB | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02257 | hp2 | a0001 | c0002 | t0124 | g0090 | AFR | ACB | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02258 | hp1 | a0001 | c0001 | t0008 | g0013 | AFR | ACB | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02258 | hp2 | a0001 | c0001 | t0011 | g0002 | AFR | ACB | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02280 | hp1 | a0001 | c0001 | t0005 | g0055 | AFR | ACB | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02280 | hp2 | a0001 | c0003 | t0007 | g0015 | AFR | ACB | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02293 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PEL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02293 | hp2 | a0001 | c0002 | t0110 | g0001 | AMR | PEL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0067 | AMR | PEL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02300 | hp2 | a0002 | c0004 | t0004 | g0002 | AMR | PEL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02523 | hp1 | a0001 | c0001 | t0010 | g0177 | EAS | KHV | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02572 | hp1 | a0001 | c0001 | t0012 | g0035 | AFR | GWD | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02572 | hp2 | a0001 | c0001 | t0030 | g0105 | AFR | GWD | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02602 | hp2 | a0001 | c0002 | t0107 | g0077 | SAS | PJL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02615 | hp1 | a0001 | c0002 | t0037 | g0069 | AFR | GWD | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02615 | hp2 | a0001 | c0001 | t0027 | g0130 | AFR | GWD | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02622 | hp1 | a0001 | c0003 | t0090 | g0152 | AFR | GWD | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02622 | hp2 | a0001 | c0001 | t0008 | g0045 | AFR | GWD | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02630 | hp1 | a0001 | c0001 | t0008 | g0013 | AFR | GWD | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02630 | hp2 | a0001 | c0001 | t0005 | g0056 | AFR | GWD | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02647 | hp1 | a0001 | c0001 | t0023 | g0025 | AFR | GWD | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02647 | hp2 | a0001 | c0001 | t0033 | g0176 | AFR | GWD | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02683 | hp1 | a0001 | c0001 | t0086 | g0095 | SAS | PJL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02683 | hp2 | a0001 | c0001 | t0010 | g0006 | SAS | PJL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0058 | SAS | PJL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02698 | hp2 | a0001 | c0002 | t0019 | g0034 | SAS | PJL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02717 | hp1 | a0001 | c0006 | t0127 | g0168 | AFR | GWD | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02717 | hp2 | a0001 | c0003 | t0007 | g0042 | AFR | GWD | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02723 | hp1 | a0001 | c0001 | t0120 | g0026 | AFR | GWD | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02723 | hp2 | a0003 | c0005 | t0018 | g0016 | AFR | GWD | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02809 | hp1 | a0001 | c0006 | t0129 | g0170 | AFR | GWD | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02809 | hp2 | a0001 | c0003 | t0088 | g0148 | AFR | GWD | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02818 | hp1 | a0001 | c0001 | t0094 | g0172 | AFR | GWD | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02818 | hp2 | a0001 | c0001 | t0008 | g0013 | AFR | GWD | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02886 | hp1 | a0001 | c0002 | t0019 | g0074 | AFR | GWD | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02886 | hp2 | a0001 | c0006 | t0128 | g0169 | AFR | GWD | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02895 | hp1 | a0001 | c0001 | t0095 | g0179 | AFR | GWD | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02895 | hp2 | a0001 | c0003 | t0007 | g0041 | AFR | GWD | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02896 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | GWD | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02896 | hp2 | a0001 | c0003 | t0007 | g0015 | AFR | GWD | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02897 | hp1 | a0001 | c0003 | t0007 | g0041 | AFR | GWD | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02897 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | GWD | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02922 | hp1 | a0001 | c0001 | t0012 | g0110 | AFR | ESN | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02922 | hp2 | a0001 | c0001 | t0012 | g0097 | AFR | ESN | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02965 | hp1 | a0001 | c0001 | t0123 | g0165 | AFR | ESN | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02970 | hp1 | a0001 | c0003 | t0036 | g0059 | AFR | ESN | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02970 | hp2 | a0001 | c0001 | t0069 | g0106 | AFR | ESN | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02976 | hp1 | a0001 | c0001 | t0029 | g0114 | AFR | ESN | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02976 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | ESN | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03017 | hp1 | a0001 | c0002 | t0111 | g0029 | SAS | PJL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03017 | hp2 | a0001 | c0001 | t0009 | g0002 | SAS | PJL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03041 | hp1 | a0003 | c0005 | t0018 | g0016 | AFR | GWD | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03041 | hp2 | a0001 | c0001 | t0096 | g0182 | AFR | GWD | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03130 | hp2 | a0001 | c0001 | t0008 | g0013 | AFR | ESN | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03139 | hp1 | a0001 | c0001 | t0027 | g0131 | AFR | ESN | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03139 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | ESN | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03195 | hp1 | a0001 | c0001 | t0041 | g0017 | AFR | ESN | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03195 | hp2 | a0001 | c0001 | t0012 | g0003 | AFR | ESN | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | MSL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03225 | hp2 | a0001 | c0001 | t0008 | g0166 | AFR | MSL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0118 | SAS | PJL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03453 | hp2 | a0001 | c0001 | t0033 | g0178 | AFR | MSL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03486 | hp1 | a0001 | c0003 | t0036 | g0149 | AFR | MSL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03486 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | MSL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03491 | hp1 | a0001 | c0001 | t0116 | g0027 | SAS | PJL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03491 | hp2 | a0001 | c0001 | t0031 | g0002 | SAS | PJL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03492 | hp1 | a0001 | c0001 | t0117 | g0027 | SAS | PJL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03516 | hp1 | a0001 | c0001 | t0025 | g0017 | AFR | ESN | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03516 | hp2 | a0001 | c0003 | t0007 | g0015 | AFR | ESN | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03540 | hp1 | a0001 | c0001 | t0077 | g0142 | AFR | GWD | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03540 | hp2 | a0001 | c0001 | t0029 | g0011 | AFR | GWD | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03579 | hp1 | a0003 | c0005 | t0018 | g0016 | AFR | MSL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03579 | hp2 | a0001 | c0001 | t0015 | g0157 | AFR | MSL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0127 | SAS | PJL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03654 | hp2 | a0001 | c0001 | t0099 | g0006 | SAS | PJL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0140 | SAS | PJL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03669 | hp2 | a0001 | c0002 | t0019 | g0034 | SAS | PJL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03688 | hp1 | a0001 | c0001 | t0009 | g0002 | SAS | STU | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03688 | hp2 | a0001 | c0001 | t0100 | g0184 | SAS | STU | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03710 | hp1 | a0001 | c0001 | t0011 | g0002 | SAS | PJL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03710 | hp2 | a0001 | c0001 | t0009 | g0133 | SAS | PJL | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0146 | SAS | BEB | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03831 | hp2 | a0001 | c0001 | t0085 | g0145 | SAS | BEB | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03834 | hp1 | a0001 | c0001 | t0080 | g0100 | SAS | BEB | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03834 | hp2 | a0001 | c0001 | t0093 | g0006 | SAS | BEB | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0022 | SAS | BEB | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03927 | hp2 | a0001 | c0001 | t0006 | g0007 | SAS | BEB | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0102 | SAS | BEB | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG03942 | hp2 | a0001 | c0001 | t0006 | g0007 | SAS | BEB | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0158 | SAS | STU | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0070 | SAS | STU | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG04199 | hp1 | a0001 | c0001 | t0006 | g0007 | SAS | STU | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG04199 | hp2 | a0005 | c0008 | t0051 | g0124 | SAS | STU | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | STU | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG04204 | hp2 | a0001 | c0002 | t0014 | g0022 | SAS | STU | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0119 | SAS | STU | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG04228 | hp2 | a0001 | c0002 | t0019 | g0029 | SAS | STU | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18522 | hp1 | a0001 | c0001 | t0023 | g0025 | AFR | YRI | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18522 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | YRI | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18612 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | CHB | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18612 | hp2 | a0001 | c0001 | t0065 | g0004 | EAS | CHB | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | CHB | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18747 | hp2 | a0001 | c0001 | t0062 | g0012 | EAS | CHB | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18906 | hp1 | a0001 | c0001 | t0015 | g0156 | AFR | YRI | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18906 | hp2 | a0001 | c0001 | t0012 | g0003 | AFR | YRI | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18939 | hp2 | a0001 | c0001 | t0006 | g0014 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18940 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18941 | hp1 | a0001 | c0001 | t0010 | g0019 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18948 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18949 | hp2 | a0001 | c0001 | t0072 | g0111 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18951 | hp2 | a0001 | c0001 | t0058 | g0012 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18956 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18959 | hp1 | a0001 | c0001 | t0006 | g0061 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18960 | hp2 | a0001 | c0001 | t0021 | g0002 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18963 | hp1 | a0001 | c0001 | t0010 | g0019 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18963 | hp2 | a0001 | c0002 | t0112 | g0001 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18964 | hp1 | a0001 | c0002 | t0038 | g0068 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18964 | hp2 | a0001 | c0001 | t0013 | g0002 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18965 | hp1 | a0001 | c0001 | t0126 | g0116 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18965 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18968 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18968 | hp2 | a0001 | c0001 | t0035 | g0046 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18969 | hp2 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18970 | hp1 | a0001 | c0001 | t0074 | g0125 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18971 | hp2 | a0001 | c0001 | t0045 | g0011 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18972 | hp2 | a0001 | c0001 | t0125 | g0109 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18973 | hp1 | a0001 | c0001 | t0006 | g0014 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18974 | hp1 | a0001 | c0002 | t0014 | g0020 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18974 | hp2 | a0001 | c0001 | t0076 | g0036 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18978 | hp1 | a0001 | c0001 | t0105 | g0008 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18978 | hp2 | a0001 | c0001 | t0097 | g0180 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18979 | hp2 | a0001 | c0001 | t0017 | g0006 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18981 | hp1 | a0001 | c0001 | t0106 | g0153 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18981 | hp2 | a0001 | c0001 | t0022 | g0006 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18982 | hp1 | a0001 | c0001 | t0013 | g0135 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18986 | hp1 | a0001 | c0001 | t0009 | g0002 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18987 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18991 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18992 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18992 | hp2 | a0001 | c0002 | t0014 | g0083 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18993 | hp1 | a0001 | c0001 | t0021 | g0018 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18995 | hp2 | a0001 | c0001 | t0101 | g0006 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18997 | hp1 | a0001 | c0001 | t0087 | g0104 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18997 | hp2 | a0001 | c0002 | t0014 | g0075 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18998 | hp1 | a0001 | c0001 | t0021 | g0002 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19002 | hp2 | a0001 | c0001 | t0031 | g0002 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19003 | hp1 | a0001 | c0001 | t0020 | g0002 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19003 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19004 | hp2 | a0001 | c0002 | t0024 | g0001 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19005 | hp1 | a0001 | c0001 | t0006 | g0014 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19007 | hp1 | a0001 | c0001 | t0010 | g0019 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19007 | hp2 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19009 | hp1 | a0001 | c0001 | t0035 | g0046 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19030 | hp1 | a0001 | c0003 | t0089 | g0044 | AFR | LWK | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19030 | hp2 | a0001 | c0001 | t0012 | g0098 | AFR | LWK | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19043 | hp1 | a0001 | c0003 | t0007 | g0044 | AFR | LWK | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19043 | hp2 | a0001 | c0001 | t0023 | g0049 | AFR | LWK | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19055 | hp1 | a0001 | c0001 | t0017 | g0171 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19055 | hp2 | a0001 | c0001 | t0040 | g0107 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19056 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19057 | hp1 | a0001 | c0001 | t0053 | g0144 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19058 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19058 | hp2 | a0001 | c0001 | t0071 | g0120 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19059 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19059 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19062 | hp1 | a0001 | c0001 | t0010 | g0048 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19062 | hp2 | a0001 | c0001 | t0032 | g0002 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19063 | hp1 | a0001 | c0001 | t0017 | g0183 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19063 | hp2 | a0001 | c0001 | t0060 | g0094 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19064 | hp1 | a0001 | c0001 | t0098 | g0048 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19064 | hp2 | a0001 | c0001 | t0016 | g0160 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19065 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19066 | hp2 | a0001 | c0001 | t0016 | g0018 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19067 | hp1 | a0001 | c0001 | t0102 | g0175 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19067 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19079 | hp2 | a0001 | c0001 | t0044 | g0161 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19081 | hp1 | a0001 | c0001 | t0010 | g0019 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19081 | hp2 | a0001 | c0001 | t0066 | g0003 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19082 | hp1 | a0001 | c0002 | t0024 | g0001 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19082 | hp2 | a0001 | c0001 | t0082 | g0002 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19084 | hp1 | a0001 | c0001 | t0040 | g0003 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19084 | hp2 | a0001 | c0001 | t0070 | g0008 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19085 | hp1 | a0001 | c0001 | t0032 | g0137 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19085 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19086 | hp1 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19087 | hp2 | a0001 | c0001 | t0075 | g0036 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19089 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19089 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19090 | hp2 | a0001 | c0002 | t0113 | g0001 | EAS | JPT | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19240 | hp1 | a0001 | c0001 | t0061 | g0003 | AFR | YRI | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | YRI | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA20129 | hp1 | a0001 | c0001 | t0039 | g0051 | AFR | ASW | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | ASW | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA20752 | hp1 | a0001 | c0001 | t0030 | g0129 | EUR | TSI | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA20752 | hp2 | a0002 | c0004 | t0054 | g0115 | EUR | TSI | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01123 | hp1 | a0001 | c0001 | t0026 | g0002 | AMR | CLM | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02109 | hp1 | a0001 | c0003 | t0007 | g0042 | AFR | ACB | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02109 | hp2 | a0001 | c0001 | t0073 | g0112 | AFR | ACB | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02486 | hp1 | a0001 | c0001 | t0025 | g0017 | AFR | ACB | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02486 | hp2 | a0001 | c0001 | t0039 | g0026 | AFR | ACB | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02559 | hp1 | a0001 | c0001 | t0121 | g0050 | AFR | ACB | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG02559 | hp2 | a0001 | c0001 | t0008 | g0045 | AFR | ACB | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG06807 | hp1 | a0001 | c0001 | t0068 | g0035 | AFR | USA | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
HG06807 | hp2 | a0001 | c0003 | t0007 | g0015 | AFR | USA | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | USA | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA20300 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | USA | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA21309 | hp1 | a0001 | c0001 | t0008 | g0013 | AFR | LWK | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
NA21309 | hp2 | a0001 | c0002 | t0037 | g0065 | AFR | LWK | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0136 | REF | REF | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0054 | REF | REF | RAB21_chr12_71749863_71805286 | RAB21 | chr12 | 71749863 | 71805286 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:71755163 | G | A | 1 | a0004 | 1 | HG02004.hp2 | missense_variant | MODERATE | c.34G>A | p.Ala12Thr | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/7 | 301/15558 | 34/678 | 12/225 | chr12 | 71755163 | |||
chr12:71782055 | A | C | 1 | a0003 | 4 | HG01891.hp1 HG02723.hp2 HG03041.hp1 others(1): Show |
missense_variant | MODERATE | c.416A>C | p.Glu139Ala | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 5/7 | 683/15558 | 416/678 | 139/225 | chr12 | 71782055 | |||
chr12:71785588 | C | T | 1 | a0005 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.593C>T | p.Pro198Leu | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 860/15558 | 593/678 | 198/225 | chr12 | 71785588 | |||
chr12:71785666 | C | T | 1 | a0002 | 4 | HG01070.hp1 HG01071.hp2 HG02300.hp2 others(1): Show |
missense_variant | MODERATE | c.671C>T | p.Ser224Phe | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 938/15558 | 671/678 | 224/225 | chr12 | 71785666 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:71770615 | C | T | 1 | a0001c0002 | 93 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(90): Show |
synonymous_variant | LOW | c.243C>T | p.Phe81Phe | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 3/7 | 510/15558 | 243/678 | 81/225 | chr12 | 71770615 | |||
chr12:71782621 | C | T | 1 | a0001c0003 | 14 | HG02109.hp1 HG02280.hp2 HG02622.hp1 others(11): Show |
synonymous_variant | LOW | c.498C>T | p.Asn166Asn | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 6/7 | 765/15558 | 498/678 | 166/225 | chr12 | 71782621 | |||
chr12:71785631 | T | C | 1 | a0001c0006 | 3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
synonymous_variant | LOW | c.636T>C | p.Pro212Pro | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 903/15558 | 636/678 | 212/225 | chr12 | 71785631 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:71755116 | C | A | 4 | a0001c0001t0015 a0001c0001t0025 a0001c0001t0041 others(1): Show |
8 | HG01069.hp1 HG01884.hp1 HG02145.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-14C>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/7 | 14 | chr12 | 71755116 | ||||||
chr12:71785675 | T | C | 1 | a0001c0001t0005 | 13 | HG01243.hp2 HG02257.hp1 HG02280.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 2 | chr12 | 71785675 | ||||||
chr12:71785682 | G | A | 1 | a0001c0001t0043 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 9 | chr12 | 71785682 | ||||||
chr12:71785727 | C | G | 3 | a0001c0006t0127 a0001c0006t0128 a0001c0006t0129 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*54C>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 54 | chr12 | 71785727 | ||||||
chr12:71785834 | A | T | 3 | a0001c0001t0040 a0001c0001t0125 a0001c0001t0126 |
4 | NA18965.hp1 NA18972.hp2 NA19055.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*161A>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 161 | chr12 | 71785834 | ||||||
chr12:71785877 | ATGTTTTT others(14): Show |
A | 4 | a0001c0001t0016 a0001c0001t0044 a0001c0001t0045 others(1): Show |
7 | HG02056.hp1 HG02080.hp1 HG02132.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*226_*246delTGTTTT others(15): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 226 | INFO_REALIGN_3_PRIME | chr12 | 71785877 | |||||
chr12:71785879 | GT | G | 2 | a0001c0001t0008 a0001c0001t0123 |
10 | HG01884.hp2 HG02258.hp1 HG02559.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*215delT | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 215 | INFO_REALIGN_3_PRIME | chr12 | 71785879 | |||||
chr12:71785879 | GTTTTTTT others(4): Show |
G | 1 | a0001c0001t0004 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*226_*236delTGTTTT others(5): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 226 | INFO_REALIGN_3_PRIME | chr12 | 71785879 | |||||
chr12:71785884 | T | C | 2 | a0001c0002t0037 a0001c0002t0109 |
2 | HG01496.hp2 HG02615.hp1 |
3_prime_UTR_variant | MODIFIER | c.*211T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 211 | chr12 | 71785884 | ||||||
chr12:71785890 | T | G | 1 | a0001c0002t0001 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*217T>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 217 | chr12 | 71785890 | ||||||
chr12:71785890 | TTTTTTTT others(3): Show |
T | 1 | a0001c0001t0002 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*238_*247delTTTTTT others(4): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 238 | INFO_REALIGN_3_PRIME | chr12 | 71785890 | |||||
chr12:71785900 | G | GT | 31 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0023 others(28): Show |
129 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*236dupT | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 237 | INFO_REALIGN_3_PRIME | chr12 | 71785900 | |||||
chr12:71785910 | G | GT | 3 | a0001c0001t0005 a0001c0001t0102 a0001c0001t0103 |
15 | HG01243.hp2 HG02027.hp1 HG02257.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*246dupT | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 247 | INFO_REALIGN_3_PRIME | chr12 | 71785910 | |||||
chr12:71785911 | T | G | 13 | a0001c0001t0004 a0001c0001t0011 a0001c0001t0026 others(10): Show |
32 | HG00408.hp1 HG00609.hp2 HG00639.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*238T>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 238 | chr12 | 71785911 | ||||||
chr12:71785912 | T | G | 3 | a0001c0001t0026 a0001c0001t0047 a0001c0001t0048 |
4 | HG01123.hp1 HG01256.hp1 HG01256.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*239T>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 239 | chr12 | 71785912 | ||||||
chr12:71785958 | C | G | 1 | a0001c0003t0036 | 2 | HG02970.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*285C>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 285 | chr12 | 71785958 | ||||||
chr12:71785988 | A | G | 4 | a0001c0001t0015 a0001c0001t0025 a0001c0001t0041 others(1): Show |
8 | HG01069.hp1 HG01884.hp1 HG02145.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*315A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 315 | chr12 | 71785988 | ||||||
chr12:71786002 | C | T | 2 | a0001c0006t0128 a0001c0006t0129 |
2 | HG02809.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*329C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 329 | chr12 | 71786002 | ||||||
chr12:71786027 | G | A | 1 | a0001c0002t0104 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*354G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 354 | chr12 | 71786027 | ||||||
chr12:71786108 | A | G | 1 | a0001c0002t0124 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*435A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 435 | chr12 | 71786108 | ||||||
chr12:71786370 | C | T | 1 | a0001c0001t0055 | 1 | HG01993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*697C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 697 | chr12 | 71786370 | ||||||
chr12:71786392 | G | T | 64 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(61): Show |
204 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*719G>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 719 | chr12 | 71786392 | ||||||
chr12:71786554 | A | G | 1 | a0001c0001t0101 | 1 | NA18995.hp2 | 3_prime_UTR_variant | MODIFIER | c.*881A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 881 | chr12 | 71786554 | ||||||
chr12:71786584 | G | A | 2 | a0001c0001t0056 a0001c0001t0057 |
2 | HG01516.hp1 HG01952.hp2 |
3_prime_UTR_variant | MODIFIER | c.*911G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 911 | chr12 | 71786584 | ||||||
chr12:71786777 | C | T | 25 | a0001c0001t0010 a0001c0001t0015 a0001c0001t0017 others(22): Show |
46 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1104C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 1104 | chr12 | 71786777 | ||||||
chr12:71786837 | A | G | 3 | a0001c0006t0127 a0001c0006t0128 a0001c0006t0129 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1164A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 1164 | chr12 | 71786837 | ||||||
chr12:71786955 | A | G | 5 | a0001c0003t0007 a0001c0003t0036 a0001c0003t0088 others(2): Show |
14 | HG02109.hp1 HG02280.hp2 HG02622.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1282A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 1282 | chr12 | 71786955 | ||||||
chr12:71786962 | G | T | 1 | a0001c0006t0127 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1289G>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 1289 | chr12 | 71786962 | ||||||
chr12:71786974 | T | A | 1 | a0001c0001t0027 | 2 | HG02615.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1301T>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 1301 | chr12 | 71786974 | ||||||
chr12:71786975 | G | A | 1 | a0001c0001t0058 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1302G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 1302 | chr12 | 71786975 | ||||||
chr12:71786984 | A | T | 3 | a0001c0006t0127 a0001c0006t0128 a0001c0006t0129 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1311A>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 1311 | chr12 | 71786984 | ||||||
chr12:71787109 | A | C | 1 | a0001c0001t0123 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1436A>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 1436 | chr12 | 71787109 | ||||||
chr12:71787166 | A | T | 1 | a0002c0004t0054 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1493A>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 1493 | chr12 | 71787166 | ||||||
chr12:71787301 | T | G | 1 | a0001c0001t0005 | 13 | HG01243.hp2 HG02257.hp1 HG02280.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1628T>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 1628 | chr12 | 71787301 | ||||||
chr12:71787305 | A | T | 1 | a0001c0001t0042 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1632A>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 1632 | chr12 | 71787305 | ||||||
chr12:71787322 | G | A | 1 | a0001c0001t0091 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1649G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 1649 | chr12 | 71787322 | ||||||
chr12:71787377 | A | T | 1 | a0001c0001t0087 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1704A>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 1704 | chr12 | 71787377 | ||||||
chr12:71787480 | A | G | 1 | a0001c0001t0053 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1807A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 1807 | chr12 | 71787480 | ||||||
chr12:71787526 | A | G | 29 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0023 others(26): Show |
127 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*1853A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 1853 | chr12 | 71787526 | ||||||
chr12:71787686 | G | A | 3 | a0001c0006t0127 a0001c0006t0128 a0001c0006t0129 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2013G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 2013 | chr12 | 71787686 | ||||||
chr12:71787792 | T | C | 1 | a0001c0001t0059 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2119T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 2119 | chr12 | 71787792 | ||||||
chr12:71787925 | T | C | 3 | a0001c0006t0127 a0001c0006t0128 a0001c0006t0129 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2252T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 2252 | chr12 | 71787925 | ||||||
chr12:71788048 | A | G | 1 | a0003c0005t0018 | 4 | HG01891.hp1 HG02723.hp2 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2375A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 2375 | chr12 | 71788048 | ||||||
chr12:71788125 | G | A | 91 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(88): Show |
282 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(279): Show |
3_prime_UTR_variant | MODIFIER | c.*2452G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 2452 | chr12 | 71788125 | ||||||
chr12:71788163 | T | A | 1 | a0001c0001t0060 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2490T>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 2490 | chr12 | 71788163 | ||||||
chr12:71788172 | G | T | 2 | a0001c0002t0024 a0001c0002t0122 |
4 | HG00423.hp1 HG00438.hp1 NA19004.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2499G>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 2499 | chr12 | 71788172 | ||||||
chr12:71788245 | C | A | 1 | a0001c0002t0107 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2572C>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 2572 | chr12 | 71788245 | ||||||
chr12:71788298 | AT | A | 18 | a0001c0002t0001 a0001c0002t0014 a0001c0002t0019 others(15): Show |
93 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*2635delT | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 2635 | INFO_REALIGN_3_PRIME | chr12 | 71788298 | |||||
chr12:71788340 | T | A | 1 | a0001c0001t0092 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2667T>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 2667 | chr12 | 71788340 | ||||||
chr12:71788388 | G | C | 64 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(61): Show |
204 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*2715G>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 2715 | chr12 | 71788388 | ||||||
chr12:71788389 | A | C | 1 | a0001c0001t0086 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2716A>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 2716 | chr12 | 71788389 | ||||||
chr12:71788431 | T | A | 1 | a0001c0001t0061 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2758T>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 2758 | chr12 | 71788431 | ||||||
chr12:71788500 | A | G | 1 | a0001c0001t0121 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2827A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 2827 | chr12 | 71788500 | ||||||
chr12:71788700 | G | A | 3 | a0001c0006t0127 a0001c0006t0128 a0001c0006t0129 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3027G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 3027 | chr12 | 71788700 | ||||||
chr12:71788812 | G | A | 25 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0028 others(22): Show |
76 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*3139G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 3139 | chr12 | 71788812 | ||||||
chr12:71788855 | A | G | 1 | a0001c0001t0100 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3182A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 3182 | chr12 | 71788855 | ||||||
chr12:71789066 | A | G | 4 | a0001c0001t0023 a0001c0001t0039 a0001c0001t0120 others(1): Show |
7 | HG02486.hp2 HG02559.hp1 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3393A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 3393 | chr12 | 71789066 | ||||||
chr12:71789126 | G | C | 1 | a0001c0001t0123 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3453G>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 3453 | chr12 | 71789126 | ||||||
chr12:71789408 | C | T | 5 | a0001c0001t0006 a0001c0001t0116 a0001c0001t0117 others(2): Show |
17 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*3735C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 3735 | chr12 | 71789408 | ||||||
chr12:71789417 | A | G | 1 | a0001c0001t0052 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3744A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 3744 | chr12 | 71789417 | ||||||
chr12:71789453 | T | C | 1 | a0001c0003t0036 | 2 | HG02970.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3780T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 3780 | chr12 | 71789453 | ||||||
chr12:71789491 | T | C | 26 | a0001c0001t0010 a0001c0001t0015 a0001c0001t0017 others(23): Show |
47 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*3818T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 3818 | chr12 | 71789491 | ||||||
chr12:71789533 | A | C | 1 | a0001c0001t0060 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3860A>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 3860 | chr12 | 71789533 | ||||||
chr12:71789707 | T | G | 1 | a0001c0001t0093 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4034T>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 4034 | chr12 | 71789707 | ||||||
chr12:71789711 | T | C | 3 | a0001c0001t0074 a0001c0001t0075 a0001c0001t0076 |
3 | NA18970.hp1 NA18974.hp2 NA19087.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4038T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 4038 | chr12 | 71789711 | ||||||
chr12:71789962 | A | G | 5 | a0001c0001t0006 a0001c0001t0116 a0001c0001t0117 others(2): Show |
17 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*4289A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 4289 | chr12 | 71789962 | ||||||
chr12:71790080 | C | A | 5 | a0001c0001t0006 a0001c0001t0116 a0001c0001t0117 others(2): Show |
17 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*4407C>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 4407 | chr12 | 71790080 | ||||||
chr12:71790115 | A | G | 3 | a0001c0001t0025 a0001c0001t0041 a0001c0001t0042 |
4 | HG01069.hp1 HG02486.hp1 HG03195.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4442A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 4442 | chr12 | 71790115 | ||||||
chr12:71790340 | C | A | 63 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(60): Show |
200 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(197): Show |
3_prime_UTR_variant | MODIFIER | c.*4667C>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 4667 | chr12 | 71790340 | ||||||
chr12:71790362 | G | A | 2 | a0001c0001t0040 a0001c0001t0125 |
3 | NA18972.hp2 NA19055.hp2 NA19084.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4689G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 4689 | chr12 | 71790362 | ||||||
chr12:71790429 | A | G | 2 | a0001c0001t0008 a0001c0001t0123 |
10 | HG01884.hp2 HG02258.hp1 HG02559.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4756A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 4756 | chr12 | 71790429 | ||||||
chr12:71790541 | T | C | 1 | a0001c0002t0108 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4868T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 4868 | chr12 | 71790541 | ||||||
chr12:71790770 | C | T | 1 | a0001c0003t0090 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5097C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 5097 | chr12 | 71790770 | ||||||
chr12:71790874 | CT | C | 60 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(57): Show |
196 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(193): Show |
3_prime_UTR_variant | MODIFIER | c.*5211delT | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 5211 | INFO_REALIGN_3_PRIME | chr12 | 71790874 | |||||
chr12:71790874 | CTTTTT | C | 4 | a0001c0001t0015 a0001c0001t0025 a0001c0001t0041 others(1): Show |
8 | HG01069.hp1 HG01884.hp1 HG02145.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5207_*5211delTTTT others(1): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 5207 | INFO_REALIGN_3_PRIME | chr12 | 71790874 | |||||
chr12:71790967 | T | C | 59 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(56): Show |
190 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*5294T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 5294 | chr12 | 71790967 | ||||||
chr12:71790984 | T | G | 1 | a0001c0001t0028 | 2 | HG00438.hp2 HG02040.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5311T>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 5311 | chr12 | 71790984 | ||||||
chr12:71791047 | G | A | 55 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(52): Show |
182 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*5374G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 5374 | chr12 | 71791047 | ||||||
chr12:71791182 | A | G | 1 | a0001c0001t0073 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5509A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 5509 | chr12 | 71791182 | ||||||
chr12:71791189 | G | A | 1 | a0001c0001t0005 | 13 | HG01243.hp2 HG02257.hp1 HG02280.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*5516G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 5516 | chr12 | 71791189 | ||||||
chr12:71791293 | G | A | 2 | a0001c0001t0041 a0001c0001t0042 |
2 | HG01069.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5620G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 5620 | chr12 | 71791293 | ||||||
chr12:71791377 | C | T | 15 | a0001c0002t0001 a0001c0002t0014 a0001c0002t0019 others(12): Show |
89 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*5704C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 5704 | chr12 | 71791377 | ||||||
chr12:71791380 | G | A | 64 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(61): Show |
204 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*5707G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 5707 | chr12 | 71791380 | ||||||
chr12:71791475 | C | T | 22 | a0001c0001t0010 a0001c0001t0017 a0001c0001t0022 others(19): Show |
39 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*5802C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 5802 | chr12 | 71791475 | ||||||
chr12:71791771 | T | C | 25 | a0001c0001t0008 a0001c0001t0023 a0001c0001t0039 others(22): Show |
111 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*6098T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 6098 | chr12 | 71791771 | ||||||
chr12:71791904 | G | A | 2 | a0001c0001t0026 a0001c0001t0048 |
3 | HG01123.hp1 HG01256.hp1 HG01433.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6231G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 6231 | chr12 | 71791904 | ||||||
chr12:71791956 | C | G | 1 | a0003c0005t0018 | 4 | HG01891.hp1 HG02723.hp2 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6283C>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 6283 | chr12 | 71791956 | ||||||
chr12:71791981 | C | G | 4 | a0001c0003t0007 a0001c0003t0036 a0001c0003t0089 others(1): Show |
13 | HG02109.hp1 HG02280.hp2 HG02622.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*6308C>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 6308 | chr12 | 71791981 | ||||||
chr12:71792029 | G | A | 1 | a0001c0001t0123 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6356G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 6356 | chr12 | 71792029 | ||||||
chr12:71792078 | G | C | 1 | a0001c0001t0077 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6405G>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 6405 | chr12 | 71792078 | ||||||
chr12:71792265 | C | T | 59 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(56): Show |
190 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*6592C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 6592 | chr12 | 71792265 | ||||||
chr12:71792274 | A | C | 22 | a0001c0001t0010 a0001c0001t0017 a0001c0001t0022 others(19): Show |
39 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*6601A>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 6601 | chr12 | 71792274 | ||||||
chr12:71792289 | T | C | 8 | a0001c0001t0006 a0001c0001t0116 a0001c0001t0117 others(5): Show |
20 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*6616T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 6616 | chr12 | 71792289 | ||||||
chr12:71792293 | G | A | 1 | a0001c0002t0038 | 2 | HG00544.hp2 NA18964.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6620G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 6620 | chr12 | 71792293 | ||||||
chr12:71792413 | C | G | 1 | a0001c0001t0005 | 13 | HG01243.hp2 HG02257.hp1 HG02280.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*6740C>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 6740 | chr12 | 71792413 | ||||||
chr12:71792703 | A | G | 1 | a0001c0001t0099 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7030A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 7030 | chr12 | 71792703 | ||||||
chr12:71792734 | T | C | 1 | a0001c0001t0078 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7061T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 7061 | chr12 | 71792734 | ||||||
chr12:71792763 | C | A | 1 | a0001c0001t0062 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7090C>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 7090 | chr12 | 71792763 | ||||||
chr12:71792877 | G | A | 59 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(56): Show |
190 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*7204G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 7204 | chr12 | 71792877 | ||||||
chr12:71792896 | T | C | 5 | a0001c0001t0006 a0001c0001t0116 a0001c0001t0117 others(2): Show |
17 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*7223T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 7223 | chr12 | 71792896 | ||||||
chr12:71793172 | G | A | 1 | a0001c0002t0110 | 1 | HG02293.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7499G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 7499 | chr12 | 71793172 | ||||||
chr12:71793319 | G | A | 1 | a0001c0001t0044 | 1 | NA19079.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7646G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 7646 | chr12 | 71793319 | ||||||
chr12:71793562 | C | A | 59 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(56): Show |
190 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*7889C>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 7889 | chr12 | 71793562 | ||||||
chr12:71793722 | A | G | 8 | a0001c0001t0006 a0001c0001t0116 a0001c0001t0117 others(5): Show |
20 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*8049A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8049 | chr12 | 71793722 | ||||||
chr12:71793776 | G | A | 1 | a0001c0003t0088 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8103G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8103 | chr12 | 71793776 | ||||||
chr12:71793850 | A | G | 19 | a0001c0001t0106 a0001c0002t0001 a0001c0002t0014 others(16): Show |
94 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*8177A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8177 | chr12 | 71793850 | ||||||
chr12:71793865 | C | T | 1 | a0005c0008t0051 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8192C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8192 | chr12 | 71793865 | ||||||
chr12:71793876 | C | G | 1 | a0001c0001t0044 | 1 | NA19079.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8203C>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8203 | chr12 | 71793876 | ||||||
chr12:71793933 | T | C | 1 | a0001c0001t0045 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8260T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8260 | chr12 | 71793933 | ||||||
chr12:71793965 | A | G | 1 | a0001c0002t0115 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8292A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8292 | chr12 | 71793965 | ||||||
chr12:71793969 | C | T | 1 | a0001c0001t0120 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8296C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8296 | chr12 | 71793969 | ||||||
chr12:71793986 | G | C | 2 | a0001c0001t0116 a0001c0001t0117 |
2 | HG03491.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8313G>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8313 | chr12 | 71793986 | ||||||
chr12:71794176 | C | T | 1 | a0001c0001t0071 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8503C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8503 | chr12 | 71794176 | ||||||
chr12:71794236 | GAAA | G | 59 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(56): Show |
190 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*8571_*8573delAAA | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8571 | INFO_REALIGN_3_PRIME | chr12 | 71794236 | |||||
chr12:71794405 | T | TTA | 2 | a0001c0001t0029 a0001c0001t0074 |
3 | HG02976.hp1 HG03540.hp2 NA18970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8754_*8755dupAT | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8756 | INFO_REALIGN_3_PRIME | chr12 | 71794405 | |||||
chr12:71794405 | TTA | T | 15 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0020 others(12): Show |
41 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*8754_*8755delAT | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8754 | INFO_REALIGN_3_PRIME | chr12 | 71794405 | |||||
chr12:71794421 | ATATATAT others(3): Show |
A | 2 | a0001c0002t0114 a0001c0006t0129 |
2 | HG01361.hp2 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8750_*8759delATAT others(6): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8750 | INFO_REALIGN_3_PRIME | chr12 | 71794421 | |||||
chr12:71794421 | ATATATAT others(5): Show |
A | 1 | a0001c0002t0109 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8750_*8761delATAT others(8): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8750 | INFO_REALIGN_3_PRIME | chr12 | 71794421 | |||||
chr12:71794423 | ATATATTT | A | 5 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(2): Show |
15 | HG01243.hp2 HG02129.hp1 HG02257.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*8752_*8758delATAT others(3): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8752 | INFO_REALIGN_3_PRIME | chr12 | 71794423 | |||||
chr12:71794423 | ATATATTT others(2): Show |
A | 4 | a0001c0001t0023 a0001c0002t0001 a0001c0002t0104 others(1): Show |
13 | HG00558.hp2 HG01071.hp1 HG01261.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*8752_*8760delATAT others(5): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8752 | INFO_REALIGN_3_PRIME | chr12 | 71794423 | |||||
chr12:71794423 | ATATATTT others(3): Show |
A | 12 | a0001c0001t0023 a0001c0001t0106 a0001c0001t0121 others(9): Show |
53 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*8752_*8761delATAT others(6): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8752 | INFO_REALIGN_3_PRIME | chr12 | 71794423 | |||||
chr12:71794423 | ATATATTT others(4): Show |
A | 3 | a0001c0001t0023 a0001c0002t0001 a0001c0002t0037 |
5 | HG02040.hp1 HG02165.hp1 HG02615.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*8752_*8762delATAT others(7): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8752 | INFO_REALIGN_3_PRIME | chr12 | 71794423 | |||||
chr12:71794423 | ATATATTT others(5): Show |
A | 1 | a0001c0001t0039 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8752_*8763delATAT others(8): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8752 | INFO_REALIGN_3_PRIME | chr12 | 71794423 | |||||
chr12:71794423 | ATATATTT others(11): Show |
A | 1 | a0001c0002t0124 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8752_*8769delATAT others(14): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8752 | INFO_REALIGN_3_PRIME | chr12 | 71794423 | |||||
chr12:71794424 | TA | T | 3 | a0001c0001t0078 a0001c0001t0083 a0001c0001t0085 |
3 | HG00140.hp1 HG02135.hp2 HG03831.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8752delA | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8752 | chr12 | 71794424 | ||||||
chr12:71794425 | A | ATT | 2 | a0001c0001t0016 a0001c0001t0081 |
3 | HG01346.hp2 HG02080.hp1 HG02132.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8753_*8754insTT | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8754 | INFO_REALIGN_3_PRIME | chr12 | 71794425 | |||||
chr12:71794425 | A | T | 1 | a0001c0001t0011 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8752A>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8752 | chr12 | 71794425 | ||||||
chr12:71794425 | ATAT | A | 6 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0013 others(3): Show |
10 | HG01081.hp1 HG01433.hp1 HG01515.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*8754_*8756delATT | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8754 | INFO_REALIGN_3_PRIME | chr12 | 71794425 | |||||
chr12:71794425 | ATATTTTT | A | 4 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0119 others(1): Show |
11 | HG00642.hp2 HG00738.hp2 HG02132.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*8754_*8760delATTT others(3): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8754 | INFO_REALIGN_3_PRIME | chr12 | 71794425 | |||||
chr12:71794425 | ATATTTTT others(1): Show |
A | 5 | a0001c0001t0005 a0001c0002t0001 a0001c0002t0019 others(2): Show |
6 | HG02886.hp2 HG03017.hp1 HG03139.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*8754_*8761delATTT others(4): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8754 | INFO_REALIGN_3_PRIME | chr12 | 71794425 | |||||
chr12:71794425 | ATATTTTT others(2): Show |
A | 8 | a0001c0001t0025 a0001c0001t0041 a0001c0001t0042 others(5): Show |
16 | HG00609.hp1 HG01069.hp1 HG01993.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*8754_*8762delATTT others(5): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8754 | INFO_REALIGN_3_PRIME | chr12 | 71794425 | |||||
chr12:71794425 | ATATTTTT others(3): Show |
A | 2 | a0001c0001t0039 a0001c0002t0001 |
4 | HG02486.hp2 NA18948.hp2 NA19058.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8754_*8763delATTT others(6): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8754 | INFO_REALIGN_3_PRIME | chr12 | 71794425 | |||||
chr12:71794426 | TA | T | 3 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0013 |
7 | HG02145.hp1 HG02258.hp2 HG02698.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*8754delA | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8754 | chr12 | 71794426 | ||||||
chr12:71794427 | A | ATATATAT others(6): Show |
1 | a0001c0003t0007 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8755_*8756insATAT others(9): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8756 | INFO_REALIGN_3_PRIME | chr12 | 71794427 | |||||
chr12:71794427 | A | ATATATAT others(7): Show |
1 | a0001c0003t0007 | 2 | HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8755_*8756insATAT others(10): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8756 | INFO_REALIGN_3_PRIME | chr12 | 71794427 | |||||
chr12:71794427 | A | ATATATAT others(14): Show |
1 | a0001c0003t0036 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8755_*8756insATAT others(17): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8756 | INFO_REALIGN_3_PRIME | chr12 | 71794427 | |||||
chr12:71794427 | A | ATATATAT others(5): Show |
2 | a0001c0003t0007 a0001c0003t0089 |
4 | HG02109.hp1 HG06807.hp2 NA19030.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8755_*8756insATAT others(8): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8756 | INFO_REALIGN_3_PRIME | chr12 | 71794427 | |||||
chr12:71794427 | A | ATATATAT others(5): Show |
1 | a0001c0003t0007 | 3 | HG02280.hp2 HG02896.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8755_*8756insATAT others(8): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8756 | INFO_REALIGN_3_PRIME | chr12 | 71794427 | |||||
chr12:71794427 | A | ATATATAT others(3): Show |
1 | a0001c0003t0036 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8755_*8756insATAT others(6): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8756 | INFO_REALIGN_3_PRIME | chr12 | 71794427 | |||||
chr12:71794427 | A | T | 15 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(12): Show |
27 | HG00140.hp1 HG00642.hp1 HG01099.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*8754A>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8754 | chr12 | 71794427 | ||||||
chr12:71794427 | AT | A | 9 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0012 others(6): Show |
13 | HG01169.hp1 HG02056.hp2 HG02523.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*8783delT | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8783 | INFO_REALIGN_3_PRIME | chr12 | 71794427 | |||||
chr12:71794427 | ATT | A | 14 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0017 others(11): Show |
23 | HG00408.hp1 HG00423.hp2 HG01123.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*8782_*8783delTT | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8782 | INFO_REALIGN_3_PRIME | chr12 | 71794427 | |||||
chr12:71794427 | ATTT | A | 9 | a0001c0001t0002 a0001c0001t0040 a0001c0001t0060 others(6): Show |
23 | HG01167.hp1 HG02027.hp2 HG02071.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*8781_*8783delTTT | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8781 | INFO_REALIGN_3_PRIME | chr12 | 71794427 | |||||
chr12:71794427 | ATTTT | A | 6 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0040 others(3): Show |
7 | HG02818.hp1 HG02895.hp1 HG03041.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*8780_*8783delTTTT | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8780 | INFO_REALIGN_3_PRIME | chr12 | 71794427 | |||||
chr12:71794427 | ATTTTTT | A | 5 | a0001c0001t0034 a0001c0001t0097 a0001c0001t0101 others(2): Show |
6 | HG00597.hp1 HG00621.hp1 HG00741.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*8778_*8783delTTTT others(2): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8778 | INFO_REALIGN_3_PRIME | chr12 | 71794427 | |||||
chr12:71794427 | ATTTTTTT others(1): Show |
A | 11 | a0001c0001t0010 a0001c0001t0015 a0001c0001t0022 others(8): Show |
22 | HG00544.hp1 HG00558.hp1 HG02027.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*8776_*8783delTTTT others(4): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8776 | INFO_REALIGN_3_PRIME | chr12 | 71794427 | |||||
chr12:71794427 | ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0015 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8774_*8783delTTTT others(6): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8774 | INFO_REALIGN_3_PRIME | chr12 | 71794427 | |||||
chr12:71794427 | ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0091 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8773_*8783delTTTT others(7): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8773 | INFO_REALIGN_3_PRIME | chr12 | 71794427 | |||||
chr12:71794428 | T | TA | 3 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0028 |
7 | HG00438.hp2 HG02040.hp2 HG02922.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*8755_*8756insA | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8756 | chr12 | 71794428 | ||||||
chr12:71794428 | T | TATA | 2 | a0001c0001t0002 a0001c0001t0033 |
3 | HG03453.hp2 NA18950.hp1 NA19086.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8755_*8756insATA | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8756 | chr12 | 71794428 | ||||||
chr12:71794429 | T | A | 6 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0012 others(3): Show |
9 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*8756T>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8756 | chr12 | 71794429 | ||||||
chr12:71794430 | T | A | 6 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0033 others(3): Show |
11 | HG02523.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*8757T>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8757 | chr12 | 71794430 | ||||||
chr12:71794431 | T | A | 5 | a0001c0001t0017 a0001c0001t0030 a0001c0001t0063 others(2): Show |
9 | HG00423.hp2 HG01346.hp1 HG01361.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*8758T>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8758 | chr12 | 71794431 | ||||||
chr12:71794432 | T | A | 3 | a0001c0001t0033 a0001c0001t0065 a0001c0001t0080 |
4 | HG02647.hp2 HG03453.hp2 HG03834.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8759T>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8759 | chr12 | 71794432 | ||||||
chr12:71794433 | T | A | 5 | a0001c0001t0017 a0001c0001t0063 a0001c0001t0094 others(2): Show |
8 | HG00423.hp2 HG01975.hp1 HG02818.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*8760T>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8760 | chr12 | 71794433 | ||||||
chr12:71794434 | T | A | 1 | a0001c0001t0033 | 2 | HG02647.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8761T>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8761 | chr12 | 71794434 | ||||||
chr12:71794435 | T | A | 8 | a0001c0001t0017 a0001c0001t0034 a0001c0001t0094 others(5): Show |
12 | HG00597.hp1 HG00621.hp1 HG01975.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*8762T>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8762 | chr12 | 71794435 | ||||||
chr12:71794436 | T | A | 3 | a0001c0001t0033 a0001c0001t0035 a0001c0001t0046 |
5 | HG02056.hp1 HG02647.hp2 HG03453.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*8763T>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8763 | chr12 | 71794436 | ||||||
chr12:71794437 | T | A | 16 | a0001c0001t0010 a0001c0001t0017 a0001c0001t0022 others(13): Show |
28 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*8764T>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8764 | chr12 | 71794437 | ||||||
chr12:71794438 | T | A | 3 | a0001c0001t0033 a0001c0001t0035 a0001c0001t0046 |
5 | HG02056.hp1 HG02647.hp2 HG03453.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*8765T>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8765 | chr12 | 71794438 | ||||||
chr12:71794439 | T | A | 15 | a0001c0001t0010 a0001c0001t0017 a0001c0001t0022 others(12): Show |
27 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*8766T>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8766 | chr12 | 71794439 | ||||||
chr12:71794440 | T | A | 3 | a0001c0001t0033 a0001c0001t0035 a0001c0001t0046 |
5 | HG02056.hp1 HG02647.hp2 HG03453.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*8767T>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8767 | chr12 | 71794440 | ||||||
chr12:71794441 | T | A | 12 | a0001c0001t0010 a0001c0001t0017 a0001c0001t0034 others(9): Show |
22 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*8768T>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8768 | chr12 | 71794441 | ||||||
chr12:71794442 | T | A | 2 | a0001c0001t0035 a0001c0001t0046 |
3 | HG02056.hp1 NA18968.hp2 NA19009.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8769T>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8769 | chr12 | 71794442 | ||||||
chr12:71794443 | T | A | 3 | a0001c0001t0017 a0001c0001t0034 a0001c0001t0098 |
7 | HG00597.hp1 HG00621.hp1 HG01975.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*8770T>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8770 | chr12 | 71794443 | ||||||
chr12:71794559 | C | G | 1 | a0001c0002t0113 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8886C>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8886 | chr12 | 71794559 | ||||||
chr12:71794570 | G | C | 1 | a0001c0002t0038 | 2 | HG00544.hp2 NA18964.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8897G>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8897 | chr12 | 71794570 | ||||||
chr12:71794582 | G | A | 1 | a0001c0001t0125 | 1 | NA18972.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8909G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8909 | chr12 | 71794582 | ||||||
chr12:71794585 | C | A | 55 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(52): Show |
182 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*8912C>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 8912 | chr12 | 71794585 | ||||||
chr12:71794690 | G | A | 1 | a0001c0001t0102 | 1 | NA19067.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9017G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 9017 | chr12 | 71794690 | ||||||
chr12:71794698 | A | G | 1 | a0001c0002t0113 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9025A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 9025 | chr12 | 71794698 | ||||||
chr12:71794717 | C | A | 59 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(56): Show |
190 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*9044C>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 9044 | chr12 | 71794717 | ||||||
chr12:71794870 | G | A | 1 | a0001c0001t0073 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9197G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 9197 | chr12 | 71794870 | ||||||
chr12:71794992 | C | G | 1 | a0001c0001t0021 | 3 | NA18960.hp2 NA18993.hp1 NA18998.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9319C>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 9319 | chr12 | 71794992 | ||||||
chr12:71795036 | G | A | 3 | a0001c0001t0025 a0001c0001t0041 a0001c0001t0042 |
4 | HG01069.hp1 HG02486.hp1 HG03195.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*9363G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 9363 | chr12 | 71795036 | ||||||
chr12:71795097 | A | T | 59 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(56): Show |
190 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*9424A>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 9424 | chr12 | 71795097 | ||||||
chr12:71795114 | T | A | 58 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0010 others(55): Show |
177 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*9441T>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 9441 | chr12 | 71795114 | ||||||
chr12:71795370 | A | T | 20 | a0001c0001t0010 a0001c0001t0017 a0001c0001t0022 others(17): Show |
34 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*9697A>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 9697 | chr12 | 71795370 | ||||||
chr12:71795378 | GGAGAAAT others(1408): Show |
G | 58 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0010 others(55): Show |
177 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*9707_*11121del | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 9707 | INFO_REALIGN_3_PRIME | chr12 | 71795378 | |||||
chr12:71795531 | G | C | 1 | a0001c0001t0005 | 13 | HG01243.hp2 HG02257.hp1 HG02280.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*9858G>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 9858 | chr12 | 71795531 | ||||||
chr12:71795818 | T | C | 1 | a0001c0001t0013 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10145T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 10145 | chr12 | 71795818 | ||||||
chr12:71795824 | G | C | 1 | a0001c0003t0036 | 2 | HG02970.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10151G>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 10151 | chr12 | 71795824 | ||||||
chr12:71796017 | T | A | 1 | a0001c0001t0002 | 3 | NA18949.hp1 NA18991.hp1 NA19011.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10344T>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 10344 | chr12 | 71796017 | ||||||
chr12:71796027 | C | G | 1 | a0001c0001t0002 | 2 | HG02965.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10354C>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 10354 | chr12 | 71796027 | ||||||
chr12:71796104 | G | A | 4 | a0001c0001t0009 a0001c0001t0031 a0001c0001t0056 others(1): Show |
5 | HG01516.hp1 HG01952.hp2 HG03017.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*10431G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 10431 | chr12 | 71796104 | ||||||
chr12:71796726 | G | A | 1 | a0001c0001t0081 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11053G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11053 | chr12 | 71796726 | ||||||
chr12:71796728 | A | C | 1 | a0001c0001t0081 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11055A>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11055 | chr12 | 71796728 | ||||||
chr12:71796729 | A | C | 1 | a0001c0001t0081 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11056A>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11056 | chr12 | 71796729 | ||||||
chr12:71796730 | C | T | 1 | a0001c0001t0081 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11057C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11057 | chr12 | 71796730 | ||||||
chr12:71796736 | G | C | 1 | a0001c0003t0088 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11063G>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11063 | chr12 | 71796736 | ||||||
chr12:71796738 | G | T | 1 | a0001c0001t0081 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11065G>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11065 | chr12 | 71796738 | ||||||
chr12:71796741 | A | T | 1 | a0001c0001t0081 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11068A>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11068 | chr12 | 71796741 | ||||||
chr12:71796744 | G | C | 1 | a0001c0001t0081 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11071G>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11071 | chr12 | 71796744 | ||||||
chr12:71796745 | T | A | 1 | a0001c0001t0081 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11072T>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11072 | chr12 | 71796745 | ||||||
chr12:71796747 | G | C | 1 | a0001c0001t0081 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11074G>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11074 | chr12 | 71796747 | ||||||
chr12:71796749 | G | T | 1 | a0001c0001t0081 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11076G>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11076 | chr12 | 71796749 | ||||||
chr12:71796751 | A | T | 1 | a0001c0001t0081 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11078A>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11078 | chr12 | 71796751 | ||||||
chr12:71796752 | T | A | 1 | a0001c0001t0081 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11079T>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11079 | chr12 | 71796752 | ||||||
chr12:71796753 | C | T | 1 | a0001c0001t0081 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11080C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11080 | chr12 | 71796753 | ||||||
chr12:71796759 | G | C | 1 | a0001c0001t0081 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11086G>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11086 | chr12 | 71796759 | ||||||
chr12:71796761 | A | C | 1 | a0001c0001t0081 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11088A>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11088 | chr12 | 71796761 | ||||||
chr12:71796763 | A | C | 1 | a0001c0001t0081 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11090A>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11090 | chr12 | 71796763 | ||||||
chr12:71796776 | T | A | 1 | a0001c0001t0081 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11103T>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11103 | chr12 | 71796776 | ||||||
chr12:71796777 | G | T | 1 | a0001c0001t0081 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11104G>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11104 | chr12 | 71796777 | ||||||
chr12:71796778 | T | A | 1 | a0001c0001t0081 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11105T>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11105 | chr12 | 71796778 | ||||||
chr12:71796784 | A | T | 1 | a0001c0001t0081 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11111A>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11111 | chr12 | 71796784 | ||||||
chr12:71796785 | A | C | 1 | a0001c0001t0081 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11112A>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11112 | chr12 | 71796785 | ||||||
chr12:71796786 | G | A | 1 | a0001c0001t0081 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11113G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11113 | chr12 | 71796786 | ||||||
chr12:71796788 | G | A | 1 | a0001c0001t0081 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11115G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11115 | chr12 | 71796788 | ||||||
chr12:71796812 | T | C | 1 | a0001c0001t0081 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11139T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11139 | chr12 | 71796812 | ||||||
chr12:71796819 | A | T | 1 | a0001c0001t0081 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11146A>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11146 | chr12 | 71796819 | ||||||
chr12:71796823 | A | C | 1 | a0001c0001t0081 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11150A>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11150 | chr12 | 71796823 | ||||||
chr12:71796824 | A | T | 1 | a0001c0001t0081 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11151A>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11151 | chr12 | 71796824 | ||||||
chr12:71796828 | A | T | 1 | a0001c0001t0081 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11155A>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11155 | chr12 | 71796828 | ||||||
chr12:71796832 | A | C | 1 | a0001c0001t0081 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11159A>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11159 | chr12 | 71796832 | ||||||
chr12:71796836 | G | A | 1 | a0001c0001t0081 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11163G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11163 | chr12 | 71796836 | ||||||
chr12:71796837 | T | C | 1 | a0001c0001t0081 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11164T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11164 | chr12 | 71796837 | ||||||
chr12:71796838 | A | C | 1 | a0001c0001t0081 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11165A>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11165 | chr12 | 71796838 | ||||||
chr12:71796839 | A | T | 1 | a0001c0001t0081 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11166A>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11166 | chr12 | 71796839 | ||||||
chr12:71796840 | G | C | 1 | a0001c0001t0081 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11167G>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11167 | chr12 | 71796840 | ||||||
chr12:71796841 | C | A | 1 | a0001c0001t0081 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11168C>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11168 | chr12 | 71796841 | ||||||
chr12:71796847 | A | G | 59 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(56): Show |
190 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*11174A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11174 | chr12 | 71796847 | ||||||
chr12:71796869 | A | C | 1 | a0001c0001t0081 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11196A>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11196 | chr12 | 71796869 | ||||||
chr12:71796887 | A | C | 1 | a0001c0001t0081 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11214A>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11214 | chr12 | 71796887 | ||||||
chr12:71797051 | A | G | 2 | a0001c0001t0023 a0001c0001t0121 |
4 | HG02559.hp1 HG02647.hp1 NA18522.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*11378A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11378 | chr12 | 71797051 | ||||||
chr12:71797055 | T | C | 59 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(56): Show |
190 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*11382T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11382 | chr12 | 71797055 | ||||||
chr12:71797086 | G | A | 1 | a0003c0005t0018 | 4 | HG01891.hp1 HG02723.hp2 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*11413G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11413 | chr12 | 71797086 | ||||||
chr12:71797119 | T | C | 1 | a0001c0001t0064 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11446T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11446 | chr12 | 71797119 | ||||||
chr12:71797168 | A | G | 1 | a0001c0001t0069 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11495A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11495 | chr12 | 71797168 | ||||||
chr12:71797440 | A | G | 1 | a0001c0001t0085 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11767A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11767 | chr12 | 71797440 | ||||||
chr12:71797579 | TAA | T | 56 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0010 others(53): Show |
175 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*11919_*11920delAA | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11919 | INFO_REALIGN_3_PRIME | chr12 | 71797579 | |||||
chr12:71797579 | TAAA | T | 2 | a0001c0001t0005 a0001c0006t0128 |
14 | HG01243.hp2 HG02257.hp1 HG02280.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*11918_*11920delAA others(1): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11918 | INFO_REALIGN_3_PRIME | chr12 | 71797579 | |||||
chr12:71797624 | GA | G | 58 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(55): Show |
188 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(185): Show |
3_prime_UTR_variant | MODIFIER | c.*11967delA | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 11967 | INFO_REALIGN_3_PRIME | chr12 | 71797624 | |||||
chr12:71797789 | T | C | 5 | a0001c0003t0007 a0001c0003t0036 a0001c0003t0088 others(2): Show |
14 | HG02109.hp1 HG02280.hp2 HG02622.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*12116T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 12116 | chr12 | 71797789 | ||||||
chr12:71797807 | G | GA | 59 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(56): Show |
190 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*12136dupA | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 12137 | INFO_REALIGN_3_PRIME | chr12 | 71797807 | |||||
chr12:71797849 | T | C | 1 | a0001c0001t0121 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12176T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 12176 | chr12 | 71797849 | ||||||
chr12:71797918 | C | A | 59 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(56): Show |
190 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*12245C>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 12245 | chr12 | 71797918 | ||||||
chr12:71798036 | G | T | 1 | a0001c0001t0005 | 13 | HG01243.hp2 HG02257.hp1 HG02280.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*12363G>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 12363 | chr12 | 71798036 | ||||||
chr12:71798045 | A | G | 1 | a0001c0001t0032 | 2 | NA19062.hp2 NA19085.hp1 |
3_prime_UTR_variant | MODIFIER | c.*12372A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 12372 | chr12 | 71798045 | ||||||
chr12:71798069 | A | T | 1 | a0001c0002t0113 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12396A>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 12396 | chr12 | 71798069 | ||||||
chr12:71798107 | G | A | 1 | a0001c0002t0113 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12434G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 12434 | chr12 | 71798107 | ||||||
chr12:71798231 | T | C | 64 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(61): Show |
204 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*12558T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 12558 | chr12 | 71798231 | ||||||
chr12:71798285 | G | A | 59 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(56): Show |
190 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*12612G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 12612 | chr12 | 71798285 | ||||||
chr12:71798365 | G | T | 1 | a0001c0001t0084 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12692G>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 12692 | chr12 | 71798365 | ||||||
chr12:71798387 | T | C | 59 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(56): Show |
190 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*12714T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 12714 | chr12 | 71798387 | ||||||
chr12:71798570 | A | T | 5 | a0001c0001t0006 a0001c0001t0116 a0001c0001t0117 others(2): Show |
17 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*12897A>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 12897 | chr12 | 71798570 | ||||||
chr12:71798606 | T | G | 1 | a0001c0001t0005 | 13 | HG01243.hp2 HG02257.hp1 HG02280.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*12933T>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 12933 | chr12 | 71798606 | ||||||
chr12:71798741 | T | C | 59 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(56): Show |
190 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*13068T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 13068 | chr12 | 71798741 | ||||||
chr12:71798799 | G | A | 1 | a0001c0003t0088 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*13126G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 13126 | chr12 | 71798799 | ||||||
chr12:71798852 | G | A | 1 | a0001c0001t0118 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13179G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 13179 | chr12 | 71798852 | ||||||
chr12:71798893 | T | TA | 5 | a0001c0001t0006 a0001c0001t0116 a0001c0001t0117 others(2): Show |
17 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*13221dupA | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 13222 | INFO_REALIGN_3_PRIME | chr12 | 71798893 | |||||
chr12:71798904 | G | A | 1 | a0001c0002t0111 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13231G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 13231 | chr12 | 71798904 | ||||||
chr12:71799421 | G | A | 13 | a0001c0002t0001 a0001c0002t0014 a0001c0002t0024 others(10): Show |
84 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*13748G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 13748 | chr12 | 71799421 | ||||||
chr12:71799429 | G | A | 1 | a0001c0001t0005 | 13 | HG01243.hp2 HG02257.hp1 HG02280.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*13756G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 13756 | chr12 | 71799429 | ||||||
chr12:71799500 | T | C | 1 | a0001c0001t0091 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13827T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 13827 | chr12 | 71799500 | ||||||
chr12:71799520 | G | T | 1 | a0001c0002t0122 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13847G>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 13847 | chr12 | 71799520 | ||||||
chr12:71799599 | A | C | 21 | a0001c0001t0010 a0001c0001t0017 a0001c0001t0022 others(18): Show |
35 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*13926A>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 13926 | chr12 | 71799599 | ||||||
chr12:71799891 | G | A | 1 | a0001c0001t0082 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*14218G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 14218 | chr12 | 71799891 | ||||||
chr12:71800072 | C | CA | 3 | a0001c0001t0020 a0001c0001t0083 a0001c0003t0007 |
13 | HG01891.hp2 HG02074.hp1 HG02109.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*14418dupA | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 14419 | INFO_REALIGN_3_PRIME | chr12 | 71800072 | |||||
chr12:71800072 | CA | C | 87 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(84): Show |
268 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(265): Show |
3_prime_UTR_variant | MODIFIER | c.*14418delA | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 14418 | INFO_REALIGN_3_PRIME | chr12 | 71800072 | |||||
chr12:71800080 | A | G | 1 | a0001c0002t0112 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*14407A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 14407 | chr12 | 71800080 | ||||||
chr12:71800081 | A | G | 48 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0015 others(45): Show |
155 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*14408A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 14408 | chr12 | 71800081 | ||||||
chr12:71800082 | A | G | 1 | a0001c0001t0102 | 1 | NA19067.hp1 | 3_prime_UTR_variant | MODIFIER | c.*14409A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 14409 | chr12 | 71800082 | ||||||
chr12:71800229 | A | T | 1 | a0001c0001t0067 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*14556A>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 7/7 | 14556 | chr12 | 71800229 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:71755360 | C | A | 6 | a0001c0001t0023g0025 a0001c0001t0023g0049 a0001c0001t0039g0026 others(3): Show |
7 | HG02486.hp2 HG02559.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.159+72C>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71755360 | |||||||
chr12:71755886 | C | A | 1 | a0001c0001t0091g0052 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.159+598C>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71755886 | |||||||
chr12:71756078 | C | T | 27 | a0001c0001t0010g0006 a0001c0001t0010g0019 a0001c0001t0010g0048 others(24): Show |
33 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.159+790C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71756078 | |||||||
chr12:71756113 | A | C | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.159+825A>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71756113 | |||||||
chr12:71756211 | C | T | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.159+923C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71756211 | |||||||
chr12:71756363 | T | G | 1 | a0001c0006t0127g0168 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.159+1075T>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71756363 | |||||||
chr12:71756367 | C | T | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.159+1079C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71756367 | |||||||
chr12:71756386 | C | A | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.159+1098C>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71756386 | |||||||
chr12:71756773 | A | G | 5 | a0001c0001t0008g0013 a0001c0001t0008g0045 a0001c0001t0008g0166 others(2): Show |
10 | HG01884.hp2 HG02258.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.159+1485A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71756773 | |||||||
chr12:71756958 | G | T | 249 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0010 others(246): Show |
365 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(362): Show |
intron_variant | MODIFIER | c.159+1670G>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71756958 | |||||||
chr12:71757155 | C | T | 3 | a0001c0001t0002g0162 a0001c0001t0002g0163 a0001c0001t0002g0164 |
3 | NA18949.hp1 NA18991.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.159+1867C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71757155 | |||||||
chr12:71757285 | T | A | 1 | a0001c0002t0001g0057 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.159+1997T>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71757285 | |||||||
chr12:71757321 | A | G | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.159+2033A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71757321 | |||||||
chr12:71757330 | G | A | 1 | a0001c0001t0003g0058 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.159+2042G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71757330 | |||||||
chr12:71757357 | A | G | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.159+2069A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71757357 | |||||||
chr12:71757435 | C | T | 6 | a0001c0001t0002g0018 a0001c0001t0016g0018 a0001c0001t0016g0159 others(3): Show |
7 | HG02080.hp1 HG02132.hp2 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.159+2147C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71757435 | |||||||
chr12:71757461 | C | A | 1 | a0001c0001t0016g0159 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.159+2173C>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71757461 | |||||||
chr12:71757487 | T | G | 1 | a0001c0003t0036g0059 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.159+2199T>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71757487 | |||||||
chr12:71757490 | T | G | 8 | a0001c0001t0006g0007 a0001c0001t0006g0014 a0001c0001t0006g0060 others(5): Show |
17 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.159+2202T>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71757490 | |||||||
chr12:71757612 | C | T | 1 | a0001c0001t0016g0159 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.159+2324C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71757612 | |||||||
chr12:71757805 | A | C | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.159+2517A>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71757805 | |||||||
chr12:71757828 | A | G | 1 | a0001c0001t0002g0158 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.159+2540A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71757828 | |||||||
chr12:71757887 | T | C | 1 | a0001c0001t0059g0063 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.159+2599T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71757887 | |||||||
chr12:71757953 | A | G | 37 | a0001c0001t0010g0006 a0001c0001t0010g0019 a0001c0001t0010g0048 others(34): Show |
47 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.159+2665A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71757953 | |||||||
chr12:71758209 | GT | G | 6 | a0001c0001t0023g0025 a0001c0001t0023g0049 a0001c0001t0039g0026 others(3): Show |
7 | HG02486.hp2 HG02559.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.159+2924delT | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 71758209 | ||||||
chr12:71758285 | G | A | 67 | a0001c0001t0008g0013 a0001c0001t0008g0045 a0001c0001t0008g0166 others(64): Show |
110 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.159+2997G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71758285 | |||||||
chr12:71758287 | C | A | 29 | a0001c0001t0010g0006 a0001c0001t0010g0019 a0001c0001t0010g0048 others(26): Show |
35 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.159+2999C>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71758287 | |||||||
chr12:71758504 | C | CT | 9 | a0001c0001t0006g0007 a0001c0001t0006g0014 a0001c0001t0006g0060 others(6): Show |
19 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.159+3229dupT | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 71758504 | ||||||
chr12:71758538 | G | A | 1 | a0001c0003t0036g0059 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.159+3250G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71758538 | |||||||
chr12:71758630 | G | A | 1 | a0001c0001t0006g0014 | 4 | HG02129.hp1 NA18939.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+3342G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71758630 | |||||||
chr12:71758647 | A | AT | 164 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0010 others(161): Show |
227 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.159+3371dupT | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 71758647 | ||||||
chr12:71758647 | A | ATT | 9 | a0001c0001t0015g0154 a0001c0001t0015g0155 a0001c0001t0015g0156 others(6): Show |
10 | HG01069.hp1 HG01884.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.159+3370_159+3371d others(4): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 71758647 | ||||||
chr12:71758647 | A | T | 1 | a0001c0003t0036g0059 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.159+3359A>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71758647 | |||||||
chr12:71758948 | G | A | 78 | a0001c0001t0006g0007 a0001c0001t0006g0014 a0001c0001t0006g0060 others(75): Show |
130 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.159+3660G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71758948 | |||||||
chr12:71758997 | T | A | 1 | a0001c0002t0001g0064 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.159+3709T>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71758997 | |||||||
chr12:71759232 | G | A | 1 | a0001c0001t0060g0094 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.159+3944G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71759232 | |||||||
chr12:71759234 | C | A | 1 | a0001c0002t0001g0057 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.159+3946C>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71759234 | |||||||
chr12:71759235 | A | G | 1 | a0001c0002t0001g0057 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.159+3947A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71759235 | |||||||
chr12:71759237 | G | T | 1 | a0001c0002t0001g0057 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.159+3949G>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71759237 | |||||||
chr12:71759373 | A | G | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.159+4085A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71759373 | |||||||
chr12:71759428 | G | A | 2 | a0001c0001t0012g0035 a0001c0001t0068g0035 |
2 | HG02572.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.159+4140G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71759428 | |||||||
chr12:71759452 | A | C | 1 | a0001c0003t0036g0059 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.159+4164A>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71759452 | |||||||
chr12:71759504 | A | G | 3 | a0001c0001t0015g0155 a0001c0001t0015g0156 a0001c0001t0015g0157 |
3 | HG02145.hp2 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.159+4216A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71759504 | |||||||
chr12:71759537 | G | A | 1 | a0001c0001t0086g0095 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.159+4249G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71759537 | |||||||
chr12:71759550 | T | C | 1 | a0001c0002t0037g0065 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.159+4262T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71759550 | |||||||
chr12:71759551 | T | G | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.159+4263T>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71759551 | |||||||
chr12:71759657 | A | G | 1 | a0001c0003t0090g0152 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.159+4369A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71759657 | |||||||
chr12:71759698 | C | T | 1 | a0001c0001t0044g0161 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.159+4410C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71759698 | |||||||
chr12:71759770 | A | G | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.159+4482A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71759770 | |||||||
chr12:71759839 | C | A | 6 | a0001c0001t0023g0025 a0001c0001t0023g0049 a0001c0001t0039g0026 others(3): Show |
7 | HG02486.hp2 HG02559.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.159+4551C>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71759839 | |||||||
chr12:71760051 | G | T | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.159+4763G>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71760051 | |||||||
chr12:71760077 | A | T | 2 | a0001c0001t0002g0043 a0001c0001t0067g0151 |
3 | HG01081.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.159+4789A>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71760077 | |||||||
chr12:71760355 | C | T | 1 | a0001c0001t0003g0150 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.159+5067C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71760355 | |||||||
chr12:71760373 | A | T | 71 | a0001c0001t0008g0013 a0001c0001t0008g0045 a0001c0001t0008g0166 others(68): Show |
114 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.159+5085A>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71760373 | |||||||
chr12:71760374 | T | A | 68 | a0001c0001t0008g0013 a0001c0001t0008g0045 a0001c0001t0008g0166 others(65): Show |
111 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.159+5086T>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71760374 | |||||||
chr12:71760375 | A | T | 68 | a0001c0001t0008g0013 a0001c0001t0008g0045 a0001c0001t0008g0166 others(65): Show |
111 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.159+5087A>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71760375 | |||||||
chr12:71760415 | G | A | 1 | a0001c0001t0002g0096 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.159+5127G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71760415 | |||||||
chr12:71760447 | G | A | 1 | a0001c0001t0044g0161 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.159+5159G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71760447 | |||||||
chr12:71760451 | A | G | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.159+5163A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71760451 | |||||||
chr12:71760480 | C | T | 2 | a0001c0001t0010g0048 a0001c0001t0098g0048 |
2 | NA19062.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.159+5192C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71760480 | |||||||
chr12:71760533 | G | A | 79 | a0001c0001t0006g0007 a0001c0001t0006g0014 a0001c0001t0006g0060 others(76): Show |
131 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.159+5245G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71760533 | |||||||
chr12:71760575 | G | C | 1 | a0001c0001t0012g0097 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.159+5287G>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71760575 | |||||||
chr12:71760718 | T | C | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.159+5430T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71760718 | |||||||
chr12:71760726 | T | C | 125 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0010 others(122): Show |
174 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.159+5438T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71760726 | |||||||
chr12:71760796 | A | G | 1 | a0001c0002t0001g0093 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.159+5508A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71760796 | |||||||
chr12:71760837 | G | T | 1 | a0001c0001t0002g0147 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.159+5549G>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71760837 | |||||||
chr12:71760838 | G | T | 1 | a0001c0001t0002g0147 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.159+5550G>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71760838 | |||||||
chr12:71760915 | C | T | 57 | a0001c0001t0106g0153 a0001c0002t0001g0001 a0001c0002t0001g0009 others(54): Show |
94 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.159+5627C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71760915 | |||||||
chr12:71760973 | G | A | 27 | a0001c0001t0010g0006 a0001c0001t0010g0019 a0001c0001t0010g0048 others(24): Show |
33 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.159+5685G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71760973 | |||||||
chr12:71761043 | T | TA | 12 | a0001c0001t0008g0013 a0001c0001t0008g0045 a0001c0001t0008g0166 others(9): Show |
22 | HG01099.hp1 HG01257.hp2 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.159+5770dupA | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 71761043 | ||||||
chr12:71761169 | A | G | 79 | a0001c0001t0006g0007 a0001c0001t0006g0014 a0001c0001t0006g0060 others(76): Show |
131 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.159+5881A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71761169 | |||||||
chr12:71761222 | A | T | 1 | a0001c0001t0100g0184 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.159+5934A>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71761222 | |||||||
chr12:71761394 | A | G | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.159+6106A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71761394 | |||||||
chr12:71761713 | A | C | 1 | a0001c0001t0005g0056 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.159+6425A>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71761713 | |||||||
chr12:71761796 | TTTTA | T | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.159+6516_159+6519d others(6): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 71761796 | ||||||
chr12:71761804 | A | G | 1 | a0001c0002t0019g0034 | 2 | HG02698.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.159+6516A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71761804 | |||||||
chr12:71761899 | G | A | 1 | a0001c0002t0038g0068 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.159+6611G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71761899 | |||||||
chr12:71761961 | A | G | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.159+6673A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71761961 | |||||||
chr12:71761999 | C | G | 1 | a0001c0001t0002g0146 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.159+6711C>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71761999 | |||||||
chr12:71762054 | A | T | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.159+6766A>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71762054 | |||||||
chr12:71762175 | A | G | 1 | a0001c0006t0129g0170 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.159+6887A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71762175 | |||||||
chr12:71762286 | G | GGTTTGGT others(3): Show |
6 | a0001c0001t0006g0007 a0001c0001t0006g0014 a0001c0001t0006g0060 others(3): Show |
15 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.159+7002_159+7003i others(12): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 71762286 | ||||||
chr12:71762286 | G | GGTTTGGT others(8): Show |
2 | a0001c0001t0116g0027 a0001c0001t0117g0027 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.159+7002_159+7003i others(17): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 71762286 | ||||||
chr12:71762286 | G | GGTTTT | 83 | a0001c0001t0003g0102 a0001c0001t0004g0101 a0001c0001t0010g0006 others(80): Show |
125 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.159+7029_159+7033d others(7): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 71762286 | ||||||
chr12:71762286 | G | GGTTTTGT others(3): Show |
3 | a0001c0002t0001g0028 a0001c0002t0037g0065 a0001c0002t0037g0069 |
4 | HG02615.hp1 NA18986.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.159+7024_159+7033d others(12): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 71762286 | ||||||
chr12:71762286 | GGTTTTGT others(3): Show |
G | 1 | a0001c0001t0008g0167 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.159+7024_159+7033d others(12): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 71762286 | ||||||
chr12:71762291 | T | G | 1 | a0001c0006t0129g0170 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.159+7003T>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71762291 | |||||||
chr12:71762345 | G | A | 67 | a0001c0001t0008g0013 a0001c0001t0008g0045 a0001c0001t0008g0166 others(64): Show |
110 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.159+7057G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71762345 | |||||||
chr12:71762374 | C | T | 8 | a0001c0001t0006g0007 a0001c0001t0006g0014 a0001c0001t0006g0060 others(5): Show |
17 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.159+7086C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71762374 | |||||||
chr12:71762399 | A | G | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.159+7111A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71762399 | |||||||
chr12:71762410 | A | C | 1 | a0001c0002t0001g0091 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.159+7122A>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71762410 | |||||||
chr12:71762460 | C | G | 1 | a0001c0002t0124g0090 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.159+7172C>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71762460 | |||||||
chr12:71762538 | C | T | 7 | a0001c0001t0015g0154 a0001c0001t0015g0155 a0001c0001t0015g0156 others(4): Show |
8 | HG01069.hp1 HG01884.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.159+7250C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71762538 | |||||||
chr12:71762645 | C | T | 78 | a0001c0001t0006g0007 a0001c0001t0006g0014 a0001c0001t0006g0060 others(75): Show |
130 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.160-7155C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71762645 | |||||||
chr12:71762646 | G | C | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.160-7154G>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71762646 | |||||||
chr12:71763005 | T | C | 1 | a0003c0005t0018g0016 | 4 | HG01891.hp1 HG02723.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-6795T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71763005 | |||||||
chr12:71763029 | A | G | 1 | a0001c0002t0001g0089 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.160-6771A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71763029 | |||||||
chr12:71763101 | G | GCA | 49 | a0001c0001t0008g0013 a0001c0001t0008g0045 a0001c0001t0008g0166 others(46): Show |
84 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.160-6672_160-6671d others(4): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 71763101 | ||||||
chr12:71763101 | G | GCACA | 8 | a0001c0001t0085g0145 a0001c0001t0091g0052 a0001c0002t0001g0022 others(5): Show |
10 | HG01496.hp2 HG02055.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.160-6674_160-6671d others(6): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 71763101 | ||||||
chr12:71763101 | G | GCACACAC others(1): Show |
26 | a0001c0001t0010g0006 a0001c0001t0010g0019 a0001c0001t0010g0048 others(23): Show |
31 | HG00544.hp1 HG00558.hp1 HG01975.hp1 others(28): Show |
intron_variant | MODIFIER | c.160-6678_160-6671d others(10): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 71763101 | ||||||
chr12:71763101 | G | GCACACAC others(3): Show |
2 | a0001c0001t0034g0047 a0001c0001t0106g0153 |
3 | HG00597.hp1 HG00621.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.160-6680_160-6671d others(12): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 71763101 | ||||||
chr12:71763101 | GCA | G | 76 | a0001c0001t0002g0018 a0001c0001t0003g0002 a0001c0001t0003g0023 others(73): Show |
110 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.160-6672_160-6671d others(4): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 71763101 | ||||||
chr12:71763101 | GCACA | G | 60 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0010 others(57): Show |
89 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.160-6674_160-6671d others(6): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 71763101 | ||||||
chr12:71763101 | GCACACA | G | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.160-6676_160-6671d others(8): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 71763101 | ||||||
chr12:71763173 | A | G | 1 | a0001c0002t0114g0086 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.160-6627A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71763173 | |||||||
chr12:71763442 | A | G | 2 | a0001c0001t0002g0096 a0001c0001t0043g0122 |
2 | HG00738.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.160-6358A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71763442 | |||||||
chr12:71763502 | A | G | 2 | a0001c0002t0001g0028 a0001c0002t0001g0085 |
3 | NA18986.hp2 NA19005.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.160-6298A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71763502 | |||||||
chr12:71763569 | G | A | 1 | a0001c0001t0121g0050 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.160-6231G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71763569 | |||||||
chr12:71763642 | G | A | 249 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0010 others(246): Show |
365 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(362): Show |
intron_variant | MODIFIER | c.160-6158G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71763642 | |||||||
chr12:71763839 | G | T | 1 | a0001c0001t0077g0142 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.160-5961G>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71763839 | |||||||
chr12:71763927 | G | C | 1 | a0001c0001t0094g0172 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.160-5873G>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71763927 | |||||||
chr12:71763935 | G | T | 6 | a0001c0001t0004g0004 a0001c0001t0011g0004 a0001c0001t0011g0141 others(3): Show |
13 | HG00408.hp1 HG00642.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.160-5865G>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71763935 | |||||||
chr12:71763954 | A | T | 6 | a0001c0001t0015g0155 a0001c0001t0015g0156 a0001c0001t0015g0157 others(3): Show |
7 | HG01069.hp1 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.160-5846A>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71763954 | |||||||
chr12:71764037 | C | T | 1 | a0001c0001t0003g0140 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.160-5763C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71764037 | |||||||
chr12:71764052 | A | G | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.160-5748A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71764052 | |||||||
chr12:71764112 | A | G | 1 | a0001c0001t0005g0055 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.160-5688A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71764112 | |||||||
chr12:71764118 | C | T | 1 | a0001c0001t0080g0100 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.160-5682C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71764118 | |||||||
chr12:71764683 | C | G | 7 | a0001c0001t0003g0024 a0001c0001t0003g0040 a0001c0001t0003g0058 others(4): Show |
7 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.160-5117C>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71764683 | |||||||
chr12:71764738 | T | G | 76 | a0001c0001t0006g0007 a0001c0001t0006g0014 a0001c0001t0006g0060 others(73): Show |
128 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.160-5062T>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71764738 | |||||||
chr12:71764866 | A | G | 1 | a0001c0006t0128g0169 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.160-4934A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71764866 | |||||||
chr12:71764923 | C | T | 1 | a0001c0001t0028g0121 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.160-4877C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71764923 | |||||||
chr12:71765095 | C | T | 1 | a0001c0002t0001g0067 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.160-4705C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71765095 | |||||||
chr12:71765378 | G | A | 1 | a0001c0001t0015g0155 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.160-4422G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71765378 | |||||||
chr12:71765535 | G | A | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.160-4265G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71765535 | |||||||
chr12:71765686 | T | C | 249 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0010 others(246): Show |
365 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(362): Show |
intron_variant | MODIFIER | c.160-4114T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71765686 | |||||||
chr12:71765879 | T | G | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.160-3921T>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71765879 | |||||||
chr12:71766089 | A | G | 1 | a0001c0003t0090g0152 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.160-3711A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71766089 | |||||||
chr12:71766094 | A | C | 5 | a0001c0001t0002g0008 a0001c0001t0063g0008 a0001c0001t0070g0008 others(2): Show |
9 | HG00423.hp2 NA18944.hp2 NA18966.hp1 others(6): Show |
intron_variant | MODIFIER | c.160-3706A>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71766094 | |||||||
chr12:71766238 | A | G | 1 | a0001c0003t0088g0148 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.160-3562A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71766238 | |||||||
chr12:71766323 | T | C | 67 | a0001c0001t0008g0013 a0001c0001t0008g0045 a0001c0001t0008g0166 others(64): Show |
110 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.160-3477T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71766323 | |||||||
chr12:71766359 | A | G | 5 | a0001c0003t0007g0015 a0001c0003t0007g0041 a0001c0003t0007g0042 others(2): Show |
10 | HG02109.hp1 HG02280.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.160-3441A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71766359 | |||||||
chr12:71766400 | T | C | 1 | a0001c0001t0081g0123 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.160-3400T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71766400 | |||||||
chr12:71766593 | T | C | 1 | a0001c0001t0002g0103 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.160-3207T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71766593 | |||||||
chr12:71766695 | C | T | 5 | a0001c0003t0007g0015 a0001c0003t0007g0041 a0001c0003t0007g0042 others(2): Show |
10 | HG02109.hp1 HG02280.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.160-3105C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71766695 | |||||||
chr12:71766696 | G | A | 1 | a0001c0001t0035g0046 | 2 | NA18968.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.160-3104G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71766696 | |||||||
chr12:71766840 | A | G | 1 | a0001c0003t0088g0148 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.160-2960A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71766840 | |||||||
chr12:71767039 | A | G | 1 | a0001c0002t0037g0069 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.160-2761A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71767039 | |||||||
chr12:71767040 | T | C | 1 | a0005c0008t0051g0124 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.160-2760T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71767040 | |||||||
chr12:71767185 | A | C | 2 | a0001c0001t0116g0027 a0001c0001t0117g0027 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.160-2615A>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71767185 | |||||||
chr12:71767189 | G | A | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.160-2611G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71767189 | |||||||
chr12:71767424 | A | G | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.160-2376A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71767424 | |||||||
chr12:71767508 | T | C | 1 | a0001c0001t0008g0045 | 2 | HG02559.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.160-2292T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71767508 | |||||||
chr12:71767988 | A | T | 1 | a0001c0001t0091g0052 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.160-1812A>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71767988 | |||||||
chr12:71768019 | G | T | 1 | a0001c0001t0004g0138 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.160-1781G>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71768019 | |||||||
chr12:71768043 | T | C | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.160-1757T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71768043 | |||||||
chr12:71768141 | A | C | 1 | a0001c0001t0032g0137 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.160-1659A>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71768141 | |||||||
chr12:71768310 | G | T | 1 | a0001c0002t0001g0092 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.160-1490G>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71768310 | |||||||
chr12:71768370 | C | T | 1 | a0001c0001t0012g0097 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.160-1430C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71768370 | |||||||
chr12:71768428 | C | T | 2 | a0001c0001t0002g0119 a0001c0001t0002g0158 |
2 | HG04115.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.160-1372C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71768428 | |||||||
chr12:71768470 | G | A | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.160-1330G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71768470 | |||||||
chr12:71768530 | A | G | 1 | a0001c0003t0007g0042 | 2 | HG02109.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.160-1270A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71768530 | |||||||
chr12:71768540 | T | C | 1 | a0001c0002t0001g0072 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.160-1260T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71768540 | |||||||
chr12:71768643 | C | A | 1 | a0001c0001t0074g0125 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.160-1157C>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71768643 | |||||||
chr12:71768923 | T | C | 4 | a0001c0001t0005g0005 a0001c0001t0005g0053 a0001c0001t0005g0055 others(1): Show |
13 | HG01243.hp2 HG02257.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.160-877T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71768923 | |||||||
chr12:71768932 | C | CGTGT | 4 | a0001c0001t0005g0005 a0001c0001t0005g0053 a0001c0001t0005g0055 others(1): Show |
13 | HG01243.hp2 HG02257.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.160-855_160-852dup others(4): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 71768932 | ||||||
chr12:71768932 | CGT | C | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.160-853_160-852del others(2): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 71768932 | ||||||
chr12:71768966 | G | A | 1 | a0001c0001t0084g0126 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.160-834G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71768966 | |||||||
chr12:71768984 | T | C | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.160-816T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71768984 | |||||||
chr12:71769176 | G | A | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.160-624G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71769176 | |||||||
chr12:71769364 | A | G | 1 | a0003c0005t0018g0016 | 4 | HG01891.hp1 HG02723.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-436A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71769364 | |||||||
chr12:71769374 | G | A | 1 | a0001c0002t0001g0066 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.160-426G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71769374 | |||||||
chr12:71769449 | T | G | 5 | a0001c0001t0008g0013 a0001c0001t0008g0045 a0001c0001t0008g0166 others(2): Show |
10 | HG01884.hp2 HG02258.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.160-351T>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71769449 | |||||||
chr12:71769453 | ATCTTAGA others(4): Show |
A | 1 | a0001c0001t0006g0014 | 4 | HG02129.hp1 NA18939.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-339_160-329del others(11): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 71769453 | ||||||
chr12:71769474 | C | G | 1 | a0001c0001t0002g0118 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.160-326C>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71769474 | |||||||
chr12:71769594 | T | C | 1 | a0001c0001t0044g0161 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.160-206T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 1/6 | chr12 | 71769594 | |||||||
chr12:71769877 | A | G | 1 | a0002c0004t0004g0039 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.219+18A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 2/6 | chr12 | 71769877 | |||||||
chr12:71769897 | C | T | 2 | a0001c0002t0037g0069 a0001c0002t0109g0088 |
2 | HG01496.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.219+38C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 2/6 | chr12 | 71769897 | |||||||
chr12:71769907 | T | C | 1 | a0001c0001t0087g0104 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.219+48T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 2/6 | chr12 | 71769907 | |||||||
chr12:71769908 | C | T | 1 | a0001c0001t0087g0104 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.219+49C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 2/6 | chr12 | 71769908 | |||||||
chr12:71769909 | T | C | 1 | a0001c0001t0087g0104 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.219+50T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 2/6 | chr12 | 71769909 | |||||||
chr12:71769943 | C | CT | 35 | a0001c0001t0010g0006 a0001c0001t0010g0019 a0001c0001t0010g0048 others(32): Show |
45 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.219+98dupT | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 71769943 | ||||||
chr12:71769943 | CT | C | 14 | a0001c0001t0012g0035 a0001c0001t0030g0105 a0001c0001t0068g0035 others(11): Show |
19 | HG02109.hp1 HG02280.hp2 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.219+98delT | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 71769943 | ||||||
chr12:71769992 | A | G | 1 | a0001c0001t0002g0117 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.219+133A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 2/6 | chr12 | 71769992 | |||||||
chr12:71770013 | A | G | 37 | a0001c0001t0010g0006 a0001c0001t0010g0019 a0001c0001t0010g0048 others(34): Show |
47 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.219+154A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 2/6 | chr12 | 71770013 | |||||||
chr12:71770155 | A | G | 78 | a0001c0001t0006g0007 a0001c0001t0006g0014 a0001c0001t0006g0060 others(75): Show |
130 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.219+296A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 2/6 | chr12 | 71770155 | |||||||
chr12:71770169 | G | T | 2 | a0001c0001t0008g0166 a0001c0001t0008g0167 |
2 | HG01884.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.219+310G>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 2/6 | chr12 | 71770169 | |||||||
chr12:71770283 | A | G | 3 | a0001c0001t0002g0162 a0001c0001t0002g0163 a0001c0001t0002g0164 |
3 | NA18949.hp1 NA18991.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.220-309A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 2/6 | chr12 | 71770283 | |||||||
chr12:71770468 | T | C | 56 | a0001c0002t0001g0001 a0001c0002t0001g0009 a0001c0002t0001g0020 others(53): Show |
93 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.220-124T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 2/6 | chr12 | 71770468 | |||||||
chr12:71770728 | A | G | 1 | a0001c0002t0001g0091 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.327+29A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 3/6 | chr12 | 71770728 | |||||||
chr12:71770807 | G | GTA | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.327+113_327+114dup others(2): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 71770807 | ||||||
chr12:71770861 | T | C | 1 | a0001c0001t0003g0127 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.327+162T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 3/6 | chr12 | 71770861 | |||||||
chr12:71770921 | C | T | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.327+222C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 3/6 | chr12 | 71770921 | |||||||
chr12:71771107 | T | A | 1 | a0001c0001t0040g0107 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.327+408T>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 3/6 | chr12 | 71771107 | |||||||
chr12:71771242 | C | T | 2 | a0001c0001t0004g0038 a0001c0001t0011g0038 |
2 | HG00639.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.327+543C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 3/6 | chr12 | 71771242 | |||||||
chr12:71771462 | T | C | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.327+763T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 3/6 | chr12 | 71771462 | |||||||
chr12:71771505 | A | G | 1 | a0001c0002t0001g0084 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.327+806A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 3/6 | chr12 | 71771505 | |||||||
chr12:71771537 | A | G | 1 | a0001c0001t0022g0173 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.327+838A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 3/6 | chr12 | 71771537 | |||||||
chr12:71771692 | G | A | 1 | a0001c0006t0128g0169 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.327+993G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 3/6 | chr12 | 71771692 | |||||||
chr12:71771740 | G | A | 1 | a0001c0002t0019g0034 | 2 | HG02698.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.327+1041G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 3/6 | chr12 | 71771740 | |||||||
chr12:71771745 | C | T | 1 | a0001c0001t0008g0045 | 2 | HG02559.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.327+1046C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 3/6 | chr12 | 71771745 | |||||||
chr12:71771932 | C | T | 1 | a0001c0003t0090g0152 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.327+1233C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 3/6 | chr12 | 71771932 | |||||||
chr12:71771975 | CA | C | 10 | a0001c0001t0069g0106 a0001c0003t0007g0015 a0001c0003t0007g0041 others(7): Show |
15 | HG02109.hp1 HG02280.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.327+1289delA | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 71771975 | ||||||
chr12:71772222 | A | G | 2 | a0001c0001t0004g0038 a0001c0001t0011g0038 |
2 | HG00639.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.327+1523A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 3/6 | chr12 | 71772222 | |||||||
chr12:71772243 | A | G | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.327+1544A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 3/6 | chr12 | 71772243 | |||||||
chr12:71772458 | A | AT | 3 | a0001c0002t0037g0065 a0001c0002t0037g0069 a0001c0002t0109g0088 |
3 | HG01496.hp2 HG02615.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.328-1500dupT | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 71772458 | ||||||
chr12:71772510 | T | G | 1 | a0001c0001t0006g0060 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.328-1449T>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 3/6 | chr12 | 71772510 | |||||||
chr12:71772556 | G | A | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.328-1403G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 3/6 | chr12 | 71772556 | |||||||
chr12:71772579 | T | A | 4 | a0001c0003t0007g0041 a0001c0006t0127g0168 a0001c0006t0128g0169 others(1): Show |
5 | HG02717.hp1 HG02809.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.328-1380T>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 3/6 | chr12 | 71772579 | |||||||
chr12:71772639 | G | A | 1 | a0001c0001t0091g0052 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.328-1320G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 3/6 | chr12 | 71772639 | |||||||
chr12:71772868 | C | G | 4 | a0001c0001t0005g0005 a0001c0001t0005g0053 a0001c0001t0005g0055 others(1): Show |
13 | HG01243.hp2 HG02257.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.328-1091C>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 3/6 | chr12 | 71772868 | |||||||
chr12:71772905 | T | A | 1 | a0001c0001t0039g0051 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.328-1054T>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 3/6 | chr12 | 71772905 | |||||||
chr12:71772997 | A | G | 1 | a0001c0001t0017g0183 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.328-962A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 3/6 | chr12 | 71772997 | |||||||
chr12:71773079 | T | G | 2 | a0001c0002t0001g0064 a0001c0002t0001g0073 |
2 | NA18940.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.328-880T>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 3/6 | chr12 | 71773079 | |||||||
chr12:71773087 | A | G | 1 | a0001c0002t0001g0087 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.328-872A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 3/6 | chr12 | 71773087 | |||||||
chr12:71773371 | A | G | 5 | a0001c0003t0007g0015 a0001c0003t0007g0041 a0001c0003t0007g0042 others(2): Show |
10 | HG02109.hp1 HG02280.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.328-588A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 3/6 | chr12 | 71773371 | |||||||
chr12:71773486 | A | G | 3 | a0001c0001t0002g0012 a0001c0001t0058g0012 a0001c0001t0062g0012 |
5 | HG00597.hp2 HG02056.hp2 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.328-473A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 3/6 | chr12 | 71773486 | |||||||
chr12:71773509 | AT | A | 66 | a0001c0001t0008g0013 a0001c0001t0008g0045 a0001c0001t0008g0166 others(63): Show |
109 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.328-441delT | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 71773509 | ||||||
chr12:71773540 | A | G | 28 | a0001c0001t0010g0006 a0001c0001t0010g0019 a0001c0001t0010g0048 others(25): Show |
34 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.328-419A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 3/6 | chr12 | 71773540 | |||||||
chr12:71773586 | A | G | 5 | a0001c0001t0008g0013 a0001c0001t0008g0045 a0001c0001t0008g0166 others(2): Show |
10 | HG01884.hp2 HG02258.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.328-373A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 3/6 | chr12 | 71773586 | |||||||
chr12:71773710 | T | G | 1 | a0001c0001t0003g0037 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.328-249T>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 3/6 | chr12 | 71773710 | |||||||
chr12:71773892 | T | G | 1 | a0001c0001t0026g0128 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.328-67T>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 3/6 | chr12 | 71773892 | |||||||
chr12:71774137 | A | C | 1 | a0001c0001t0126g0116 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.391+115A>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71774137 | |||||||
chr12:71774289 | TACAAAAA others(90): Show |
T | 1 | a0001c0006t0127g0168 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.391+269_391+365del others(97): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr12 | 71774289 | ||||||
chr12:71774291 | C | CA | 21 | a0001c0001t0005g0005 a0001c0001t0005g0053 a0001c0001t0005g0056 others(18): Show |
31 | HG00438.hp1 HG00741.hp1 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.391+296dupA | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr12 | 71774291 | ||||||
chr12:71774291 | CA | C | 142 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0010 others(139): Show |
182 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(179): Show |
intron_variant | MODIFIER | c.391+296delA | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr12 | 71774291 | ||||||
chr12:71774291 | CAA | C | 16 | a0001c0001t0002g0010 a0001c0001t0002g0043 a0001c0001t0010g0019 others(13): Show |
23 | HG01167.hp1 HG01993.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.391+295_391+296del others(2): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr12 | 71774291 | ||||||
chr12:71774461 | A | G | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.391+439A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71774461 | |||||||
chr12:71774585 | C | T | 1 | a0001c0003t0090g0152 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.391+563C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71774585 | |||||||
chr12:71774682 | A | G | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.391+660A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71774682 | |||||||
chr12:71774756 | T | TA | 103 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0010 others(100): Show |
160 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.391+751dupA | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr12 | 71774756 | ||||||
chr12:71774756 | T | TAA | 16 | a0001c0001t0002g0108 a0001c0001t0002g0162 a0001c0001t0006g0007 others(13): Show |
23 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.391+750_391+751dup others(2): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr12 | 71774756 | ||||||
chr12:71774756 | TA | T | 7 | a0001c0001t0003g0150 a0001c0001t0013g0135 a0001c0001t0060g0094 others(4): Show |
7 | HG02717.hp1 HG02809.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.391+751delA | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr12 | 71774756 | ||||||
chr12:71774797 | A | G | 1 | a0001c0002t0001g0087 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.391+775A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71774797 | |||||||
chr12:71774813 | A | C | 1 | a0001c0002t0001g0081 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.391+791A>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71774813 | |||||||
chr12:71774861 | G | GGCTTCAA others(13): Show |
3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.391+847_391+866dup others(20): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr12 | 71774861 | ||||||
chr12:71774862 | G | A | 3 | a0001c0001t0002g0162 a0001c0001t0002g0163 a0001c0001t0002g0164 |
3 | NA18949.hp1 NA18991.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.391+840G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71774862 | |||||||
chr12:71775004 | T | C | 248 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0010 others(245): Show |
371 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(368): Show |
intron_variant | MODIFIER | c.391+982T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71775004 | |||||||
chr12:71775186 | A | G | 1 | a0001c0001t0046g0181 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.391+1164A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71775186 | |||||||
chr12:71775192 | G | T | 1 | a0001c0002t0001g0080 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.391+1170G>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71775192 | |||||||
chr12:71775567 | C | T | 1 | a0001c0001t0081g0123 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.391+1545C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71775567 | |||||||
chr12:71775620 | T | TCC | 8 | a0001c0001t0006g0007 a0001c0001t0006g0014 a0001c0001t0006g0060 others(5): Show |
17 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.391+1599_391+1600d others(4): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr12 | 71775620 | ||||||
chr12:71775677 | C | T | 1 | a0001c0002t0001g0066 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.391+1655C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71775677 | |||||||
chr12:71775683 | C | T | 1 | a0001c0001t0002g0108 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.391+1661C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71775683 | |||||||
chr12:71775816 | T | C | 1 | a0001c0001t0074g0125 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.391+1794T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71775816 | |||||||
chr12:71775839 | AT | A | 66 | a0001c0001t0008g0013 a0001c0001t0008g0045 a0001c0001t0008g0166 others(63): Show |
109 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.391+1825delT | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr12 | 71775839 | ||||||
chr12:71776183 | A | G | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.391+2161A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71776183 | |||||||
chr12:71776273 | C | T | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.391+2251C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71776273 | |||||||
chr12:71776396 | C | G | 1 | a0003c0005t0018g0016 | 4 | HG01891.hp1 HG02723.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.391+2374C>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71776396 | |||||||
chr12:71776418 | G | A | 4 | a0001c0001t0005g0005 a0001c0001t0005g0053 a0001c0001t0005g0055 others(1): Show |
13 | HG01243.hp2 HG02257.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.391+2396G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71776418 | |||||||
chr12:71776484 | A | G | 1 | a0001c0001t0006g0014 | 4 | HG02129.hp1 NA18939.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.391+2462A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71776484 | |||||||
chr12:71776709 | G | A | 28 | a0001c0001t0010g0006 a0001c0001t0010g0019 a0001c0001t0010g0048 others(25): Show |
34 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.391+2687G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71776709 | |||||||
chr12:71776740 | T | A | 1 | a0001c0001t0003g0037 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.391+2718T>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71776740 | |||||||
chr12:71776771 | T | C | 2 | a0001c0001t0023g0025 a0001c0001t0121g0050 |
3 | HG02559.hp1 HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.391+2749T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71776771 | |||||||
chr12:71776781 | G | T | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.391+2759G>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71776781 | |||||||
chr12:71776910 | C | G | 4 | a0001c0001t0002g0010 a0001c0001t0002g0143 a0001c0001t0028g0010 others(1): Show |
8 | HG00438.hp2 HG02040.hp2 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.391+2888C>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71776910 | |||||||
chr12:71777007 | G | A | 36 | a0001c0001t0010g0006 a0001c0001t0010g0019 a0001c0001t0010g0048 others(33): Show |
46 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.391+2985G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71777007 | |||||||
chr12:71777112 | C | A | 2 | a0001c0001t0027g0130 a0001c0001t0027g0131 |
2 | HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.391+3090C>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71777112 | |||||||
chr12:71777197 | A | C | 1 | a0001c0001t0097g0180 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.391+3175A>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71777197 | |||||||
chr12:71777214 | C | G | 1 | a0001c0001t0003g0140 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.391+3192C>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71777214 | |||||||
chr12:71777233 | C | T | 75 | a0001c0001t0006g0007 a0001c0001t0006g0014 a0001c0001t0006g0060 others(72): Show |
127 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.391+3211C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71777233 | |||||||
chr12:71777234 | G | A | 1 | a0001c0001t0035g0046 | 2 | NA18968.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.391+3212G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71777234 | |||||||
chr12:71777347 | A | G | 1 | a0001c0002t0037g0065 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.391+3325A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71777347 | |||||||
chr12:71777792 | G | A | 1 | a0001c0006t0128g0169 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.391+3770G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71777792 | |||||||
chr12:71778035 | T | C | 1 | a0001c0001t0057g0132 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.392-3996T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71778035 | |||||||
chr12:71778083 | A | G | 6 | a0001c0001t0023g0025 a0001c0001t0023g0049 a0001c0001t0039g0026 others(3): Show |
7 | HG02486.hp2 HG02559.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.392-3948A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71778083 | |||||||
chr12:71778624 | C | T | 1 | a0001c0001t0073g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.392-3407C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71778624 | |||||||
chr12:71778826 | A | C | 1 | a0002c0004t0054g0115 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.392-3205A>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71778826 | |||||||
chr12:71778947 | A | G | 1 | a0001c0003t0090g0152 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.392-3084A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71778947 | |||||||
chr12:71778965 | T | A | 1 | a0001c0002t0001g0030 | 2 | NA18991.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.392-3066T>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71778965 | |||||||
chr12:71778991 | T | C | 4 | a0001c0001t0005g0005 a0001c0001t0005g0053 a0001c0001t0005g0055 others(1): Show |
13 | HG01243.hp2 HG02257.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.392-3040T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71778991 | |||||||
chr12:71779034 | A | T | 4 | a0001c0001t0005g0005 a0001c0001t0005g0053 a0001c0001t0005g0055 others(1): Show |
13 | HG01243.hp2 HG02257.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.392-2997A>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71779034 | |||||||
chr12:71779111 | G | T | 1 | a0001c0001t0119g0062 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.392-2920G>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71779111 | |||||||
chr12:71779125 | C | T | 2 | a0001c0001t0072g0111 a0001c0002t0019g0074 |
2 | HG02886.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.392-2906C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71779125 | |||||||
chr12:71779186 | G | A | 3 | a0001c0001t0015g0154 a0001c0002t0001g0064 a0001c0002t0001g0073 |
3 | HG01884.hp1 NA18940.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.392-2845G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71779186 | |||||||
chr12:71779345 | A | C | 6 | a0001c0001t0023g0025 a0001c0001t0023g0049 a0001c0001t0039g0026 others(3): Show |
7 | HG02486.hp2 HG02559.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.392-2686A>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71779345 | |||||||
chr12:71779369 | G | A | 1 | a0001c0001t0039g0051 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.392-2662G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71779369 | |||||||
chr12:71779379 | G | A | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.392-2652G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71779379 | |||||||
chr12:71779411 | G | A | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.392-2620G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71779411 | |||||||
chr12:71779471 | A | C | 74 | a0001c0001t0006g0007 a0001c0001t0006g0014 a0001c0001t0006g0060 others(71): Show |
126 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.392-2560A>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71779471 | |||||||
chr12:71779500 | G | A | 1 | a0001c0001t0005g0053 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.392-2531G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71779500 | |||||||
chr12:71779514 | GT | G | 4 | a0001c0001t0005g0005 a0001c0001t0005g0053 a0001c0001t0005g0055 others(1): Show |
13 | HG01243.hp2 HG02257.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.392-2513delT | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr12 | 71779514 | ||||||
chr12:71779600 | T | G | 6 | a0001c0001t0023g0025 a0001c0001t0023g0049 a0001c0001t0039g0026 others(3): Show |
7 | HG02486.hp2 HG02559.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.392-2431T>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71779600 | |||||||
chr12:71779601 | A | G | 1 | a0001c0001t0027g0131 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.392-2430A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71779601 | |||||||
chr12:71779610 | G | A | 8 | a0001c0001t0006g0007 a0001c0001t0006g0014 a0001c0001t0006g0060 others(5): Show |
17 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.392-2421G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71779610 | |||||||
chr12:71779632 | A | G | 8 | a0001c0003t0007g0015 a0001c0003t0007g0041 a0001c0003t0007g0042 others(5): Show |
13 | HG02109.hp1 HG02280.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.392-2399A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71779632 | |||||||
chr12:71779801 | T | G | 1 | a0001c0001t0008g0166 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.392-2230T>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71779801 | |||||||
chr12:71779831 | A | C | 1 | a0001c0002t0001g0087 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.392-2200A>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71779831 | |||||||
chr12:71779839 | A | G | 2 | a0001c0001t0003g0040 a0001c0001t0009g0040 |
2 | HG01070.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.392-2192A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71779839 | |||||||
chr12:71779917 | T | C | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.392-2114T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71779917 | |||||||
chr12:71779924 | T | C | 1 | a0001c0002t0001g0080 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.392-2107T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71779924 | |||||||
chr12:71779980 | A | G | 1 | a0001c0001t0016g0160 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.392-2051A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71779980 | |||||||
chr12:71780123 | T | C | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.392-1908T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71780123 | |||||||
chr12:71780290 | C | G | 67 | a0001c0001t0008g0013 a0001c0001t0008g0045 a0001c0001t0008g0166 others(64): Show |
110 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.392-1741C>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71780290 | |||||||
chr12:71780337 | T | C | 37 | a0001c0001t0010g0006 a0001c0001t0010g0019 a0001c0001t0010g0048 others(34): Show |
47 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.392-1694T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71780337 | |||||||
chr12:71780373 | T | C | 4 | a0001c0001t0005g0005 a0001c0001t0005g0053 a0001c0001t0005g0055 others(1): Show |
13 | HG01243.hp2 HG02257.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.392-1658T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71780373 | |||||||
chr12:71780429 | A | T | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.392-1602A>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71780429 | |||||||
chr12:71780785 | CTTATCTG others(4): Show |
C | 1 | a0001c0001t0026g0128 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.392-1233_392-1223d others(13): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr12 | 71780785 | ||||||
chr12:71780789 | T | G | 5 | a0001c0003t0007g0015 a0001c0003t0007g0041 a0001c0003t0007g0042 others(2): Show |
10 | HG02109.hp1 HG02280.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.392-1242T>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71780789 | |||||||
chr12:71780887 | G | A | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.392-1144G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71780887 | |||||||
chr12:71780972 | A | G | 3 | a0001c0001t0012g0098 a0001c0001t0012g0110 a0001c0001t0029g0114 |
3 | HG02922.hp1 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.392-1059A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71780972 | |||||||
chr12:71781142 | A | G | 5 | a0001c0002t0001g0030 a0001c0002t0001g0031 a0001c0002t0001g0032 others(2): Show |
8 | HG00621.hp2 NA18944.hp1 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.392-889A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71781142 | |||||||
chr12:71781175 | A | G | 3 | a0001c0002t0001g0021 a0001c0002t0001g0064 a0001c0002t0001g0073 |
5 | HG00408.hp2 HG02040.hp1 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.392-856A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71781175 | |||||||
chr12:71781225 | T | G | 1 | a0001c0002t0001g0076 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.392-806T>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71781225 | |||||||
chr12:71781286 | A | G | 3 | a0001c0002t0037g0065 a0001c0002t0037g0069 a0001c0002t0109g0088 |
3 | HG01496.hp2 HG02615.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.392-745A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71781286 | |||||||
chr12:71781336 | GCAGGCAC | G | 8 | a0001c0001t0006g0007 a0001c0001t0006g0014 a0001c0001t0006g0060 others(5): Show |
17 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.392-693_392-687del others(7): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr12 | 71781336 | ||||||
chr12:71781345 | T | C | 1 | a0001c0001t0091g0052 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.392-686T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71781345 | |||||||
chr12:71781401 | G | A | 1 | a0001c0002t0107g0077 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.392-630G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71781401 | |||||||
chr12:71781466 | C | CA | 7 | a0001c0001t0003g0134 a0001c0001t0015g0154 a0001c0003t0036g0059 others(4): Show |
7 | HG01884.hp1 HG01978.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.392-550dupA | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr12 | 71781466 | ||||||
chr12:71781466 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0095g0179 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.392-559_392-550del others(10): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr12 | 71781466 | ||||||
chr12:71781488 | A | G | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.392-543A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71781488 | |||||||
chr12:71781605 | T | A | 1 | a0001c0001t0012g0097 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.392-426T>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71781605 | |||||||
chr12:71781718 | A | G | 1 | a0001c0001t0033g0178 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.392-313A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71781718 | |||||||
chr12:71781732 | A | G | 8 | a0001c0003t0007g0015 a0001c0003t0007g0041 a0001c0003t0007g0042 others(5): Show |
13 | HG02109.hp1 HG02280.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.392-299A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71781732 | |||||||
chr12:71781743 | A | G | 1 | a0001c0001t0125g0109 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.392-288A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71781743 | |||||||
chr12:71781917 | G | C | 8 | a0001c0001t0006g0007 a0001c0001t0006g0014 a0001c0001t0006g0060 others(5): Show |
17 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.392-114G>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 4/6 | chr12 | 71781917 | |||||||
chr12:71782186 | A | G | 2 | a0001c0001t0010g0019 a0001c0001t0010g0177 |
5 | HG02523.hp1 NA18941.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.446+101A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 5/6 | chr12 | 71782186 | |||||||
chr12:71782334 | G | C | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.447-236G>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 5/6 | chr12 | 71782334 | |||||||
chr12:71782432 | T | C | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.447-138T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 5/6 | chr12 | 71782432 | |||||||
chr12:71782532 | A | G | 2 | a0001c0002t0019g0029 a0001c0002t0111g0029 |
2 | HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.447-38A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 5/6 | chr12 | 71782532 | |||||||
chr12:71782721 | G | A | 2 | a0001c0001t0027g0130 a0001c0001t0027g0131 |
2 | HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.535+63G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 6/6 | chr12 | 71782721 | |||||||
chr12:71782762 | C | G | 1 | a0001c0001t0003g0150 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.535+104C>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 6/6 | chr12 | 71782762 | |||||||
chr12:71782875 | A | G | 1 | a0001c0001t0048g0113 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.535+217A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 6/6 | chr12 | 71782875 | |||||||
chr12:71782882 | T | C | 3 | a0001c0002t0001g0030 a0001c0002t0001g0031 a0001c0002t0001g0081 |
5 | NA18956.hp2 NA18969.hp1 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.535+224T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 6/6 | chr12 | 71782882 | |||||||
chr12:71782897 | A | G | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.535+239A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 6/6 | chr12 | 71782897 | |||||||
chr12:71782908 | T | C | 1 | a0001c0001t0008g0045 | 2 | HG02559.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.535+250T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 6/6 | chr12 | 71782908 | |||||||
chr12:71783033 | T | G | 1 | a0001c0002t0001g0066 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.535+375T>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 6/6 | chr12 | 71783033 | |||||||
chr12:71783282 | A | G | 63 | a0001c0001t0023g0025 a0001c0001t0023g0049 a0001c0001t0039g0026 others(60): Show |
101 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.535+624A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 6/6 | chr12 | 71783282 | |||||||
chr12:71783424 | C | T | 1 | a0001c0003t0090g0152 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.535+766C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 6/6 | chr12 | 71783424 | |||||||
chr12:71783461 | TACAC | T | 5 | a0001c0001t0033g0176 a0001c0001t0033g0178 a0001c0001t0094g0172 others(2): Show |
5 | HG02647.hp2 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.535+815_535+818del others(4): Show |
RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 71783461 | ||||||
chr12:71783616 | C | G | 36 | a0001c0001t0010g0006 a0001c0001t0010g0019 a0001c0001t0010g0048 others(33): Show |
46 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.535+958C>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 6/6 | chr12 | 71783616 | |||||||
chr12:71783631 | A | G | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.535+973A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 6/6 | chr12 | 71783631 | |||||||
chr12:71783667 | A | C | 1 | a0001c0001t0009g0133 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.535+1009A>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 6/6 | chr12 | 71783667 | |||||||
chr12:71783797 | AC | A | 2 | a0001c0002t0001g0020 a0001c0002t0014g0020 |
3 | NA18974.hp1 NA18982.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.535+1140delC | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 6/6 | chr12 | 71783797 | |||||||
chr12:71783814 | G | A | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.535+1156G>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 6/6 | chr12 | 71783814 | |||||||
chr12:71784236 | C | G | 7 | a0001c0001t0015g0154 a0001c0001t0015g0155 a0001c0001t0015g0156 others(4): Show |
8 | HG01069.hp1 HG01884.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.536-1295C>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 6/6 | chr12 | 71784236 | |||||||
chr12:71784362 | T | C | 28 | a0001c0001t0010g0006 a0001c0001t0010g0019 a0001c0001t0010g0048 others(25): Show |
34 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.536-1169T>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 6/6 | chr12 | 71784362 | |||||||
chr12:71784515 | A | AT | 43 | a0001c0001t0006g0061 a0001c0001t0010g0006 a0001c0001t0010g0019 others(40): Show |
54 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.536-1004dupT | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 71784515 | ||||||
chr12:71784707 | T | A | 1 | a0001c0003t0088g0148 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.536-824T>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 6/6 | chr12 | 71784707 | |||||||
chr12:71784719 | C | G | 1 | a0001c0001t0015g0157 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.536-812C>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 6/6 | chr12 | 71784719 | |||||||
chr12:71784825 | C | T | 1 | a0001c0002t0024g0079 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.536-706C>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 6/6 | chr12 | 71784825 | |||||||
chr12:71784844 | T | A | 1 | a0001c0001t0008g0166 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.536-687T>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 6/6 | chr12 | 71784844 | |||||||
chr12:71784930 | C | CA | 13 | a0001c0001t0002g0163 a0001c0001t0006g0007 a0001c0001t0006g0060 others(10): Show |
19 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.536-589dupA | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 71784930 | ||||||
chr12:71785145 | A | G | 1 | a0001c0002t0001g0078 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.536-386A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 6/6 | chr12 | 71785145 | |||||||
chr12:71785257 | T | A | 1 | a0001c0001t0002g0043 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.536-274T>A | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 6/6 | chr12 | 71785257 | |||||||
chr12:71785269 | A | G | 1 | a0001c0003t0090g0152 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.536-262A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 6/6 | chr12 | 71785269 | |||||||
chr12:71785274 | A | T | 4 | a0001c0001t0005g0005 a0001c0001t0005g0053 a0001c0001t0005g0055 others(1): Show |
13 | HG01243.hp2 HG02257.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.536-257A>T | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 6/6 | chr12 | 71785274 | |||||||
chr12:71785292 | A | G | 128 | a0001c0001t0005g0005 a0001c0001t0005g0053 a0001c0001t0005g0055 others(125): Show |
204 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.536-239A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 6/6 | chr12 | 71785292 | |||||||
chr12:71785378 | A | G | 1 | a0003c0005t0018g0016 | 4 | HG01891.hp1 HG02723.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.536-153A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 6/6 | chr12 | 71785378 | |||||||
chr12:71785387 | A | C | 4 | a0001c0001t0005g0005 a0001c0001t0005g0053 a0001c0001t0005g0055 others(1): Show |
13 | HG01243.hp2 HG02257.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.536-144A>C | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 6/6 | chr12 | 71785387 | |||||||
chr12:71785449 | A | G | 3 | a0001c0006t0127g0168 a0001c0006t0128g0169 a0001c0006t0129g0170 |
3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.536-82A>G | RAB21 | ENSG00000080371.6 | transcript | ENST00000261263.5 | protein_coding | 6/6 | chr12 | 71785449 |