Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g31470 | A02 | 18913675 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.289-1G>A| |
S144 |
2 | BAA02g31470 | A02 | 18915507 | G | A | missense_variant | MODERATE | c.994G>A|p.Glu332Lys |
S229 |
3 | BAA02g31470 | A02 | 18918193 | C | A | intron_variant | MODIFIER | c.1300+1635C>A| |
S182 |
4 | BAA02g31470 | A02 | 18918982 | C | T | intron_variant | MODIFIER | c.1301-1039C>T| |
S92 |
5 | BAA02g31470 | A02 | 18919061 | C | T | intron_variant | MODIFIER | c.1301-960C>T| |
S284 |
6 | BAA02g31470 | A02 | 18919149 | C | T | intron_variant | MODIFIER | c.1301-872C>T| |
S107 |
7 | BAA02g31470 | A02 | 18919894 | C | T | intron_variant | MODIFIER | c.1301-127C>T| |
S122 |
8 | BAA02g31470 | A02 | 18920299 | G | A | missense_variant | MODERATE | c.1579G>A|p.Glu527Lys |
S126 |
9 | BAA02g31470 | A02 | 18920767 | C | T | missense_variant | MODERATE | c.2047C>T|p.Pro683Ser |
S112 |
10 | BAA02g31470 | A02 | 18920859 | C | T | synonymous_variant | LOW | c.2139C>T|p.Phe713Phe |
S164 |
11 | BAA02g31470 | A02 | 18921198 | C | T | synonymous_variant | LOW | c.2397C>T|p.Arg799Arg |
S224 |
12 | BAA02g31470 | A02 | 18921709 | C | T | missense_variant | MODERATE | c.2872C>T|p.Pro958Ser |
S140 |
13 | BAA02g31470 | A02 | 18921872 | G | A | missense_variant&splice_region_variant | MODERATE | c.3035G>A|p.Arg1012Gln |
S125 |
14 | BAA02g31470 | A02 | 18927411 | G | A | downstream_gene_variant | MODIFIER | c.*1475G>A| |
S72 S78 |
15 | BAA02g31470 | A02 | 18927581 | G | A | downstream_gene_variant | MODIFIER | c.*1645G>A| |
S136 |
16 | BAA02g31470 | A02 | 18927599 | G | A | downstream_gene_variant | MODIFIER | c.*1663G>A| |
S230 |
17 | BAA02g31470 | A02 | 18929444 | C | T | downstream_gene_variant | MODIFIER | c.*3508C>T| |
S138 |