Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g09490 | A02 | 4177261 | G | A | synonymous_variant | LOW | c.1212C>T|p.Cys404Cys |
S275 |
2 | BAA02g09490 | A02 | 4177859 | C | T | missense_variant&splice_region_variant | MODERATE | c.916G>A|p.Glu306Lys |
S90 |
3 | BAA02g09490 | A02 | 4178072 | G | A | splice_region_variant&intron_variant | LOW | c.915+7C>T| |
S235 |
4 | BAA02g09490 | A02 | 4179651 | T | C | missense_variant | MODERATE | c.448A>G|p.Ser150Gly |
S290 |
5 | BAA02g09490 | A02 | 4181148 | G | A | upstream_gene_variant | MODIFIER | c.-533C>T| |
S4 |
6 | BAA02g09490 | A02 | 4181894 | C | T | upstream_gene_variant | MODIFIER | c.-1279G>A| |
S270 |
7 | BAA02g09490 | A02 | 4182345 | G | A | upstream_gene_variant | MODIFIER | c.-1730C>T| |
S276 |
8 | BAA02g09490 | A02 | 4182621 | C | T | upstream_gene_variant | MODIFIER | c.-2006G>A| |
S278 |
9 | BAA02g09490 | A02 | 4183915 | C | T | upstream_gene_variant | MODIFIER | c.-3300G>A| |
S13 |
10 | BAA02g09490 | A02 | 4184280 | G | A | upstream_gene_variant | MODIFIER | c.-3665C>T| |
S69 |