Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g31080 | A08 | 20791498 | G | A | missense_variant | MODERATE | c.352C>T|p.Pro118Ser |
S124 |
2 | BAA08g31080 | A08 | 20791524 | G | A | missense_variant | MODERATE | c.326C>T|p.Ser109Phe |
S272 |
3 | BAA08g31080 | A08 | 20791547 | T | G | synonymous_variant | LOW | c.303A>C|p.Leu101Leu |
S220 |
4 | BAA08g31080 | A08 | 20791559 | G | A | synonymous_variant | LOW | c.291C>T|p.Ala97Ala |
S220 |
5 | BAA08g31080 | A08 | 20791688 | C | T | synonymous_variant | LOW | c.162G>A|p.Ala54Ala |
S201 S213 S220 S226 |
6 | BAA08g31080 | A08 | 20791706 | G | A | synonymous_variant | LOW | c.144C>T|p.Ala48Ala |
S201 S213 S226 |
7 | BAA08g31080 | A08 | 20791724 | A | T | synonymous_variant | LOW | c.126T>A|p.Ala42Ala |
S201 S213 |
8 | BAA08g31080 | A08 | 20791738 | A | C | missense_variant | MODERATE | c.112T>G|p.Ser38Ala |
S201 |
9 | BAA08g31080 | A08 | 20794441 | C | T | upstream_gene_variant | MODIFIER | c.-2592G>A| |
S132 S137 S138 S89 |
10 | BAA08g31080 | A08 | 20795167 | G | A | upstream_gene_variant | MODIFIER | c.-3318C>T| |
S64 |