Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g16030 | A08 | 13393604 | G | A | synonymous_variant | LOW | c.186G>A|p.Ala62Ala |
S146 |
2 | BAA08g16030 | A08 | 13394384 | C | T | missense_variant | MODERATE | c.694C>T|p.Pro232Ser |
S148 S210 S31 |
3 | BAA08g16030 | A08 | 13395102 | C | T | missense_variant&splice_region_variant | MODERATE | c.1139C>T|p.Thr380Met |
S296 |
4 | BAA08g16030 | A08 | 13395452 | C | T | missense_variant | MODERATE | c.1286C>T|p.Ala429Val |
S1 S90 |
5 | BAA08g16030 | A08 | 13398272 | G | A | downstream_gene_variant | MODIFIER | c.*2448G>A| |
S218 S268 S269 |
6 | BAA08g16030 | A08 | 13398749 | G | A | downstream_gene_variant | MODIFIER | c.*2925G>A| |
S100 |
7 | BAA08g16030 | A08 | 13398937 | G | A | downstream_gene_variant | MODIFIER | c.*3113G>A| |
S125 |
8 | BAA08g16030 | A08 | 13399626 | C | T | downstream_gene_variant | MODIFIER | c.*3802C>T| |
S135 |