Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g01270 | A09 | 928593 | G | A | missense_variant&splice_region_variant | MODERATE | c.211G>A|p.Val71Ile |
S23 |
2 | BAA09g01270 | A09 | 929477 | T | A | synonymous_variant | LOW | c.744T>A|p.Ala248Ala |
S91 |
3 | BAA09g01270 | A09 | 929481 | A | G | missense_variant | MODERATE | c.748A>G|p.Ile250Val |
S91 |
4 | BAA09g01270 | A09 | 929486 | C | T | synonymous_variant | LOW | c.753C>T|p.Tyr251Tyr |
S91 |
5 | BAA09g01270 | A09 | 929510 | G | T | synonymous_variant | LOW | c.777G>T|p.Ser259Ser |
S91 |
6 | BAA09g01270 | A09 | 929513 | C | T | synonymous_variant | LOW | c.780C>T|p.Phe260Phe |
S91 |
7 | BAA09g01270 | A09 | 929516 | A | C | synonymous_variant | LOW | c.783A>C|p.Thr261Thr |
S91 |