Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g00910 | A10 | 421911 | C | T | synonymous_variant | LOW | c.1767G>A|p.Glu589Glu |
S287 |
2 | BAA10g00910 | A10 | 422153 | G | A | missense_variant | MODERATE | c.1525C>T|p.Pro509Ser |
S267 |
3 | BAA10g00910 | A10 | 422864 | G | A | missense_variant | MODERATE | c.961C>T|p.Pro321Ser |
S99 |
4 | BAA10g00910 | A10 | 423105 | G | A | synonymous_variant | LOW | c.720C>T|p.Asp240Asp |
S219 S72 |
5 | BAA10g00910 | A10 | 423133 | C | T | missense_variant | MODERATE | c.692G>A|p.Gly231Glu |
S177 |
6 | BAA10g00910 | A10 | 423378 | C | T | synonymous_variant | LOW | c.447G>A|p.Glu149Glu |
S233 |
7 | BAA10g00910 | A10 | 423396 | C | T | synonymous_variant | LOW | c.429G>A|p.Gln143Gln |
S260 |
8 | BAA10g00910 | A10 | 423936 | G | A | missense_variant | MODERATE | c.43C>T|p.Leu15Phe |
S2 |
9 | BAA10g00910 | A10 | 425572 | C | T | upstream_gene_variant | MODIFIER | c.-1594G>A| |
S298 |