Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g14510 | A10 | 15181672 | C | T | missense_variant | MODERATE | c.634G>A|p.Val212Met |
S28 |
2 | BAA10g14510 | A10 | 15181760 | G | A | synonymous_variant | LOW | c.546C>T|p.Ile182Ile |
S295 |
3 | BAA10g14510 | A10 | 15182071 | G | A | missense_variant | MODERATE | c.325C>T|p.Leu109Phe |
S148 S30 S31 |
4 | BAA10g14510 | A10 | 15182256 | G | A | missense_variant | MODERATE | c.140C>T|p.Ala47Val |
S203 |
5 | BAA10g14510 | A10 | 15184416 | G | A | upstream_gene_variant | MODIFIER | c.-2021C>T| |
S18 |
6 | BAA10g14510 | A10 | 15185892 | C | T | upstream_gene_variant | MODIFIER | c.-3497G>A| |
S28 |
7 | BAA10g14510 | A10 | 15186488 | G | A | upstream_gene_variant | MODIFIER | c.-4093C>T| |
S80 |