Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g07000 | A10 | 3792172 | G | A | missense_variant | MODERATE | c.733C>T|p.Pro245Ser |
S167 |
2 | BAA10g07000 | A10 | 3792378 | C | T | missense_variant | MODERATE | c.527G>A|p.Arg176Lys |
S84 S93 |
3 | BAA10g07000 | A10 | 3792597 | G | A | missense_variant | MODERATE | c.308C>T|p.Ala103Val |
S207 |
4 | BAA10g07000 | A10 | 3792772 | G | A | missense_variant | MODERATE | c.211C>T|p.Leu71Phe |
S158 |
5 | BAA10g07000 | A10 | 3792813 | G | A | missense_variant | MODERATE | c.170C>T|p.Thr57Ile |
S267 |
6 | BAA10g07000 | A10 | 3792839 | G | A | synonymous_variant | LOW | c.144C>T|p.Val48Val |
S221 |
7 | BAA10g07000 | A10 | 3795243 | C | T | upstream_gene_variant | MODIFIER | c.-2261G>A| |
S247 |