Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g12500 | A10 | 13893481 | C | T | missense_variant | MODERATE | c.1516G>A|p.Ala506Thr |
S96 |
2 | BAA10g12500 | A10 | 13894014 | G | A | missense_variant | MODERATE | c.1069C>T|p.Pro357Ser |
S181 |
3 | BAA10g12500 | A10 | 13894047 | G | A | missense_variant | MODERATE | c.1036C>T|p.Pro346Ser |
S105 S106 |
4 | BAA10g12500 | A10 | 13894297 | G | A | synonymous_variant | LOW | c.786C>T|p.Tyr262Tyr |
S68 |
5 | BAA10g12500 | A10 | 13894800 | C | T | missense_variant | MODERATE | c.374G>A|p.Arg125Lys |
S34 |
6 | BAA10g12500 | A10 | 13895120 | C | T | missense_variant | MODERATE | c.133G>A|p.Gly45Arg |
S84 S93 |
7 | BAA10g12500 | A10 | 13897328 | G | A | upstream_gene_variant | MODIFIER | c.-2076C>T| |
S139 |
8 | BAA10g12500 | A10 | 13898037 | G | A | upstream_gene_variant | MODIFIER | c.-2785C>T| |
S128 |