Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g01950 | A10 | 930475 | G | T | missense_variant | MODERATE | c.2420C>A|p.Ser807Tyr |
S1 S107 S251 S258 S264 S37 S47 S48 S97 |
2 | BAA10g01950 | A10 | 930663 | C | T | synonymous_variant | LOW | c.2232G>A|p.Pro744Pro |
S206 S26 |
3 | BAA10g01950 | A10 | 930695 | C | T | missense_variant | MODERATE | c.2200G>A|p.Val734Met |
S87 |
4 | BAA10g01950 | A10 | 930777 | G | A | synonymous_variant | LOW | c.2118C>T|p.Phe706Phe |
S192 |
5 | BAA10g01950 | A10 | 930828 | C | T | synonymous_variant | LOW | c.2067G>A|p.Thr689Thr |
S263 |
6 | BAA10g01950 | A10 | 931759 | G | A | missense_variant | MODERATE | c.1235C>T|p.Ala412Val |
S33 |
7 | BAA10g01950 | A10 | 932026 | G | A | missense_variant | MODERATE | c.968C>T|p.Thr323Ile |
S107 |
8 | BAA10g01950 | A10 | 932725 | G | A | missense_variant | MODERATE | c.610C>T|p.Pro204Ser |
S118 |
9 | BAA10g01950 | A10 | 935091 | C | T | upstream_gene_variant | MODIFIER | c.-1067G>A| |
S182 |