Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g29240 | A10 | 22086740 | C | T | missense_variant | MODERATE | c.1498G>A|p.Ala500Thr |
S176 |
2 | BAA10g29240 | A10 | 22086925 | C | T | missense_variant | MODERATE | c.1313G>A|p.Ser438Asn |
S2 |
3 | BAA10g29240 | A10 | 22086954 | C | T | missense_variant | MODERATE | c.1284G>A|p.Met428Ile |
S105 |
4 | BAA10g29240 | A10 | 22087150 | G | A | missense_variant | MODERATE | c.1088C>T|p.Thr363Met |
S43 |
5 | BAA10g29240 | A10 | 22087231 | G | A | missense_variant | MODERATE | c.1007C>T|p.Ala336Val |
S289 S290 |
6 | BAA10g29240 | A10 | 22087311 | C | T | synonymous_variant | LOW | c.927G>A|p.Arg309Arg |
S206 S26 |
7 | BAA10g29240 | A10 | 22087711 | C | T | missense_variant | MODERATE | c.627G>A|p.Met209Ile |
S301 S304 |
8 | BAA10g29240 | A10 | 22087810 | C | T | synonymous_variant | LOW | c.528G>A|p.Lys176Lys |
S196 |
9 | BAA10g29240 | A10 | 22092089 | C | T | upstream_gene_variant | MODIFIER | c.-3488G>A| |
S133 |