Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g14380 | A02 | 6725619 | G | A | missense_variant | MODERATE | c.238G>A|p.Glu80Lys |
S148 |
2 | BAA02g14380 | A02 | 6725767 | C | T | missense_variant | MODERATE | c.386C>T|p.Ser129Phe |
S212 |
3 | BAA02g14380 | A02 | 6727535 | C | T | synonymous_variant | LOW | c.1038C>T|p.Cys346Cys |
S183 S198 |
4 | BAA02g14380 | A02 | 6727784 | G | A | missense_variant | MODERATE | c.1208G>A|p.Gly403Asp |
S308 |
5 | BAA02g14380 | A02 | 6728460 | G | A | missense_variant | MODERATE | c.1795G>A|p.Asp599Asn |
S190 |
6 | BAA02g14380 | A02 | 6730194 | G | A | missense_variant | MODERATE | c.2539G>A|p.Glu847Lys |
S67 |
7 | BAA02g14380 | A02 | 6730339 | G | A | missense_variant | MODERATE | c.2582G>A|p.Gly861Glu |
S303 |
8 | BAA02g14380 | A02 | 6730751 | G | A | synonymous_variant | LOW | c.2994G>A|p.Arg998Arg |
S168 |
9 | BAA02g14380 | A02 | 6730856 | C | A | synonymous_variant | LOW | c.3099C>A|p.Ser1033Ser |
S279 |
10 | BAA02g14380 | A02 | 6731199 | C | T | missense_variant | MODERATE | c.3442C>T|p.His1148Tyr |
S130 |
11 | BAA02g14380 | A02 | 6731273 | G | A | synonymous_variant | LOW | c.3516G>A|p.Pro1172Pro |
S153 S213 |