Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g46230 | A01 | 30861425 | C | T | missense_variant | MODERATE | c.37C>T|p.Leu13Phe |
S174 |
2 | BAA01g46230 | A01 | 30861716 | C | T | missense_variant | MODERATE | c.77C>T|p.Ser26Leu |
S303 |
3 | BAA01g46230 | A01 | 30864237 | C | T | synonymous_variant | LOW | c.1326C>T|p.Val442Val |
S216 |
4 | BAA01g46230 | A01 | 30864502 | G | A | missense_variant | MODERATE | c.1411G>A|p.Gly471Arg |
S172 |
5 | BAA01g46230 | A01 | 30865716 | G | A | downstream_gene_variant | MODIFIER | c.*1113G>A| |
S185 |
6 | BAA01g46230 | A01 | 30865975 | C | T | downstream_gene_variant | MODIFIER | c.*1372C>T| |
S37 |
7 | BAA01g46230 | A01 | 30868407 | C | T | downstream_gene_variant | MODIFIER | c.*3804C>T| |
S134 |
8 | BAA01g46230 | A01 | 30868998 | G | A | downstream_gene_variant | MODIFIER | c.*4395G>A| |
S173 |