Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g36450 | A01 | 24413750 | G | A | missense_variant | MODERATE | c.2045C>T|p.Ala682Val |
S185 |
2 | BAA01g36450 | A01 | 24414013 | C | T | missense_variant | MODERATE | c.1879G>A|p.Val627Ile |
S136 |
3 | BAA01g36450 | A01 | 24415672 | C | T | missense_variant | MODERATE | c.865G>A|p.Val289Met |
S192 |
4 | BAA01g36450 | A01 | 24416094 | C | T | missense_variant | MODERATE | c.748G>A|p.Glu250Lys |
S303 |
5 | BAA01g36450 | A01 | 24416199 | C | T | missense_variant | MODERATE | c.643G>A|p.Glu215Lys |
S234 |
6 | BAA01g36450 | A01 | 24416290 | C | T | synonymous_variant | LOW | c.552G>A|p.Lys184Lys |
S75 S81 |
7 | BAA01g36450 | A01 | 24417025 | C | T | upstream_gene_variant | MODIFIER | c.-184G>A| |
S266 |
8 | BAA01g36450 | A01 | 24417545 | C | T | upstream_gene_variant | MODIFIER | c.-704G>A| |
S213 |
9 | BAA01g36450 | A01 | 24420440 | C | T | upstream_gene_variant | MODIFIER | c.-3599G>A| |
S4 |