Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g00910 | A05 | 549400 | G | A | upstream_gene_variant | MODIFIER | c.-4902G>A| |
S274 |
2 | BAA05g00910 | A05 | 549651 | G | A | upstream_gene_variant | MODIFIER | c.-4651G>A| |
S305 |
3 | BAA05g00910 | A05 | 554484 | C | T | synonymous_variant | LOW | c.183C>T|p.Asp61Asp |
S128 |
4 | BAA05g00910 | A05 | 554578 | G | A | missense_variant | MODERATE | c.277G>A|p.Gly93Ser |
S25 |
5 | BAA05g00910 | A05 | 555993 | G | A | synonymous_variant | LOW | c.1692G>A|p.Ala564Ala |
S277 |
6 | BAA05g00910 | A05 | 556008 | C | T | synonymous_variant | LOW | c.1707C>T|p.Cys569Cys |
S221 |
7 | BAA05g00910 | A05 | 556266 | C | T | synonymous_variant | LOW | c.1965C>T|p.Tyr655Tyr |
S38 |
8 | BAA05g00910 | A05 | 556418 | G | A | missense_variant | MODERATE | c.2053G>A|p.Glu685Lys |
S241 |
9 | BAA05g00910 | A05 | 556431 | C | T | missense_variant | MODERATE | c.2066C>T|p.Ser689Phe |
S263 |
10 | BAA05g00910 | A05 | 556579 | C | T | missense_variant&splice_region_variant | MODERATE | c.2137C>T|p.Pro713Ser |
S19 |
11 | BAA05g00910 | A05 | 558375 | C | T | downstream_gene_variant | MODIFIER | c.*1291C>T| |
S161 |
12 | BAA05g00910 | A05 | 560178 | C | T | downstream_gene_variant | MODIFIER | c.*3094C>T| |
S280 |