Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g18990 | A08 | 15057007 | C | T | missense_variant | MODERATE | c.1228G>A|p.Glu410Lys |
S236 |
2 | BAA08g18990 | A08 | 15057597 | G | A | synonymous_variant | LOW | c.990C>T|p.Leu330Leu |
S153 |
3 | BAA08g18990 | A08 | 15057612 | G | A | synonymous_variant | LOW | c.975C>T|p.Ala325Ala |
S292 |
4 | BAA08g18990 | A08 | 15057620 | C | T | missense_variant&splice_region_variant | MODERATE | c.967G>A|p.Asp323Asn |
S44 |
5 | BAA08g18990 | A08 | 15059872 | G | A | synonymous_variant | LOW | c.645C>T|p.Val215Val |
S103 |
6 | BAA08g18990 | A08 | 15060006 | G | A | synonymous_variant | LOW | c.511C>T|p.Leu171Leu |
S72 S78 |
7 | BAA08g18990 | A08 | 15060251 | G | A | missense_variant | MODERATE | c.266C>T|p.Ser89Leu |
S162 |
8 | BAA08g18990 | A08 | 15060653 | G | A | missense_variant | MODERATE | c.32C>T|p.Ala11Val |
S297 |
9 | BAA08g18990 | A08 | 15060819 | C | T | upstream_gene_variant | MODIFIER | c.-135G>A| |
S134 |
10 | BAA08g18990 | A08 | 15061312 | C | T | upstream_gene_variant | MODIFIER | c.-628G>A| |
S192 |
11 | BAA08g18990 | A08 | 15065084 | G | A | upstream_gene_variant | MODIFIER | c.-4400C>T| |
S133 |