Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g23660 | A09 | 15044906 | C | T | missense_variant | MODERATE | c.1187G>A|p.Gly396Glu |
S269 |
2 | BAA09g23660 | A09 | 15044980 | G | A | synonymous_variant | LOW | c.1113C>T|p.Ser371Ser |
S116 |
3 | BAA09g23660 | A09 | 15046566 | C | T | synonymous_variant | LOW | c.105G>A|p.Leu35Leu |
S107 |
4 | BAA09g23660 | A09 | 15047199 | G | A | upstream_gene_variant | MODIFIER | c.-529C>T| |
S1 S228 S90 |
5 | BAA09g23660 | A09 | 15047399 | G | A | upstream_gene_variant | MODIFIER | c.-729C>T| |
S240 |
6 | BAA09g23660 | A09 | 15047711 | C | T | upstream_gene_variant | MODIFIER | c.-1041G>A| |
S161 |
7 | BAA09g23660 | A09 | 15048324 | C | T | upstream_gene_variant | MODIFIER | c.-1654G>A| |
S174 S27 |
8 | BAA09g23660 | A09 | 15049011 | G | A | upstream_gene_variant | MODIFIER | c.-2341C>T| |
S217 |
9 | BAA09g23660 | A09 | 15051138 | C | T | upstream_gene_variant | MODIFIER | c.-4468G>A| |
S32 |