Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g01400 | A06 | 894033 | G | A | missense_variant | MODERATE | c.3154C>T|p.Arg1052Cys |
S139 |
2 | BAA06g01400 | A06 | 895183 | C | T | missense_variant | MODERATE | c.2314G>A|p.Ala772Thr |
S53 |
3 | BAA06g01400 | A06 | 895662 | C | T | missense_variant | MODERATE | c.1906G>A|p.Glu636Lys |
S183 S198 |
4 | BAA06g01400 | A06 | 900291 | C | T | upstream_gene_variant | MODIFIER | c.-1678G>A| |
S94 |
5 | BAA06g01400 | A06 | 900526 | G | A | upstream_gene_variant | MODIFIER | c.-1913C>T| |
S187 |
6 | BAA06g01400 | A06 | 901575 | G | A | upstream_gene_variant | MODIFIER | c.-2962C>T| |
S169 |
7 | BAA06g01400 | A06 | 901585 | G | A | upstream_gene_variant | MODIFIER | c.-2972C>T| |
S45 |