Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g40290 | A06 | 26203289 | C | T | missense_variant | MODERATE | c.1388G>A|p.Gly463Asp |
S18 |
2 | BAA06g40290 | A06 | 26203420 | C | T | synonymous_variant | LOW | c.1257G>A|p.Val419Val |
S272 |
3 | BAA06g40290 | A06 | 26203638 | C | T | missense_variant | MODERATE | c.1132G>A|p.Val378Ile |
S262 |
4 | BAA06g40290 | A06 | 26204072 | G | A | synonymous_variant | LOW | c.804C>T|p.Leu268Leu |
S246 |
5 | BAA06g40290 | A06 | 26204794 | G | A | synonymous_variant | LOW | c.768C>T|p.Tyr256Tyr |
S151 |
6 | BAA06g40290 | A06 | 26204802 | G | A | missense_variant | MODERATE | c.760C>T|p.Leu254Phe |
S219 S72 |
7 | BAA06g40290 | A06 | 26204805 | C | T | missense_variant | MODERATE | c.757G>A|p.Glu253Lys |
S109 |
8 | BAA06g40290 | A06 | 26206397 | C | T | upstream_gene_variant | MODIFIER | c.-294G>A| |
S132 S137 S89 |
9 | BAA06g40290 | A06 | 26206618 | G | A | upstream_gene_variant | MODIFIER | c.-515C>T| |
S295 |
10 | BAA06g40290 | A06 | 26206991 | G | A | upstream_gene_variant | MODIFIER | c.-888C>T| |
S208 S219 |
11 | BAA06g40290 | A06 | 26209525 | G | A | upstream_gene_variant | MODIFIER | c.-3422C>T| |
S199 |