Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g57930 | A09 | 56941566 | G | A | missense_variant | MODERATE | c.1940C>T|p.Ala647Val |
S255 |
2 | BAA09g57930 | A09 | 56941868 | G | A | synonymous_variant | LOW | c.1719C>T|p.Asn573Asn |
S65 |
3 | BAA09g57930 | A09 | 56941909 | G | A | missense_variant | MODERATE | c.1678C>T|p.Arg560Trp |
S54 |
4 | BAA09g57930 | A09 | 56942380 | C | T | missense_variant | MODERATE | c.1496G>A|p.Arg499Gln |
S77 S82 |
5 | BAA09g57930 | A09 | 56942588 | C | T | missense_variant | MODERATE | c.1381G>A|p.Val461Ile |
S120 |
6 | BAA09g57930 | A09 | 56943190 | G | A | missense_variant | MODERATE | c.1018C>T|p.Leu340Phe |
S39 |
7 | BAA09g57930 | A09 | 56943885 | G | A | missense_variant | MODERATE | c.476C>T|p.Ala159Val |
S46 |
8 | BAA09g57930 | A09 | 56943929 | G | A | synonymous_variant | LOW | c.432C>T|p.Phe144Phe |
S177 |
9 | BAA09g57930 | A09 | 56944716 | A | C | upstream_gene_variant | MODIFIER | c.-356T>G| |
S217 S248 |
10 | BAA09g57930 | A09 | 56947259 | G | A | upstream_gene_variant | MODIFIER | c.-2899C>T| |
S73 S91 |
11 | BAA09g57930 | A09 | 56947329 | C | A | upstream_gene_variant | MODIFIER | c.-2969G>T| |
S151 |