Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g11860 | A08 | 10456916 | C | T | missense_variant | MODERATE | c.604C>T|p.Leu202Phe |
S132 S137 S89 |
2 | BAA08g11860 | A08 | 10457490 | A | C | splice_acceptor_variant&intron_variant | HIGH | c.925-2A>C| |
S94 |
3 | BAA08g11860 | A08 | 10457677 | G | A | synonymous_variant | LOW | c.1110G>A|p.Lys370Lys |
S72 |
4 | BAA08g11860 | A08 | 10458123 | G | A | synonymous_variant | LOW | c.1272G>A|p.Lys424Lys |
S255 |
5 | BAA08g11860 | A08 | 10458144 | G | A | synonymous_variant | LOW | c.1293G>A|p.Ala431Ala |
S11 |
6 | BAA08g11860 | A08 | 10458412 | G | A | missense_variant | MODERATE | c.1561G>A|p.Asp521Asn |
S297 |