Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g21190 | A09 | 13213197 | C | T | missense_variant | MODERATE | c.1570C>T|p.Leu524Phe |
S177 |
2 | BAA09g21190 | A09 | 13213321 | C | T | missense_variant | MODERATE | c.1694C>T|p.Pro565Leu |
S143 |
3 | BAA09g21190 | A09 | 13214534 | C | T | synonymous_variant | LOW | c.2907C>T|p.Ile969Ile |
S183 |
4 | BAA09g21190 | A09 | 13214770 | G | A | missense_variant | MODERATE | c.3143G>A|p.Ser1048Asn |
S55 |
5 | BAA09g21190 | A09 | 13216849 | G | A | downstream_gene_variant | MODIFIER | c.*2012G>A| |
S33 |