Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g45650 | A06 | 29092292 | C | T | missense_variant | MODERATE | c.569C>T|p.Pro190Leu |
S252 |
2 | BAA06g45650 | A06 | 29093304 | C | T | synonymous_variant | LOW | c.765C>T|p.Gly255Gly |
S257 |
3 | BAA06g45650 | A06 | 29096093 | C | T | downstream_gene_variant | MODIFIER | c.*245C>T| |
S293 |