Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g69840 | A09 | 62168112 | C | T | synonymous_variant | LOW | c.855C>T|p.Ser285Ser |
S211 S227 |
2 | BAA09g69840 | A09 | 62168437 | C | T | missense_variant | MODERATE | c.1094C>T|p.Thr365Ile |
S2 |
3 | BAA09g69840 | A09 | 62170565 | G | A | missense_variant | MODERATE | c.2291G>A|p.Gly764Asp |
S247 |
4 | BAA09g69840 | A09 | 62170772 | G | A | missense_variant&splice_region_variant | MODERATE | c.2407G>A|p.Val803Met |
S167 |
5 | BAA09g69840 | A09 | 62174429 | C | T | downstream_gene_variant | MODIFIER | c.*3273C>T| |
S283 |
6 | BAA09g69840 | A09 | 62174448 | G | A | downstream_gene_variant | MODIFIER | c.*3292G>A| |
S12 |