Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g06460 | A09 | 3608092 | C | T | missense_variant | MODERATE | c.485C>T|p.Pro162Leu |
S13 |
2 | BAA09g06460 | A09 | 3609084 | G | A | missense_variant&splice_region_variant | MODERATE | c.838G>A|p.Glu280Lys |
S245 |
3 | BAA09g06460 | A09 | 3610407 | G | A | missense_variant&splice_region_variant | MODERATE | c.1417G>A|p.Glu473Lys |
S283 |
4 | BAA09g06460 | A09 | 3611833 | C | T | missense_variant | MODERATE | c.2426C>T|p.Ser809Phe |
S51 |
5 | BAA09g06460 | A09 | 3615026 | C | T | downstream_gene_variant | MODIFIER | c.*2648C>T| |
S261 |
6 | BAA09g06460 | A09 | 3615349 | C | T | downstream_gene_variant | MODIFIER | c.*2971C>T| |
S138 |
7 | BAA09g06460 | A09 | 3615643 | C | T | downstream_gene_variant | MODIFIER | c.*3265C>T| |
S104 S52 |
8 | BAA09g06460 | A09 | 3616244 | C | T | downstream_gene_variant | MODIFIER | c.*3866C>T| |
S119 |
9 | BAA09g06460 | A09 | 3616526 | C | T | downstream_gene_variant | MODIFIER | c.*4148C>T| |
S85 |