Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g26700 | A08 | 19007537 | G | A | missense_variant | MODERATE | c.1222G>A|p.Asp408Asn |
S211 S227 |
2 | BAA08g26700 | A08 | 19007665 | C | T | synonymous_variant | LOW | c.1350C>T|p.Leu450Leu |
S25 |
3 | BAA08g26700 | A08 | 19007736 | C | T | missense_variant | MODERATE | c.1421C>T|p.Ala474Val |
S71 |
4 | BAA08g26700 | A08 | 19007828 | G | A | missense_variant | MODERATE | c.1513G>A|p.Gly505Arg |
S286 |
5 | BAA08g26700 | A08 | 19009000 | C | T | synonymous_variant | LOW | c.2532C>T|p.Leu844Leu |
S176 |
6 | BAA08g26700 | A08 | 19009106 | G | A | missense_variant | MODERATE | c.2638G>A|p.Glu880Lys |
S32 |
7 | BAA08g26700 | A08 | 19010037 | G | A | missense_variant | MODERATE | c.3569G>A|p.Gly1190Asp |
S151 S263 |
8 | BAA08g26700 | A08 | 19010781 | G | A | downstream_gene_variant | MODIFIER | c.*66G>A| |
S37 |
9 | BAA08g26700 | A08 | 19011012 | G | A | downstream_gene_variant | MODIFIER | c.*297G>A| |
S218 |
10 | BAA08g26700 | A08 | 19011419 | C | T | downstream_gene_variant | MODIFIER | c.*704C>T| |
S299 |