Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g04960 | A03 | 2089255 | C | T | missense_variant | MODERATE | c.253C>T|p.Leu85Phe |
S180 |
2 | BAA03g04960 | A03 | 2091215 | G | A | missense_variant | MODERATE | c.1573G>A|p.Gly525Arg |
S282 |
3 | BAA03g04960 | A03 | 2091716 | G | A | missense_variant | MODERATE | c.1870G>A|p.Glu624Lys |
S246 |
4 | BAA03g04960 | A03 | 2092078 | G | A | splice_region_variant&synonymous_variant | LOW | c.2232G>A|p.Gln744Gln |
S95 |
5 | BAA03g04960 | A03 | 2092174 | G | A | synonymous_variant | LOW | c.2244G>A|p.Val748Val |
S132 S137 S89 |
6 | BAA03g04960 | A03 | 2092319 | G | A | missense_variant | MODERATE | c.2389G>A|p.Asp797Asn |
S206 S26 |
7 | BAA03g04960 | A03 | 2092404 | C | T | missense_variant | MODERATE | c.2474C>T|p.Ala825Val |
S46 |
8 | BAA03g04960 | A03 | 2093281 | G | A | downstream_gene_variant | MODIFIER | c.*828G>A| |
S261 |
9 | BAA03g04960 | A03 | 2093680 | G | A | downstream_gene_variant | MODIFIER | c.*1227G>A| |
S283 |