Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g05260 | A01 | 2309132 | G | A | missense_variant | MODERATE | c.277G>A|p.Val93Ile |
S17 |
2 | BAA01g05260 | A01 | 2309423 | C | T | missense_variant | MODERATE | c.482C>T|p.Thr161Ile |
S211 S227 |
3 | BAA01g05260 | A01 | 2309803 | C | T | synonymous_variant | LOW | c.774C>T|p.Arg258Arg |
S58 |
4 | BAA01g05260 | A01 | 2310311 | C | T | missense_variant | MODERATE | c.1124C>T|p.Pro375Leu |
S195 |
5 | BAA01g05260 | A01 | 2310680 | C | T | missense_variant | MODERATE | c.1493C>T|p.Ser498Leu |
S155 S211 |
6 | BAA01g05260 | A01 | 2311245 | G | A | missense_variant | MODERATE | c.1861G>A|p.Ala621Thr |
S288 |
7 | BAA01g05260 | A01 | 2311267 | G | A | missense_variant | MODERATE | c.1883G>A|p.Ser628Asn |
S15 S3 |
8 | BAA01g05260 | A01 | 2311379 | G | A | synonymous_variant | LOW | c.1995G>A|p.Glu665Glu |
S247 |