Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g05980 | A01 | 2682450 | C | T | missense_variant | MODERATE | c.77C>T|p.Pro26Leu |
S4 |
2 | BAA01g05980 | A01 | 2682556 | G | A | synonymous_variant | LOW | c.183G>A|p.Ala61Ala |
S281 |
3 | BAA01g05980 | A01 | 2683102 | C | T | missense_variant | MODERATE | c.560C>T|p.Ala187Val |
S267 |
4 | BAA01g05980 | A01 | 2683218 | G | A | missense_variant | MODERATE | c.595G>A|p.Asp199Asn |
S156 |
5 | BAA01g05980 | A01 | 2683935 | C | T | stop_gained&splice_region_variant | HIGH | c.1045C>T|p.Gln349* |
S265 |
6 | BAA01g05980 | A01 | 2684083 | G | A | synonymous_variant | LOW | c.1104G>A|p.Gln368Gln |
S116 |