Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g40890 | A01 | 27071963 | G | A | missense_variant | MODERATE | c.106G>A|p.Asp36Asn |
S42 |
2 | BAA01g40890 | A01 | 27073160 | G | A | missense_variant | MODERATE | c.1009G>A|p.Glu337Lys |
S187 |
3 | BAA01g40890 | A01 | 27073330 | T | C | synonymous_variant | LOW | c.1179T>C|p.Pro393Pro |
S88 |
4 | BAA01g40890 | A01 | 27073600 | G | A | missense_variant | MODERATE | c.1363G>A|p.Glu455Lys |
S108 |
5 | BAA01g40890 | A01 | 27073630 | C | T | missense_variant | MODERATE | c.1393C>T|p.Pro465Ser |
S136 |
6 | BAA01g40890 | A01 | 27073719 | G | A | synonymous_variant | LOW | c.1482G>A|p.Arg494Arg |
S308 |
7 | BAA01g40890 | A01 | 27074373 | G | A | missense_variant&splice_region_variant | MODERATE | c.1612G>A|p.Asp538Asn |
S221 |
8 | BAA01g40890 | A01 | 27074445 | G | A | missense_variant | MODERATE | c.1684G>A|p.Glu562Lys |
S177 |