Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g09900 | A01 | 4431721 | G | A | synonymous_variant | LOW | c.165G>A|p.Glu55Glu |
S241 |
2 | BAA01g09900 | A01 | 4432060 | C | T | splice_region_variant&intron_variant | LOW | c.339+7C>T| |
S218 |
3 | BAA01g09900 | A01 | 4433049 | G | A | missense_variant | MODERATE | c.674G>A|p.Cys225Tyr |
S10 |
4 | BAA01g09900 | A01 | 4433591 | G | A | missense_variant&splice_region_variant | MODERATE | c.890G>A|p.Gly297Asp |
S131 |
5 | BAA01g09900 | A01 | 4433602 | G | A | missense_variant | MODERATE | c.901G>A|p.Glu301Lys |
S239 |
6 | BAA01g09900 | A01 | 4434505 | G | A | missense_variant | MODERATE | c.1454G>A|p.Gly485Asp |
S139 |
7 | BAA01g09900 | A01 | 4434974 | C | T | missense_variant | MODERATE | c.1745C>T|p.Ala582Val |
S171 |
8 | BAA01g09900 | A01 | 4435645 | C | T | synonymous_variant | LOW | c.2175C>T|p.Gly725Gly |
S200 |
9 | BAA01g09900 | A01 | 4436258 | G | A | synonymous_variant | LOW | c.2511G>A|p.Gln837Gln |
S208 S219 |