Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g46020 | A06 | 29291984 | G | A | missense_variant | MODERATE | c.3091C>T|p.Leu1031Phe |
S247 |
2 | BAA06g46020 | A06 | 29292103 | G | A | missense_variant | MODERATE | c.2972C>T|p.Pro991Leu |
S173 |
3 | BAA06g46020 | A06 | 29292599 | C | T | missense_variant | MODERATE | c.2476G>A|p.Ala826Thr |
S149 |
4 | BAA06g46020 | A06 | 29292680 | G | A | missense_variant | MODERATE | c.2395C>T|p.Pro799Ser |
S33 |
5 | BAA06g46020 | A06 | 29293389 | T | G | synonymous_variant | LOW | c.1686A>C|p.Ile562Ile |
S33 |
6 | BAA06g46020 | A06 | 29293924 | G | A | missense_variant | MODERATE | c.1151C>T|p.Ser384Leu |
S237 |
7 | BAA06g46020 | A06 | 29294863 | G | A | missense_variant | MODERATE | c.332C>T|p.Ala111Val |
S117 |
8 | BAA06g46020 | A06 | 29296862 | C | T | upstream_gene_variant | MODIFIER | c.-1238G>A| |
S279 |