Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g01200 | A08 | 857316 | G | A | synonymous_variant | LOW | c.813C>T|p.Phe271Phe |
S97 |
2 | BAA08g01200 | A08 | 857369 | C | T | missense_variant | MODERATE | c.760G>A|p.Glu254Lys |
S167 |
3 | BAA08g01200 | A08 | 857651 | C | T | missense_variant | MODERATE | c.478G>A|p.Glu160Lys |
S245 |
4 | BAA08g01200 | A08 | 857712 | C | T | synonymous_variant | LOW | c.417G>A|p.Lys139Lys |
S189 |
5 | BAA08g01200 | A08 | 857780 | C | T | missense_variant | MODERATE | c.349G>A|p.Gly117Arg |
S148 S30 S31 |
6 | BAA08g01200 | A08 | 857840 | C | T | missense_variant | MODERATE | c.289G>A|p.Glu97Lys |
S275 |
7 | BAA08g01200 | A08 | 858113 | C | T | missense_variant | MODERATE | c.16G>A|p.Glu6Lys |
S80 |
8 | BAA08g01200 | A08 | 859143 | G | A | upstream_gene_variant | MODIFIER | c.-1015C>T| |
S221 |
9 | BAA08g01200 | A08 | 860536 | G | A | upstream_gene_variant | MODIFIER | c.-2408C>T| |
S19 |