Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g28660 | A10 | 21876777 | C | T | missense_variant | MODERATE | c.100C>T|p.His34Tyr |
S148 S210 S30 S31 |
2 | BAA10g28660 | A10 | 21876829 | C | T | missense_variant | MODERATE | c.152C>T|p.Ser51Phe |
S155 |
3 | BAA10g28660 | A10 | 21876920 | G | A | synonymous_variant | LOW | c.243G>A|p.Glu81Glu |
S236 |
4 | BAA10g28660 | A10 | 21877163 | G | A | synonymous_variant | LOW | c.414G>A|p.Gln138Gln |
S15 S156 S3 S34 S4 S6 |
5 | BAA10g28660 | A10 | 21877488 | C | T | missense_variant | MODERATE | c.605C>T|p.Pro202Leu |
S123 S210 S225 |
6 | BAA10g28660 | A10 | 21877688 | C | T | missense_variant | MODERATE | c.730C>T|p.Pro244Ser |
S206 S26 |
7 | BAA10g28660 | A10 | 21881012 | G | A | downstream_gene_variant | MODIFIER | c.*2868G>A| |
S259 |