Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g42650 | A06 | 27602277 | G | A | synonymous_variant | LOW | c.1254C>T|p.Leu418Leu |
S32 |
2 | BAA06g42650 | A06 | 27602519 | C | T | missense_variant | MODERATE | c.1012G>A|p.Glu338Lys |
S221 |
3 | BAA06g42650 | A06 | 27602527 | G | A | missense_variant | MODERATE | c.1004C>T|p.Thr335Met |
S35 |
4 | BAA06g42650 | A06 | 27603754 | C | T | missense_variant | MODERATE | c.553G>A|p.Glu185Lys |
S274 |
5 | BAA06g42650 | A06 | 27603873 | C | T | missense_variant | MODERATE | c.434G>A|p.Gly145Glu |
S136 |
6 | BAA06g42650 | A06 | 27605140 | C | T | upstream_gene_variant | MODIFIER | c.-418G>A| |
S142 |
7 | BAA06g42650 | A06 | 27606596 | A | G | upstream_gene_variant | MODIFIER | c.-1874T>C| |
S296 |
8 | BAA06g42650 | A06 | 27606767 | C | T | upstream_gene_variant | MODIFIER | c.-2045G>A| |
S62 |
9 | BAA06g42650 | A06 | 27608465 | G | A | upstream_gene_variant | MODIFIER | c.-3743C>T| |
S19 |