Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g30180 | A06 | 20554776 | C | T | missense_variant | MODERATE | c.635C>T|p.Ser212Phe |
S115 |
2 | BAA06g30180 | A06 | 20554969 | G | A | synonymous_variant | LOW | c.732G>A|p.Lys244Lys |
S295 |
3 | BAA06g30180 | A06 | 20556266 | C | T | splice_region_variant&intron_variant | LOW | c.1456-6C>T| |
S136 |
4 | BAA06g30180 | A06 | 20556653 | G | A | missense_variant | MODERATE | c.1732G>A|p.Ala578Thr |
S271 |
5 | BAA06g30180 | A06 | 20556852 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.1848-1G>A| |
S256 |
6 | BAA06g30180 | A06 | 20557804 | G | A | missense_variant | MODERATE | c.2332G>A|p.Glu778Lys |
S251 |
7 | BAA06g30180 | A06 | 20558326 | C | T | downstream_gene_variant | MODIFIER | c.*472C>T| |
S96 |
8 | BAA06g30180 | A06 | 20558362 | G | A | downstream_gene_variant | MODIFIER | c.*508G>A| |
S206 S26 |