Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g32770 | A10 | 23447065 | C | T | missense_variant | MODERATE | c.104C>T|p.Ala35Val |
S97 |
2 | BAA10g32770 | A10 | 23447388 | G | A | missense_variant | MODERATE | c.427G>A|p.Glu143Lys |
S66 |
3 | BAA10g32770 | A10 | 23447946 | G | A | missense_variant | MODERATE | c.985G>A|p.Gly329Arg |
S57 |
4 | BAA10g32770 | A10 | 23448068 | C | T | synonymous_variant | LOW | c.1107C>T|p.Asn369Asn |
S156 |
5 | BAA10g32770 | A10 | 23448566 | G | A | synonymous_variant | LOW | c.1605G>A|p.Thr535Thr |
S9 |
6 | BAA10g32770 | A10 | 23451945 | G | A | downstream_gene_variant | MODIFIER | c.*3196G>A| |
S1 S90 |