Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g23940 | A01 | 12533812 | C | T | synonymous_variant | LOW | c.2325G>A|p.Glu775Glu |
S223 |
2 | BAA01g23940 | A01 | 12534373 | G | A | synonymous_variant | LOW | c.1830C>T|p.Pro610Pro |
S245 |
3 | BAA01g23940 | A01 | 12534497 | T | C | missense_variant | MODERATE | c.1706A>G|p.Tyr569Cys |
S127 |
4 | BAA01g23940 | A01 | 12534794 | G | A | missense_variant | MODERATE | c.1409C>T|p.Ser470Phe |
S114 |
5 | BAA01g23940 | A01 | 12534930 | C | T | missense_variant | MODERATE | c.1273G>A|p.Asp425Asn |
S273 |
6 | BAA01g23940 | A01 | 12535439 | G | A | missense_variant | MODERATE | c.910C>T|p.Pro304Ser |
S172 S217 |
7 | BAA01g23940 | A01 | 12535640 | C | T | splice_donor_variant&intron_variant | HIGH | c.793+1G>A| |
S47 |
8 | BAA01g23940 | A01 | 12536121 | T | C | intron_variant | MODIFIER | c.502-111A>G| |
S293 |
9 | BAA01g23940 | A01 | 12536316 | G | A | missense_variant | MODERATE | c.455C>T|p.Ser152Phe |
S45 |
10 | BAA01g23940 | A01 | 12538384 | G | A | upstream_gene_variant | MODIFIER | c.-1296C>T| |
S37 |