Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g11720 | A10 | 13302165 | G | A | missense_variant | MODERATE | c.236G>A|p.Ser79Asn |
S280 |
2 | BAA10g11720 | A10 | 13302615 | C | T | missense_variant | MODERATE | c.686C>T|p.Ser229Phe |
S305 |
3 | BAA10g11720 | A10 | 13302854 | G | A | missense_variant&splice_region_variant | MODERATE | c.925G>A|p.Glu309Lys |
S245 |
4 | BAA10g11720 | A10 | 13303213 | G | A | missense_variant | MODERATE | c.1046G>A|p.Ser349Asn |
S159 S187 S188 S276 |
5 | BAA10g11720 | A10 | 13305616 | C | T | synonymous_variant | LOW | c.2128C>T|p.Leu710Leu |
S225 S73 |
6 | BAA10g11720 | A10 | 13306755 | G | A | downstream_gene_variant | MODIFIER | c.*494G>A| |
S192 |
7 | BAA10g11720 | A10 | 13307279 | G | A | downstream_gene_variant | MODIFIER | c.*1018G>A| |
S178 |