Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g02980 | A10 | 1444635 | G | A | synonymous_variant | LOW | c.48G>A|p.Lys16Lys |
S20 |
2 | BAA10g02980 | A10 | 1444912 | C | T | missense_variant | MODERATE | c.325C>T|p.Leu109Phe |
S291 S47 |
3 | BAA10g02980 | A10 | 1445064 | G | A | synonymous_variant | LOW | c.477G>A|p.Glu159Glu |
S274 |
4 | BAA10g02980 | A10 | 1446685 | G | A | missense_variant | MODERATE | c.530G>A|p.Ser177Asn |
S105 S106 |
5 | BAA10g02980 | A10 | 1446695 | C | T | synonymous_variant | LOW | c.540C>T|p.Asp180Asp |
S23 |
6 | BAA10g02980 | A10 | 1453675 | G | A | downstream_gene_variant | MODIFIER | c.*3374G>A| |
S45 |
7 | BAA10g02980 | A10 | 1453723 | G | A | downstream_gene_variant | MODIFIER | c.*3422G>A| |
S60 |
8 | BAA10g02980 | A10 | 1455028 | C | T | downstream_gene_variant | MODIFIER | c.*4727C>T| |
S260 |
9 | BAA10g02980 | A10 | 1455066 | C | T | downstream_gene_variant | MODIFIER | c.*4765C>T| |
S247 |