Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g39900 | A09 | 47268186 | C | T | missense_variant | MODERATE | c.1177G>A|p.Glu393Lys |
S179 |
2 | BAA09g39900 | A09 | 47268276 | C | T | missense_variant | MODERATE | c.1087G>A|p.Asp363Asn |
S25 S264 |
3 | BAA09g39900 | A09 | 47268536 | C | T | missense_variant | MODERATE | c.910G>A|p.Val304Ile |
S6 |
4 | BAA09g39900 | A09 | 47268811 | G | A | synonymous_variant | LOW | c.720C>T|p.Cys240Cys |
S239 S33 |
5 | BAA09g39900 | A09 | 47268828 | C | T | missense_variant | MODERATE | c.703G>A|p.Val235Ile |
S183 |
6 | BAA09g39900 | A09 | 47269032 | G | A | missense_variant | MODERATE | c.499C>T|p.Leu167Phe |
S10 |
7 | BAA09g39900 | A09 | 47269286 | C | T | missense_variant | MODERATE | c.245G>A|p.Cys82Tyr |
S66 |
8 | BAA09g39900 | A09 | 47269414 | C | T | synonymous_variant | LOW | c.117G>A|p.Ser39Ser |
S297 |
9 | BAA09g39900 | A09 | 47269441 | G | A | synonymous_variant | LOW | c.90C>T|p.Ile30Ile |
S270 |
10 | BAA09g39900 | A09 | 47273859 | G | A | upstream_gene_variant | MODIFIER | c.-4329C>T| |
S11 |