Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g63290 | A09 | 59310940 | G | A | upstream_gene_variant | MODIFIER | c.-4922G>A| |
S260 |
2 | BAA09g63290 | A09 | 59315999 | C | T | synonymous_variant | LOW | c.138C>T|p.Tyr46Tyr |
S58 |
3 | BAA09g63290 | A09 | 59316313 | A | C | missense_variant | MODERATE | c.452A>C|p.Asn151Thr |
S110 S166 S196 S6 |
4 | BAA09g63290 | A09 | 59316391 | C | T | missense_variant | MODERATE | c.530C>T|p.Pro177Leu |
S206 |
5 | BAA09g63290 | A09 | 59316452 | G | A | missense_variant | MODERATE | c.591G>A|p.Met197Ile |
S188 |
6 | BAA09g63290 | A09 | 59317656 | G | A | missense_variant | MODERATE | c.1600G>A|p.Asp534Asn |
S46 |
7 | BAA09g63290 | A09 | 59317716 | G | A | missense_variant | MODERATE | c.1660G>A|p.Val554Ile |
S246 |
8 | BAA09g63290 | A09 | 59318889 | C | T | missense_variant | MODERATE | c.2513C>T|p.Ser838Phe |
S56 |
9 | BAA09g63290 | A09 | 59319454 | C | T | missense_variant | MODERATE | c.2906C>T|p.Ser969Phe |
S146 |
10 | BAA09g63290 | A09 | 59319777 | C | T | synonymous_variant | LOW | c.3141C>T|p.Ile1047Ile |
S5 |