Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g14150 | A02 | 6635502 | C | T | upstream_gene_variant | MODIFIER | c.-3983C>T| |
S58 |
2 | BAA02g14150 | A02 | 6639554 | G | A | missense_variant | MODERATE | c.70G>A|p.Asp24Asn |
S280 |
3 | BAA02g14150 | A02 | 6640020 | C | T | missense_variant | MODERATE | c.536C>T|p.Ser179Phe |
S270 |
4 | BAA02g14150 | A02 | 6640913 | C | T | synonymous_variant | LOW | c.810C>T|p.Ser270Ser |
S165 |
5 | BAA02g14150 | A02 | 6641067 | G | A | missense_variant | MODERATE | c.964G>A|p.Gly322Arg |
S202 |
6 | BAA02g14150 | A02 | 6641190 | A | C | missense_variant | MODERATE | c.1087A>C|p.Ser363Arg |
S137 S175 S221 S222 S234 S259 S286 S5 S97 |
7 | BAA02g14150 | A02 | 6641322 | C | T | missense_variant | MODERATE | c.1219C>T|p.Pro407Ser |
S178 |
8 | BAA02g14150 | A02 | 6641436 | G | A | missense_variant | MODERATE | c.1333G>A|p.Glu445Lys |
S122 |