Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g41890 | A07 | 36584280 | G | A | missense_variant | MODERATE | c.1721C>T|p.Ala574Val |
S136 |
2 | BAA07g41890 | A07 | 36584933 | G | A | synonymous_variant | LOW | c.1068C>T|p.Asn356Asn |
S126 |
3 | BAA07g41890 | A07 | 36585145 | G | A | missense_variant | MODERATE | c.856C>T|p.Arg286Trp |
S155 |
4 | BAA07g41890 | A07 | 36585545 | G | A | synonymous_variant | LOW | c.456C>T|p.Ile152Ile |
S246 |
5 | BAA07g41890 | A07 | 36585673 | C | T | missense_variant | MODERATE | c.328G>A|p.Glu110Lys |
S281 |
6 | BAA07g41890 | A07 | 36585818 | C | T | synonymous_variant | LOW | c.183G>A|p.Gln61Gln |
S207 |
7 | BAA07g41890 | A07 | 36588436 | G | A | upstream_gene_variant | MODIFIER | c.-2436C>T| |
S6 |
8 | BAA07g41890 | A07 | 36590750 | G | A | upstream_gene_variant | MODIFIER | c.-4750C>T| |
S45 |
9 | BAA07g41890 | A07 | 36590853 | C | T | upstream_gene_variant | MODIFIER | c.-4853G>A| |
S192 |