Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g11480 | A01 | 5319504 | C | T | synonymous_variant | LOW | c.2991G>A|p.Ser997Ser |
S42 |
2 | BAA01g11480 | A01 | 5319800 | C | T | missense_variant | MODERATE | c.2695G>A|p.Asp899Asn |
S171 |
3 | BAA01g11480 | A01 | 5319839 | C | T | missense_variant | MODERATE | c.2656G>A|p.Glu886Lys |
S61 |
4 | BAA01g11480 | A01 | 5320784 | G | A | missense_variant | MODERATE | c.1711C>T|p.Leu571Phe |
S138 |
5 | BAA01g11480 | A01 | 5321246 | C | T | missense_variant | MODERATE | c.1249G>A|p.Gly417Arg |
S182 |
6 | BAA01g11480 | A01 | 5322455 | C | T | missense_variant | MODERATE | c.40G>A|p.Glu14Lys |
S295 |
7 | BAA01g11480 | A01 | 5323219 | G | A | upstream_gene_variant | MODIFIER | c.-725C>T| |
S273 |
8 | BAA01g11480 | A01 | 5325415 | G | A | upstream_gene_variant | MODIFIER | c.-2921C>T| |
S180 |
9 | BAA01g11480 | A01 | 5325470 | G | A | upstream_gene_variant | MODIFIER | c.-2976C>T| |
S293 |
10 | BAA01g11480 | A01 | 5325665 | G | A | upstream_gene_variant | MODIFIER | c.-3171C>T| |
S121 |