Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g05800 | A02 | 2472064 | G | A | missense_variant | MODERATE | c.1297C>T|p.Pro433Ser |
S260 |
2 | BAA02g05800 | A02 | 2472198 | G | A | synonymous_variant | LOW | c.1251C>T|p.Cys417Cys |
S174 |
3 | BAA02g05800 | A02 | 2472577 | G | A | splice_region_variant&intron_variant | LOW | c.1010+7C>T| |
S197 S30 |
4 | BAA02g05800 | A02 | 2473540 | C | T | missense_variant | MODERATE | c.688G>A|p.Asp230Asn |
S32 |
5 | BAA02g05800 | A02 | 2473778 | C | T | synonymous_variant | LOW | c.531G>A|p.Arg177Arg |
S229 |
6 | BAA02g05800 | A02 | 2474396 | C | T | synonymous_variant | LOW | c.87G>A|p.Gln29Gln |
S180 |
7 | BAA02g05800 | A02 | 2477211 | G | A | upstream_gene_variant | MODIFIER | c.-2729C>T| |
S157 |
8 | BAA02g05800 | A02 | 2477736 | C | T | upstream_gene_variant | MODIFIER | c.-3254G>A| |
S123 |
9 | BAA02g05800 | A02 | 2477864 | G | A | upstream_gene_variant | MODIFIER | c.-3382C>T| |
S266 |
10 | BAA02g05800 | A02 | 2478312 | G | A | upstream_gene_variant | MODIFIER | c.-3830C>T| |
S202 |
11 | BAA02g05800 | A02 | 2478540 | C | T | upstream_gene_variant | MODIFIER | c.-4058G>A| |
S277 |