Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g15070 | A05 | 8039065 | G | A | missense_variant | MODERATE | c.2392C>T|p.Leu798Phe |
S153 S213 |
2 | BAA05g15070 | A05 | 8039446 | G | A | missense_variant | MODERATE | c.2161C>T|p.His721Tyr |
S294 |
3 | BAA05g15070 | A05 | 8040070 | G | A | splice_region_variant&intron_variant | LOW | c.1877-8C>T| |
S244 |
4 | BAA05g15070 | A05 | 8040700 | C | T | synonymous_variant | LOW | c.1572G>A|p.Arg524Arg |
S44 |
5 | BAA05g15070 | A05 | 8041656 | C | T | missense_variant | MODERATE | c.1081G>A|p.Val361Met |
S177 |
6 | BAA05g15070 | A05 | 8041906 | G | A | missense_variant | MODERATE | c.896C>T|p.Thr299Ile |
S308 |
7 | BAA05g15070 | A05 | 8042693 | C | T | synonymous_variant | LOW | c.324G>A|p.Glu108Glu |
S165 |
8 | BAA05g15070 | A05 | 8044054 | C | T | upstream_gene_variant | MODIFIER | c.-792G>A| |
S59 |
9 | BAA05g15070 | A05 | 8044587 | G | A | upstream_gene_variant | MODIFIER | c.-1325C>T| |
S293 |
10 | BAA05g15070 | A05 | 8048237 | C | T | upstream_gene_variant | MODIFIER | c.-4975G>A| |
S206 S26 |