Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g16740 | A05 | 9307902 | G | A | synonymous_variant | LOW | c.1956C>T|p.Phe652Phe |
S156 |
2 | BAA05g16740 | A05 | 9307952 | C | T | missense_variant | MODERATE | c.1906G>A|p.Glu636Lys |
S162 |
3 | BAA05g16740 | A05 | 9308490 | G | A | synonymous_variant | LOW | c.1368C>T|p.Thr456Thr |
S178 |
4 | BAA05g16740 | A05 | 9309018 | C | T | synonymous_variant | LOW | c.996G>A|p.Glu332Glu |
S17 |
5 | BAA05g16740 | A05 | 9309680 | G | A | synonymous_variant | LOW | c.489C>T|p.Tyr163Tyr |
S261 |
6 | BAA05g16740 | A05 | 9309892 | G | A | missense_variant | MODERATE | c.277C>T|p.Pro93Ser |
S152 |
7 | BAA05g16740 | A05 | 9309902 | G | A | synonymous_variant | LOW | c.267C>T|p.Leu89Leu |
S144 |
8 | BAA05g16740 | A05 | 9310056 | G | A | missense_variant | MODERATE | c.113C>T|p.Ser38Leu |
S80 |
9 | BAA05g16740 | A05 | 9310061 | C | A | synonymous_variant | LOW | c.108G>T|p.Ala36Ala |
S199 |
10 | BAA05g16740 | A05 | 9313202 | G | A | upstream_gene_variant | MODIFIER | c.-3034C>T| |
S124 |
11 | BAA05g16740 | A05 | 9315107 | G | A | upstream_gene_variant | MODIFIER | c.-4939C>T| |
S183 S32 |