Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g17430 | A10 | 16765850 | C | T | upstream_gene_variant | MODIFIER | c.-3757C>T| |
S5 |
2 | BAA10g17430 | A10 | 16769581 | G | A | upstream_gene_variant | MODIFIER | c.-26G>A| |
S5 |
3 | BAA10g17430 | A10 | 16769803 | C | T | missense_variant | MODERATE | c.131C>T|p.Thr44Ile |
S305 |
4 | BAA10g17430 | A10 | 16770397 | C | T | missense_variant | MODERATE | c.503C>T|p.Ala168Val |
S45 |
5 | BAA10g17430 | A10 | 16770398 | G | A | synonymous_variant | LOW | c.504G>A|p.Ala168Ala |
S129 |
6 | BAA10g17430 | A10 | 16770796 | C | T | missense_variant | MODERATE | c.677C>T|p.Ala226Val |
S18 |
7 | BAA10g17430 | A10 | 16771933 | G | A | missense_variant | MODERATE | c.1315G>A|p.Asp439Asn |
S184 |
8 | BAA10g17430 | A10 | 16772329 | C | T | synonymous_variant | LOW | c.1539C>T|p.Asn513Asn |
S6 |
9 | BAA10g17430 | A10 | 16772780 | G | A | missense_variant | MODERATE | c.1804G>A|p.Asp602Asn |
S88 |