Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g08040 | A09 | 4491335 | G | A | missense_variant | MODERATE | c.3043C>T|p.Pro1015Ser |
S149 |
2 | BAA09g08040 | A09 | 4491350 | G | A | stop_gained | HIGH | c.3028C>T|p.Gln1010* |
S228 |
3 | BAA09g08040 | A09 | 4491466 | G | A | missense_variant | MODERATE | c.2912C>T|p.Ser971Leu |
S188 |
4 | BAA09g08040 | A09 | 4492088 | C | T | missense_variant | MODERATE | c.2290G>A|p.Asp764Asn |
S143 |
5 | BAA09g08040 | A09 | 4492548 | C | T | synonymous_variant | LOW | c.1830G>A|p.Arg610Arg |
S183 S198 |
6 | BAA09g08040 | A09 | 4493061 | G | A | synonymous_variant | LOW | c.1317C>T|p.Ser439Ser |
S262 |
7 | BAA09g08040 | A09 | 4494478 | G | A | missense_variant | MODERATE | c.65C>T|p.Ser22Leu |
S235 |
8 | BAA09g08040 | A09 | 4495016 | C | T | upstream_gene_variant | MODIFIER | c.-474G>A| |
S270 |
9 | BAA09g08040 | A09 | 4495310 | G | A | upstream_gene_variant | MODIFIER | c.-768C>T| |
S108 |
10 | BAA09g08040 | A09 | 4495746 | C | T | upstream_gene_variant | MODIFIER | c.-1204G>A| |
S244 |
11 | BAA09g08040 | A09 | 4495752 | C | T | upstream_gene_variant | MODIFIER | c.-1210G>A| |
S158 |
12 | BAA09g08040 | A09 | 4497509 | G | A | upstream_gene_variant | MODIFIER | c.-2967C>T| |
S30 S31 |
13 | BAA09g08040 | A09 | 4498075 | C | T | upstream_gene_variant | MODIFIER | c.-3533G>A| |
S156 |