Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g01180 | A08 | 850394 | C | T | missense_variant | MODERATE | c.982G>A|p.Asp328Asn |
S120 |
2 | BAA08g01180 | A08 | 850496 | G | A | stop_gained | HIGH | c.880C>T|p.Gln294* |
S38 |
3 | BAA08g01180 | A08 | 850533 | C | T | synonymous_variant | LOW | c.843G>A|p.Glu281Glu |
S276 |
4 | BAA08g01180 | A08 | 850629 | C | T | synonymous_variant | LOW | c.747G>A|p.Arg249Arg |
S275 |
5 | BAA08g01180 | A08 | 850752 | G | A | synonymous_variant | LOW | c.624C>T|p.Leu208Leu |
S38 |
6 | BAA08g01180 | A08 | 851188 | G | A | missense_variant | MODERATE | c.188C>T|p.Ser63Phe |
S242 |
7 | BAA08g01180 | A08 | 853269 | C | T | upstream_gene_variant | MODIFIER | c.-1894G>A| |
S148 S210 S30 S31 |
8 | BAA08g01180 | A08 | 853358 | G | A | upstream_gene_variant | MODIFIER | c.-1983C>T| |
S190 |
9 | BAA08g01180 | A08 | 855297 | G | A | upstream_gene_variant | MODIFIER | c.-3922C>T| |
S282 |