Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g40380 | A02 | 34069617 | C | T | missense_variant | MODERATE | c.565G>A|p.Asp189Asn |
S97 |
2 | BAA02g40380 | A02 | 34069921 | G | A | missense_variant | MODERATE | c.341C>T|p.Ser114Phe |
S256 |
3 | BAA02g40380 | A02 | 34070580 | G | A | intron_variant | MODIFIER | c.318-636C>T| |
S136 |
4 | BAA02g40380 | A02 | 34071326 | G | A | intron_variant | MODIFIER | c.317+1323C>T| |
S196 |
5 | BAA02g40380 | A02 | 34071985 | G | A | intron_variant | MODIFIER | c.317+664C>T| |
S37 |
6 | BAA02g40380 | A02 | 34072669 | G | A | synonymous_variant | LOW | c.297C>T|p.Ser99Ser |
S279 |
7 | BAA02g40380 | A02 | 34072720 | G | A | synonymous_variant | LOW | c.246C>T|p.Tyr82Tyr |
S138 |
8 | BAA02g40380 | A02 | 34073139 | G | A | missense_variant | MODERATE | c.134C>T|p.Thr45Ile |
S281 |
9 | BAA02g40380 | A02 | 34073142 | C | T | missense_variant | MODERATE | c.131G>A|p.Gly44Glu |
S54 |
10 | BAA02g40380 | A02 | 34073792 | C | T | upstream_gene_variant | MODIFIER | c.-251G>A| |
S6 |
11 | BAA02g40380 | A02 | 34076483 | C | T | upstream_gene_variant | MODIFIER | c.-2942G>A| |
S194 |
12 | BAA02g40380 | A02 | 34078466 | A | G | upstream_gene_variant | MODIFIER | c.-4925T>C| |
S301 S304 |