Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g14350 | A10 | 15093886 | C | T | missense_variant | MODERATE | c.1696G>A|p.Ala566Thr |
S176 |
2 | BAA10g14350 | A10 | 15094761 | G | A | missense_variant | MODERATE | c.892C>T|p.Pro298Ser |
S198 |
3 | BAA10g14350 | A10 | 15094891 | C | T | synonymous_variant | LOW | c.762G>A|p.Gly254Gly |
S284 |
4 | BAA10g14350 | A10 | 15097277 | C | T | upstream_gene_variant | MODIFIER | c.-103G>A| |
S173 |
5 | BAA10g14350 | A10 | 15097880 | G | T | upstream_gene_variant | MODIFIER | c.-706C>A| |
S153 S213 |
6 | BAA10g14350 | A10 | 15098797 | C | T | upstream_gene_variant | MODIFIER | c.-1623G>A| |
S70 |
7 | BAA10g14350 | A10 | 15098830 | G | A | upstream_gene_variant | MODIFIER | c.-1656C>T| |
S112 |
8 | BAA10g14350 | A10 | 15101665 | C | T | upstream_gene_variant | MODIFIER | c.-4491G>A| |
S259 |