Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g35060 | A05 | 35909783 | C | T | missense_variant | MODERATE | c.2062G>A|p.Asp688Asn |
S132 S137 S215 |
2 | BAA05g35060 | A05 | 35910302 | C | T | missense_variant | MODERATE | c.1712G>A|p.Ser571Asn |
S114 |
3 | BAA05g35060 | A05 | 35911195 | G | A | synonymous_variant | LOW | c.1309C>T|p.Leu437Leu |
S267 |
4 | BAA05g35060 | A05 | 35913006 | G | A | missense_variant | MODERATE | c.722C>T|p.Pro241Leu |
S181 |
5 | BAA05g35060 | A05 | 35913596 | G | A | missense_variant | MODERATE | c.596C>T|p.Ser199Phe |
S236 |
6 | BAA05g35060 | A05 | 35914689 | C | T | splice_region_variant&intron_variant | LOW | c.258-7G>A| |
S225 |
7 | BAA05g35060 | A05 | 35914851 | G | A | synonymous_variant | LOW | c.177C>T|p.Phe59Phe |
S223 |
8 | BAA05g35060 | A05 | 35915221 | C | T | upstream_gene_variant | MODIFIER | c.-194G>A| |
S297 |
9 | BAA05g35060 | A05 | 35915704 | G | A | upstream_gene_variant | MODIFIER | c.-677C>T| |
S39 |
10 | BAA05g35060 | A05 | 35917686 | C | T | upstream_gene_variant | MODIFIER | c.-2659G>A| |
S70 |
11 | BAA05g35060 | A05 | 35917821 | G | T | upstream_gene_variant | MODIFIER | c.-2794C>A| |
S225 |