Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g43860 | A06 | 28191386 | C | T | missense_variant | MODERATE | c.1856G>A|p.Arg619Gln |
S290 |
2 | BAA06g43860 | A06 | 28191781 | G | A | splice_region_variant&synonymous_variant | LOW | c.1461C>T|p.Ser487Ser |
S207 |
3 | BAA06g43860 | A06 | 28192416 | G | A | missense_variant | MODERATE | c.1199C>T|p.Ala400Val |
S226 |
4 | BAA06g43860 | A06 | 28193536 | G | A | missense_variant | MODERATE | c.670C>T|p.Arg224Cys |
S233 |
5 | BAA06g43860 | A06 | 28194199 | C | T | missense_variant | MODERATE | c.272G>A|p.Gly91Glu |
S126 |
6 | BAA06g43860 | A06 | 28194710 | C | T | upstream_gene_variant | MODIFIER | c.-159G>A| |
S130 |
7 | BAA06g43860 | A06 | 28197326 | G | A | upstream_gene_variant | MODIFIER | c.-2775C>T| |
S193 |
8 | BAA06g43860 | A06 | 28197665 | G | A | upstream_gene_variant | MODIFIER | c.-3114C>T| |
S152 |
9 | BAA06g43860 | A06 | 28197794 | C | T | upstream_gene_variant | MODIFIER | c.-3243G>A| |
S39 |
10 | BAA06g43860 | A06 | 28198907 | G | A | upstream_gene_variant | MODIFIER | c.-4356C>T| |
S171 |
11 | BAA06g43860 | A06 | 28199262 | G | A | upstream_gene_variant | MODIFIER | c.-4711C>T| |
S11 |