Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g06140 | A10 | 3174252 | C | T | downstream_gene_variant | MODIFIER | c.*3757G>A| |
S119 |
2 | BAA10g06140 | A10 | 3174762 | C | T | downstream_gene_variant | MODIFIER | c.*3247G>A| |
S170 |
3 | BAA10g06140 | A10 | 3178319 | C | T | missense_variant | MODERATE | c.1066G>A|p.Val356Met |
S41 |
4 | BAA10g06140 | A10 | 3179596 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.421-1G>A| |
S277 |
5 | BAA10g06140 | A10 | 3179777 | G | A | missense_variant | MODERATE | c.326C>T|p.Ala109Val |
S308 |
6 | BAA10g06140 | A10 | 3180012 | G | A | synonymous_variant | LOW | c.201C>T|p.Ser67Ser |
S125 |
7 | BAA10g06140 | A10 | 3180526 | G | A | synonymous_variant | LOW | c.45C>T|p.Ile15Ile |
S202 |
8 | BAA10g06140 | A10 | 3180964 | C | T | upstream_gene_variant | MODIFIER | c.-394G>A| |
S202 |
9 | BAA10g06140 | A10 | 3181182 | G | A | upstream_gene_variant | MODIFIER | c.-612C>T| |
S120 |
10 | BAA10g06140 | A10 | 3181332 | C | T | upstream_gene_variant | MODIFIER | c.-762G>A| |
S40 S49 |
11 | BAA10g06140 | A10 | 3183039 | G | A | upstream_gene_variant | MODIFIER | c.-2469C>T| |
S136 |