Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g01290 | A06 | 849602 | C | T | upstream_gene_variant | MODIFIER | c.-3138C>T| |
S48 |
2 | BAA06g01290 | A06 | 849612 | G | A | upstream_gene_variant | MODIFIER | c.-3128G>A| |
S77 S82 |
3 | BAA06g01290 | A06 | 851863 | C | T | upstream_gene_variant | MODIFIER | c.-877C>T| |
S202 |
4 | BAA06g01290 | A06 | 851874 | C | T | upstream_gene_variant | MODIFIER | c.-866C>T| |
S111 |
5 | BAA06g01290 | A06 | 852139 | C | T | upstream_gene_variant | MODIFIER | c.-601C>T| |
S34 |
6 | BAA06g01290 | A06 | 852922 | G | A | synonymous_variant | LOW | c.183G>A|p.Lys61Lys |
S264 |
7 | BAA06g01290 | A06 | 854166 | G | A | missense_variant | MODERATE | c.1342G>A|p.Val448Met |
S115 |
8 | BAA06g01290 | A06 | 854587 | G | A | synonymous_variant | LOW | c.1593G>A|p.Lys531Lys |
S39 |
9 | BAA06g01290 | A06 | 855299 | C | T | missense_variant | MODERATE | c.2027C>T|p.Pro676Leu |
S31 |
10 | BAA06g01290 | A06 | 855759 | C | T | synonymous_variant | LOW | c.2301C>T|p.Phe767Phe |
S278 |
11 | BAA06g01290 | A06 | 855827 | C | T | missense_variant | MODERATE | c.2369C>T|p.Ala790Val |
S266 |