Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g20470 | A10 | 18405120 | G | A | missense_variant | MODERATE | c.1948C>T|p.Pro650Ser |
S67 |
2 | BAA10g20470 | A10 | 18405770 | G | A | missense_variant | MODERATE | c.1457C>T|p.Ser486Phe |
S202 |
3 | BAA10g20470 | A10 | 18406077 | G | A | missense_variant | MODERATE | c.1150C>T|p.Leu384Phe |
S136 |
4 | BAA10g20470 | A10 | 18407265 | C | T | splice_region_variant&synonymous_variant | LOW | c.504G>A|p.Arg168Arg |
S142 |
5 | BAA10g20470 | A10 | 18408561 | C | T | missense_variant | MODERATE | c.262G>A|p.Glu88Lys |
S114 |
6 | BAA10g20470 | A10 | 18411567 | C | T | upstream_gene_variant | MODIFIER | c.-2745G>A| |
S10 |
7 | BAA10g20470 | A10 | 18411606 | C | T | upstream_gene_variant | MODIFIER | c.-2784G>A| |
S277 |
8 | BAA10g20470 | A10 | 18411645 | C | T | upstream_gene_variant | MODIFIER | c.-2823G>A| |
S206 |
9 | BAA10g20470 | A10 | 18412796 | C | T | upstream_gene_variant | MODIFIER | c.-3974G>A| |
S135 |
10 | BAA10g20470 | A10 | 18413150 | T | C | upstream_gene_variant | MODIFIER | c.-4328A>G| |
S274 |
11 | BAA10g20470 | A10 | 18413814 | C | T | upstream_gene_variant | MODIFIER | c.-4992G>A| |
S291 |