Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g13640 | A10 | 14613659 | G | A | missense_variant | MODERATE | c.1189G>A|p.Val397Ile |
S198 |
2 | BAA10g13640 | A10 | 14618059 | C | T | downstream_gene_variant | MODIFIER | c.*3453C>T| |
S185 |
3 | BAA10g13640 | A10 | 14618266 | G | A | downstream_gene_variant | MODIFIER | c.*3660G>A| |
S112 |
4 | BAA10g13640 | A10 | 14618303 | G | A | downstream_gene_variant | MODIFIER | c.*3697G>A| |
S136 S61 |
5 | BAA10g13640 | A10 | 14618594 | G | A | downstream_gene_variant | MODIFIER | c.*3988G>A| |
S4 |
6 | BAA10g13640 | A10 | 14618836 | G | A | downstream_gene_variant | MODIFIER | c.*4230G>A| |
S136 |
7 | BAA10g13640 | A10 | 14618938 | G | A | downstream_gene_variant | MODIFIER | c.*4332G>A| |
S295 |
8 | BAA10g13640 | A10 | 14619136 | G | A | downstream_gene_variant | MODIFIER | c.*4530G>A| |
S236 |