Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g20060 | A10 | 18203128 | G | A | synonymous_variant | LOW | c.99G>A|p.Glu33Glu |
S216 |
2 | BAA10g20060 | A10 | 18203199 | C | T | missense_variant | MODERATE | c.170C>T|p.Ala57Val |
S195 |
3 | BAA10g20060 | A10 | 18206605 | G | A | downstream_gene_variant | MODIFIER | c.*3117G>A| |
S67 |
4 | BAA10g20060 | A10 | 18207516 | C | T | downstream_gene_variant | MODIFIER | c.*4028C>T| |
S292 |
5 | BAA10g20060 | A10 | 18207544 | C | T | downstream_gene_variant | MODIFIER | c.*4056C>T| |
S133 |
6 | BAA10g20060 | A10 | 18207645 | G | A | downstream_gene_variant | MODIFIER | c.*4157G>A| |
S298 |
7 | BAA10g20060 | A10 | 18207764 | C | T | downstream_gene_variant | MODIFIER | c.*4276C>T| |
S230 |
8 | BAA10g20060 | A10 | 18207831 | C | T | downstream_gene_variant | MODIFIER | c.*4343C>T| |
S298 |
9 | BAA10g20060 | A10 | 18208465 | C | T | downstream_gene_variant | MODIFIER | c.*4977C>T| |
S68 |