Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g26930 | A10 | 21161461 | G | A | missense_variant | MODERATE | c.1402C>T|p.Pro468Ser |
S189 |
2 | BAA10g26930 | A10 | 21161926 | G | A | stop_gained&splice_region_variant | HIGH | c.1102C>T|p.Gln368* |
S298 |
3 | BAA10g26930 | A10 | 21162680 | G | A | synonymous_variant | LOW | c.429C>T|p.Asp143Asp |
S94 |
4 | BAA10g26930 | A10 | 21163650 | C | T | upstream_gene_variant | MODIFIER | c.-181G>A| |
S277 |
5 | BAA10g26930 | A10 | 21163991 | C | T | upstream_gene_variant | MODIFIER | c.-522G>A| |
S165 |
6 | BAA10g26930 | A10 | 21164653 | C | T | upstream_gene_variant | MODIFIER | c.-1184G>A| |
S36 |
7 | BAA10g26930 | A10 | 21166678 | G | A | upstream_gene_variant | MODIFIER | c.-3209C>T| |
S179 |
8 | BAA10g26930 | A10 | 21166818 | C | T | upstream_gene_variant | MODIFIER | c.-3349G>A| |
S244 |
9 | BAA10g26930 | A10 | 21168438 | G | A | upstream_gene_variant | MODIFIER | c.-4969C>T| |
S71 |