Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g26200 | A10 | 20878154 | G | A | synonymous_variant | LOW | c.1243C>T|p.Leu415Leu |
S109 |
2 | BAA10g26200 | A10 | 20879141 | C | T | missense_variant | MODERATE | c.547G>A|p.Glu183Lys |
S308 |
3 | BAA10g26200 | A10 | 20879679 | G | A | splice_region_variant&intron_variant | LOW | c.200-4C>T| |
S278 |
4 | BAA10g26200 | A10 | 20879807 | G | A | missense_variant | MODERATE | c.145C>T|p.Leu49Phe |
S288 |
5 | BAA10g26200 | A10 | 20879848 | G | A | missense_variant | MODERATE | c.104C>T|p.Ser35Leu |
S263 |
6 | BAA10g26200 | A10 | 20882419 | C | T | upstream_gene_variant | MODIFIER | c.-2468G>A| |
S199 |
7 | BAA10g26200 | A10 | 20883879 | C | T | upstream_gene_variant | MODIFIER | c.-3928G>A| |
S107 |