Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g21810 | A10 | 19051865 | C | T | missense_variant | MODERATE | c.1207G>A|p.Val403Met |
S204 |
2 | BAA10g21810 | A10 | 19051967 | C | T | missense_variant | MODERATE | c.1105G>A|p.Gly369Arg |
S60 |
3 | BAA10g21810 | A10 | 19052682 | C | T | synonymous_variant | LOW | c.390G>A|p.Pro130Pro |
S245 |
4 | BAA10g21810 | A10 | 19052723 | G | A | missense_variant | MODERATE | c.349C>T|p.Leu117Phe |
S9 |
5 | BAA10g21810 | A10 | 19052932 | C | T | missense_variant | MODERATE | c.140G>A|p.Gly47Glu |
S124 |
6 | BAA10g21810 | A10 | 19056034 | C | T | upstream_gene_variant | MODIFIER | c.-2963G>A| |
S306 S308 |
7 | BAA10g21810 | A10 | 19057566 | G | A | upstream_gene_variant | MODIFIER | c.-4495C>T| |
S263 |
8 | BAA10g21810 | A10 | 19057945 | C | T | upstream_gene_variant | MODIFIER | c.-4874G>A| |
S176 |
9 | BAA10g21810 | A10 | 19057968 | G | A | upstream_gene_variant | MODIFIER | c.-4897C>T| |
S198 |