Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g15900 | A10 | 16040346 | G | A | missense_variant | MODERATE | c.1750C>T|p.Leu584Phe |
S279 |
2 | BAA10g15900 | A10 | 16040473 | G | A | synonymous_variant | LOW | c.1623C>T|p.Asp541Asp |
S262 |
3 | BAA10g15900 | A10 | 16040828 | C | T | missense_variant | MODERATE | c.1307G>A|p.Gly436Asp |
S92 |
4 | BAA10g15900 | A10 | 16040886 | C | T | missense_variant | MODERATE | c.1249G>A|p.Glu417Lys |
S73 |
5 | BAA10g15900 | A10 | 16041787 | C | T | synonymous_variant | LOW | c.447G>A|p.Val149Val |
S33 |
6 | BAA10g15900 | A10 | 16043976 | C | T | upstream_gene_variant | MODIFIER | c.-1574G>A| |
S269 |
7 | BAA10g15900 | A10 | 16045370 | G | A | upstream_gene_variant | MODIFIER | c.-2968C>T| |
S164 |
8 | BAA10g15900 | A10 | 16046097 | C | T | upstream_gene_variant | MODIFIER | c.-3695G>A| |
S38 |
9 | BAA10g15900 | A10 | 16046139 | G | A | upstream_gene_variant | MODIFIER | c.-3737C>T| |
S286 |