Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g16660 | A09 | 9764330 | G | A | missense_variant | MODERATE | c.631C>T|p.Arg211Trp |
S130 |
2 | BAA09g16660 | A09 | 9764415 | G | A | synonymous_variant | LOW | c.546C>T|p.Gly182Gly |
S142 |
3 | BAA09g16660 | A09 | 9764701 | G | A | missense_variant | MODERATE | c.260C>T|p.Ala87Val |
S277 |
4 | BAA09g16660 | A09 | 9764967 | G | A | upstream_gene_variant | MODIFIER | c.-7C>T| |
S57 |
5 | BAA09g16660 | A09 | 9766599 | G | A | upstream_gene_variant | MODIFIER | c.-1639C>T| |
S280 |
6 | BAA09g16660 | A09 | 9767337 | C | T | upstream_gene_variant | MODIFIER | c.-2377G>A| |
S174 S216 |
7 | BAA09g16660 | A09 | 9769763 | G | A | upstream_gene_variant | MODIFIER | c.-4803C>T| |
S112 |