Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g09150 | A06 | 4678814 | G | A | missense_variant | MODERATE | c.232G>A|p.Glu78Lys |
S52 |
2 | BAA06g09150 | A06 | 4679018 | G | A | missense_variant | MODERATE | c.436G>A|p.Gly146Arg |
S236 |
3 | BAA06g09150 | A06 | 4680815 | G | A | missense_variant | MODERATE | c.1579G>A|p.Asp527Asn |
S190 |
4 | BAA06g09150 | A06 | 4681257 | G | A | missense_variant | MODERATE | c.1876G>A|p.Gly626Arg |
S208 S219 |
5 | BAA06g09150 | A06 | 4681272 | G | A | missense_variant | MODERATE | c.1891G>A|p.Glu631Lys |
S178 |
6 | BAA06g09150 | A06 | 4681477 | C | T | missense_variant | MODERATE | c.2096C>T|p.Thr699Ile |
S175 |
7 | BAA06g09150 | A06 | 4681828 | G | A | missense_variant | MODERATE | c.2308G>A|p.Asp770Asn |
S269 |
8 | BAA06g09150 | A06 | 4682804 | C | T | missense_variant | MODERATE | c.2992C>T|p.Leu998Phe |
S171 |
9 | BAA06g09150 | A06 | 4684807 | C | T | downstream_gene_variant | MODIFIER | c.*1371C>T| |
S67 |
10 | BAA06g09150 | A06 | 4684826 | G | A | downstream_gene_variant | MODIFIER | c.*1390G>A| |
S155 S211 |
11 | BAA06g09150 | A06 | 4685830 | G | A | downstream_gene_variant | MODIFIER | c.*2394G>A| |
S218 |
12 | BAA06g09150 | A06 | 4686040 | C | T | downstream_gene_variant | MODIFIER | c.*2604C>T| |
S189 |