Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g29950 | A01 | 19015207 | C | T | upstream_gene_variant | MODIFIER | c.-555C>T| |
S57 |
2 | BAA01g29950 | A01 | 19015338 | C | T | upstream_gene_variant | MODIFIER | c.-424C>T| |
S208 S93 |
3 | BAA01g29950 | A01 | 19015359 | C | T | upstream_gene_variant | MODIFIER | c.-403C>T| |
S231 |
4 | BAA01g29950 | A01 | 19015503 | C | T | upstream_gene_variant | MODIFIER | c.-259C>T| |
S28 |
5 | BAA01g29950 | A01 | 19015572 | C | T | upstream_gene_variant | MODIFIER | c.-190C>T| |
S112 |
6 | BAA01g29950 | A01 | 19015779 | G | A | synonymous_variant | LOW | c.18G>A|p.Lys6Lys |
S99 |
7 | BAA01g29950 | A01 | 19015880 | G | A | missense_variant | MODERATE | c.119G>A|p.Ser40Asn |
S138 |
8 | BAA01g29950 | A01 | 19016035 | C | T | missense_variant | MODERATE | c.274C>T|p.Pro92Ser |
S130 |
9 | BAA01g29950 | A01 | 19016093 | C | T | missense_variant | MODERATE | c.332C>T|p.Pro111Leu |
S128 |
10 | BAA01g29950 | A01 | 19017258 | G | A | missense_variant | MODERATE | c.880G>A|p.Asp294Asn |
S25 |
11 | BAA01g29950 | A01 | 19017284 | G | A | synonymous_variant | LOW | c.906G>A|p.Glu302Glu |
S271 |