Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g21000 | A09 | 13012439 | C | T | missense_variant | MODERATE | c.779G>A|p.Ser260Asn |
S60 |
2 | BAA09g21000 | A09 | 13013387 | C | T | intron_variant | MODIFIER | c.331-414G>A| |
S129 S206 S26 |
3 | BAA09g21000 | A09 | 13013452 | G | A | intron_variant | MODIFIER | c.331-479C>T| |
S201 |
4 | BAA09g21000 | A09 | 13013823 | C | T | intron_variant | MODIFIER | c.330+208G>A| |
S104 S52 |
5 | BAA09g21000 | A09 | 13014186 | C | T | missense_variant | MODERATE | c.175G>A|p.Ala59Thr |
S245 |
6 | BAA09g21000 | A09 | 13014650 | C | T | upstream_gene_variant | MODIFIER | c.-290G>A| |
S118 |
7 | BAA09g21000 | A09 | 13014871 | G | A | upstream_gene_variant | MODIFIER | c.-511C>T| |
S20 |
8 | BAA09g21000 | A09 | 13016310 | C | T | upstream_gene_variant | MODIFIER | c.-1950G>A| |
S269 |
9 | BAA09g21000 | A09 | 13016521 | G | A | upstream_gene_variant | MODIFIER | c.-2161C>T| |
S80 |
10 | BAA09g21000 | A09 | 13017286 | C | T | upstream_gene_variant | MODIFIER | c.-2926G>A| |
S168 |
11 | BAA09g21000 | A09 | 13017561 | G | A | upstream_gene_variant | MODIFIER | c.-3201C>T| |
S162 |