Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g04160 | A08 | 2946427 | C | T | missense_variant | MODERATE | c.73C>T|p.Leu25Phe |
S53 |
2 | BAA08g04160 | A08 | 2946448 | G | A | missense_variant | MODERATE | c.94G>A|p.Ala32Thr |
S260 |
3 | BAA08g04160 | A08 | 2946998 | G | A | missense_variant | MODERATE | c.421G>A|p.Asp141Asn |
S87 |
4 | BAA08g04160 | A08 | 2947491 | C | T | missense_variant | MODERATE | c.643C>T|p.Pro215Ser |
S157 S163 |
5 | BAA08g04160 | A08 | 2948886 | G | A | missense_variant | MODERATE | c.1373G>A|p.Arg458Gln |
S130 |
6 | BAA08g04160 | A08 | 2948970 | G | A | missense_variant | MODERATE | c.1457G>A|p.Gly486Glu |
S275 |
7 | BAA08g04160 | A08 | 2949920 | G | A | downstream_gene_variant | MODIFIER | c.*877G>A| |
S62 |
8 | BAA08g04160 | A08 | 2950117 | C | T | downstream_gene_variant | MODIFIER | c.*1074C>T| |
S167 |