Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g18110 | A09 | 10863705 | C | T | missense_variant | MODERATE | c.196C>T|p.Pro66Ser |
S157 |
2 | BAA09g18110 | A09 | 10863913 | C | T | missense_variant | MODERATE | c.295C>T|p.Leu99Phe |
S174 |
3 | BAA09g18110 | A09 | 10864669 | G | A | missense_variant | MODERATE | c.797G>A|p.Arg266Lys |
S233 |
4 | BAA09g18110 | A09 | 10866113 | C | T | missense_variant | MODERATE | c.1564C>T|p.Leu522Phe |
S204 |
5 | BAA09g18110 | A09 | 10867357 | G | A | missense_variant | MODERATE | c.2362G>A|p.Asp788Asn |
S38 |
6 | BAA09g18110 | A09 | 10868823 | C | T | downstream_gene_variant | MODIFIER | c.*1386C>T| |
S41 |
7 | BAA09g18110 | A09 | 10869971 | C | T | downstream_gene_variant | MODIFIER | c.*2534C>T| |
S71 |
8 | BAA09g18110 | A09 | 10870275 | G | A | downstream_gene_variant | MODIFIER | c.*2838G>A| |
S221 |