Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g47200 | A09 | 51588515 | G | A | missense_variant | MODERATE | c.2540C>T|p.Ala847Val |
S45 |
2 | BAA09g47200 | A09 | 51589472 | C | T | synonymous_variant | LOW | c.1896G>A|p.Thr632Thr |
S100 |
3 | BAA09g47200 | A09 | 51589750 | G | A | missense_variant | MODERATE | c.1618C>T|p.Leu540Phe |
S84 S93 |
4 | BAA09g47200 | A09 | 51592469 | C | T | synonymous_variant | LOW | c.522G>A|p.Arg174Arg |
S18 |
5 | BAA09g47200 | A09 | 51592970 | G | A | synonymous_variant | LOW | c.21C>T|p.Val7Val |
S136 |
6 | BAA09g47200 | A09 | 51593047 | G | A | upstream_gene_variant | MODIFIER | c.-57C>T| |
S150 |
7 | BAA09g47200 | A09 | 51593222 | G | A | upstream_gene_variant | MODIFIER | c.-232C>T| |
S190 |
8 | BAA09g47200 | A09 | 51593992 | G | A | upstream_gene_variant | MODIFIER | c.-1002C>T| |
S194 |
9 | BAA09g47200 | A09 | 51594222 | G | A | upstream_gene_variant | MODIFIER | c.-1232C>T| |
S272 |
10 | BAA09g47200 | A09 | 51594406 | C | T | upstream_gene_variant | MODIFIER | c.-1416G>A| |
S170 |
11 | BAA09g47200 | A09 | 51594433 | C | T | upstream_gene_variant | MODIFIER | c.-1443G>A| |
S208 |
12 | BAA09g47200 | A09 | 51594904 | C | T | upstream_gene_variant | MODIFIER | c.-1914G>A| |
S130 |