Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g46390 | A09 | 51159484 | G | A | synonymous_variant | LOW | c.651C>T|p.His217His |
S79 S91 |
2 | BAA09g46390 | A09 | 51159513 | G | A | missense_variant | MODERATE | c.622C>T|p.Pro208Ser |
S46 |
3 | BAA09g46390 | A09 | 51159700 | C | T | missense_variant | MODERATE | c.512G>A|p.Gly171Glu |
S208 |
4 | BAA09g46390 | A09 | 51159908 | G | A | synonymous_variant | LOW | c.387C>T|p.Ile129Ile |
S137 |
5 | BAA09g46390 | A09 | 51160194 | C | T | missense_variant | MODERATE | c.275G>A|p.Arg92Lys |
S25 |
6 | BAA09g46390 | A09 | 51160391 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.79-1G>A| |
S186 |
7 | BAA09g46390 | A09 | 51162246 | C | T | upstream_gene_variant | MODIFIER | c.-1033G>A| |
S216 |
8 | BAA09g46390 | A09 | 51162261 | C | T | upstream_gene_variant | MODIFIER | c.-1048G>A| |
S60 |
9 | BAA09g46390 | A09 | 51162382 | C | T | upstream_gene_variant | MODIFIER | c.-1169G>A| |
S232 |
10 | BAA09g46390 | A09 | 51162389 | C | T | upstream_gene_variant | MODIFIER | c.-1176G>A| |
S168 |
11 | BAA09g46390 | A09 | 51163686 | C | T | upstream_gene_variant | MODIFIER | c.-2473G>A| |
S261 |
12 | BAA09g46390 | A09 | 51165661 | G | A | upstream_gene_variant | MODIFIER | c.-4448C>T| |
S59 |