Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g19690 | A01 | 9694508 | G | A | missense_variant | MODERATE | c.2423C>T|p.Pro808Leu |
S187 |
2 | BAA01g19690 | A01 | 9694970 | C | T | synonymous_variant | LOW | c.2145G>A|p.Lys715Lys |
S269 |
3 | BAA01g19690 | A01 | 9695782 | C | T | missense_variant | MODERATE | c.1888G>A|p.Asp630Asn |
S279 |
4 | BAA01g19690 | A01 | 9696248 | G | A | missense_variant | MODERATE | c.1561C>T|p.Leu521Phe |
S121 |
5 | BAA01g19690 | A01 | 9696723 | C | T | synonymous_variant | LOW | c.1251G>A|p.Leu417Leu |
S51 |
6 | BAA01g19690 | A01 | 9696758 | C | T | missense_variant | MODERATE | c.1216G>A|p.Gly406Ser |
S35 |
7 | BAA01g19690 | A01 | 9697250 | G | A | synonymous_variant | LOW | c.801C>T|p.His267His |
S117 |
8 | BAA01g19690 | A01 | 9697994 | C | T | missense_variant | MODERATE | c.287G>A|p.Arg96Lys |
S233 |
9 | BAA01g19690 | A01 | 9698371 | T | C | upstream_gene_variant | MODIFIER | c.-5A>G| |
S134 |
10 | BAA01g19690 | A01 | 9698426 | G | A | upstream_gene_variant | MODIFIER | c.-60C>T| |
S129 |
11 | BAA01g19690 | A01 | 9698458 | G | A | upstream_gene_variant | MODIFIER | c.-92C>T| |
S156 |
12 | BAA01g19690 | A01 | 9700312 | G | A | upstream_gene_variant | MODIFIER | c.-1946C>T| |
S228 |
13 | BAA01g19690 | A01 | 9702811 | G | A | upstream_gene_variant | MODIFIER | c.-4445C>T| |
S165 |
14 | BAA01g19690 | A01 | 9703064 | C | T | upstream_gene_variant | MODIFIER | c.-4698G>A| |
S36 |