Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g10070 | A01 | 4553565 | C | T | synonymous_variant | LOW | c.1530G>A|p.Gln510Gln |
S185 |
2 | BAA01g10070 | A01 | 4553603 | C | T | missense_variant | MODERATE | c.1492G>A|p.Val498Ile |
S208 S93 |
3 | BAA01g10070 | A01 | 4553780 | C | T | missense_variant | MODERATE | c.1315G>A|p.Val439Met |
S98 |
4 | BAA01g10070 | A01 | 4553845 | G | A | missense_variant | MODERATE | c.1250C>T|p.Pro417Leu |
S142 |
5 | BAA01g10070 | A01 | 4553989 | C | T | missense_variant | MODERATE | c.1106G>A|p.Ser369Asn |
S231 |
6 | BAA01g10070 | A01 | 4554469 | G | A | missense_variant | MODERATE | c.811C>T|p.Leu271Phe |
S217 |
7 | BAA01g10070 | A01 | 4554617 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.664-1G>A| |
S252 |
8 | BAA01g10070 | A01 | 4554735 | C | T | missense_variant | MODERATE | c.631G>A|p.Ala211Thr |
S35 |
9 | BAA01g10070 | A01 | 4555264 | G | A | synonymous_variant | LOW | c.102C>T|p.Thr34Thr |
S95 |
10 | BAA01g10070 | A01 | 4556189 | G | A | upstream_gene_variant | MODIFIER | c.-824C>T| |
S294 |
11 | BAA01g10070 | A01 | 4559092 | G | A | upstream_gene_variant | MODIFIER | c.-3727C>T| |
S124 |
12 | BAA01g10070 | A01 | 4559957 | C | T | upstream_gene_variant | MODIFIER | c.-4592G>A| |
S100 |