Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g12770 | A01 | 6036572 | T | A | downstream_gene_variant | MODIFIER | c.*4833A>T| |
S209 |
2 | BAA01g12770 | A01 | 6036655 | G | A | downstream_gene_variant | MODIFIER | c.*4750C>T| |
S32 |
3 | BAA01g12770 | A01 | 6037166 | G | A | downstream_gene_variant | MODIFIER | c.*4239C>T| |
S180 |
4 | BAA01g12770 | A01 | 6037294 | G | A | downstream_gene_variant | MODIFIER | c.*4111C>T| |
S202 |
5 | BAA01g12770 | A01 | 6037652 | C | T | downstream_gene_variant | MODIFIER | c.*3753G>A| |
S7 |
6 | BAA01g12770 | A01 | 6042444 | C | T | synonymous_variant | LOW | c.1296G>A|p.Lys432Lys |
S18 |
7 | BAA01g12770 | A01 | 6042602 | C | T | missense_variant | MODERATE | c.1138G>A|p.Ala380Thr |
S50 |
8 | BAA01g12770 | A01 | 6042664 | G | A | missense_variant | MODERATE | c.1076C>T|p.Ser359Phe |
S297 |
9 | BAA01g12770 | A01 | 6043465 | G | A | missense_variant | MODERATE | c.356C>T|p.Thr119Ile |
S109 |
10 | BAA01g12770 | A01 | 6043467 | T | A | synonymous_variant | LOW | c.354A>T|p.Ala118Ala |
S109 |
11 | BAA01g12770 | A01 | 6043480 | C | T | missense_variant | MODERATE | c.341G>A|p.Ser114Asn |
S62 |