Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g08610 | A02 | 3733632 | G | A | upstream_gene_variant | MODIFIER | c.-3097G>A| |
S5 |
2 | BAA02g08610 | A02 | 3737184 | C | T | synonymous_variant | LOW | c.456C>T|p.His152His |
S15 S3 |
3 | BAA02g08610 | A02 | 3737573 | C | T | missense_variant | MODERATE | c.767C>T|p.Ser256Phe |
S46 |
4 | BAA02g08610 | A02 | 3737636 | G | A | missense_variant | MODERATE | c.830G>A|p.Ser277Asn |
S52 |
5 | BAA02g08610 | A02 | 3737869 | C | T | missense_variant | MODERATE | c.1063C>T|p.Pro355Ser |
S138 |
6 | BAA02g08610 | A02 | 3737947 | G | A | missense_variant | MODERATE | c.1141G>A|p.Val381Ile |
S86 |
7 | BAA02g08610 | A02 | 3738746 | C | T | missense_variant | MODERATE | c.1858C>T|p.Leu620Phe |
S120 |
8 | BAA02g08610 | A02 | 3738751 | G | A | stop_gained | HIGH | c.1863G>A|p.Trp621* |
S125 |
9 | BAA02g08610 | A02 | 3738992 | C | T | missense_variant | MODERATE | c.2024C>T|p.Thr675Ile |
S211 S227 |
10 | BAA02g08610 | A02 | 3741300 | C | T | synonymous_variant | LOW | c.2902C>T|p.Leu968Leu |
S103 |