Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g03720 | A01 | 1693228 | C | T | missense_variant | MODERATE | c.1522C>T|p.Leu508Phe |
S211 S227 |
2 | BAA01g03720 | A01 | 1694079 | G | A | missense_variant | MODERATE | c.2057G>A|p.Gly686Glu |
S63 |
3 | BAA01g03720 | A01 | 1694376 | C | T | missense_variant | MODERATE | c.2191C>T|p.Pro731Ser |
S58 |
4 | BAA01g03720 | A01 | 1694806 | G | A | missense_variant | MODERATE | c.2500G>A|p.Ala834Thr |
S115 |
5 | BAA01g03720 | A01 | 1695558 | G | A | synonymous_variant | LOW | c.3060G>A|p.Lys1020Lys |
S177 |
6 | BAA01g03720 | A01 | 1696100 | C | T | missense_variant | MODERATE | c.3416C>T|p.Ala1139Val |
S262 |
7 | BAA01g03720 | A01 | 1696674 | C | T | synonymous_variant | LOW | c.3810C>T|p.Asn1270Asn |
S168 |
8 | BAA01g03720 | A01 | 1697641 | G | A | downstream_gene_variant | MODIFIER | c.*623G>A| |
S289 S290 |
9 | BAA01g03720 | A01 | 1697898 | G | A | downstream_gene_variant | MODIFIER | c.*880G>A| |
S308 |
10 | BAA01g03720 | A01 | 1698664 | C | T | downstream_gene_variant | MODIFIER | c.*1646C>T| |
S11 |