Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g27530 | A01 | 16012963 | G | A | missense_variant | MODERATE | c.23G>A|p.Gly8Asp |
S13 |
2 | BAA01g27530 | A01 | 16013847 | A | C | missense_variant | MODERATE | c.684A>C|p.Lys228Asn |
S37 S62 |
3 | BAA01g27530 | A01 | 16013886 | G | A | synonymous_variant | LOW | c.723G>A|p.Ala241Ala |
S271 |
4 | BAA01g27530 | A01 | 16013962 | G | A | missense_variant | MODERATE | c.799G>A|p.Glu267Lys |
S180 |
5 | BAA01g27530 | A01 | 16014026 | G | A | missense_variant | MODERATE | c.863G>A|p.Gly288Glu |
S84 S93 |
6 | BAA01g27530 | A01 | 16014228 | C | T | intron_variant | MODIFIER | c.1026+39C>T| |
S196 |
7 | BAA01g27530 | A01 | 16016403 | C | T | downstream_gene_variant | MODIFIER | c.*1933C>T| |
S142 |
8 | BAA01g27530 | A01 | 16018143 | C | T | downstream_gene_variant | MODIFIER | c.*3673C>T| |
S50 |
9 | BAA01g27530 | A01 | 16018751 | G | A | downstream_gene_variant | MODIFIER | c.*4281G>A| |
S70 |
10 | BAA01g27530 | A01 | 16018947 | C | T | downstream_gene_variant | MODIFIER | c.*4477C>T| |
S183 |