Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g04540 | A01 | 2013807 | C | T | missense_variant | MODERATE | c.2260G>A|p.Ala754Thr |
S44 |
2 | BAA01g04540 | A01 | 2013978 | G | A | missense_variant | MODERATE | c.2089C>T|p.Arg697Trp |
S173 |
3 | BAA01g04540 | A01 | 2014451 | G | A | missense_variant | MODERATE | c.1783C>T|p.Leu595Phe |
S161 |
4 | BAA01g04540 | A01 | 2014898 | C | T | missense_variant | MODERATE | c.1336G>A|p.Asp446Asn |
S107 |
5 | BAA01g04540 | A01 | 2015519 | C | T | synonymous_variant | LOW | c.807G>A|p.Glu269Glu |
S133 |
6 | BAA01g04540 | A01 | 2015582 | C | T | synonymous_variant | LOW | c.744G>A|p.Glu248Glu |
S62 |
7 | BAA01g04540 | A01 | 2015763 | C | T | missense_variant | MODERATE | c.563G>A|p.Gly188Asp |
S59 |
8 | BAA01g04540 | A01 | 2016165 | C | T | missense_variant | MODERATE | c.332G>A|p.Ser111Asn |
S111 |
9 | BAA01g04540 | A01 | 2016882 | C | T | upstream_gene_variant | MODIFIER | c.-386G>A| |
S238 |
10 | BAA01g04540 | A01 | 2019047 | C | T | upstream_gene_variant | MODIFIER | c.-2551G>A| |
S249 |