Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g02980 | A02 | 1324175 | G | A | missense_variant | MODERATE | c.1222G>A|p.Glu408Lys |
S266 |
2 | BAA02g02980 | A02 | 1324180 | G | A | synonymous_variant | LOW | c.1227G>A|p.Lys409Lys |
S7 |
3 | BAA02g02980 | A02 | 1324426 | G | A | missense_variant | MODERATE | c.1361G>A|p.Ser454Asn |
S226 |
4 | BAA02g02980 | A02 | 1324431 | G | A | missense_variant | MODERATE | c.1366G>A|p.Val456Met |
S236 |
5 | BAA02g02980 | A02 | 1325678 | G | A | missense_variant | MODERATE | c.2078G>A|p.Arg693Lys |
S134 |
6 | BAA02g02980 | A02 | 1325808 | G | A | missense_variant | MODERATE | c.2141G>A|p.Gly714Asp |
S10 |
7 | BAA02g02980 | A02 | 1326098 | G | A | synonymous_variant | LOW | c.2349G>A|p.Thr783Thr |
S96 |
8 | BAA02g02980 | A02 | 1327166 | C | T | missense_variant | MODERATE | c.2962C>T|p.Arg988Cys |
S95 |
9 | BAA02g02980 | A02 | 1327356 | G | A | synonymous_variant | LOW | c.3069G>A|p.Lys1023Lys |
S308 |
10 | BAA02g02980 | A02 | 1327490 | C | T | missense_variant | MODERATE | c.3203C>T|p.Ala1068Val |
S185 |
11 | BAA02g02980 | A02 | 1329195 | C | T | downstream_gene_variant | MODIFIER | c.*1433C>T| |
S153 |
12 | BAA02g02980 | A02 | 1332056 | G | A | downstream_gene_variant | MODIFIER | c.*4294G>A| |
S288 |
13 | BAA02g02980 | A02 | 1332236 | C | T | downstream_gene_variant | MODIFIER | c.*4474C>T| |
S241 |