Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g44250 | A01 | 29309209 | G | A | missense_variant | MODERATE | c.286G>A|p.Glu96Lys |
S209 |
2 | BAA01g44250 | A01 | 29312300 | C | T | missense_variant | MODERATE | c.1054C>T|p.Leu352Phe |
S191 |
3 | BAA01g44250 | A01 | 29312514 | C | T | missense_variant | MODERATE | c.1136C>T|p.Thr379Ile |
S231 |
4 | BAA01g44250 | A01 | 29312896 | G | A | missense_variant | MODERATE | c.1295G>A|p.Arg432Gln |
S209 |
5 | BAA01g44250 | A01 | 29313333 | G | A | missense_variant | MODERATE | c.1387G>A|p.Asp463Asn |
S293 |
6 | BAA01g44250 | A01 | 29313376 | C | T | missense_variant | MODERATE | c.1430C>T|p.Ser477Phe |
S221 |
7 | BAA01g44250 | A01 | 29313575 | G | A | missense_variant | MODERATE | c.1535G>A|p.Ser512Asn |
S86 |
8 | BAA01g44250 | A01 | 29314835 | C | T | synonymous_variant | LOW | c.2169C>T|p.Asp723Asp |
S25 |
9 | BAA01g44250 | A01 | 29314893 | C | T | missense_variant | MODERATE | c.2227C>T|p.Leu743Phe |
S188 |
10 | BAA01g44250 | A01 | 29314994 | G | A | synonymous_variant | LOW | c.2328G>A|p.Val776Val |
S117 |
11 | BAA01g44250 | A01 | 29315247 | G | A | missense_variant | MODERATE | c.2581G>A|p.Glu861Lys |
S225 |
12 | BAA01g44250 | A01 | 29315339 | C | T | downstream_gene_variant | MODIFIER | c.*69C>T| |
S88 |
13 | BAA01g44250 | A01 | 29315824 | A | C | downstream_gene_variant | MODIFIER | c.*554A>C| |
S176 |
14 | BAA01g44250 | A01 | 29316183 | G | A | downstream_gene_variant | MODIFIER | c.*913G>A| |
S108 |