Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g45330 | A01 | 30199455 | G | A | missense_variant | MODERATE | c.1223C>T|p.Ala408Val |
S144 |
2 | BAA01g45330 | A01 | 30200067 | C | T | missense_variant | MODERATE | c.692G>A|p.Gly231Glu |
S191 |
3 | BAA01g45330 | A01 | 30200555 | G | A | missense_variant | MODERATE | c.472C>T|p.Pro158Ser |
S278 |
4 | BAA01g45330 | A01 | 30200569 | C | T | missense_variant | MODERATE | c.458G>A|p.Ser153Asn |
S241 |
5 | BAA01g45330 | A01 | 30200575 | G | A | missense_variant | MODERATE | c.452C>T|p.Ser151Phe |
S204 |
6 | BAA01g45330 | A01 | 30200879 | C | T | synonymous_variant | LOW | c.228G>A|p.Leu76Leu |
S130 |
7 | BAA01g45330 | A01 | 30203192 | C | T | upstream_gene_variant | MODIFIER | c.-1355G>A| |
S56 |
8 | BAA01g45330 | A01 | 30203521 | T | A | upstream_gene_variant | MODIFIER | c.-1684A>T| |
S13 S80 |
9 | BAA01g45330 | A01 | 30204119 | C | T | upstream_gene_variant | MODIFIER | c.-2282G>A| |
S18 |
10 | BAA01g45330 | A01 | 30204754 | G | A | upstream_gene_variant | MODIFIER | c.-2917C>T| |
S287 |