Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g13490 | A02 | 6209345 | C | T | missense_variant | MODERATE | c.2005G>A|p.Ala669Thr |
S240 |
2 | BAA02g13490 | A02 | 6210253 | C | T | missense_variant | MODERATE | c.1097G>A|p.Arg366Lys |
S156 |
3 | BAA02g13490 | A02 | 6211033 | G | A | missense_variant | MODERATE | c.317C>T|p.Ser106Phe |
S12 |
4 | BAA02g13490 | A02 | 6211187 | C | T | missense_variant | MODERATE | c.163G>A|p.Asp55Asn |
S221 |
5 | BAA02g13490 | A02 | 6212968 | G | A | upstream_gene_variant | MODIFIER | c.-1619C>T| |
S279 |
6 | BAA02g13490 | A02 | 6213257 | G | A | upstream_gene_variant | MODIFIER | c.-1908C>T| |
S225 S50 S73 |
7 | BAA02g13490 | A02 | 6213701 | C | T | upstream_gene_variant | MODIFIER | c.-2352G>A| |
S180 |
8 | BAA02g13490 | A02 | 6215079 | G | A | upstream_gene_variant | MODIFIER | c.-3730C>T| |
S92 |
9 | BAA02g13490 | A02 | 6216152 | C | T | upstream_gene_variant | MODIFIER | c.-4803G>A| |
S116 |
10 | BAA02g13490 | A02 | 6216229 | G | A | upstream_gene_variant | MODIFIER | c.-4880C>T| |
S294 |