Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g44260 | A09 | 50027109 | G | A | upstream_gene_variant | MODIFIER | c.-4457G>A| |
S190 |
2 | BAA09g44260 | A09 | 50027334 | C | T | upstream_gene_variant | MODIFIER | c.-4232C>T| |
S276 |
3 | BAA09g44260 | A09 | 50027497 | G | A | upstream_gene_variant | MODIFIER | c.-4069G>A| |
S23 |
4 | BAA09g44260 | A09 | 50027851 | G | A | upstream_gene_variant | MODIFIER | c.-3715G>A| |
S111 |
5 | BAA09g44260 | A09 | 50028045 | G | A | upstream_gene_variant | MODIFIER | c.-3521G>A| |
S16 |
6 | BAA09g44260 | A09 | 50029606 | C | T | upstream_gene_variant | MODIFIER | c.-1960C>T| |
S37 S57 |
7 | BAA09g44260 | A09 | 50029642 | C | T | upstream_gene_variant | MODIFIER | c.-1924C>T| |
S18 |
8 | BAA09g44260 | A09 | 50031974 | G | A | missense_variant | MODERATE | c.232G>A|p.Val78Met |
S210 S225 |
9 | BAA09g44260 | A09 | 50031986 | G | A | missense_variant | MODERATE | c.244G>A|p.Glu82Lys |
S246 |
10 | BAA09g44260 | A09 | 50033596 | C | T | missense_variant | MODERATE | c.758C>T|p.Thr253Ile |
S90 |
11 | BAA09g44260 | A09 | 50034943 | G | A | stop_gained | HIGH | c.1371G>A|p.Trp457* |
S249 |
12 | BAA09g44260 | A09 | 50034973 | C | T | synonymous_variant | LOW | c.1401C>T|p.Asn467Asn |
S183 |
13 | BAA09g44260 | A09 | 50035594 | G | A | synonymous_variant | LOW | c.1692G>A|p.Arg564Arg |
S1 S90 |