Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g02180 | A03 | 970498 | G | A | synonymous_variant | LOW | c.2955C>T|p.Tyr985Tyr |
S122 |
2 | BAA03g02180 | A03 | 971253 | G | A | synonymous_variant | LOW | c.2277C>T|p.Ile759Ile |
S112 |
3 | BAA03g02180 | A03 | 972304 | C | T | missense_variant&splice_region_variant | MODERATE | c.1588G>A|p.Val530Ile |
S81 S85 |
4 | BAA03g02180 | A03 | 972428 | C | T | synonymous_variant | LOW | c.1566G>A|p.Lys522Lys |
S174 S27 |
5 | BAA03g02180 | A03 | 972967 | G | A | missense_variant | MODERATE | c.1192C>T|p.Arg398Cys |
S226 |
6 | BAA03g02180 | A03 | 973646 | C | T | splice_region_variant&intron_variant | LOW | c.710+5G>A| |
S51 |
7 | BAA03g02180 | A03 | 973670 | G | A | missense_variant | MODERATE | c.691C>T|p.Leu231Phe |
S236 |
8 | BAA03g02180 | A03 | 977526 | C | T | upstream_gene_variant | MODIFIER | c.-2794G>A| |
S159 S243 S299 |
9 | BAA03g02180 | A03 | 977631 | G | A | upstream_gene_variant | MODIFIER | c.-2899C>T| |
S162 |
10 | BAA03g02180 | A03 | 977690 | G | A | upstream_gene_variant | MODIFIER | c.-2958C>T| |
S236 |