Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g18950 | A05 | 11018230 | C | T | upstream_gene_variant | MODIFIER | c.-3274C>T| |
S89 |
2 | BAA05g18950 | A05 | 11020467 | G | A | upstream_gene_variant | MODIFIER | c.-1037G>A| |
S23 |
3 | BAA05g18950 | A05 | 11020749 | G | A | upstream_gene_variant | MODIFIER | c.-755G>A| |
S104 S52 |
4 | BAA05g18950 | A05 | 11020862 | G | A | upstream_gene_variant | MODIFIER | c.-642G>A| |
S236 |
5 | BAA05g18950 | A05 | 11021115 | C | T | upstream_gene_variant | MODIFIER | c.-389C>T| |
S53 |
6 | BAA05g18950 | A05 | 11021689 | C | T | synonymous_variant | LOW | c.186C>T|p.Ile62Ile |
S269 |
7 | BAA05g18950 | A05 | 11023587 | C | T | synonymous_variant | LOW | c.1176C>T|p.Ile392Ile |
S35 |
8 | BAA05g18950 | A05 | 11024695 | G | A | missense_variant | MODERATE | c.1840G>A|p.Asp614Asn |
S132 S137 S89 |
9 | BAA05g18950 | A05 | 11024742 | C | T | synonymous_variant | LOW | c.1887C>T|p.Phe629Phe |
S292 |
10 | BAA05g18950 | A05 | 11025370 | C | T | downstream_gene_variant | MODIFIER | c.*436C>T| |
S295 |
11 | BAA05g18950 | A05 | 11027721 | C | T | downstream_gene_variant | MODIFIER | c.*2787C>T| |
S74 |