Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g41440 | A05 | 39603157 | C | T | upstream_gene_variant | MODIFIER | c.-248C>T| |
S112 |
2 | BAA05g41440 | A05 | 39603388 | G | A | upstream_gene_variant | MODIFIER | c.-17G>A| |
S223 |
3 | BAA05g41440 | A05 | 39603614 | C | T | synonymous_variant | LOW | c.210C>T|p.Ile70Ile |
S247 |
4 | BAA05g41440 | A05 | 39604944 | G | A | missense_variant | MODERATE | c.1288G>A|p.Glu430Lys |
S273 |
5 | BAA05g41440 | A05 | 39606328 | C | T | missense_variant | MODERATE | c.1802C>T|p.Ser601Phe |
S267 |
6 | BAA05g41440 | A05 | 39606711 | C | T | missense_variant | MODERATE | c.2185C>T|p.Pro729Ser |
S122 |
7 | BAA05g41440 | A05 | 39606884 | G | A | synonymous_variant | LOW | c.2358G>A|p.Glu786Glu |
S63 |
8 | BAA05g41440 | A05 | 39607451 | C | T | synonymous_variant | LOW | c.2925C>T|p.Leu975Leu |
S123 |
9 | BAA05g41440 | A05 | 39607594 | C | T | missense_variant | MODERATE | c.3068C>T|p.Thr1023Met |
S256 |
10 | BAA05g41440 | A05 | 39609464 | G | A | downstream_gene_variant | MODIFIER | c.*1494G>A| |
S72 S78 |
11 | BAA05g41440 | A05 | 39609703 | C | T | downstream_gene_variant | MODIFIER | c.*1733C>T| |
S192 |
12 | BAA05g41440 | A05 | 39612741 | G | A | downstream_gene_variant | MODIFIER | c.*4771G>A| |
S6 |