Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g12440 | A05 | 6386605 | G | A | upstream_gene_variant | MODIFIER | c.-3887G>A| |
S187 |
2 | BAA05g12440 | A05 | 6386618 | C | T | upstream_gene_variant | MODIFIER | c.-3874C>T| |
S193 |
3 | BAA05g12440 | A05 | 6387292 | C | T | upstream_gene_variant | MODIFIER | c.-3200C>T| |
S184 |
4 | BAA05g12440 | A05 | 6387372 | G | A | upstream_gene_variant | MODIFIER | c.-3120G>A| |
S218 |
5 | BAA05g12440 | A05 | 6387536 | G | A | upstream_gene_variant | MODIFIER | c.-2956G>A| |
S138 |
6 | BAA05g12440 | A05 | 6388495 | G | A | upstream_gene_variant | MODIFIER | c.-1997G>A| |
S240 |
7 | BAA05g12440 | A05 | 6388897 | G | A | upstream_gene_variant | MODIFIER | c.-1595G>A| |
S134 |
8 | BAA05g12440 | A05 | 6390316 | G | A | upstream_gene_variant | MODIFIER | c.-176G>A| |
S13 S202 |
9 | BAA05g12440 | A05 | 6391261 | G | A | missense_variant | MODERATE | c.770G>A|p.Cys257Tyr |
S296 |
10 | BAA05g12440 | A05 | 6391985 | G | A | downstream_gene_variant | MODIFIER | c.*174G>A| |
S125 |
11 | BAA05g12440 | A05 | 6392286 | G | A | downstream_gene_variant | MODIFIER | c.*475G>A| |
S189 S272 |
12 | BAA05g12440 | A05 | 6393377 | C | T | downstream_gene_variant | MODIFIER | c.*1566C>T| |
S281 |
13 | BAA05g12440 | A05 | 6394294 | G | A | downstream_gene_variant | MODIFIER | c.*2483G>A| |
S132 S137 |