Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g31760 | A10 | 23073559 | T | A | upstream_gene_variant | MODIFIER | c.-1916T>A| |
S296 |
2 | BAA10g31760 | A10 | 23073906 | G | A | upstream_gene_variant | MODIFIER | c.-1569G>A| |
S264 |
3 | BAA10g31760 | A10 | 23074289 | C | T | upstream_gene_variant | MODIFIER | c.-1186C>T| |
S246 |
4 | BAA10g31760 | A10 | 23074587 | C | T | upstream_gene_variant | MODIFIER | c.-888C>T| |
S4 |
5 | BAA10g31760 | A10 | 23074968 | C | T | upstream_gene_variant | MODIFIER | c.-507C>T| |
S135 |
6 | BAA10g31760 | A10 | 23075276 | C | T | upstream_gene_variant | MODIFIER | c.-199C>T| |
S204 |
7 | BAA10g31760 | A10 | 23075300 | G | A | upstream_gene_variant | MODIFIER | c.-175G>A| |
S262 |
8 | BAA10g31760 | A10 | 23076369 | C | T | missense_variant | MODERATE | c.506C>T|p.Ser169Phe |
S156 |
9 | BAA10g31760 | A10 | 23076398 | C | T | missense_variant | MODERATE | c.535C>T|p.Pro179Ser |
S169 |
10 | BAA10g31760 | A10 | 23080196 | G | A | downstream_gene_variant | MODIFIER | c.*3055G>A| |
S263 |
11 | BAA10g31760 | A10 | 23080834 | C | T | downstream_gene_variant | MODIFIER | c.*3693C>T| |
S33 |
12 | BAA10g31760 | A10 | 23081544 | G | A | downstream_gene_variant | MODIFIER | c.*4403G>A| |
S38 |