Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g26150 | A10 | 20854167 | C | T | upstream_gene_variant | MODIFIER | c.-4801C>T| |
S221 |
2 | BAA10g26150 | A10 | 20854257 | T | A | upstream_gene_variant | MODIFIER | c.-4711T>A| |
S257 |
3 | BAA10g26150 | A10 | 20854286 | G | A | upstream_gene_variant | MODIFIER | c.-4682G>A| |
S262 |
4 | BAA10g26150 | A10 | 20854528 | G | A | upstream_gene_variant | MODIFIER | c.-4440G>A| |
S267 |
5 | BAA10g26150 | A10 | 20856424 | G | T | upstream_gene_variant | MODIFIER | c.-2544G>T| |
S156 |
6 | BAA10g26150 | A10 | 20856543 | G | A | upstream_gene_variant | MODIFIER | c.-2425G>A| |
S190 |
7 | BAA10g26150 | A10 | 20857547 | G | A | upstream_gene_variant | MODIFIER | c.-1421G>A| |
S219 S72 |
8 | BAA10g26150 | A10 | 20857809 | C | T | upstream_gene_variant | MODIFIER | c.-1159C>T| |
S275 |
9 | BAA10g26150 | A10 | 20857980 | G | A | upstream_gene_variant | MODIFIER | c.-988G>A| |
S179 |
10 | BAA10g26150 | A10 | 20858267 | C | T | upstream_gene_variant | MODIFIER | c.-701C>T| |
S18 |
11 | BAA10g26150 | A10 | 20858689 | C | T | upstream_gene_variant | MODIFIER | c.-279C>T| |
S38 |
12 | BAA10g26150 | A10 | 20860597 | G | A | missense_variant | MODERATE | c.647G>A|p.Arg216Lys |
S59 |
13 | BAA10g26150 | A10 | 20860829 | C | T | synonymous_variant | LOW | c.879C>T|p.Ala293Ala |
S195 |