Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g24390 | A10 | 20109608 | C | T | upstream_gene_variant | MODIFIER | c.-2409C>T| |
S282 |
2 | BAA10g24390 | A10 | 20109826 | G | A | upstream_gene_variant | MODIFIER | c.-2191G>A| |
S198 |
3 | BAA10g24390 | A10 | 20110127 | C | T | upstream_gene_variant | MODIFIER | c.-1890C>T| |
S244 |
4 | BAA10g24390 | A10 | 20110198 | C | T | upstream_gene_variant | MODIFIER | c.-1819C>T| |
S47 |
5 | BAA10g24390 | A10 | 20110403 | C | T | upstream_gene_variant | MODIFIER | c.-1614C>T| |
S195 |
6 | BAA10g24390 | A10 | 20110723 | G | A | upstream_gene_variant | MODIFIER | c.-1294G>A| |
S209 |
7 | BAA10g24390 | A10 | 20112147 | G | T | missense_variant | MODERATE | c.131G>T|p.Gly44Val |
S134 |
8 | BAA10g24390 | A10 | 20113164 | C | T | missense_variant | MODERATE | c.764C>T|p.Thr255Met |
S292 |
9 | BAA10g24390 | A10 | 20114387 | C | T | synonymous_variant | LOW | c.1917C>T|p.Val639Val |
S103 |
10 | BAA10g24390 | A10 | 20114757 | C | T | synonymous_variant | LOW | c.2199C>T|p.Phe733Phe |
S96 |