Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g10430 | A10 | 12165804 | G | A | missense_variant&splice_region_variant | MODERATE | c.158C>T|p.Thr53Met |
S265 |
2 | BAA10g10430 | A10 | 12166832 | G | A | upstream_gene_variant | MODIFIER | c.-804C>T| |
S71 |
3 | BAA10g10430 | A10 | 12166876 | C | T | upstream_gene_variant | MODIFIER | c.-848G>A| |
S282 |
4 | BAA10g10430 | A10 | 12167289 | G | A | upstream_gene_variant | MODIFIER | c.-1261C>T| |
S202 |
5 | BAA10g10430 | A10 | 12168512 | C | T | upstream_gene_variant | MODIFIER | c.-2484G>A| |
S272 |
6 | BAA10g10430 | A10 | 12168568 | G | A | upstream_gene_variant | MODIFIER | c.-2540C>T| |
S16 |
7 | BAA10g10430 | A10 | 12168575 | C | T | upstream_gene_variant | MODIFIER | c.-2547G>A| |
S206 S26 |
8 | BAA10g10430 | A10 | 12168647 | G | A | upstream_gene_variant | MODIFIER | c.-2619C>T| |
S136 |
9 | BAA10g10430 | A10 | 12169450 | C | T | upstream_gene_variant | MODIFIER | c.-3422G>A| |
S180 |
10 | BAA10g10430 | A10 | 12170441 | C | T | upstream_gene_variant | MODIFIER | c.-4413G>A| |
S210 S225 |