Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g19600 | A10 | 17923558 | C | T | downstream_gene_variant | MODIFIER | c.*2346G>A| |
S117 |
2 | BAA10g19600 | A10 | 17924545 | C | T | downstream_gene_variant | MODIFIER | c.*1359G>A| |
S136 |
3 | BAA10g19600 | A10 | 17927062 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.2130-1G>A| |
S115 |
4 | BAA10g19600 | A10 | 17927219 | G | A | splice_region_variant&intron_variant | LOW | c.2064-8C>T| |
S25 |
5 | BAA10g19600 | A10 | 17929348 | C | T | missense_variant | MODERATE | c.818G>A|p.Arg273Lys |
S51 |
6 | BAA10g19600 | A10 | 17929511 | C | T | missense_variant | MODERATE | c.736G>A|p.Asp246Asn |
S84 S93 |
7 | BAA10g19600 | A10 | 17929709 | C | T | missense_variant | MODERATE | c.641G>A|p.Arg214Lys |
S25 |
8 | BAA10g19600 | A10 | 17930288 | A | G | synonymous_variant | LOW | c.159T>C|p.Arg53Arg |
S62 |
9 | BAA10g19600 | A10 | 17932620 | G | A | upstream_gene_variant | MODIFIER | c.-1979C>T| |
S94 |
10 | BAA10g19600 | A10 | 17934173 | T | A | upstream_gene_variant | MODIFIER | c.-3532A>T| |
S63 |
11 | BAA10g19600 | A10 | 17935604 | C | T | upstream_gene_variant | MODIFIER | c.-4963G>A| |
S306 S308 |