Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g02920 | A10 | 1423098 | G | A | missense_variant | MODERATE | c.1367C>T|p.Pro456Leu |
S302 |
2 | BAA10g02920 | A10 | 1423613 | G | A | missense_variant | MODERATE | c.944C>T|p.Ser315Leu |
S4 |
3 | BAA10g02920 | A10 | 1425636 | G | A | missense_variant | MODERATE | c.341C>T|p.Thr114Ile |
S133 |
4 | BAA10g02920 | A10 | 1426684 | G | A | splice_region_variant&intron_variant | LOW | c.25+7C>T| |
S242 |
5 | BAA10g02920 | A10 | 1428597 | G | A | upstream_gene_variant | MODIFIER | c.-1882C>T| |
S15 S3 |
6 | BAA10g02920 | A10 | 1429003 | G | A | upstream_gene_variant | MODIFIER | c.-2288C>T| |
S120 |
7 | BAA10g02920 | A10 | 1429773 | C | T | upstream_gene_variant | MODIFIER | c.-3058G>A| |
S2 |