Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g26850 | A10 | 21124165 | G | A | missense_variant&splice_region_variant | MODERATE | c.383C>T|p.Ser128Phe |
S178 |
2 | BAA10g26850 | A10 | 21124377 | G | A | missense_variant | MODERATE | c.247C>T|p.Pro83Ser |
S219 S72 |
3 | BAA10g26850 | A10 | 21124383 | G | A | missense_variant | MODERATE | c.241C>T|p.Pro81Ser |
S172 S217 |
4 | BAA10g26850 | A10 | 21124974 | C | T | upstream_gene_variant | MODIFIER | c.-351G>A| |
S292 |
5 | BAA10g26850 | A10 | 21126489 | C | T | upstream_gene_variant | MODIFIER | c.-1866G>A| |
S162 |