Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g42460 | A05 | 40218218 | C | T | upstream_gene_variant | MODIFIER | c.-163C>T| |
S260 |
2 | BAA05g42460 | A05 | 40218700 | C | T | missense_variant | MODERATE | c.320C>T|p.Ala107Val |
S219 |
3 | BAA05g42460 | A05 | 40219116 | C | T | stop_gained | HIGH | c.736C>T|p.Arg246* |
S54 |
4 | BAA05g42460 | A05 | 40219479 | C | T | missense_variant | MODERATE | c.1099C>T|p.Pro367Ser |
S179 |
5 | BAA05g42460 | A05 | 40219653 | G | A | missense_variant | MODERATE | c.1273G>A|p.Glu425Lys |
S278 |
6 | BAA05g42460 | A05 | 40219882 | C | T | missense_variant | MODERATE | c.1502C>T|p.Pro501Leu |
S201 |
7 | BAA05g42460 | A05 | 40220211 | G | A | missense_variant | MODERATE | c.1831G>A|p.Glu611Lys |
S182 |
8 | BAA05g42460 | A05 | 40221481 | C | T | synonymous_variant | LOW | c.2583C>T|p.Asn861Asn |
S172 S217 |
9 | BAA05g42460 | A05 | 40222206 | G | A | missense_variant | MODERATE | c.3053G>A|p.Arg1018Lys |
S144 |