Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g17660 | A02 | 8797646 | G | A | splice_region_variant&intron_variant | LOW | c.3009+8C>T| |
S17 |
2 | BAA02g17660 | A02 | 8797782 | G | A | splice_region_variant&synonymous_variant | LOW | c.2881C>T|p.Leu961Leu |
S205 |
3 | BAA02g17660 | A02 | 8800117 | C | T | missense_variant | MODERATE | c.1232G>A|p.Cys411Tyr |
S18 |
4 | BAA02g17660 | A02 | 8800530 | C | T | stop_gained | HIGH | c.852G>A|p.Trp284* |
S79 |
5 | BAA02g17660 | A02 | 8800717 | C | T | missense_variant | MODERATE | c.665G>A|p.Gly222Glu |
S234 |
6 | BAA02g17660 | A02 | 8801115 | G | A | synonymous_variant | LOW | c.267C>T|p.Asn89Asn |
S37 |
7 | BAA02g17660 | A02 | 8801787 | G | A | upstream_gene_variant | MODIFIER | c.-406C>T| |
S256 |
8 | BAA02g17660 | A02 | 8802619 | C | T | upstream_gene_variant | MODIFIER | c.-1238G>A| |
S165 |
9 | BAA02g17660 | A02 | 8803887 | G | A | upstream_gene_variant | MODIFIER | c.-2506C>T| |
S188 |
10 | BAA02g17660 | A02 | 8803888 | G | A | upstream_gene_variant | MODIFIER | c.-2507C>T| |
S33 |