Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g00200 | A05 | 117226 | C | T | missense_variant | MODERATE | c.1319G>A|p.Arg440Lys |
S15 S3 |
2 | BAA05g00200 | A05 | 117561 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.985-1G>A| |
S287 |
3 | BAA05g00200 | A05 | 117728 | C | T | missense_variant | MODERATE | c.881G>A|p.Gly294Glu |
S171 |
4 | BAA05g00200 | A05 | 117967 | G | A | missense_variant | MODERATE | c.706C>T|p.Pro236Ser |
S122 |
5 | BAA05g00200 | A05 | 118248 | G | A | splice_region_variant&intron_variant | LOW | c.433-8C>T| |
S186 |
6 | BAA05g00200 | A05 | 118465 | C | T | splice_region_variant&intron_variant | LOW | c.307-4G>A| |
S139 |
7 | BAA05g00200 | A05 | 118868 | G | A | missense_variant | MODERATE | c.181C>T|p.Arg61Cys |
S274 |
8 | BAA05g00200 | A05 | 120403 | G | A | upstream_gene_variant | MODIFIER | c.-1239C>T| |
S295 |
9 | BAA05g00200 | A05 | 120819 | C | T | upstream_gene_variant | MODIFIER | c.-1655G>A| |
S94 |
10 | BAA05g00200 | A05 | 121391 | G | A | upstream_gene_variant | MODIFIER | c.-2227C>T| |
S47 |
11 | BAA05g00200 | A05 | 123415 | C | T | upstream_gene_variant | MODIFIER | c.-4251G>A| |
S10 |