Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g65490 | A09 | 60319476 | G | A | missense_variant | MODERATE | c.1114C>T|p.Pro372Ser |
S42 |
2 | BAA09g65490 | A09 | 60319709 | C | T | splice_region_variant&intron_variant | LOW | c.968-4G>A| |
S65 |
3 | BAA09g65490 | A09 | 60320579 | C | T | missense_variant | MODERATE | c.530G>A|p.Gly177Glu |
S8 |
4 | BAA09g65490 | A09 | 60323845 | C | T | upstream_gene_variant | MODIFIER | c.-2415G>A| |
S279 |
5 | BAA09g65490 | A09 | 60324868 | C | T | upstream_gene_variant | MODIFIER | c.-3438G>A| |
S18 S60 |
6 | BAA09g65490 | A09 | 60325976 | G | A | upstream_gene_variant | MODIFIER | c.-4546C>T| |
S246 |
7 | BAA09g65490 | A09 | 60326149 | C | T | upstream_gene_variant | MODIFIER | c.-4719G>A| |
S163 |