Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g04770 | A06 | 2706592 | C | T | missense_variant | MODERATE | c.1034G>A|p.Arg345Lys |
S17 |
2 | BAA06g04770 | A06 | 2706684 | C | T | synonymous_variant | LOW | c.942G>A|p.Gly314Gly |
S144 |
3 | BAA06g04770 | A06 | 2706692 | C | T | missense_variant | MODERATE | c.934G>A|p.Ala312Thr |
S293 |
4 | BAA06g04770 | A06 | 2707589 | G | A | splice_region_variant&intron_variant | LOW | c.368-8C>T| |
S88 |
5 | BAA06g04770 | A06 | 2708322 | C | T | upstream_gene_variant | MODIFIER | c.-107G>A| |
S266 |