Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g11940 | A06 | 6027880 | G | A | missense_variant | MODERATE | c.977C>T|p.Ala326Val |
S13 |
2 | BAA06g11940 | A06 | 6028111 | C | T | missense_variant | MODERATE | c.829G>A|p.Glu277Lys |
S278 |
3 | BAA06g11940 | A06 | 6028443 | C | T | synonymous_variant | LOW | c.756G>A|p.Lys252Lys |
S94 |
4 | BAA06g11940 | A06 | 6028630 | C | T | synonymous_variant | LOW | c.654G>A|p.Leu218Leu |
S148 |
5 | BAA06g11940 | A06 | 6028654 | C | T | synonymous_variant | LOW | c.630G>A|p.Leu210Leu |
S11 |
6 | BAA06g11940 | A06 | 6029197 | G | A | missense_variant | MODERATE | c.563C>T|p.Ala188Val |
S136 |
7 | BAA06g11940 | A06 | 6030214 | C | T | missense_variant | MODERATE | c.41G>A|p.Arg14Gln |
S95 |
8 | BAA06g11940 | A06 | 6032164 | G | A | upstream_gene_variant | MODIFIER | c.-1910C>T| |
S146 |
9 | BAA06g11940 | A06 | 6034701 | C | T | upstream_gene_variant | MODIFIER | c.-4447G>A| |
S250 |