Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g21800 | A10 | 19045282 | G | A | missense_variant | MODERATE | c.521G>A|p.Gly174Glu |
S182 |
2 | BAA10g21800 | A10 | 19045401 | C | T | synonymous_variant | LOW | c.640C>T|p.Leu214Leu |
S148 S210 S30 S31 |
3 | BAA10g21800 | A10 | 19045551 | G | A | missense_variant | MODERATE | c.790G>A|p.Gly264Arg |
S239 |
4 | BAA10g21800 | A10 | 19045917 | G | A | missense_variant | MODERATE | c.1156G>A|p.Gly386Ser |
S195 |
5 | BAA10g21800 | A10 | 19046297 | C | T | synonymous_variant | LOW | c.1536C>T|p.Pro512Pro |
S201 |
6 | BAA10g21800 | A10 | 19046419 | C | T | missense_variant | MODERATE | c.1658C>T|p.Ser553Leu |
S70 |
7 | BAA10g21800 | A10 | 19046592 | G | A | missense_variant | MODERATE | c.1831G>A|p.Ala611Thr |
S139 |
8 | BAA10g21800 | A10 | 19047025 | G | A | missense_variant | MODERATE | c.2264G>A|p.Arg755Gln |
S109 |
9 | BAA10g21800 | A10 | 19048301 | G | A | synonymous_variant | LOW | c.3075G>A|p.Glu1025Glu |
S66 |
10 | BAA10g21800 | A10 | 19048800 | G | A | synonymous_variant | LOW | c.3210G>A|p.Glu1070Glu |
S208 |
11 | BAA10g21800 | A10 | 19050987 | G | A | synonymous_variant | LOW | c.4728G>A|p.Glu1576Glu |
S126 |
12 | BAA10g21800 | A10 | 19051228 | G | A | downstream_gene_variant | MODIFIER | c.*88G>A| |
S202 |