Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g18860 | A10 | 17506674 | G | A | synonymous_variant | LOW | c.2022C>T|p.Ile674Ile |
S4 |
2 | BAA10g18860 | A10 | 17507512 | C | T | synonymous_variant | LOW | c.1269G>A|p.Lys423Lys |
S249 |
3 | BAA10g18860 | A10 | 17507679 | G | A | missense_variant | MODERATE | c.1102C>T|p.Leu368Phe |
S195 |
4 | BAA10g18860 | A10 | 17507908 | C | T | missense_variant | MODERATE | c.947G>A|p.Arg316Lys |
S95 |
5 | BAA10g18860 | A10 | 17508599 | G | A | missense_variant | MODERATE | c.523C>T|p.His175Tyr |
S132 S137 S215 |
6 | BAA10g18860 | A10 | 17508832 | G | A | missense_variant | MODERATE | c.290C>T|p.Ser97Phe |
S176 |
7 | BAA10g18860 | A10 | 17508902 | C | T | missense_variant | MODERATE | c.220G>A|p.Glu74Lys |
S140 |
8 | BAA10g18860 | A10 | 17511173 | G | A | upstream_gene_variant | MODIFIER | c.-2052C>T| |
S144 |
9 | BAA10g18860 | A10 | 17512277 | C | T | upstream_gene_variant | MODIFIER | c.-3156G>A| |
S274 |
10 | BAA10g18860 | A10 | 17513748 | C | T | upstream_gene_variant | MODIFIER | c.-4627G>A| |
S249 |