Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g02490 | A10 | 1206126 | C | T | missense_variant | MODERATE | c.2246G>A|p.Arg749Lys |
S192 |
2 | BAA10g02490 | A10 | 1206449 | G | A | missense_variant | MODERATE | c.2083C>T|p.Arg695Cys |
S277 |
3 | BAA10g02490 | A10 | 1207316 | G | A | splice_region_variant&synonymous_variant | LOW | c.1575C>T|p.Leu525Leu |
S158 |
4 | BAA10g02490 | A10 | 1207326 | G | A | splice_region_variant&intron_variant | LOW | c.1573-8C>T| |
S163 |
5 | BAA10g02490 | A10 | 1207724 | C | T | missense_variant | MODERATE | c.1346G>A|p.Arg449Lys |
S288 |
6 | BAA10g02490 | A10 | 1208727 | G | A | missense_variant | MODERATE | c.772C>T|p.Pro258Ser |
S19 |
7 | BAA10g02490 | A10 | 1209098 | T | G | synonymous_variant | LOW | c.564A>C|p.Ile188Ile |
S126 |
8 | BAA10g02490 | A10 | 1209386 | G | A | missense_variant | MODERATE | c.377C>T|p.Pro126Leu |
S38 |
9 | BAA10g02490 | A10 | 1209929 | C | T | missense_variant | MODERATE | c.101G>A|p.Gly34Glu |
S173 |
10 | BAA10g02490 | A10 | 1210759 | C | T | upstream_gene_variant | MODIFIER | c.-730G>A| |
S27 |
11 | BAA10g02490 | A10 | 1211846 | G | A | upstream_gene_variant | MODIFIER | c.-1817C>T| |
S197 |