Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g14110 | A10 | 14954644 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1328-1G>A| |
S177 |
2 | BAA10g14110 | A10 | 14954964 | G | A | missense_variant | MODERATE | c.1088C>T|p.Thr363Met |
S239 |
3 | BAA10g14110 | A10 | 14955005 | C | T | synonymous_variant | LOW | c.1047G>A|p.Gly349Gly |
S42 |
4 | BAA10g14110 | A10 | 14955230 | C | T | missense_variant | MODERATE | c.973G>A|p.Glu325Lys |
S260 |
5 | BAA10g14110 | A10 | 14955290 | G | A | missense_variant | MODERATE | c.913C>T|p.Pro305Ser |
S34 |
6 | BAA10g14110 | A10 | 14955694 | C | T | missense_variant | MODERATE | c.788G>A|p.Gly263Asp |
S60 |
7 | BAA10g14110 | A10 | 14955848 | C | T | missense_variant | MODERATE | c.634G>A|p.Glu212Lys |
S121 |
8 | BAA10g14110 | A10 | 14958255 | C | T | upstream_gene_variant | MODIFIER | c.-995G>A| |
S44 |
9 | BAA10g14110 | A10 | 14959084 | G | A | upstream_gene_variant | MODIFIER | c.-1824C>T| |
S257 |
10 | BAA10g14110 | A10 | 14959428 | G | A | upstream_gene_variant | MODIFIER | c.-2168C>T| |
S17 |