Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g16170 | A10 | 16120738 | C | T | upstream_gene_variant | MODIFIER | c.-4191C>T| |
S174 S27 S39 |
2 | BAA10g16170 | A10 | 16125749 | G | A | missense_variant | MODERATE | c.520G>A|p.Glu174Lys |
S205 |
3 | BAA10g16170 | A10 | 16125798 | C | T | missense_variant | MODERATE | c.569C>T|p.Ser190Phe |
S46 |
4 | BAA10g16170 | A10 | 16126025 | G | A | missense_variant | MODERATE | c.694G>A|p.Asp232Asn |
S59 |
5 | BAA10g16170 | A10 | 16126705 | C | T | missense_variant | MODERATE | c.980C>T|p.Thr327Ile |
S84 S93 |
6 | BAA10g16170 | A10 | 16127576 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.1435-1G>A| |
S245 |
7 | BAA10g16170 | A10 | 16128481 | G | A | missense_variant | MODERATE | c.1924G>A|p.Gly642Arg |
S289 |
8 | BAA10g16170 | A10 | 16128883 | G | A | missense_variant | MODERATE | c.2162G>A|p.Cys721Tyr |
S223 |
9 | BAA10g16170 | A10 | 16129773 | C | T | synonymous_variant | LOW | c.2976C>T|p.Leu992Leu |
S204 |