Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g09870 | A07 | 18740401 | C | T | missense_variant | MODERATE | c.1150G>A|p.Glu384Lys |
S277 |
2 | BAA07g09870 | A07 | 18740684 | C | T | missense_variant | MODERATE | c.958G>A|p.Val320Ile |
S267 |
3 | BAA07g09870 | A07 | 18740887 | C | T | missense_variant&splice_region_variant | MODERATE | c.755G>A|p.Gly252Glu |
S165 |
4 | BAA07g09870 | A07 | 18740888 | C | T | missense_variant&splice_region_variant | MODERATE | c.754G>A|p.Gly252Arg |
S162 |
5 | BAA07g09870 | A07 | 18741079 | C | T | missense_variant | MODERATE | c.638G>A|p.Gly213Glu |
S16 |
6 | BAA07g09870 | A07 | 18741194 | C | T | missense_variant | MODERATE | c.523G>A|p.Glu175Lys |
|
7 | BAA07g09870 | A07 | 18741290 | C | T | missense_variant | MODERATE | c.427G>A|p.Gly143Arg |
S230 |
8 | BAA07g09870 | A07 | 18741513 | C | T | synonymous_variant | LOW | c.204G>A|p.Thr68Thr |
S146 |
9 | BAA07g09870 | A07 | 18742463 | G | A | missense_variant | MODERATE | c.41C>T|p.Ser14Leu |
S159 S243 S299 |
10 | BAA07g09870 | A07 | 18742671 | G | A | upstream_gene_variant | MODIFIER | c.-168C>T| |
S208 |
11 | BAA07g09870 | A07 | 18743149 | C | T | upstream_gene_variant | MODIFIER | c.-646G>A| |
S162 |
12 | BAA07g09870 | A07 | 18745527 | C | T | upstream_gene_variant | MODIFIER | c.-3024G>A| |
S136 S186 S275 |