Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g32850 | A10 | 23486152 | C | T | synonymous_variant | LOW | c.2169G>A|p.Leu723Leu |
S152 |
2 | BAA10g32850 | A10 | 23487104 | G | A | synonymous_variant | LOW | c.1398C>T|p.Leu466Leu |
S50 |
3 | BAA10g32850 | A10 | 23487177 | G | A | missense_variant | MODERATE | c.1325C>T|p.Thr442Ile |
S276 |
4 | BAA10g32850 | A10 | 23487987 | C | T | missense_variant | MODERATE | c.928G>A|p.Gly310Arg |
S242 |
5 | BAA10g32850 | A10 | 23488501 | C | T | synonymous_variant | LOW | c.414G>A|p.Gly138Gly |
S36 |
6 | BAA10g32850 | A10 | 23488573 | C | T | synonymous_variant | LOW | c.342G>A|p.Glu114Glu |
S67 |
7 | BAA10g32850 | A10 | 23488601 | G | A | missense_variant | MODERATE | c.314C>T|p.Ser105Phe |
S197 |
8 | BAA10g32850 | A10 | 23488863 | G | A | missense_variant | MODERATE | c.52C>T|p.Arg18Cys |
S262 |
9 | BAA10g32850 | A10 | 23489370 | C | T | upstream_gene_variant | MODIFIER | c.-456G>A| |
S177 |
10 | BAA10g32850 | A10 | 23489700 | C | T | upstream_gene_variant | MODIFIER | c.-786G>A| |
S67 |
11 | BAA10g32850 | A10 | 23490911 | G | A | upstream_gene_variant | MODIFIER | c.-1997C>T| |
S289 S290 S77 S82 |
12 | BAA10g32850 | A10 | 23493846 | C | T | upstream_gene_variant | MODIFIER | c.-4932G>A| |
S225 |