Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g27100 | A10 | 21213175 | C | T | missense_variant | MODERATE | c.181C>T|p.Pro61Ser |
S86 |
2 | BAA10g27100 | A10 | 21215773 | G | A | missense_variant | MODERATE | c.1555G>A|p.Gly519Arg |
S95 |
3 | BAA10g27100 | A10 | 21218749 | C | T | missense_variant | MODERATE | c.2969C>T|p.Ala990Val |
S68 |
4 | BAA10g27100 | A10 | 21218865 | C | T | stop_gained | HIGH | c.3085C>T|p.Gln1029* |
S297 S302 |
5 | BAA10g27100 | A10 | 21219408 | C | T | synonymous_variant | LOW | c.3412C>T|p.Leu1138Leu |
S165 |
6 | BAA10g27100 | A10 | 21220629 | C | T | synonymous_variant | LOW | c.4146C>T|p.Leu1382Leu |
S54 |
7 | BAA10g27100 | A10 | 21221174 | G | A | downstream_gene_variant | MODIFIER | c.*224G>A| |
S279 |
8 | BAA10g27100 | A10 | 21221891 | G | A | downstream_gene_variant | MODIFIER | c.*941G>A| |
S219 S72 |
9 | BAA10g27100 | A10 | 21222658 | G | A | downstream_gene_variant | MODIFIER | c.*1708G>A| |
S109 |
10 | BAA10g27100 | A10 | 21222854 | G | A | downstream_gene_variant | MODIFIER | c.*1904G>A| |
S202 |
11 | BAA10g27100 | A10 | 21223176 | C | T | downstream_gene_variant | MODIFIER | c.*2226C>T| |
S305 |