Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g20710 | A10 | 18503982 | G | A | missense_variant | MODERATE | c.1042C>T|p.Pro348Ser |
S62 |
2 | BAA10g20710 | A10 | 18504511 | C | T | missense_variant | MODERATE | c.601G>A|p.Ala201Thr |
S206 |
3 | BAA10g20710 | A10 | 18504526 | C | T | missense_variant | MODERATE | c.586G>A|p.Glu196Lys |
S183 |
4 | BAA10g20710 | A10 | 18504737 | C | T | synonymous_variant | LOW | c.447G>A|p.Leu149Leu |
S301 S304 |
5 | BAA10g20710 | A10 | 18506463 | G | A | stop_gained | HIGH | c.271C>T|p.Gln91* |
S213 |
6 | BAA10g20710 | A10 | 18507516 | G | A | upstream_gene_variant | MODIFIER | c.-709C>T| |
S165 |
7 | BAA10g20710 | A10 | 18507537 | C | T | upstream_gene_variant | MODIFIER | c.-730G>A| |
S9 |
8 | BAA10g20710 | A10 | 18507604 | G | A | upstream_gene_variant | MODIFIER | c.-797C>T| |
S66 |
9 | BAA10g20710 | A10 | 18508031 | G | A | upstream_gene_variant | MODIFIER | c.-1224C>T| |
S293 |
10 | BAA10g20710 | A10 | 18508426 | C | T | upstream_gene_variant | MODIFIER | c.-1619G>A| |
S143 |
11 | BAA10g20710 | A10 | 18508577 | G | A | upstream_gene_variant | MODIFIER | c.-1770C>T| |
S128 |
12 | BAA10g20710 | A10 | 18510122 | C | T | upstream_gene_variant | MODIFIER | c.-3315G>A| |
S86 |
13 | BAA10g20710 | A10 | 18510486 | C | T | upstream_gene_variant | MODIFIER | c.-3679G>A| |
S175 |