Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g15080 | A10 | 15593611 | G | A | downstream_gene_variant | MODIFIER | c.*2628C>T| |
S112 |
2 | BAA10g15080 | A10 | 15594842 | G | A | downstream_gene_variant | MODIFIER | c.*1397C>T| |
S139 |
3 | BAA10g15080 | A10 | 15596665 | C | T | stop_gained | HIGH | c.1914G>A|p.Trp638* |
S302 |
4 | BAA10g15080 | A10 | 15597053 | C | T | missense_variant | MODERATE | c.1526G>A|p.Ser509Asn |
S297 |
5 | BAA10g15080 | A10 | 15597093 | G | A | missense_variant | MODERATE | c.1486C>T|p.Pro496Ser |
S271 |
6 | BAA10g15080 | A10 | 15597553 | C | T | synonymous_variant | LOW | c.1026G>A|p.Leu342Leu |
S124 |
7 | BAA10g15080 | A10 | 15597939 | C | T | missense_variant | MODERATE | c.640G>A|p.Glu214Lys |
S11 |
8 | BAA10g15080 | A10 | 15598933 | C | T | missense_variant | MODERATE | c.104G>A|p.Gly35Glu |
S117 |
9 | BAA10g15080 | A10 | 15600503 | C | T | upstream_gene_variant | MODIFIER | c.-1467G>A| |
S210 |
10 | BAA10g15080 | A10 | 15600913 | G | A | upstream_gene_variant | MODIFIER | c.-1877C>T| |
S241 |
11 | BAA10g15080 | A10 | 15602795 | G | A | upstream_gene_variant | MODIFIER | c.-3759C>T| |
S139 |