Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g20900 | A10 | 18587798 | C | T | missense_variant | MODERATE | c.1393G>A|p.Asp465Asn |
S173 S176 |
2 | BAA10g20900 | A10 | 18587876 | C | T | missense_variant | MODERATE | c.1315G>A|p.Glu439Lys |
S149 |
3 | BAA10g20900 | A10 | 18587899 | C | T | missense_variant | MODERATE | c.1292G>A|p.Ser431Asn |
S229 S247 |
4 | BAA10g20900 | A10 | 18590576 | G | A | upstream_gene_variant | MODIFIER | c.-339C>T| |
S32 |
5 | BAA10g20900 | A10 | 18590847 | C | T | upstream_gene_variant | MODIFIER | c.-610G>A| |
S190 |
6 | BAA10g20900 | A10 | 18591921 | C | T | upstream_gene_variant | MODIFIER | c.-1684G>A| |
S91 |
7 | BAA10g20900 | A10 | 18592266 | G | A | upstream_gene_variant | MODIFIER | c.-2029C>T| |
S105 S106 |
8 | BAA10g20900 | A10 | 18592447 | C | T | upstream_gene_variant | MODIFIER | c.-2210G>A| |
S45 |
9 | BAA10g20900 | A10 | 18593131 | C | T | upstream_gene_variant | MODIFIER | c.-2894G>A| |
S107 |
10 | BAA10g20900 | A10 | 18593504 | C | T | upstream_gene_variant | MODIFIER | c.-3267G>A| |
S37 |