Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g26350 | A10 | 20932760 | C | T | missense_variant | MODERATE | c.991G>A|p.Gly331Ser |
S260 |
2 | BAA10g26350 | A10 | 20932783 | C | T | missense_variant | MODERATE | c.968G>A|p.Ser323Asn |
S244 |
3 | BAA10g26350 | A10 | 20933418 | G | A | synonymous_variant | LOW | c.333C>T|p.Leu111Leu |
S1 |
4 | BAA10g26350 | A10 | 20933537 | G | A | missense_variant | MODERATE | c.214C>T|p.Pro72Ser |
S82 S92 |
5 | BAA10g26350 | A10 | 20935365 | G | A | upstream_gene_variant | MODIFIER | c.-1615C>T| |
S34 |
6 | BAA10g26350 | A10 | 20935611 | G | A | upstream_gene_variant | MODIFIER | c.-1861C>T| |
S32 |
7 | BAA10g26350 | A10 | 20937774 | G | A | upstream_gene_variant | MODIFIER | c.-4024C>T| |
S32 |
8 | BAA10g26350 | A10 | 20937965 | C | T | upstream_gene_variant | MODIFIER | c.-4215G>A| |
S166 |