Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g16780 | A10 | 16436104 | C | T | upstream_gene_variant | MODIFIER | c.-2077C>T| |
S275 |
2 | BAA10g16780 | A10 | 16437873 | C | T | upstream_gene_variant | MODIFIER | c.-308C>T| |
S11 |
3 | BAA10g16780 | A10 | 16438707 | C | T | synonymous_variant | LOW | c.450C>T|p.Asp150Asp |
S162 |
4 | BAA10g16780 | A10 | 16438819 | C | T | missense_variant | MODERATE | c.562C>T|p.Pro188Ser |
S47 |
5 | BAA10g16780 | A10 | 16439764 | C | T | downstream_gene_variant | MODIFIER | c.*475C>T| |
S130 S152 |
6 | BAA10g16780 | A10 | 16439777 | C | T | downstream_gene_variant | MODIFIER | c.*488C>T| |
S259 |
7 | BAA10g16780 | A10 | 16440558 | G | A | downstream_gene_variant | MODIFIER | c.*1269G>A| |
S8 |
8 | BAA10g16780 | A10 | 16442853 | G | A | downstream_gene_variant | MODIFIER | c.*3564G>A| |
S126 |
9 | BAA10g16780 | A10 | 16443535 | C | T | downstream_gene_variant | MODIFIER | c.*4246C>T| |
S260 |