Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g48050 | A09 | 52032006 | G | A | upstream_gene_variant | MODIFIER | c.-3547G>A| |
S88 |
2 | BAA09g48050 | A09 | 52032435 | C | T | upstream_gene_variant | MODIFIER | c.-3118C>T| |
S19 |
3 | BAA09g48050 | A09 | 52033017 | G | A | upstream_gene_variant | MODIFIER | c.-2536G>A| |
S11 S153 |
4 | BAA09g48050 | A09 | 52033047 | G | A | upstream_gene_variant | MODIFIER | c.-2506G>A| |
S89 |
5 | BAA09g48050 | A09 | 52033110 | G | A | upstream_gene_variant | MODIFIER | c.-2443G>A| |
S2 |
6 | BAA09g48050 | A09 | 52034024 | G | A | upstream_gene_variant | MODIFIER | c.-1529G>A| |
S267 |
7 | BAA09g48050 | A09 | 52035657 | G | A | synonymous_variant | LOW | c.105G>A|p.Glu35Glu |
S298 |
8 | BAA09g48050 | A09 | 52036354 | C | T | missense_variant | MODERATE | c.626C>T|p.Ser209Leu |
S235 |
9 | BAA09g48050 | A09 | 52037104 | C | T | synonymous_variant | LOW | c.996C>T|p.Ser332Ser |
S122 |
10 | BAA09g48050 | A09 | 52038179 | G | A | missense_variant | MODERATE | c.1280G>A|p.Ser427Asn |
S217 |
11 | BAA09g48050 | A09 | 52039391 | C | T | intron_variant | MODIFIER | c.2252+88C>T| |
S60 |