Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 13 of 13 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g16780 A02 8278230 G A upstream_gene_variant MODIFIER c.-2824G>A| S70
2 BAA02g16780 A02 8278510 C T upstream_gene_variant MODIFIER c.-2544C>T| S283
3 BAA02g16780 A02 8278601 G A upstream_gene_variant MODIFIER c.-2453G>A| S62
4 BAA02g16780 A02 8279911 G A upstream_gene_variant MODIFIER c.-1143G>A| S87
5 BAA02g16780 A02 8282733 G A missense_variant MODERATE c.275G>A|p.Ser92Asn S10
6 BAA02g16780 A02 8283021 C T missense_variant MODERATE c.563C>T|p.Pro188Leu S209
7 BAA02g16780 A02 8283068 G A missense_variant MODERATE c.610G>A|p.Val204Ile S148
S30
S31
8 BAA02g16780 A02 8284049 C T missense_variant MODERATE c.1298C>T|p.Ser433Leu S73
S91
9 BAA02g16780 A02 8284115 G A missense_variant MODERATE c.1364G>A|p.Gly455Asp S7
10 BAA02g16780 A02 8284306 G A missense_variant MODERATE c.1555G>A|p.Glu519Lys S256
11 BAA02g16780 A02 8284401 G A synonymous_variant LOW c.1650G>A|p.Glu550Glu S69
12 BAA02g16780 A02 8284460 C T missense_variant MODERATE c.1709C>T|p.Pro570Leu S270
13 BAA02g16780 A02 8284488 G A synonymous_variant LOW c.1737G>A|p.Pro579Pro S297