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 BAA09g01900 A09 1316827 G A upstream_gene_variant MODIFIER c.-246G>A| S201
2 BAA09g01900 A09 1316856 G A upstream_gene_variant MODIFIER c.-217G>A| S33
3 BAA09g01900 A09 1317191 G A missense_variant MODERATE c.13G>A|p.Glu5Lys S223
4 BAA09g01900 A09 1317340 G A synonymous_variant LOW c.162G>A|p.Leu54Leu S237
5 BAA09g01900 A09 1317387 G A missense_variant MODERATE c.209G>A|p.Gly70Glu S240
6 BAA09g01900 A09 1317444 C T missense_variant MODERATE c.266C>T|p.Ala89Val S53
7 BAA09g01900 A09 1317467 G T missense_variant MODERATE c.289G>T|p.Ala97Ser S118
8 BAA09g01900 A09 1317664 G A stop_gained HIGH c.486G>A|p.Trp162* S153
S213
9 BAA09g01900 A09 1317851 G A missense_variant MODERATE c.673G>A|p.Glu225Lys S202
10 BAA09g01900 A09 1317935 G A missense_variant MODERATE c.757G>A|p.Glu253Lys S262
11 BAA09g01900 A09 1317937 G A synonymous_variant LOW c.759G>A|p.Glu253Glu S231
12 BAA09g01900 A09 1318449 G A missense_variant MODERATE c.1187G>A|p.Gly396Glu S224
13 BAA09g01900 A09 1318843 G A synonymous_variant LOW c.1503G>A|p.Gln501Gln S127