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


Gene ID

Results: 1 - 15 of 15 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g18990 A10 17584660 G A missense_variant MODERATE c.1108C>T|p.Pro370Ser S167
2 BAA10g18990 A10 17584702 G A missense_variant MODERATE c.1066C>T|p.Arg356Cys S233
3 BAA10g18990 A10 17584763 G A synonymous_variant LOW c.1005C>T|p.Tyr335Tyr S63
4 BAA10g18990 A10 17586053 C T missense_variant MODERATE c.229G>A|p.Glu77Lys S60
5 BAA10g18990 A10 17586069 C T synonymous_variant LOW c.213G>A|p.Arg71Arg S269
6 BAA10g18990 A10 17588115 G A upstream_gene_variant MODIFIER c.-714C>T| S295
7 BAA10g18990 A10 17588634 C T upstream_gene_variant MODIFIER c.-1233G>A| S202
8 BAA10g18990 A10 17589597 C T upstream_gene_variant MODIFIER c.-2196G>A| S119
9 BAA10g18990 A10 17589681 C T upstream_gene_variant MODIFIER c.-2280G>A| S108
10 BAA10g18990 A10 17589748 C T upstream_gene_variant MODIFIER c.-2347G>A| S160
11 BAA10g18990 A10 17590334 C T upstream_gene_variant MODIFIER c.-2933G>A| S2
12 BAA10g18990 A10 17590653 G A upstream_gene_variant MODIFIER c.-3252C>T| S180
13 BAA10g18990 A10 17590865 A C upstream_gene_variant MODIFIER c.-3464T>G| S54
14 BAA10g18990 A10 17592117 C T upstream_gene_variant MODIFIER c.-4716G>A| S146
15 BAA10g18990 A10 17592277 C T upstream_gene_variant MODIFIER c.-4876G>A| S10