Product Details

SNP ID
rs855795
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:37052333 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGCTCTTTGGGATGTGGGTGGCGGA[G/T]GGGTGCAGGGAGCTAGCTGGATGGA
Phenotype
MIM: 616386
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
KCTD17 PubMed Links

Gene Details

Gene
KCTD17
Gene Name
potassium channel tetramerization domain containing 17
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001282684.1 Intron NP_001269613.1
NM_001282685.1 Intron NP_001269614.1
NM_001282686.1 Intron NP_001269615.1
NM_024681.3 Intron NP_078957.2
XM_005261741.3 Intron XP_005261798.2
XM_005261742.2 Intron XP_005261799.2
XM_005261743.2 Intron XP_005261800.2
XM_005261744.2 Intron XP_005261801.1
XM_011530374.2 Intron XP_011528676.1
XM_011530377.2 Intron XP_011528679.1

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