Product Details

SNP ID
rs4499086
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:64270696 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGACCCCTCACCACTTGTTTCACAA[G/T]ACTGGCCACAAAAGTAATCTAGACA
Phenotype
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
C12orf56 PubMed Links

Gene Details

Gene
C12orf56
Gene Name
chromosome 12 open reading frame 56
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001099676.2 1123 Missense Mutation ATT,CTT I375L NP_001093146.1
NM_001170633.1 1123 Missense Mutation ATT,CTT I535L NP_001164104.1
XM_017018770.1 1123 Intron XP_016874259.1

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