Product Details

SNP ID

rs200912589

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:92706978 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTGACCTCTGAACCTGAAAGGGCCC[C/T]GAATGCAGCTGACTCACTGGAGCCC

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

C12orf74 PubMed Links

Gene Details

Gene

C12orf74

Gene Name

chromosome 12 open reading frame 74

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001037671.3	798	Missense Mutation	CCG,CTG	P116L	NP_001032760.1
NM_001178097.2	798	Missense Mutation	CCG,CTG	P116L	NP_001171568.1

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