Product Details

SNP ID

rs139845028

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:96982082 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCATTGGCATCAGAGGCAGTTTTCA[A/C]TCCTAAGCAGACCCTTACAATTCCA

Phenotype

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

C10orf12 PubMed Links

Gene Details

Gene

C10orf12

Gene Name

chromosome 10 open reading frame 12

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015652.2	799	Missense Mutation	AAT,ACT	N231T	NP_056467.2

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