Product Details

SNP ID

rs146360818

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:96981832 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAAGACAGCTCGGAAAAGTAAAAGG[C/G]CATCAGGGCTGAGGATAAATGATTA

Phenotype

Polymorphism

C/G, 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	549	Missense Mutation	CCA,GCA	P148A	NP_056467.2

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