Product Details

SNP ID

rs187232235

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:110057270 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCTGCAGGGAGGATGTGCCTTTCA[A/G]CAAAGTTCCTCTCCCCCTTACAGCT

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

C12orf76 PubMed Links

Gene Details

Gene

C12orf76

Gene Name

chromosome 12 open reading frame 76

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_207435.2	251	Missense Mutation	GCT,GTT	A73V	NP_997318.1
XM_017019297.1	251	Missense Mutation	GCT,GTT	A84V	XP_016874786.1

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