Product Details

SNP ID

rs189761707

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:9092948 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGAGTGTGTCAGCAGCCAGGACTTT[C/G]TCTCTGGGTCCCCTTCCAAAACGCA

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

C16orf72 PubMed Links

Gene Details

Gene

C16orf72

Gene Name

chromosome 16 open reading frame 72

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014117.2	619	Missense Mutation	TCT,TGT	S85C	NP_054836.2
XM_011522462.2	619	Missense Mutation	TCT,TGT	S85C	XP_011520764.1

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