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SNP ID

rs146699813

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:40335247 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTTGGCTGCCTCCTCTCGTGGGCC[A/G]GCTTCTCGGGGCCAGGCCCTGCTGG

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

C15orf52 PubMed Links

Gene Details

Gene

C15orf52

Gene Name

chromosome 15 open reading frame 52

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_207380.2	1532	Missense Mutation	CGG,TGG	R506W	NP_997263.2

Gene

INAFM2

Gene Name

InaF motif containing 2

There are no transcripts associated with this gene.

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