Product Details

SNP ID: rs12587155
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.14:77763646 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: CTGGGATGCAGGATTGAAAGAACAG[A/G]GTGGAGAAGAGCTTTTGCAATCCAC
Phenotype: MIM: 603055
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: C14orf178 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001173978.1		Intron			NP_001167449.1
NM_174943.3		Intron			NP_777603.1

There are no transcripts associated with this gene.