Product Details

SNP ID: rs8015313
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.14:77768453 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: ATTTTTATTTTTTATTTTTTACAGG[C/T]ATGATCAACCAGGTACAGAATCAGT
Phenotype: MIM: 603055
Polymorphism: C/T, 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	289	Intron			NP_001167449.1
NM_174943.3	289	Missense Mutation	CAT,TAT	H26Y	NP_777603.1

There are no transcripts associated with this gene.