Product Details

SNP ID: rs999474
Assay Type: Validated
NCBI dbSNP Submissions: NA
Location: Chr.17:48910303 on Build GRCh38
Set Membership: HapMap Validated
Context Sequence [VIC/FAM]: CCTGGGCAAGAAGGCCACCATGATA[A/G]TCTTACTCTCTGCTGGCTGGCTTGC
Phenotype: MIM: 611362
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: LOC105371814 PubMed Links

Gene Details

There are no transcripts associated with this gene.

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_023079.4		Intron			NP_075567.2