Product Details

SNP ID: rs9323435
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.14:63313747 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: CATTCTTCTCCCGTATGATTCACTC[C/T]TTCACCAACCTTGGGTTTTTGTTAG
Phenotype: MIM: 609652
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: GPHB5 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_145171.3		Intron			NP_660154.3