Product Details

SNP ID: rs10134462
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.14:63314797 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TCAAATGACAGTACCTTTGCTTTTT[G/T]GTTCTTCTTTGTTCTAGGCAAAAAA
Phenotype: MIM: 609652
Polymorphism: G/T, Transversion 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