Product Details

SNP ID: rs1055410
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.5:141100595 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: GTGGGGCAAAAGACTGTTTCCCAGC[G/T]CTGTCTGAGGTTCAGCTTGGCGACA
Phenotype: MIM: 606328 MIM: 606329
Polymorphism: G/T, Transversion substitution
Allele Nomenclature
Literature Links: PCDHB2 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_018937.4	354	UTR 5			NP_061760.1