Product Details

SNP ID: rs17844385
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.5:141100752 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TGGGTCCGAGTCAAGACGCTATTCT[A/G]TGGCTGAGGAAAAAGAGAAGGGCTT
Phenotype: MIM: 606328 MIM: 606329
Polymorphism: A/G, Transition 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	511	Missense Mutation	ATG,GTG	M35V	NP_061760.1