Product Details

SNP ID: rs140168051
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.5:141100986 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: ACATTTTCAGATATTACTGCAAAAC[A/C]CTTTGCAATTCGTTACAAACGAGCT
Phenotype: MIM: 606328 MIM: 606329
Polymorphism: A/C, 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	745	Missense Mutation	ACT,CCT	T113P	NP_061760.1