Product Details

SNP ID: rs141476251
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.5:141150357 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GGGTTCTGAATCGATTCAGTATTCC[A/G]TATTGGAGGAGACAGAAAGTGGCAC
Phenotype: MIM: 606332
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: PCDHB17P 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_001303145.1	336	Intron			NP_001290074.1
NM_018939.3	336	Missense Mutation	ATA,GTA	I34V	NP_061762.2