Product Details

SNP ID: rs143226291
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.5:141150305 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: ACAAGAAAAGGCAAGTGGCTTTCTT[C/T]ATTTTATTGATGCTTTGGGGAGAGG
Phenotype: MIM: 606332
Polymorphism: C/T, 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	284	Intron			NP_001290074.1
NM_018939.3	284	Silent Mutation	TTC,TTT	F16F	NP_061762.2