Product Details

SNP ID: rs149588398
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.9:97309517 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CCCATGATGAAGAAGGTGGAGACTC[C/G]TGAAGGGGAGGTGATGTCTCCCCGA
Phenotype
Polymorphism: C/G, Transversion substitution
Allele Nomenclature
Literature Links: CCDC180 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_020893.2	433	Missense Mutation	CCT,CGT	P102R	NP_065944.2

There are no transcripts associated with this gene.