Product Details

SNP ID: rs202055986
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.5:77630511 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CAGGCCCATGGAGTTGGGCGGCGGA[A/C]CGGCCGCCAGGCTGCACTGGGACAG
Phenotype: MIM: 604529
Polymorphism: A/C, Transversion substitution
Allele Nomenclature
Literature Links: OTP PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_032109.2	879	Missense Mutation	GGT,GTT	G244V	NP_115485.1

There are no transcripts associated with this gene.