Product Details

SNP ID: hCV58519998
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.6:87086413 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CGGCTGGGAGAAGAATGGGTTTTCC[C/T]GTAGCGTGCATTCTGGGCAATCTAT
Phenotype: MIM: 118850
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: CGA PubMed Links

Gene Details

There are no transcripts associated with this gene.