Product Details

SNP ID
rs6503932
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.17:59626139 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGCAGATGAGGAACTGTGTTAGACT[C/T]TAGGGACAAGGTGGTAAACAAGATG
Phenotype
MIM: 118955
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
CLTC PubMed Links
Additional Information
For this assay, SNP(s) [rs371311395] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene
CLTC
Gene Name
clathrin heavy chain
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001288653.1 Intron NP_001275582.1
NM_004859.3 Intron NP_004850.1
XM_005257012.3 Intron XP_005257069.1

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