Product Details

SNP ID

rs3765975

Assay Type

Functionally Tested

NCBI dbSNP Submissions

59

Location

Chr.1:86427136 on Build GRCh38

Set Membership

HapMap JSNP

Context Sequence [VIC/FAM]

TGTCCTTCCAAGTCTACAATGAGAT[G/T]TAGGTAGGAATCATGGAAGGGGGAA

Phenotype

MIM: 604003

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

CLCA2 PubMed Links

Additional Information

For this assay, SNP(s) [rs111331175] 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

CLCA2

Gene Name

chloride channel accessory 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006536.5		Intron			NP_006527.1
XM_011542448.2		Intron			XP_011540750.1

View Full Product Details