Product Details

SNP ID

rs28670063

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:169630222 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GATGCTGCGGTTTGGGGTACAGTTG[C/T]ACCCATTACCCAGGAAGTGGGTATA

Phenotype

MIM: 600580

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

CLCN3 PubMed Links

Additional Information

For this assay, SNP(s) [rs113109873] 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

CLCN3

Gene Name

chloride voltage-gated channel 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001243372.1		Intron			NP_001230301.1
NM_001243374.1		Intron			NP_001230303.1
NM_001829.3		Intron			NP_001820.2
NM_173872.3		Intron			NP_776297.2
XM_005262726.2		Intron			XP_005262783.1
XM_011531586.2		Intron			XP_011529888.1

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