Product Details

SNP ID

rs1786194

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:118136104 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCTCTCAGGTAGGAGGGGGAGAAGC[A/G]GGGGAGAGCTGGGCTCAGGAGTGCC

Phenotype

MIM: 608256

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SCN4B PubMed Links

Additional Information

For this assay, SNP(s) [rs59423170] 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

SCN4B

Gene Name

sodium voltage-gated channel beta subunit 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001142348.1	1450	UTR 3			NP_001135820.1
NM_001142349.1	1450	UTR 3			NP_001135821.1
NM_174934.3	1450	UTR 3			NP_777594.1

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