Product Details

SNP ID

rs1062844

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.2:166196526 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AATAGAAAATTACACACGAACCTGT[C/G]AAACATCTTGTCTTACTACATTATG

Phenotype

MIM: 603415

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

LOC101929680 PubMed Links

Additional Information

For this assay, SNP(s) [rs77050817] are located under a probe 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

LOC101929680

Gene Name

uncharacterized LOC101929680

There are no transcripts associated with this gene.

Gene

SCN9A

Gene Name

sodium voltage-gated channel alpha subunit 9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002977.3	8421	UTR 3			NP_002968.1
XM_005246757.2	8421	UTR 3			XP_005246814.1
XM_011511616.2	8421	Intron			XP_011509918.1
XM_011511617.2	8421	Intron			XP_011509919.1
XM_011511618.2	8421	Intron			XP_011509920.1
XM_011511619.2	8421	Intron			XP_011509921.1
XM_017004668.1	8421	Intron			XP_016860157.1
XM_017004669.1	8421	Intron			XP_016860158.1

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