Product Details

SNP ID

rs4981084

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.14:30898855 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCTTAAGCCCTTTTACTGGCTAACA[C/T]TGTGGGCCTCTATTAAATGGAGAGA

Phenotype

MIM: 603196 MIM: 614766

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

COCH PubMed Links

Additional Information

For this assay, SNP(s) [rs10047928] 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

COCH

Gene Name

cochlin

There are no transcripts associated with this gene.

Gene

LOC100506071

Gene Name

uncharacterized LOC100506071

There are no transcripts associated with this gene.

Gene

STRN3

Gene Name

striatin 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001083893.1		Intron			NP_001077362.1
NM_014574.3		Intron			NP_055389.3
XM_005267569.3		Intron			XP_005267626.1
XM_005267570.3		Intron			XP_005267627.1

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