Product Details

SNP ID

rs9324068

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.14:103935613 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGCTAGACACTGGGAAGTTTAACTT[C/T]GAGAATGATGAGATCCCTTAACTAG

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

RD3L PubMed Links

Additional Information

For this assay, SNP(s) [rs75340877] 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

RD3L

Gene Name

retinal degeneration 3-like

There are no transcripts associated with this gene.

Gene

TDRD9

Gene Name

tudor domain containing 9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_153046.2		Intron			NP_694591.2
XM_005267309.3		Intron			XP_005267366.1
XM_006720019.3		Intron			XP_006720082.1
XM_006720020.3		Intron			XP_006720083.1
XM_011536397.2		Intron			XP_011534699.1
XM_011536398.2		Intron			XP_011534700.1
XM_011536400.2		Intron			XP_011534702.1
XM_011536401.2		Intron			XP_011534703.1
XM_011536402.2		Intron			XP_011534704.1
XM_017020955.1		Intron			XP_016876444.1

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