Product Details

SNP ID

rs57238032

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:123903225 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTATTGGGCTGGCTGATGGACACAC[A/G]GAAGTTCACTAGGCTATTTGCCTTT

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

CCDC14 PubMed Links

Additional Information

For this assay, SNP(s) [rs139167722] 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

CCDC14

Gene Name

coiled-coil domain containing 14

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001308317.1		Intron			NP_001295246.1
NM_022757.4		Intron			NP_073594.4
XM_005247710.4		Intron			XP_005247767.1
XM_005247711.4		Intron			XP_005247768.1
XM_005247713.2		Intron			XP_005247770.1
XM_005247714.2		Intron			XP_005247771.1
XM_005247715.4		Intron			XP_005247772.1
XM_005247716.4		Intron			XP_005247773.1
XM_006713731.3		Intron			XP_006713794.1
XM_006713733.3		Intron			XP_006713796.1
XM_011513081.2		Intron			XP_011511383.1
XM_017007056.1		Intron			XP_016862545.1
XM_017007057.1		Intron			XP_016862546.1
XM_017007058.1		Intron			XP_016862547.1
XM_017007059.1		Intron			XP_016862548.1
XM_017007060.1		Intron			XP_016862549.1
XM_017007061.1		Intron			XP_016862550.1

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