Product Details

SNP ID

rs14332

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.22:17179611 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAAGACAAAAGGGGAAAGAAGGAAT[C/G]TTCCAGGCAGAGAGAAAGAGAAAAG

Phenotype

MIM: 607575

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

CECR1 PubMed Links

Additional Information

For this assay, SNP(s) [rs76206943] 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

CECR1

Gene Name

cat eye syndrome chromosome region, candidate 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001282225.1	3559	UTR 3			NP_001269154.1
NM_001282226.1	3559	UTR 3			NP_001269155.1
NM_001282227.1	3559	UTR 3			NP_001269156.1
NM_001282228.1	3559	UTR 3			NP_001269157.1
NM_001282229.1	3559	UTR 3			NP_001269158.1
NM_177405.2	3559	UTR 3			NP_803124.1
XM_006724080.3	3559	UTR 3			XP_006724143.1
XM_011546133.1	3559	UTR 3			XP_011544435.1

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