Product Details

SNP ID
rs1265099
Assay Type
Validated
NCBI dbSNP Submissions
NA
Location
Chr.6:31137636 on Build GRCh38
Set Membership
HapMap Validated
Context Sequence [VIC/FAM]
AGGTGGCAGAAGGGAACACAGTACC[A/G]TAGCCCTGCCCCAGCGATCGCGCGG
Phenotype
MIM: 605310 MIM: 613525 MIM: 613526
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
CCHCR1 PubMed Links
Additional Information
For this assay, SNP(s) [rs201861237] 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
CCHCR1
Gene Name
coiled-coil alpha-helical rod protein 1
There are no transcripts associated with this gene.

Gene
PSORS1C1
Gene Name
psoriasis susceptibility 1 candidate 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_014068.2 1050 Intron NP_054787.2
Gene
PSORS1C2
Gene Name
psoriasis susceptibility 1 candidate 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_014069.2 1050 UTR 3 NP_054788.2

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