Product Details

SNP ID

rs2575695

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.8:103373488 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GACATTTATTGAGAGTACTAAGCAT[A/G]TGTTGGGTTAGCATTTTAAAGTAGA

Phenotype

MIM: 610635

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

CTHRC1 PubMed Links

Additional Information

For this assay, SNP(s) [rs77776607] are located under a probe and SNP(s) [rs33982219] 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

CTHRC1

Gene Name

collagen triple helix repeat containing 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001256099.1		Intron			NP_001243028.1
NM_138455.3		Intron			NP_612464.1
XM_011516824.2		Intron			XP_011515126.1

View Full Product Details