Product Details

SNP ID

rs10801582

Assay Type

Functionally Tested

NCBI dbSNP Submissions

31

Location

Chr.1:196975227 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GGTGACTGTTACAAGAGGGGTTTAA[A/G]CGTAGTGTTGGGAATGAAAAAATGA

Phenotype

MIM: 608593

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

CFHR5 PubMed Links

Additional Information

For this assay, SNP(s) [rs77948462] 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

CFHR5

Gene Name

complement factor H related 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_030787.3		Intron			NP_110414.1
XM_011510020.2		Intron			XP_011508322.1

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