Product Details

SNP ID

rs214484

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.21:25881968 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

CAGTTACACAGATGCTGTGCTCCAT[C/G]TAGCCACCAGGTGGCGGTGGAAACC

Phenotype

MIM: 104760

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

APP PubMed Links

Additional Information

For this assay, SNP(s) [rs17001455] 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

APP

Gene Name

amyloid beta precursor protein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000484.3		Intron			NP_000475.1
NM_001136016.3		Intron			NP_001129488.1
NM_001136129.2		Intron			NP_001129601.1
NM_001136130.2		Intron			NP_001129602.1
NM_001136131.2		Intron			NP_001129603.1
NM_001204301.1		Intron			NP_001191230.1
NM_001204302.1		Intron			NP_001191231.1
NM_001204303.1		Intron			NP_001191232.1
NM_201413.2		Intron			NP_958816.1
NM_201414.2		Intron			NP_958817.1

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