Product Details

SNP ID

rs201411134

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.21:25881763 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGTGGCGCTCCTCTGGGGTGACAGC[A/G]GCGTCAACCTGAAAAACAAGAGGAG

Phenotype

MIM: 104760

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

APP PubMed Links

Additional Information

For this assay, SNP(s) [rs41276546] 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	2309	Silent Mutation	GCC,GCT	A740A	NP_000475.1
NM_001136016.3	2309	Silent Mutation	GCC,GCT	A716A	NP_001129488.1
NM_001136129.2	2309	Silent Mutation	GCC,GCT	A609A	NP_001129601.1
NM_001136130.2	2309	Silent Mutation	GCC,GCT	A684A	NP_001129602.1
NM_001136131.2	2309	Silent Mutation	GCC,GCT	A630A	NP_001129603.1
NM_001204301.1	2309	Silent Mutation	GCC,GCT	A722A	NP_001191230.1
NM_001204302.1	2309	Silent Mutation	GCC,GCT	A703A	NP_001191231.1
NM_001204303.1	2309	Silent Mutation	GCC,GCT	A647A	NP_001191232.1
NM_201413.2	2309	Silent Mutation	GCC,GCT	A721A	NP_958816.1
NM_201414.2	2309	Silent Mutation	GCC,GCT	A665A	NP_958817.1

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