Product Details

SNP ID

rs7819103

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.8:42155171 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AAATGGAATACTTTTGAACCTCTTG[C/T]GTGGGAAAGTCATCCTATTTGCGAT

Phenotype

MIM: 610469

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

AP3M2 PubMed Links

Additional Information

For this assay, SNP(s) [rs145444960] are located under a probe 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

AP3M2

Gene Name

adaptor related protein complex 3 mu 2 subunit

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001134296.1	662	Intron			NP_001127768.1
NM_006803.3	662	Intron			NP_006794.1
XM_017012977.1	662	Intron			XP_016868466.1
XM_017012978.1	662	UTR 5			XP_016868467.1
XM_017012979.1	662	Intron			XP_016868468.1

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