Product Details

SNP ID

rs8138476

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.22:43961284 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTGATTTGTAAGAATCGCTTGGTGC[C/T]ACACTAGACCTTCTGTGTCCATCTC

Phenotype

MIM: 612058

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

SAMM50 PubMed Links

Additional Information

For this assay, SNP(s) [rs201208438] 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

SAMM50

Gene Name

SAMM50 sorting and assembly machinery component

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015380.4		Intron			NP_056195.3

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