Product Details

SNP ID

rs151171858

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:147509280 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCTCGCGGCCACACGACCGCCCCC[C/T]GCAGCAGGGAGCTGGTGAGCTACCC

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

SAMD5 PubMed Links

Additional Information

For this assay, SNP(s) [rs535026861] 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

SAMD5

Gene Name

sterile alpha motif domain containing 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001030060.2	589	Missense Mutation	CGC,TGC	R118C	NP_001025231.1
XM_017010850.1	589	Missense Mutation	CGC,TGC	R118C	XP_016866339.1

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