Product Details

SNP ID

rs28742272

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.16:11668900 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGGCATTTCGGGGTTCTTCAAAATT[C/T]TGGGAGCTCCGGGGAGGGCTCCGGG

Phenotype

MIM: 603032

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

SNN PubMed Links

Additional Information

For this assay, SNP(s) [rs141298508] 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

SNN

Gene Name

stannin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003498.5		Intron			NP_003489.1
XM_017023741.1		Intron			XP_016879230.1
XM_017023742.1		Intron			XP_016879231.1

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