Product Details

SNP ID

rs9722

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.21:46599326 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

TTGCTGTCTGCTTTCTTGCATGACC[A/G]TCTCTGTTACAGGAAAGGTTTGGCT

Phenotype

MIM: 176990

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

S100B PubMed Links

Additional Information

For this assay, SNP(s) [rs116960944] 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

S100B

Gene Name

S100 calcium binding protein B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006272.2	554	UTR 3			NP_006263.1
XM_017028424.1	554	UTR 3			XP_016883913.1

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