Product Details

SNP ID

rs2257906

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.21:17791486 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GGCTCATATTCTGGAAATATGCTAC[C/T]ATTGATATCAAATGCAACATATCCC

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

C21orf91 PubMed Links

Additional Information

For this assay, SNP(s) [rs2257907] 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

C21orf91

Gene Name

chromosome 21 open reading frame 91

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001100420.1	2911	UTR 3			NP_001093890.1
NM_001100421.1	2911	UTR 3			NP_001093891.1
NM_017447.3	2911	UTR 3			NP_059143.3

Gene

C21orf91-OT1

Gene Name

C21orf91 overlapping transcript 1

There are no transcripts associated with this gene.

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