Product Details

SNP ID

rs58661272

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.22:45416886 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGGTGATCATCCTTTCATAATTGT[A/G]TTGATTACTCAGGTTTTTTTTTTTT

Phenotype

MIM: 608685

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

RIBC2 PubMed Links

Additional Information

For this assay, SNP(s) [rs34961526] 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

RIBC2

Gene Name

RIB43A domain with coiled-coils 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015653.4		Intron			NP_056468.3
XM_005261524.4		Intron			XP_005261581.1
XM_011530126.2		Intron			XP_011528428.1
XM_017028766.1		Intron			XP_016884255.1

Gene

SMC1B

Gene Name

structural maintenance of chromosomes 1B

There are no transcripts associated with this gene.

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