Product Details

SNP ID

rs11211460

Assay Type

Functionally Tested

NCBI dbSNP Submissions

48

Location

Chr.1:38843435 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TATATCTGAACTATTCCATTAAAAA[C/T]TCAGGCCGGGCGCAGTGGCTCACTC

Phenotype

MIM: 608267

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

RRAGC PubMed Links

Additional Information

For this assay, SNP(s) [rs115651987] 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

RRAGC

Gene Name

Ras related GTP binding C

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001271851.1		Intron			NP_001258780.1
NM_022157.3		Intron			NP_071440.1

View Full Product Details