Product Details

SNP ID

rs9344929

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:89366077 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGAGGAAAGGAGTTAGGGCACCTTA[A/C]TTATTTTTAGAAATCTCCTTTCAAA

Phenotype

MIM: 608268

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

RRAGD PubMed Links

Additional Information

For this assay, SNP(s) [rs854908] 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

RRAGD

Gene Name

Ras related GTP binding D

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_021244.4	3237	UTR 3			NP_067067.1
XM_005248755.4	3237	UTR 3			XP_005248812.1
XM_011536022.2	3237	UTR 3			XP_011534324.1

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