Product Details

SNP ID

rs138886317

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.11:14281687 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCCTCCATGTATGTTACCTTAAGCT[A/G]CCGTGCTAACTGTTGTCCTTCTTCC

Phenotype

MIM: 600098

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

RRAS2 PubMed Links

Additional Information

For this assay, SNP(s) [rs2303972] 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

RRAS2

Gene Name

related RAS viral (r-ras) oncogene homolog 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001102669.2	605	Nonsense Mutation	CAG,TAG	Q71*	NP_001096139.1
NM_001177314.1	605	Intron			NP_001170785.1
NM_001177315.1	605	Intron			NP_001170786.1
NM_012250.5	605	Nonsense Mutation	CAG,TAG	Q148*	NP_036382.2
XM_017017363.1	605	Intron			XP_016872852.1

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