Product Details

SNP ID: rs12064849
Assay Type: Functionally tested
NCBI dbSNP Submissions: 8
Location: Chr.1:114705886 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GAACATACTTGGAAAACTCTAAGTA[C/T]ATACATACAAGGGCTATTGGCACAA
Phenotype: MIM: 164790
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: NRAS PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002524.4	3032	UTR 3			NP_002515.1