Product Details

SNP ID: rs76263916
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.9:90613407 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TCCATGAAGGCACACTTCCATGTGC[G/A]GGCCAAGGCCTCCGCCTCGCTGCTC
Phenotype: MIM: 607863
Polymorphism: G/A, Transition substitution
Allele Nomenclature
Literature Links: DIRAS2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_017594.4	811	Missense Mutation	CGC,TGC	R141C	NP_060064.2