Product Details

SNP ID: rs2231777
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.9:90612268 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: CACTACAAAAATGGATGTGCTTCTG[A/G]TTGTCTGATGGCCTTTGCTGGCTGC
Phenotype: MIM: 607863
Polymorphism: A/G, 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	1950	UTR 3			NP_060064.2