Product Details

SNP ID: rs201919906
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.9:90613255 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: ACATGATCACGCACTTGCCTTTGAG[C/T]TTCTCTTTCCTTTTCTGCTGCTTGC
Phenotype: MIM: 607863
Polymorphism: C/T, 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	963	Silent Mutation	AAA,AAG	K191K	NP_060064.2