Product Details

SNP ID: rs146390181
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.8:56113575 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CGTTGCCACCGAACTCCATGATGAT[A/G]GTCCCTAGGCTATTGGACCCTGCGG
Phenotype: MIM: 190060
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: MOS PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005372.1	408	Silent Mutation	ACC,ACT	T136T	NP_005363.1