Product Details

SNP ID: rs144426877
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.8:56113782 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TGTACACCGAGCCAAACCCTCCAGC[A/T]CCCAGCCTCTGCAGCAAGCACACCT
Phenotype: MIM: 190060
Polymorphism: A/T, Transversion 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	201	Silent Mutation	GGA,GGT	G67G	NP_005363.1