Product Details

SNP ID: rs74737097
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.6:96525298 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: ATAGATTTTGTATTTGTTTTCCAGG[G/T]AATTAATGTGGACCTGATTCATATT
Phenotype: MIM: 613372
Polymorphism: G/T, Transversion substitution
Allele Nomenclature
Literature Links: UFL1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015323.4	302	Missense Mutation	GGA,GTA	G85V	NP_056138.1