Product Details

SNP ID: rs1480274
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.4:121668495 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AGTCATCTTCTCCACAGAGCAGCAG[A/C]AGAGCTTTCTTATAGTCCCCAGATG
Phenotype: MIM: 131230
Polymorphism: A/C, Transversion substitution
Allele Nomenclature
Literature Links: ANXA5 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001154.3	1101	Silent Mutation	CTG,CTT	L312L	NP_001145.1