Product Details

SNP ID: rs7686966
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.4:121668734 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: GTATTCCCTCTGGTAACACAAAGAA[C/T]CAGGCAACTTTAACAACTATAGTCA
Phenotype: MIM: 131230
Polymorphism: C/T, Transition 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		Intron			NP_001145.1
XM_017008141.1		Intron			XP_016863630.1