Product Details

SNP ID: hCV326811
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.22:37341421 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CTGTACCTGCCTTTCCTCTCCAGCT[A/C]TGGGCCAAGCCCACTGTGCTCACCC
Phenotype
Polymorphism: A/C, Transversion substitution
Allele Nomenclature
Literature Links: ELFN2 PubMed Links

Gene Details

Gene: ELFN2
Gene Name: extracellular leucine rich repeat and fibronectin type III domain containing 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_052906.4		Intron			NP_443138.2