Product Details

SNP ID: rs190357072
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.4:184089229 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GCGCTTTTAAAACACATTACATAAA[T/C]CTTTAGAAATCTTTTGTGAAGGTAA
Phenotype: MIM: 616983
Polymorphism: T/C, Transition substitution
Allele Nomenclature
Literature Links: ENPP6 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_153343.3	3413	UTR 3			NP_699174.1