Product Details

SNP ID: rs10784339
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.12:63144866 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: ACATTTAAAAGGAGAAAATACAACT[C/G]GGTAGGGTGATATGCACTTTTTTTT
Phenotype: MIM: 600821
Polymorphism: C/G, Transversion substitution
Allele Nomenclature
Literature Links: AVPR1A PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000706.4	5724	UTR 3			NP_000697.1