Product Details

SNP ID
rs121964883
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.20:3083156 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCTGGGCCCGAAGCAGCGGCCTTTG[C/A]CCCCGGGGCCGCAGGGGAGGCACTG
Phenotype
MIM: 192340
Polymorphism
C/A, Transversion substitution
Allele Nomenclature
Literature Links
AVP PubMed Links

Gene Details

Gene
AVP
Gene Name
arginine vasopressin
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000490.4 193 Missense Mutation GGC,GTC G48V NP_000481.2
XM_011529267.1 193 Missense Mutation GGC,GTC G48V XP_011527569.1

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