Product Details

SNP ID

rs202246953

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.20:3084578 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACCTGTCTCAGCTCCAGGTCGGACA[C/T]GGCCCTCTTGCCGCCCCTCGGGCAG

Phenotype

MIM: 192340

Polymorphism

C/T, Transition 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	147	Missense Mutation	ATG,GTG	M33V	NP_000481.2
XM_011529267.1	147	Missense Mutation	ATG,GTG	M33V	XP_011527569.1

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