Product Details

SNP ID: rs199817559
Assay Type: Functionally tested
NCBI dbSNP Submissions: 4
Location: Chr.1:230704236 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GTCATTGCTCAATTTTTGCAGGTTC[A/G]GCTCGGTGTGCAGAATGGCGGGCAG
Phenotype: MIM: 106150
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: AGT PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000029.3	1734	Missense Mutation	CCG,CTG	P409L	NP_000020.1