Product Details

SNP ID: rs11568044
Assay Type: Functionally tested
NCBI dbSNP Submissions: 26
Location: Chr.1:230704075 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: CTCTCCCACCTTTGGCCCTACTCTC[C/T]GCTCCCTCTTGCCCTGCTGGCCCCA
Phenotype: MIM: 106150
Polymorphism: C/T, 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		Intron			NP_000020.1