Product Details

SNP ID

rs141179680

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:142911989 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGGTGCAGATGCAAGACTAGTTAAT[C/T]GCTCTGAAAGTGAGGAGGGGGGACG

Phenotype

MIM: 124080

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

CYP11B2 PubMed Links

Gene Details

Gene

CYP11B2

Gene Name

cytochrome P450 family 11 subfamily B member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000498.3	1506	Silent Mutation	GCA,GCG	A501A	NP_000489.3

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