Product Details

SNP ID

rs56160784

Assay Type

DME

NCBI dbSNP Submissions

NA

Location

Chr.15:74749801 on Build GRCh38

Set Membership

DME Validated Inventoried

Context Sequence [VIC/FAM]

AGCTTCTCCTGGCCTCTGCCATCTT[C/G]TGCCTGGTATTCTGGGTGCTCAAGG

Phenotype

MIM: 124060

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

CYP1A2*2,g.63C>G

Literature Links

CYP1A2 PubMed Links

Gene Details

Gene

CYP1A2

Gene Name

cytochrome P450 family 1 subfamily A member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000761.4	127	Missense Mutation	TTC,TTG	F21L	NP_000752.2

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