Product Details

SNP ID

rs67927428

Assay Type

DME

NCBI dbSNP Submissions

NA

Location

Chr.19:41090365 on Build GRCh38

Set Membership

DME Validated Inventoried

Context Sequence [VIC/FAM]

CTGACTCTCCTCAGACCTCTGAGTT[G/T]ACTCTCTCCCCAACCCCCTTCTCCC

Phenotype

MIM: 608055

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

CYP2A13*1E,g.1894G>T

Literature Links

CYP2A13 PubMed Links

Gene Details

Gene

CYP2A13

Gene Name

cytochrome P450 family 2 subfamily A member 13

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000766.4		Intron			NP_000757.2

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