Product Details

SNP ID

hCV33845966

Assay Type

DME

NCBI dbSNP Submissions

NA

Location

Chr.19:41091747 on Build GRCh38

Set Membership

DME Validated Inventoried

Context Sequence [VIC/FAM]

GCAACCCCAGCTCTATGAGATGTTC[C/T]CTTCGGTGATGAAACACCTGCCAGG

Phenotype

MIM: 608055

Polymorphism

C/T, Transition substitution

Allele Nomenclature

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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