Product Details

SNP ID

rs33926104

Assay Type

DME

NCBI dbSNP Submissions

NA

Location

Chr.19:40991390 on Build GRCh38

Set Membership

DME Validated Inventoried

Context Sequence [VIC/FAM]

TCAGCGCCACCCTAACACCCATGAC[A/C]GCCTCCCACCAGGGCCCCGCCCTCT

Phenotype

MIM: 123930

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

CYP2B6*17A,c.85C>A CYP2B6*17A,g.85C>A CYP2B6*17B,c.85C>A CYP2B6*17B,g.85C>A

Literature Links

CYP2B6 PubMed Links

Gene Details

Gene

CYP2B6

Gene Name

cytochrome P450 family 2 subfamily B member 6

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000767.4	188	Missense Mutation	AGC,CGC	S29R	NP_000758.1
XM_005258569.4	188	Missense Mutation	AGC,CGC	S29R	XP_005258626.1
XM_006723050.3	188	Missense Mutation	AGC,CGC	S29R	XP_006723113.1
XM_011526546.2	188	Missense Mutation	AGC,CGC	S29R	XP_011524848.1
XM_011526547.2	188	Intron			XP_011524849.1
XM_011526548.2	188	Missense Mutation	AGC,CGC	S29R	XP_011524850.1
XM_011526549.2	188	Intron			XP_011524851.1
XM_011526550.2	188	Intron			XP_011524852.1

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