Product Details

SNP ID

rs16974794

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:40993189 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCATTTGTAGTTGGCCTGGTAACAT[A/G]TAGTATCCTGGAGACCCACTAGAAG

Phenotype

MIM: 123930

Polymorphism

A/G, Transition substitution

Allele Nomenclature

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		Intron			NP_000758.1
XM_005258569.4		Intron			XP_005258626.1
XM_006723050.3		Intron			XP_006723113.1
XM_011526546.2		Intron			XP_011524848.1
XM_011526547.2		Intron			XP_011524849.1
XM_011526548.2		Intron			XP_011524850.1
XM_011526549.2		Intron			XP_011524851.1
XM_011526550.2		Intron			XP_011524852.1

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