Product Details

SNP ID

rs305968

Assay Type

DME

NCBI dbSNP Submissions

NA

Location

Chr.19:41116284 on Build GRCh38

Set Membership

HapMap DME Validated Inventoried

Context Sequence [VIC/FAM]

CAAGAGATAAGGGAAAGCTGCCTCC[A/G]GGACCCAGACCCCTCTCAATCCTGG

Phenotype

MIM: 124070

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

CYP2F1 PubMed Links

Gene Details

Gene

CYP2F1

Gene Name

cytochrome P450 family 2 subfamily F member 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000774.4	308	Silent Mutation	CCA,CCG	P32P	NP_000765.2
XM_011526551.2	308	Silent Mutation	CCA,CCG	P32P	XP_011524853.1
XM_011526552.2	308	Silent Mutation	CCA,CCG	P32P	XP_011524854.1
XM_011526553.2	308	Silent Mutation	CCA,CCG	P107P	XP_011524855.1
XM_011526554.2	308	Intron			XP_011524856.1
XM_011526555.2	308	Silent Mutation	CCA,CCG	P107P	XP_011524857.1
XM_017026384.1	308	Silent Mutation	CCA,CCG	P107P	XP_016881873.1
XM_017026385.1	308	Silent Mutation	CCA,CCG	P107P	XP_016881874.1
XM_017026386.1	308	Silent Mutation	CCA,CCG	P107P	XP_016881875.1
XM_017026387.1	308	Silent Mutation	CCA,CCG	P107P	XP_016881876.1

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