Product Details

SNP ID

rs16995378

Assay Type

DME

NCBI dbSNP Submissions

NA

Location

Chr.19:15673576 on Build GRCh38

Set Membership

HapMap DME Validated Inventoried

Context Sequence [VIC/FAM]

TGGCTGGGCCTCAGACCGGTGGCAA[C/T]GTCCCCATGGCTACTCCTGCTGCTG

Phenotype

MIM: 611485

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

CYP4F12 PubMed Links

Gene Details

Gene

CYP4F12

Gene Name

cytochrome P450 family 4 subfamily F member 12

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_023944.3	161	Intron			NP_076433.3
XM_006722850.3	161	UTR 5			XP_006722913.1
XM_011528202.2	161	Intron			XP_011526504.1
XM_011528203.2	161	Intron			XP_011526505.1
XM_011528204.2	161	Intron			XP_011526506.1
XM_011528205.2	161	Intron			XP_011526507.1
XM_011528207.2	161	Intron			XP_011526509.1
XM_011528208.2	161	Intron			XP_011526510.1
XM_017027172.1	161	Missense Mutation	ACG,ATG	T16M	XP_016882661.1

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