Product Details

SNP ID

rs3917630

Assay Type

Functionally tested

NCBI dbSNP Submissions

8

Location

Chr.1:94530966 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AAAGTGGGAGATCCAAAGTGCTACC[A/C]GGATTTGGGTGAAGAAGAGATAGTA

Phenotype

MIM: 134390

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

F3 PubMed Links

Gene Details

Gene

F3

Gene Name

coagulation factor III, tissue factor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001178096.1		Intron			NP_001171567.1
NM_001993.4		Intron			NP_001984.1

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