Product Details

SNP ID

rs5901

Assay Type

Functionally tested

NCBI dbSNP Submissions

48

Location

Chr.1:94533194 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GTGTTGTTCCTTCTGACTAAAGTCC[A/G]TTCATCTTCTACGGTCACATTCACT

Phenotype

MIM: 134390

Polymorphism

A/G, Transition 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	708	Silent Mutation			NP_001171567.1
NM_001993.4	708	Silent Mutation			NP_001984.1

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