Product Details

SNP ID

rs143207556

Assay Type

Functionally tested

NCBI dbSNP Submissions

16

Location

Chr.1:94532378 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCTACCGGGCTGTCTGTACTCTTCC[A/G]GTTAACTGTTCGGGAGGGAATCACT

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	915	Intron			NP_001171567.1
NM_001993.4	915	Missense Mutation			NP_001984.1

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