Product Details

SNP ID

rs199637318

Assay Type

Functionally tested

NCBI dbSNP Submissions

3

Location

Chr.1:94533131 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GATTTCCAATAATAAAGTGTATAAA[C/T]TAAGTCCTTGCCAAAAACATCCCGG

Phenotype

MIM: 134390

Polymorphism

C/T, 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	771	Missense Mutation	ATT,GTT	I184V	NP_001171567.1
NM_001993.4	771	Missense Mutation	ATT,GTT	I184V	NP_001984.1

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