Product Details

SNP ID

rs3789683

Assay Type

Functionally tested

NCBI dbSNP Submissions

43

Location

Chr.1:94530506 on Build GRCh38

Set Membership

HapMap JSNP

Context Sequence [VIC/FAM]

GTTCTCCTTCCAGCTCTGCCCCACT[C/T]CTGCCTTTCTACACTTGTGTAGAGA

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	1063	Missense Mutation	AAG,GAG	K228E	NP_001171567.1
NM_001993.4	1063	Missense Mutation	GAA,GGA	E281G	NP_001984.1

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