Product Details

SNP ID

rs143872295

Assay Type

Functionally tested

NCBI dbSNP Submissions

11

Location

Chr.1:94530477 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGCTTCCTTTATGAAACATTCAGTG[A/G]GGAGTTCTCCTTCCAGCTCTGCCCC

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	1092	Silent Mutation	CCC,CCT	P237P	NP_001171567.1
NM_001993.4	1092	Missense Mutation	CCA,TCA	P291S	NP_001984.1

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