Product Details

SNP ID

rs9332701

Assay Type

Functionally tested

NCBI dbSNP Submissions

47

Location

Chr.1:169515529 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GTGGATGGTATAGCTCTTTACATAC[A/G]TTTCAGAGGACAGAGACTTGCAGCC

Phenotype

MIM: 612309

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

F5 PubMed Links

Gene Details

Gene

F5

Gene Name

coagulation factor V

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000130.4	6588	Missense Mutation	ACG,ATG	T2148M	NP_000121.2
XM_017000660.1	6588	Missense Mutation	ACG,ATG	T2011M	XP_016856149.1

View Full Product Details