Product Details

SNP ID

rs200904690

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:46720814 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTTGTGAGACAGCGAGGACGCCTC[A/G]AGATAAGCTTGCTGCATGTCTGGAA

Phenotype

MIM: 176930

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

F2 PubMed Links

Gene Details

Gene

F2

Gene Name

coagulation factor II, thrombin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000506.4	312	Missense Mutation	CAA,CGA	Q97R	NP_000497.1
NM_001311257.1	312	Missense Mutation	CAA,CGA	Q81R	NP_001298186.1

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