Product Details

SNP ID
rs144785536
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.11:46719725 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGTGTTCCTGGCTCCTCAGCAAGCA[C/T]GGTCGCTGCTCCAGCGGGTCCGGCG
Phenotype
MIM: 176930
Polymorphism
C/T, 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_000506.4 125 Missense Mutation CGG,TGG R35W NP_000497.1
NM_001311257.1 125 Missense Mutation CGG,TGG R19W NP_001298186.1

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