Product Details

SNP ID
rs113727256
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:187467875 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGAATTGTAGTAGAATCTGTTCTCA[C/T]TGGCACGACACAATCCTCTGTCTGC
Phenotype
MIM: 152310
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
TFPI PubMed Links

Gene Details

Gene
TFPI
Gene Name
tissue factor pathway inhibitor
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
XM_005246818.1 1012 Missense Mutation AAT,AGT N229S XP_005246875.1
XM_005246819.1 1012 Missense Mutation AAT,AGT N229S XP_005246876.1
XM_006712720.3 1012 Missense Mutation AAT,AGT N229S XP_006712783.1
XM_011511707.2 1012 Missense Mutation AAT,AGT N229S XP_011510009.1
XM_011511708.1 1012 Missense Mutation AAT,AGT N229S XP_011510010.1
XM_011511709.2 1012 Missense Mutation AAT,AGT N229S XP_011510011.1

View Full Product Details