Product Details

SNP ID
rs211694396
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:186271672 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGAGGGGACATTACTACGGTCTTCA[C/T]ACCAAGCGCCAAGTACTGCCAGGTA
Phenotype
MIM: 264900
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
F11 PubMed Links

Gene Details

Gene
F11
Gene Name
coagulation factor XI
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000128.3 471 Missense Mutation ACA,ATA T40I NP_000119.1
XM_005262821.3 471 Missense Mutation ACA,ATA T40I XP_005262878.1
XM_005262822.3 471 Missense Mutation ACA,ATA T40I XP_005262879.1
XM_005262823.3 471 Missense Mutation ACA,ATA T40I XP_005262880.1
XM_006714137.2 471 Missense Mutation ACA,ATA T40I XP_006714200.1
XM_017007884.1 471 Missense Mutation ACA,ATA T40I XP_016863373.1
XM_017007885.1 471 Missense Mutation ACA,ATA T40I XP_016863374.1
XM_017007886.1 471 Missense Mutation ACA,ATA T40I XP_016863375.1

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