Product Details

SNP ID
rs3917851
Assay Type
Functionally tested
NCBI dbSNP Submissions
27
Location
Chr.1:169590397 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GCTCTGGGTAATTTGCATTGCATTT[C/T]GCACCCACACTAAGTTATTGTTCAT
Phenotype
MIM: 612309 MIM: 173610
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
F5 PubMed Links

Gene Details

Gene
F5
Gene Name
coagulation factor V
There are no transcripts associated with this gene.

Gene
SELP
Gene Name
selectin P
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_003005.3 Intron NP_002996.2
XM_005245435.1 Intron XP_005245492.1
XM_005245436.3 Intron XP_005245493.1
XM_005245438.1 Intron XP_005245495.1
XM_005245439.1 Intron XP_005245496.1
XM_005245440.1 Intron XP_005245497.1

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