Product Details

SNP ID

rs138021584

Assay Type

Functionally tested

NCBI dbSNP Submissions

7

Location

Chr.1:169515483 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGGATTTCAGCCTGTATGGTTTCCA[C/T]TCCACTCCCTGCTCACTGTAGTGGA

Phenotype

MIM: 612309

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

F5 PubMed Links

Gene Details

Gene

F5

Gene Name

coagulation factor V

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000130.4	6634	Silent Mutation	GAA,GAG	E2163E	NP_000121.2
XM_017000660.1	6634	Silent Mutation	GAA,GAG	E2026E	XP_016856149.1

View Full Product Details