Product Details

SNP ID

rs4253829

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:186270130 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTCACAGATGATGTGATTGAGTACC[C/T]AGAAAAATCCAAAATTAACCATCAC

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		Intron			NP_000119.1
XM_005262821.3		Intron			XP_005262878.1
XM_005262822.3		Intron			XP_005262879.1
XM_005262823.3		Intron			XP_005262880.1
XM_006714137.2		Intron			XP_006714200.1
XM_017007884.1		Intron			XP_016863373.1
XM_017007885.1		Intron			XP_016863374.1
XM_017007886.1		Intron			XP_016863375.1

View Full Product Details