Product Details

SNP ID

rs4149658

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:139531271 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GGGAAACAAAAGCACAAACAATGGC[C/T]TTATTTACACAAAAAGTCTGATTTT

Phenotype

MIM: 300746

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

F9 PubMed Links

Gene Details

Gene

F9

Gene Name

coagulation factor IX

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000133.3		Intron			NP_000124.1
NM_001313913.1		Intron			NP_001300842.1
XM_005262397.4		Intron			XP_005262454.1

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