Product Details

SNP ID

rs11099960

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:154563097 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATTATTGCTACTATTGTGTGTTTTT[C/T]TAGTTAAGTCCCAAGGTGTCAACGA

Phenotype

MIM: 134830

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FGB PubMed Links

Gene Details

Gene

FGB

Gene Name

fibrinogen beta chain

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001184741.1	118	Silent Mutation	CTA,TTA	L27L	NP_001171670.1
NM_005141.4	118	Silent Mutation	CTA,TTA	L27L	NP_005132.2

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