NM_000132.4(F8):c.2149C>T (p.Arg717Trp) AND Thrombophilia, X-linked, due to factor 8 defect

Germline classification:: Pathogenic (1 submission)
Last evaluated:: May 4, 2022
Review status:: 1 star out of maximum of 4 stars
criteria provided, single submitter

Somatic classification of clinical impact:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Somatic classification of oncogenicity:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Record status:: current
Accession:: RCV002247321.1

Allele description [Variation Report for NM_000132.4(F8):c.2149C>T (p.Arg717Trp)]

NM_000132.4(F8):c.2149C>T (p.Arg717Trp)

Gene:

F8:coagulation factor VIII [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

Xq28

Genomic location:

Preferred name:

NM_000132.4(F8):c.2149C>T (p.Arg717Trp)

Other names:

F8, ARG698TRP; R698W

HGVS:

NC_000023.11:g.154931641G>A
NG_011403.2:g.96083C>T
NM_000132.4:c.2149C>TMANE SELECT
NP_000123.1:p.Arg717Trp
NP_000123.1:p.Arg717Trp
LRG_555t1:c.2149C>T
LRG_555:g.96083C>T
LRG_555p1:p.Arg717Trp
NC_000023.10:g.154159916G>A
NG_011403.1:g.96083C>T
NM_000132.3:c.2149C>T
P00451:p.Arg717Trp

Protein change:

R717W; ARG698TRP

Links:

UniProtKB: P00451#VAR_001130; OMIM: 300841.0162; dbSNP: rs137852435

NCBI 1000 Genomes Browser:

rs137852435

Molecular consequence:

NM_000132.4:c.2149C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Thrombophilia, X-linked, due to factor 8 defect
Synonyms:: THROMBOPHILIA, X-LINKED, DUE TO FACTOR VIII DEFECT; Thrombophilia 13, X-linked, due to factor VIII defect
Identifiers:: MONDO: MONDO:0859082; MedGen: C5676879; OMIM: 301071

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002519673	Mendelics	criteria provided, single submitter (Mendelics Assertion Criteria 2019)	Pathogenic (May 4, 2022)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV002519673

Mendelics

criteria provided, single submitter

(Mendelics Assertion Criteria 2019)

Pathogenic
(May 4, 2022)

germline

clinical testing

Citation Link

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Mendelics, SCV002519673.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not provided

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Apr 20, 2025

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