NM_000128.4(F11):c.1843G>A (p.Val615Met) AND Plasma factor XI deficiency

Germline classification:: Likely benign (1 submission)
Last evaluated:: Apr 20, 2020
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

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:: RCV001275733.1

Allele description [Variation Report for NM_000128.4(F11):c.1843G>A (p.Val615Met)]

NM_000128.4(F11):c.1843G>A (p.Val615Met)

Genes:

F11-AS1:F11 antisense RNA 1 [Gene - HGNC]
F11:coagulation factor XI [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

4q35.2

Genomic location:

Preferred name:

NM_000128.4(F11):c.1843G>A (p.Val615Met)

HGVS:

NC_000004.12:g.186288579G>A
NG_008051.1:g.27616G>A
NM_000128.4:c.1843G>AMANE SELECT
NP_000119.1:p.Val615Met
LRG_583t1:c.1843G>A
LRG_583:g.27616G>A
NC_000004.11:g.187209733G>A
NM_000128.3:c.1843G>A
NR_033900.1:n.915C>T

Protein change:

V615M

Links:

dbSNP: rs202061241

NCBI 1000 Genomes Browser:

rs202061241

Molecular consequence:

NM_000128.4:c.1843G>A - missense variant - [Sequence Ontology: SO:0001583]
NR_033900.1:n.915C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Name:: Plasma factor XI deficiency
Identifiers:

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001461162	Natera, Inc.	no assertion criteria provided	Likely benign (Apr 20, 2020)	germline	clinical testing

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001461162

Natera, Inc.

no assertion criteria provided

Likely benign
(Apr 20, 2020)

germline

clinical testing

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 Natera, Inc., SCV001461162.1

#	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: Sep 29, 2024

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