NM_000128.4(F11):c.1204C>T (p.Gln402Ter) AND Cerebral hemorrhage

Germline classification:: Likely pathogenic (1 submission)
Last evaluated:: Jul 17, 2019
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:: RCV001281447.1

Allele description [Variation Report for NM_000128.4(F11):c.1204C>T (p.Gln402Ter)]

NM_000128.4(F11):c.1204C>T (p.Gln402Ter)

Gene:

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.1204C>T (p.Gln402Ter)

HGVS:

NC_000004.12:g.186284160C>T
NG_008051.1:g.23197C>T
NM_000128.4:c.1204C>TMANE SELECT
NP_000119.1:p.Gln402Ter
LRG_583t1:c.1204C>T
LRG_583:g.23197C>T
NC_000004.11:g.187205314C>T
NM_000128.3:c.1204C>T

Protein change:

Q402*

Links:

dbSNP: rs1741002305

NCBI 1000 Genomes Browser:

rs1741002305

Molecular consequence:

NM_000128.4:c.1204C>T - nonsense - [Sequence Ontology: SO:0001587]

Observations:

Condition(s)

Name:: Cerebral hemorrhage
Synonyms:: Intracerebral hemorrhage
Identifiers:: MONDO: MONDO:0013792; MedGen: C2937358; Human Phenotype Ontology: HP:0001342

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

Help

Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001468755	New York Genome Center - CSER-NYCKidSeq	criteria provided, single submitter (NYGC Assertion Criteria 2020)	Likely pathogenic (Jul 17, 2019)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001468755

New York Genome Center - CSER-NYCKidSeq

criteria provided, single submitter

(NYGC Assertion Criteria 2020)

Likely pathogenic
(Jul 17, 2019)

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	yes	1	not provided	not provided	1	not provided	clinical testing

Details of each submission

From New York Genome Center - CSER-NYCKidSeq, SCV001468755.1

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

Last Updated: Sep 29, 2024

ClinVar

Relating variation to medicine