NM_004380.3(CREBBP):c.5602C>T (p.Arg1868Trp) AND See cases

Germline classification:: Pathogenic (1 submission)
Last evaluated:: Dec 21, 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:: RCV003156089.2

Allele description [Variation Report for NM_004380.3(CREBBP):c.5602C>T (p.Arg1868Trp)]

NM_004380.3(CREBBP):c.5602C>T (p.Arg1868Trp)

Gene:

CREBBP:CREB binding protein [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

16p13.3

Genomic location:

Preferred name:

NM_004380.3(CREBBP):c.5602C>T (p.Arg1868Trp)

HGVS:

NC_000016.10:g.3729445G>A
NG_009873.2:g.156269C>T
NM_001079846.1:c.5488C>T
NM_004380.3:c.5602C>TMANE SELECT
NP_001073315.1:p.Arg1830Trp
NP_004371.2:p.Arg1868Trp
NP_004371.2:p.Arg1868Trp
LRG_1426t1:c.5602C>T
LRG_1426:g.156269C>T
LRG_1426p1:p.Arg1868Trp
NC_000016.9:g.3779446G>A
NG_009873.1:g.155676C>T
NM_004380.2:c.5602C>T

Protein change:

R1830W; ARG1868TRP

Links:

OMIM: 600140.0011; dbSNP: rs886039491

NCBI 1000 Genomes Browser:

rs886039491

Molecular consequence:

NM_001079846.1:c.5488C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_004380.3:c.5602C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: See cases [See the Variation display for details]
Identifiers:

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003845234	Center for Personalized Medicine, Children's Hospital Los Angeles	criteria provided, single submitter (ACMG Guidelines, 2015)	Pathogenic (Dec 21, 2022)	unknown	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003845234

Center for Personalized Medicine, Children's Hospital Los Angeles

criteria provided, single submitter

(ACMG Guidelines, 2015)

Pathogenic
(Dec 21, 2022)

unknown

clinical testing

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

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

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]

PMID:: 25741868
PMCID:: PMC4544753

Details of each submission

From Center for Personalized Medicine, Children's Hospital Los Angeles, SCV003845234.1

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

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

Last Updated: Oct 20, 2024

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