NM_004380.3(CREBBP):c.6169C>T (p.Gln2057Ter) AND Rubinstein-Taybi syndrome due to CREBBP mutations

Germline classification:: Likely pathogenic (1 submission)
Last evaluated:: Apr 29, 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:: RCV003148514.1

Allele description [Variation Report for NM_004380.3(CREBBP):c.6169C>T (p.Gln2057Ter)]

NM_004380.3(CREBBP):c.6169C>T (p.Gln2057Ter)

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.6169C>T (p.Gln2057Ter)

HGVS:

NC_000016.10:g.3728878G>A
NG_009873.2:g.156836C>T
NM_001079846.1:c.6055C>T
NM_004380.3:c.6169C>TMANE SELECT
NP_001073315.1:p.Gln2019Ter
NP_004371.2:p.Gln2057Ter
LRG_1426t1:c.6169C>T
LRG_1426:g.156836C>T
LRG_1426p1:p.Gln2057Ter
NC_000016.9:g.3778879G>A

Protein change:

Q2019*

Molecular consequence:

NM_001079846.1:c.6055C>T - nonsense - [Sequence Ontology: SO:0001587]
NM_004380.3:c.6169C>T - nonsense - [Sequence Ontology: SO:0001587]

Condition(s)

Name:: Rubinstein-Taybi syndrome due to CREBBP mutations
Synonyms:: Rubinstein syndrome; Broad thumbs and great toes, characteristic facies, and mental retardation; RUBINSTEIN-TAYBI SYNDROME 1, INCOMPLETE; See all synonyms [MedGen]
Identifiers:: MONDO: MONDO:0008393; MedGen: C4551859; Orphanet: 783; OMIM: 180849

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003836424	Baylor Genetics	criteria provided, single submitter (ACMG Guidelines, 2015)	Likely pathogenic (Apr 29, 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

SCV003836424

Baylor Genetics

criteria provided, single submitter

(ACMG Guidelines, 2015)

Likely pathogenic
(Apr 29, 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	unknown	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 Baylor Genetics, SCV003836424.1

#	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	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Mar 11, 2023

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