VCV001690699.4 - ClinVar

NM_004380.3(CREBBP):c.3974G>T (p.Ser1325Ile)

Germline

Classification

The aggregate germline classification for this variant, typically for a monogenic or Mendelian disorder as in the ACMG/AMP guidelines, or for response to a drug. This value is calculated by NCBI based on data from submitters. Read our rules for calculating the aggregate classification.

(3)

Stars represent the aggregate review status, or the level of review supporting the aggregate germline classification for this VCV record. This value is calculated by NCBI based on data from submitters. Read our rules for calculating the review status. The number of submissions which contribute to this review status is shown in parentheses.

Uncertain significance

criteria provided, multiple submitters, no conflicts

Somatic

No data submitted for somatic clinical impact

Somatic

No data submitted for oncogenicity

Variant Details

Identifiers

NM_004380.3(CREBBP):c.3974G>T (p.Ser1325Ile)

Variation ID: 1690699 Accession: VCV001690699.4

Type and length

single nucleotide variant, 1 bp

Location

Cytogenetic: 16p13.3 16: 3744902 (GRCh38) [ NCBI UCSC ] 16: 3794903 (GRCh37) [ NCBI UCSC ]

Timeline in ClinVar

	First in ClinVar Help The date this variant first appeared in ClinVar with each type of classification.	Last submission Help The date of the most recent submission for each type of classification for this variant.	Last evaluated Help The most recent date that a submitter evaluated this variant for each type of classification.
Germline	Jun 9, 2022	Nov 20, 2023	Jan 25, 2023

HGVS

Nucleotide	Protein	Molecular consequence
NM_004380.3:c.3974G>T MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.	NP_004371.2:p.Ser1325Ile	missense
NM_001079846.1:c.3860G>T	NP_001073315.1:p.Ser1287Ile	missense
NM_004380.2:c.3974G>T
NC_000016.10:g.3744902C>A
NC_000016.9:g.3794903C>A
NG_009873.2:g.140812G>T
LRG_1426:g.140812G>T
LRG_1426t1:c.3974G>T	LRG_1426p1:p.Ser1325Ile

... more HGVS ... less HGVS

Protein change

S1287I, S1325I

Other names

Canonical SPDI

NC_000016.10:3744901:C:A

Functional consequence Help The effect of the variant on RNA or protein function, based on experimental evidence from submitters.

Global minor allele frequency (GMAF) Help The global minor allele frequency calculated by the 1000 Genomes Project. The minor allele at this location is indicated in parentheses and may be different from the allele represented by this VCV record.

Allele frequency Help The frequency of the allele represented by this VCV record.

Links

dbSNP: rs760292945 VarSome

Genes

Gene	OMIM	ClinGen Gene Dosage Sensitivity Curation		Variation Viewer Help Links to Variation Viewer, a genome browser to view variation data from NCBI databases.	Related variants
Gene	OMIM	HI score Help The haploinsufficiency score for the gene, curated by ClinGen’s Dosage Sensitivity Curation task team.	TS score Help The triplosensitivity score for the gene, curated by ClinGen’s Dosage Sensitivity Curation task team.		Within gene Help The number of variants in ClinVar that are contained within this gene, with a link to view the list of variants.	All Help The number of variants in ClinVar for this gene, including smaller variants within the gene and larger CNVs that overlap or fully contain the gene.
CREBBP		Sufficient evidence for dosage pathogenicity	No evidence available	GRCh38 GRCh37	2427	2545

Conditions - Germline

Condition Help The condition for this variant-condition (RCV) record in ClinVar.	Classification Help The aggregate germline classification for this variant-condition (RCV) record in ClinVar. The number of submissions that contribute to this aggregate classification is shown in parentheses. (# of submissions)	Review status Help The aggregate review status for this variant-condition (RCV) record in ClinVar. This value is calculated by NCBI based on data from submitters. Read our rules for calculating the review status.	Last evaluated Help The most recent date that a submitter evaluated this variant for the condition.	Variation/condition record Help The RCV accession number, with most recent version number, for the variant-condition record, with a link to the RCV web page.
See cases	Uncertain significance (1)	criteria provided, single submitter	Oct 7, 2019	RCV002253117.2
Menke-Hennekam syndrome 1 Rubinstein-Taybi syndrome due to CREBBP mutations	Uncertain significance (1)	criteria provided, single submitter	Aug 17, 2021	RCV002481058.1
CREBBP-related disorder	Uncertain significance (1)	criteria provided, single submitter	Jan 25, 2023	RCV003403756.4

Submissions - Germline

Classification Help The submitted germline classification for each SCV record. (Last evaluated)	Review status Help Stars represent the review status, or the level of review supporting the submitted (SCV) record. This value is calculated by NCBI based on data from the submitter. Read our rules for calculating the review status. This column also includes a link to the submitter’s assertion criteria if provided, and the collection method. (Assertion criteria)	Condition Help The condition for the classification, provided by the submitter for this submitted (SCV) record. This column also includes the affected status and allele origin of individuals observed with this variant.	Submitter Help The submitting organization for this submitted (SCV) record. This column also includes the SCV accession and version number, the date this SCV first appeared in ClinVar, and the date that this SCV was last updated in ClinVar.	More information Help This column includes more information supporting the classification, including citations, the comment on classification, and detailed evidence provided as observations of the variant by the submitter.
Uncertain significance (Oct 07, 2019)	criteria provided, single submitter (ACMG Guidelines, 2015) Method: clinical testing	See cases Affected status: yes Allele origin: germline	Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein Accession: SCV002523283.1 First in ClinVar: Jun 09, 2022 Last updated: Jun 09, 2022	Comment: ACMG classification criteria: PM2, PP3 Clinical Features: Neurodevelopmental abnormality (present) , Atypical behavior (present) , Abnormal facial shape (present) Geographic origin: Brazil
Uncertain significance (Aug 17, 2021)	criteria provided, single submitter (ACMG Guidelines, 2015) Method: clinical testing	Rubinstein-Taybi syndrome due to CREBBP mutations Menke-Hennekam syndrome 1 Affected status: unknown Allele origin: unknown	Fulgent Genetics, Fulgent Genetics Accession: SCV002793044.1 First in ClinVar: Dec 31, 2022 Last updated: Dec 31, 2022
Uncertain significance (Jan 25, 2023)	criteria provided, single submitter (ACMG Guidelines, 2015) Method: clinical testing	CREBBP-related condition Affected status: unknown Allele origin: germline	PreventionGenetics, part of Exact Sciences Accession: SCV004111140.1 First in ClinVar: Nov 20, 2023 Last updated: Nov 20, 2023	Comment: The CREBBP c.3974G>T variant is predicted to result in the amino acid substitution p.Ser1325Ile. To our knowledge, this variant has not been reported in the … (more) The CREBBP c.3974G>T variant is predicted to result in the amino acid substitution p.Ser1325Ile. To our knowledge, this variant has not been reported in the literature or in a large population database (http://gnomad.broadinstitute.org), indicating this variant is rare. At this time, the clinical significance of this variant is uncertain due to the absence of conclusive functional and genetic evidence. (less)

Comment:

The CREBBP c.3974G>T variant is predicted to result in the amino acid substitution p.Ser1325Ile. To our knowledge, this variant has not been reported in the literature or in a large population database (http://gnomad.broadinstitute.org), indicating this variant is rare. At this time, the clinical significance of this variant is uncertain due to the absence of conclusive functional and genetic evidence.

Germline Functional Evidence

There is no functional evidence in ClinVar for this variation. If you have generated functional data for this variation, please consider submitting that data to ClinVar.

Comment:

Citations for germline classification of this variant

There are no citations for germline classification of this variant in ClinVar. If you know of citations for this variation, please consider submitting that information to ClinVar.

Text-mined citations for rs760292945 ...

These citations are identified by LitVar using the rs number, so they may include citations for more than one variant at this location. Please review the LitVar results carefully for your variant of interest.

Record last updated May 12, 2024

ClinVar Genomic variation as it relates to human health

NM_004380.3(CREBBP):c.3974G>T (p.Ser1325Ile)

Variant Details

Genes

Conditions - Germline

Submissions - Germline

Germline Functional Evidence

Citations for germline classification of this variant

Text-mined citations for rs760292945 ...