VCV000456990.17 - ClinVar

NM_000719.7(CACNA1C):c.6039C>T (p.Pro2013=)

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.

(4)

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.

Likely benign

criteria provided, multiple submitters, no conflicts

Somatic

No data submitted for somatic clinical impact

Somatic

No data submitted for oncogenicity

Variant Details

Identifiers

NM_000719.7(CACNA1C):c.6039C>T (p.Pro2013=)

Variation ID: 456990 Accession: VCV000456990.17

Type and length

single nucleotide variant, 1 bp

Location

Cytogenetic: 12p13.33 12: 2688701 (GRCh38) [ NCBI UCSC ] 12: 2797867 (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	Dec 26, 2017	May 1, 2024	May 11, 2023

HGVS

Nucleotide	Protein	Molecular consequence
NM_000719.7:c.6039C>T MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.	NP_000710.5:p.Pro2013=	synonymous
NM_001167623.2:c.6039C>T MANE Plus Clinical Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.	NP_001161095.1:p.Pro2013=	synonymous
NM_001129827.2:c.6183C>T	NP_001123299.1:p.Pro2061=	synonymous
NM_001129829.2:c.6162C>T	NP_001123301.1:p.Pro2054=	synonymous
NM_001129830.3:c.6144C>T	NP_001123302.2:p.Pro2048=	synonymous
NM_001129831.2:c.6123C>T	NP_001123303.1:p.Pro2041=	synonymous
NM_001129832.2:c.6099C>T	NP_001123304.1:p.Pro2033=	synonymous
NM_001129833.2:c.6096C>T	NP_001123305.1:p.Pro2032=	synonymous
NM_001129834.2:c.6096C>T	NP_001123306.1:p.Pro2032=	synonymous
NM_001129835.2:c.6096C>T	NP_001123307.1:p.Pro2032=	synonymous
NM_001129836.2:c.6090C>T	NP_001123308.1:p.Pro2030=	synonymous
NM_001129837.2:c.6063C>T	NP_001123309.1:p.Pro2021=	synonymous
NM_001129838.2:c.6063C>T	NP_001123310.1:p.Pro2021=	synonymous
NM_001129839.2:c.6057C>T	NP_001123311.1:p.Pro2019=	synonymous
NM_001129840.2:c.6039C>T	NP_001123312.1:p.Pro2013=	synonymous
NM_001129841.2:c.6039C>T	NP_001123313.1:p.Pro2013=	synonymous
NM_001129842.2:c.6039C>T	NP_001123314.1:p.Pro2013=	synonymous
NM_001129843.2:c.6039C>T	NP_001123315.1:p.Pro2013=	synonymous
NM_001129844.2:c.6030C>T	NP_001123316.1:p.Pro2010=	synonymous
NM_001129846.2:c.6006C>T	NP_001123318.1:p.Pro2002=	synonymous
NM_001167624.3:c.6144C>T	NP_001161096.2:p.Pro2048=	synonymous
NM_001167625.2:c.6219C>T	NP_001161097.1:p.Pro2073=	synonymous
NM_199460.4:c.6288C>T	NP_955630.3:p.Pro2096=	synonymous
NC_000012.12:g.2688701C>T
NC_000012.11:g.2797867C>T
NG_008801.2:g.722916C>T
LRG_334:g.722916C>T
LRG_334t1:c.6039C>T

... more HGVS ... less HGVS

Protein change

Other names

Canonical SPDI

NC_000012.12:2688700:C:T

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.

The Genome Aggregation Database (gnomAD) 0.00001

Trans-Omics for Precision Medicine (TOPMed) 0.00004

Links

ClinGen: CA6390062 dbSNP: rs780157730 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.
CACNA1C		Little evidence for dosage pathogenicity	No evidence available	GRCh38 GRCh38 GRCh37	2116	3091
CACNA1C-AS1	-	-	-	GRCh38 GRCh38	-	857

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.
Long QT syndrome	Likely benign (1)	criteria provided, single submitter	Dec 13, 2022	RCV000558521.15
not provided	Likely benign (1)	criteria provided, single submitter	Apr 28, 2021	RCV001811029.13
Brugada syndrome 3 Long qt syndrome 8 Timothy syndrome	Likely benign (1)	criteria provided, single submitter	Mar 28, 2022	RCV002490957.8
Cardiovascular phenotype	Likely benign (1)	criteria provided, single submitter	May 11, 2023	RCV003278879.9

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.
Likely benign (Apr 28, 2021)	criteria provided, single submitter (ARUP Molecular Germline Variant Investigation Process 2021) Method: clinical testing	not provided Affected status: unknown Allele origin: germline	ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories Accession: SCV002048210.1 First in ClinVar: Jan 08, 2022 Last updated: Jan 08, 2022
Likely benign (Mar 28, 2022)	criteria provided, single submitter (ACMG Guidelines, 2015) Method: clinical testing	Timothy syndrome Brugada syndrome 3 Long qt syndrome 8 Affected status: unknown Allele origin: unknown	Fulgent Genetics, Fulgent Genetics Accession: SCV002798788.1 First in ClinVar: Dec 31, 2022 Last updated: Dec 31, 2022
Likely benign (Dec 13, 2022)	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015)) Method: clinical testing	Long QT syndrome Affected status: unknown Allele origin: germline	Labcorp Genetics (formerly Invitae), Labcorp Accession: SCV000627582.4 First in ClinVar: Dec 26, 2017 Last updated: Feb 28, 2024
Likely benign (May 11, 2023)	criteria provided, single submitter (Ambry Variant Classification Scheme 2023) Method: clinical testing	Cardiovascular phenotype Affected status: unknown Allele origin: germline	Ambry Genetics Accession: SCV004005083.2 First in ClinVar: Jul 08, 2023 Last updated: May 01, 2024	Comment: This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of … (more) This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity. (less)

Comment:

This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

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 rs780157730 ...

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 Nov 10, 2024

ClinVar Genomic variation as it relates to human health

NM_000719.7(CACNA1C):c.6039C>T (p.Pro2013=)

Variant Details

Genes

Conditions - Germline

Submissions - Germline

Germline Functional Evidence

Citations for germline classification of this variant

Text-mined citations for rs780157730 ...