VCV002058730.2 - ClinVar

NM_000719.7(CACNA1C):c.4942G>C (p.Ala1648Pro)

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.

(1)

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, single submitter

Somatic

No data submitted for somatic clinical impact

Somatic

No data submitted for oncogenicity

Variant Details

Identifiers

NM_000719.7(CACNA1C):c.4942G>C (p.Ala1648Pro)

Variation ID: 2058730 Accession: VCV002058730.2

Type and length

single nucleotide variant, 1 bp

Location

Cytogenetic: 12p13.33 12: 2677207 (GRCh38) [ NCBI UCSC ] 12: 2786373 (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	Feb 8, 2023	Feb 20, 2024	Dec 24, 2021

HGVS

Nucleotide	Protein	Molecular consequence
NM_000719.7:c.4942G>C MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.	NP_000710.5:p.Ala1648Pro	missense
NM_001167623.2:c.4942G>C MANE Plus Clinical Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.	NP_001161095.1:p.Ala1648Pro	missense
NM_001129827.2:c.5086G>C	NP_001123299.1:p.Ala1696Pro	missense
NM_001129829.2:c.5065G>C	NP_001123301.1:p.Ala1689Pro	missense
NM_001129830.3:c.4942G>C	NP_001123302.2:p.Ala1648Pro	missense
NM_001129831.2:c.5026G>C	NP_001123303.1:p.Ala1676Pro	missense
NM_001129832.2:c.5002G>C	NP_001123304.1:p.Ala1668Pro	missense
NM_001129833.2:c.4999G>C	NP_001123305.1:p.Ala1667Pro	missense
NM_001129834.2:c.4999G>C	NP_001123306.1:p.Ala1667Pro	missense
NM_001129835.2:c.4999G>C	NP_001123307.1:p.Ala1667Pro	missense
NM_001129836.2:c.4993G>C	NP_001123308.1:p.Ala1665Pro	missense
NM_001129837.2:c.4966G>C	NP_001123309.1:p.Ala1656Pro	missense
NM_001129838.2:c.4966G>C	NP_001123310.1:p.Ala1656Pro	missense
NM_001129839.2:c.4960G>C	NP_001123311.1:p.Ala1654Pro	missense
NM_001129840.2:c.4942G>C	NP_001123312.1:p.Ala1648Pro	missense
NM_001129841.2:c.4942G>C	NP_001123313.1:p.Ala1648Pro	missense
NM_001129842.2:c.4942G>C	NP_001123314.1:p.Ala1648Pro	missense
NM_001129843.2:c.4942G>C	NP_001123315.1:p.Ala1648Pro	missense
NM_001129844.2:c.4933G>C	NP_001123316.1:p.Ala1645Pro	missense
NM_001129846.2:c.4909G>C	NP_001123318.1:p.Ala1637Pro	missense
NM_001167624.3:c.4942G>C	NP_001161096.2:p.Ala1648Pro	missense
NM_001167625.2:c.4909G>C	NP_001161097.1:p.Ala1637Pro	missense
NM_199460.4:c.5086G>C	NP_955630.3:p.Ala1696Pro	missense
NR_045725.1:n.1024C>G		non-coding transcript variant
NC_000012.12:g.2677207G>C
NC_000012.11:g.2786373G>C
NG_008801.2:g.711422G>C
NG_124864.1:g.271G>C
LRG_334:g.711422G>C
LRG_334t1:c.4942G>C	LRG_334p1:p.Ala1648Pro
LRG_334t2:c.5086G>C	LRG_334p2:p.Ala1696Pro
LRG_334t3:c.4942G>C	LRG_334p3:p.Ala1648Pro
LRG_334t4:c.4942G>C	LRG_334p4:p.Ala1648Pro

... more HGVS ... less HGVS

Protein change

A1645P, A1648P, A1654P, A1668P, A1676P, A1656P, A1637P, A1667P, A1696P, A1665P, A1689P

Other names

Canonical SPDI

NC_000012.12:2677206:G:C

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

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	Uncertain significance (1)	criteria provided, single submitter	Dec 24, 2021	RCV002928664.3

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 (Dec 24, 2021)	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: SCV003267964.2 First in ClinVar: Feb 07, 2023 Last updated: Feb 20, 2024	Comment: This variant has not been reported in the literature in individuals affected with CACNA1C-related conditions. In summary, the available evidence is currently insufficient to determine … (more) This variant has not been reported in the literature in individuals affected with CACNA1C-related conditions. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Possibly Damaging"; Align-GVGD: "Class C0"). This variant is not present in population databases (gnomAD no frequency). This sequence change replaces alanine, which is neutral and non-polar, with proline, which is neutral and non-polar, at codon 1648 of the CACNA1C protein (p.Ala1648Pro). (less)

Comment:

This variant has not been reported in the literature in individuals affected with CACNA1C-related conditions. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Possibly Damaging"; Align-GVGD: "Class C0"). This variant is not present in population databases (gnomAD no frequency). This sequence change replaces alanine, which is neutral and non-polar, with proline, which is neutral and non-polar, at codon 1648 of the CACNA1C protein (p.Ala1648Pro).

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 this variant ...

Record last updated Sep 29, 2024

ClinVar Genomic variation as it relates to human health

NM_000719.7(CACNA1C):c.4942G>C (p.Ala1648Pro)

Variant Details

Genes

Conditions - Germline

Submissions - Germline

Germline Functional Evidence

Citations for germline classification of this variant

Text-mined citations for this variant ...