U.S. flag

An official website of the United States government

NM_018896.5(CACNA1G):c.1699C>T (p.Arg567Cys) AND not provided

Germline classification:
Benign/Likely benign (2 submissions)
Last evaluated:
Jan 22, 2024
Review status:
2 stars out of maximum of 4 stars
criteria provided, multiple submitters, no conflicts
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:
RCV000957636.8

Allele description [Variation Report for NM_018896.5(CACNA1G):c.1699C>T (p.Arg567Cys)]

NM_018896.5(CACNA1G):c.1699C>T (p.Arg567Cys)

Gene:
CACNA1G:calcium voltage-gated channel subunit alpha1 G [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
17q21.33
Genomic location:
Preferred name:
NM_018896.5(CACNA1G):c.1699C>T (p.Arg567Cys)
HGVS:
  • NC_000017.11:g.50576101C>T
  • NG_032024.1:g.20034C>T
  • NM_001256324.2:c.1699C>T
  • NM_001256325.2:c.1699C>T
  • NM_001256326.2:c.1699C>T
  • NM_001256327.2:c.1699C>T
  • NM_001256328.2:c.1699C>T
  • NM_001256329.2:c.1699C>T
  • NM_001256330.2:c.1699C>T
  • NM_001256331.2:c.1699C>T
  • NM_001256332.2:c.1699C>T
  • NM_001256333.2:c.1699C>T
  • NM_001256334.2:c.1699C>T
  • NM_001256359.2:c.1699C>T
  • NM_001256360.2:c.1699C>T
  • NM_001256361.2:c.1699C>T
  • NM_018896.5:c.1699C>TMANE SELECT
  • NM_198376.3:c.1699C>T
  • NM_198377.3:c.1699C>T
  • NM_198378.3:c.1699C>T
  • NM_198379.3:c.1699C>T
  • NM_198380.3:c.1699C>T
  • NM_198382.3:c.1699C>T
  • NM_198383.3:c.1699C>T
  • NM_198384.3:c.1699C>T
  • NM_198385.3:c.1699C>T
  • NM_198386.3:c.1699C>T
  • NM_198387.3:c.1699C>T
  • NM_198388.3:c.1699C>T
  • NM_198396.3:c.1699C>T
  • NP_001243253.1:p.Arg567Cys
  • NP_001243254.1:p.Arg567Cys
  • NP_001243255.1:p.Arg567Cys
  • NP_001243256.1:p.Arg567Cys
  • NP_001243257.1:p.Arg567Cys
  • NP_001243258.1:p.Arg567Cys
  • NP_001243259.1:p.Arg567Cys
  • NP_001243260.1:p.Arg567Cys
  • NP_001243261.1:p.Arg567Cys
  • NP_001243262.1:p.Arg567Cys
  • NP_001243263.1:p.Arg567Cys
  • NP_001243288.1:p.Arg567Cys
  • NP_001243289.1:p.Arg567Cys
  • NP_001243290.1:p.Arg567Cys
  • NP_061496.2:p.Arg567Cys
  • NP_938190.1:p.Arg567Cys
  • NP_938191.2:p.Arg567Cys
  • NP_938192.1:p.Arg567Cys
  • NP_938193.1:p.Arg567Cys
  • NP_938194.1:p.Arg567Cys
  • NP_938196.1:p.Arg567Cys
  • NP_938197.1:p.Arg567Cys
  • NP_938198.1:p.Arg567Cys
  • NP_938199.1:p.Arg567Cys
  • NP_938200.1:p.Arg567Cys
  • NP_938201.1:p.Arg567Cys
  • NP_938202.1:p.Arg567Cys
  • NP_938406.1:p.Arg567Cys
  • NC_000017.10:g.48653462C>T
  • NC_000017.10:g.48653462C>T
  • NM_018896.4:c.1699C>T
  • NR_046054.2:n.2444C>T
  • NR_046055.2:n.2444C>T
  • NR_046056.2:n.2444C>T
  • NR_046057.2:n.2444C>T
  • NR_046058.2:n.2444C>T
Protein change:
R567C
Links:
dbSNP: rs60802569
NCBI 1000 Genomes Browser:
rs60802569
Molecular consequence:
  • NM_001256324.2:c.1699C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001256325.2:c.1699C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001256326.2:c.1699C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001256327.2:c.1699C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001256328.2:c.1699C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001256329.2:c.1699C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001256330.2:c.1699C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001256331.2:c.1699C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001256332.2:c.1699C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001256333.2:c.1699C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001256334.2:c.1699C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001256359.2:c.1699C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001256360.2:c.1699C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001256361.2:c.1699C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_018896.5:c.1699C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_198376.3:c.1699C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_198377.3:c.1699C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_198378.3:c.1699C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_198379.3:c.1699C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_198380.3:c.1699C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_198382.3:c.1699C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_198383.3:c.1699C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_198384.3:c.1699C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_198385.3:c.1699C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_198386.3:c.1699C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_198387.3:c.1699C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_198388.3:c.1699C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_198396.3:c.1699C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NR_046054.2:n.2444C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_046055.2:n.2444C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_046056.2:n.2444C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_046057.2:n.2444C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_046058.2:n.2444C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV001104449Invitae
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))
Benign
(Jan 22, 2024)
germlineclinical testing

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

SCV001982779GeneDx
criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)
Likely benign
(Apr 13, 2021)
germlineclinical testing

Citation Link

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyesnot providednot providednot providednot providednot providedclinical testing
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical testing

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]
PMID:
28492532
PMCID:
PMC5632818

Details of each submission

From Invitae, SCV001104449.4

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

From GeneDx, SCV001982779.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Feb 28, 2024