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NM_018896.5(CACNA1G):c.1589G>A (p.Arg530His) AND not provided

Germline classification:
Benign/Likely benign (3 submissions)
Last evaluated:
Dec 1, 2023
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:
RCV000972919.13

Allele description [Variation Report for NM_018896.5(CACNA1G):c.1589G>A (p.Arg530His)]

NM_018896.5(CACNA1G):c.1589G>A (p.Arg530His)

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.1589G>A (p.Arg530His)
HGVS:
  • NC_000017.11:g.50575991G>A
  • NG_032024.1:g.19924G>A
  • NM_001256324.2:c.1589G>A
  • NM_001256325.2:c.1589G>A
  • NM_001256326.2:c.1589G>A
  • NM_001256327.2:c.1589G>A
  • NM_001256328.2:c.1589G>A
  • NM_001256329.2:c.1589G>A
  • NM_001256330.2:c.1589G>A
  • NM_001256331.2:c.1589G>A
  • NM_001256332.2:c.1589G>A
  • NM_001256333.2:c.1589G>A
  • NM_001256334.2:c.1589G>A
  • NM_001256359.2:c.1589G>A
  • NM_001256360.2:c.1589G>A
  • NM_001256361.2:c.1589G>A
  • NM_018896.5:c.1589G>AMANE SELECT
  • NM_198376.3:c.1589G>A
  • NM_198377.3:c.1589G>A
  • NM_198378.3:c.1589G>A
  • NM_198379.3:c.1589G>A
  • NM_198380.3:c.1589G>A
  • NM_198382.3:c.1589G>A
  • NM_198383.3:c.1589G>A
  • NM_198384.3:c.1589G>A
  • NM_198385.3:c.1589G>A
  • NM_198386.3:c.1589G>A
  • NM_198387.3:c.1589G>A
  • NM_198388.3:c.1589G>A
  • NM_198396.3:c.1589G>A
  • NP_001243253.1:p.Arg530His
  • NP_001243254.1:p.Arg530His
  • NP_001243255.1:p.Arg530His
  • NP_001243256.1:p.Arg530His
  • NP_001243257.1:p.Arg530His
  • NP_001243258.1:p.Arg530His
  • NP_001243259.1:p.Arg530His
  • NP_001243260.1:p.Arg530His
  • NP_001243261.1:p.Arg530His
  • NP_001243262.1:p.Arg530His
  • NP_001243263.1:p.Arg530His
  • NP_001243288.1:p.Arg530His
  • NP_001243289.1:p.Arg530His
  • NP_001243290.1:p.Arg530His
  • NP_061496.2:p.Arg530His
  • NP_938190.1:p.Arg530His
  • NP_938191.2:p.Arg530His
  • NP_938192.1:p.Arg530His
  • NP_938193.1:p.Arg530His
  • NP_938194.1:p.Arg530His
  • NP_938196.1:p.Arg530His
  • NP_938197.1:p.Arg530His
  • NP_938198.1:p.Arg530His
  • NP_938199.1:p.Arg530His
  • NP_938200.1:p.Arg530His
  • NP_938201.1:p.Arg530His
  • NP_938202.1:p.Arg530His
  • NP_938406.1:p.Arg530His
  • NC_000017.10:g.48653352G>A
  • NC_000017.10:g.48653352G>A
  • NM_018896.4:c.1589G>A
  • NR_046054.2:n.2334G>A
  • NR_046055.2:n.2334G>A
  • NR_046056.2:n.2334G>A
  • NR_046057.2:n.2334G>A
  • NR_046058.2:n.2334G>A
Protein change:
R530H
Links:
dbSNP: rs7222276
NCBI 1000 Genomes Browser:
rs7222276
Molecular consequence:
  • NM_001256324.2:c.1589G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001256325.2:c.1589G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001256326.2:c.1589G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001256327.2:c.1589G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001256328.2:c.1589G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001256329.2:c.1589G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001256330.2:c.1589G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001256331.2:c.1589G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001256332.2:c.1589G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001256333.2:c.1589G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001256334.2:c.1589G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001256359.2:c.1589G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001256360.2:c.1589G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001256361.2:c.1589G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_018896.5:c.1589G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_198376.3:c.1589G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_198377.3:c.1589G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_198378.3:c.1589G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_198379.3:c.1589G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_198380.3:c.1589G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_198382.3:c.1589G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_198383.3:c.1589G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_198384.3:c.1589G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_198385.3:c.1589G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_198386.3:c.1589G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_198387.3:c.1589G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_198388.3:c.1589G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_198396.3:c.1589G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NR_046054.2:n.2334G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_046055.2:n.2334G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_046056.2:n.2334G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_046057.2:n.2334G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_046058.2:n.2334G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
Observations:
1

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV001120649Invitae
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))
Benign
(Nov 27, 2023)
germlineclinical testing

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

SCV001982992GeneDx
criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)
Likely benign
(Apr 11, 2021)
germlineclinical testing

Citation Link,

SCV004699766CeGaT Center for Human Genetics Tuebingen
criteria provided, single submitter

(CeGaT Center For Human Genetics Tuebingen Variant Classification Criteria Version 2)
Benign
(Dec 1, 2023)
germlineclinical testing

Citation Link

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical testing
not providedgermlineyes1not 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, SCV001120649.4

#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, SCV001982992.2

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

From CeGaT Center for Human Genetics Tuebingen, SCV004699766.5

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testingnot provided

Description

CACNA1G: BS1, BS2

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot provided1not providednot providednot provided

Last Updated: Jul 15, 2024