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NM_020297.4(ABCC9):c.4512+777_4512+778delinsAA AND Dilated cardiomyopathy 1O

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Jan 15, 2024
Review status:
1 star out of maximum of 4 stars
criteria provided, single submitter
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:
RCV003094784.3

Allele description [Variation Report for NM_020297.4(ABCC9):c.4512+777_4512+778delinsAA]

NM_020297.4(ABCC9):c.4512+777_4512+778delinsAA

Gene:
ABCC9:ATP binding cassette subfamily C member 9 [Gene - OMIM - HGNC]
Variant type:
Indel
Cytogenetic location:
12p12.1
Genomic location:
Preferred name:
NM_020297.4(ABCC9):c.4512+777_4512+778delinsAA
HGVS:
  • NC_000012.12:g.21805220_21805221delinsTT
  • NG_012819.1:g.136474_136475delinsAA
  • NM_001377273.1:c.4512+777_4512+778delinsAA
  • NM_001377274.1:c.3645+777_3645+778delinsAA
  • NM_005691.4:c.4603_4604delinsAA
  • NM_020297.4:c.4512+777_4512+778delinsAAMANE SELECT
  • NP_005682.2:p.Ala1535Asn
  • NP_005682.2:p.Ala1535Asn
  • LRG_377t2:c.4603_4604delGCinsAA
  • LRG_377:g.136474_136475delinsAA
  • LRG_377p2:p.Ala1535Asn
  • NC_000012.11:g.21958154_21958155delinsTT
  • NM_005691.2:c.4603_4604delGCinsAA
Protein change:
A1535N
Molecular consequence:
  • NM_001377273.1:c.4512+777_4512+778delinsAA - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001377274.1:c.3645+777_3645+778delinsAA - intron variant - [Sequence Ontology: SO:0001627]
  • NM_020297.4:c.4512+777_4512+778delinsAA - intron variant - [Sequence Ontology: SO:0001627]
  • NM_005691.4:c.4603_4604delinsAA - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Dilated cardiomyopathy 1O (CMD1O)
Synonyms:
CARDIOMYOPATHY, DILATED, WITH VENTRICULAR TACHYCARDIA
Identifiers:
MONDO: MONDO:0012062; MedGen: C1837839; Orphanet: 154; OMIM: 608569

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV003501056Invitae
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Uncertain significance
(Jan 15, 2024) 		germlineclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
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, SCV003501056.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)

Description

This sequence change replaces alanine, which is neutral and non-polar, with asparagine, which is neutral and polar, at codon 1535 of the ABCC9 protein (p.Ala1535Asn). Information on the frequency of this variant in the gnomAD database is not available, as this variant may be reported differently in the database. This variant has not been reported in the literature in individuals affected with ABCC9-related conditions. ClinVar contains an entry for this variant (Variation ID: 1741831). An algorithm developed to predict the effect of missense changes on protein structure and function (PolyPhen-2) suggests that this variant is likely to be tolerated. 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.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Jun 23, 2024