NM_020297.4(ABCC9):c.4512+765C>T AND not provided

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Oct 21, 2022
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:: RCV001551013.4

Allele description [Variation Report for NM_020297.4(ABCC9):c.4512+765C>T]

NM_020297.4(ABCC9):c.4512+765C>T

Gene:

ABCC9:ATP binding cassette subfamily C member 9 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

12p12.1

Genomic location:

Preferred name:

NM_020297.4(ABCC9):c.4512+765C>T

HGVS:

NC_000012.12:g.21805233G>A
NG_012819.1:g.136462C>T
NM_001377273.1:c.4512+765C>T
NM_001377274.1:c.3645+765C>T
NM_005691.4:c.4591C>T
NM_020297.4:c.4512+765C>TMANE SELECT
NP_005682.2:p.Pro1531Ser
NP_005682.2:p.Pro1531Ser
LRG_377t2:c.4591C>T
LRG_377:g.136462C>T
NC_000012.11:g.21958167G>A
NM_005691.2:c.4591C>T
NM_005691.3:c.4591C>T

Protein change:

P1531S

Links:

dbSNP: rs142875103

NCBI 1000 Genomes Browser:

rs142875103

Molecular consequence:

NM_001377273.1:c.4512+765C>T - intron variant - [Sequence Ontology: SO:0001627]
NM_001377274.1:c.3645+765C>T - intron variant - [Sequence Ontology: SO:0001627]
NM_020297.4:c.4512+765C>T - intron variant - [Sequence Ontology: SO:0001627]
NM_005691.4:c.4591C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001771428	GeneDx	criteria provided, single submitter (GeneDx Variant Classification Process June 2021)	Uncertain significance (Oct 21, 2022)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001771428

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)

Uncertain significance
(Oct 21, 2022)

germline

clinical testing

Citation Link

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	yes	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From GeneDx, SCV001771428.3

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not provided

Description

Identified in a patient with DCM in published literature (Mazzarotto et al., 2020); In silico analysis supports that this missense variant does not alter protein structure/function; Reported using an alternate transcript of the gene; This variant is associated with the following publications: (PMID: 31983221)

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	yes	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: May 1, 2024

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