NM_001134363.3(RBM20):c.2072C>T (p.Ala691Val) AND Cardiovascular phenotype

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Dec 19, 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:: RCV003167075.2

Allele description [Variation Report for NM_001134363.3(RBM20):c.2072C>T (p.Ala691Val)]

NM_001134363.3(RBM20):c.2072C>T (p.Ala691Val)

Gene:

RBM20:RNA binding motif protein 20 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

10q25.2

Genomic location:

Preferred name:

NM_001134363.3(RBM20):c.2072C>T (p.Ala691Val)

HGVS:

NC_000010.11:g.110812469C>T
NG_021177.1:g.173073C>T
NM_001134363.1:c.2072C>T
NM_001134363.3:c.2072C>TMANE SELECT
NP_001127835.2:p.Ala691Val
LRG_382t1:c.2072C>T
LRG_382:g.173073C>T
NC_000010.10:g.112572227C>T

Protein change:

A691V

Links:

dbSNP: rs1293517489

NCBI 1000 Genomes Browser:

rs1293517489

Molecular consequence:

NM_001134363.3:c.2072C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Cardiovascular phenotype
Identifiers:: MedGen: CN230736

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control protein E1B 55K [Human mastadenovirus C]
control protein E1B 55K [Human mastadenovirus C]
gi|9626164|ref|NP_040511.1|

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003856971	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Dec 19, 2022)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003856971

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Dec 19, 2022)

germline

clinical testing

Citation Link

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Summary from all submissions

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

Details of each submission

From Ambry Genetics, SCV003856971.2

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

Description

The p.A691V variant (also known as c.2072C>T), located in coding exon 9 of the RBM20 gene, results from a C to T substitution at nucleotide position 2072. The alanine at codon 691 is replaced by valine, an amino acid with similar properties. This amino acid position is conserved. In addition, this alteration is predicted to be tolerated by in silico analysis. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.

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

Last Updated: Sep 29, 2024

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