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NM_001134363.3(RBM20):c.2070G>A (p.Pro690=) AND not specified

Germline classification:
Likely benign (1 submission)
Last evaluated:
Jan 12, 2018
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:
RCV000606061.4

Allele description [Variation Report for NM_001134363.3(RBM20):c.2070G>A (p.Pro690=)]

NM_001134363.3(RBM20):c.2070G>A (p.Pro690=)

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.2070G>A (p.Pro690=)
HGVS:
  • NC_000010.11:g.110812467G>A
  • NG_021177.1:g.173071G>A
  • NM_001134363.3:c.2070G>AMANE SELECT
  • NP_001127835.2:p.Pro690=
  • LRG_382t1:c.2070G>A
  • LRG_382:g.173071G>A
  • NC_000010.10:g.112572225G>A
  • NM_001134363.1:c.2070G>A
  • p.Pro690Pro
Links:
dbSNP: rs890520365
NCBI 1000 Genomes Browser:
rs890520365
Molecular consequence:
  • NM_001134363.3:c.2070G>A - synonymous variant - [Sequence Ontology: SO:0001819]
Observations:
1

Condition(s)

Synonyms:
AllHighlyPenetrant
Identifiers:
MedGen: CN169374

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000713832Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine
criteria provided, single submitter

(LMM Criteria)		Likely benign
(Jan 12, 2018) 		germlineclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlinenot provided11not providednot providednot providedclinical testing

Citations

PubMed

A systematic approach to assessing the clinical significance of genetic variants.

Duzkale H, Shen J, McLaughlin H, Alfares A, Kelly MA, Pugh TJ, Funke BH, Rehm HL, Lebo MS.

Clin Genet. 2013 Nov;84(5):453-63. doi: 10.1111/cge.12257.

PubMed [citation]
PMID:
24033266
PMCID:
PMC3995020

Details of each submission

From Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine, SCV000713832.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testing PubMed (1)

Description

The p.Pro690Pro variant in RBM20 is not expected to have clinical significance b ecause it does not alter an amino acid residue and is not located within the spl ice consensus sequence. ACMG/AMP Criteria applied: PM2, BP4, BP7.

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

Last Updated: Sep 29, 2024