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NM_001374828.1(ARID1B):c.1950del (p.Ala652fs) AND not provided

Germline classification:
Pathogenic (1 submission)
Last evaluated:
Jan 13, 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:
RCV002267522.2

Allele description [Variation Report for NM_001374828.1(ARID1B):c.1950del (p.Ala652fs)]

NM_001374828.1(ARID1B):c.1950del (p.Ala652fs)

Gene:
ARID1B:AT-rich interaction domain 1B [Gene - OMIM - HGNC]
Variant type:
Deletion
Cytogenetic location:
6q25.3
Genomic location:
Preferred name:
NM_001374828.1(ARID1B):c.1950del (p.Ala652fs)
HGVS:
  • NC_000006.12:g.156829385del
  • NG_066624.1:g.58360del
  • NM_001371656.1:c.1950del
  • NM_001374820.1:c.1950del
  • NM_001374828.1:c.1950delMANE SELECT
  • NM_017519.3:c.1950del
  • NM_020732.3:c.1701del
  • NP_001358585.1:p.Ala652fs
  • NP_001361749.1:p.Ala652fs
  • NP_001361757.1:p.Ala652fs
  • NP_059989.3:p.Ala652fs
  • NC_000006.11:g.157150519del
Protein change:
A652fs
Links:
dbSNP: rs2128046981
NCBI 1000 Genomes Browser:
rs2128046981
Molecular consequence:
  • NM_001371656.1:c.1950del - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001374820.1:c.1950del - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001374828.1:c.1950del - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_017519.3:c.1950del - frameshift variant - [Sequence Ontology: SO:0001589]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV002549639GeneDx
criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)		Pathogenic
(Jan 13, 2022) 		germlineclinical testing

Citation Link

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyesnot providednot providednot providednot providednot providedclinical testing

Details of each submission

From GeneDx, SCV002549639.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

Observed in a patient with Coffin-Siris syndrome in published literature (Aref-Eshghi et al., 2018); Not observed at significant frequency in large population cohorts (gnomAD); Frameshift variant predicted to result in protein truncation or nonsense mediated decay in a gene for which loss-of-function is a known mechanism of disease; This variant is associated with the following publications: (PMID: 30459321)

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

Last Updated: Sep 1, 2024