NM_025219.3(DNAJC5):c.*1197_*1249del AND not provided

NM_025219.3(DNAJC5):c.1197_1249del AND not provided

Germline classification:: Likely benign (1 submission)
Last evaluated:: Sep 22, 2021
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:: RCV002052328.2

Allele description [Variation Report for NM_025219.3(DNAJC5):c.1197_1249del]

NM_025219.3(DNAJC5):c.1197_1249del

Gene:

DNAJC5:DnaJ heat shock protein family (Hsp40) member C5 [Gene - OMIM - HGNC]

Variant type:

Deletion

Cytogenetic location:

20q13.33

Genomic location:

Preferred name:

NM_025219.3(DNAJC5):c.*1197_*1249del

HGVS:

NC_000020.11:g.63932765_63932817del
NG_029805.2:g.42664_42716del
NM_025219.3:c.*1197_*1249delMANE SELECT
LRG_831t1:c.*1197_*1249del
LRG_831:g.42664_42716del
NC_000020.10:g.62564118_62564170del

Links:

dbSNP: rs1568991776

NCBI 1000 Genomes Browser:

rs1568991776

Molecular consequence:

NM_025219.3:c.*1197_*1249del - 3 prime UTR variant - [Sequence Ontology: SO:0001624]

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
SCV002319049	GeneDx	criteria provided, single submitter (GeneDx Variant Classification Process June 2021)	Likely benign (Sep 22, 2021)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV002319049

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)

Likely benign
(Sep 22, 2021)

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, SCV002319049.2

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

#	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: Dec 24, 2023

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