NM_001376.5(DYNC1H1):c.92_124dup (p.Leu41_Leu42insGlnLysHisLeuArgLysLeuValProLeuLeu) AND not provided

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Dec 8, 2023
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:: RCV004768158.1

Allele description [Variation Report for NM_001376.5(DYNC1H1):c.92_124dup (p.Leu41_Leu42insGlnLysHisLeuArgLysLeuValProLeuLeu)]

NM_001376.5(DYNC1H1):c.92_124dup (p.Leu41_Leu42insGlnLysHisLeuArgLysLeuValProLeuLeu)

Gene:

DYNC1H1:dynein cytoplasmic 1 heavy chain 1 [Gene - OMIM - HGNC]

Variant type:

Duplication

Cytogenetic location:

14q32.31

Genomic location:

Preferred name:

NM_001376.5(DYNC1H1):c.92_124dup (p.Leu41_Leu42insGlnLysHisLeuArgLysLeuValProLeuLeu)

HGVS:

NC_000014.9:g.101964783_101964815dup
NG_008777.1:g.5256_5288dup
NG_130187.1:g.574_606dup
NM_001376.5:c.92_124dupMANE SELECT
NP_001367.2:p.Leu41_Leu42insGlnLysHisLeuArgLysLeuValProLeuLeu
NP_001367.2:p.Leu41_Leu42insGlnLysHisLeuArgLysLeuValProLeuLeu
NC_000014.8:g.102431120_102431152dup
NM_001376.4:c.92_124dup

Molecular consequence:

NM_001376.5:c.92_124dup - inframe insertion - [Sequence Ontology: SO:0001821]

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
SCV005376024	GeneDx	criteria provided, single submitter (GeneDx Variant Classification Process June 2021)	Uncertain significance (Dec 8, 2023)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV005376024

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)

Uncertain significance
(Dec 8, 2023)

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, SCV005376024.1

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

Description

Not observed at significant frequency in large population cohorts (gnomAD); In-frame duplication of 11 amino acids in a non-repeat region; Has not been previously published as pathogenic or benign to our knowledge

#	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: Oct 26, 2024

ClinVar

Relating variation to medicine