NM_000531.6(OTC):c.299-8del AND not provided

Germline classification:: Likely benign (1 submission)
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

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:: RCV001699143.2

Allele description [Variation Report for NM_000531.6(OTC):c.299-8del]

NM_000531.6(OTC):c.299-8del

Gene:

OTC:ornithine transcarbamylase [Gene - OMIM - HGNC]

Variant type:

Deletion

Cytogenetic location:

Xp11.4

Genomic location:

Preferred name:

NM_000531.6(OTC):c.299-8del

HGVS:

NC_000023.11:g.38381334del
NG_008471.1:g.33852del
NM_000531.6:c.299-8delMANE SELECT
LRG_846t1:c.299-8del
LRG_846:g.33852del
NC_000023.10:g.38240578del
NC_000023.10:g.38240587del

Links:

dbSNP: rs764551624

NCBI 1000 Genomes Browser:

rs764551624

Molecular consequence:

NM_000531.6:c.299-8del - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

Recent activity

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FHF complex subunit HOOK-interacting protein 1B isoform X4 [Homo sapiens]
FHF complex subunit HOOK-interacting protein 1B isoform X4 [Homo sapiens]
gi|1370460358|ref|XP_024304478.1|

Protein
phosphatidylinositol-3-phosphate phosphatase MTMR7 [Homo sapiens]
phosphatidylinositol-3-phosphate phosphatase MTMR7 [Homo sapiens]
gi|225543474|ref|NP_004677.3|

Protein
ACTL7A actin like 7A [Homo sapiens]
ACTL7A actin like 7A [Homo sapiens]
Gene ID:10881

Gene

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001925680	Clinical Genetics, Academic Medical Center - VKGL Data-share Consensus See additional submitters Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen	no assertion criteria provided	Likely benign	germline	clinical testing

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001925680

Clinical Genetics, Academic Medical Center - VKGL Data-share Consensus

See additional submitters

no assertion criteria provided

Likely benign

germline

clinical testing

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 Clinical Genetics, Academic Medical Center - VKGL Data-share Consensus, SCV001925680.1

#	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: Sep 29, 2024

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