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NM_001376342.1(ZC3H11A):c.798C>A (p.Leu266=) AND not provided

Germline classification:
Likely benign (1 submission)
Last evaluated:
Jan 1, 2024
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:
RCV003885883.9

Allele description [Variation Report for NM_001376342.1(ZC3H11A):c.798C>A (p.Leu266=)]

NM_001376342.1(ZC3H11A):c.798C>A (p.Leu266=)

Genes:
ZBED6:zinc finger BED-type containing 6 [Gene - OMIM - HGNC]
ZC3H11A:zinc finger CCCH-type containing 11A [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
1q32.1
Genomic location:
Preferred name:
NM_001376342.1(ZC3H11A):c.798C>A (p.Leu266=)
HGVS:
  • NC_000001.11:g.203831758C>A
  • NM_001319238.2:c.798C>A
  • NM_001319239.2:c.798C>A
  • NM_001350261.2:c.798C>A
  • NM_001350262.2:c.798C>A
  • NM_001350263.2:c.798C>A
  • NM_001350264.2:c.798C>A
  • NM_001350265.2:c.798C>A
  • NM_001350266.2:c.798C>A
  • NM_001376334.1:c.798C>A
  • NM_001376335.1:c.798C>A
  • NM_001376336.1:c.798C>A
  • NM_001376337.1:c.798C>A
  • NM_001376338.1:c.798C>A
  • NM_001376339.1:c.798C>A
  • NM_001376340.1:c.798C>A
  • NM_001376341.1:c.798C>A
  • NM_001376342.1:c.798C>AMANE SELECT
  • NM_001376343.1:c.798C>A
  • NM_001376344.1:c.798C>A
  • NM_001376345.1:c.798C>A
  • NM_001376346.1:c.798C>A
  • NM_001376347.1:c.798C>A
  • NM_001376348.1:c.798C>A
  • NM_001376349.1:c.798C>A
  • NM_001376350.1:c.798C>A
  • NM_001376351.1:c.798C>A
  • NM_001376352.1:c.798C>A
  • NM_001376353.1:c.798C>A
  • NM_001376354.1:c.798C>A
  • NM_001376355.1:c.798C>A
  • NM_001376356.1:c.798C>A
  • NM_001376357.1:c.798C>A
  • NM_001376358.1:c.798C>A
  • NM_001376359.1:c.798C>A
  • NM_001376360.1:c.798C>A
  • NM_001376361.1:c.798C>A
  • NM_001376362.1:c.798C>A
  • NM_001376363.1:c.798C>A
  • NM_001376364.1:c.798C>A
  • NM_001376365.1:c.798C>A
  • NM_001376366.1:c.798C>A
  • NM_001376367.1:c.798C>A
  • NM_001395895.1:c.*3497C>AMANE SELECT
  • NM_014827.6:c.798C>A
  • NP_001306167.1:p.Leu266=
  • NP_001306168.1:p.Leu266=
  • NP_001337190.1:p.Leu266=
  • NP_001337191.1:p.Leu266=
  • NP_001337192.1:p.Leu266=
  • NP_001337193.1:p.Leu266=
  • NP_001337194.1:p.Leu266=
  • NP_001337195.1:p.Leu266=
  • NP_001363263.1:p.Leu266=
  • NP_001363264.1:p.Leu266=
  • NP_001363265.1:p.Leu266=
  • NP_001363266.1:p.Leu266=
  • NP_001363267.1:p.Leu266=
  • NP_001363268.1:p.Leu266=
  • NP_001363269.1:p.Leu266=
  • NP_001363270.1:p.Leu266=
  • NP_001363271.1:p.Leu266=
  • NP_001363272.1:p.Leu266=
  • NP_001363273.1:p.Leu266=
  • NP_001363274.1:p.Leu266=
  • NP_001363275.1:p.Leu266=
  • NP_001363276.1:p.Leu266=
  • NP_001363277.1:p.Leu266=
  • NP_001363278.1:p.Leu266=
  • NP_001363279.1:p.Leu266=
  • NP_001363280.1:p.Leu266=
  • NP_001363281.1:p.Leu266=
  • NP_001363282.1:p.Leu266=
  • NP_001363283.1:p.Leu266=
  • NP_001363284.1:p.Leu266=
  • NP_001363285.1:p.Leu266=
  • NP_001363286.1:p.Leu266=
  • NP_001363287.1:p.Leu266=
  • NP_001363288.1:p.Leu266=
  • NP_001363289.1:p.Leu266=
  • NP_001363290.1:p.Leu266=
  • NP_001363291.1:p.Leu266=
  • NP_001363292.1:p.Leu266=
  • NP_001363293.1:p.Leu266=
  • NP_001363294.1:p.Leu266=
  • NP_001363295.1:p.Leu266=
  • NP_001363296.1:p.Leu266=
  • NP_055642.3:p.Leu266=
  • NC_000001.10:g.203800886C>A
Molecular consequence:
  • NM_001395895.1:c.*3497C>A - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001319238.2:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001319239.2:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001350261.2:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001350262.2:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001350263.2:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001350264.2:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001350265.2:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001350266.2:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001376334.1:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001376335.1:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001376336.1:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001376337.1:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001376338.1:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001376339.1:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001376340.1:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001376341.1:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001376342.1:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001376343.1:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001376344.1:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001376345.1:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001376346.1:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001376347.1:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001376348.1:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001376349.1:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001376350.1:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001376351.1:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001376352.1:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001376353.1:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001376354.1:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001376355.1:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001376356.1:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001376357.1:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001376358.1:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001376359.1:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001376360.1:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001376361.1:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001376362.1:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001376363.1:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001376364.1:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001376365.1:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001376366.1:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001376367.1:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_014827.6:c.798C>A - synonymous variant - [Sequence Ontology: SO:0001819]
Observations:
1

Condition(s)

Synonyms:
none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV004701447CeGaT Center for Human Genetics Tuebingen
criteria provided, single submitter

(CeGaT Center For Human Genetics Tuebingen Variant Classification Criteria Version 2)		Likely benign
(Jan 1, 2024) 		germlineclinical testing

Citation Link

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyes1not providednot providednot providednot providedclinical testing

Details of each submission

From CeGaT Center for Human Genetics Tuebingen, SCV004701447.9

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testingnot provided

Description

ZC3H11A: BP4, BP7, BS2

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

Last Updated: Dec 22, 2024