U.S. flag

An official website of the United States government

NM_001348716.2(KDM6B):c.753ACC[16] (p.Pro262_Pro264dup) AND not provided

Germline classification:
Benign (2 submissions)
Last evaluated:
Feb 17, 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:
RCV001573304.3

Allele description [Variation Report for NM_001348716.2(KDM6B):c.753ACC[16] (p.Pro262_Pro264dup)]

NM_001348716.2(KDM6B):c.753ACC[16] (p.Pro262_Pro264dup)

Gene:
KDM6B:lysine demethylase 6B [Gene - OMIM - HGNC]
Variant type:
Microsatellite
Cytogenetic location:
17p13.1
Genomic location:
Preferred name:
NM_001348716.2(KDM6B):c.753ACC[16] (p.Pro262_Pro264dup)
HGVS:
  • NC_000017.11:g.7846860ACC[16]
  • NG_053032.1:g.17661ACC[16]
  • NM_001080424.2:c.753ACC[16]
  • NM_001348716.2:c.753ACC[16]MANE SELECT
  • NP_001073893.1:p.Pro262_Pro264dup
  • NP_001335645.1:p.Pro262_Pro264dup
  • NC_000017.10:g.7750178ACC[16]
  • NM_001080424.1:c.783_791dup
  • NM_001080424.1:c.783_791dup9
Links:
dbSNP: rs61462443
NCBI 1000 Genomes Browser:
rs61462443
Molecular consequence:
  • NM_001080424.2:c.753ACC[16] - inframe_insertion - [Sequence Ontology: SO:0001821]
  • NM_001348716.2:c.753ACC[16] - inframe_insertion - [Sequence Ontology: SO:0001821]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV001798968Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) - VKGL Data-share Consensus
no assertion criteria provided
Likely benigngermlineclinical testing

SCV001862861GeneDx
criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)
Benign
(Feb 17, 2021)
germlineclinical testing

Citation Link

Summary from all submissions

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

Details of each submission

From Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) - VKGL Data-share Consensus, SCV001798968.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot providednot providednot providednot providednot provided

From GeneDx, SCV001862861.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Oct 13, 2024