NM_015443.4(KANSL1):c.-90+500_-90+501dup AND not provided

Germline classification:: Benign (1 submission)
Last evaluated:: Sep 17, 2019
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:: RCV001680862.1

Allele description [Variation Report for NM_015443.4(KANSL1):c.-90+500_-90+501dup]

NM_015443.4(KANSL1):c.-90+500_-90+501dup

Gene:

KANSL1:KAT8 regulatory NSL complex subunit 1 [Gene - OMIM - HGNC]

Variant type:

Duplication

Cytogenetic location:

17q21.31

Genomic location:

Preferred name:

NM_015443.4(KANSL1):c.-90+500_-90+501dup

HGVS:

NC_000017.11:g.46192322_46192323dup
NG_032784.1:g.38063_38064dup
NM_001193465.2:c.-89-20091_-89-20090dup
NM_001193466.2:c.-90+96_-90+97dup
NM_001379198.1:c.-89-20091_-89-20090dup
NM_015443.4:c.-90+500_-90+501dupMANE SELECT
NC_000017.10:g.44269688_44269689dup

Links:

dbSNP: rs373582551

NCBI 1000 Genomes Browser:

rs373582551

Molecular consequence:

NM_001193465.2:c.-89-20091_-89-20090dup - intron variant - [Sequence Ontology: SO:0001627]
NM_001193466.2:c.-90+96_-90+97dup - intron variant - [Sequence Ontology: SO:0001627]
NM_001379198.1:c.-89-20091_-89-20090dup - intron variant - [Sequence Ontology: SO:0001627]
NM_015443.4:c.-90+500_-90+501dup - intron variant - [Sequence Ontology: SO:0001627]

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
SCV001895916	GeneDx	criteria provided, single submitter (GeneDx Variant Classification Process June 2021)	Benign (Sep 17, 2019)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001895916

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)

Benign
(Sep 17, 2019)

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, SCV001895916.1

#	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: Dec 24, 2023

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