NM_015443.4(KANSL1):c.*359_*360insAGAGGGC AND Syndromic intellectual disability

NM_015443.4(KANSL1):c.359_360insAGAGGGC AND Syndromic intellectual disability

Germline classification:: Benign (1 submission)
Last evaluated:: Jun 14, 2016
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:: RCV000352928.5

Allele description [Variation Report for NM_015443.4(KANSL1):c.359_360insAGAGGGC]

NM_015443.4(KANSL1):c.359_360insAGAGGGC

Genes:

MAPT:microtubule associated protein tau [Gene - OMIM - HGNC]
KANSL1:KAT8 regulatory NSL complex subunit 1 [Gene - OMIM - HGNC]

Variant type:

Insertion

Cytogenetic location:

17q21.31

Genomic location:

Preferred name:

NM_015443.4(KANSL1):c.*359_*360insAGAGGGC

HGVS:

NC_000017.11:g.46031120_46031121insTCTGCCC
NG_032784.1:g.199258_199259insAGAGGGC
NM_001193465.2:c.*359_*360insAGAGGGC
NM_001193466.2:c.*359_*360insAGAGGGC
NM_001379198.1:c.*359_*360insAGAGGGC
NM_015443.4:c.*359_*360insAGAGGGCMANE SELECT
NC_000017.10:g.44108486_44108487insTCTGCCC
NM_001193466.1:c.*359_*360insAGAGGGC

Links:

dbSNP: rs113448888

NCBI 1000 Genomes Browser:

rs113448888

Molecular consequence:

NM_001193465.2:c.*359_*360insAGAGGGC - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
NM_001193466.2:c.*359_*360insAGAGGGC - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
NM_001379198.1:c.*359_*360insAGAGGGC - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
NM_015443.4:c.*359_*360insAGAGGGC - 3 prime UTR variant - [Sequence Ontology: SO:0001624]

Condition(s)

Name:: Syndromic intellectual disability
Synonyms:: Intellectual disability syndrome
Identifiers:: MONDO: MONDO:0000508; MedGen: C5680525

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000403600	Illumina Laboratory Services, Illumina	criteria provided, single submitter (ICSL Variant Classification 20161018)	Benign (Jun 14, 2016)	germline	clinical testing	ICSL_Variant_Classification_20161018.pdf Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000403600

Illumina Laboratory Services, Illumina

criteria provided, single submitter

(ICSL Variant Classification 20161018)

Benign
(Jun 14, 2016)

germline

clinical testing

ICSL_Variant_Classification_20161018.pdf

Citation Link

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Illumina Laboratory Services, Illumina, SCV000403600.2

#	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	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Dec 24, 2023

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