NM_033547.4(INTS4):c.2692C>T (p.Leu898Phe) AND not specified

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: May 2, 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:: RCV004630865.1

Allele description [Variation Report for NM_033547.4(INTS4):c.2692C>T (p.Leu898Phe)]

NM_033547.4(INTS4):c.2692C>T (p.Leu898Phe)

Genes:

AAMDC:adipogenesis associated Mth938 domain containing [Gene - OMIM - HGNC]
INTS4:integrator complex subunit 4 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11q14.1

Genomic location:

Preferred name:

NM_033547.4(INTS4):c.2692C>T (p.Leu898Phe)

HGVS:

NC_000011.10:g.77883853G>A
NM_001316957.3:c.328+6804G>A
NM_001316958.3:c.383+5097G>A
NM_001392034.1:c.383+5097G>A
NM_001392068.1:c.228+14036G>A
NM_033547.4:c.2692C>TMANE SELECT
NP_291025.3:p.Leu898Phe
NC_000011.9:g.77594899G>A
NM_033547.3:c.2692C>T

Protein change:

L898F

Molecular consequence:

NM_001316957.3:c.328+6804G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001316958.3:c.383+5097G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001392034.1:c.383+5097G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001392068.1:c.228+14036G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_033547.4:c.2692C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

Recent activity

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Sequence 5 from Patent EP1988166
Sequence 5 from Patent EP1988166
gi|218055971|emb|GM869032.1||pat|EP 166|5

Nucleotide

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV005129245	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (May 2, 2024)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV005129245

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(May 2, 2024)

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	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Ambry Genetics, SCV005129245.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not provided

Description

The c.2692C>T (p.L898F) alteration is located in exon 22 (coding exon 22) of the INTS4 gene. This alteration results from a C to T substitution at nucleotide position 2692, causing the leucine (L) at amino acid position 898 to be replaced by a phenylalanine (F). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

#	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: Nov 10, 2024

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