NM_006035.4(CDC42BPB):c.4682C>T (p.Pro1561Leu) AND Inborn genetic diseases

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Mar 23, 2023
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:: RCV003280323.2

Allele description [Variation Report for NM_006035.4(CDC42BPB):c.4682C>T (p.Pro1561Leu)]

NM_006035.4(CDC42BPB):c.4682C>T (p.Pro1561Leu)

Gene:

CDC42BPB:CDC42 binding protein kinase beta [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

14q32.32

Genomic location:

Preferred name:

NM_006035.4(CDC42BPB):c.4682C>T (p.Pro1561Leu)

HGVS:

NC_000014.9:g.102939857G>A
NM_001411054.1:c.4604C>T
NM_006035.4:c.4682C>TMANE SELECT
NP_001397983.1:p.Pro1535Leu
NP_006026.3:p.Pro1561Leu
NC_000014.8:g.103406194G>A
NM_006035.3:c.4682C>T

Protein change:

P1535L

Molecular consequence:

NM_001411054.1:c.4604C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_006035.4:c.4682C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Inborn genetic diseases
Identifiers:: MeSH: D030342; MedGen: C0950123

Recent activity

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Metanephrops armatus NTOU:M00081 12S ribosomal RNA gene, partial sequence; mitoc...
Metanephrops armatus NTOU:M00081 12S ribosomal RNA gene, partial sequence; mitochondrial
gi|224714967|gb|FJ455534.1|

Nucleotide
Gene Links for Protein (Select 1370475075) (1)
Gene
NDUFS7 NADH:ubiquinone oxidoreductase core subunit S7 [Homo sapiens]
NDUFS7 NADH:ubiquinone oxidoreductase core subunit S7 [Homo sapiens]
Gene ID:374291

Gene

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003963299	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Mar 23, 2023)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003963299

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Mar 23, 2023)

germline

clinical testing

Citation Link

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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, SCV003963299.2

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

Description

The c.4682C>T (p.P1561L) alteration is located in exon 33 (coding exon 33) of the CDC42BPB gene. This alteration results from a C to T substitution at nucleotide position 4682, causing the proline (P) at amino acid position 1561 to be replaced by a leucine (L). 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: May 1, 2024

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