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NM_005188.4(CBL):c.2345C>T (p.Pro782Leu) AND not provided

Germline classification:
Benign (3 submissions)
Last evaluated:
Oct 1, 2023
Review status:
2 stars out of maximum of 4 stars
criteria provided, multiple submitters, no conflicts
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:
RCV000680286.25

Allele description [Variation Report for NM_005188.4(CBL):c.2345C>T (p.Pro782Leu)]

NM_005188.4(CBL):c.2345C>T (p.Pro782Leu)

Gene:
CBL:Cbl proto-oncogene [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
11q23.3
Genomic location:
Preferred name:
NM_005188.4(CBL):c.2345C>T (p.Pro782Leu)
Other names:
p.P782L:CCG>CTG
HGVS:
  • NC_000011.10:g.119298451C>T
  • NG_016808.1:g.97172C>T
  • NM_005188.4:c.2345C>TMANE SELECT
  • NP_005179.2:p.Pro782Leu
  • NP_005179.2:p.Pro782Leu
  • LRG_608t1:c.2345C>T
  • LRG_608:g.97172C>T
  • LRG_608p1:p.Pro782Leu
  • NC_000011.9:g.119169161C>T
  • NM_005188.2:c.2345C>T
  • NM_005188.3:c.2345C>T
  • P22681:p.Pro782Leu
  • c.2345C>T
Protein change:
P782L
Links:
UniProtKB: P22681#VAR_057212; dbSNP: rs2229073
NCBI 1000 Genomes Browser:
rs2229073
Molecular consequence:
  • NM_005188.4:c.2345C>T - missense variant - [Sequence Ontology: SO:0001583]
Observations:
1

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000057274GeneDx
criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)
Benign
(Mar 5, 2021)
germlineclinical testing

Citation Link,

SCV001471960ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories
criteria provided, single submitter

(ARUP Molecular Germline Variant Investigation Process)
Benign
(May 22, 2020)
germlineclinical testing

Citation Link,

SCV004129487CeGaT Center for Human Genetics Tuebingen
criteria provided, single submitter

(CeGaT Center For Human Genetics Tuebingen Variant Classification Criteria Version 2)
Benign
(Oct 1, 2023)
germlineclinical testing

Citation Link

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyes1not providednot providednot providednot providedclinical testing
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical testing

Details of each submission

From GeneDx, SCV000057274.14

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

This variant is associated with the following publications: (PMID: 27244893, 24896146, 31057598, 32604168)

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot providednot providednot providednot providednot provided

From ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories, SCV001471960.1

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

From CeGaT Center for Human Genetics Tuebingen, SCV004129487.8

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testingnot provided

Description

CBL: BS1, BS2

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot provided1not providednot providednot provided

Last Updated: Sep 29, 2024