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NM_002834.5(PTPN11):c.923A>C (p.Asn308Thr) AND See cases

Germline classification:
Pathogenic (1 submission)
Last evaluated:
Dec 20, 2021
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:
RCV002287350.1

Allele description [Variation Report for NM_002834.5(PTPN11):c.923A>C (p.Asn308Thr)]

NM_002834.5(PTPN11):c.923A>C (p.Asn308Thr)

Gene:
PTPN11:protein tyrosine phosphatase non-receptor type 11 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
12q24.13
Genomic location:
Preferred name:
NM_002834.5(PTPN11):c.923A>C (p.Asn308Thr)
Other names:
p.N308T:AAT>ACT
HGVS:
  • NC_000012.12:g.112477720A>C
  • NG_007459.1:g.63989A>C
  • NM_001330437.2:c.923A>C
  • NM_001374625.1:c.920A>C
  • NM_002834.5:c.923A>CMANE SELECT
  • NM_080601.3:c.923A>C
  • NP_001317366.1:p.Asn308Thr
  • NP_001361554.1:p.Asn307Thr
  • NP_002825.3:p.Asn308Thr
  • NP_542168.1:p.Asn308Thr
  • LRG_614t1:c.923A>C
  • LRG_614:g.63989A>C
  • NC_000012.11:g.112915524A>C
  • NM_002834.3:c.923A>C
  • NM_002834.4:c.923A>C
  • NM_080601.1:c.923A>C
  • c.923A>C
Protein change:
N307T
Links:
dbSNP: rs121918455
NCBI 1000 Genomes Browser:
rs121918455
Molecular consequence:
  • NM_001330437.2:c.923A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001374625.1:c.920A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_002834.5:c.923A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_080601.3:c.923A>C - missense variant - [Sequence Ontology: SO:0001583]
Observations:
1

Condition(s)

Name:
See cases [See the Variation display for details]
Identifiers:

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV002577919Institute of Human Genetics, University Hospital Muenster
criteria provided, single submitter

(ACMG Guidelines, 2015)		Pathogenic
(Dec 20, 2021) 		unknownclinical testing

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedunknownyes1not providednot providednot providednot providedclinical testing

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]
PMID:
25741868
PMCID:
PMC4544753

Details of each submission

From Institute of Human Genetics, University Hospital Muenster, SCV002577919.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testing PubMed (1)

Description

ACMG categories: PS1,PM2,PM7,PP3,PP5

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownyesnot providedbloodnot provided1not providednot providednot provided

Last Updated: Nov 3, 2024