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NM_002390.6(ADAM11):c.2153C>T (p.Ser718Phe) AND not specified

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
May 15, 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:
RCV004282226.1

Allele description [Variation Report for NM_002390.6(ADAM11):c.2153C>T (p.Ser718Phe)]

NM_002390.6(ADAM11):c.2153C>T (p.Ser718Phe)

Gene:
ADAM11:ADAM metallopeptidase domain 11 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
17q21.31
Genomic location:
Preferred name:
NM_002390.6(ADAM11):c.2153C>T (p.Ser718Phe)
HGVS:
  • NC_000017.11:g.44778034C>T
  • NM_001318933.2:c.1553C>T
  • NM_002390.6:c.2153C>TMANE SELECT
  • NP_001305862.1:p.Ser518Phe
  • NP_002381.2:p.Ser718Phe
  • NC_000017.10:g.42855402C>T
  • NM_002390.4:c.2153C>T
Protein change:
S518F
Molecular consequence:
  • NM_001318933.2:c.1553C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_002390.6:c.2153C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:
AllHighlyPenetrant
Identifiers:
MedGen: CN169374

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Assertion and evidence details

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Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV003938807Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Uncertain significance
(May 15, 2023) 		germlineclinical testing

Citation Link

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Summary from all submissions

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

Details of each submission

From Ambry Genetics, SCV003938807.2

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

Description

The c.2153C>T (p.S718F) alteration is located in exon 24 (coding exon 24) of the ADAM11 gene. This alteration results from a C to T substitution at nucleotide position 2153, causing the serine (S) at amino acid position 718 to be replaced by a phenylalanine (F). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

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

Last Updated: Nov 3, 2024