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NM_002428.4(MMP15):c.877G>A (p.Glu293Lys) AND not specified

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Oct 29, 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:
RCV004235991.1

Allele description [Variation Report for NM_002428.4(MMP15):c.877G>A (p.Glu293Lys)]

NM_002428.4(MMP15):c.877G>A (p.Glu293Lys)

Gene:
MMP15:matrix metallopeptidase 15 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
16q21
Genomic location:
Preferred name:
NM_002428.4(MMP15):c.877G>A (p.Glu293Lys)
HGVS:
  • NC_000016.10:g.58040665G>A
  • NM_002428.4:c.877G>AMANE SELECT
  • NP_002419.1:p.Glu293Lys
  • NC_000016.9:g.58074569G>A
  • NM_002428.2:c.877G>A
Protein change:
E293K
Molecular consequence:
  • NM_002428.4:c.877G>A - 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
SCV003749692Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Uncertain significance
(Oct 29, 2021) 		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, SCV003749692.2

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

Description

The c.877G>A (p.E293K) alteration is located in exon 5 (coding exon 5) of the MMP15 gene. This alteration results from a G to A substitution at nucleotide position 877, causing the glutamic acid (E) at amino acid position 293 to be replaced by a lysine (K). 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 10, 2024