NM_002388.6(MCM3):c.540G>C (p.Glu180Asp) AND not specified

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Nov 21, 2022
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:: RCV004176517.1

Allele description [Variation Report for NM_002388.6(MCM3):c.540G>C (p.Glu180Asp)]

NM_002388.6(MCM3):c.540G>C (p.Glu180Asp)

Gene:

MCM3:minichromosome maintenance complex component 3 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

6p12.2

Genomic location:

Preferred name:

NM_002388.6(MCM3):c.540G>C (p.Glu180Asp)

HGVS:

NC_000006.12:g.52279591C>G
NM_001270472.3:c.402G>C
NM_001366369.2:c.540G>C
NM_001366370.2:c.540G>C
NM_001366371.2:c.532-43G>C
NM_001366372.2:c.532-43G>C
NM_001366373.2:c.21G>C
NM_001366374.2:c.-70G>C
NM_001366375.2:c.531+2454G>C
NM_002388.6:c.540G>CMANE SELECT
NP_001257401.2:p.Glu134Asp
NP_001353298.1:p.Glu180Asp
NP_001353299.1:p.Glu180Asp
NP_001353302.1:p.Glu7Asp
NP_002379.4:p.Glu180Asp
NC_000006.11:g.52144389C>G
NM_002388.3:c.540G>C
NR_158963.2:n.495G>C
NR_158964.2:n.608G>C
NR_158965.2:n.608G>C
NR_158966.2:n.608G>C

Protein change:

E134D

Molecular consequence:

NM_001366374.2:c.-70G>C - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001366371.2:c.532-43G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001366372.2:c.532-43G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001366375.2:c.531+2454G>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001270472.3:c.402G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001366369.2:c.540G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001366370.2:c.540G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001366373.2:c.21G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_002388.6:c.540G>C - missense variant - [Sequence Ontology: SO:0001583]
NR_158963.2:n.495G>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_158964.2:n.608G>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_158965.2:n.608G>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_158966.2:n.608G>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

Recent activity

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cytochrome oxidase subunit 1, partial (mitochondrion) [Leptotila verreauxi]
cytochrome oxidase subunit 1, partial (mitochondrion) [Leptotila verreauxi]
gi|197255740|gb|ACH55012.1|

Protein

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003665072	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Nov 21, 2022)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003665072

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Nov 21, 2022)

germline

clinical testing

Citation Link

Help

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, SCV003665072.2

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

Description

The c.540G>C (p.E180D) alteration is located in exon 5 (coding exon 5) of the MCM3 gene. This alteration results from a G to C substitution at nucleotide position 540, causing the glutamic acid (E) at amino acid position 180 to be replaced by an aspartic acid (D). 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: Nov 10, 2024

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