NM_004006.3(DMD):c.7455G>T (p.Trp2485Cys) AND not provided

Germline classification:: Uncertain significance (3 submissions)
Last evaluated:: Jun 3, 2021
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:: RCV000734758.10

Allele description [Variation Report for NM_004006.3(DMD):c.7455G>T (p.Trp2485Cys)]

NM_004006.3(DMD):c.7455G>T (p.Trp2485Cys)

Gene:

DMD:dystrophin [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

Xp21.1

Genomic location:

Preferred name:

NM_004006.3(DMD):c.7455G>T (p.Trp2485Cys)

HGVS:

NC_000023.11:g.31774047C>A
NG_012232.1:g.1570563G>T
NM_000109.4:c.7431G>T
NM_004006.3:c.7455G>TMANE SELECT
NM_004009.3:c.7443G>T
NM_004010.3:c.7086G>T
NM_004011.4:c.3432G>T
NM_004012.4:c.3423G>T
NM_004013.3:c.75G>T
NM_004020.4:c.75G>T
NM_004021.3:c.75G>T
NM_004022.3:c.75G>T
NM_004023.3:c.75G>T
NP_000100.3:p.Trp2477Cys
NP_003997.1:p.Trp2485Cys
NP_003997.2:p.Trp2485Cys
NP_004000.1:p.Trp2481Cys
NP_004001.1:p.Trp2362Cys
NP_004002.3:p.Trp1144Cys
NP_004003.2:p.Trp1141Cys
NP_004004.2:p.Trp25Cys
NP_004011.3:p.Trp25Cys
NP_004012.2:p.Trp25Cys
NP_004013.2:p.Trp25Cys
NP_004014.2:p.Trp25Cys
LRG_199t1:c.7455G>T
LRG_199:g.1570563G>T
LRG_199p1:p.Trp2485Cys
NC_000023.10:g.31792164C>A
NM_004006.2:c.7455G>T

Protein change:

W1141C

Links:

dbSNP: rs765207227

NCBI 1000 Genomes Browser:

rs765207227

Molecular consequence:

NM_000109.4:c.7431G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_004006.3:c.7455G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_004009.3:c.7443G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_004010.3:c.7086G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_004011.4:c.3432G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_004012.4:c.3423G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_004013.3:c.75G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_004020.4:c.75G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_004021.3:c.75G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_004022.3:c.75G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_004023.3:c.75G>T - missense variant - [Sequence Ontology: SO:0001583]

Observations:

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000862926	Eurofins Ntd Llc (ga)	criteria provided, single submitter (EGL ClinVar v180209 classification definitions)	Uncertain significance (Aug 16, 2018)	germline	clinical testing	Citation Link,
SCV000987677	Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute	criteria provided, single submitter (ACMG Guidelines, 2015)	Uncertain significance	germline	clinical testing	PubMed (1) [See all records that cite this PMID]
SCV003829495	Revvity Omics, Revvity	criteria provided, single submitter (ACMG Guidelines, 2015)	Uncertain significance (Jun 3, 2021)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000862926

Eurofins Ntd Llc (ga)

criteria provided, single submitter

(EGL ClinVar v180209 classification definitions)

Uncertain significance
(Aug 16, 2018)

germline

clinical testing

Citation Link,

SCV000987677

Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute

criteria provided, single submitter

(ACMG Guidelines, 2015)

Uncertain significance

germline

clinical testing

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

SCV003829495

Revvity Omics, Revvity

criteria provided, single submitter

(ACMG Guidelines, 2015)

Uncertain significance
(Jun 3, 2021)

germline

clinical testing

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

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	yes	not provided	not provided	not provided	not provided	not provided	clinical testing
not provided	germline	unknown	1	not provided	not provided	not provided	not provided	clinical 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 Eurofins Ntd Llc (ga), SCV000862926.1

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

#	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		1	not provided	not provided	not provided

From Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute, SCV000987677.1

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

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	yes	not provided	not provided	not provided		not provided	not provided	not provided	not provided

From Revvity Omics, Revvity, SCV003829495.2

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

#	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: Sep 29, 2024

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