NM_001018005.2(TPM1):c.*76A>G AND not provided

This record was updated by the submitter. Please see the current version.

Germline classification:: Benign (3 submissions)
Last evaluated:: Mar 3, 2015
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:: RCV001660654.4

Allele description

NM_001018005.2(TPM1):c.*76A>G

Gene:

TPM1:tropomyosin 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

15q22.2

Genomic location:

Preferred name:

NM_001018005.2(TPM1):c.*76A>G

HGVS:

NC_000015.10:g.63065975A>G
NG_007557.1:g.28337A>G
NM_000366.6:c.*124A>G
NM_001018004.2:c.772+3330A>G
NM_001018005.2:c.*76A>GMANE SELECT
NM_001018006.2:c.772+3330A>G
NM_001018007.2:c.772+3330A>G
NM_001018008.2:c.664+3330A>G
NM_001018020.2:c.772+3330A>G
NM_001301244.2:c.*76A>G
NM_001301289.2:c.664+3330A>G
NM_001330344.2:c.664+3330A>G
NM_001330346.2:c.*76A>G
NM_001330351.2:c.664+3330A>G
NM_001365776.1:c.772+3330A>G
NM_001365777.1:c.852A>G
NM_001365778.1:c.898+3330A>G
NM_001365779.1:c.*124A>G
NM_001365780.1:c.744A>G
NM_001365781.2:c.*1829A>G
NM_001365782.1:c.*1829A>G
NP_001352706.1:p.Leu284=
NP_001352709.1:p.Leu248=
LRG_387t1:c.*76A>G
LRG_387:g.28337A>G
NC_000015.9:g.63358174A>G
NM_001018005.1:c.*76A>G

Links:

dbSNP: rs140658011

NCBI 1000 Genomes Browser:

rs140658011

Molecular consequence:

NM_000366.6:c.*124A>G - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
NM_001018005.2:c.*76A>G - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
NM_001301244.2:c.*76A>G - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
NM_001330346.2:c.*76A>G - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
NM_001365779.1:c.*124A>G - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
NM_001365781.2:c.*1829A>G - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
NM_001365782.1:c.*1829A>G - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
NM_001018004.2:c.772+3330A>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001018006.2:c.772+3330A>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001018007.2:c.772+3330A>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001018008.2:c.664+3330A>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001018020.2:c.772+3330A>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001301289.2:c.664+3330A>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001330344.2:c.664+3330A>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001330351.2:c.664+3330A>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001365776.1:c.772+3330A>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001365778.1:c.898+3330A>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001365777.1:c.852A>G - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001365780.1:c.744A>G - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

Help

Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001881888	GeneDx	criteria provided, single submitter (GeneDx Variant Classification Process June 2021)	Benign (Mar 3, 2015)	germline	clinical testing	Citation Link,
SCV001977962	Genome Diagnostics Laboratory, University Medical Center Utrecht - VKGL Data-share Consensus See additional submitters Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen	no assertion criteria provided	Likely benign	germline	clinical testing
SCV001979439	Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ - VKGL Data-share Consensus See additional submitters Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen	no assertion criteria provided	Likely benign	germline	clinical testing

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001881888

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)

Benign
(Mar 3, 2015)

germline

clinical testing

Citation Link,

SCV001977962

Genome Diagnostics Laboratory, University Medical Center Utrecht - VKGL Data-share Consensus

See additional submitters

no assertion criteria provided

Likely benign

germline

clinical testing

SCV001979439

Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ - VKGL Data-share Consensus

See additional submitters

no assertion criteria provided

Likely benign

germline

clinical testing

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

Details of each submission

From GeneDx, SCV001881888.1

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

From Genome Diagnostics Laboratory, University Medical Center Utrecht - VKGL Data-share Consensus, SCV001977962.1

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

From Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ - VKGL Data-share Consensus, SCV001979439.1

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

Last Updated: Dec 24, 2023

ClinVar

Relating variation to medicine