NM_000051.4(ATM):c.2610C>T (p.Asn870=) AND not specified

Germline classification:: Likely benign (2 submissions)
Last evaluated:: Aug 20, 2019
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:: RCV000586240.4

Allele description [Variation Report for NM_000051.4(ATM):c.2610C>T (p.Asn870=)]

NM_000051.4(ATM):c.2610C>T (p.Asn870=)

Gene:

ATM:ATM serine/threonine kinase [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11q22.3

Genomic location:

Preferred name:

NM_000051.4(ATM):c.2610C>T (p.Asn870=)

HGVS:

NC_000011.10:g.108267314C>T
NG_009830.1:g.49483C>T
NM_000051.4:c.2610C>TMANE SELECT
NM_001351834.2:c.2610C>T
NP_000042.3:p.Asn870=
NP_000042.3:p.Asn870=
NP_001338763.1:p.Asn870=
LRG_135t1:c.2610C>T
LRG_135:g.49483C>T
LRG_135p1:p.Asn870=
NC_000011.9:g.108138041C>T
NM_000051.3:c.2610C>T
p.N870N

Links:

dbSNP: rs587780618

NCBI 1000 Genomes Browser:

rs587780618

Molecular consequence:

NM_000051.4:c.2610C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001351834.2:c.2610C>T - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000694232	Women's Health and Genetics/Laboratory Corporation of America, LabCorp	criteria provided, single submitter (LabCorp Variant Classification Summary - May 2015)	Likely benign (Aug 20, 2019)	germline	clinical testing	Citation Link,
SCV003840059	Genetic Services Laboratory, University of Chicago	no assertion criteria provided	Likely benign (Jun 6, 2022)	germline	clinical testing

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000694232

Women's Health and Genetics/Laboratory Corporation of America, LabCorp

criteria provided, single submitter

(LabCorp Variant Classification Summary - May 2015)

Likely benign
(Aug 20, 2019)

germline

clinical testing

Citation Link,

SCV003840059

Genetic Services Laboratory, University of Chicago

no assertion criteria provided

Likely benign
(Jun 6, 2022)

germline

clinical testing

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	no	not provided	not provided	not provided	not provided	not provided	clinical testing
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Women's Health and Genetics/Laboratory Corporation of America, LabCorp, SCV000694232.2

#	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	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

From Genetic Services Laboratory, University of Chicago, SCV003840059.1

#	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	no	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Nov 3, 2024

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