NM_000124.4(ERCC6):c.1659G>T (p.Lys553Asn) AND not specified

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jul 29, 2013
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:: RCV000170369.11

Allele description [Variation Report for NM_000124.4(ERCC6):c.1659G>T (p.Lys553Asn)]

NM_000124.4(ERCC6):c.1659G>T (p.Lys553Asn)

Gene:

ERCC6:ERCC excision repair 6, chromatin remodeling factor [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

10q11.23

Genomic location:

Preferred name:

NM_000124.4(ERCC6):c.1659G>T (p.Lys553Asn)

HGVS:

NC_000010.11:g.49500564C>A
NG_009442.1:g.43538G>T
NM_000124.4:c.1659G>TMANE SELECT
NM_001346440.2:c.1659G>T
NP_000115.1:p.Lys553Asn
NP_001333369.1:p.Lys553Asn
LRG_465t1:c.1659G>T
LRG_465:g.43538G>T
NC_000010.10:g.50708610C>A
NM_000124.2:c.1659G>T
NM_000124.3:c.1659G>T

Protein change:

K553N

Links:

dbSNP: rs116373975

NCBI 1000 Genomes Browser:

rs116373975

Molecular consequence:

NM_000124.4:c.1659G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001346440.2:c.1659G>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

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
SCV000222784	Claritas Genomics	criteria provided, single submitter (ACMG Guidelines, 2007)	Uncertain significance (Jul 29, 2013)	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

SCV000222784

Claritas Genomics

criteria provided, single submitter

(ACMG Guidelines, 2007)

Uncertain significance
(Jul 29, 2013)

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	not provided	not provided	not provided	not provided	not provided	not provided	clinical testing

Citations

PubMed

ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007.

Richards CS, Bale S, Bellissimo DB, Das S, Grody WW, Hegde MR, Lyon E, Ward BE; Molecular Subcommittee of the ACMG Laboratory Quality Assurance Committee.

Genet Med. 2008 Apr;10(4):294-300. doi: 10.1097/GIM.0b013e31816b5cae.

PubMed [citation]

PMID:: 18414213

Details of each submission

From Claritas Genomics, SCV000222784.1

#	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	not provided	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Nov 24, 2024

ClinVar

Relating variation to medicine