NM_000083.3(CLCN1):c.921_932del (p.Ala308_Phe311del) AND not provided

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jun 14, 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:: RCV003144304.3

Allele description [Variation Report for NM_000083.3(CLCN1):c.921_932del (p.Ala308_Phe311del)]

NM_000083.3(CLCN1):c.921_932del (p.Ala308_Phe311del)

Gene:

CLCN1:chloride voltage-gated channel 1 [Gene - OMIM - HGNC]

Variant type:

Deletion

Cytogenetic location:

7q34

Genomic location:

Preferred name:

NM_000083.3(CLCN1):c.921_932del (p.Ala308_Phe311del)

HGVS:

NC_000007.14:g.143330839_143330850del
NG_009815.2:g.19714_19725del
NM_000083.3:c.921_932delMANE SELECT
NP_000074.3:p.Ala308_Phe311del
NC_000007.13:g.143027930_143027941del
NC_000007.13:g.143027932_143027943del
NG_009815.1:g.19714_19725del
NM_000083.2:c.921_932delTGCAGCCACGTT
NR_046453.2:n.1026_1037del

Links:

dbSNP: rs766116662

NCBI 1000 Genomes Browser:

rs766116662

Molecular consequence:

NM_000083.3:c.921_932del - inframe_deletion - [Sequence Ontology: SO:0001822]
NR_046453.2:n.1026_1037del - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

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next to BRCA1 gene 1 protein isoform X2 [Homo sapiens]
next to BRCA1 gene 1 protein isoform X2 [Homo sapiens]
gi|2462555262|ref|XP_054172092.1|

Protein
next to BRCA1 gene 1 protein isoform a [Homo sapiens]
next to BRCA1 gene 1 protein isoform a [Homo sapiens]
gi|14110375|ref|NP_005890.2|

Protein

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003830727	Revvity Omics, Revvity	criteria provided, single submitter (ACMG Guidelines, 2015)	Uncertain significance (Jun 14, 2022)	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

SCV003830727

Revvity Omics, Revvity

criteria provided, single submitter

(ACMG Guidelines, 2015)

Uncertain significance
(Jun 14, 2022)

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	unknown	not provided	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 Revvity Omics, Revvity, SCV003830727.2

#	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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