VCV001726436.2 - ClinVar

NM_001130987.2(DYSF):c.5255del (p.Ala1752fs)

Germline

Classification

The aggregate germline classification for this variant, typically for a monogenic or Mendelian disorder as in the ACMG/AMP guidelines, or for response to a drug. This value is calculated by NCBI based on data from submitters. Read our rules for calculating the aggregate classification.

(1)

Stars represent the aggregate review status, or the level of review supporting the aggregate germline classification for this VCV record. This value is calculated by NCBI based on data from submitters. Read our rules for calculating the review status. The number of submissions which contribute to this review status is shown in parentheses.

Likely pathogenic

criteria provided, single submitter

Somatic

No data submitted for somatic clinical impact

Somatic

No data submitted for oncogenicity

Variant Details

Identifiers

NM_001130987.2(DYSF):c.5255del (p.Ala1752fs)

Variation ID: 1726436 Accession: VCV001726436.2

Type and length

Deletion, 1 bp

Location

Cytogenetic: 2p13.2 2: 71665242 (GRCh38) [ NCBI UCSC ] 2: 71892372 (GRCh37) [ NCBI UCSC ]

Timeline in ClinVar

	First in ClinVar Help The date this variant first appeared in ClinVar with each type of classification.	Last submission Help The date of the most recent submission for each type of classification for this variant.	Last evaluated Help The most recent date that a submitter evaluated this variant for each type of classification.
Germline	Nov 19, 2022	Dec 24, 2022	Dec 17, 2021

HGVS

Nucleotide	Protein	Molecular consequence
NM_001130987.2:c.5255del MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.	NP_001124459.1:p.Ala1752fs	frameshift
NM_003494.4:c.5138del MANE Plus Clinical Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.	NP_003485.1:p.Ala1713fs	frameshift
NM_001130455.2:c.5141del	NP_001123927.1:p.Ala1714fs	frameshift
NM_001130976.2:c.5096del	NP_001124448.1:p.Ala1699fs	frameshift
NM_001130977.2:c.5159del	NP_001124449.1:p.Ala1720fs	frameshift
NM_001130978.2:c.5201del	NP_001124450.1:p.Ala1734fs	frameshift
NM_001130979.2:c.5231del	NP_001124451.1:p.Ala1744fs	frameshift
NM_001130980.2:c.5189del	NP_001124452.1:p.Ala1730fs	frameshift
NM_001130981.2:c.5252del	NP_001124453.1:p.Ala1751fs	frameshift
NM_001130982.2:c.5234del	NP_001124454.1:p.Ala1745fs	frameshift
NM_001130983.2:c.5204del	NP_001124455.1:p.Ala1735fs	frameshift
NM_001130984.2:c.5162del	NP_001124456.1:p.Ala1721fs	frameshift
NM_001130985.2:c.5192del	NP_001124457.1:p.Ala1731fs	frameshift
NM_001130986.2:c.5099del	NP_001124458.1:p.Ala1700fs	frameshift
NC_000002.12:g.71665242del
NC_000002.11:g.71892372del
NG_008694.1:g.216620del
LRG_845:g.216620del
LRG_845t1:c.5138del	LRG_845p1:p.Ala1713fs
LRG_845t2:c.5255del	LRG_845p2:p.Ala1752fs

... more HGVS ... less HGVS

Protein change

A1699fs, A1700fs, A1713fs, A1714fs, A1720fs, A1721fs, A1730fs, A1731fs, A1734fs, A1735fs, A1744fs, A1745fs, A1751fs, A1752fs

Other names

Canonical SPDI

NC_000002.12:71665241:C:

Functional consequence Help The effect of the variant on RNA or protein function, based on experimental evidence from submitters.

Global minor allele frequency (GMAF) Help The global minor allele frequency calculated by the 1000 Genomes Project. The minor allele at this location is indicated in parentheses and may be different from the allele represented by this VCV record.

Allele frequency Help The frequency of the allele represented by this VCV record.

Links

VarSome

Genes

Gene	OMIM	ClinGen Gene Dosage Sensitivity Curation		Variation Viewer Help Links to Variation Viewer, a genome browser to view variation data from NCBI databases.	Related variants
Gene	OMIM	HI score Help The haploinsufficiency score for the gene, curated by ClinGen’s Dosage Sensitivity Curation task team.	TS score Help The triplosensitivity score for the gene, curated by ClinGen’s Dosage Sensitivity Curation task team.		Within gene Help The number of variants in ClinVar that are contained within this gene, with a link to view the list of variants.	All Help The number of variants in ClinVar for this gene, including smaller variants within the gene and larger CNVs that overlap or fully contain the gene.
DYSF		-	-	GRCh38 GRCh37	4062	4111

Conditions - Germline

Condition Help The condition for this variant-condition (RCV) record in ClinVar.	Classification Help The aggregate germline classification for this variant-condition (RCV) record in ClinVar. The number of submissions that contribute to this aggregate classification is shown in parentheses. (# of submissions)	Review status Help The aggregate review status for this variant-condition (RCV) record in ClinVar. This value is calculated by NCBI based on data from submitters. Read our rules for calculating the review status.	Last evaluated Help The most recent date that a submitter evaluated this variant for the condition.	Variation/condition record Help The RCV accession number, with most recent version number, for the variant-condition record, with a link to the RCV web page.
Autosomal recessive limb-girdle muscular dystrophy type 2B Distal myopathy with anterior tibial onset Miyoshi muscular dystrophy 1	Likely pathogenic (1)	criteria provided, single submitter	Dec 17, 2021	RCV002310120.2

Submissions - Germline

Classification Help The submitted germline classification for each SCV record. (Last evaluated)	Review status Help Stars represent the review status, or the level of review supporting the submitted (SCV) record. This value is calculated by NCBI based on data from the submitter. Read our rules for calculating the review status. This column also includes a link to the submitter’s assertion criteria if provided, and the collection method. (Assertion criteria)	Condition Help The condition for the classification, provided by the submitter for this submitted (SCV) record. This column also includes the affected status and allele origin of individuals observed with this variant.	Submitter Help The submitting organization for this submitted (SCV) record. This column also includes the SCV accession and version number, the date this SCV first appeared in ClinVar, and the date that this SCV was last updated in ClinVar.	More information Help This column includes more information supporting the classification, including citations, the comment on classification, and detailed evidence provided as observations of the variant by the submitter.
Likely pathogenic (Dec 17, 2021)	criteria provided, single submitter (Myriad Women's Health Autosomal Recessive and X-Linked Classification Criteria (2021)) Method: clinical testing	Autosomal recessive limb-girdle muscular dystrophy type 2B Miyoshi muscular dystrophy 1 Distal myopathy with anterior tibial onset Affected status: unknown Allele origin: unknown	Myriad Genetics, Inc. Accession: SCV002604879.2 First in ClinVar: Nov 19, 2022 Last updated: Dec 24, 2022	Comment: NM_003494.3(DYSF):c.5138delC(A1713Dfs9) is expected to be pathogenic in the context of dysferlinopathy. This variant is predicted to lead to an abnormal or absent protein product due … (more) NM_003494.3(DYSF):c.5138delC(A1713Dfs9) is expected to be pathogenic in the context of dysferlinopathy. This variant is predicted to lead to an abnormal or absent protein product due to the creation of a premature termination codon in DYSF, a gene where loss-of-function variants are known to be pathogenic. Please note: this variant was assessed in the context of healthy population screening. (less)

Comment:

NM_003494.3(DYSF):c.5138delC(A1713Dfs*9) is expected to be pathogenic in the context of dysferlinopathy. This variant is predicted to lead to an abnormal or absent protein product due to the creation of a premature termination codon in DYSF, a gene where loss-of-function variants are known to be pathogenic. Please note: this variant was assessed in the context of healthy population screening.

Germline Functional Evidence

There is no functional evidence in ClinVar for this variation. If you have generated functional data for this variation, please consider submitting that data to ClinVar.

Comment:

Citations for germline classification of this variant

There are no citations for germline classification of this variant in ClinVar. If you know of citations for this variation, please consider submitting that information to ClinVar.

Text-mined citations for this variant ...

Record last updated Aug 06, 2023

ClinVar Genomic variation as it relates to human health

NM_001130987.2(DYSF):c.5255del (p.Ala1752fs)

Variant Details

Genes

Conditions - Germline

Submissions - Germline

Germline Functional Evidence

Citations for germline classification of this variant

Text-mined citations for this variant ...