VCV002127493.2 - ClinVar

NM_001077365.2(POMT1):c.2162T>G (p.Leu721Trp)

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.

Uncertain significance

criteria provided, single submitter

Somatic

No data submitted for somatic clinical impact

Somatic

No data submitted for oncogenicity

Variant Details

Identifiers

NM_001077365.2(POMT1):c.2162T>G (p.Leu721Trp)

Variation ID: 2127493 Accession: VCV002127493.2

Type and length

single nucleotide variant, 1 bp

Location

Cytogenetic: 9q34.13 9: 131523090 (GRCh38) [ NCBI UCSC ] 9: 134398477 (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	Feb 8, 2023	Feb 28, 2024	Oct 4, 2022

HGVS

Nucleotide	Protein	Molecular consequence
NM_001077365.2:c.2162T>G MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.	NP_001070833.1:p.Leu721Trp	missense
NM_001077366.2:c.2000T>G	NP_001070834.1:p.Leu667Trp	missense
NM_001136113.2:c.2162T>G	NP_001129585.1:p.Leu721Trp	missense
NM_001136114.2:c.1811T>G	NP_001129586.1:p.Leu604Trp	missense
NM_001353193.2:c.2228T>G	NP_001340122.2:p.Leu743Trp	missense
NM_001353194.2:c.2000T>G	NP_001340123.1:p.Leu667Trp	missense
NM_001353195.2:c.1811T>G	NP_001340124.1:p.Leu604Trp	missense
NM_001353196.2:c.2072T>G	NP_001340125.1:p.Leu691Trp	missense
NM_001353197.2:c.2066T>G	NP_001340126.2:p.Leu689Trp	missense
NM_001353198.2:c.2066T>G	NP_001340127.2:p.Leu689Trp	missense
NM_001353199.2:c.1877T>G	NP_001340128.2:p.Leu626Trp	missense
NM_001353200.2:c.1706T>G	NP_001340129.1:p.Leu569Trp	missense
NM_001374689.1:c.2150T>G	NP_001361618.1:p.Leu717Trp	missense
NM_001374690.1:c.1943T>G	NP_001361619.1:p.Leu648Trp	missense
NM_001374691.1:c.1811T>G	NP_001361620.1:p.Leu604Trp	missense
NM_001374692.1:c.1811T>G	NP_001361621.1:p.Leu604Trp	missense
NM_001374693.1:c.1811T>G	NP_001361622.1:p.Leu604Trp	missense
NM_001374695.1:c.1772T>G	NP_001361624.1:p.Leu591Trp	missense
NM_001411024.1:c.1031T>G	NP_001397953.1:p.Leu344Trp	missense
NM_007171.4:c.2228T>G	NP_009102.4:p.Leu743Trp	missense
NR_148391.2:n.2196T>G		non-coding transcript variant
NR_148392.2:n.2414T>G		non-coding transcript variant
NR_148393.2:n.2335T>G		non-coding transcript variant
NR_148394.2:n.2089T>G		non-coding transcript variant
NR_148395.2:n.2487T>G		non-coding transcript variant
NR_148396.2:n.2121T>G		non-coding transcript variant
NR_148397.2:n.2246T>G		non-coding transcript variant
NR_148398.2:n.2201T>G		non-coding transcript variant
NR_148399.2:n.2727T>G		non-coding transcript variant
NR_148400.2:n.2326T>G		non-coding transcript variant
NC_000009.12:g.131523090T>G
NC_000009.11:g.134398477T>G
NG_008896.2:g.25189T>G
LRG_842:g.25189T>G
LRG_842t1:c.2228T>G	LRG_842p1:p.Leu743Trp
LRG_842t2:c.2162T>G	LRG_842p2:p.Leu721Trp

... more HGVS ... less HGVS

Protein change

L591W, L604W, L569W, L626W, L667W, L721W, L691W, L717W, L344W, L648W, L689W, L743W

Other names

Canonical SPDI

NC_000009.12:131523089:T:G

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.
POMT1		-	-	GRCh38 GRCh37	1161	1202

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 2K Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B1 Walker-Warburg congenital muscular dystrophy	Uncertain significance (1)	criteria provided, single submitter	Oct 4, 2022	RCV003047817.3

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.
Uncertain significance (Oct 04, 2022)	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015)) Method: clinical testing	Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B1 Walker-Warburg congenital muscular dystrophy Autosomal recessive limb-girdle muscular dystrophy type 2K Explanation for multiple conditions: Uncertain. The variant was classified for several related diseases, possibly a spectrum of disease; the variant may be associated with one or more the diseases. Affected status: unknown Allele origin: germline	Labcorp Genetics (formerly Invitae), Labcorp Accession: SCV003345040.2 First in ClinVar: Feb 07, 2023 Last updated: Feb 28, 2024	Comment: In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant … (more) In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Probably Damaging"; Align-GVGD: "Class C0"). This variant has not been reported in the literature in individuals affected with POMT1-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change replaces leucine, which is neutral and non-polar, with tryptophan, which is neutral and slightly polar, at codon 743 of the POMT1 protein (p.Leu743Trp). (less)

Comment:

In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Probably Damaging"; Align-GVGD: "Class C0"). This variant has not been reported in the literature in individuals affected with POMT1-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change replaces leucine, which is neutral and non-polar, with tryptophan, which is neutral and slightly polar, at codon 743 of the POMT1 protein (p.Leu743Trp).

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 Sep 29, 2024

ClinVar Genomic variation as it relates to human health

NM_001077365.2(POMT1):c.2162T>G (p.Leu721Trp)

Variant Details

Genes

Conditions - Germline

Submissions - Germline

Germline Functional Evidence

Citations for germline classification of this variant

Text-mined citations for this variant ...