VCV000003532.1 - ClinVar

NM_021939.4(FKBP10):c.321_353del (p.Met107_Leu117del)

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.

Pathogenic

no assertion criteria provided

Somatic

No data submitted for somatic clinical impact

Somatic

No data submitted for oncogenicity

Variant Details

Identifiers

NM_021939.4(FKBP10):c.321_353del (p.Met107_Leu117del)

Variation ID: 3532 Accession: VCV000003532.1

Type and length

Deletion, 33 bp

Location

Cytogenetic: 17q21.2 17: 41817126-41817158 (GRCh38) [ NCBI UCSC ] 17: 39973378-39973410 (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	Oct 11, 2015	Oct 11, 2015	Apr 9, 2010

HGVS

Nucleotide	Protein	Molecular consequence
NM_021939.4:c.321_353del MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.	NP_068758.3:p.Met107_Leu117del	inframe deletion
NC_000017.11:g.41817133_41817165del
NC_000017.10:g.39973385_39973417del
NG_015860.1:g.9424_9456del
LRG_12:g.9424_9456del
LRG_12t1:c.321_353del33	LRG_12p1:p.Met107_Leu117del

... more HGVS ... less HGVS

Protein change

Other names

Canonical SPDI

NC_000017.11:41817125:GCCTCATGGGCATGTGTGTCAACGAGCGGCGACGCCTCAT:GCCTCAT

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

LOVD 3: FKBP10_000001 OMIM: 607063.0001 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.
FKBP10		-	-	GRCh38 GRCh37	598	606

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.
Osteogenesis imperfecta type 12	Pathogenic (1)	no assertion criteria provided	Apr 9, 2010	RCV000003710.4

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.
Pathogenic (Apr 09, 2010)	no assertion criteria provided Method: literature only	OSTEOGENESIS IMPERFECTA, TYPE XI Affected status: not provided Allele origin: germline	OMIM Accession: SCV000023873.4 First in ClinVar: Apr 04, 2013 Last updated: Oct 11, 2015	Publications: PubMed (1) PubMed: 20362275 Comment on evidence: In all affected members of 5 consanguineous Turkish families with OI type XI (OI11; 610698), Alanay et al. (2010) identified homozygosity for an in-frame deletion … (more) In all affected members of 5 consanguineous Turkish families with OI type XI (OI11; 610698), Alanay et al. (2010) identified homozygosity for an in-frame deletion in FKBP10 (321_353del), predicted to result in deletion of 11 amino acids (met107_leu117del). RT-PCR products derived from fibroblasts of 1 affected individual showed that this mutation leads to synthesis of FKBP65 mRNA containing the deletion. (less)

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.

Citations for germline classification of this variant

Title	Author	Journal	Year	Link
Mutations in the gene encoding the RER protein FKBP65 cause autosomal-recessive osteogenesis imperfecta.	Alanay Y	American journal of human genetics	2010	PMID: 20362275

Text-mined citations for this variant ...

Record last updated Apr 06, 2024

ClinVar Genomic variation as it relates to human health

NM_021939.4(FKBP10):c.321_353del (p.Met107_Leu117del)

Variant Details

Genes

Conditions - Germline

Submissions - Germline

Germline Functional Evidence

Citations for germline classification of this variant

Text-mined citations for this variant ...