VCV000324076.7 - ClinVar

NM_000088.4(COL1A1):c.681_682insAGCA

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.

(4)

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.

Benign/Likely benign

criteria provided, multiple submitters, no conflicts

Somatic

No data submitted for somatic clinical impact

Somatic

No data submitted for oncogenicity

Variant Details

Identifiers

NM_000088.4(COL1A1):c.*681_*682insAGCA

Variation ID: 324076 Accession: VCV000324076.7

Type and length

Insertion, 4 bp

Location

Cytogenetic: 17q21.33 17: 50184820-50184821 (GRCh38) [ NCBI UCSC ] 17: 48262181-48262182 (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	Dec 6, 2016	Sep 19, 2021	May 10, 2021

HGVS

Nucleotide	Protein	Molecular consequence
NM_000088.4:c.681_682insAGCA MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.		3 prime UTR
NC_000017.11:g.50184822_50184823insCTTG
NC_000017.10:g.48262183_48262184insCTTG
NG_007400.1:g.21819_21820insAGCA
LRG_1:g.21819_21820insAGCA
LRG_1t1:c.681_682insAGCA

... more HGVS ... less HGVS

Protein change

Other names

Canonical SPDI

NC_000017.11:50184820:TG:TGCTTG

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.

0.41973 (TG)

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

Links

ClinGen: CA10640052 dbSNP: rs3840870 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.
COL1A1		Sufficient evidence for dosage pathogenicity	No evidence available	GRCh38 GRCh37	2747	2951

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, Dominant	Likely benign (1)	criteria provided, single submitter	Jun 14, 2016	RCV000311883.5
Infantile cortical hyperostosis	Likely benign (1)	criteria provided, single submitter	Jun 14, 2016	RCV000351512.5
Ehlers-Danlos syndrome type 7A	Likely benign (1)	criteria provided, single submitter	Jun 14, 2016	RCV000403912.5
not provided	Benign (1)	criteria provided, single submitter	May 10, 2021	RCV001643011.2

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.
Likely benign (Jun 14, 2016)	criteria provided, single submitter (ICSL Variant Classification 20161018) Method: clinical testing	Ehlers-Danlos Syndrome, Type VIIA Affected status: unknown Allele origin: germline	Illumina Laboratory Services, Illumina Accession: SCV000404033.2 First in ClinVar: Dec 06, 2016 Last updated: Dec 06, 2016
Likely benign (Jun 14, 2016)	criteria provided, single submitter (ICSL Variant Classification 20161018) Method: clinical testing	Caffey Disease Affected status: unknown Allele origin: germline	Illumina Laboratory Services, Illumina Accession: SCV000404032.2 First in ClinVar: Dec 06, 2016 Last updated: Dec 06, 2016
Likely benign (Jun 14, 2016)	criteria provided, single submitter (ICSL Variant Classification 20161018) Method: clinical testing	Osteogenesis Imperfecta, Dominant Affected status: unknown Allele origin: germline	Illumina Laboratory Services, Illumina Accession: SCV000404034.2 First in ClinVar: Dec 06, 2016 Last updated: Dec 06, 2016
Benign (May 10, 2021)	criteria provided, single submitter (GeneDx Variant Classification Process June 2021) Method: clinical testing	Not Provided Affected status: yes Allele origin: germline	GeneDx Accession: SCV001857033.1 First in ClinVar: Sep 19, 2021 Last updated: Sep 19, 2021

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

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 rs3840870 ...

These citations are identified by LitVar using the rs number, so they may include citations for more than one variant at this location. Please review the LitVar results carefully for your variant of interest.

Record last updated Sep 01, 2024

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