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NM_032119.4(ADGRV1):c.9907-35A>C

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Interpretation:
Benign​

Review status:
criteria provided, single submitter
Submissions:
2 (Most recent: Apr 12, 2019)
Last evaluated:
Jun 14, 2018
Accession:
VCV000158656.1
Variation ID:
158656
Description:
single nucleotide variant
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NM_032119.4(ADGRV1):c.9907-35A>C

Allele ID
168553
Variant type
single nucleotide variant
Variant length
1 bp
Cytogenetic location
5q14.3
Genomic location
5: 90725051 (GRCh38) GRCh38 UCSC
5: 90020868 (GRCh37) GRCh37 UCSC
HGVS
Nucleotide Protein Molecular
consequence
NC_000005.10:g.90725051A>C
NC_000005.9:g.90020868A>C
NM_032119.4:c.9907-35A>C MANE Select
... more HGVS
Protein change
-
Other names
-
Canonical SPDI
NC_000005.10:90725050:A:C
Functional consequence
-
Global minor allele frequency (GMAF)
0.20188 (A)

Allele frequency
Exome Aggregation Consortium (ExAC) 0.71052
The Genome Aggregation Database (gnomAD), exomes 0.70256
The Genome Aggregation Database (gnomAD) 0.71289
1000 Genomes Project 0.79812
Trans-Omics for Precision Medicine (TOPMed) 0.73711
NHLBI Exome Sequencing Project (ESP) Exome Variant Server 0.71721
Links
ClinGen: CA172281
dbSNP: rs7723259
Varsome
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Aggregate interpretations per condition

Interpreted condition Interpretation Number of submissions Review status Last evaluated Variation/condition record
Benign 1 criteria provided, single submitter Jun 14, 2018 RCV000833699.1
Likely benign 1 no assertion criteria provided - RCV000146085.1
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Gene OMIM ClinGen Gene Dosage Sensitivity Curation Variation viewer Related variants
HI score Help TS score Help Within gene All
ADGRV1 - - GRCh38
GRCh37
2305 2336

Submitted interpretations and evidence

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Interpretation
(Last evaluated)
Review status
(Assertion criteria)
Condition
(Inheritance)
Submitter Supporting information
Benign
(Jun 14, 2018)
criteria provided, single submitter
Method: clinical testing
Not Provided
Allele origin: germline
GeneDx
Accession: SCV000975463.1
Submitted: (Apr 12, 2019)
Evidence details
Comment:
This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at … (more)
Likely benign
(-)
no assertion criteria provided
Method: clinical testing
not specified
(Autosomal dominant inheritance)
Allele origin: germline
Genetic Services Laboratory, University of Chicago
Accession: SCV000193301.1
Submitted: (Sep 11, 2014)
Comment:
Likely benign based on allele frequency in 1000 Genomes Project or ESP global frequency and its presence in a patient with a rare or unrelated … (more)
Evidence details

Functional evidence

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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 this variant

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

Text-mined citations for rs7723259...

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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 May 27, 2021