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NM_000260.4(MYO7A):c.3109-68G>A

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Interpretation:
Benign​

Review status:
criteria provided, single submitter
Submissions:
2 (Most recent: Dec 28, 2020)
Last evaluated:
Jun 13, 2018
Accession:
VCV000678829.2
Variation ID:
678829
Description:
single nucleotide variant
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NM_000260.4(MYO7A):c.3109-68G>A

Allele ID
666262
Variant type
single nucleotide variant
Variant length
1 bp
Cytogenetic location
11q13.5
Genomic location
11: 77182356 (GRCh38) GRCh38 UCSC
11: 76893401 (GRCh37) GRCh37 UCSC
HGVS
Nucleotide Protein Molecular
consequence
NC_000011.10:g.77182356G>A
NC_000011.9:g.76893401G>A
NG_009086.1:g.59092G>A
... more HGVS
Protein change
-
Other names
-
Canonical SPDI
NC_000011.10:77182355:G:A
Functional consequence
-
Global minor allele frequency (GMAF)
0.47504 (G)

Allele frequency
1000 Genomes Project 0.52496
Trans-Omics for Precision Medicine (TOPMed) 0.56807
The Genome Aggregation Database (gnomAD) 0.57804
The Genome Aggregation Database (gnomAD) 0.57823
Trans-Omics for Precision Medicine (TOPMed) 0.56076
Links
dbSNP: rs2276287
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 13, 2018 RCV000838439.1
Benign 1 no assertion criteria provided Sep 16, 2020 RCV001272509.1
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Gene OMIM ClinGen Gene Dosage Sensitivity Curation Variation viewer Related variants
HI score Help TS score Help Within gene All
MYO7A - - GRCh38
GRCh37
2211 2221

Submitted interpretations and evidence

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Interpretation
(Last evaluated)
Review status
(Assertion criteria)
Condition
(Inheritance)
Submitter Supporting information
Benign
(Jun 13, 2018)
criteria provided, single submitter
Method: clinical testing
Not Provided
Allele origin: germline
GeneDx
Accession: SCV000980306.1
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)
Benign
(Sep 16, 2020)
no assertion criteria provided
Method: clinical testing
Usher syndrome type 1B
Allele origin: germline
Natera, Inc.
Accession: SCV001454581.1
Submitted: (Dec 28, 2020)
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 rs2276287...

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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 Nov 27, 2021