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NM_020549.4(CHAT):c.1511+167C>T

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Interpretation:
Benign​

Review status:
criteria provided, single submitter
Submissions:
1 (Most recent: Apr 12, 2019)
Last evaluated:
Jun 16, 2018
Accession:
VCV000678351.1
Variation ID:
678351
Description:
single nucleotide variant
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NM_020549.4(CHAT):c.1511+167C>T

Allele ID
665158
Variant type
single nucleotide variant
Variant length
1 bp
Cytogenetic location
10q11.23
Genomic location
10: 49649803 (GRCh38) GRCh38 UCSC
10: 50857849 (GRCh37) GRCh37 UCSC
HGVS
Nucleotide Protein Molecular
consequence
NC_000010.10:g.50857849C>T
NC_000010.11:g.49649803C>T
NM_020984.3:c.1157+167C>T
... more HGVS
Protein change
-
Other names
-
Canonical SPDI
NC_000010.11:49649802:C:T
Functional consequence
-
Global minor allele frequency (GMAF)
0.17193 (C)

Allele frequency
The Genome Aggregation Database (gnomAD) 0.81066
Trans-Omics for Precision Medicine (TOPMed) 0.81839
1000 Genomes Project 0.82808
Links
dbSNP: rs3793797
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 16, 2018 RCV000837931.1
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Gene OMIM ClinGen Gene Dosage Sensitivity Curation Variation viewer Related variants
HI score Help TS score Help Within gene All
CHAT - - GRCh38
GRCh37
401 499

Submitted interpretations and evidence

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Interpretation
(Last evaluated)
Review status
(Assertion criteria)
Condition
(Inheritance)
Submitter Supporting information
Benign
(Jun 16, 2018)
criteria provided, single submitter
Method: clinical testing
Not Provided
Allele origin: germline
GeneDx
Accession: SCV000979793.1
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)

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 rs3793797...

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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 Feb 27, 2021