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NM_054027.6(ANKH):c.*840G>C

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Interpretation:
Benign​

Review status:
criteria provided, single submitter
Submissions:
2 (Most recent: Feb 20, 2020)
Last evaluated:
Jan 13, 2018
Accession:
VCV000351478.2
Variation ID:
351478
Description:
single nucleotide variant
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NM_054027.6(ANKH):c.*840G>C

Allele ID
297689
Variant type
single nucleotide variant
Variant length
1 bp
Cytogenetic location
5p15.2
Genomic location
5: 14710357 (GRCh38) GRCh38 UCSC
5: 14710466 (GRCh37) GRCh37 UCSC
HGVS
Nucleotide Protein Molecular
consequence
LRG_1362:g.166429G>C
LRG_1362t1:c.*840G>C
NC_000005.10:g.14710357C>G
... more HGVS
Protein change
-
Other names
-
Canonical SPDI
NC_000005.10:14710356:C:G
Functional consequence
-
Global minor allele frequency (GMAF)
0.00220 (G)

Allele frequency
The Genome Aggregation Database (gnomAD) 0.00013
1000 Genomes Project 0.00220
Trans-Omics for Precision Medicine (TOPMed) 0.00022
Links
ClinGen: CA10620511
dbSNP: rs568699300
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 Jan 13, 2018 RCV000294478.2
Benign 1 criteria provided, single submitter Jan 13, 2018 RCV000387535.2
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Gene OMIM ClinGen Gene Dosage Sensitivity Curation Variation viewer Related variants
HI score Help TS score Help Within gene All
ANKH - - GRCh38
GRCh37
115 405
OTULIN - - GRCh38
GRCh37
25 318

Submitted interpretations and evidence

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Interpretation
(Last evaluated)
Review status
(Assertion criteria)
Condition
(Inheritance)
Submitter Supporting information
Benign
(Jan 13, 2018)
criteria provided, single submitter
Method: clinical testing
Craniometaphyseal dysplasia, autosomal dominant
Allele origin: germline
Illumina Clinical Services Laboratory,Illumina
Accession: SCV000453663.3
Submitted: (Feb 20, 2020)
Evidence details
Comment:
This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated … (more)
Benign
(Jan 13, 2018)
criteria provided, single submitter
Method: clinical testing
Chondrocalcinosis 2
Allele origin: germline
Illumina Clinical Services Laboratory,Illumina
Accession: SCV000453662.3
Submitted: (Feb 20, 2020)
Evidence details
Comment:
This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated … (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 rs568699300...

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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 Oct 08, 2021