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NM_194456.1(KRIT1):c.-312A>G

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Interpretation:
Benign/Likely benign​

Review status:
criteria provided, single submitter
Submissions:
2 (Most recent: Feb 20, 2020)
Last evaluated:
Jan 13, 2018
Accession:
VCV000360895.2
Variation ID:
360895
Description:
single nucleotide variant
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NM_194456.1(KRIT1):c.-312A>G

Allele ID
311931
Variant type
single nucleotide variant
Variant length
1 bp
Cytogenetic location
7q21.2
Genomic location
7: 92245063 (GRCh38) GRCh38 UCSC
7: 91874377 (GRCh37) GRCh37 UCSC
HGVS
Nucleotide Protein Molecular
consequence
LRG_650t1:c.-312A>G
LRG_650:g.6038A>G
NC_000007.13:g.91874377T>C
... more HGVS
Protein change
-
Other names
-
Canonical SPDI
NC_000007.14:92245062:T:C
Functional consequence
-
Global minor allele frequency (GMAF)
0.00100 (C)

Allele frequency
1000 Genomes Project 0.00100
Trans-Omics for Precision Medicine (TOPMed) 0.00002
Links
ClinGen: CA10629627
dbSNP: rs538102163
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 RCV000298591.2
Likely benign 1 criteria provided, single submitter Jan 13, 2018 RCV000334812.2
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Gene OMIM ClinGen Gene Dosage Sensitivity Curation Variation viewer Related variants
HI score Help TS score Help Within gene All
KRIT1 - - GRCh38
GRCh37
362 393

Submitted interpretations and evidence

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Interpretation
(Last evaluated)
Review status
(Assertion criteria)
Condition
(Inheritance)
Submitter Supporting information
Likely benign
(Jan 13, 2018)
criteria provided, single submitter
Method: clinical testing
Cerebral cavernous malformation
Allele origin: germline
Illumina Clinical Services Laboratory,Illumina
Accession: SCV000470461.3
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
Angiokeratoma corporis diffusum with arteriovenous fistulas
Allele origin: germline
Illumina Clinical Services Laboratory,Illumina
Accession: SCV000470460.3
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 rs538102163...

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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