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NM_019616.4(F7):c.*639G>A

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Interpretation:
Likely benign​

Review status:
criteria provided, single submitter
Submissions:
2 (Most recent: Oct 18, 2016)
Last evaluated:
Jun 14, 2016
Accession:
VCV000311246.2
Variation ID:
311246
Description:
single nucleotide variant
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NM_019616.4(F7):c.*639G>A

Allele ID
327504
Variant type
single nucleotide variant
Variant length
1 bp
Cytogenetic location
13q34
Genomic location
13: 113119647 (GRCh38) GRCh38 UCSC
13: 113773961 (GRCh37) GRCh37 UCSC
HGVS
Nucleotide Protein Molecular
consequence
NC_000013.10:g.113773961G>A
NC_000013.11:g.113119647G>A
NG_009258.1:g.1849G>A
... more HGVS
Protein change
-
Other names
-
Canonical SPDI
NC_000013.11:113119646:G:A
Functional consequence
-
Global minor allele frequency (GMAF)
0.02736 (A)

Allele frequency
The Genome Aggregation Database (gnomAD) 0.02557
1000 Genomes Project 0.02736
Trans-Omics for Precision Medicine (TOPMed) 0.02935
Links
ClinGen: CA10639058
dbSNP: rs3093250
Varsome
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Aggregate interpretations per condition

Interpreted condition Interpretation Number of submissions Review status Last evaluated Variation/condition record
Likely benign 1 criteria provided, single submitter Jun 14, 2016 RCV000283131.2
Likely benign 1 criteria provided, single submitter Jun 14, 2016 RCV000406253.2
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Gene OMIM ClinGen Gene Dosage Sensitivity Curation Variation viewer Related variants
HI score Help TS score Help Within gene All
F10 - - GRCh38
GRCh37
78 216
F7 - - GRCh38
GRCh37
160 282

Submitted interpretations and evidence

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Interpretation
(Last evaluated)
Review status
(Assertion criteria)
Condition
(Inheritance)
Submitter Supporting information
Likely benign
(Jun 14, 2016)
criteria provided, single submitter
Method: clinical testing
Factor VII Deficiency
Allele origin: germline
Illumina Clinical Services Laboratory,Illumina
Accession: SCV000382762.2
Submitted: (Oct 18, 2016)
Evidence details
Likely benign
(Jun 14, 2016)
criteria provided, single submitter
Method: clinical testing
Factor X Deficiency
Allele origin: germline
Illumina Clinical Services Laboratory,Illumina
Accession: SCV000483429.2
Submitted: (Oct 18, 2016)
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 rs3093250...

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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 Sep 29, 2021