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NM_000128.4(F11):c.127G>A (p.Ala43Thr)

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Interpretation:
not provided​

Review status:
no assertion provided
Submissions:
1 (Most recent: Jun 7, 2012)
Accession:
VCV000068174.1
Variation ID:
68174
Description:
single nucleotide variant
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NM_000128.4(F11):c.127G>A (p.Ala43Thr)

Allele ID
79065
Variant type
single nucleotide variant
Variant length
1 bp
Cytogenetic location
4q35.2
Genomic location
4: 186271680 (GRCh38) GRCh38 UCSC
4: 187192834 (GRCh37) GRCh37 UCSC
HGVS
Nucleotide Protein Molecular
consequence
P03951:p.Ala43Thr
NC_000004.11:g.187192834G>A
NC_000004.12:g.186271680G>A
... more HGVS
Protein change
A43T
Other names
-
Canonical SPDI
NC_000004.12:186271679:G:A
Functional consequence
-
Global minor allele frequency (GMAF)
-

Allele frequency
Exome Aggregation Consortium (ExAC) 0.00001
The Genome Aggregation Database (gnomAD), exomes 0.00004
Links
UniProtKB/Swiss-Prot: VAR_067930
dbSNP: rs281875264
ClinGen: CA219104
UniProtKB: P03951#VAR_067930
VarSome
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Aggregate interpretations per condition

Interpreted condition Interpretation Number of submissions Review status Last evaluated Variation/condition record
not provided 1 no assertion provided - RCV000059006.1
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Gene OMIM ClinGen Gene Dosage Sensitivity Curation Variation viewer Related variants
HI score Help TS score Help Within gene All
F11 - - GRCh38
GRCh37
268 510

Submitted interpretations and evidence

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Interpretation
(Last evaluated)
Review status
(Assertion criteria)
Condition
(Inheritance)
Submitter Supporting information
not provided
(-)
no assertion provided
Method: not provided
not provided
Allele origin: not provided
UniProtKB/Swiss-Prot
Accession: SCV000090527.1
Submitted: (Jun 07, 2012)
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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Title Author Journal Year Link
Three dominant-negative mutations in factor XI-deficient patients. Dai L Haemophilia : the official journal of the World Federation of Hemophilia 2011 PMID: 21457405

Text-mined citations for rs281875264...

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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 24, 2021