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NM_000128.3(F11):c.965C>T (p.Thr322Ile)

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Interpretation:
not provided​

Review status:
no assertion provided
Submissions:
1 (Most recent: Jun 7, 2012)
Accession:
VCV000068207.1
Variation ID:
68207
Description:
single nucleotide variant
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NM_000128.3(F11):c.965C>T (p.Thr322Ile)

Allele ID
79098
Variant type
single nucleotide variant
Variant length
1 bp
Cytogenetic location
4q35.2
Genomic location
4: 186280322 (GRCh38) GRCh38 UCSC
4: 187201476 (GRCh37) GRCh37 UCSC
HGVS
Nucleotide Protein Molecular
consequence
NC_000004.11:g.187201476C>T
NC_000004.12:g.186280322C>T
NM_000128.3:c.965C>T NP_000119.1:p.Thr322Ile missense
... more HGVS
Protein change
T322I
Other names
-
Canonical SPDI
NC_000004.12:186280321:C:T
Functional consequence
-
Global minor allele frequency (GMAF)
-

Allele frequency
NHLBI Exome Sequencing Project (ESP) Exome Variant Server 0.00008
The Genome Aggregation Database (gnomAD), exomes 0.00002
Exome Aggregation Consortium (ExAC) 0.00003
Trans-Omics for Precision Medicine (TOPMed) 0.00002
Links
ClinGen: CA219168
UniProtKB: P03951#VAR_012089
UniProtKB/Swiss-Prot: VAR_012089
dbSNP: rs281875269
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 - RCV000059040.1
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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: SCV000090561.1
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
Six point mutations that cause factor XI deficiency. Pugh RE Blood 1995 PMID: 7888672

Text-mined citations for rs281875269...

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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 27, 2019