NM_000545.8(HNF1A):c.866C>G (p.Pro289Arg) AND not provided

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jun 13, 2022
Review status:: 1 star out of maximum of 4 stars
criteria provided, single submitter

Somatic classification of clinical impact:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Somatic classification of oncogenicity:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Record status:: current
Accession:: RCV001751507.4

Allele description [Variation Report for NM_000545.8(HNF1A):c.866C>G (p.Pro289Arg)]

NM_000545.8(HNF1A):c.866C>G (p.Pro289Arg)

Gene:

HNF1A:HNF1 homeobox A [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

12q24.31

Genomic location:

Preferred name:

NM_000545.8(HNF1A):c.866C>G (p.Pro289Arg)

Other names:

NM_000545.8(HNF1A):c.866C>G; p.Pro289Arg

HGVS:

NC_000012.12:g.120994316C>G
NG_011731.2:g.20571C>G
NM_000545.8:c.866C>GMANE SELECT
NM_001306179.2:c.866C>G
NP_000536.6:p.Pro289Arg
NP_001293108.2:p.Pro289Arg
LRG_522t1:c.866C>G
LRG_522:g.20571C>G
NC_000012.11:g.121432119C>G
NM_000545.5:c.866C>G
NM_001306179.1:c.866C>G

Protein change:

P289R

Links:

dbSNP: rs267603343

NCBI 1000 Genomes Browser:

rs267603343

Molecular consequence:

NM_000545.8:c.866C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001306179.2:c.866C>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

Help

Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002007738	GeneDx	criteria provided, single submitter (GeneDx Variant Classification Process June 2021)	Uncertain significance (Jun 13, 2022)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV002007738

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)

Uncertain significance
(Jun 13, 2022)

germline

clinical testing

Citation Link

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	yes	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From GeneDx, SCV002007738.3

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not provided

Description

Identified in a family with MODY in published literature (Ellard et al., 2000); In silico analysis, which includes protein predictors and evolutionary conservation, supports that this variant does not alter protein structure/function; Not observed at significant frequency in large population cohorts (gnomAD); This variant is associated with the following publications: (PMID: 11058894)

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	yes	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Mar 30, 2024

ClinVar

Relating variation to medicine