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NM_000525.4(KCNJ11):c.1044G>C (p.Gln348His) AND Monogenic diabetes

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Feb 22, 2019
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:
RCV001174373.4

Allele description [Variation Report for NM_000525.4(KCNJ11):c.1044G>C (p.Gln348His)]

NM_000525.4(KCNJ11):c.1044G>C (p.Gln348His)

Gene:
KCNJ11:potassium inwardly rectifying channel subfamily J member 11 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
11p15.1
Genomic location:
Preferred name:
NM_000525.4(KCNJ11):c.1044G>C (p.Gln348His)
HGVS:
  • NC_000011.10:g.17387048C>G
  • NG_012446.1:g.6612G>C
  • NM_000525.4:c.1044G>CMANE SELECT
  • NM_001166290.2:c.783G>C
  • NM_001377296.1:c.783G>C
  • NM_001377297.1:c.783G>C
  • NP_000516.3:p.Gln348His
  • NP_001159762.1:p.Gln261His
  • NP_001364225.1:p.Gln261His
  • NP_001364226.1:p.Gln261His
  • NC_000011.9:g.17408595C>G
  • NM_000525.3:c.1044G>C
Protein change:
Q261H
Links:
dbSNP: rs745379486
NCBI 1000 Genomes Browser:
rs745379486
Molecular consequence:
  • NM_000525.4:c.1044G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001166290.2:c.783G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001377296.1:c.783G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001377297.1:c.783G>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Monogenic diabetes
Identifiers:
MONDO: MONDO:0015967; MedGen: C3888631

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001337511Personalized Diabetes Medicine Program, University of Maryland School of Medicine
criteria provided, single submitter

(ACMG Guidelines, 2015)		Uncertain significance
(Feb 22, 2019) 		unknownresearch

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedunknownunknown1not providednot providednot providednot providedresearch

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]
PMID:
25741868
PMCID:
PMC4544753

Details of each submission

From Personalized Diabetes Medicine Program, University of Maryland School of Medicine, SCV001337511.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedresearch PubMed (1)

Description

ACMG criteria: PM2 (extremely low frequency in gnomAD)= VUS (REVEL 0.513 + PP3/7 predictors + BP4/2 predictors= conflicting evidence, not using)

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownunknownnot providednot providednot provided1not providednot providednot provided

Last Updated: Sep 16, 2024