NM_000352.6(ABCC8):c.878A>C (p.His293Pro) AND Hyperinsulinemic hypoglycemia, familial, 1

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jan 17, 2014
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:: RCV000145007.6

Allele description [Variation Report for NM_000352.6(ABCC8):c.878A>C (p.His293Pro)]

NM_000352.6(ABCC8):c.878A>C (p.His293Pro)

Gene:

ABCC8:ATP binding cassette subfamily C member 8 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11p15.1

Genomic location:

Preferred name:

NM_000352.6(ABCC8):c.878A>C (p.His293Pro)

HGVS:

NC_000011.10:g.17460621T>G
NG_008867.1:g.21282A>C
NM_000352.6:c.878A>CMANE SELECT
NM_001287174.3:c.878A>C
NM_001351295.2:c.878A>C
NM_001351296.2:c.875A>C
NM_001351297.2:c.875A>C
NP_000343.2:p.His293Pro
NP_001274103.1:p.His293Pro
NP_001338224.1:p.His293Pro
NP_001338225.1:p.His292Pro
NP_001338226.1:p.His292Pro
LRG_790t1:c.878A>C
LRG_790t2:c.878A>C
LRG_790:g.21282A>C
LRG_790p1:p.His293Pro
LRG_790p2:p.His293Pro
NC_000011.9:g.17482168T>G
NM_000352.3:c.878A>C
NR_147094.2:n.944A>C

Protein change:

H292P

Links:

dbSNP: rs587783175

NCBI 1000 Genomes Browser:

rs587783175

Molecular consequence:

NM_000352.6:c.878A>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001287174.3:c.878A>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001351295.2:c.878A>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001351296.2:c.875A>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001351297.2:c.875A>C - missense variant - [Sequence Ontology: SO:0001583]
NR_147094.2:n.944A>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Name:: Hyperinsulinemic hypoglycemia, familial, 1 (HHF1)
Synonyms:: HYPERINSULINISM, FAMILIAL, WITH PANCREATIC NESIDIOBLASTOSIS; HYPOGLYCEMIA, HYPERINSULINEMIC, OF INFANCY; NESIDIOBLASTOSIS OF PANCREAS; See all synonyms [MedGen]
Identifiers:: MONDO: MONDO:0009734; MedGen: C2931832; Orphanet: 276575; Orphanet: 276598; OMIM: 256450

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000192043	Genetic Services Laboratory, University of Chicago	criteria provided, single submitter (ACMG Guidelines, 2007)	Uncertain significance (Jan 17, 2014)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000192043

Genetic Services Laboratory, University of Chicago

criteria provided, single submitter

(ACMG Guidelines, 2007)

Uncertain significance
(Jan 17, 2014)

germline

clinical testing

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

Help

Summary from all submissions

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

Citations

PubMed

ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007.

Richards CS, Bale S, Bellissimo DB, Das S, Grody WW, Hegde MR, Lyon E, Ward BE; Molecular Subcommittee of the ACMG Laboratory Quality Assurance Committee.

Genet Med. 2008 Apr;10(4):294-300. doi: 10.1097/GIM.0b013e31816b5cae.

PubMed [citation]

PMID:: 18414213

Details of each submission

From Genetic Services Laboratory, University of Chicago, SCV000192043.1

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

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

Last Updated: Apr 9, 2023

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