NM_000352.6(ABCC8):c.4412-4T>G AND Hyperinsulinemic hypoglycemia, familial, 1

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jan 10, 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:: RCV003227877.2

Allele description [Variation Report for NM_000352.6(ABCC8):c.4412-4T>G]

NM_000352.6(ABCC8):c.4412-4T>G

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.4412-4T>G

HGVS:

NC_000011.10:g.17394403A>C
NG_008867.1:g.87500T>G
NM_000352.6:c.4412-4T>GMANE SELECT
NM_001287174.3:c.4415-4T>G
NM_001351295.2:c.4478-4T>G
NM_001351296.2:c.4412-4T>G
NM_001351297.2:c.4409-4T>G
LRG_790t1:c.4412-4T>G
LRG_790t2:c.4415-4T>G
LRG_790:g.87500T>G
NC_000011.9:g.17415950A>C
NM_000352.4:c.4412-4T>G

Links:

dbSNP: rs1476016104

NCBI 1000 Genomes Browser:

rs1476016104

Molecular consequence:

NM_000352.6:c.4412-4T>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001287174.3:c.4415-4T>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001351295.2:c.4478-4T>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001351296.2:c.4412-4T>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001351297.2:c.4409-4T>G - intron variant - [Sequence Ontology: SO:0001627]

Observations:

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
SCV003925176	New York Genome Center	criteria provided, single submitter (NYGC Assertion Criteria 2020)	Uncertain significance (Jan 10, 2022)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003925176

New York Genome Center

criteria provided, single submitter

(NYGC Assertion Criteria 2020)

Uncertain significance
(Jan 10, 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	unknown	1	not provided	not provided	1	not provided	clinical testing

Details of each submission

From New York Genome Center, SCV003925176.2

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

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

Last Updated: Feb 25, 2025

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