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NM_000352.6(ABCC8):c.208G>A (p.Gly70Arg) AND ABCC8-related disorder

Germline classification:
Pathogenic (1 submission)
Last evaluated:
May 18, 2023
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:
RCV004533977.1

Allele description [Variation Report for NM_000352.6(ABCC8):c.208G>A (p.Gly70Arg)]

NM_000352.6(ABCC8):c.208G>A (p.Gly70Arg)

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.208G>A (p.Gly70Arg)
HGVS:
  • NC_000011.10:g.17474968C>T
  • NG_008867.1:g.6935G>A
  • NM_000352.5:c.208G>A
  • NM_000352.6:c.208G>AMANE SELECT
  • NM_001287174.3:c.208G>A
  • NM_001351295.2:c.208G>A
  • NM_001351296.2:c.208G>A
  • NM_001351297.2:c.208G>A
  • NP_000343.2:p.Gly70Arg
  • NP_001274103.1:p.Gly70Arg
  • NP_001338224.1:p.Gly70Arg
  • NP_001338225.1:p.Gly70Arg
  • NP_001338226.1:p.Gly70Arg
  • LRG_790t1:c.208G>A
  • LRG_790t2:c.208G>A
  • LRG_790:g.6935G>A
  • LRG_790p1:p.Gly70Arg
  • LRG_790p2:p.Gly70Arg
  • NC_000011.9:g.17496515C>T
  • NM_000352.3:c.208G>A
  • NM_000352.4:c.208G>A
  • NM_000352.6:c.208G>A
  • NR_147094.2:n.277G>A
Protein change:
G70R
Links:
dbSNP: rs764349043
NCBI 1000 Genomes Browser:
rs764349043
Molecular consequence:
  • NM_000352.6:c.208G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001287174.3:c.208G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001351295.2:c.208G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001351296.2:c.208G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001351297.2:c.208G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NR_147094.2:n.277G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Name:
ABCC8-related disorder
Identifiers:

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV004115091PreventionGenetics, part of Exact Sciences
criteria provided, single submitter

(ACMG Guidelines, 2015)		Pathogenic
(May 18, 2023) 		germlineclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical testing

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 PreventionGenetics, part of Exact Sciences, SCV004115091.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)

Description

The ABCC8 c.208G>A variant is predicted to result in the amino acid substitution p.Gly70Arg. This variant was reported to be causative for congenital hyperinsulinism (Banerjee et al. 2011. PubMed ID: 21378087; Vajravelu et al. 2019. PubMed ID: 30086540). This variant is reported in 0.0056% of alleles in individuals of Latino descent in gnomAD (http://gnomad.broadinstitute.org/variant/11-17496515-C-T). A different nucleotide substitution affecting the same amino acid residue (c.209G>A, p.Gly70Glu) has also been reported to be pathogenic for congenital hyperinsulinism (Tornovsky et al. 2004. PubMed ID: 15579781). The c.208G>A (p.Gly70Arg) variant is interpreted as pathogenic.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Nov 24, 2024