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NM_000352.6(ABCC8):c.1973G>T (p.Gly658Val) AND multiple conditions

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Oct 29, 2021
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:
RCV002478056.3

Allele description [Variation Report for NM_000352.6(ABCC8):c.1973G>T (p.Gly658Val)]

NM_000352.6(ABCC8):c.1973G>T (p.Gly658Val)

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.1973G>T (p.Gly658Val)
HGVS:
  • NC_000011.10:g.17428356C>A
  • NG_008867.1:g.53547G>T
  • NM_000352.6:c.1973G>TMANE SELECT
  • NM_001287174.3:c.1973G>T
  • NM_001351295.2:c.2039G>T
  • NM_001351296.2:c.1970G>T
  • NM_001351297.2:c.1970G>T
  • NP_000343.2:p.Gly658Val
  • NP_001274103.1:p.Gly658Val
  • NP_001338224.1:p.Gly680Val
  • NP_001338225.1:p.Gly657Val
  • NP_001338226.1:p.Gly657Val
  • LRG_790t1:c.1973G>T
  • LRG_790t2:c.1973G>T
  • LRG_790:g.53547G>T
  • LRG_790p1:p.Gly658Val
  • LRG_790p2:p.Gly658Val
  • NC_000011.9:g.17449903C>A
  • NM_000352.3:c.1973G>T
  • NM_000352.4:c.1973G>T
  • NR_147094.2:n.2039G>T
Protein change:
G657V
Links:
dbSNP: rs149400972
NCBI 1000 Genomes Browser:
rs149400972
Molecular consequence:
  • NM_000352.6:c.1973G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001287174.3:c.1973G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001351295.2:c.2039G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001351296.2:c.1970G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001351297.2:c.1970G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NR_147094.2:n.2039G>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Name:
Diabetes mellitus, transient neonatal, 2 (TNDM2)
Identifiers:
MONDO: MONDO:0012480; MedGen: C1835887; Orphanet: 99886; OMIM: 610374
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
Name:
Leucine-induced hypoglycemia (LIH)
Synonyms:
Leucine-sensitive hypoglycemia of infancy; Familial infantile hypoglycemia precipitated by leucine
Identifiers:
MONDO: MONDO:0009415; MedGen: C0271714; OMIM: 240800
Name:
Type 2 diabetes mellitus
Synonyms:
DIABETES MELLITUS, TYPE 2, PROTECTION AGAINST; Type II diabetes mellitus; Diabetes mellitus, noninsulin-dependent, late onset
Identifiers:
MONDO: MONDO:0005148; MeSH: D003924; MedGen: C0011860; OMIM: 125853; Human Phenotype Ontology: HP:0005978
Name:
Diabetes mellitus, permanent neonatal 3
Identifiers:
MONDO: MONDO:0030088; MedGen: C5394303; OMIM: 618857

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV002792018Fulgent Genetics, Fulgent Genetics
criteria provided, single submitter

(ACMG Guidelines, 2015)		Uncertain significance
(Oct 29, 2021) 		unknownclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedunknownunknownnot 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 Fulgent Genetics, Fulgent Genetics, SCV002792018.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Sep 29, 2024