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NM_005257.6(GATA6):c.551G>A (p.Ser184Asn) AND multiple conditions

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Mar 18, 2024
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:
RCV005025078.1

Allele description [Variation Report for NM_005257.6(GATA6):c.551G>A (p.Ser184Asn)]

NM_005257.6(GATA6):c.551G>A (p.Ser184Asn)

Gene:
GATA6:GATA binding protein 6 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
18q11.2
Genomic location:
Preferred name:
NM_005257.6(GATA6):c.551G>A (p.Ser184Asn)
HGVS:
  • NC_000018.10:g.22171695G>A
  • NG_032677.2:g.7259G>A
  • NM_005257.6:c.551G>AMANE SELECT
  • NP_005248.2:p.Ser184Asn
  • NP_005248.2:p.Ser184Asn
  • NC_000018.9:g.19751656G>A
  • NM_005257.4:c.551G>A
  • NM_005257.5:c.551G>A
  • Q92908:p.Ser184Asn
Protein change:
S184N; SER184ASN
Links:
UniProtKB: Q92908#VAR_067382; OMIM: 601656.0005; dbSNP: rs387906816
NCBI 1000 Genomes Browser:
rs387906816
Molecular consequence:
  • NM_005257.6:c.551G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Conotruncal heart malformations (CTHM)
Identifiers:
MONDO: MONDO:0016581; MedGen: C1857586; Orphanet: 3384; Orphanet: 3426; OMIM: 217095
Name:
Pancreatic hypoplasia-diabetes-congenital heart disease syndrome
Synonyms:
PANCREATIC HYPOPLASIA, CONGENITAL, WITH DIABETES MELLITUS AND CONGENITAL HEART DISEASE; HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES
Identifiers:
MONDO: MONDO:0010802; MedGen: C2931296; Orphanet: 2255; OMIM: 600001
Name:
Tetralogy of Fallot (TOF)
Identifiers:
MONDO: MONDO:0008542; MedGen: C0039685; Orphanet: 3303; OMIM: 187500; Human Phenotype Ontology: HP:0001636
Name:
Atrioventricular septal defect 5 (AVSD5)
Identifiers:
MONDO: MONDO:0013769; MedGen: C3280939; OMIM: 614474
Name:
Atrial septal defect 9 (ASD9)
Identifiers:
MONDO: MONDO:0013770; MedGen: C3280943; Orphanet: 1478; OMIM: 614475

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV005655045Fulgent Genetics, Fulgent Genetics
criteria provided, single submitter

(ACMG Guidelines, 2015)		Uncertain significance
(Mar 18, 2024) 		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 Fulgent Genetics, Fulgent Genetics, SCV005655045.1

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

Last Updated: May 16, 2025