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NM_005629.4(SLC6A8):c.130G>T (p.Gly44Cys) AND Developmental disorder

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Feb 17, 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:
RCV001843769.1

Allele description [Variation Report for NM_005629.4(SLC6A8):c.130G>T (p.Gly44Cys)]

NM_005629.4(SLC6A8):c.130G>T (p.Gly44Cys)

Gene:
SLC6A8:solute carrier family 6 member 8 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
Xq28
Genomic location:
Preferred name:
NM_005629.4(SLC6A8):c.130G>T (p.Gly44Cys)
HGVS:
  • NC_000023.11:g.153688704G>T
  • NG_012016.2:g.5408G>T
  • NM_001142805.2:c.130G>T
  • NM_005629.4:c.130G>TMANE SELECT
  • NP_001136277.1:p.Gly44Cys
  • NP_005620.1:p.Gly44Cys
  • NC_000023.10:g.152954159G>T
  • NM_001142805.1:c.130G>T
Protein change:
G44C
Links:
dbSNP: rs2091437228
NCBI 1000 Genomes Browser:
rs2091437228
Molecular consequence:
  • NM_001142805.2:c.130G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_005629.4:c.130G>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Developmental disorder
Identifiers:
MedGen: C0008073

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV002102908Department of Genetics, Rouen University Hospital, Normandy Center for Genomic and Personalized Medicine
criteria provided, single submitter

(ACMG Guidelines, 2015)		Uncertain significance
(Feb 17, 2021) 		maternalclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedmaternalyesnot 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 Department of Genetics, Rouen University Hospital, Normandy Center for Genomic and Personalized Medicine, SCV002102908.1

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

Last Updated: Dec 24, 2023