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NM_016204.4(GDF2):c.911C>T (p.Thr304Met) AND not provided

Germline classification:
Likely benign (1 submission)
Last evaluated:
Dec 17, 2019
Review status:
2 stars out of maximum of 4 stars
criteria provided, multiple submitters, no conflicts
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:
RCV000757325.14

Allele description

NM_016204.4(GDF2):c.911C>T (p.Thr304Met)

Gene:
GDF2:growth differentiation factor 2 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
10q11.22
Genomic location:
Preferred name:
NM_016204.4(GDF2):c.911C>T (p.Thr304Met)
HGVS:
  • NC_000010.11:g.47325405C>T
  • NG_033916.1:g.7916C>T
  • NM_016204.4:c.911C>TMANE SELECT
  • NP_057288.1:p.Thr304Met
  • NC_000010.10:g.48413957G>A
  • NM_016204.1:c.911C>T
  • NM_016204.2:c.911C>T
  • NM_016204.4:c.911C>T
Protein change:
T304M
Links:
dbSNP: rs75024165
NCBI 1000 Genomes Browser:
rs75024165
Molecular consequence:
  • NM_016204.4:c.911C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001822797GeneDx
criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)		Likely benign
(Dec 17, 2019) 		germlineclinical testing

Citation Link

Help

Summary from all submissions

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

Details of each submission

From GeneDx, SCV001822797.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot providednot providednot providednot providednot provided

Last Updated: May 1, 2024