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NM_001160148.2(DDHD1):c.2299C>T (p.Arg767Cys) AND not specified

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Dec 2, 2016
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:
RCV000414377.1

Allele description [Variation Report for NM_001160148.2(DDHD1):c.2299C>T (p.Arg767Cys)]

NM_001160148.2(DDHD1):c.2299C>T (p.Arg767Cys)

Gene:
DDHD1:DDHD domain containing 1 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
14q22.1
Genomic location:
Preferred name:
NM_001160148.2(DDHD1):c.2299C>T (p.Arg767Cys)
HGVS:
  • NC_000014.9:g.53054576G>A
  • NG_042832.1:g.103753C>T
  • NM_001160147.2:c.2320C>T
  • NM_001160148.2:c.2299C>TMANE SELECT
  • NM_030637.3:c.2299C>T
  • NP_001153619.1:p.Arg774Cys
  • NP_001153620.1:p.Arg767Cys
  • NP_085140.2:p.Arg767Cys
  • NC_000014.8:g.53521294G>A
  • NM_001160147.1:c.2320C>T
Protein change:
R767C
Links:
dbSNP: rs1057518484
NCBI 1000 Genomes Browser:
rs1057518484
Molecular consequence:
  • NM_001160147.2:c.2320C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001160148.2:c.2299C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_030637.3:c.2299C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:
AllHighlyPenetrant
Identifiers:
MedGen: CN169374

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Assertion and evidence details

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Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000492163GeneDx
criteria provided, single submitter

(GeneDx Variant Classification (06012015))		Uncertain significance
(Dec 2, 2016) 		germlineclinical testing

Citation Link

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Summary from all submissions

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

Details of each submission

From GeneDx, SCV000492163.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

The R774C variant in the DDHD1 gene has not been reported previously as a pathogenic variant, nor as a benign variant, to our knowledge. The R774C variant was not observed in approximately 6,500 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project, indicating it is not a common benign variant in these populations. The R774C variant is a non-conservative amino acid substitution, which is likely to impact secondary protein structure as these residues differ in polarity, charge, size and/or other properties. This substitution occurs at a position that is conserved across species. In silico analysis predicts this variant is probably damaging to the protein structure/function. We interpret R774C as a variant of uncertain significance.

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

Last Updated: Sep 29, 2024