NM_001080414.4(CCDC88C):c.322G>A (p.Gly108Ser) AND Inborn genetic diseases

Clinical significance:Uncertain significance (Last evaluated: Oct 2, 2018)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV001265961.1

Allele description [Variation Report for NM_001080414.4(CCDC88C):c.322G>A (p.Gly108Ser)]

NM_001080414.4(CCDC88C):c.322G>A (p.Gly108Ser)

Gene:
CCDC88C:coiled-coil domain containing 88C [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
14q32.11
Genomic location:
Preferred name:
NM_001080414.4(CCDC88C):c.322G>A (p.Gly108Ser)
HGVS:
  • NC_000014.9:g.91359660C>T
  • NG_033118.1:g.63185G>A
  • NG_033118.2:g.63185G>A
  • NM_001080414.4:c.322G>AMANE SELECT
  • NP_001073883.2:p.Gly108Ser
  • NC_000014.8:g.91826004C>T
  • NM_001080414.2:c.322G>A
  • NM_001080414.3:c.322G>A
Protein change:
G108S
Links:
dbSNP: rs61745604
NCBI 1000 Genomes Browser:
rs61745604
Molecular consequence:
  • NM_001080414.4:c.322G>A - missense variant - [Sequence Ontology: SO:0001583]
Observations:
1

Condition(s)

Name:
Inborn genetic diseases
Identifiers:
MeSH: D030342; MedGen: C0950123

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV001444133Ambry Geneticscriteria provided, single submitter
Uncertain significance
(Oct 2, 2018)
germlineclinical testing

Citation Link

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
Caucasiangermlineyes1not providednot provided1not providedclinical testing

Details of each submission

From Ambry Genetics, SCV001444133.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1Caucasian1not providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyes1not providednot provided1not providednot providednot provided

Last Updated: Jul 10, 2021

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