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NM_001243279.3(ACSF3):c.1614-10G>C AND not specified

Germline classification:
Likely benign (1 submission)
Last evaluated:
Feb 5, 2018
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:
RCV000431797.2

Allele description [Variation Report for NM_001243279.3(ACSF3):c.1614-10G>C]

NM_001243279.3(ACSF3):c.1614-10G>C

Gene:
ACSF3:acyl-CoA synthetase family member 3 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
16q24.3
Genomic location:
Preferred name:
NM_001243279.3(ACSF3):c.1614-10G>C
HGVS:
  • NC_000016.10:g.89154080G>C
  • NG_031961.1:g.65272G>C
  • NM_001127214.4:c.1614-10G>C
  • NM_001243279.3:c.1614-10G>CMANE SELECT
  • NM_001284316.2:c.819-10G>C
  • NM_174917.5:c.1614-10G>C
  • NC_000016.9:g.89220488G>C
  • NM_174917.3:c.1614-10G>C
  • NM_174917.4:c.1614-10G>C
Links:
dbSNP: rs370941606
NCBI 1000 Genomes Browser:
rs370941606
Molecular consequence:
  • NM_001127214.4:c.1614-10G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001243279.3:c.1614-10G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001284316.2:c.819-10G>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_174917.5:c.1614-10G>C - intron variant - [Sequence Ontology: SO:0001627]

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
SCV000521514GeneDx
criteria provided, single submitter

(GeneDx Variant Classification (06012015))		Likely benign
(Feb 5, 2018) 		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, SCV000521514.4

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

Description

This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.

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

Last Updated: Sep 29, 2024