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NM_002880.4(RAF1):c.845G>A (p.Arg282Gln) AND not provided

Germline classification:
Likely benign (1 submission)
Last evaluated:
Sep 25, 2020
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:
RCV001547003.2

Allele description [Variation Report for NM_002880.4(RAF1):c.845G>A (p.Arg282Gln)]

NM_002880.4(RAF1):c.845G>A (p.Arg282Gln)

Gene:
RAF1:Raf-1 proto-oncogene, serine/threonine kinase [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
3p25.2
Genomic location:
Preferred name:
NM_002880.4(RAF1):c.845G>A (p.Arg282Gln)
HGVS:
  • NC_000003.12:g.12600405C>T
  • NG_007467.1:g.68775G>A
  • NM_001354689.3:c.905G>A
  • NM_001354690.3:c.845G>A
  • NM_001354691.3:c.602G>A
  • NM_001354692.3:c.602G>A
  • NM_001354693.3:c.746G>A
  • NM_001354694.3:c.662G>A
  • NM_001354695.3:c.503G>A
  • NM_002880.4:c.845G>AMANE SELECT
  • NP_001341618.1:p.Arg302Gln
  • NP_001341619.1:p.Arg282Gln
  • NP_001341620.1:p.Arg201Gln
  • NP_001341621.1:p.Arg201Gln
  • NP_001341622.1:p.Arg249Gln
  • NP_001341623.1:p.Arg221Gln
  • NP_001341624.1:p.Arg168Gln
  • NP_002871.1:p.Arg282Gln
  • NP_002871.1:p.Arg282Gln
  • LRG_413t1:c.845G>A
  • LRG_413t2:c.905G>A
  • LRG_413:g.68775G>A
  • LRG_413p1:p.Arg282Gln
  • LRG_413p2:p.Arg302Gln
  • NC_000003.11:g.12641904C>T
  • NM_002880.3:c.845G>A
  • NR_148940.3:n.1176G>A
  • NR_148941.3:n.1176G>A
  • NR_148942.3:n.1176G>A
Protein change:
R168Q
Links:
dbSNP: rs752713997
NCBI 1000 Genomes Browser:
rs752713997
Molecular consequence:
  • NM_001354689.3:c.905G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354690.3:c.845G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354691.3:c.602G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354692.3:c.602G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354693.3:c.746G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354694.3:c.662G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354695.3:c.503G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_002880.4:c.845G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NR_148940.3:n.1176G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_148941.3:n.1176G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_148942.3:n.1176G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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Assertion and evidence details

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Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001766619GeneDx
criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)		Likely benign
(Sep 25, 2020) 		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, SCV001766619.1

#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: Sep 29, 2024