U.S. flag

An official website of the United States government

NM_023110.3(FGFR1):c.2359A>G (p.Thr787Ala) AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Mar 31, 2023
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:
RCV003332914.1

Allele description [Variation Report for NM_023110.3(FGFR1):c.2359A>G (p.Thr787Ala)]

NM_023110.3(FGFR1):c.2359A>G (p.Thr787Ala)

Gene:
FGFR1:fibroblast growth factor receptor 1 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
8p11.23
Genomic location:
Preferred name:
NM_023110.3(FGFR1):c.2359A>G (p.Thr787Ala)
HGVS:
  • NC_000008.11:g.38413738T>C
  • NG_007729.1:g.60097A>G
  • NG_113979.1:g.753T>C
  • NM_000604.2:c.2359A>G
  • NM_001174063.2:c.2353A>G
  • NM_001174064.2:c.2329A>G
  • NM_001174065.2:c.2353A>G
  • NM_001174066.2:c.2092A>G
  • NM_001174067.2:c.2452A>G
  • NM_001354367.2:c.2286+180A>G
  • NM_001354368.2:c.2080A>G
  • NM_001354369.2:c.2280+180A>G
  • NM_001354370.2:c.2019+180A>G
  • NM_001410922.1:c.2347A>G
  • NM_015850.4:c.2353A>G
  • NM_023105.3:c.2092A>G
  • NM_023106.3:c.2086A>G
  • NM_023110.3:c.2359A>GMANE SELECT
  • NP_000595.1:p.Thr787Ala
  • NP_001167534.1:p.Thr785Ala
  • NP_001167535.1:p.Thr777Ala
  • NP_001167536.1:p.Thr785Ala
  • NP_001167537.1:p.Thr698Ala
  • NP_001167538.1:p.Thr818Ala
  • NP_001341297.1:p.Thr694Ala
  • NP_001397851.1:p.Thr783Ala
  • NP_056934.2:p.Thr785Ala
  • NP_075593.1:p.Thr698Ala
  • NP_075594.1:p.Thr696Ala
  • NP_075598.2:p.Thr787Ala
  • NP_075598.2:p.Thr787Ala
  • LRG_993t1:c.2359A>G
  • LRG_993:g.60097A>G
  • LRG_993p1:p.Thr787Ala
  • NC_000008.10:g.38271256T>C
  • NM_023110.2:c.2359A>G
Protein change:
T694A
Molecular consequence:
  • NM_001354367.2:c.2286+180A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354369.2:c.2280+180A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354370.2:c.2019+180A>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_000604.2:c.2359A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001174063.2:c.2353A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001174064.2:c.2329A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001174065.2:c.2353A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001174066.2:c.2092A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001174067.2:c.2452A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354368.2:c.2080A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001410922.1:c.2347A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_015850.4:c.2353A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_023105.3:c.2092A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_023106.3:c.2086A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_023110.3:c.2359A>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: CN517202

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV004040443GeneDx
criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)		Uncertain significance
(Mar 31, 2023) 		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, SCV004040443.1

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

Description

Not observed at significant frequency in large population cohorts (gnomAD); In silico analysis supports that this missense variant does not alter protein structure/function; Has not been previously published as pathogenic or benign to our knowledge

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

Last Updated: Oct 7, 2023