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NM_000141.5(FGFR2):c.1440-248C>T AND not provided

Germline classification:
Likely benign (1 submission)
Last evaluated:
Dec 10, 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:
RCV001576075.3

Allele description [Variation Report for NM_000141.5(FGFR2):c.1440-248C>T]

NM_000141.5(FGFR2):c.1440-248C>T

Gene:
FGFR2:fibroblast growth factor receptor 2 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
10q26.13
Genomic location:
Preferred name:
NM_000141.5(FGFR2):c.1440-248C>T
HGVS:
  • NC_000010.11:g.121501195G>A
  • NG_012449.2:g.102264C>T
  • NM_000141.5:c.1440-248C>TMANE SELECT
  • NM_001144913.1:c.1443-248C>T
  • NM_001144914.1:c.1104-248C>T
  • NM_001144915.2:c.1173-248C>T
  • NM_001144916.2:c.1095-248C>T
  • NM_001144917.2:c.1092-248C>T
  • NM_001144918.2:c.1089-248C>T
  • NM_001144919.2:c.1176-248C>T
  • NM_001320654.2:c.756-248C>T
  • NM_001320658.2:c.1434-248C>T
  • NM_022970.4:c.1443-248C>T
  • NM_023029.2:c.1173-248C>T
  • LRG_994:g.102264C>T
  • NC_000010.10:g.123260709G>A
Links:
dbSNP: rs41295621
NCBI 1000 Genomes Browser:
rs41295621
Molecular consequence:
  • NM_000141.5:c.1440-248C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001144913.1:c.1443-248C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001144914.1:c.1104-248C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001144915.2:c.1173-248C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001144916.2:c.1095-248C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001144917.2:c.1092-248C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001144918.2:c.1089-248C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001144919.2:c.1176-248C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001320654.2:c.756-248C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001320658.2:c.1434-248C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_022970.4:c.1443-248C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_023029.2:c.1173-248C>T - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001803189GeneDx
criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)		Likely benign
(Dec 10, 2018) 		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, SCV001803189.1

#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: Dec 24, 2023