NM_023110.3(FGFR1):c.2314C>T (p.Pro772Ser) AND not specified

Germline classification:: Benign (5 submissions)
Last evaluated:: Mar 25, 2020
Review status:: 2 stars out of maximum of 4 stars
criteria provided, multiple submitters, no conflicts

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:: RCV000175365.19

Allele description [Variation Report for NM_023110.3(FGFR1):c.2314C>T (p.Pro772Ser)]

NM_023110.3(FGFR1):c.2314C>T (p.Pro772Ser)

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.2314C>T (p.Pro772Ser)

Other names:

NM_001174063.1(FGFR1):c.2308C>T(p.Pro770Ser); NM_001174064.1(FGFR1):c.2284C>T(p.Pro762Ser); NM_001174065.1(FGFR1):c.2308C>T(p.Pro770Ser); NM_001174066.1(FGFR1):c.2047C>T(p.Pro683Ser); NM_001174067.1(FGFR1):c.2407C>T(p.Pro803Ser); NM_015850.3(FGFR1):c.2308C>T(p.Pro770Ser); NM_023105.2(FGFR1):c.2047C>T(p.Pro683Ser); NM_023106.2(FGFR1):c.2041C>T(p.Pro681Ser); NM_023110.2(FGFR1):c.2314C>T(p.Pro772Ser)

HGVS:

NC_000008.11:g.38413783G>A
NG_007729.1:g.60052C>T
NM_001174063.2:c.2308C>T
NM_001174064.2:c.2284C>T
NM_001174065.2:c.2308C>T
NM_001174066.2:c.2047C>T
NM_001174067.2:c.2407C>T
NM_001354367.2:c.2286+135C>T
NM_001354368.2:c.2035C>T
NM_001354369.2:c.2280+135C>T
NM_001354370.2:c.2019+135C>T
NM_015850.4:c.2308C>T
NM_023105.3:c.2047C>T
NM_023106.3:c.2041C>T
NM_023110.3:c.2314C>TMANE SELECT
NP_001167534.1:p.Pro770Ser
NP_001167535.1:p.Pro762Ser
NP_001167536.1:p.Pro770Ser
NP_001167537.1:p.Pro683Ser
NP_001167538.1:p.Pro803Ser
NP_001341297.1:p.Pro679Ser
NP_056934.2:p.Pro770Ser
NP_075593.1:p.Pro683Ser
NP_075594.1:p.Pro681Ser
NP_075598.2:p.Pro772Ser
NP_075598.2:p.Pro772Ser
LRG_993t1:c.2314C>T
LRG_993:g.60052C>T
LRG_993p1:p.Pro772Ser
NC_000008.10:g.38271301G>A
NM_023110.2:c.2314C>T
P11362:p.Pro772Ser

Protein change:

P679S

Links:

UniProtKB: P11362#VAR_017892; dbSNP: rs56234888

NCBI 1000 Genomes Browser:

rs56234888

Molecular consequence:

NM_001354367.2:c.2286+135C>T - intron variant - [Sequence Ontology: SO:0001627]
NM_001354369.2:c.2280+135C>T - intron variant - [Sequence Ontology: SO:0001627]
NM_001354370.2:c.2019+135C>T - intron variant - [Sequence Ontology: SO:0001627]
NM_001174063.2:c.2308C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001174064.2:c.2284C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001174065.2:c.2308C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001174066.2:c.2047C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001174067.2:c.2407C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001354368.2:c.2035C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_015850.4:c.2308C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_023105.3:c.2047C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_023106.3:c.2041C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_023110.3:c.2314C>T - missense variant - [Sequence Ontology: SO:0001583]

Observations:

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000226838	Eurofins Ntd Llc (ga)	criteria provided, single submitter (EGL Classification Definitions 2015)	Benign (Feb 26, 2015)	germline	clinical testing	Citation Link,
SCV000517335	GeneDx	criteria provided, single submitter (GeneDx Variant Classification (06012015))	Benign (Aug 31, 2015)	germline	clinical testing	Citation Link,
SCV001924260	Clinical Genetics, Academic Medical Center - VKGL Data-share Consensus See additional submitters Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen	no assertion criteria provided	Benign	germline	clinical testing
SCV001927970	Genome Diagnostics Laboratory, University Medical Center Utrecht - VKGL Data-share Consensus See additional submitters Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen	no assertion criteria provided	Benign	germline	clinical testing
SCV001984548	Al Jalila Children’s Genomics Center, Al Jalila Childrens Speciality Hospital	criteria provided, single submitter (ACMG Guidelines, 2015)	Benign (Mar 25, 2020)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	yes	not provided	not provided	not provided	not provided	not provided	clinical testing
not provided	germline	unknown	2	not provided	not provided	not provided	not provided	clinical testing

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]

PMID:: 25741868
PMCID:: PMC4544753

Details of each submission

From Eurofins Ntd Llc (ga), SCV000226838.5

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	2	not provided	not provided	clinical testing	not provided

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		2	not provided	not provided	not provided

From GeneDx, SCV000517335.4

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not 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.

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	yes	not provided	not provided	not provided		not provided	not provided	not provided	not provided

From Clinical Genetics, Academic Medical Center - VKGL Data-share Consensus, SCV001924260.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not provided

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	yes	not provided	not provided	not provided		not provided	not provided	not provided	not provided

From Genome Diagnostics Laboratory, University Medical Center Utrecht - VKGL Data-share Consensus, SCV001927970.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not provided

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	yes	not provided	not provided	not provided		not provided	not provided	not provided	not provided

From Al Jalila Children’s Genomics Center, Al Jalila Childrens Speciality Hospital, SCV001984548.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	PubMed (1)

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	yes	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Nov 10, 2024

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