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

Germline classification:: Likely benign (1 submission)
Last evaluated:: Apr 27, 2017
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:: RCV000356059.13

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]

Condition(s)

Name:: Craniosynostosis syndrome
Synonyms:: Craniosynostosis
Identifiers:: MONDO: MONDO:0015469; MeSH: D003398; MedGen: C0010278; OMIM: PS123100; Human Phenotype Ontology: HP:0001363

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000473590	Illumina Laboratory Services, Illumina	criteria provided, single submitter (ICSL Variant Classification Criteria 13 December 2019)	Likely benign (Apr 27, 2017)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000473590

Illumina Laboratory Services, Illumina

criteria provided, single submitter

(ICSL Variant Classification Criteria 13 December 2019)

Likely benign
(Apr 27, 2017)

germline

clinical testing

Citation Link

Help

Summary from all submissions

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

Details of each submission

From Illumina Laboratory Services, Illumina, SCV000473590.3

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

Description

This variant was observed as part of a predisposition screen in an ostensibly healthy population. A literature search was performed for the gene, cDNA change, and amino acid change (where applicable). No publications were found based on this search. Allele frequency data from public databases allowed determination this variant is unlikely to cause disease. Therefore, this variant is classified as likely benign.

#	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		not provided	not provided	not provided	not provided

Last Updated: Nov 10, 2024

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