NM_001379081.2(FREM1):c.1640C>G (p.Ala547Gly) AND Chronic kidney disease

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: May 28, 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:: RCV001171324.1

Allele description [Variation Report for NM_001379081.2(FREM1):c.1640C>G (p.Ala547Gly)]

NM_001379081.2(FREM1):c.1640C>G (p.Ala547Gly)

Gene:

FREM1:FRAS1 related extracellular matrix 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

9p22.3

Genomic location:

Preferred name:

NM_001379081.2(FREM1):c.1640C>G (p.Ala547Gly)

HGVS:

NC_000009.12:g.14842414G>C
NG_017005.2:g.72823C>G
NM_001379081.2:c.1640C>GMANE SELECT
NM_144966.7:c.1640C>G
NP_001366010.1:p.Ala547Gly
NP_659403.4:p.Ala547Gly
NP_659403.4:p.Ala547Gly
NC_000009.11:g.14842412G>C
NM_144966.5:c.1640C>G
NR_163238.2:n.2456C>G
NR_163239.2:n.2400C>G
p.A547G

Protein change:

A547G

Links:

dbSNP: rs201056172

NCBI 1000 Genomes Browser:

rs201056172

Molecular consequence:

NM_001379081.2:c.1640C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_144966.7:c.1640C>G - missense variant - [Sequence Ontology: SO:0001583]
NR_163238.2:n.2456C>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_163239.2:n.2400C>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Name:: Chronic kidney disease
Identifiers:: MONDO: MONDO:0005300; MedGen: C1561643; Human Phenotype Ontology: HP:0012622

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001328271	Cavalleri Lab, Royal College of Surgeons in Ireland	criteria provided, single submitter (ACMG Guidelines, 2015)	Uncertain significance (May 28, 2020)	unknown	research	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001328271

Cavalleri Lab, Royal College of Surgeons in Ireland

criteria provided, single submitter

(ACMG Guidelines, 2015)

Uncertain significance
(May 28, 2020)

unknown

research

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	unknown	yes	not provided	not provided	not provided	not provided	not provided	research

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 Cavalleri Lab, Royal College of Surgeons in Ireland, SCV001328271.1

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

Description

PP3, BS1

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

Last Updated: May 7, 2024

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Relating variation to medicine