NM_024301.5(FKRP):c.962_970dup (p.Ala321_Arg323dup) AND not provided

Germline classification:: Uncertain significance (2 submissions)
Last evaluated:: Apr 5, 2022
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:: RCV000394003.7

Allele description [Variation Report for NM_024301.5(FKRP):c.962_970dup (p.Ala321_Arg323dup)]

NM_024301.5(FKRP):c.962_970dup (p.Ala321_Arg323dup)

Gene:

FKRP:fukutin related protein [Gene - OMIM - HGNC]

Variant type:

Duplication

Cytogenetic location:

19q13.32

Genomic location:

Preferred name:

NM_024301.5(FKRP):c.962_970dup (p.Ala321_Arg323dup)

HGVS:

NC_000019.10:g.46756412_46756420dup
NG_008898.2:g.15367_15375dup
NM_001039885.3:c.962_970dup
NM_024301.5:c.962_970dupMANE SELECT
NP_001034974.1:p.Ala321_Arg323dup
NP_077277.1:p.Ala321_Arg323dup
LRG_761t1:c.962_970dup
LRG_761:g.15367_15375dup
LRG_761p1:p.Ala321_Arg323dup
NC_000019.9:g.47259669_47259677dup

Links:

dbSNP: rs886044307

NCBI 1000 Genomes Browser:

rs886044307

Molecular consequence:

NM_001039885.3:c.962_970dup - inframe_insertion - [Sequence Ontology: SO:0001821]
NM_024301.5:c.962_970dup - inframe_insertion - [Sequence Ontology: SO:0001821]

Observations:

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000344366	Eurofins Ntd Llc (ga)	criteria provided, single submitter (EGL Classification Definitions)	Uncertain significance (Aug 31, 2016)	germline	clinical testing	Citation Link,
SCV003832658	Revvity Omics, Revvity	criteria provided, single submitter (ACMG Guidelines, 2015)	Uncertain significance (Apr 5, 2022)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000344366

Eurofins Ntd Llc (ga)

criteria provided, single submitter

(EGL Classification Definitions)

Uncertain significance
(Aug 31, 2016)

germline

clinical testing

Citation Link,

SCV003832658

Revvity Omics, Revvity

criteria provided, single submitter

(ACMG Guidelines, 2015)

Uncertain significance
(Apr 5, 2022)

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	unknown	1	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), SCV000344366.3

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

From Revvity Omics, Revvity, SCV003832658.2

#	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	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Mar 16, 2024

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