NM_024301.5(FKRP):c.1136G>C (p.Arg379Pro) AND Autosomal recessive limb-girdle muscular dystrophy type 2I

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Aug 7, 2020
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

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:: RCV001832510.1

Allele description [Variation Report for NM_024301.5(FKRP):c.1136G>C (p.Arg379Pro)]

NM_024301.5(FKRP):c.1136G>C (p.Arg379Pro)

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

19q13.32

Genomic location:

Preferred name:

NM_024301.5(FKRP):c.1136G>C (p.Arg379Pro)

HGVS:

NC_000019.10:g.46756586G>C
NG_008898.2:g.15541G>C
NM_001039885.3:c.1136G>C
NM_024301.5:c.1136G>CMANE SELECT
NP_001034974.1:p.Arg379Pro
NP_077277.1:p.Arg379Pro
LRG_761t1:c.1136G>C
LRG_761:g.15541G>C
LRG_761p1:p.Arg379Pro
NC_000019.9:g.47259843G>C
NC_000019.9:g.47259843G>C
NM_024301.4:c.1136G>C

Protein change:

R379P

Links:

dbSNP: rs140217866

NCBI 1000 Genomes Browser:

rs140217866

Molecular consequence:

NM_001039885.3:c.1136G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_024301.5:c.1136G>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Autosomal recessive limb-girdle muscular dystrophy type 2I
Synonyms:: MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5; MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I; MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, FRKP-RELATED; See all synonyms [MedGen]
Identifiers:: MONDO: MONDO:0011787; MedGen: C1846672; Orphanet: 34515; OMIM: 607155

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002091338	Natera, Inc.	no assertion criteria provided	Uncertain significance (Aug 7, 2020)	germline	clinical testing

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV002091338

Natera, Inc.

no assertion criteria provided

Uncertain significance
(Aug 7, 2020)

germline

clinical testing

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 Natera, Inc., SCV002091338.1

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

Last Updated: Sep 29, 2024

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