NM_213720.3(CHCHD10):c.44G>T (p.Arg15Leu) AND Frontotemporal dementia and/or amyotrophic lateral sclerosis 2

Germline classification:: Pathogenic (1 submission)
Last evaluated:: Sep 14, 2022
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:: RCV002463652.8

Allele description [Variation Report for NM_213720.3(CHCHD10):c.44G>T (p.Arg15Leu)]

NM_213720.3(CHCHD10):c.44G>T (p.Arg15Leu)

Gene:

CHCHD10:coiled-coil-helix-coiled-coil-helix domain containing 10 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

22q11.23

Genomic location:

Preferred name:

NM_213720.3(CHCHD10):c.44G>T (p.Arg15Leu)

HGVS:

NC_000022.11:g.23767591C>A
NG_034223.1:g.5382G>T
NM_001301339.2:c.44G>T
NM_213720.3:c.44G>TMANE SELECT
NP_001288268.1:p.Arg15Leu
NP_001288268.1:p.Arg15Leu
NP_998885.1:p.Arg15Leu
NC_000022.10:g.24109778C>A
NM_001301339.1:c.44G>T
NM_213720.2:c.44G>T

Protein change:

R15L; ARG15LEU

Links:

OMIM: 615903.0002; dbSNP: rs730880030

NCBI 1000 Genomes Browser:

rs730880030

Molecular consequence:

NM_001301339.2:c.44G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_213720.3:c.44G>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Frontotemporal dementia and/or amyotrophic lateral sclerosis 2
Synonyms:: FTDALS2
Identifiers:: MONDO: MONDO:0014395; MedGen: C4014648; Orphanet: 275872; OMIM: 615911

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002758619	Human Genetics Bochum, Ruhr University Bochum	criteria provided, single submitter (ACMG Guidelines, 2015)	Pathogenic (Sep 14, 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

SCV002758619

Human Genetics Bochum, Ruhr University Bochum

criteria provided, single submitter

(ACMG Guidelines, 2015)

Pathogenic
(Sep 14, 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	yes	not provided	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 Human Genetics Bochum, Ruhr University Bochum, SCV002758619.1

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

Description

ACMG criteria used to clasify this variant: PS3, PM2, PS4, PP1

#	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: Jan 19, 2025

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