NM_000466.3(PEX1):c.3455_3456del (p.Ser1152fs) AND Heimler syndrome 1

Germline classification:: Likely pathogenic (1 submission)
Last evaluated:: Apr 2, 2023
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:: RCV003475989.1

Allele description [Variation Report for NM_000466.3(PEX1):c.3455_3456del (p.Ser1152fs)]

NM_000466.3(PEX1):c.3455_3456del (p.Ser1152fs)

Genes:

GATAD1:GATA zinc finger domain containing 1 [Gene - OMIM - HGNC]
PEX1:peroxisomal biogenesis factor 1 [Gene - OMIM - HGNC]

Variant type:

Microsatellite

Cytogenetic location:

7q21.2

Genomic location:

Preferred name:

NM_000466.3(PEX1):c.3455_3456del (p.Ser1152fs)

HGVS:

NC_000007.14:g.92489895GA[2]
NG_008341.2:g.43633CT[2]
NM_000466.3:c.3455_3456delMANE SELECT
NM_001282677.2:c.3284_3285del
NM_001282678.2:c.2831_2832del
NP_000457.1:p.Ser1152fs
NP_001269606.1:p.Ser1095fs
NP_001269607.1:p.Ser944fs
NC_000007.13:g.92119208_92119209del
NC_000007.13:g.92119209GA[2]
NM_000466.2:c.3455_3456del
NM_000466.2:c.3455_3456delCT

Protein change:

S1095fs

Links:

dbSNP: rs759183382

NCBI 1000 Genomes Browser:

rs759183382

Molecular consequence:

NM_000466.3:c.3455_3456del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001282677.2:c.3284_3285del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001282678.2:c.2831_2832del - frameshift variant - [Sequence Ontology: SO:0001589]

Condition(s)

Name:: Heimler syndrome 1 (HMLR1)
Synonyms:: PEROXISOME BIOGENESIS DISORDER 1C
Identifiers:: MedGen: C4551980; Orphanet: 3220; OMIM: 234580

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004203353	Baylor Genetics	criteria provided, single submitter (ACMG Guidelines, 2015)	Likely pathogenic (Apr 2, 2023)	unknown	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

SCV004203353

Baylor Genetics

criteria provided, single submitter

(ACMG Guidelines, 2015)

Likely pathogenic
(Apr 2, 2023)

unknown

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	unknown	unknown	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 Baylor Genetics, SCV004203353.1

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

Last Updated: Oct 13, 2024

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