NM_000287.4(PEX6):c.406delinsAT (p.Pro136fs) AND multiple conditions

Germline classification:: Likely pathogenic (1 submission)
Last evaluated:: Apr 4, 2018
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:: RCV000673737.1

Allele description [Variation Report for NM_000287.4(PEX6):c.406delinsAT (p.Pro136fs)]

NM_000287.4(PEX6):c.406delinsAT (p.Pro136fs)

Gene:

PEX6:peroxisomal biogenesis factor 6 [Gene - OMIM - HGNC]

Variant type:

Indel

Cytogenetic location:

6p21.1

Genomic location:

Preferred name:

NM_000287.4(PEX6):c.406delinsAT (p.Pro136fs)

HGVS:

NC_000006.12:g.42978745delinsAT
NG_008370.1:g.5499delinsAT
NM_000287.4:c.406delinsATMANE SELECT
NM_001316313.2:c.406delinsAT
NP_000278.3:p.Pro136fs
NP_001303242.1:p.Pro136fs
NC_000006.11:g.42946483delinsAT
NM_000287.3:c.406delCinsAT
NR_133009.2:n.437delinsAT

Protein change:

P136fs

Links:

dbSNP: rs1554128488

NCBI 1000 Genomes Browser:

rs1554128488

Molecular consequence:

NM_000287.4:c.406delinsAT - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001316313.2:c.406delinsAT - frameshift variant - [Sequence Ontology: SO:0001589]
NR_133009.2:n.437delinsAT - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Name:: Peroxisome biogenesis disorder 4A (Zellweger) (PBD4A)
Synonyms:: Zellweger syndrome spectrum (PEX6-related)
Identifiers:: MONDO: MONDO:0013930; MedGen: C3553936; Orphanet: 912; OMIM: 614862

Name:: Peroxisome biogenesis disorder 4B (PBD4B)
Identifiers:: MONDO: MONDO:0013931; MedGen: C3553937; Orphanet: 44; OMIM: 614863

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000798974	Counsyl	criteria provided, single submitter (Counsyl Autosomal Recessive and X-Linked Classification Criteria (2018))	Likely pathogenic (Apr 4, 2018)	unknown	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000798974

Counsyl

criteria provided, single submitter

(Counsyl Autosomal Recessive and X-Linked Classification Criteria (2018))

Likely pathogenic
(Apr 4, 2018)

unknown

clinical testing

Citation Link

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

Details of each submission

From Counsyl, SCV000798974.1

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

Last Updated: Dec 30, 2023

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