6-42964123-G-A

Position:

• chr6-42964123-G-A

Variant summary

Our verdict is Benign. Variant got -20 ACMG points: 0P and 20B. BP4_Strong BP6_Very_Strong BS1 BS2

The NM_000287.4(PEX6):​c.*212C>T variant causes a 3 prime UTR change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0277 in 612,356 control chromosomes in the GnomAD database, including 331 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Likely benign (★★).

• Frequency:
  • Genomes: 𝑓 0.023 (60 hom., cov: 32)
  • Exomes 𝑓: 0.029 (271 hom.)
• Consequence: PEX6 NM_000287.4 3_prime_UTR
• Clinical Significance: Likely benign criteria provided, multiple submitters, no conflicts B:3
• Conservation: PhyloP100: 0.113

Genes affected

PEX6 (HGNC:8859): (peroxisomal biogenesis factor 6) This gene encodes a member of the AAA (ATPases associated with diverse cellular activities) family of ATPases. This member is a predominantly cytoplasmic protein, which plays a direct role in peroxisomal protein import and is required for PTS1 (peroxisomal targeting signal 1, a C-terminal tripeptide of the sequence ser-lys-leu) receptor activity. Mutations in this gene cause peroxisome biogenesis disorders of complementation group 4 and complementation group 6. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015]

ACMG classification

Verdict is Benign. Variant got -20 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.91).
• BP6: Variant 6-42964123-G-A is Benign according to our data. Variant chr6-42964123-G-A is described in ClinVar as [Likely_benign]. Clinvar id is 356790.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars.
• BS1: Variant frequency is greater than expected in population nfe. gnomad4 allele frequency = 0.0229 (3484/152336) while in subpopulation NFE AF= 0.0337 (2290/68034). AF 95% confidence interval is 0.0325. There are 60 homozygotes in gnomad4. There are 1626 alleles in male gnomad4 subpopulation. Median coverage is 32. This position pass quality control queck.
• BS2: High Homozygotes in GnomAd4 at 60 AR gene

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
PEX6	NM_000287.4	c.*212C>T		3_prime_UTR_variant	17/17	ENST00000304611.13	NP_000278.3

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
PEX6	ENST00000304611.13	c.*212C>T		3_prime_UTR_variant	17/17	1	NM_000287.4	ENSP00000303511	P1

Frequencies

GnomAD3 genomes AF: 0.0229 AC: 3485 AN: 152218 Hom.: 60 Cov.: 32

Gnomad AFR AF: 0.00545

Gnomad AMI AF: 0.0373

Gnomad AMR AF: 0.0163

Gnomad ASJ AF: 0.0901

Gnomad EAS AF: 0.000962

Gnomad SAS AF: 0.0188

Gnomad FIN AF: 0.0217

Gnomad MID AF: 0.00949

Gnomad NFE AF: 0.0337

Gnomad OTH AF: 0.0206

GnomAD4 exome AF: 0.0293 AC: 13460 AN: 460020 Hom.: 271 Cov.: 5 AF XY: 0.0292 AC XY: 7069 AN XY: 242422

Gnomad4 AFR exome AF: 0.00534

Gnomad4 AMR exome AF: 0.0148

Gnomad4 ASJ exome AF: 0.0968

Gnomad4 EAS exome AF: 0.0000324

Gnomad4 SAS exome AF: 0.0254

Gnomad4 FIN exome AF: 0.0234

Gnomad4 NFE exome AF: 0.0324

Gnomad4 OTH exome AF: 0.0310

GnomAD4 genome AF: 0.0229 AC: 3484 AN: 152336 Hom.: 60 Cov.: 32 AF XY: 0.0218 AC XY: 1626 AN XY: 74486

Gnomad4 AFR AF: 0.00544

Gnomad4 AMR AF: 0.0163

Gnomad4 ASJ AF: 0.0901

Gnomad4 EAS AF: 0.000964

Gnomad4 SAS AF: 0.0190

Gnomad4 FIN AF: 0.0217

Gnomad4 NFE AF: 0.0337

Gnomad4 OTH AF: 0.0204

Alfa AF: 0.0279 Hom.: 10

Bravo AF: 0.0220

Asia WGS AF: 0.00924 AC: 33 AN: 3478

ClinVar

Significance: Likely benign

Submissions summary: Benign:3

Revision: criteria provided, multiple submitters, no conflicts

Submissions by phenotype

not provided Benign:2

Likely benign, criteria provided, single submitter	not provided	Breakthrough Genomics, Breakthrough Genomics	-	- -
Likely benign, criteria provided, single submitter	clinical testing	GeneDx	Mar 10, 2019	- -

Peroxisome biogenesis disorder 4A (Zellweger) Benign:1

Likely benign, criteria provided, single submitter

clinical testing

Illumina Laboratory Services, Illumina

Jan 13, 2018

This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated by ICSL or reported in the Human Gene Mutation Database (HGMD: prior to June 1st, 2018), and was therefore a candidate for classification through an automated scoring system. Utilizing variant allele frequency, disease prevalence and penetrance estimates, and inheritance mode, an automated score was calculated to assess if this variant is too frequent to cause the disease. Based on the score and internal cut-off values, a variant classified as likely benign is not then subjected to further curation. The score for this variant resulted in a classification of likely benign for this disease. -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
CADD	Benign	7.3
DANN	Benign	0.41

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.0		Details are displayed if max score is > 0.2

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

LitVar

Other links and lift over

dbSNP: rs1051218; hg19: chr6-42931861;