rs481453

Positions:

• chr1-10612878-A-G

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_004565.3(PEX14):​c.299-5454A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.212 in 152,208 control chromosomes in the GnomAD database, including 4,470 homozygotes. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: 𝑓 0.21 (4470 hom., cov: 33)
• Consequence: PEX14 NM_004565.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.435

Genes affected

PEX14 (HGNC:8856): (peroxisomal biogenesis factor 14) This gene encodes an essential component of the peroxisomal import machinery. The protein is integrated into peroxisome membranes with its C-terminus exposed to the cytosol, and interacts with the cytosolic receptor for proteins containing a PTS1 peroxisomal targeting signal. The protein also functions as a transcriptional corepressor and interacts with a histone deacetylase. A mutation in this gene results in one form of Zellweger syndrome. [provided by RefSeq, Jul 2008]

(HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.92).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.391 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
PEX14	NM_004565.3	c.299-5454A>G		intron_variant		ENST00000356607.9	NP_004556.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
PEX14	ENST00000356607.9	c.299-5454A>G		intron_variant		1	NM_004565.3	ENSP00000349016	P1
	ENST00000663738.1	n.2220T>C		non_coding_transcript_exon_variant	2/2
PEX14	ENST00000491661.2	c.284-5454A>G		intron_variant		2		ENSP00000465473

Frequencies

GnomAD3 genomes AF: 0.212 AC: 32255 AN: 152090 Hom.: 4458 Cov.: 33

Gnomad AFR AF: 0.396

Gnomad AMI AF: 0.144

Gnomad AMR AF: 0.146

Gnomad ASJ AF: 0.202

Gnomad EAS AF: 0.121

Gnomad SAS AF: 0.193

Gnomad FIN AF: 0.178

Gnomad MID AF: 0.253

Gnomad NFE AF: 0.130

Gnomad OTH AF: 0.198

We have no GnomAD4 exomes data on this position. Probably position not covered by the project.

GnomAD4 genome AF: 0.212 AC: 32308 AN: 152208 Hom.: 4470 Cov.: 33 AF XY: 0.213 AC XY: 15886 AN XY: 74420

Gnomad4 AFR AF: 0.396

Gnomad4 AMR AF: 0.146

Gnomad4 ASJ AF: 0.202

Gnomad4 EAS AF: 0.122

Gnomad4 SAS AF: 0.194

Gnomad4 FIN AF: 0.178

Gnomad4 NFE AF: 0.130

Gnomad4 OTH AF: 0.196

Alfa AF: 0.145 Hom.: 1960

Bravo AF: 0.214

Asia WGS AF: 0.151 AC: 526 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.92
CADD	Benign	5.6
DANN	Benign	0.37

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: rs481453; hg19: chr1-10672935;