rs163030

Positions:

• chr5-77485646-A-C
• chr5-77485646-A-G
• chr5-77485646-A-T

Variant summary

Our verdict is Benign. Variant got -10 ACMG points: 0P and 10B. BP4_Moderate BA1

The NM_018268.4(WDR41):​c.167+3811T>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.627 in 152,106 control chromosomes in the GnomAD database, including 31,500 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 0.63 (31500 hom., cov: 32)
• Consequence: WDR41 NM_018268.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.448

Genes affected

WDR41 (HGNC:25601): (WD repeat domain 41) Contributes to guanyl-nucleotide exchange factor activity. Involved in regulation of autophagy. Located in cytoplasm. Part of guanyl-nucleotide exchange factor complex. Colocalizes with Atg1/ULK1 kinase complex. [provided by Alliance of Genome Resources, Apr 2022]

WDR41 (HGNC:):

ACMG classification

Verdict is Benign. Variant got -10 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.33).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.826 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
WDR41	NM_018268.4	c.167+3811T>G		intron_variant		ENST00000296679.9	NP_060738.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
WDR41	ENST00000296679.9	c.167+3811T>G		intron_variant		1	NM_018268.4	ENSP00000296679.4

Frequencies

GnomAD3 genomes AF: 0.627 AC: 95329 AN: 151988 Hom.: 31448 Cov.: 32

Gnomad AFR AF: 0.833

Gnomad AMI AF: 0.590

Gnomad AMR AF: 0.673

Gnomad ASJ AF: 0.717

Gnomad EAS AF: 0.592

Gnomad SAS AF: 0.656

Gnomad FIN AF: 0.485

Gnomad MID AF: 0.668

Gnomad NFE AF: 0.510

Gnomad OTH AF: 0.633

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

GnomAD4 genome AF: 0.627 AC: 95439 AN: 152106 Hom.: 31500 Cov.: 32 AF XY: 0.627 AC XY: 46614 AN XY: 74344

Gnomad4 AFR AF: 0.833

Gnomad4 AMR AF: 0.673

Gnomad4 ASJ AF: 0.717

Gnomad4 EAS AF: 0.592

Gnomad4 SAS AF: 0.656

Gnomad4 FIN AF: 0.485

Gnomad4 NFE AF: 0.510

Gnomad4 OTH AF: 0.632

Alfa AF: 0.537 Hom.: 32744

Bravo AF: 0.656

Asia WGS AF: 0.628 AC: 2186 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.33
CADD	Benign	17
DANN	Benign	0.70

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: rs163030; hg19: chr5-76781471;