15-53514585-T-C

Variant summary

Our verdict is Benign. Variant got -14 ACMG points: 0P and 14B. BP4_Strong BP6_Moderate BA1

The NM_182758.4(WDR72):c.*3114A>G variant causes a 3 prime UTR change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.091 in 152,170 control chromosomes in the GnomAD database, including 720 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Likely benign (★).

• Frequency:
  • Genomes: 𝑓 0.091 (720 hom., cov: 32)
  • Failed GnomAD Quality Control
• Consequence: WDR72 NM_182758.4 3_prime_UTR
• Clinical Significance: Likely benign criteria provided, single submitter B:1
• Conservation: PhyloP100: 0.499

Genes affected

WDR72 (HGNC:26790): (WD repeat domain 72) This gene encodes a protein with eight WD-40 repeats. Mutations in this gene have been associated with amelogenesis imperfecta hypomaturation type 2A3. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2013]

LOC105370826 (HGNC:):

ACMG classification

Verdict is Benign. Variant got -14 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.88).
• BP6: Variant 15-53514585-T-C is Benign according to our data. Variant chr15-53514585-T-C is described in ClinVar as [Likely_benign]. Clinvar id is 316499.Status of the report is criteria_provided_single_submitter, 1 stars.
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.111 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
WDR72	NM_182758.4	c.*3114A>G		3_prime_UTR_variant	20/20	ENST00000360509.10
LOC105370826	XR_007064645.1	n.256-186T>C		intron_variant, non_coding_transcript_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
WDR72	ENST00000360509.10	c.*3114A>G		3_prime_UTR_variant	20/20	1	NM_182758.4	P4
WDR72	ENST00000396328.5	c.*3114A>G		3_prime_UTR_variant	20/20	1		P4
WDR72	ENST00000567224.1	n.3489A>G		non_coding_transcript_exon_variant	3/3	1
WDR72	ENST00000614174.4	c.*3114A>G		3_prime_UTR_variant	3/3	2

Frequencies

GnomAD3 genomes AF: 0.0911 AC: 13851 AN: 152056 Hom.: 719 Cov.: 32

Gnomad AFR AF: 0.0462

Gnomad AMI AF: 0.0758

Gnomad AMR AF: 0.0999

Gnomad ASJ AF: 0.0664

Gnomad EAS AF: 0.0873

Gnomad SAS AF: 0.0961

Gnomad FIN AF: 0.124

Gnomad MID AF: 0.0510

Gnomad NFE AF: 0.113

Gnomad OTH AF: 0.0865

GnomAD4 exome Data not reliable, filtered out with message: AC0 AC: 0 AN: 0 Hom.: 0 Cov.: 0 AC XY: 0 AN XY: 0

GnomAD4 genome AF: 0.0910 AC: 13846 AN: 152170 Hom.: 720 Cov.: 32 AF XY: 0.0915 AC XY: 6809 AN XY: 74398

Gnomad4 AFR AF: 0.0461

Gnomad4 AMR AF: 0.0997

Gnomad4 ASJ AF: 0.0664

Gnomad4 EAS AF: 0.0871

Gnomad4 SAS AF: 0.0962

Gnomad4 FIN AF: 0.124

Gnomad4 NFE AF: 0.113

Gnomad4 OTH AF: 0.0870

Alfa AF: 0.0776 Hom.: 121

Bravo AF: 0.0868

ClinVar

Significance: Likely benign

Submissions summary: Benign:1

Revision: criteria provided, single submitter

Submissions by phenotype

Amelogenesis Imperfecta, Recessive Benign:1

Likely benign, criteria provided, single submitter

clinical testing

Illumina Laboratory Services, Illumina

Jun 14, 2016

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Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.88
Cadd	Benign	1.8
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: rs72745122; hg19: chr15-53806782;