rs1441027

Positions:

• chr10-34294769-G-A
• chr10-34294769-G-T

Variant summary

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

The NM_001184785.2(PARD3):​c.3066-10524C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.489 in 151,970 control chromosomes in the GnomAD database, including 18,269 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 0.49 (18269 hom., cov: 32)
• Consequence: PARD3 NM_001184785.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.833

Genes affected

PARD3 (HGNC:16051): (par-3 family cell polarity regulator) This gene encodes a member of the PARD protein family. PARD family members interact with other PARD family members and other proteins; they affect asymmetrical cell division and direct polarized cell growth. Multiple alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Oct 2011]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.84).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.535 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
PARD3	NM_001184785.2	c.3066-10524C>T		intron_variant		ENST00000374788.8

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
PARD3	ENST00000374788.8	c.3066-10524C>T		intron_variant		1	NM_001184785.2	A1

Frequencies

GnomAD3 genomes AF: 0.489 AC: 74270 AN: 151850 Hom.: 18253 Cov.: 32

Gnomad AFR AF: 0.484

Gnomad AMI AF: 0.442

Gnomad AMR AF: 0.473

Gnomad ASJ AF: 0.537

Gnomad EAS AF: 0.381

Gnomad SAS AF: 0.554

Gnomad FIN AF: 0.490

Gnomad MID AF: 0.580

Gnomad NFE AF: 0.497

Gnomad OTH AF: 0.511

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

GnomAD4 genome AF: 0.489 AC: 74326 AN: 151970 Hom.: 18269 Cov.: 32 AF XY: 0.489 AC XY: 36332 AN XY: 74264

Gnomad4 AFR AF: 0.484

Gnomad4 AMR AF: 0.473

Gnomad4 ASJ AF: 0.537

Gnomad4 EAS AF: 0.382

Gnomad4 SAS AF: 0.552

Gnomad4 FIN AF: 0.490

Gnomad4 NFE AF: 0.497

Gnomad4 OTH AF: 0.512

Alfa AF: 0.499 Hom.: 18472

Bravo AF: 0.488

Asia WGS AF: 0.485 AC: 1684 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.84
CADD	Benign	4.0
DANN	Benign	0.63

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: rs1441027; hg19: chr10-34583697;