rs10763984

Variant names:

• chr10-34369919-C-T
• rs10763984
• NM_001184785.2:c.1707+2579G>A

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_001184785.2(PARD3):​c.1707+2579G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.593 in 152,036 control chromosomes in the GnomAD database, including 28,778 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 0.59 (28778 hom., cov: 31)
• Consequence: PARD3 NM_001184785.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.254
• Publications: 2 publications found

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

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.93).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.843 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001184785.2. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	PARD3	NM_001184785.2	MANE Select	c.1707+2579G>A		intron	N/A	NP_001171714.1	Q8TEW0-2
	PARD3	NM_019619.4		c.1707+2579G>A		intron	N/A	NP_062565.2
	PARD3	NM_001184786.2		c.1668+4955G>A		intron	N/A	NP_001171715.1	Q8TEW0-11

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	PARD3	ENST00000374788.8	TSL:1 MANE Select	c.1707+2579G>A		intron	N/A	ENSP00000363920.3	Q8TEW0-2
	PARD3	ENST00000374789.8	TSL:1	c.1707+2579G>A		intron	N/A	ENSP00000363921.3	Q8TEW0-1
	PARD3	ENST00000545693.5	TSL:1	c.1668+4955G>A		intron	N/A	ENSP00000443147.1	Q8TEW0-11

Frequencies

GnomAD3 genomes AF: 0.593 AC: 90032 AN: 151918 Hom.: 28712 Cov.: 31

Gnomad AFR AF: 0.850

Gnomad AMI AF: 0.426

Gnomad AMR AF: 0.529

Gnomad ASJ AF: 0.543

Gnomad EAS AF: 0.488

Gnomad SAS AF: 0.581

Gnomad FIN AF: 0.517

Gnomad MID AF: 0.484

Gnomad NFE AF: 0.477

Gnomad OTH AF: 0.557

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

GnomAD4 genome AF: 0.593 AC: 90160 AN: 152036 Hom.: 28778 Cov.: 31 AF XY: 0.594 AC XY: 44143 AN XY: 74286

African (AFR) AF: 0.850 AC: 35286 AN: 41512

American (AMR) AF: 0.529 AC: 8074 AN: 15274

Ashkenazi Jewish (ASJ) AF: 0.543 AC: 1884 AN: 3472

East Asian (EAS) AF: 0.488 AC: 2518 AN: 5162

South Asian (SAS) AF: 0.580 AC: 2793 AN: 4812

European-Finnish (FIN) AF: 0.517 AC: 5446 AN: 10534

Middle Eastern (MID) AF: 0.503 AC: 148 AN: 294

European-Non Finnish (NFE) AF: 0.477 AC: 32447 AN: 67958

Other (OTH) AF: 0.558 AC: 1176 AN: 2108

Alfa AF: 0.554 Hom.: 4084

Bravo AF: 0.605

Asia WGS AF: 0.566 AC: 1970 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.93
CADD	Benign	0.62
DANN	Benign	0.79
PhyloP100		-0.25
Mutation Taster		=100/0	polymorphism (auto)

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

Other links and lift over

dbSNP: rs10763984; hg19: chr10-34658847;