NM_015569.5:c.2522+8857A>G

Variant names:

• chr1-172397666-A-G
• rs9286854
• NM_015569.5:c.2522+8857A>G

Variant summary

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

The NM_015569.5(DNM3):​c.2522+8857A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.483 in 152,074 control chromosomes in the GnomAD database, including 20,509 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 0.48 (20509 hom., cov: 33)
• Consequence: DNM3 NM_015569.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.612
• Publications: 7 publications found

Genes affected

DNM3 (HGNC:29125): (dynamin 3) This gene encodes a member of a family of guanosine triphosphate (GTP)-binding proteins that associate with microtubules and are involved in vesicular transport. The encoded protein functions in the development of megakaryocytes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2013]

PIGC (HGNC:8960): (phosphatidylinositol glycan anchor biosynthesis class C) This gene encodes an endoplasmic reticulum associated protein that is involved in glycosylphosphatidylinositol (GPI) lipid anchor biosynthesis. The GPI lipid anchor is a glycolipid found on many blood cells and serves to anchor proteins to the cell surface. The encoded protein is one subunit of the GPI N-acetylglucosaminyl (GlcNAc) transferase that transfers GlcNAc to phosphatidylinositol (PI) on the cytoplasmic side of the endoplasmic reticulum. Two alternatively spliced transcripts that encode the same protein have been found for this gene. A pseudogene on chromosome 11 has also been characterized. [provided by RefSeq, Jul 2008]

PIGC Gene-Disease associations (from GenCC):

• glycosylphosphatidylinositol biosynthesis defect 16

  Inheritance: AR Classification: STRONG, LIMITED Submitted by: Labcorp Genetics (formerly Invitae), Ambry Genetics
• autosomal recessive non-syndromic intellectual disability

  Inheritance: AR Classification: SUPPORTIVE Submitted by: Orphanet

LOC102724528 (HGNC:):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.87).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.85 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_015569.5. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	DNM3	NM_015569.5	MANE Select	c.2522+8857A>G		intron	N/A	NP_056384.2
	DNM3	NM_001350204.2		c.2540+8857A>G		intron	N/A	NP_001337133.1
	DNM3	NM_001136127.3		c.2510+8857A>G		intron	N/A	NP_001129599.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	DNM3	ENST00000627582.3	TSL:1 MANE Select	c.2522+8857A>G		intron	N/A	ENSP00000486701.1
	DNM3	ENST00000367731.5	TSL:1	c.2510+8857A>G		intron	N/A	ENSP00000356705.1
	DNM3	ENST00000485254.3	TSL:1	c.2540+8857A>G		intron	N/A	ENSP00000429165.2

Frequencies

GnomAD3 genomes AF: 0.483 AC: 73459 AN: 151956 Hom.: 20506 Cov.: 33

Gnomad AFR AF: 0.193

Gnomad AMI AF: 0.654

Gnomad AMR AF: 0.637

Gnomad ASJ AF: 0.551

Gnomad EAS AF: 0.872

Gnomad SAS AF: 0.563

Gnomad FIN AF: 0.548

Gnomad MID AF: 0.596

Gnomad NFE AF: 0.572

Gnomad OTH AF: 0.534

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

GnomAD4 genome AF: 0.483 AC: 73481 AN: 152074 Hom.: 20509 Cov.: 33 AF XY: 0.489 AC XY: 36377 AN XY: 74326

African (AFR) AF: 0.193 AC: 8009 AN: 41492

American (AMR) AF: 0.637 AC: 9741 AN: 15286

Ashkenazi Jewish (ASJ) AF: 0.551 AC: 1911 AN: 3466

East Asian (EAS) AF: 0.871 AC: 4512 AN: 5178

South Asian (SAS) AF: 0.563 AC: 2714 AN: 4818

European-Finnish (FIN) AF: 0.548 AC: 5774 AN: 10544

Middle Eastern (MID) AF: 0.592 AC: 173 AN: 292

European-Non Finnish (NFE) AF: 0.572 AC: 38913 AN: 67974

Other (OTH) AF: 0.539 AC: 1139 AN: 2114

Alfa AF: 0.537 Hom.: 37943

Bravo AF: 0.480

Asia WGS AF: 0.691 AC: 2396 AN: 3470

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.87
CADD	Benign	0.014
DANN	Benign	0.64
PhyloP100		-0.61
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: rs9286854; hg19: chr1-172366806;