chr1-34868798-G-A

Variant names:

• chr1-34868798-G-A
• rs201441073
• NM_001080418.3:c.2292C>T

Variant summary

Our verdict is Benign. The variant received -21 ACMG points: 0P and 21B. BP4_Strong BP6_Very_Strong BP7 BS1 BS2

The NM_001080418.3(DLGAP3):​c.2292C>T​(p.Pro764Pro) variant causes a synonymous change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00128 in 1,582,906 control chromosomes in the GnomAD database, including 17 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★★).

• Frequency:
  • Genomes: 𝑓 0.0064 (9 hom., cov: 32)
  • Exomes 𝑓: 0.00074 (8 hom.)
• Consequence: DLGAP3 NM_001080418.3 synonymous
• Clinical Significance: Benign criteria provided, multiple submitters, no conflicts B:2
• Conservation: PhyloP100: -2.52
• Publications: 0 publications found

Genes affected

DLGAP3 (HGNC:30368): (DLG associated protein 3) Predicted to enable PDZ domain binding activity; molecular adaptor activity; and scaffold protein binding activity. Predicted to be involved in protein-containing complex assembly and regulation of postsynaptic neurotransmitter receptor activity. Predicted to be located in synapse. Predicted to be part of postsynaptic density. Predicted to be active in several cellular components, including cholinergic synapse; glutamatergic synapse; and neuromuscular junction. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Our verdict: Benign. The variant received -21 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.73).
• BP6: Variant 1-34868798-G-A is Benign according to our data. Variant chr1-34868798-G-A is described in ClinVar as Benign. ClinVar VariationId is 786723.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars.
• BP7: Synonymous conserved (PhyloP=-2.52 with no splicing effect.
• BS1: Variant frequency is greater than expected in population afr. GnomAd4 allele frequency = 0.00637 (969/152220) while in subpopulation AFR AF = 0.0219 (911/41552). AF 95% confidence interval is 0.0207. There are 9 homozygotes in GnomAd4. There are 481 alleles in the male GnomAd4 subpopulation. Median coverage is 32. This position passed quality control check.
• BS2: High Homozygotes in GnomAd4 at 9 gene

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001080418.3. 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
	DLGAP3	NM_001080418.3	MANE Select	c.2292C>T	p.Pro764Pro	synonymous	Exon 9 of 12	NP_001073887.1	O95886

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	DLGAP3	ENST00000373347.6	TSL:5 MANE Select	c.2292C>T	p.Pro764Pro	synonymous	Exon 9 of 12	ENSP00000362444.1	O95886
	DLGAP3	ENST00000235180.4	TSL:2	c.2292C>T	p.Pro764Pro	synonymous	Exon 7 of 10	ENSP00000235180.4	O95886

Frequencies

GnomAD3 genomes AF: 0.00636 AC: 968 AN: 152108 Hom.: 9 Cov.: 32

Gnomad AFR AF: 0.0219

Gnomad AMI AF: 0.00

Gnomad AMR AF: 0.00164

Gnomad ASJ AF: 0.00144

Gnomad EAS AF: 0.00

Gnomad SAS AF: 0.000207

Gnomad FIN AF: 0.00

Gnomad MID AF: 0.00318

Gnomad NFE AF: 0.000265

Gnomad OTH AF: 0.00430

GnomAD2 exomes AF: 0.00170 AC: 345 AN: 203030 AF XY: 0.00129

Gnomad AFR exome AF: 0.0241

Gnomad AMR exome AF: 0.00112

Gnomad ASJ exome AF: 0.000791

Gnomad EAS exome AF: 0.0000608

Gnomad FIN exome AF: 0.00

Gnomad NFE exome AF: 0.000144

Gnomad OTH exome AF: 0.00133

GnomAD4 exome AF: 0.000735 AC: 1052 AN: 1430686 Hom.: 8 Cov.: 32 AF XY: 0.000682 AC XY: 484 AN XY: 709638

African (AFR) AF: 0.0227 AC: 749 AN: 33044

American (AMR) AF: 0.00113 AC: 49 AN: 43228

Ashkenazi Jewish (ASJ) AF: 0.00129 AC: 33 AN: 25538

East Asian (EAS) AF: 0.0000256 AC: 1 AN: 39040

South Asian (SAS) AF: 0.000106 AC: 9 AN: 84514

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 39460

Middle Eastern (MID) AF: 0.00161 AC: 9 AN: 5574

European-Non Finnish (NFE) AF: 0.0000926 AC: 102 AN: 1100972

Other (OTH) AF: 0.00169 AC: 100 AN: 59316

GnomAD4 genome AF: 0.00637 AC: 969 AN: 152220 Hom.: 9 Cov.: 32 AF XY: 0.00646 AC XY: 481 AN XY: 74430

African (AFR) AF: 0.0219 AC: 911 AN: 41552

American (AMR) AF: 0.00163 AC: 25 AN: 15298

Ashkenazi Jewish (ASJ) AF: 0.00144 AC: 5 AN: 3470

East Asian (EAS) AF: 0.00 AC: 0 AN: 5170

South Asian (SAS) AF: 0.000207 AC: 1 AN: 4824

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 10606

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 292

European-Non Finnish (NFE) AF: 0.000265 AC: 18 AN: 67982

Other (OTH) AF: 0.00426 AC: 9 AN: 2114

Alfa AF: 0.00108 Hom.: 1

Bravo AF: 0.00688

Asia WGS AF: 0.000577 AC: 2 AN: 3478

ClinVar

ClinVar submissions

Significance: Benign

Revision: criteria provided, multiple submitters, no conflicts

Pathogenic	VUS	Benign	Condition
-	-	2	not provided (2)

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.73
CADD	Benign	0.92
DANN	Benign	0.83
PhyloP100		-2.5
Mutation Taster		=100/0	polymorphism

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: rs201441073; hg19: chr1-35334399;