NM_018981.4:c.2265+3992G>A

Variant names:

• chr2-182766793-G-A
• rs288293
• NM_018981.4:c.2265+3992G>A

Variant summary

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

The NM_018981.4(DNAJC10):​c.2265+3992G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.644 in 151,888 control chromosomes in the GnomAD database, including 31,876 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 0.64 (31876 hom., cov: 30)
• Consequence: DNAJC10 NM_018981.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.11
• Publications: 2 publications found

Genes affected

DNAJC10 (HGNC:24637): (DnaJ heat shock protein family (Hsp40) member C10) This gene encodes an endoplasmic reticulum co-chaperone which is part of the endoplasmic reticulum-associated degradation complex involved in recognizing and degrading misfolded proteins. The encoded protein reduces incorrect disulfide bonds in misfolded glycoproteins. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Oct 2012]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.03).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.697 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_018981.4. 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
	DNAJC10	NM_018981.4	MANE Select	c.2265+3992G>A		intron	N/A	NP_061854.1
	DNAJC10	NM_001271581.3		c.2127+3992G>A		intron	N/A	NP_001258510.1
	DNAJC10	NR_073365.2		n.3449+3992G>A		intron	N/A

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	DNAJC10	ENST00000264065.12	TSL:1 MANE Select	c.2265+3992G>A		intron	N/A	ENSP00000264065.6
	DNAJC10	ENST00000616986.5	TSL:1	c.2127+3992G>A		intron	N/A	ENSP00000479930.1
	DNAJC10	ENST00000418559.6	TSL:1	n.*1330+3992G>A		intron	N/A	ENSP00000389483.1

Frequencies

GnomAD3 genomes AF: 0.645 AC: 97824 AN: 151770 Hom.: 31853 Cov.: 30

Gnomad AFR AF: 0.704

Gnomad AMI AF: 0.569

Gnomad AMR AF: 0.567

Gnomad ASJ AF: 0.780

Gnomad EAS AF: 0.502

Gnomad SAS AF: 0.639

Gnomad FIN AF: 0.625

Gnomad MID AF: 0.718

Gnomad NFE AF: 0.633

Gnomad OTH AF: 0.676

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

GnomAD4 genome AF: 0.644 AC: 97883 AN: 151888 Hom.: 31876 Cov.: 30 AF XY: 0.641 AC XY: 47632 AN XY: 74264

African (AFR) AF: 0.704 AC: 29139 AN: 41418

American (AMR) AF: 0.566 AC: 8638 AN: 15250

Ashkenazi Jewish (ASJ) AF: 0.780 AC: 2705 AN: 3470

East Asian (EAS) AF: 0.503 AC: 2586 AN: 5140

South Asian (SAS) AF: 0.639 AC: 3080 AN: 4820

European-Finnish (FIN) AF: 0.625 AC: 6591 AN: 10554

Middle Eastern (MID) AF: 0.731 AC: 215 AN: 294

European-Non Finnish (NFE) AF: 0.633 AC: 42992 AN: 67922

Other (OTH) AF: 0.673 AC: 1418 AN: 2108

Alfa AF: 0.613 Hom.: 11858

Bravo AF: 0.638

Asia WGS AF: 0.587 AC: 2047 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
CADD	Benign	0.74
DANN	Benign	0.65
PhyloP100		-1.1
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: rs288293; hg19: chr2-183631520;