rs9525570

Variant names:

• chr13-42100870-T-C
• rs9525570
• NM_178009.5:c.193-26593T>C

Variant summary

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

The NM_178009.5(DGKH):​c.193-26593T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.135 in 152,234 control chromosomes in the GnomAD database, including 1,592 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 0.14 (1592 hom., cov: 32)
• Consequence: DGKH NM_178009.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.0600
• Publications: 0 publications found

Genes affected

DGKH (HGNC:2854): (diacylglycerol kinase eta) This gene encodes a member of the diacylglycerol kinase (DGK) enzyme family. Members of this family are involved in regulating intracellular concentrations of diacylglycerol and phosphatidic acid. Variation in this gene has been associated with bipolar disorder. Alternatively spliced transcript variants have been identified. [provided by RefSeq, Jul 2014]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.55).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.174 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_178009.5. 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
	DGKH	NM_178009.5	MANE Select	c.193-26593T>C		intron	N/A	NP_821077.1	Q86XP1-1
	DGKH	NM_001204504.3		c.193-26593T>C		intron	N/A	NP_001191433.1	Q86XP1-2
	DGKH	NM_152910.6		c.193-26593T>C		intron	N/A	NP_690874.2

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	DGKH	ENST00000337343.9	TSL:1 MANE Select	c.193-26593T>C		intron	N/A	ENSP00000337572.4	Q86XP1-1
	DGKH	ENST00000261491.9	TSL:1	c.193-26593T>C		intron	N/A	ENSP00000261491.4	Q86XP1-2
	DGKH	ENST00000916518.1		c.193-26593T>C		intron	N/A	ENSP00000586577.1

Frequencies

GnomAD3 genomes AF: 0.135 AC: 20604 AN: 152116 Hom.: 1590 Cov.: 32

Gnomad AFR AF: 0.0848

Gnomad AMI AF: 0.138

Gnomad AMR AF: 0.153

Gnomad ASJ AF: 0.172

Gnomad EAS AF: 0.0868

Gnomad SAS AF: 0.184

Gnomad FIN AF: 0.0991

Gnomad MID AF: 0.158

Gnomad NFE AF: 0.165

Gnomad OTH AF: 0.174

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

GnomAD4 genome AF: 0.135 AC: 20622 AN: 152234 Hom.: 1592 Cov.: 32 AF XY: 0.135 AC XY: 10028 AN XY: 74450

African (AFR) AF: 0.0850 AC: 3530 AN: 41546

American (AMR) AF: 0.153 AC: 2337 AN: 15282

Ashkenazi Jewish (ASJ) AF: 0.172 AC: 598 AN: 3470

East Asian (EAS) AF: 0.0866 AC: 449 AN: 5182

South Asian (SAS) AF: 0.184 AC: 890 AN: 4832

European-Finnish (FIN) AF: 0.0991 AC: 1051 AN: 10606

Middle Eastern (MID) AF: 0.163 AC: 48 AN: 294

European-Non Finnish (NFE) AF: 0.165 AC: 11222 AN: 68004

Other (OTH) AF: 0.176 AC: 371 AN: 2108

Alfa AF: 0.164 Hom.: 3544

Bravo AF: 0.138

Asia WGS AF: 0.132 AC: 459 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.55
CADD	Benign	12
DANN	Benign	0.94
PhyloP100		-0.060
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: rs9525570; hg19: chr13-42675006;