rs645112

chr5-79106724-C-Achr5-79106724-C-T

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The ENST00000520388.5(DMGDH):n.492-2446G>T variant causes a intron, non coding transcript change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.512 in 152,080 control chromosomes in the GnomAD database, including 21,410 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 0.51 (21410 hom., cov: 32)
• Consequence: DMGDH ENST00000520388.5 intron, non_coding_transcript
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.404

Genes affected

DMGDH (HGNC:24475): (dimethylglycine dehydrogenase) This gene encodes an enzyme involved in the catabolism of choline, catalyzing the oxidative demethylation of dimethylglycine to form sarcosine. The enzyme is found as a monomer in the mitochondrial matrix, and uses flavin adenine dinucleotide and folate as cofactors. Mutation in this gene causes dimethylglycine dehydrogenase deficiency, characterized by a fishlike body odor, chronic muscle fatigue, and elevated levels of the muscle form of creatine kinase in serum. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.89).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.593 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
DMGDH	ENST00000520388.5	n.492-2446G>T		intron_variant, non_coding_transcript_variant		4

Frequencies

GnomAD3 genomes AF: 0.512 AC: 77786 AN: 151962 Hom.: 21399 Cov.: 32

Gnomad AFR AF: 0.298

Gnomad AMI AF: 0.746

Gnomad AMR AF: 0.574

Gnomad ASJ AF: 0.434

Gnomad EAS AF: 0.610

Gnomad SAS AF: 0.503

Gnomad FIN AF: 0.666

Gnomad MID AF: 0.573

Gnomad NFE AF: 0.598

Gnomad OTH AF: 0.515

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

GnomAD4 genome AF: 0.512 AC: 77833 AN: 152080 Hom.: 21410 Cov.: 32 AF XY: 0.514 AC XY: 38233 AN XY: 74340

Gnomad4 AFR AF: 0.298

Gnomad4 AMR AF: 0.575

Gnomad4 ASJ AF: 0.434

Gnomad4 EAS AF: 0.609

Gnomad4 SAS AF: 0.505

Gnomad4 FIN AF: 0.666

Gnomad4 NFE AF: 0.598

Gnomad4 OTH AF: 0.513

Alfa AF: 0.546 Hom.: 3902

Bravo AF: 0.496

Asia WGS AF: 0.531 AC: 1850 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.89
Cadd	Benign	2.0
Dann	Benign	0.60

Splicing

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

LitVar

Other links and lift over

dbSNP: rs645112; hg19: chr5-78402547;