NM_000794.5:c.*863A>G

Variant names:

• chr5-175440896-T-C
• rs4867798
• NM_000794.5:c.*863A>G

Variant summary

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

The NM_000794.5(DRD1):​c.*863A>G variant causes a 3 prime UTR change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.312 in 152,422 control chromosomes in the GnomAD database, including 7,613 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 0.31 (7600 hom., cov: 33)
  • Exomes 𝑓: 0.34 (13 hom.)
• Consequence: DRD1 NM_000794.5 3_prime_UTR
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.28
• Publications: 47 publications found

Genes affected

DRD1 (HGNC:3020): (dopamine receptor D1) This gene encodes the D1 subtype of the dopamine receptor. The D1 subtype is the most abundant dopamine receptor in the central nervous system. This G-protein coupled receptor stimulates adenylyl cyclase and activates cyclic AMP-dependent protein kinases. D1 receptors regulate neuronal growth and development, mediate some behavioral responses, and modulate dopamine receptor D2-mediated events. Alternate transcription initiation sites result in two transcript variants of this gene. [provided by RefSeq, Jul 2008]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.83).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.454 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_000794.5. 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
	DRD1	NM_000794.5	MANE Select	c.*863A>G		3_prime_UTR	Exon 2 of 2	NP_000785.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	DRD1	ENST00000393752.3	TSL:2 MANE Select	c.*863A>G		3_prime_UTR	Exon 2 of 2	ENSP00000377353.1

Frequencies

GnomAD3 genomes AF: 0.312 AC: 47469 AN: 152032 Hom.: 7601 Cov.: 33

Gnomad AFR AF: 0.295

Gnomad AMI AF: 0.243

Gnomad AMR AF: 0.318

Gnomad ASJ AF: 0.388

Gnomad EAS AF: 0.471

Gnomad SAS AF: 0.303

Gnomad FIN AF: 0.355

Gnomad MID AF: 0.418

Gnomad NFE AF: 0.299

Gnomad OTH AF: 0.326

GnomAD4 exome AF: 0.342 AC: 93 AN: 272 Hom.: 13 Cov.: 0 AF XY: 0.360 AC XY: 59 AN XY: 164

African (AFR) AC: 0 AN: 0

American (AMR) AC: 0 AN: 0

Ashkenazi Jewish (ASJ) AC: 0 AN: 0

East Asian (EAS) AC: 0 AN: 0

South Asian (SAS) AC: 0 AN: 0

European-Finnish (FIN) AF: 0.343 AC: 92 AN: 268

Middle Eastern (MID) AC: 0 AN: 0

European-Non Finnish (NFE) AC: 0 AN: 0

Other (OTH) AF: 0.250 AC: 1 AN: 4

GnomAD4 genome AF: 0.312 AC: 47483 AN: 152150 Hom.: 7600 Cov.: 33 AF XY: 0.314 AC XY: 23377 AN XY: 74372

African (AFR) AF: 0.295 AC: 12250 AN: 41506

American (AMR) AF: 0.318 AC: 4858 AN: 15286

Ashkenazi Jewish (ASJ) AF: 0.388 AC: 1348 AN: 3472

East Asian (EAS) AF: 0.469 AC: 2431 AN: 5180

South Asian (SAS) AF: 0.303 AC: 1461 AN: 4824

European-Finnish (FIN) AF: 0.355 AC: 3766 AN: 10604

Middle Eastern (MID) AF: 0.425 AC: 125 AN: 294

European-Non Finnish (NFE) AF: 0.299 AC: 20327 AN: 67966

Other (OTH) AF: 0.330 AC: 695 AN: 2106

Alfa AF: 0.312 Hom.: 16718

Bravo AF: 0.316

Asia WGS AF: 0.380 AC: 1322 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.83
CADD	Benign	6.5
DANN	Benign	0.78
PhyloP100		1.3
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: rs4867798; hg19: chr5-174867899;