rs2033654

Variant names:

• chr2-24880239-C-A
• rs2033654
• NM_004036.5:c.676-7520G>T

Your query was ambiguous. Multiple possible variants found:

• chr2-24880239-C-A
• chr2-24880239-C-G
• chr2-24880239-C-T

Variant summary

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

The NM_004036.5(ADCY3):​c.676-7520G>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.537 in 152,148 control chromosomes in the GnomAD database, including 24,546 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 0.54 (24546 hom., cov: 33)
• Consequence: ADCY3 NM_004036.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.399
• Publications: 21 publications found

Genes affected

ADCY3 (HGNC:234): (adenylate cyclase 3) This gene encodes adenylyl cyclase 3 which is a membrane-associated enzyme and catalyzes the formation of the secondary messenger cyclic adenosine monophosphate (cAMP). This protein appears to be widely expressed in various human tissues and may be involved in a number of physiological and pathophysiological metabolic processes. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2016]

ADCY3 Gene-Disease associations (from GenCC):

• body mass index quantitative trait locus 19

  Inheritance: AR Classification: STRONG Submitted by: Labcorp Genetics (formerly Invitae)

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.96).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.819 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
ADCY3	NM_004036.5	c.676-7520G>T		intron_variant	Intron 2 of 21	ENST00000679454.1	NP_004027.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
ADCY3	ENST00000679454.1	c.676-7520G>T		intron_variant	Intron 2 of 21		NM_004036.5	ENSP00000505261.1
ADCY3	ENST00000405392.6	c.676-7520G>T		intron_variant	Intron 1 of 20	1		ENSP00000384484.2
ADCY3	ENST00000260600.9	c.676-7520G>T		intron_variant	Intron 1 of 20	1		ENSP00000260600.5
ADCY3	ENST00000435135.5	c.676-37855G>T		intron_variant	Intron 2 of 7	5		ENSP00000389799.1

Frequencies

GnomAD3 genomes AF: 0.536 AC: 81551 AN: 152030 Hom.: 24500 Cov.: 33

Gnomad AFR AF: 0.826

Gnomad AMI AF: 0.360

Gnomad AMR AF: 0.376

Gnomad ASJ AF: 0.395

Gnomad EAS AF: 0.465

Gnomad SAS AF: 0.476

Gnomad FIN AF: 0.395

Gnomad MID AF: 0.430

Gnomad NFE AF: 0.439

Gnomad OTH AF: 0.509

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

GnomAD4 genome AF: 0.537 AC: 81649 AN: 152148 Hom.: 24546 Cov.: 33 AF XY: 0.529 AC XY: 39348 AN XY: 74376

African (AFR) AF: 0.826 AC: 34308 AN: 41524

American (AMR) AF: 0.375 AC: 5739 AN: 15294

Ashkenazi Jewish (ASJ) AF: 0.395 AC: 1370 AN: 3466

East Asian (EAS) AF: 0.466 AC: 2407 AN: 5166

South Asian (SAS) AF: 0.479 AC: 2304 AN: 4814

European-Finnish (FIN) AF: 0.395 AC: 4185 AN: 10582

Middle Eastern (MID) AF: 0.429 AC: 126 AN: 294

European-Non Finnish (NFE) AF: 0.439 AC: 29820 AN: 67984

Other (OTH) AF: 0.503 AC: 1062 AN: 2112

Alfa AF: 0.489 Hom.: 22899

Bravo AF: 0.544

Asia WGS AF: 0.472 AC: 1641 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.96
CADD	Benign	2.2
DANN	Benign	0.45
PhyloP100		0.40
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: rs2033654; hg19: chr2-25103108;