5-7634119-G-C

Variant names:

• chr5-7634119-G-C
• rs1544938
• NM_020546.3:c.720+7803G>C

Variant summary

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

The NM_020546.3(ADCY2):​c.720+7803G>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.15 in 151,992 control chromosomes in the GnomAD database, including 2,100 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 0.15 (2100 hom., cov: 32)
• Consequence: ADCY2 NM_020546.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.906
• Publications: 4 publications found

Genes affected

ADCY2 (HGNC:233): (adenylate cyclase 2) This gene encodes a member of the family of adenylate cyclases, which are membrane-associated enzymes that catalyze the formation of the secondary messenger cyclic adenosine monophosphate (cAMP). This enzyme is insensitive to Ca(2+)/calmodulin, and is stimulated by the G protein beta and gamma subunit complex. [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=-0.92).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.423 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_020546.3. 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
	ADCY2	NM_020546.3	MANE Select	c.720+7803G>C		intron	N/A	NP_065433.2

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ADCY2	ENST00000338316.9	TSL:1 MANE Select	c.720+7803G>C		intron	N/A	ENSP00000342952.4
	ADCY2	ENST00000515681.1	TSL:4	c.87+7803G>C		intron	N/A	ENSP00000425069.1
	ADCY2	ENST00000498598.1	TSL:5	n.419+7803G>C		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.150 AC: 22752 AN: 151874 Hom.: 2097 Cov.: 32

Gnomad AFR AF: 0.0941

Gnomad AMI AF: 0.212

Gnomad AMR AF: 0.161

Gnomad ASJ AF: 0.277

Gnomad EAS AF: 0.438

Gnomad SAS AF: 0.0948

Gnomad FIN AF: 0.162

Gnomad MID AF: 0.190

Gnomad NFE AF: 0.153

Gnomad OTH AF: 0.170

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

GnomAD4 genome AF: 0.150 AC: 22758 AN: 151992 Hom.: 2100 Cov.: 32 AF XY: 0.151 AC XY: 11226 AN XY: 74298

African (AFR) AF: 0.0940 AC: 3897 AN: 41468

American (AMR) AF: 0.161 AC: 2464 AN: 15262

Ashkenazi Jewish (ASJ) AF: 0.277 AC: 960 AN: 3466

East Asian (EAS) AF: 0.438 AC: 2260 AN: 5158

South Asian (SAS) AF: 0.0950 AC: 457 AN: 4808

European-Finnish (FIN) AF: 0.162 AC: 1716 AN: 10562

Middle Eastern (MID) AF: 0.197 AC: 58 AN: 294

European-Non Finnish (NFE) AF: 0.153 AC: 10395 AN: 67954

Other (OTH) AF: 0.170 AC: 358 AN: 2110

Alfa AF: 0.0751 Hom.: 107

Bravo AF: 0.153

Asia WGS AF: 0.257 AC: 892 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.92
CADD	Benign	0.70
DANN	Benign	0.64
PhyloP100		0.91
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: rs1544938; hg19: chr5-7634232;