chr19-605985-A-G

Position:

• chr19-605985-A-G

Variant summary

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

The NM_001194.4(HCN2):​c.1218+763A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.618 in 148,552 control chromosomes in the GnomAD database, including 29,412 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 0.62 (29412 hom., cov: 34)
• Consequence: HCN2 NM_001194.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -2.66

Genes affected

HCN2 (HGNC:4846): (hyperpolarization activated cyclic nucleotide gated potassium and sodium channel 2) The protein encoded by this gene is a hyperpolarization-activated cation channel involved in the generation of native pacemaker activity in the heart and in the brain. The encoded protein is activated by cAMP and can produce a fast, large current. Defects in this gene were noted as a possible cause of some forms of epilepsy. [provided by RefSeq, Jan 2017]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.91).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.78 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
HCN2	NM_001194.4	c.1218+763A>G		intron_variant		ENST00000251287.3	NP_001185.3

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
HCN2	ENST00000251287.3	c.1218+763A>G		intron_variant		1	NM_001194.4	ENSP00000251287	P1

Frequencies

GnomAD3 genomes AF: 0.618 AC: 91777 AN: 148428 Hom.: 29376 Cov.: 34

Gnomad AFR AF: 0.727

Gnomad AMI AF: 0.458

Gnomad AMR AF: 0.703

Gnomad ASJ AF: 0.479

Gnomad EAS AF: 0.800

Gnomad SAS AF: 0.708

Gnomad FIN AF: 0.383

Gnomad MID AF: 0.583

Gnomad NFE AF: 0.563

Gnomad OTH AF: 0.631

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

GnomAD4 genome AF: 0.618 AC: 91864 AN: 148552 Hom.: 29412 Cov.: 34 AF XY: 0.615 AC XY: 44611 AN XY: 72596

Gnomad4 AFR AF: 0.727

Gnomad4 AMR AF: 0.703

Gnomad4 ASJ AF: 0.479

Gnomad4 EAS AF: 0.801

Gnomad4 SAS AF: 0.707

Gnomad4 FIN AF: 0.383

Gnomad4 NFE AF: 0.563

Gnomad4 OTH AF: 0.633

Alfa AF: 0.579 Hom.: 18385

Bravo AF: 0.654

Asia WGS AF: 0.725 AC: 2475 AN: 3426

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
CADD	Benign	1.2
DANN	Benign	0.18

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

Publications

LitVar

Other links and lift over

dbSNP: rs7255568; hg19: chr19-605985;