16-84399428-C-T

Position:

• chr16-84399428-C-T

Variant summary

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

The NM_014861.4(ATP2C2):​c.210+819C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.467 in 152,034 control chromosomes in the GnomAD database, including 17,421 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 0.47 (17421 hom., cov: 33)
• Consequence: ATP2C2 NM_014861.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.90

Genes affected

ATP2C2 (HGNC:29103): (ATPase secretory pathway Ca2+ transporting 2) Enables P-type calcium transporter activity and P-type manganese transporter activity. Predicted to be involved in calcium ion transmembrane transport; cellular calcium ion homeostasis; and manganese ion transport. Predicted to act upstream of or within mammary gland epithelium development; positive regulation of calcium ion import; and protein localization to plasma membrane. Predicted to be located in trans-Golgi network membrane. Predicted to be active in Golgi membrane; endoplasmic reticulum; and plasma membrane. Predicted to be integral component of membrane. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.05).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.595 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
ATP2C2	NM_014861.4	c.210+819C>T		intron_variant		ENST00000262429.9	NP_055676.3
ATP2C2	NM_001286527.3	c.210+819C>T		intron_variant			NP_001273456.2
ATP2C2	XM_011523486.3	c.141+819C>T		intron_variant			XP_011521788.1
ATP2C2	XM_047434994.1	c.141+819C>T		intron_variant			XP_047290950.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
ATP2C2	ENST00000262429.9	c.210+819C>T		intron_variant		1	NM_014861.4	ENSP00000262429.4
ATP2C2	ENST00000416219.6	c.210+819C>T		intron_variant		1		ENSP00000397925.2

Frequencies

GnomAD3 genomes AF: 0.467 AC: 70914 AN: 151916 Hom.: 17410 Cov.: 33

Gnomad AFR AF: 0.316

Gnomad AMI AF: 0.586

Gnomad AMR AF: 0.590

Gnomad ASJ AF: 0.679

Gnomad EAS AF: 0.455

Gnomad SAS AF: 0.612

Gnomad FIN AF: 0.443

Gnomad MID AF: 0.576

Gnomad NFE AF: 0.511

Gnomad OTH AF: 0.520

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

GnomAD4 genome AF: 0.467 AC: 70950 AN: 152034 Hom.: 17421 Cov.: 33 AF XY: 0.468 AC XY: 34769 AN XY: 74310

Gnomad4 AFR AF: 0.316

Gnomad4 AMR AF: 0.590

Gnomad4 ASJ AF: 0.679

Gnomad4 EAS AF: 0.455

Gnomad4 SAS AF: 0.613

Gnomad4 FIN AF: 0.443

Gnomad4 NFE AF: 0.511

Gnomad4 OTH AF: 0.520

Alfa AF: 0.516 Hom.: 41031

Bravo AF: 0.475

Asia WGS AF: 0.513 AC: 1786 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.1
CADD	Benign	0.0070
DANN	Benign	0.67

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: rs922450; hg19: chr16-84433034;