rs12149426

Variant names:

• chr16-84431500-C-A
• rs12149426
• NM_014861.4:c.986+5699C>A

Your query was ambiguous. Multiple possible variants found:

• chr16-84431500-C-A
• chr16-84431500-C-G
• chr16-84431500-C-T

Variant summary

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

The NM_014861.4(ATP2C2):​c.986+5699C>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.209 in 150,230 control chromosomes in the GnomAD database, including 3,429 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 0.21 (3429 hom., cov: 31)
• Consequence: ATP2C2 NM_014861.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.721
• Publications: 1 publications found

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

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.02).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.282 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
ATP2C2	NM_014861.4	c.986+5699C>A		intron_variant	Intron 11 of 26	ENST00000262429.9	NP_055676.3

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
ATP2C2	ENST00000262429.9	c.986+5699C>A		intron_variant	Intron 11 of 26	1	NM_014861.4	ENSP00000262429.4
ATP2C2	ENST00000416219.7	c.986+5699C>A		intron_variant	Intron 11 of 27	1		ENSP00000397925.2
ATP2C2	ENST00000420010.6	n.659+5699C>A		intron_variant	Intron 8 of 23	2
ATP2C2	ENST00000565631.5	n.1477+5699C>A		intron_variant	Intron 9 of 24	2

Frequencies

GnomAD3 genomes AF: 0.209 AC: 31307 AN: 150112 Hom.: 3414 Cov.: 31

Gnomad AFR AF: 0.265

Gnomad AMI AF: 0.118

Gnomad AMR AF: 0.204

Gnomad ASJ AF: 0.185

Gnomad EAS AF: 0.157

Gnomad SAS AF: 0.295

Gnomad FIN AF: 0.134

Gnomad MID AF: 0.217

Gnomad NFE AF: 0.187

Gnomad OTH AF: 0.211

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

GnomAD4 genome AF: 0.209 AC: 31373 AN: 150230 Hom.: 3429 Cov.: 31 AF XY: 0.208 AC XY: 15241 AN XY: 73240

African (AFR) AF: 0.265 AC: 10836 AN: 40870

American (AMR) AF: 0.205 AC: 3091 AN: 15112

Ashkenazi Jewish (ASJ) AF: 0.185 AC: 641 AN: 3458

East Asian (EAS) AF: 0.157 AC: 796 AN: 5066

South Asian (SAS) AF: 0.295 AC: 1396 AN: 4732

European-Finnish (FIN) AF: 0.134 AC: 1366 AN: 10172

Middle Eastern (MID) AF: 0.223 AC: 65 AN: 292

European-Non Finnish (NFE) AF: 0.187 AC: 12631 AN: 67538

Other (OTH) AF: 0.213 AC: 445 AN: 2088

Alfa AF: 0.112 Hom.: 199

Bravo AF: 0.211

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
CADD	Benign	1.4
DANN	Benign	0.55
PhyloP100		-0.72
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: rs12149426; hg19: chr16-84465106;