rs403630

Variant names:

• chr2-40265648-A-C
• rs403630
• NM_021097.5:c.1809-87155T>G

Your query was ambiguous. Multiple possible variants found:

• chr2-40265648-A-C
• chr2-40265648-A-G
• chr2-40265648-A-T

Variant summary

Our verdict is Benign. The variant received -10 ACMG points: 0P and 10B. BP4_Moderate BA1

The NM_021097.5(SLC8A1):​c.1809-87155T>G variant causes a intron change. The variant allele was found at a frequency of 0.811 in 151,968 control chromosomes in the GnomAD database, including 50,410 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 0.81 (50410 hom., cov: 31)
• Consequence: SLC8A1 NM_021097.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 3.79
• Publications: 4 publications found

Genes affected

SLC8A1 (HGNC:11068): (solute carrier family 8 member A1) In cardiac myocytes, Ca(2+) concentrations alternate between high levels during contraction and low levels during relaxation. The increase in Ca(2+) concentration during contraction is primarily due to release of Ca(2+) from intracellular stores. However, some Ca(2+) also enters the cell through the sarcolemma (plasma membrane). During relaxation, Ca(2+) is sequestered within the intracellular stores. To prevent overloading of intracellular stores, the Ca(2+) that entered across the sarcolemma must be extruded from the cell. The Na(+)-Ca(2+) exchanger is the primary mechanism by which the Ca(2+) is extruded from the cell during relaxation. In the heart, the exchanger may play a key role in digitalis action. The exchanger is the dominant mechanism in returning the cardiac myocyte to its resting state following excitation.[supplied by OMIM, Apr 2004]

ACMG classification

Our verdict: Benign. The variant received -10 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.27).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.872 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
SLC8A1	NM_021097.5	c.1809-87155T>G		intron_variant	Intron 2 of 10	ENST00000332839.9	NP_066920.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
SLC8A1	ENST00000332839.9	c.1809-87155T>G		intron_variant	Intron 2 of 10	1	NM_021097.5	ENSP00000332931.4

Frequencies

GnomAD3 genomes AF: 0.812 AC: 123236 AN: 151852 Hom.: 50384 Cov.: 31

Gnomad AFR AF: 0.880

Gnomad AMI AF: 0.783

Gnomad AMR AF: 0.690

Gnomad ASJ AF: 0.809

Gnomad EAS AF: 0.781

Gnomad SAS AF: 0.884

Gnomad FIN AF: 0.663

Gnomad MID AF: 0.839

Gnomad NFE AF: 0.818

Gnomad OTH AF: 0.804

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

GnomAD4 genome AF: 0.811 AC: 123316 AN: 151968 Hom.: 50410 Cov.: 31 AF XY: 0.804 AC XY: 59711 AN XY: 74266

African (AFR) AF: 0.879 AC: 36447 AN: 41444

American (AMR) AF: 0.689 AC: 10517 AN: 15256

Ashkenazi Jewish (ASJ) AF: 0.809 AC: 2804 AN: 3466

East Asian (EAS) AF: 0.781 AC: 4038 AN: 5170

South Asian (SAS) AF: 0.884 AC: 4258 AN: 4816

European-Finnish (FIN) AF: 0.663 AC: 6998 AN: 10548

Middle Eastern (MID) AF: 0.827 AC: 243 AN: 294

European-Non Finnish (NFE) AF: 0.818 AC: 55592 AN: 67946

Other (OTH) AF: 0.806 AC: 1705 AN: 2116

Alfa AF: 0.816 Hom.: 22056

Bravo AF: 0.812

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.27
CADD	Benign	22
DANN	Benign	0.84
PhyloP100		3.8
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: rs403630; hg19: chr2-40492788;