rs877087

Positions:

• chr15-33582074-T-C
• chr15-33582074-T-G

Variant summary

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

The NM_001036.6(RYR3):​c.1573+431T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.51 in 152,106 control chromosomes in the GnomAD database, including 20,793 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 0.51 (20793 hom., cov: 33)
• Consequence: RYR3 NM_001036.6 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.73

Genes affected

RYR3 (HGNC:10485): (ryanodine receptor 3) The protein encoded by this gene is a ryanodine receptor, which functions to release calcium from intracellular storage for use in many cellular processes. For example, the encoded protein is involved in skeletal muscle contraction by releasing calcium from the sarcoplasmic reticulum followed by depolarization of T-tubules. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.89).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.567 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
RYR3	NM_001036.6	c.1573+431T>C		intron_variant		ENST00000634891.2	NP_001027.3

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
RYR3	ENST00000634891.2	c.1573+431T>C		intron_variant		1	NM_001036.6	ENSP00000489262	P4
RYR3	ENST00000389232.9	c.1573+431T>C		intron_variant		5		ENSP00000373884	A1
RYR3	ENST00000415757.7	c.1573+431T>C		intron_variant		2		ENSP00000399610	A2
RYR3	ENST00000634418.1	c.1573+431T>C		intron_variant		5		ENSP00000489529

Frequencies

GnomAD3 genomes AF: 0.510 AC: 77501 AN: 151988 Hom.: 20780 Cov.: 33

Gnomad AFR AF: 0.574

Gnomad AMI AF: 0.707

Gnomad AMR AF: 0.420

Gnomad ASJ AF: 0.631

Gnomad EAS AF: 0.0486

Gnomad SAS AF: 0.297

Gnomad FIN AF: 0.464

Gnomad MID AF: 0.570

Gnomad NFE AF: 0.539

Gnomad OTH AF: 0.521

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

GnomAD4 genome AF: 0.510 AC: 77536 AN: 152106 Hom.: 20793 Cov.: 33 AF XY: 0.499 AC XY: 37133 AN XY: 74364

Gnomad4 AFR AF: 0.573

Gnomad4 AMR AF: 0.419

Gnomad4 ASJ AF: 0.631

Gnomad4 EAS AF: 0.0484

Gnomad4 SAS AF: 0.298

Gnomad4 FIN AF: 0.464

Gnomad4 NFE AF: 0.539

Gnomad4 OTH AF: 0.516

Alfa AF: 0.529 Hom.: 21422

Bravo AF: 0.511

Asia WGS AF: 0.177 AC: 617 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.89
CADD	Benign	0.23
DANN	Benign	0.66

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: rs877087; hg19: chr15-33874275;