rs1879282

Variant names:

• chr2-30806969-C-T
• rs1879282
• NM_144575.3:c.-33+333G>A

Variant summary

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

The NM_144575.3(CAPN13):​c.-33+333G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.739 in 152,196 control chromosomes in the GnomAD database, including 42,176 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 0.74 (42176 hom., cov: 32)
• Consequence: CAPN13 NM_144575.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.88
• Publications: 8 publications found

Genes affected

CAPN13 (HGNC:16663): (calpain 13) The calpains, calcium-activated neutral proteases, are nonlysosomal, intracellular cysteine proteases. The mammalian calpains include ubiquitous, stomach-specific, and muscle-specific proteins. The ubiquitous enzymes consist of heterodimers with distinct large, catalytic subunits associated with a common small, regulatory subunit. This gene encodes a member of the calpain large subunit family. [provided by RefSeq, Jun 2012]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.91).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.833 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_144575.3. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	CAPN13	NM_144575.3	MANE Select	c.-33+333G>A		intron	N/A	NP_653176.2

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	CAPN13	ENST00000295055.12	TSL:5 MANE Select	c.-33+333G>A		intron	N/A	ENSP00000295055.8	Q6MZZ7-1
	CAPN13	ENST00000946473.1		c.-119+333G>A		intron	N/A	ENSP00000616532.1
	CAPN13	ENST00000946475.1		c.-147+333G>A		intron	N/A	ENSP00000616534.1

Frequencies

GnomAD3 genomes AF: 0.739 AC: 112376 AN: 152078 Hom.: 42130 Cov.: 32

Gnomad AFR AF: 0.841

Gnomad AMI AF: 0.750

Gnomad AMR AF: 0.563

Gnomad ASJ AF: 0.642

Gnomad EAS AF: 0.780

Gnomad SAS AF: 0.635

Gnomad FIN AF: 0.794

Gnomad MID AF: 0.712

Gnomad NFE AF: 0.718

Gnomad OTH AF: 0.699

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

GnomAD4 genome AF: 0.739 AC: 112473 AN: 152196 Hom.: 42176 Cov.: 32 AF XY: 0.736 AC XY: 54731 AN XY: 74404

African (AFR) AF: 0.841 AC: 34919 AN: 41536

American (AMR) AF: 0.562 AC: 8605 AN: 15298

Ashkenazi Jewish (ASJ) AF: 0.642 AC: 2227 AN: 3470

East Asian (EAS) AF: 0.781 AC: 4042 AN: 5178

South Asian (SAS) AF: 0.635 AC: 3059 AN: 4814

European-Finnish (FIN) AF: 0.794 AC: 8398 AN: 10578

Middle Eastern (MID) AF: 0.721 AC: 212 AN: 294

European-Non Finnish (NFE) AF: 0.718 AC: 48845 AN: 68000

Other (OTH) AF: 0.700 AC: 1482 AN: 2116

Alfa AF: 0.709 Hom.: 66023

Bravo AF: 0.724

Asia WGS AF: 0.715 AC: 2488 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
CADD	Benign	0.057
DANN	Benign	0.38
PhyloP100		-1.9
PromoterAI		-0.024	Neutral
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

MaxEntScan Visualizer can be used to analyze the impact of this mutation on the neighboring sequence.

Other links and lift over

dbSNP: rs1879282;

hg19: chr2-31029835;