rs9513227

chr13-97287048-T-A

Variant summary

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

The NM_001382683.1(MBNL2):c.174+10639T>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.128 in 152,212 control chromosomes in the GnomAD database, including 1,331 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 0.13 (1331 hom., cov: 32)
• Consequence: MBNL2 NM_001382683.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.0670

Genes affected

MBNL2 (HGNC:16746): (muscleblind like splicing regulator 2) This gene is a member of the muscleblind protein family which was initially described in Drosophila melanogaster. This gene encodes a C3H-type zinc finger protein that modulates alternative splicing of pre-mRNAs. Muscleblind proteins bind specifically to expanded dsCUG RNA but not to normal size CUG repeats and may thereby play a role in the pathophysiology of myotonic dystrophy. Several alternatively spliced transcript variants have been described but the full-length natures of only some have been determined. [provided by RefSeq, Mar 2012]

(HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.86).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.153 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
MBNL2	NM_001382683.1	c.174+10639T>A		intron_variant		ENST00000679496.1
LOC101927385	XR_001749966.2	n.3102+7474A>T		intron_variant, non_coding_transcript_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
MBNL2	ENST00000679496.1	c.174+10639T>A		intron_variant			NM_001382683.1
	ENST00000665007.1	n.274+7489A>T		intron_variant, non_coding_transcript_variant

Frequencies

GnomAD3 genomes AF: 0.128 AC: 19528 AN: 152096 Hom.: 1326 Cov.: 32

Gnomad AFR AF: 0.139

Gnomad AMI AF: 0.248

Gnomad AMR AF: 0.151

Gnomad ASJ AF: 0.134

Gnomad EAS AF: 0.0857

Gnomad SAS AF: 0.162

Gnomad FIN AF: 0.0645

Gnomad MID AF: 0.130

Gnomad NFE AF: 0.126

Gnomad OTH AF: 0.121

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

GnomAD4 genome AF: 0.128 AC: 19556 AN: 152212 Hom.: 1331 Cov.: 32 AF XY: 0.127 AC XY: 9480 AN XY: 74424

Gnomad4 AFR AF: 0.139

Gnomad4 AMR AF: 0.152

Gnomad4 ASJ AF: 0.134

Gnomad4 EAS AF: 0.0857

Gnomad4 SAS AF: 0.163

Gnomad4 FIN AF: 0.0645

Gnomad4 NFE AF: 0.126

Gnomad4 OTH AF: 0.121

Alfa AF: 0.127 Hom.: 162

Bravo AF: 0.134

Asia WGS AF: 0.156 AC: 542 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.86
Cadd	Benign	2.8
Dann	Benign	0.49

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: rs9513227; hg19: chr13-97939302;