10-68121288-A-T

Variant summary

Our verdict is Benign. Variant got -14 ACMG points: 0P and 14B. BP4_Strong BP6_Moderate BA1

The NM_032578.4(MYPN):c.-1-150A>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.115 in 730,496 control chromosomes in the GnomAD database, including 5,683 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★).

• Frequency:
  • Genomes: 𝑓 0.12 (1192 hom., cov: 32)
  • Exomes 𝑓: 0.11 (4491 hom.)
• Consequence: MYPN NM_032578.4 intron
• Clinical Significance: Benign criteria provided, single submitter B:1
• Conservation: PhyloP100: 0.151

Genes affected

MYPN (HGNC:23246): (myopalladin) Striated muscle in vertebrates comprises large proteins which must be organized properly to contract efficiently. Z-lines in striated muscle are a sign of this organization, representing the ends of actin thin filaments, titin, nebulin or nebulette and accessory proteins required for structure and function. This gene encodes a protein which interacts with nebulin in skeletal muscle or nebulette in cardiac muscle and alpha-actinin. In addition, this gene product can interact with a protein with the I-band indicating it has a regulatory as well as structural function. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2011]

ACMG classification

Verdict is Benign. Variant got -14 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.85).
• BP6: Variant 10-68121288-A-T is Benign according to our data. Variant chr10-68121288-A-T is described in ClinVar as [Benign]. Clinvar id is 1241484.Status of the report is criteria_provided_single_submitter, 1 stars.
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.203 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
MYPN	NM_032578.4	c.-1-150A>T		intron_variant		ENST00000358913.10

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
MYPN	ENST00000358913.10	c.-1-150A>T		intron_variant		1	NM_032578.4	P1

Frequencies

GnomAD3 genomes AF: 0.122 AC: 18542 AN: 152062 Hom.: 1187 Cov.: 32

Gnomad AFR AF: 0.114

Gnomad AMI AF: 0.163

Gnomad AMR AF: 0.104

Gnomad ASJ AF: 0.164

Gnomad EAS AF: 0.120

Gnomad SAS AF: 0.214

Gnomad FIN AF: 0.143

Gnomad MID AF: 0.168

Gnomad NFE AF: 0.118

Gnomad OTH AF: 0.131

GnomAD4 exome AF: 0.114 AC: 65656 AN: 578316 Hom.: 4491 AF XY: 0.117 AC XY: 34706 AN XY: 296116

Gnomad4 AFR exome AF: 0.106

Gnomad4 AMR exome AF: 0.102

Gnomad4 ASJ exome AF: 0.143

Gnomad4 EAS exome AF: 0.124

Gnomad4 SAS exome AF: 0.207

Gnomad4 FIN exome AF: 0.129

Gnomad4 NFE exome AF: 0.101

Gnomad4 OTH exome AF: 0.119

GnomAD4 genome AF: 0.122 AC: 18564 AN: 152180 Hom.: 1192 Cov.: 32 AF XY: 0.123 AC XY: 9154 AN XY: 74416

Gnomad4 AFR AF: 0.115

Gnomad4 AMR AF: 0.104

Gnomad4 ASJ AF: 0.164

Gnomad4 EAS AF: 0.120

Gnomad4 SAS AF: 0.214

Gnomad4 FIN AF: 0.143

Gnomad4 NFE AF: 0.118

Gnomad4 OTH AF: 0.131

Alfa AF: 0.116 Hom.: 123

Bravo AF: 0.118

Asia WGS AF: 0.140 AC: 486 AN: 3478

ClinVar

Significance: Benign

Submissions summary: Benign:1

Revision: criteria provided, single submitter

Submissions by phenotype

not provided Benign:1

Benign, criteria provided, single submitter

clinical testing

GeneDx

Jun 19, 2018

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Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.85
Cadd	Benign	2.5
Dann	Benign	0.61

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: rs71578985; hg19: chr10-69881045;