NM_001018100.5:c.163-67G>A

Variant names:

• chr15-57617966-G-A
• rs937254
• NM_001018100.5:c.163-67G>A

Variant summary

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

The NM_001018100.5(MYZAP):​c.163-67G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.423 in 1,539,032 control chromosomes in the GnomAD database, including 141,119 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 0.47 (17324 hom., cov: 32)
  • Exomes 𝑓: 0.42 (123795 hom.)
• Consequence: MYZAP NM_001018100.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.99
• Publications: 20 publications found

Genes affected

MYZAP (HGNC:43444): (myocardial zonula adherens protein) This gene encodes a protein that is abundantly expressed in cardiac tissue. The encoded protein localizes to intercalated discs in cardiomyocytes and functions as an activator of Rho-dependent serum-response factor signaling. Alternative splicing results in multiple transcript variants. Readthrough transcription also exists between this gene and the neighboring downstream gene POLR2M (polymerase (RNA) II (DNA directed) polypeptide M) and is represented with GeneID: 145781. [provided by RefSeq, Mar 2014]

GCOM1 (HGNC:26424): (GCOM1, MYZAP-POLR2M combined locus) This locus represents naturally occurring readthrough transcription between the neighboring MYZAP (myocardial zonula adherens protein) and POLR2M (polymerase (RNA) II (DNA directed) polypeptide M) genes on chromosome 15. Alternative splicing results in multiple readthrough transcript variants. Readthrough variants may encode proteins that share sequence identity with the upstream gene product or with both the upstream and downstream gene products. Some readthrough transcript variants are also expected to be candidates for nonsense-mediated decay (NMD). [provided by RefSeq, Oct 2013]

GCOM1 Gene-Disease associations (from GenCC):

• dilated cardiomyopathy

  Inheritance: AR Classification: MODERATE Submitted by: Ambry Genetics

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.92).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.567 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001018100.5. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	MYZAP	NM_001018100.5	MANE Select	c.163-67G>A		intron	N/A	NP_001018110.1
	GCOM1	NM_001285900.3		c.163-67G>A		intron	N/A	NP_001272829.1
	GCOM1	NM_001018090.6		c.163-67G>A		intron	N/A	NP_001018100.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	MYZAP	ENST00000267853.10	TSL:1 MANE Select	c.163-67G>A		intron	N/A	ENSP00000267853.5
	GCOM1	ENST00000587652.5	TSL:2	c.163-67G>A		intron	N/A	ENSP00000465231.1
	MYZAP	ENST00000380565.8	TSL:1	c.163-67G>A		intron	N/A	ENSP00000369939.4

Frequencies

GnomAD3 genomes AF: 0.470 AC: 71357 AN: 151894 Hom.: 17307 Cov.: 32

Gnomad AFR AF: 0.573

Gnomad AMI AF: 0.364

Gnomad AMR AF: 0.541

Gnomad ASJ AF: 0.415

Gnomad EAS AF: 0.561

Gnomad SAS AF: 0.558

Gnomad FIN AF: 0.418

Gnomad MID AF: 0.525

Gnomad NFE AF: 0.390

Gnomad OTH AF: 0.463

GnomAD4 exome AF: 0.417 AC: 578843 AN: 1387020 Hom.: 123795 AF XY: 0.420 AC XY: 287344 AN XY: 683600

African (AFR) AF: 0.586 AC: 18169 AN: 30992

American (AMR) AF: 0.611 AC: 21101 AN: 34538

Ashkenazi Jewish (ASJ) AF: 0.417 AC: 9105 AN: 21854

East Asian (EAS) AF: 0.534 AC: 20690 AN: 38748

South Asian (SAS) AF: 0.564 AC: 40398 AN: 71566

European-Finnish (FIN) AF: 0.427 AC: 20609 AN: 48228

Middle Eastern (MID) AF: 0.470 AC: 2487 AN: 5286

European-Non Finnish (NFE) AF: 0.391 AC: 421576 AN: 1078460

Other (OTH) AF: 0.431 AC: 24708 AN: 57348

GnomAD4 genome AF: 0.470 AC: 71426 AN: 152012 Hom.: 17324 Cov.: 32 AF XY: 0.475 AC XY: 35322 AN XY: 74284

African (AFR) AF: 0.573 AC: 23736 AN: 41426

American (AMR) AF: 0.541 AC: 8269 AN: 15278

Ashkenazi Jewish (ASJ) AF: 0.415 AC: 1439 AN: 3466

East Asian (EAS) AF: 0.560 AC: 2894 AN: 5164

South Asian (SAS) AF: 0.558 AC: 2695 AN: 4826

European-Finnish (FIN) AF: 0.418 AC: 4404 AN: 10548

Middle Eastern (MID) AF: 0.517 AC: 152 AN: 294

European-Non Finnish (NFE) AF: 0.390 AC: 26531 AN: 67984

Other (OTH) AF: 0.461 AC: 974 AN: 2114

Alfa AF: 0.429 Hom.: 30636

Bravo AF: 0.483

Asia WGS AF: 0.531 AC: 1850 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.92
CADD	Benign	0.0010
DANN	Benign	0.43
PhyloP100		-2.0
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: rs937254; hg19: chr15-57910164; COSMIC: COSV51089983;