rs1557540

chr22-36336492-C-T

Variant summary

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

The NM_002473.6(MYH9):c.490+4878G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.601 in 152,184 control chromosomes in the GnomAD database, including 28,438 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 0.60 (28438 hom., cov: 34)
• Consequence: MYH9 NM_002473.6 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -2.11

Genes affected

MYH9 (HGNC:7579): (myosin heavy chain 9) This gene encodes a conventional non-muscle myosin; this protein should not be confused with the unconventional myosin-9a or 9b (MYO9A or MYO9B). The encoded protein is a myosin IIA heavy chain that contains an IQ domain and a myosin head-like domain which is involved in several important functions, including cytokinesis, cell motility and maintenance of cell shape. Defects in this gene have been associated with non-syndromic sensorineural deafness autosomal dominant type 17, Epstein syndrome, Alport syndrome with macrothrombocytopenia, Sebastian syndrome, Fechtner syndrome and macrothrombocytopenia with progressive sensorineural deafness. [provided by RefSeq, Dec 2011]

(HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.97).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.69 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
MYH9	NM_002473.6	c.490+4878G>A		intron_variant		ENST00000216181.11

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
MYH9	ENST00000216181.11	c.490+4878G>A		intron_variant		1	NM_002473.6	P1
	ENST00000663925.1	n.86+986C>T		intron_variant, non_coding_transcript_variant

Frequencies

GnomAD3 genomes AF: 0.601 AC: 91388 AN: 152066 Hom.: 28410 Cov.: 34

Gnomad AFR AF: 0.697

Gnomad AMI AF: 0.686

Gnomad AMR AF: 0.616

Gnomad ASJ AF: 0.491

Gnomad EAS AF: 0.156

Gnomad SAS AF: 0.370

Gnomad FIN AF: 0.593

Gnomad MID AF: 0.599

Gnomad NFE AF: 0.596

Gnomad OTH AF: 0.575

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

GnomAD4 genome AF: 0.601 AC: 91455 AN: 152184 Hom.: 28438 Cov.: 34 AF XY: 0.595 AC XY: 44283 AN XY: 74394

Gnomad4 AFR AF: 0.697

Gnomad4 AMR AF: 0.615

Gnomad4 ASJ AF: 0.491

Gnomad4 EAS AF: 0.156

Gnomad4 SAS AF: 0.371

Gnomad4 FIN AF: 0.593

Gnomad4 NFE AF: 0.596

Gnomad4 OTH AF: 0.570

Alfa AF: 0.588 Hom.: 36036

Bravo AF: 0.609

Asia WGS AF: 0.286 AC: 997 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.97
Cadd	Benign	0.0040
Dann	Benign	0.57

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: rs1557540; hg19: chr22-36732537;