11-77156915-TACATCG-T

Position:

• chr11-77156915-TACATCG-T

Variant summary

Our verdict is Likely pathogenic. Variant got 6 ACMG points: 6P and 0B. PM2 PM4 PP3 PP5

The NM_000260.4(MYO7A):​c.652_657del​(p.Asp218_Ile219del) variant causes a inframe deletion change involving the alteration of a conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. Variant has been reported in ClinVar as Pathogenic (no stars).

• Frequency: Genomes: not found (cov: 33)
• Consequence: MYO7A NM_000260.4 inframe_deletion
• Clinical Significance: Pathogenic no assertion criteria provided P:1
• Conservation: PhyloP100: 9.92

Genes affected

MYO7A (HGNC:7606): (myosin VIIA) This gene is a member of the myosin gene family. Myosins are mechanochemical proteins characterized by the presence of a motor domain, an actin-binding domain, a neck domain that interacts with other proteins, and a tail domain that serves as an anchor. This gene encodes an unconventional myosin with a very short tail. Defects in this gene are associated with the mouse shaker-1 phenotype and the human Usher syndrome 1B which are characterized by deafness, reduced vestibular function, and (in human) retinal degeneration. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Likely_pathogenic. Variant got 6 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• PM4: Nonframeshift variant in NON repetitive region in NM_000260.4.
• PP3: No computational evidence supports a deleterious effect, but strongly conserved according to phyloP
• PP5: Variant 11-77156915-TACATCG-T is Pathogenic according to our data. Variant chr11-77156915-TACATCG-T is described in ClinVar as [Pathogenic]. Clinvar id is 11849.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr11-77156915-TACATCG-T is described in Lovd as [Pathogenic]. Variant chr11-77156915-TACATCG-T is described in Lovd as [Likely_pathogenic].

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
MYO7A	NM_000260.4	c.652_657del	p.Asp218_Ile219del	inframe_deletion	7/49	ENST00000409709.9	NP_000251.3

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
MYO7A	ENST00000409709.9	c.652_657del	p.Asp218_Ile219del	inframe_deletion	7/49	1	NM_000260.4	ENSP00000386331
MYO7A	ENST00000409619.6	c.619_624del	p.Asp207_Ile208del	inframe_deletion	8/50	1		ENSP00000386635
MYO7A	ENST00000458637.6	c.652_657del	p.Asp218_Ile219del	inframe_deletion	7/49	1		ENSP00000392185	P1

Frequencies

GnomAD3 genomes Cov.: 33

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

GnomAD4 genome Cov.: 33

ClinVar

Significance: Pathogenic

Submissions summary: Pathogenic:1

Revision: no assertion criteria provided

Submissions by phenotype

Usher syndrome type 1B Pathogenic:1

Pathogenic, no assertion criteria provided

literature only

OMIM

Oct 10, 1995

- -

Computational scores

Source: dbNSFP v4.3

Splicing

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

LitVar

Other links and lift over

dbSNP: rs1555062984; hg19: chr11-76867961;