Evidence Repository - Clinical Genome Resources

The ClinGen Evidence Repository is an FDA-recognized human genetic variant database containing expert-curated assertions regarding variants' pathogenicity and supporting evidence summaries. [Disclaimer]

Variant: NM_000257.3(MYH7):c.327C>T (p.Tyr109=)

Curation History

CA013536

42952 (ClinVar)

Gene: MYH7

Condition: cardiomyopathy

Inheritance Mode: Autosomal dominant inheritance

Link to MONDO

UUID: 0569b019-28db-4569-b243-bcc906486bd5

Approved on: 2016-12-15

Published on: 2018-11-16

HGVS expressions

NM_000257.3:c.327C>T

NM_000257.3(MYH7):c.327C>T (p.Tyr109=)

NM_000257.4:c.327C>T

ENST00000355349.3:c.327C>T

NC_000014.9:g.23433102G>A

CM000676.2:g.23433102G>A

NC_000014.8:g.23902311G>A

CM000676.1:g.23902311G>A

NC_000014.7:g.22972151G>A

NG_007884.1:g.7560C>T

Benign

BA1 BP7

Evidence Links 0

Expert Panel

Cardiomyopathy VCEP

Criteria Specification Information

Criteria Specifications for this VCEP

Evidence submitted by expert panel

Cardiomyopathy VCEP

The filtering allele frequency of the c.327C>T (p.Tyr109=) silent variant in the MYH7 gene is 0.13% (31/16512) of South Asian chromosomes by the Exome Aggregation Consortium (http://exac.broadinstitute.org), which is a high enough frequency to be classified as benign based on thresholds defined by the ClinGen Inherited Cardiomyopathy Expert Panel (BA1, BP7; PMID:29300372).

BA1

Variant found in 0.188% (31/16512) of South Asian chromosomes in ExAC

BP7

No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline

Curation History

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