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_030662.3(MAP2K2):c.453C>T (p.Asp151=)

Curation History

CA137943

46237 (ClinVar)

Gene: MAP2K2

Condition: RASopathy

Inheritance Mode: Autosomal dominant inheritance

Link to MONDO

UUID: b79aa141-9bf2-4854-99cb-72cca42926e8

Approved on: 2017-05-09

Published on: 2018-12-10

HGVS expressions

NM_030662.3:c.453C>T

NM_030662.3(MAP2K2):c.453C>T (p.Asp151=)

NC_000019.10:g.4102451G>A

CM000681.2:g.4102451G>A

NC_000019.9:g.4102449G>A

CM000681.1:g.4102449G>A

NC_000019.8:g.4053449G>A

NG_007996.1:g.26678C>T

ENST00000262948.9:c.453C>T

ENST00000394867.8:c.162C>T

ENST00000593364.5:n.400C>T

ENST00000597008.5:n.54C>T

ENST00000599345.1:n.723C>T

ENST00000601786.5:n.754C>T

ENST00000602167.5:n.173C>T

Benign

BA1

Evidence Links 0

Expert Panel

RASopathy VCEP

Criteria Specification Information

Criteria Specifications for this VCEP

Evidence submitted by expert panel

RASopathy VCEP

The filtering allele frequency of the c.453C>T (p.Asp151=) variant in the MAP2K2 gene is 27.128% (10569/38338) of European chromosomes by the Exome Aggregation Consortium, which is a high enough frequency to be classified as benign based on thresholds defined by the ClinGen RASopathy Expert Panel (BA1; PMID:29493581)

BA1

Curation History

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