NM_145690.3(YWHAZ):c.689C>G (p.Ser230Trp) AND Noonan-like disorder

Germline classification:: Likely pathogenic (1 submission)
Last evaluated:: Sep 29, 2023
Review status:: 1 star out of maximum of 4 stars
criteria provided, single submitter

Somatic classification of clinical impact:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Somatic classification of oncogenicity:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Record status:: current
Accession:: RCV003987577.1

Allele description [Variation Report for NM_145690.3(YWHAZ):c.689C>G (p.Ser230Trp)]

NM_145690.3(YWHAZ):c.689C>G (p.Ser230Trp)

Gene:

YWHAZ:tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

8q22.3

Genomic location:

Preferred name:

NM_145690.3(YWHAZ):c.689C>G (p.Ser230Trp)

HGVS:

NC_000008.11:g.100920742G>C
NM_001135699.2:c.689C>G
NM_001135700.2:c.689C>G
NM_001135701.2:c.689C>G
NM_001135702.2:c.689C>G
NM_003406.4:c.689C>G
NM_145690.3:c.689C>GMANE SELECT
NP_001129171.1:p.Ser230Trp
NP_001129171.1:p.Ser230Trp
NP_001129172.1:p.Ser230Trp
NP_001129173.1:p.Ser230Trp
NP_001129174.1:p.Ser230Trp
NP_003397.1:p.Ser230Trp
NP_663723.1:p.Ser230Trp
NC_000008.10:g.101932970G>C
NM_001135699.1:c.689C>G
NM_145690.2:c.689C>G

Protein change:

S230W; SER230TRP

Links:

OMIM: 601288.0001; dbSNP: rs1554612377

NCBI 1000 Genomes Browser:

rs1554612377

Molecular consequence:

NM_001135699.2:c.689C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001135700.2:c.689C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001135701.2:c.689C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001135702.2:c.689C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_003406.4:c.689C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_145690.3:c.689C>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Noonan-like disorder
Identifiers:

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004804812	Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues	criteria provided, single submitter (ACGS Guidelines, 2020)	Likely pathogenic (Sep 29, 2023)	de novo	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV004804812

Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues

criteria provided, single submitter

(ACGS Guidelines, 2020)

Likely pathogenic
(Sep 29, 2023)

de novo

clinical testing

Citation Link

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	de novo	yes	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues, SCV004804812.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not provided

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	de novo	yes	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Mar 30, 2024

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