NM_178012.5(TUBB2B):c.602G>T (p.Cys201Phe) AND Complex cortical dysplasia with other brain malformations 7

Germline classification:: Likely pathogenic (1 submission)
Last evaluated:: Jan 1, 2020
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:: RCV001072151.1

Allele description [Variation Report for NM_178012.5(TUBB2B):c.602G>T (p.Cys201Phe)]

NM_178012.5(TUBB2B):c.602G>T (p.Cys201Phe)

Gene:

TUBB2B:tubulin beta 2B class IIb [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

6p25.2

Genomic location:

Preferred name:

NM_178012.5(TUBB2B):c.602G>T (p.Cys201Phe)

HGVS:

NC_000006.12:g.3225487C>A
NG_016715.1:g.7248G>T
NM_178012.5:c.602G>TMANE SELECT
NP_821080.1:p.Cys201Phe
NC_000006.11:g.3225721C>A

Protein change:

C201F

Links:

dbSNP: rs201922441

NCBI 1000 Genomes Browser:

rs201922441

Molecular consequence:

NM_178012.5:c.602G>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Complex cortical dysplasia with other brain malformations 7
Synonyms:: Polymicrogyria, asymmetric
Identifiers:: MONDO: MONDO:0012399; MedGen: C3552236; Orphanet: 300573; OMIM: 610031

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001235717	Bruce Lefroy Centre, Murdoch Childrens Research Institute	criteria provided, single submitter (ACMG Guidelines, 2015)	Likely pathogenic (Jan 1, 2020)	de novo	research	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001235717

Bruce Lefroy Centre, Murdoch Childrens Research Institute

criteria provided, single submitter

(ACMG Guidelines, 2015)

Likely pathogenic
(Jan 1, 2020)

de novo

research

PubMed (1)
[See all records that cite this PMID]

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	research

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]

PMID:: 25741868
PMCID:: PMC4544753

Details of each submission

From Bruce Lefroy Centre, Murdoch Childrens Research Institute, SCV001235717.2

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	research	PubMed (1)

Description

PM2, PM6, PP2, PP3

#	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: Apr 23, 2022

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