NM_178014.4(TUBB):c.*127del AND not provided

Germline classification:: Benign (1 submission)
Last evaluated:: Oct 22, 2019
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:: RCV001668026.2

Allele description [Variation Report for NM_178014.4(TUBB):c.*127del]

NM_178014.4(TUBB):c.*127del

Gene:

TUBB:tubulin beta class I [Gene - OMIM - HGNC]

Variant type:

Deletion

Cytogenetic location:

6p21.33

Genomic location:

Preferred name:

NM_178014.4(TUBB):c.*127del

HGVS:

NC_000006.12:g.30724524del
NG_034142.1:g.9324del
NM_001293212.2:c.*127del
NM_001293213.2:c.*127del
NM_001293214.2:c.*127del
NM_001293215.2:c.*127del
NM_001293216.2:c.*127del
NM_178014.4:c.*127delMANE SELECT
NC_000006.11:g.30692301del
NR_120608.2:n.1018del

Links:

dbSNP: rs3214320

NCBI 1000 Genomes Browser:

rs3214320

Molecular consequence:

NM_001293212.2:c.*127del - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
NM_001293213.2:c.*127del - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
NM_001293214.2:c.*127del - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
NM_001293215.2:c.*127del - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
NM_001293216.2:c.*127del - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
NM_178014.4:c.*127del - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
NR_120608.2:n.1018del - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001891132	GeneDx	criteria provided, single submitter (GeneDx Variant Classification Process June 2021)	Benign (Oct 22, 2019)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001891132

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)

Benign
(Oct 22, 2019)

germline

clinical testing

Citation Link

Help

Summary from all submissions

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

Details of each submission

From GeneDx, SCV001891132.1

#	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	germline	yes	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Dec 24, 2023

ClinVar

Relating variation to medicine