NM_001353694.2(TIAM1):c.4444C>G (p.Arg1482Gly) AND not specified

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jan 23, 2024
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:: RCV004467154.1

Allele description [Variation Report for NM_001353694.2(TIAM1):c.4444C>G (p.Arg1482Gly)]

NM_001353694.2(TIAM1):c.4444C>G (p.Arg1482Gly)

Gene:

TIAM1:TIAM Rac1 associated GEF 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

21q22.11

Genomic location:

Preferred name:

NM_001353694.2(TIAM1):c.4444C>G (p.Arg1482Gly)

HGVS:

NC_000021.9:g.31120700G>C
NM_001353684.2:c.1543C>G
NM_001353685.2:c.1468C>G
NM_001353686.2:c.4369C>G
NM_001353687.2:c.4369C>G
NM_001353688.1:c.4444C>G
NM_001353689.1:c.4444C>G
NM_001353690.1:c.4444C>G
NM_001353691.1:c.4444C>G
NM_001353692.1:c.4444C>G
NM_001353693.1:c.4444C>G
NM_001353694.2:c.4444C>GMANE SELECT
NM_003253.3:c.4444C>G
NP_001340613.1:p.Arg515Gly
NP_001340614.1:p.Arg490Gly
NP_001340615.1:p.Arg1457Gly
NP_001340616.1:p.Arg1457Gly
NP_001340617.1:p.Arg1482Gly
NP_001340618.1:p.Arg1482Gly
NP_001340619.1:p.Arg1482Gly
NP_001340620.1:p.Arg1482Gly
NP_001340621.1:p.Arg1482Gly
NP_001340622.1:p.Arg1482Gly
NP_001340623.1:p.Arg1482Gly
NP_003244.2:p.Arg1482Gly
NC_000021.8:g.32493018G>C
NM_003253.2:c.4444C>G

Protein change:

R1457G

Molecular consequence:

NM_001353684.2:c.1543C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001353685.2:c.1468C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001353686.2:c.4369C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001353687.2:c.4369C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001353688.1:c.4444C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001353689.1:c.4444C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001353690.1:c.4444C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001353691.1:c.4444C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001353692.1:c.4444C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001353693.1:c.4444C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001353694.2:c.4444C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_003253.3:c.4444C>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004964958	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Jan 23, 2024)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV004964958

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Jan 23, 2024)

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	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Ambry Genetics, SCV004964958.1

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

Description

The c.4444C>G (p.R1482G) alteration is located in exon 29 (coding exon 25) of the TIAM1 gene. This alteration results from a C to G substitution at nucleotide position 4444, causing the arginine (R) at amino acid position 1482 to be replaced by a glycine (G). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

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

Last Updated: May 7, 2024

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