NM_012108.4(STAP1):c.221T>C (p.Leu74Pro) AND not specified

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jan 22, 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:: RCV004243234.1

Allele description [Variation Report for NM_012108.4(STAP1):c.221T>C (p.Leu74Pro)]

NM_012108.4(STAP1):c.221T>C (p.Leu74Pro)

Genes:

LOC123477751:Sharpr-MPRA regulatory region 12077 [Gene]
STAP1:signal transducing adaptor family member 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

4q13.2

Genomic location:

Preferred name:

NM_012108.4(STAP1):c.221T>C (p.Leu74Pro)

HGVS:

NC_000004.12:g.67575413T>C
NG_047142.1:g.21686T>C
NG_077554.1:g.203T>C
NM_001317769.2:c.221T>C
NM_012108.4:c.221T>CMANE SELECT
NP_001304698.1:p.Leu74Pro
NP_036240.1:p.Leu74Pro
NC_000004.11:g.68441131T>C
NM_012108.2:c.221T>C

Protein change:

L74P

Molecular consequence:

NM_001317769.2:c.221T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_012108.4:c.221T>C - 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
SCV003858000	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Jan 22, 2023)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003858000

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Jan 22, 2023)

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, SCV003858000.2

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

Description

The p.L74P variant (also known as c.221T>C), located in coding exon 3 of the STAP1 gene, results from a T to C substitution at nucleotide position 221. The leucine at codon 74 is replaced by proline, an amino acid with similar properties. This amino acid position is conserved. In addition, this alteration is predicted to be deleterious by in silico analysis. Since supporting evidence is limited at this time, 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 19, 2024

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