NM_002451.4(MTAP):c.154A>G (p.Asn52Asp) AND not provided

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Oct 1, 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:: RCV003425638.10

Allele description [Variation Report for NM_002451.4(MTAP):c.154A>G (p.Asn52Asp)]

NM_002451.4(MTAP):c.154A>G (p.Asn52Asp)

Gene:

MTAP:methylthioadenosine phosphorylase [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

9p21.3

Genomic location:

Preferred name:

NM_002451.4(MTAP):c.154A>G (p.Asn52Asp)

HGVS:

NC_000009.12:g.21816747A>G
NG_032650.2:g.19112A>G
NM_001396040.1:c.205A>G
NM_001396041.1:c.154A>G
NM_001396042.1:c.154A>G
NM_001396043.1:c.154A>G
NM_001396044.1:c.154A>G
NM_001396045.1:c.154A>G
NM_002451.4:c.154A>GMANE SELECT
NP_001382969.1:p.Asn69Asp
NP_001382970.1:p.Asn52Asp
NP_001382971.1:p.Asn52Asp
NP_001382972.1:p.Asn52Asp
NP_001382973.1:p.Asn52Asp
NP_001382974.1:p.Asn52Asp
NP_002442.2:p.Asn52Asp
NC_000009.11:g.21816746A>G
NR_173242.1:n.267A>G

Protein change:

N52D

Molecular consequence:

NM_001396040.1:c.205A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001396041.1:c.154A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001396042.1:c.154A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001396043.1:c.154A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001396044.1:c.154A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001396045.1:c.154A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_002451.4:c.154A>G - missense variant - [Sequence Ontology: SO:0001583]
NR_173242.1:n.267A>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Observations:

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

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Gene ID:122928112

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004157605	CeGaT Center for Human Genetics Tuebingen	criteria provided, single submitter (CeGaT Center For Human Genetics Tuebingen Variant Classification Criteria Version 2)	Uncertain significance (Oct 1, 2023)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV004157605

CeGaT Center for Human Genetics Tuebingen

criteria provided, single submitter

(CeGaT Center For Human Genetics Tuebingen Variant Classification Criteria Version 2)

Uncertain significance
(Oct 1, 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	yes	1	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From CeGaT Center for Human Genetics Tuebingen, SCV004157605.10

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

Description

MTAP: PM2

#	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		1	not provided	not provided	not provided

Last Updated: Oct 20, 2024

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Relating variation to medicine