NM_000038.6(APC):c.7504G>A (p.Gly2502Ser) AND not specified

Germline classification:: Benign (10 submissions)
Last evaluated:: Aug 15, 2023
Review status:: 2 stars out of maximum of 4 stars
criteria provided, multiple submitters, no conflicts

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:: RCV000077994.39

Allele description [Variation Report for NM_000038.6(APC):c.7504G>A (p.Gly2502Ser)]

NM_000038.6(APC):c.7504G>A (p.Gly2502Ser)

Gene:

APC:APC regulator of WNT signaling pathway [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

5q22.2

Genomic location:

Preferred name:

NM_000038.6(APC):c.7504G>A (p.Gly2502Ser)

Other names:

p.G2502S:GGT>AGT; CCDS4107.1:c.7504G>A

HGVS:

NC_000005.10:g.112843098G>A
NG_008481.4:g.155578G>A
NM_000038.6:c.7504G>AMANE SELECT
NM_001127510.3:c.7504G>A
NM_001127511.3:c.7450G>A
NM_001354895.2:c.7504G>A
NM_001354896.2:c.7558G>A
NM_001354897.2:c.7534G>A
NM_001354898.2:c.7429G>A
NM_001354899.2:c.7420G>A
NM_001354900.2:c.7381G>A
NM_001354901.2:c.7327G>A
NM_001354902.2:c.7231G>A
NM_001354903.2:c.7201G>A
NM_001354904.2:c.7126G>A
NM_001354905.2:c.7024G>A
NM_001354906.2:c.6655G>A
NP_000029.2:p.Gly2502Ser
NP_000029.2:p.Gly2502Ser
NP_001120982.1:p.Gly2502Ser
NP_001120983.2:p.Gly2484Ser
NP_001341824.1:p.Gly2502Ser
NP_001341825.1:p.Gly2520Ser
NP_001341826.1:p.Gly2512Ser
NP_001341827.1:p.Gly2477Ser
NP_001341828.1:p.Gly2474Ser
NP_001341829.1:p.Gly2461Ser
NP_001341830.1:p.Gly2443Ser
NP_001341831.1:p.Gly2411Ser
NP_001341832.1:p.Gly2401Ser
NP_001341833.1:p.Gly2376Ser
NP_001341834.1:p.Gly2342Ser
NP_001341835.1:p.Gly2219Ser
LRG_130t1:c.7504G>A
LRG_130:g.155578G>A
LRG_130p1:p.Gly2502Ser
NC_000005.9:g.112178795G>A
NM_000038.4:c.7504G>A
NM_000038.5:c.7504G>A
NM_001127510.2:c.7504G>A
NM_001127511.2:c.7450G>A
P25054:p.Gly2502Ser
p.G2502S

Protein change:

G2219S

Links:

UniProtKB: P25054#VAR_005055; dbSNP: rs2229995

NCBI 1000 Genomes Browser:

rs2229995

Molecular consequence:

NM_000038.6:c.7504G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001127510.3:c.7504G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001127511.3:c.7450G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001354895.2:c.7504G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001354896.2:c.7558G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001354897.2:c.7534G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001354898.2:c.7429G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001354899.2:c.7420G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001354900.2:c.7381G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001354901.2:c.7327G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001354902.2:c.7231G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001354903.2:c.7201G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001354904.2:c.7126G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001354905.2:c.7024G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001354906.2:c.6655G>A - missense variant - [Sequence Ontology: SO:0001583]

Observations:

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

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cytochrome b, partial (mitochondrion) [Apomys sacobianus]
cytochrome b, partial (mitochondrion) [Apomys sacobianus]
gi|1569270109|gb|QBB01192.1|

Protein
Related gene-specific medical variations for Gene (Select 53407) (1)
ClinVar
PMC Links for Gene (Select 53407) (46)
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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000084177	ITMI	no classification provided	not provided	germline	reference population	PubMed (1) [See all records that cite this PMID]
SCV000109831	Eurofins Ntd Llc (ga)	criteria provided, single submitter (EGL Classification Definitions 2015)	Benign (Aug 22, 2012)	germline	clinical testing	Citation Link,
SCV000167015	GeneDx	criteria provided, single submitter (GeneDx Variant Classification (06012015))	Benign (Oct 14, 2013)	germline	clinical testing	Citation Link,
SCV000301605	PreventionGenetics, part of Exact Sciences	criteria provided, single submitter (ACMG Guidelines, 2015)	Benign	germline	clinical testing	PubMed (1) [See all records that cite this PMID]
SCV000691766	Mayo Clinic Laboratories, Mayo Clinic	no assertion criteria provided	Benign	unknown	clinical testing
SCV001798965	Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) - VKGL Data-share Consensus	no assertion criteria provided	Benign	germline	clinical testing
SCV001807757	Genome Diagnostics Laboratory, Amsterdam University Medical Center - VKGL Data-share Consensus	no assertion criteria provided	Benign	germline	clinical testing
SCV001958192	Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ - VKGL Data-share Consensus See additional submitters Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen	no assertion criteria provided	Benign	germline	clinical testing
SCV001971045	Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center - VKGL Data-share Consensus See additional submitters Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen	no assertion criteria provided	Benign	germline	clinical testing
SCV002550658	Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital	criteria provided, single submitter (ACMG Guidelines, 2015)	Benign (Aug 15, 2023)	germline	clinical testing	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	germline	yes	not provided	not provided	not provided	not provided	not provided	clinical testing
not provided	unknown	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing
not provided	germline	unknown	2	not provided	not provided	not provided	not provided	clinical testing
African	germline	unknown	not provided	not provided	not provided	43	not provided	reference population
African_European	germline	unknown	not provided	not provided	not provided	46	not provided	reference population
Central_Asian	germline	unknown	not provided	not provided	not provided	50	not provided	reference population
East_Asian	germline	unknown	not provided	not provided	not provided	62	not provided	reference population
European	germline	unknown	not provided	not provided	not provided	331	not provided	reference population
Hispanic	germline	unknown	not provided	not provided	not provided	118	not provided	reference population
Whole_cohort	germline	unknown	not provided	not provided	not provided	681	not provided	reference population

Citations

PubMed

Germline variation in cancer-susceptibility genes in a healthy, ancestrally diverse cohort: implications for individual genome sequencing.

Bodian DL, McCutcheon JN, Kothiyal P, Huddleston KC, Iyer RK, Vockley JG, Niederhuber JE.

PLoS One. 2014;9(4):e94554. doi: 10.1371/journal.pone.0094554.

PubMed [citation]

PMID:: 24728327
PMCID:: PMC3984285

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 ITMI, SCV000084177.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	African	not provided	not provided	not provided	reference population	PubMed (1)
2	African_European	not provided	not provided	not provided	reference population	PubMed (1)
3	Central_Asian	not provided	not provided	not provided	reference population	PubMed (1)
4	East_Asian	not provided	not provided	not provided	reference population	PubMed (1)
5	European	not provided	not provided	not provided	reference population	PubMed (1)
6	Hispanic	not provided	not provided	not provided	reference population	PubMed (1)
7	Whole_cohort	not provided	not provided	not provided	reference population	PubMed (1)

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	43	not provided	discovery		not provided	0	not provided	not provided
2	germline	unknown	46	not provided	discovery		not provided	0.0109	not provided	not provided
3	germline	unknown	50	not provided	discovery		not provided	0.01	not provided	not provided
4	germline	unknown	62	not provided	discovery		not provided	0	not provided	not provided
5	germline	unknown	331	not provided	discovery		not provided	0.0242	not provided	not provided
6	germline	unknown	118	not provided	discovery		not provided	0.0169	not provided	not provided
7	germline	unknown	681	not provided	discovery		not provided	0.0169	not provided	not provided

From Eurofins Ntd Llc (ga), SCV000109831.8

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	2	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	unknown	not provided	not provided	not provided		2	not provided	not provided	not provided

From GeneDx, SCV000167015.11

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

Description

This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.

#	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

From PreventionGenetics, part of Exact Sciences, SCV000301605.1

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

#	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

From Mayo Clinic Laboratories, Mayo Clinic, SCV000691766.1

#	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	unknown	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

From Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) - VKGL Data-share Consensus, SCV001798965.1

#	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

From Genome Diagnostics Laboratory, Amsterdam University Medical Center - VKGL Data-share Consensus, SCV001807757.1

#	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

From Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ - VKGL Data-share Consensus, SCV001958192.1

#	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

From Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center - VKGL Data-share Consensus, SCV001971045.1

#	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

From Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital, SCV002550658.4

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

#	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: Sep 29, 2024

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