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NM_000038.6(APC):c.6895C>T (p.Pro2299Ser) AND Familial adenomatous polyposis 1

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Dec 10, 2022
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:
RCV003766557.2

Allele description [Variation Report for NM_000038.6(APC):c.6895C>T (p.Pro2299Ser)]

NM_000038.6(APC):c.6895C>T (p.Pro2299Ser)

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.6895C>T (p.Pro2299Ser)
HGVS:
  • NC_000005.10:g.112842489C>T
  • NG_008481.4:g.154969C>T
  • NM_000038.6:c.6895C>TMANE SELECT
  • NM_001127510.3:c.6895C>T
  • NM_001127511.3:c.6841C>T
  • NM_001354895.2:c.6895C>T
  • NM_001354896.2:c.6949C>T
  • NM_001354897.2:c.6925C>T
  • NM_001354898.2:c.6820C>T
  • NM_001354899.2:c.6811C>T
  • NM_001354900.2:c.6772C>T
  • NM_001354901.2:c.6718C>T
  • NM_001354902.2:c.6622C>T
  • NM_001354903.2:c.6592C>T
  • NM_001354904.2:c.6517C>T
  • NM_001354905.2:c.6415C>T
  • NM_001354906.2:c.6046C>T
  • NP_000029.2:p.Pro2299Ser
  • NP_001120982.1:p.Pro2299Ser
  • NP_001120983.2:p.Pro2281Ser
  • NP_001341824.1:p.Pro2299Ser
  • NP_001341825.1:p.Pro2317Ser
  • NP_001341826.1:p.Pro2309Ser
  • NP_001341827.1:p.Pro2274Ser
  • NP_001341828.1:p.Pro2271Ser
  • NP_001341829.1:p.Pro2258Ser
  • NP_001341830.1:p.Pro2240Ser
  • NP_001341831.1:p.Pro2208Ser
  • NP_001341832.1:p.Pro2198Ser
  • NP_001341833.1:p.Pro2173Ser
  • NP_001341834.1:p.Pro2139Ser
  • NP_001341835.1:p.Pro2016Ser
  • LRG_130:g.154969C>T
  • NC_000005.9:g.112178186C>T
  • NM_000038.5:c.6895C>T
Protein change:
P2016S
Links:
dbSNP: rs1060503267
NCBI 1000 Genomes Browser:
rs1060503267
Molecular consequence:
  • NM_000038.6:c.6895C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001127510.3:c.6895C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001127511.3:c.6841C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354895.2:c.6895C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354896.2:c.6949C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354897.2:c.6925C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354898.2:c.6820C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354899.2:c.6811C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354900.2:c.6772C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354901.2:c.6718C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354902.2:c.6622C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354903.2:c.6592C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354904.2:c.6517C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354905.2:c.6415C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354906.2:c.6046C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Familial adenomatous polyposis 1 (FAP1)
Synonyms:
POLYPOSIS, ADENOMATOUS INTESTINAL; FAMILIAL ADENOMATOUS POLYPOSIS 1, ATTENUATED; APC-Associated Polyposis Conditions
Identifiers:
MONDO: MONDO:0021056; MedGen: C2713442; OMIM: 175100

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000552474Labcorp Genetics (formerly Invitae), Labcorp
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Uncertain significance
(Dec 10, 2022) 		germlineclinical testing

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical testing

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]
PMID:
28492532
PMCID:
PMC5632818

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV000552474.5

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)

Description

In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is not expected to disrupt APC protein function. ClinVar contains an entry for this variant (Variation ID: 411353). This variant has not been reported in the literature in individuals affected with APC-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change replaces proline, which is neutral and non-polar, with serine, which is neutral and polar, at codon 2299 of the APC protein (p.Pro2299Ser).

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Nov 10, 2024