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NM_004360.5(CDH1):c.328T>C (p.Phe110Leu) AND Hereditary cancer-predisposing syndrome

Germline classification:
Likely benign (1 submission)
Last evaluated:
Mar 3, 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:
RCV002322060.2

Allele description [Variation Report for NM_004360.5(CDH1):c.328T>C (p.Phe110Leu)]

NM_004360.5(CDH1):c.328T>C (p.Phe110Leu)

Gene:
CDH1:cadherin 1 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
16q22.1
Genomic location:
Preferred name:
NM_004360.5(CDH1):c.328T>C (p.Phe110Leu)
HGVS:
  • NC_000016.10:g.68801834T>C
  • NG_008021.1:g.69543T>C
  • NM_001317184.2:c.328T>C
  • NM_001317185.2:c.-1288T>C
  • NM_001317186.2:c.-1492T>C
  • NM_004360.5:c.328T>CMANE SELECT
  • NP_001304113.1:p.Phe110Leu
  • NP_004351.1:p.Phe110Leu
  • LRG_301t1:c.328T>C
  • LRG_301:g.69543T>C
  • NC_000016.9:g.68835737T>C
  • NM_004360.3:c.328T>C
Protein change:
F110L
Links:
dbSNP: rs1960519396
NCBI 1000 Genomes Browser:
rs1960519396
Molecular consequence:
  • NM_001317185.2:c.-1288T>C - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001317186.2:c.-1492T>C - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001317184.2:c.328T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_004360.5:c.328T>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Hereditary cancer-predisposing syndrome
Synonyms:
Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672

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Assertion and evidence details

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Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV002606952Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Likely benign
(Mar 3, 2022) 		germlineclinical testing

Citation Link

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Summary from all submissions

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

Details of each submission

From Ambry Genetics, SCV002606952.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

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

Last Updated: Sep 29, 2024