NM_000136.3(FANCC):c.436_438del (p.Tyr146del) AND Hereditary cancer-predisposing syndrome

Germline classification:: Likely benign (1 submission)
Last evaluated:: Sep 28, 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:: RCV000566915.5

Allele description [Variation Report for NM_000136.3(FANCC):c.436_438del (p.Tyr146del)]

NM_000136.3(FANCC):c.436_438del (p.Tyr146del)

Gene:

FANCC:FA complementation group C [Gene - OMIM - HGNC]

Variant type:

Deletion

Cytogenetic location:

9q22.32

Genomic location:

Preferred name:

NM_000136.3(FANCC):c.436_438del (p.Tyr146del)

HGVS:

NC_000009.12:g.95172055_95172057del
NG_011707.1:g.150653_150655del
NM_000136.3:c.436_438delMANE SELECT
NM_001243743.2:c.436_438del
NM_001243744.2:c.436_438del
NP_000127.2:p.Tyr146del
NP_001230672.1:p.Tyr146del
NP_001230673.1:p.Tyr146del
LRG_497t1:c.436_438del
LRG_497:g.150653_150655del
NC_000009.11:g.97934337_97934339del
NM_000136.2:c.436_438del
NM_000136.2:c.436_438delTAT
NM_000136.3:c.436_438delTATMANE SELECT

Protein change:

Y146del

Links:

dbSNP: rs761347179

NCBI 1000 Genomes Browser:

rs761347179

Molecular consequence:

NM_000136.3:c.436_438del - inframe_deletion - [Sequence Ontology: SO:0001822]
NM_001243743.2:c.436_438del - inframe_deletion - [Sequence Ontology: SO:0001822]
NM_001243744.2:c.436_438del - inframe_deletion - [Sequence Ontology: SO:0001822]

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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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000673325	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Likely benign (Sep 28, 2022)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000673325

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Likely benign
(Sep 28, 2022)

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, SCV000673325.5

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

#	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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