NM_004629.2(FANCG):c.552_585del (p.Thr183_Trp184insTer) AND Fanconi anemia complementation group G

Germline classification:: Likely pathogenic (1 submission)
Last evaluated:: Apr 14, 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:: RCV003461497.1

Allele description [Variation Report for NM_004629.2(FANCG):c.552_585del (p.Thr183_Trp184insTer)]

NM_004629.2(FANCG):c.552_585del (p.Thr183_Trp184insTer)

Gene:

FANCG:FA complementation group G [Gene - OMIM - HGNC]

Variant type:

Deletion

Cytogenetic location:

9p13.3

Genomic location:

Preferred name:

NM_004629.2(FANCG):c.552_585del (p.Thr183_Trp184insTer)

HGVS:

NC_000009.12:g.35077328_35077361del
NG_007312.1:g.7659_7692del
NG_007887.1:g.385_418del
NM_004629.2:c.552_585delMANE SELECT
NP_004620.1:p.Thr183_Trp184insTer
NP_004620.1:p.Trp184Terfs
LRG_499t1:c.549_582del34
LRG_499:g.7659_7692del
LRG_499p1:p.Trp184Terfs
LRG_657:g.385_418del
NC_000009.11:g.35077325_35077358del
NM_004629.1:c.549_582del34

Molecular consequence:

NM_004629.2:c.552_585del - nonsense - [Sequence Ontology: SO:0001587]

Condition(s)

Name:: Fanconi anemia complementation group G
Synonyms:: Fanconi anemia group G
Identifiers:: MONDO: MONDO:0013565; MedGen: C3469527; Orphanet: 84; OMIM: 614082

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004199158	Baylor Genetics	criteria provided, single submitter (ACMG Guidelines, 2015)	Likely pathogenic (Apr 14, 2023)	unknown	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV004199158

Baylor Genetics

criteria provided, single submitter

(ACMG Guidelines, 2015)

Likely pathogenic
(Apr 14, 2023)

unknown

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	unknown	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Citations

PubMed

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 Baylor Genetics, SCV004199158.1

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

Last Updated: Dec 30, 2023

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