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NM_018062.4(FANCL):c.1093-10_1093-8del AND Fanconi anemia

Germline classification:
Likely benign (1 submission)
Last evaluated:
Dec 24, 2021
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:
RCV002923035.2

Allele description

NM_018062.4(FANCL):c.1093-10_1093-8del

Genes:
FANCL:FA complementation group L [Gene - OMIM - HGNC]
VRK2:VRK serine/threonine kinase 2 [Gene - OMIM - HGNC]
Variant type:
Deletion
Cytogenetic location:
2p16.1
Genomic location:
Preferred name:
NM_018062.4(FANCL):c.1093-10_1093-8del
HGVS:
  • NC_000002.12:g.58159809_58159811del
  • NG_007418.1:g.86570_86572del
  • NG_029717.2:g.257069_257071del
  • NM_001114636.2:c.1108-10_1108-8del
  • NM_001130480.2:c.*116_*118del
  • NM_001130481.2:c.*116_*118del
  • NM_001130482.2:c.*116_*118del
  • NM_001130483.2:c.*501_*503del
  • NM_001288836.1:c.*116_*118del
  • NM_001288837.2:c.*116_*118del
  • NM_001288838.2:c.*501_*503del
  • NM_001288839.2:c.*116_*118del
  • NM_001374615.1:c.1138-10_1138-8del
  • NM_001410792.1:c.1153-10_1153-8del
  • NM_006296.7:c.*116_*118delMANE SELECT
  • NM_018062.4:c.1093-10_1093-8delMANE SELECT
  • LRG_501:g.86570_86572del
  • NC_000002.11:g.58386943_58386945del
  • NC_000002.11:g.58386944_58386946del
Molecular consequence:
  • NM_001130480.2:c.*116_*118del - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001130481.2:c.*116_*118del - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001130482.2:c.*116_*118del - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001130483.2:c.*501_*503del - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001288836.1:c.*116_*118del - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001288837.2:c.*116_*118del - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001288838.2:c.*501_*503del - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001288839.2:c.*116_*118del - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_006296.7:c.*116_*118del - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001114636.2:c.1108-10_1108-8del - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001374615.1:c.1138-10_1138-8del - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001410792.1:c.1153-10_1153-8del - intron variant - [Sequence Ontology: SO:0001627]
  • NM_018062.4:c.1093-10_1093-8del - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Name:
Fanconi anemia (FA)
Synonyms:
Fanconi pancytopenia; Fanconi's anemia
Identifiers:
MONDO: MONDO:0019391; MeSH: D005199; MedGen: C0015625; Orphanet: 84; OMIM: PS227650

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV003264353Invitae
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Likely benign
(Dec 24, 2021) 		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 Invitae, SCV003264353.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Sep 1, 2024