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NM_001113378.2(FANCI):c.3255+6dup AND not specified

Germline classification:
Benign (1 submission)
Last evaluated:
Mar 16, 2018
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:
RCV001818583.4

Allele description [Variation Report for NM_001113378.2(FANCI):c.3255+6dup]

NM_001113378.2(FANCI):c.3255+6dup

Gene:
FANCI:FA complementation group I [Gene - OMIM - HGNC]
Variant type:
Duplication
Cytogenetic location:
15q26.1
Genomic location:
Preferred name:
NM_001113378.2(FANCI):c.3255+6dup
HGVS:
  • NC_000015.10:g.89305415dup
  • NG_008218.2:g.34381dup
  • NG_011736.1:g.66453dup
  • NM_001113378.2:c.3255+6dupMANE SELECT
  • NM_001376910.1:c.2976+6dup
  • NM_001376911.1:c.3255+6dup
  • NM_018193.3:c.3075+6dup
  • LRG_500t1:c.3255+6dup
  • LRG_500:g.66453dup
  • LRG_765:g.34381dup
  • NC_000015.9:g.89848645_89848646insT
  • NC_000015.9:g.89848646dup
  • NM_001113378.1:c.3255+6dup
  • NM_001113378.1:c.3255+6dupT
Links:
dbSNP: rs878854178
NCBI 1000 Genomes Browser:
rs878854178
Molecular consequence:
  • NM_001113378.2:c.3255+6dup - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001376910.1:c.2976+6dup - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001376911.1:c.3255+6dup - intron variant - [Sequence Ontology: SO:0001627]
  • NM_018193.3:c.3075+6dup - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Synonyms:
AllHighlyPenetrant
Identifiers:
MedGen: CN169374

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV002069537Genetic Services Laboratory, University of Chicago
criteria provided, single submitter

(ACMG Guidelines, 2015)
Benign
(Mar 16, 2018)
germlineclinical testing

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

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlinenonot providednot providednot providednot providednot providedclinical 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 Genetic Services Laboratory, University of Chicago, SCV002069537.1

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

Last Updated: Jul 15, 2024