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NM_004523.4(KIF11):c.211-17_211-16dup AND not provided

Germline classification:
Likely benign (1 submission)
Last evaluated:
Sep 29, 2019
Review status:
Somatic classification
of clinical impact:
None
Review status:
no assertion criteria provided
Somatic classification
of oncogenicity:
None
Review status:
no assertion criteria provided
Record status:
current
Accession:
RCV001577040.3

Allele description [Variation Report for NM_004523.4(KIF11):c.211-17_211-16dup]

NM_004523.4(KIF11):c.211-17_211-16dup

Gene:
KIF11:kinesin family member 11 [Gene - OMIM - HGNC]
Variant type:
Duplication
Cytogenetic location:
10q23.33
Genomic location:
Preferred name:
NM_004523.4(KIF11):c.211-17_211-16dup
HGVS:
  • NC_000010.11:g.92606602_92606603dup
  • NG_032580.1:g.18535_18536dup
  • NM_004523.4:c.211-17_211-16dupMANE SELECT
  • NC_000010.10:g.94366359_94366360dup
Links:
dbSNP: rs11393423
NCBI 1000 Genomes Browser:
rs11393423
Molecular consequence:
  • NM_004523.4:c.211-17_211-16dup - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV001804357GeneDx
criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)
Likely benign
(Sep 29, 2019)
germlineclinical testing

Citation Link

Last Updated: Dec 24, 2023

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