NM_001365951.3(KIF1B):c.2115+6835C>T AND not provided

Clinical significance:Uncertain significance (Last evaluated: Jun 1, 2016)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
3 submissions [Details]
Record status:
current
Accession:
RCV000993906.3

Allele description [Variation Report for NM_001365951.3(KIF1B):c.2115+6835C>T]

NM_001365951.3(KIF1B):c.2115+6835C>T

Gene:
KIF1B:kinesin family member 1B [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
1p36.22
Genomic location:
Preferred name:
NM_001365951.3(KIF1B):c.2115+6835C>T
HGVS:
  • NC_000001.11:g.10304081C>T
  • NG_008069.1:g.98376C>T
  • NM_001365951.3:c.2115+6835C>TMANE SELECT
  • NM_001365952.1:c.2115+6835C>T
  • NM_001365953.1:c.2896C>T
  • NM_015074.3:c.1977+6835C>T
  • NM_183416.4:c.2896C>T
  • NP_001352882.1:p.Pro966Ser
  • NP_904325.2:p.Pro966Ser
  • LRG_252t1:c.1977+6835C>T
  • LRG_252t2:c.2115+6835C>T
  • LRG_252:g.98376C>T
  • NC_000001.10:g.10364139C>T
Protein change:
P966S
Links:
dbSNP: rs140733878
NCBI 1000 Genomes Browser:
rs140733878
Molecular consequence:
  • NM_001365951.3:c.2115+6835C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001365952.1:c.2115+6835C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_015074.3:c.1977+6835C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001365953.1:c.2896C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_183416.4:c.2896C>T - missense variant - [Sequence Ontology: SO:0001583]
Observations:
1

Condition(s)

Identifiers:
MedGen: CN517202

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV001147131CeGaT Praxis fuer Humangenetik Tuebingencriteria provided, single submitter
Uncertain significance
(Jun 1, 2016)
germlineclinical testing

Citation Link,

SCV001979122Clinical Genetics,Academic Medical Center - VKGL Data-share Consensus

See additional submitters

no assertion criteria providedLikely benigngermlineclinical testing

SCV001979809Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) - VKGL Data-share Consensus

See additional submitters

no assertion criteria providedLikely benigngermlineclinical testing

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyes1not providednot providednot providednot providedclinical testing

Details of each submission

From CeGaT Praxis fuer Humangenetik Tuebingen, SCV001147131.7

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot provided1not providednot providednot provided

From Clinical Genetics,Academic Medical Center - VKGL Data-share Consensus, SCV001979122.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot providednot providednot providednot providednot provided

From Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) - VKGL Data-share Consensus, SCV001979809.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Oct 16, 2021

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