Full data view for gene FKBP10


Osteogenesis Imperfecta Variant Database
Information The variants shown are described using the NM_021939.3 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

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Remarks     

Gender     

Consanguinity     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/. 7 c.1086del r.(?) p.(Val363Cysfs*2) Parent #2 - pathogenic (recessive) g.39976543del g.41820291del 1085_1086delC - FKBP10_000034 - PubMed: Liu 2017 - - Germline - 1/101 cases OI - - - DNA SEQ-NG - targeted 14-gene panel OI OI Fam30 PubMed: Liu 2017 analysis 101 unrelated OI families - - China - - - - - 1 Johan den Dunnen
+/+ 7 c.1086del r.(?) p.(Val363Cysfs*2) Paternal (confirmed) - pathogenic g.39976543del - 1086delC - FKBP10_000034 The protein-level variant description for the paternal allele is incorrectly described by the authors as p.A362fsX1.; The family in this study was presented again as Family 30 by {PMID28725987:Liu et al., 2017} with a phenotype of OI III. PubMed: Xu 2017 - - Germline - - - - - DNA SEQ-NG, PCR, SEQ - custom gene panel OI Family 1 PubMed: Xu 2017 - - - China Han - - - - 1 Raymond Dalgleish
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