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     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/+ 5 c.743dup r.(?) p.(Gln249Thrfs*12) Both (homozygous) - pathogenic g.39975477dup - 743dupC - FKBP10_000010 - PubMed: Shaheen 2011 - - Germline - - - - - DNA PCR, SEQ - - BRKS Family 1 PubMed: Shaheen 2011 The parents are consanguineous and there is phenotypic variability between the proband and her older sister as well as with affected cousins.; This patients family has the ID OI_F1 ({PMID23054245:Shaheen et al., 2012}). - yes Saudi Arabia - - - - - 1 Raymond Dalgleish
+/+ 5 c.743dup r.(?) p.(Gln249Thrfs*12) Both (homozygous) - pathogenic g.39975477dup - 743dupC - FKBP10_000010 - PubMed: Schwarze 2013 - - Germline - - - - - DNA PCR, SEQ - - OI Family M PubMed: Schwarze 2013 Both affected individuals in this family are described as having OI III rather than Bruck syndrome. - - - - - - - - 1 Peter Byers
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