Full data view for gene SERPINF1


Osteogenesis Imperfecta Variant Database
Information The variants shown are described using the NM_002615.5 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     
+/. 3 c.184G>A r.(?) p.(Gly62Ser) Parent #2 - pathogenic (recessive) g.1673245G>A g.1769951G>A - - SERPINF1_000033 - PubMed: Liu 2017 - - Germline - 1/101 cases OI - - - DNA SEQ-NG - targeted 14-gene panel OI OI Fam33 PubMed: Liu 2017 analysis 101 unrelated OI families - - China - - - - - 1 Johan den Dunnen
+/+ 3 c.184G>A r.(?) p.(Gly62Ser) Maternal (confirmed) - pathogenic g.1673245G>A - - - SERPINF1_000033 - PubMed: Wang 2017 - - Germline - - - - - DNA SEQ-NG, PCR, SEQ - custom gene panel OI Patient 4 PubMed: Wang 2017 The patient in this study was presented again as Family 33 by {PMID28725987:Liu et al., 2017} but with a phenotype of OI III. - - China - - - - - 1 Raymond Dalgleish
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