Full data view for gene F9

Information The variants shown are described using the NM_000133.3 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     
+/+? _1 c.-34A>T r.(=) p.(=) Maternal (inferred) EAHAD-CFDB unclassified g.138612890A>T g.139530731A>T - - F9_000014 - PubMed: Picketts et al., 1992 - - Unknown ? - - 0 - DNA PCR, SEQ - - HEMB - PubMed: Picketts et al., 1992 - M ? (Canada) - - 0 - - 1 Geoffrey Kemball-Cook
+/+? _1 c.-34A>T r.(=) p.(=) Maternal (inferred) EAHAD-CFDB unclassified g.138612890A>T g.139530731A>T - - F9_000014 - PubMed: Belvini et al., 2005 - - Unknown ? - - 0 - DNA CSCE, DHPLC, PCR, SEQ - - HEMB - PubMed: Belvini et al., 2005 - M ? Italy - - 0 - - 1 Geoffrey Kemball-Cook
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