All variants in the F9 gene

Information The variants shown are described using the NM_000133.3 transcript reference sequence.

6 entries on 1 page. Showing entries 1 - 6.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

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     

Owner     
?/. - c.19A>T r.(?) p.(Ile7Phe) - VUS g.138612942A>T g.139530783A>T F9(NM_000133.3):c.19A>T (p.I7F, p.(Ile7Phe)) - F9_000026 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Leiden
+/+? 1 c.19A>T r.(?) p.(Ile7Phe) EAHAD-CFDB unclassified g.138612942A>T g.139530783A>T - - F9_000026 - Unpublished - - Unknown ? - - 0 - Geoffrey Kemball-Cook
+/+? 1 c.19A>T r.(?) p.(Ile7Phe) EAHAD-CFDB unclassified g.138612942A>T g.139530783A>T - - F9_000026 - PubMed: Montejo et al., 1999 - - Unknown ? - - 0 - Geoffrey Kemball-Cook
+/+? 1 c.19A>T r.(?) p.(Ile7Phe) EAHAD-CFDB unclassified g.138612942A>T g.139530783A>T - - F9_000026 - Wulff et al., 2001 - - Unknown ? - - 0 - Geoffrey Kemball-Cook
+?/. 1 c.19A>T r.(?) p.(Ile7Phe) EAHAD-CFDB unclassified g.138612942A>T g.139530783A>T - - F9_000026 - PubMed: Poon et al., 1993 - - Unknown ? - - 0 - Geoffrey Kemball-Cook
-?/. - c.19A>T r.(?) p.(Ile7Phe) - likely benign g.138612942A>T g.139530783A>T F9(NM_000133.3):c.19A>T (p.I7F, p.(Ile7Phe)) - F9_000026 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Rotterdam
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