All variants in the F9 gene

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     

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     
+/+? 1 c.8G>A r.(?) p.(Arg3His) EAHAD-CFDB unclassified g.138612931G>A g.139530772G>A - - F9_000025 - PubMed: Ludwig et al., 1992a - - Unknown ? - - 0 - Geoffrey Kemball-Cook
-?/. - c.8G>A r.(?) p.(Arg3His) - likely benign g.138612931G>A g.139530772G>A F9(NM_000133.3):c.8G>A (p.R3H) - F9_000025 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Rotterdam
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