All variants in the FAH gene

Information The variants shown are described using the NM_000137.2 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     
-/. - c.181G>T r.(?) p.(Val61Phe) - benign g.80450501G>T g.80158159G>T FAH(NM_000137.2):c.181G>T (p.V61F, p.(Val61Phe)) - FAH_000035 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Rotterdam
-?/. - c.181G>T r.(?) p.(Val61Phe) - likely benign g.80450501G>T g.80158159G>T FAH(NM_000137.2):c.181G>T (p.V61F, p.(Val61Phe)) - FAH_000035 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Leiden
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