All variants in the FH gene

Information The variants shown are described using the NM_000143.3 transcript reference sequence.

5 entries on 1 page. Showing entries 1 - 5.
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Effect     

Exon     

AscendingDNA change (cDNA)     

Protein     

Zygosity     

Co_ocurrence     

RNA change     

Review status     

DNA change (genomic) (hg38)     

Reference     

DB-ID     

dbSNP ID     

Variant remarks     

Owner     
-/- 7 c.927G>A p.(=) Hetero no r.(=) - g.241504223C>T - FH_000002 - - Jesica Ramirez-Hospital Central de Mendoza
?/+? 8 c.1157A>C p.(Gln386Pro) Hetero no r.(?) - g.241502522T>G - FH_000001 - - Jesica Ramirez-Hospital Central de Mendoza
-?/-? 8i c.1237-14_1237-13dup p.(=) Hetero no r.(=) - g.241500603_241500604dup - FH_000003 - - Pablo Kalfayan-Hospital Italiano
?/? 10 c.1431_1433dup p.(Lys477dup) Hetero no r.(?) - g.241497928_241497930dup - FH_000004 - This is an in-frame duplication that has been observed with several different pathogenic FH variants in multiple affected individuals with FHD. In the homozygous state, this variant does not likely cause FHD, but additional data are needed to prove that conclusively. Although it has been observed as heterozygous in individuals with features of HLRCC, it occurs in the general population too frequently given the rarity of this condition. For these reasons, this variant has been classified as Likely Pathogenic for FHD. However, it is not likely to confer risk for HLRCC. Jesica Ramirez-Hospital Central de Mendoza
+?/? 10 c.1431_1433dup p.(Lys477dup) Hetero no r.(?) - g.241497928_241497930dup - FH_000004 - - Silvina Sisterna-Hospital de Comunidad
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