All variants in the FH gene

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

198 entries on 2 pages. Showing entries 1 - 100.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Type     

DNA change (genomic) (hg19)     

Reference     

DB-ID     

Frequency     

Variant remarks     

ClassClinical     

Owner     
./. 01 c.-?_132+?del - - This mutation is novel, not a frequent cause of HLRCC syndrome. The mitochondrial signal peptide of - GenBank FH_00144 - blood samples or cultured lymphocytes - Qi Ming
./. 07 c.? - p.? both cytosolic and mitochondrial fumarase were markedly deficient;exhibited half the expected fumara - GenBank FH_00027 - cultured skin fibroblasts - Qi Ming
./. 07 c.? - - The changes occurred at sites of residues which are generally conserved across species - GenBank FH_00136 - blood - Qi Ming
./. 01 c.1-?_1404+?del - p.Met1-?_X468+?del complete deletion of FH - GenBank FH_00090 - peripheral blood leucocytes - Qi Ming
./. 00 c.1_1533del - p.? whole gene deletion - GenBank FH_00148 - blood - Qi Ming
./. 01 c.4T>C - p.Tyr2His - - GenBank FH_00179 NA unknown - Qi Ming
./. 01 c.15dup - p.Arg6SerfsX50 - - GenBank FH_00181 NA unknown - Qi Ming
./. 01 c.50C>T - p.Ala17Val - - GenBank FH_00177 NA unknown - Qi Ming
./. 01 c.77C>T - p.Pro26Leu - - GenBank FH_00176 NA unknown - Qi Ming
./. 02 c.139C>T - p.Gln47X Disease-associated missense FH changes map to highly conserved residues, mostly in or around the e - GenBank FH_00028 - blood - Qi Ming
./. 02 c.139C>T - p.Gln47X a founder effect - GenBank FH_00028 - peripheral blood - Qi Ming
./. 02 c.143dup - p.Arg6SerfsX50 - - GenBank FH_00180 NA unknown - Qi Ming
./. 02 c.157G>T - p.Glu53X novel - GenBank FH_00149 - blood - Qi Ming
./. 02 c.172G>T - p.Gly58Cys - - GenBank FH_00174 NA unknown - Qi Ming
./. 02 c.178delC - p.Leu60X Disease-associated missense FH changes map to highly conserved residues, mostly in or around the enz - GenBank FH_00065 - blood - Qi Ming
./. 02 c.191A>C - p.Asn64Thr - - GenBank FH_00112 - blood - Qi Ming
./. 02 c.191A>C - p.Asn64Thr Sequence analysis revealed the germline mutation in the familial case to be homozygous/hemizygous in - GenBank FH_00112 - tummor - Qi Ming
./. 02 c.194A>G - p.Asp65Gly - - GenBank FH_00173 NA unknown - Qi Ming
./. 02 c.222A>T - p.Arg74Ser - - GenBank FH_00172 NA unknown - Qi Ming
./. 02 c.233del - p.Asn78ThrfsX7 - - GenBank FH_00082 - blood - Qi Ming
./. 02 c.239dupA - p.Ile81AspfsX14 confirmed by subcloning a frameshift mutation produce a truncated protein - GenBank FH_00001 - peripheral blood - Qi Ming
./. 02 c.256_257del - p.Glu86ThrfsX8 novel - GenBank FH_00091 - peripheral blood lymphocytes - Qi Ming
./. 02 c.259C>T - p.Arg87Cys - - GenBank FH_00171 NA unknown - Qi Ming
./. 02 c.267+1G>C - - splice site mutation - GenBank FH_00002 - peripheral blood - Qi Ming
./. 02 c.267+1G>C - - - - GenBank FH_00002 - peripheral blood lymphocytes - Qi Ming
./. 02 c.267+1_267+10del - p.= novel - GenBank FH_00093 - peripheral blood lymphocytes - Qi Ming
./. 03 c.276del - p.Ile93LeufsX7 novel - GenBank FH_00092 - peripheral blood lymphocytes - Qi Ming
./. 03 c.301C>T - p.Arg101X - - GenBank FH_00003 - peripheral blood - Qi Ming
./. 03 c.301C>T - p.Arg101X Disease-associated missense FH changes map to highly conserved residues, mostly in or around the enz - GenBank FH_00003 - blood - Qi Ming
./. 03 c.301C>T - p.Arg101X - - GenBank FH_00003 - peripheral blood lymphocytes - Qi Ming
./. 03 c.301C>T - p.Arg101X previously reported - GenBank FH_00003 - peripheral blood lymphocytes - Qi Ming
./. 03 c.305C>T - p.Ala102Val - - GenBank FH_00170 NA unknown - Qi Ming
./. 03 c.320A>C - p.Asn107Thr The most frequent FH germline mutations reported in series of patients with HLRCC in Europe.Haplotyp - GenBank FH_00004 - peripheral blood - Qi Ming
./. 03 c.320A>C - p.Asn107Thr Disease-associated missense FH changes map to highly conserved residues, mostly in or around the enz - GenBank FH_00004 - blood - Qi Ming
./. 03 c.320A>C - p.Asn107Thr - - GenBank FH_00004 - peripheral blood lymphocytes - Qi Ming
./. 03 c.349G>C - p.Ala117Pro Disease-associated missense FH changes map to highly conserved residues, mostly in or around the enz - GenBank FH_00030 - blood - Qi Ming
./. 03 c.349G>C - p.Ala117Pro previously reported - GenBank FH_00030 - peripheral blood lymphocytes - Qi Ming
./. 03 c.349G>C - p.Ala117Pro previously reported - GenBank FH_00030 - peripheral blood lymphocytes - Qi Ming
./. 03 c.349G>C - p.Ala117Pro - - GenBank FH_00030 - blood - Qi Ming
./. 03 c.361A>C - p.Met121Leu - - GenBank FH_00169 NA unknown - Qi Ming
./. 03 c.376_378+1 delinsA - p.Glu126del novel - GenBank FH_00095 - peripheral blood lymphocytes - Qi Ming
./. 03 c.376_378+1delinsA - p.Glu126del novel - GenBank FH_00124 - peripheral blood lymphocytes - Qi Ming
./. 04 c.379-22A>T - - - - GenBank FH_00142 - tummor - Qi Ming
./. 04 c.379-2A>G - p.= novel - GenBank FH_00097 - peripheral blood lymphocytes - Qi Ming
./. 04 c.395T>C - p.Leu132Ser FH activity was significantly decreased compared to matched normal controls: L89S (mean 118 nmol - GenBank FH_00005 - peripheral blood - Qi Ming
./. 04 c.395T>C - p.Leu132Ser - - GenBank FH_00005 - peripheral blood lymphocytes - Qi Ming
./. 04 c.404A>G - p.His135Arg a founder effect; novel - GenBank FH_00131 - peripheral blood - Qi Ming
./. 04 c.427del - p.Thr143LeufsX9 novel - GenBank FH_00099 - peripheral blood lymphocytes - Qi Ming
./. 04 c.434C>G - p.Ser145X de novo mutation; mutations associated with an absence of cutaneous leiomyomas; lower FH enzyme - GenBank FH_00006 - peripheral blood - Qi Ming
./. 04 c.434C>G - p.Ser145X - - GenBank FH_00006 - peripheral blood lymphocytes - Qi Ming
./. 04 c.437G>A - p.Gly146Glu - - GenBank FH_00168 NA unknown - Qi Ming
./. 04 c.473G>T - p.Ser158Ile new - GenBank FH_00071 - peripheral blood - Qi Ming
./. 04 c.473G>T - p.Ser158Ile - - GenBank FH_00071 - blood - Qi Ming
./. 04 c.478A>G - p.Arg160Gly de novo - GenBank FH_00007 - peripheral blood - Qi Ming
./. 04 c.539A>G - p.His180Arg Disease-associated missense FH changes map to highly conserved residues, mostly in or around the enz - GenBank FH_00031 - blood - Qi Ming
./. 04 c.539A>G - p.His180Arg previously reported - GenBank FH_00031 - peripheral blood lymphocytes - Qi Ming
./. 04 c.539A>G - p.His180Arg - - GenBank FH_00031 - blood - Qi Ming
./. 04 c.553C>T - p.Gln185X new - GenBank FH_00072 - peripheral blood - Qi Ming
./. 04 c.554A>G - p.Gln185Arg Disease-associated missense FH changes map to highly conserved residues, mostly in or around the enz - GenBank FH_00032 - blood - Qi Ming
./. 04 c.554A>G - p.Gln185Arg - - GenBank FH_00032 - blood - Qi Ming
./. 04 c.555+1G>A - p.= novel - GenBank FH_00110 - peripheral blood lymphocytes - Qi Ming
./. 05 c.556-941_556-16dup - p.= an enzymatic activity less than half that of nonaffected family members - GenBank FH_00089 - blood? - Qi Ming
./. 05 c.560C>T - p.Ser187Leu - - GenBank FH_00046 - blood - Qi Ming
./. 05 c.563A>G - p.Asn188Ser - - GenBank FH_00047 - blood - Qi Ming
./. 05 c.575C>T - p.Pro192Leu a founder effect; novel - GenBank FH_00133 - peripheral blood - Qi Ming
./. 05 c.584T>C - p.Met195Thr - - GenBank FH_00048 - blood - Qi Ming
./. 05 c.587A>G - p.His196Arg also found in the patient - GenBank FH_00024 - Tumors - Qi Ming
./. 05 c.587A>G - p.His196Arg - - GenBank FH_00024 - blood - Qi Ming
./. 05 c.587A>G - p.His196Arg - - GenBank FH_00024 - blood? - Qi Ming
./. 05 c.632T>C - p.Leu211Pro novel - GenBank FH_00104 - peripheral blood lymphocytes - Qi Ming
./. 05 c.655G>T - p.Asp219Tyr - - GenBank FH_00167 NA unknown - Qi Ming
./. 05 c.671_672del - p.Glu224ValfsX25 - - GenBank FH_00127 - blood? - Qi Ming
./. 05 c.671_672delAG - p.Glu224ValfsX25 Disease-associated missense FH changes map to highly conserved residues, mostly in or around the enz - GenBank FH_00066 - blood - Qi Ming
./. 05 c.674T>C - p.Phe225Ser - - GenBank FH_00166 NA unknown - Qi Ming
./. 05 c.679C>T - p.Gln227Ter - - GenBank FH_00165 NA unknown - Qi Ming
./. 05 c.686T>C - p.Ile229Thr Disease-associated missense FH changes map to highly conserved residues, mostly in or around the enz - GenBank FH_00039 - blood - Qi Ming
./. 05 c.686T>C - p.Ile229Thr - - GenBank FH_00039 - blood - Qi Ming
./. 05 c.686_688delTCA - p.Ile229del - - GenBank FH_00067 - blood - Qi Ming
./. 05 c.689A>G - p.Lys230Arg Disease-associated missense FH changes map to highly conserved residues, mostly in or around the enz - GenBank FH_00034 - blood - Qi Ming
./. 05 c.689A>G - p.Lys230Arg - - GenBank FH_00034 - blood - Qi Ming
./. 05 c.689A>G - p.Lys230Arg a founder effect - GenBank FH_00034 - peripheral blood - Qi Ming
./. 05 c.695del - p.Gly232AspfsX24 novel - GenBank FH_00147 - peripheral blood - Qi Ming
./. 05 c.697C>T - p.Arg233Cys de novo - GenBank FH_00008 - peripheral blood - Qi Ming
./. 05 c.697C>T - p.Arg233Cys - - GenBank FH_00008 - peripheral blood lymphocytes - Qi Ming
./. 05 c.697C>T - p.Arg233Cys previously reported - GenBank FH_00008 - peripheral blood lymphocytes - Qi Ming
./. 05 c.697C>T - p.Arg233Cys previously reported - GenBank FH_00008 - peripheral blood lymphocytes - Qi Ming
./. 05 c.697C>T - p.Arg233Cys a founder effect; novel - GenBank FH_00008 - peripheral blood - Qi Ming
./. 05 c.698G>A - p.Arg233His led to changes in highly conserved amino acids; a high frequency of kidney tumours - GenBank FH_00009 - peripheral blood - Qi Ming
./. 05 c.698G>A - p.Arg233His Disease-associated missense FH changes map to highly conserved residues, mostly in or around the enz - GenBank FH_00009 - blood - Qi Ming
./. 05 c.698G>A - p.Arg233His - - GenBank FH_00009 - peripheral blood lymphocytes - Qi Ming
./. 05 c.698G>A - p.Arg233His - - GenBank FH_00009 - blood - Qi Ming
./. 05 c.698G>A - p.Arg233His a founder effect - GenBank FH_00009 - peripheral blood - Qi Ming
./. 05 c.698G>A - p.Arg233His novel - GenBank FH_00009 - blood - Qi Ming
./. 05 c.698G>A - p.Arg233His has previously been shown to reduce the activity of FH - GenBank FH_00009 - peripheral blood - Qi Ming
./. 05 c.698G>A - p.Arg233His - - GenBank FH_00009 - blood - Qi Ming
./. 05 c.698G>T - p.Arg233Leu R190 residue may represent a mutational hotspot. - GenBank FH_00049 - peripheral blood lymphocytes - Qi Ming
./. 05 c.698G>T - p.Arg233Leu - - GenBank FH_00049 - blood - Qi Ming
./. 05 c.715G>A - p.Ala239Thr - - GenBank FH_00140 - Malignant tumors - Qi Ming
./. 04 c.738+3A>G - p.= - - GenBank FH_00188 - Malignant tumors - Qi Ming
./. 06 c.761A>G - p.Gln254Arg novel - GenBank FH_00106 - peripheral blood lymphocytes - Qi Ming
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