All variants in the CDC73 gene

Information The variants shown are described using the NM_024529.4 transcript reference sequence.

125 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.-11G>A - - 5' UTR - GenBank CDC73_00019 - HRPT2 polymorphisms - Qi Ming
./. 07 c.729+33GA(8) - - Intron - GenBank CDC73_00094 - Presumptive Polymorphisms - Qi Ming
./. 01 c.4G>T - p.Ala2Ser Exon - GenBank CDC73_00056 - The A2S mutation was found only in the LI gland. May likely lead to deleterious structural alterations of parafibromin that may affect its function. - Qi Ming
./. 01 c.16delA - p.Ser6AlafsX15 Exon - GenBank CDC73_00041 - - - Qi Ming
./. 01 c.23_25delTGCinsGT - p.Leu8ArgfsX13 Exon - GenBank CDC73_00038 - - - Qi Ming
./. 01 c.25C>T - p.Arg9X Exon - GenBank CDC73_00004 - - - Qi Ming
./. 01 c.26_149del - p.Arg9HisfsX9 Exon - GenBank CDC73_00071 - - - Qi Ming
./. 01 c.30del - p.Gln10HisfsX11 Exon - GenBank CDC73_00028 - available for identification of LOH and HRPT2 somatic mutations - Qi Ming
./. 01 c.30delG - p.Gln10HisfsX11 Exon - GenBank CDC73_00006 - - - Qi Ming
./. 01 c.33C>T - p.Tyr11Tyr Exon - GenBank CDC73_00015 - - - Qi Ming
./. 01 c.33C>T - p.Tyr11Tyr Exon - GenBank CDC73_00015 - Is considered a polymorphism - Qi Ming
./. 01 c.33C>T - p.Tyr11Tyr Exon - GenBank CDC73_00015 - Presumptive Polymorphisms - Qi Ming
./. 01 c.34_40del - p.Asn12ArgfsX7 Exon - GenBank CDC73_00005 - - - Qi Ming
./. 01 c.39del - p.Gln14ArgfsX7 Exon - GenBank CDC73_00049 - - - Qi Ming
./. 01 c.39delC - p.Gln14ArgfsX7 Exon - GenBank CDC73_00007 - - - Qi Ming
./. 01 c.39delC - p.Gln14ArgfsX7 Exon - GenBank CDC73_00007 - - - Qi Ming
./. 01 c.53delT - p.Ile18MetfsX3 Exon - GenBank CDC73_00073 - - - Qi Ming
./. 01 c.60_69del - p.Gly22X Exon - GenBank CDC73_00043 - - - Qi Ming
./. 01 c.61_64del - p.Lys21GlufsX4 Exon - GenBank CDC73_00054 - - - Qi Ming
./. 01 c.62_66del - p.Lys21ArgfsX43 Exon - GenBank CDC73_00048 - - - Qi Ming
./. 01 c.70G>T - p.Glu24X Exon - GenBank CDC73_00035 - - - Qi Ming
./. 01 c.70_73del - p.Glu24X Exon - GenBank CDC73_00050 - - - Qi Ming
./. 01 c.76del - p.Ile26SerfsX11 Exon - GenBank CDC73_00058 - Presumptive Polymorphisms - Qi Ming
./. 01 c.76delA - p.Ile26SerfsX11 Exon - GenBank CDC73_00016 - - - Qi Ming
./. 01 c.82_85del - p.Gly28SerfsX8 Exon - GenBank CDC73_00033 - - - Qi Ming
./. 01 c.85G>T - p.Glu29* Exon - GenBank CDC73_00095 - - - Qi Ming
./. 01 c.95_102del - p.Trp32X Exon - GenBank CDC73_00051 - - - Qi Ming
./. 01 c.96G>A - p.Trp32X Exon - GenBank CDC73_00062 - No HRPT2 transcript was detected. - Qi Ming
./. 01 c.96G>A - p.Trp32X Exon - GenBank CDC73_00062 - It is necessary to individualize the surgical approach for HRPT2-related hyperparathyroidism until we can gather a better phenotypegenotype correlation in larger series, to best define their treatment. - Qi Ming
./. 01 c.100A>C - p.Lys34Gln Exon - GenBank CDC73_00031 - Revealed a defect in the ability of this mutant to suppress cyclin D1 expression. - Qi Ming
./. 01 c.128G>A - p.Trp43X Exon - GenBank CDC73_00072 - - - Qi Ming
./. 01 c.131+1G>A - - Intron - GenBank CDC73_00003 - - - Qi Ming
./. 02 c.140_144del - p.Lys47ArgfsX17 Exon - GenBank CDC73_00053 - - - Qi Ming
./. 02 c.162C>A - p.Tyr54X Exon - GenBank CDC73_00057 - It could also be c.162C>G. The Y54X was found only in the RS. - Qi Ming
./. 02 c.162C>G - p.Tyr54X Exon - GenBank CDC73_00017 - - - Qi Ming
./. 02 c.162C>G - p.Tyr54X Exon - GenBank CDC73_00017 - Presumptive Polymorphisms - Qi Ming
./. 02 c.162C>G - p.Tyr54X Exon - GenBank CDC73_00017 - - - Qi Ming
./. 02 c.162C>G - p.Tyr54X Exon - GenBank CDC73_00017 - - - Qi Ming
./. 02 c.165C>A - p.Tyr55X Exon - GenBank CDC73_00067 - - - Qi Ming
./. 02 c.165C>G - p.Tyr55X Exon - GenBank CDC73_00008 - - - Qi Ming
./. 02 c.165C>G - p.Tyr55X Exon - GenBank CDC73_00008 - - - Qi Ming
./. 02 c.165C>G - p.Tyr55X Exon - GenBank CDC73_00008 - Presumptive Polymorphisms - Qi Ming
./. 02 c.165C>G - p.Tyr55X Exon - GenBank CDC73_00008 - - - Qi Ming
./. 02 c.165del - p.Tyr55X Exon - GenBank CDC73_00061 - Presumptive Polymorphisms - Qi Ming
./. 02 c.165del - p.Tyr55X Exon - GenBank CDC73_00061 - - - Qi Ming
./. 02 c.191T>C - p.Leu64Pro Exon - GenBank CDC73_00044 - - - Qi Ming
./. 02 c.191T>C - p.Leu64Pro Exon - GenBank CDC73_00044 - Presumptive Polymorphisms - Qi Ming
./. 02 c.191T>C - p.Leu64Pro Exon - GenBank CDC73_00044 - - - Qi Ming
./. 02 c.194dupA - p.Asn65LysfsX2 Exon - GenBank CDC73_00088 - - - Qi Ming
./. 02 c.195dupT - p.Asn66X Exon - GenBank CDC73_00087 - - - Qi Ming
./. 02 c.195_196insA - p.Asn66LysfsX16 Exon - GenBank CDC73_00068 - - - Qi Ming
./. 02 c.195_196insT - p.Asn66X Exon - GenBank CDC73_00075 - - - Qi Ming
./. 02 c.226C>T - p.Arg76X Exon - GenBank CDC73_00037 - - - Qi Ming
./. 02 c.226C>T - p.Arg76X Exon - GenBank CDC73_00037 - - - Qi Ming
./. 02 c.237+1G>C - = Intron - GenBank CDC73_00045 - - - Qi Ming
./. 02 c.237+1G>C - - Intron - GenBank CDC73_00045 - - - Qi Ming
./. 02 c.237+28T>C - - Intron - GenBank CDC73_00095 - HRPT2 polymorphisms - Qi Ming
./. 02 c.237+28T>C - - Intron - GenBank CDC73_00020 - Presumptive Polymorphisms - Qi Ming
./. 02 c.237+28_237+31delCCTA - - Intron - GenBank CDC73_00024 - HRPT2 polymorphisms - Qi Ming
./. 02 c.237+28_237+31delCCTA - - Intron - GenBank CDC73_00093 - Presumptive Polymorphisms - Qi Ming
./. 03 c.238-1G>A - - Intron - GenBank CDC73_00002 - - - Qi Ming
./. 03 c.272G>C - p.Arg91Pro Exon - GenBank CDC73_00055 - May likely lead to deleterious structural alterations of parafibromin that may affect its function. - Qi Ming
./. 03 c.284T>C - p.Leu95Pro Exon - GenBank CDC73_00018 5.2% - - Qi Ming
./. 03 c.284T>C - p.Leu95Pro Exon - GenBank CDC73_00018 5.2% - - Qi Ming
./. 03 c.306_307+13del15 - - Exon - GenBank CDC73_00089 - - - Qi Ming
./. 04 c.356del - p.Gln119ArgfsX14 Exon - GenBank CDC73_00030 - - - Qi Ming
./. 04 c.356delA - p.Gln119ArgfsX14 Exon - GenBank CDC73_00010 - - - Qi Ming
./. 04 c.356delA - p.Gln119ArgfsX14 Exon - GenBank CDC73_00010 - available for identification of LOH and HRPT2 somatic mutations - Qi Ming
./. 05 c.371-2A>G - - Intron - GenBank CDC73_00076 - - - Qi Ming
./. 05 c.373dupA - p.Arg126ThrfsX5 Exon - GenBank CDC73_00040 - - - Qi Ming
./. 05 c.373_374insA - p.Arg126ThrfsX5 Exon - GenBank CDC73_00069 - - - Qi Ming
./. 05 c.406A>T - p.Lys136X Exon - GenBank CDC73_00011 - - - Qi Ming
./. 05 c.423+1G>T - - Intron - GenBank CDC73_00077 - - - Qi Ming
./. 06 c.449A>G - p.Lys150Arg Exon - GenBank CDC73_00080 NA - - Qi Ming
./. 07 c.513-1del - - Intron - GenBank CDC73_00074 - Presumptive Polymorphisms - Qi Ming
./. 07 c.513-1delG - - Intron - GenBank CDC73_00078 - - - Qi Ming
./. 07 c.518_521del - p.Ser174LysfsX27 Exon - GenBank CDC73_00047 - - - Qi Ming
./. 07 c.636del - p.Phe213LeufsX6 Exon - GenBank CDC73_00065 - Presumptive Polymorphisms - Qi Ming
./. 07 c.636del - p.Phe213LeufsX6 Exon - GenBank CDC73_00065 - - - Qi Ming
./. 07 c.636delT - p.Phe213LeufsX6 Exon - GenBank CDC73_00012 - - - Qi Ming
./. 07 c.664C>T - p.Arg222X Exon - GenBank CDC73_00039 - - - Qi Ming
./. 07 c.664C>T - p.Arg222X Exon - GenBank CDC73_00039 - - - Qi Ming
./. 07 c.664C>T - p.Arg222X Exon - GenBank CDC73_00039 - The altered expression of parafibromin caused by HRPT2 gene mutation is one of the molecular mechanisms for explaining the clinical manifestations of this patient. - Qi Ming
./. 07 c.670_671delATinsG - p.Ile224ValfsX33 Exon - GenBank CDC73_00065 - leads to a frameshift encoding 33 missense amino acids before encountering a premature Stop at codon 256 - Qi Ming
./. 07 c.679dupAG - p.Arg227LysfsX40 Exon - GenBank CDC73_00013 - - - Qi Ming
./. 07 c.679_680del - p.Arg229SerfsX37 Exon - GenBank CDC73_00064 - Only the normal HRPT2 transcript was found in patient. - Qi Ming
./. 07 c.679_680del - p.Arg229SerfsX37 Exon - GenBank CDC73_00064 - Presumptive Polymorphisms - Qi Ming
./. 07 c.679_680del - p.Arg229SerfsX37 Exon - GenBank CDC73_00064 - - - Qi Ming
./. 07 c.679_680delAG - p.Arg229SerfsX37 Exon - GenBank CDC73_00019 - - - Qi Ming
./. 07 c.679_680insAG - p.Arg227LysfsX31 Exon - GenBank CDC73_00070 - - - Qi Ming
./. 07 c.679_680insAG - p.Arg227LysfsX31 Exon - GenBank CDC73_00070 - - - Qi Ming
./. 07 c.680G>A - p.Arg227Lys Exon - GenBank CDC73_00081 NA - - Qi Ming
./. 07 c.685_688del - p.Arg229TyrfsX27 Exon - GenBank CDC73_00046 - longitudinal surveillance by serum biochemistry alone may not be 100% sensitive, and addition of routine neck ultrasonography is a readily accepted adjunct that may facilitate earlier disease detection in some families - Qi Ming
./. 07 c.686_689del - p.Arg229AsnfsX27 Exon - GenBank CDC73_00063 - - - Qi Ming
./. 07 c.686_689del - p.Arg229AsnfsX27 Exon - GenBank CDC73_00063 - A more aggressive operative approach should be undertaken in these patients. - Qi Ming
./. 07 c.686_689del - p.Arg229AsnfsX27 Exon - GenBank CDC73_00063 - Presumptive Polymorphisms - Qi Ming
./. 07 c.686_689del - p.Arg229AsnfsX27 Exon - GenBank CDC73_00063 - - - Qi Ming
./. 07 c.687_688dup - p.Val230GlufsX28 Exon - GenBank CDC73_00091 - - - Qi Ming
./. 07 c.687_688dupAG - p.Val230GlufsX28 Exon - GenBank CDC73_00090 - - - Qi Ming
./. 07 c.700C>T - p.Arg234X Exon - GenBank CDC73_00016 - - - Qi Ming
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