Full data view for gene FGF1

Information The variants shown are described using the NM_000800.3 transcript reference sequence.

39 entries on 1 page. Showing entries 1 - 39.
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Effect     

AscendingDNA change (cDNA)     

RNA change     

Protein     

DNA change (genomic) (hg19)     

Reference     

DB-ID     

Frequency     

Freq. EA     

Freq. AA     

Template     

Technique     

Disease     

Reference     

Remarks     

Panel size     

Owner     
?/? c.-30G>A r.(=) p.(=) g.141993722C>T Copied from the Exome Variant Server FGF1_000039 4/13006 4/8600 0/4406 - - - - - - -
?/? c.-25C>T r.(=) p.(=) g.141993717G>A Copied from the Exome Variant Server FGF1_000038 1/13006 1/8600 0/4406 - - - - - - -
?/? c.20C>T r.(?) p.(Thr7Ile) g.141993673G>A Copied from the Exome Variant Server FGF1_000037 1/13006 1/8600 0/4406 - - - - - - -
?/? c.38C>T r.(?) p.(Thr13Ile) g.141993655G>A Copied from the Exome Variant Server FGF1_000036 1/13006 0/8600 1/4406 - - - - - - -
?/? c.62G>A r.(?) p.(Gly21Glu) g.141993631C>T Copied from the Exome Variant Server FGF1_000035 35/13006 29/8600 6/4406 - - - - - - -
?/? c.140del r.(?) p.(Asp47Valfs*25) g.141993553del Copied from the Exome Variant Server FGF1_000034 1/12518 1/8254 0/4264 - - - - - - -
?/? c.168C>T r.(=) p.(=) g.141993525G>A Copied from the Exome Variant Server FGF1_000033 2/13006 2/8600 0/4406 - - - - - - -
?/? c.169+26C>A r.(=) p.(=) g.141993498G>T Copied from the Exome Variant Server FGF1_000032 156/13006 140/8600 16/4406 - - - - - - -
?/? c.169+50G>A r.(=) p.(=) g.141993474C>T Copied from the Exome Variant Server FGF1_000031 1/13006 1/8600 0/4406 - - - - - - -
?/? c.170-358G>A r.(=) p.(=) g.141980728C>T Copied from the Exome Variant Server FGF1_000029 1/5734 0/3982 1/1752 - - - - - - -
?/? c.170-351T>A r.(=) p.(=) g.141980721A>T Copied from the Exome Variant Server FGF1_000026 28/5734 0/3982 28/1752 - - - - - - -
?/? c.170-288G>A r.(=) p.(=) g.141980658C>T Copied from the Exome Variant Server FGF1_000024 6/5734 0/3982 6/1752 - - - - - - -
?/? c.170-258C>G r.(=) p.(=) g.141980628G>C Copied from the Exome Variant Server FGF1_000023 1/5734 1/3982 0/1752 - - - - - - -
?/? c.170-36G>A r.(=) p.(=) g.141980406C>T Copied from the Exome Variant Server FGF1_000021 1/13006 1/8600 0/4406 - - - - - - -
?/? c.170-18G>A r.(=) p.(=) g.141980388C>T Copied from the Exome Variant Server FGF1_000030 1/13006 1/8600 0/4406 - - - - - - -
?/? c.170-12T>C r.(=) p.(=) g.141980382A>G Copied from the Exome Variant Server FGF1_000028 1/13006 1/8600 0/4406 - - - - - - -
?/? c.218G>A r.(?) p.(Ser73Asn) g.141980322C>T Copied from the Exome Variant Server FGF1_000027 1/13006 1/8600 0/4406 - - - - - - -
?/? c.223G>A r.(?) p.(Glu75Lys) g.141980317C>T Copied from the Exome Variant Server FGF1_000025 4/13006 4/8600 0/4406 - - - - - - -
?/? c.229G>A r.(?) p.(Gly77Ser) g.141980311C>T Copied from the Exome Variant Server FGF1_000022 1/13006 0/8600 1/4406 - - - - - - -
?/? c.233A>G r.(?) p.(Gln78Arg) g.141980307T>C Copied from the Exome Variant Server FGF1_000020 1/13006 1/8600 0/4406 - - - - - - -
?/? c.255C>T r.(=) p.(=) g.141980285G>A Copied from the Exome Variant Server FGF1_000019 1/13006 0/8600 1/4406 - - - - - - -
?/? c.273+29C>T r.(=) p.(=) g.141980238G>A Copied from the Exome Variant Server FGF1_000018 11/13006 0/8600 11/4406 - - - - - - -
?/? c.273+45G>C r.(=) p.(=) g.141980222C>G Copied from the Exome Variant Server FGF1_000017 1/13006 0/8600 1/4406 - - - - - - -
?/? c.274-35G>A r.(=) p.(=) g.141975084C>T Copied from the Exome Variant Server FGF1_000016 2/13006 2/8600 0/4406 - - - - - - -
?/? c.274-18T>G r.(=) p.(=) g.141975067A>C Copied from the Exome Variant Server FGF1_000015 6976/13006 3842/8600 3134/4406 - - - - - - -
?/? c.274-3T>C r.spl? p.? g.141975052A>G Copied from the Exome Variant Server FGF1_000014 6/13006 0/8600 6/4406 - - - - - - -
?/? c.295T>C r.(=) p.(=) g.141975028A>G Copied from the Exome Variant Server FGF1_000013 1/13006 0/8600 1/4406 - - - - - - -
?/? c.300C>T r.(=) p.(=) g.141975023G>A Copied from the Exome Variant Server FGF1_000012 1/13006 0/8600 1/4406 - - - - - - -
?/? c.333C>G r.(=) p.(=) g.141974990G>C Copied from the Exome Variant Server FGF1_000011 2/13006 2/8600 0/4406 - - - - - - -
?/? c.352G>C r.(?) p.(Ala118Pro) g.141974971C>G Copied from the Exome Variant Server FGF1_000010 1/13006 1/8600 0/4406 - - - - - - -
?/? c.369T>C r.(=) p.(=) g.141974954A>G Copied from the Exome Variant Server FGF1_000009 1/13006 1/8600 0/4406 - - - - - - -
?/? c.401G>A r.(?) p.(Arg134His) g.141974922C>T Copied from the Exome Variant Server FGF1_000008 1/13006 1/8600 0/4406 - - - - - - -
?/? c.402C>T r.(=) p.(=) g.141974921G>A Copied from the Exome Variant Server FGF1_000007 2/13006 2/8600 0/4406 - - - - - - -
?/? c.410G>A r.(?) p.(Arg137Gln) g.141974913C>T Copied from the Exome Variant Server FGF1_000006 5/13006 4/8600 1/4406 - - - - - - -
?/? c.417C>T r.(=) p.(=) g.141974906G>A Copied from the Exome Variant Server FGF1_000005 1/13006 0/8600 1/4406 - - - - - - -
?/? c.453A>G r.(=) p.(=) g.141974870T>C Copied from the Exome Variant Server FGF1_000004 2/13006 1/8600 1/4406 - - - - - - -
?/? c.*29C>T r.(=) p.(=) g.141974826G>A Copied from the Exome Variant Server FGF1_000003 2/13006 0/8600 2/4406 - - - - - - -
?/? c.*40C>T r.(=) p.(=) g.141974815G>A Copied from the Exome Variant Server FGF1_000002 11/13006 1/8600 10/4406 - - - - - - -
?/? c.*41G>A r.(=) p.(=) g.141974814C>T Copied from the Exome Variant Server FGF1_000001 63/13006 55/8600 8/4406 - - - - - - -
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