ClinVar Miner

List of variants in gene GIPC3 reported by GeneDx

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Gene type:
ClinVar version:
Total variants: 85
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HGVS dbSNP gnomAD frequency
NM_133261.3(GIPC3):c.*146A>G rs17348907 0.47552
NM_133261.3(GIPC3):c.226-22A>G rs8100350 0.34728
NM_133261.3(GIPC3):c.225+219A>G rs35181970 0.23716
NM_133261.3(GIPC3):c.276G>A (p.Leu92=) rs8113232 0.23044
NM_133261.3(GIPC3):c.593-6C>T rs10426399 0.21701
NM_133261.3(GIPC3):c.593-28T>C rs10406702 0.14805
NM_133261.3(GIPC3):c.593-102G>A rs4806942 0.13362
NC_000019.10:g.3585336C>T rs112835547 0.09754
NM_133261.3(GIPC3):c.225+126C>T rs77070566 0.04059
NM_133261.3(GIPC3):c.705+116T>C rs114579321 0.02417
NM_133261.3(GIPC3):c.592+255G>A rs193020058 0.01538
NM_133261.3(GIPC3):c.593-151G>A rs116092698 0.01368
NM_133261.3(GIPC3):c.787+43G>A rs114801367 0.01137
NM_133261.3(GIPC3):c.593-167C>T rs74364412 0.00481
NM_133261.3(GIPC3):c.*83G>A rs543815063 0.00360
NM_133261.3(GIPC3):c.592+279T>C rs374671510 0.00354
NM_133261.3(GIPC3):c.225+11C>T rs185551765 0.00351
NM_133261.3(GIPC3):c.706-12G>A rs112949777 0.00222
NM_133261.3(GIPC3):c.132G>C (p.Ala44=) rs80060313 0.00180
NM_133261.3(GIPC3):c.856G>A (p.Val286Ile) rs138339125 0.00121
NM_133261.3(GIPC3):c.4G>A (p.Glu2Lys) rs764467903 0.00110
NM_133261.3(GIPC3):c.906C>T (p.Ala302=) rs140960269 0.00086
NM_133261.3(GIPC3):c.207C>T (p.Phe69=) rs727504653 0.00060
NM_133261.3(GIPC3):c.788-45C>T rs370162131 0.00050
NM_133261.3(GIPC3):c.592+10G>T rs557737423 0.00042
NM_133261.3(GIPC3):c.613C>T (p.Arg205Trp) rs182473859 0.00039
NM_133261.3(GIPC3):c.440G>A (p.Arg147Gln) rs141293401 0.00031
NM_133261.3(GIPC3):c.20G>A (p.Arg7Gln) rs998073430 0.00028
NM_133261.3(GIPC3):c.807G>A (p.Thr269=) rs141419242 0.00017
NM_133261.3(GIPC3):c.788-43C>T rs35385787 0.00015
NM_133261.3(GIPC3):c.50C>G (p.Ala17Gly) rs876657815 0.00014
NM_133261.3(GIPC3):c.842G>A (p.Arg281His) rs371599478 0.00012
NM_133261.3(GIPC3):c.871G>A (p.Ala291Thr) rs199951984 0.00009
NM_133261.3(GIPC3):c.639G>A (p.Ala213=) rs371566042 0.00008
NM_133261.3(GIPC3):c.411+25G>A rs557145939 0.00006
NM_133261.3(GIPC3):c.667C>T (p.Arg223Trp) rs200322282 0.00006
NM_133261.3(GIPC3):c.772C>T (p.Arg258Trp) rs772316969 0.00006
NM_133261.3(GIPC3):c.788-4G>A rs372583605 0.00006
NM_133261.3(GIPC3):c.913G>A (p.Gly305Ser) rs774440451 0.00004
NM_133261.3(GIPC3):c.172G>A (p.Val58Ile) rs889681720 0.00003
NM_133261.3(GIPC3):c.213C>A (p.Ile71=) rs876657467 0.00003
NM_133261.3(GIPC3):c.826G>A (p.Ala276Thr) rs779376305 0.00003
NM_133261.3(GIPC3):c.592+7C>T rs537708164 0.00002
NM_133261.3(GIPC3):c.122C>A (p.Thr41Lys) rs727503062 0.00001
NM_133261.3(GIPC3):c.174C>T (p.Val58=) rs942647950 0.00001
NM_133261.3(GIPC3):c.241C>T (p.Leu81Phe) rs1487341857 0.00001
NM_133261.3(GIPC3):c.279G>A (p.Gly93=) rs755720741 0.00001
NM_133261.3(GIPC3):c.723G>C (p.Glu241Asp) rs200355546 0.00001
NM_133261.3(GIPC3):c.908C>T (p.Ala303Val) rs772816799 0.00001
NM_133261.3(GIPC3):c.916G>A (p.Glu306Lys) rs772055400 0.00001
NM_133261.3(GIPC3):c.*15del rs761229176
NM_133261.3(GIPC3):c.-46G>C rs545605260
NM_133261.3(GIPC3):c.-77G>A rs34722692
NM_133261.3(GIPC3):c.101G>A (p.Arg34His)
NM_133261.3(GIPC3):c.226-12T>C rs2145269341
NM_133261.3(GIPC3):c.226-2A>G
NM_133261.3(GIPC3):c.277G>A (p.Gly93Arg)
NM_133261.3(GIPC3):c.281G>T (p.Gly94Val) rs763523474
NM_133261.3(GIPC3):c.325G>A (p.Glu109Lys)
NM_133261.3(GIPC3):c.335A>G (p.Glu112Gly)
NM_133261.3(GIPC3):c.410A>G (p.Lys137Arg)
NM_133261.3(GIPC3):c.411+10A>G rs779727957
NM_133261.3(GIPC3):c.411+55dup rs531054314
NM_133261.3(GIPC3):c.494T>C (p.Ile165Thr) rs1441513340
NM_133261.3(GIPC3):c.546G>T (p.Lys182Asn)
NM_133261.3(GIPC3):c.592+277TTTG[7] rs112236623
NM_133261.3(GIPC3):c.592+277TTTG[8] rs112236623
NM_133261.3(GIPC3):c.592+277TTTG[9] rs112236623
NM_133261.3(GIPC3):c.592G>A (p.Asp198Asn) rs1320335674
NM_133261.3(GIPC3):c.679G>T (p.Gly227Trp) rs202075236
NM_133261.3(GIPC3):c.69G>A (p.Ala23=) rs150473323
NM_133261.3(GIPC3):c.69G>C (p.Ala23=) rs150473323
NM_133261.3(GIPC3):c.705G>A (p.Ala235=)
NM_133261.3(GIPC3):c.706-3dup rs200925508
NM_133261.3(GIPC3):c.706-61G>A rs28532669
NM_133261.3(GIPC3):c.712G>C (p.Glu238Gln) rs1477018298
NM_133261.3(GIPC3):c.733C>G (p.Arg245Gly) rs766991127
NM_133261.3(GIPC3):c.763A>C (p.Met255Leu)
NM_133261.3(GIPC3):c.764T>G (p.Met255Arg) rs2032449513
NM_133261.3(GIPC3):c.787+31G>T rs78077103
NM_133261.3(GIPC3):c.821C>G (p.Ala274Gly) rs149028750
NM_133261.3(GIPC3):c.821C>T (p.Ala274Val) rs149028750
NM_133261.3(GIPC3):c.85del (p.Ala29fs) rs756840753
NM_133261.3(GIPC3):c.891G>A (p.Val297=) rs1419316711
NM_133261.3(GIPC3):c.899T>C (p.Val300Ala) rs2512427928

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