ClinVar Miner

List of variants in gene GPC6 reported as likely benign for not provided

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Gene type:
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Total variants: 69
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HGVS dbSNP gnomAD frequency
NM_005708.5(GPC6):c.256C>T (p.Leu86Phe) rs143872144 0.00684
NM_005708.5(GPC6):c.*1261G>A rs141909370 0.00569
NM_005708.5(GPC6):c.710A>G (p.Lys237Arg) rs201337600 0.00059
NM_005708.5(GPC6):c.10T>A (p.Trp4Arg) rs200925249 0.00021
NM_005708.5(GPC6):c.576A>G (p.Lys192=) rs371970199 0.00012
NM_005708.5(GPC6):c.1524G>A (p.Thr508=) rs767667871 0.00011
NM_005708.5(GPC6):c.160+11G>A rs561808356 0.00011
NM_005708.5(GPC6):c.1428C>T (p.Asn476=) rs146868653 0.00009
NM_005708.5(GPC6):c.78G>A (p.Lys26=) rs146638721 0.00009
NM_005708.5(GPC6):c.984A>G (p.Glu328=) rs373334264 0.00004
NM_005708.5(GPC6):c.132G>C (p.Leu44=) rs745879189 0.00003
NM_005708.5(GPC6):c.1512C>T (p.Asp504=) rs776151903 0.00003
NM_005708.5(GPC6):c.510A>G (p.Glu170=) rs200921215 0.00003
NM_005708.5(GPC6):c.712-5T>C rs367561725 0.00003
NM_005708.5(GPC6):c.942G>A (p.Pro314=) rs138238361 0.00003
NM_005708.5(GPC6):c.1289+14G>A rs775197869 0.00002
NM_005708.5(GPC6):c.43C>T (p.Leu15=) rs779429225 0.00002
NM_005708.5(GPC6):c.878-12G>C rs945738025 0.00002
NM_005708.5(GPC6):c.1554C>T (p.Pro518=) rs1030400337 0.00001
NM_005708.5(GPC6):c.192T>C (p.Tyr64=) rs775977695 0.00001
NM_005708.5(GPC6):c.474G>A (p.Glu158=) rs759835794 0.00001
NM_005708.5(GPC6):c.712-11T>C rs1468624248 0.00001
NM_005708.5(GPC6):c.712-16T>C rs1196201785 0.00001
NM_005708.5(GPC6):c.909G>A (p.Glu303=) rs762276356 0.00001
NM_005708.5(GPC6):c.930G>A (p.Ser310=) rs754858999 0.00001
NM_005708.5(GPC6):c.1009-16T>C
NM_005708.5(GPC6):c.1083T>C (p.Asn361=)
NM_005708.5(GPC6):c.111C>T (p.Tyr37=)
NM_005708.5(GPC6):c.1152+9T>A rs794727797
NM_005708.5(GPC6):c.1179G>A (p.Lys393=)
NM_005708.5(GPC6):c.1200A>G (p.Ser400=)
NM_005708.5(GPC6):c.1227C>T (p.Asp409=)
NM_005708.5(GPC6):c.1233C>T (p.Ser411=)
NM_005708.5(GPC6):c.1239A>G (p.Thr413=)
NM_005708.5(GPC6):c.1245C>T (p.Gly415=)
NM_005708.5(GPC6):c.1254C>T (p.Asn418=)
NM_005708.5(GPC6):c.1289+7G>T
NM_005708.5(GPC6):c.1290-12T>C
NM_005708.5(GPC6):c.1290-8C>T
NM_005708.5(GPC6):c.130C>T (p.Leu44=)
NM_005708.5(GPC6):c.1320C>T (p.Leu440=)
NM_005708.5(GPC6):c.1338T>C (p.Asn446=) rs1594241632
NM_005708.5(GPC6):c.1465+11C>A rs375762690
NM_005708.5(GPC6):c.1465+14T>A
NM_005708.5(GPC6):c.1466-10T>C
NM_005708.5(GPC6):c.1466-17C>T
NM_005708.5(GPC6):c.1466-18T>G
NM_005708.5(GPC6):c.1466-6C>T
NM_005708.5(GPC6):c.1605C>T (p.Gly535=)
NM_005708.5(GPC6):c.161-7A>G
NM_005708.5(GPC6):c.195A>G (p.Thr65=) rs759121273
NM_005708.5(GPC6):c.24G>C (p.Val8=)
NM_005708.5(GPC6):c.285C>A (p.Arg95=)
NM_005708.5(GPC6):c.300C>T (p.Ser100=)
NM_005708.5(GPC6):c.320-13G>T
NM_005708.5(GPC6):c.320-4G>T
NM_005708.5(GPC6):c.435G>A (p.Glu145=)
NM_005708.5(GPC6):c.453T>G (p.Thr151=) rs2138980051
NM_005708.5(GPC6):c.489C>T (p.Asp163=)
NM_005708.5(GPC6):c.606C>T (p.Asp202=)
NM_005708.5(GPC6):c.60C>T (p.Pro20=)
NM_005708.5(GPC6):c.639C>T (p.Arg213=)
NM_005708.5(GPC6):c.672G>A (p.Gly224=)
NM_005708.5(GPC6):c.729G>A (p.Gly243=)
NM_005708.5(GPC6):c.816C>T (p.Asn272=)
NM_005708.5(GPC6):c.852C>T (p.Leu284=)
NM_005708.5(GPC6):c.877+13T>C
NM_005708.5(GPC6):c.877+8G>T
NM_005708.5(GPC6):c.93A>G (p.Gly31=) rs531412902

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