ClinVar Miner

List of variants in gene GRN reported as not provided for not provided

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Gene type:
ClinVar version:
Total variants: 81
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HGVS dbSNP gnomAD frequency
NM_002087.4(GRN):c.384T>C (p.Asp128=) rs25646 0.02616
NM_002087.4(GRN):c.55C>T (p.Arg19Trp) rs63750723 0.01303
NM_002087.4(GRN):c.1544G>C (p.Gly515Ala) rs25647 0.00781
NM_002087.4(GRN):c.1297C>T (p.Arg433Trp) rs63750412 0.00523
NM_002087.4(GRN):c.545C>T (p.Thr182Met) rs63750479 0.00356
NM_002087.4(GRN):c.970G>A (p.Ala324Thr) rs63750541 0.00112
NM_002087.4(GRN):c.359C>A (p.Ser120Tyr) rs63750043 0.00076
NM_002087.4(GRN):c.903G>A (p.Ser301=) rs63750142 0.00044
NM_002087.4(GRN):c.635G>A (p.Arg212Gln) rs63750787 0.00029
NM_002087.4(GRN):c.1253G>A (p.Arg418Gln) rs63751100 0.00022
NM_002087.4(GRN):c.279G>A (p.Gly93=) rs63751088 0.00014
NM_002087.4(GRN):c.1341C>T (p.His447=) rs63750775 0.00008
NM_002087.4(GRN):c.102C>T (p.Pro34=) rs63751074 0.00005
NM_002087.4(GRN):c.1648G>A (p.Val550Ile) rs63750754 0.00004
NM_002087.4(GRN):c.1695C>T (p.Cys565=) rs63751248 0.00004
NM_002087.4(GRN):c.1176A>C (p.Pro392=) rs63750448 0.00003
NM_002087.4(GRN):c.1294C>T (p.Arg432Cys) rs63750130 0.00003
NM_002087.4(GRN):c.1485C>T (p.Cys495=) rs63750576 0.00003
NM_002087.4(GRN):c.861G>C (p.Glu287Asp) rs63750565 0.00003
NM_002087.4(GRN):c.1373C>T (p.Pro458Leu) rs63750537 0.00002
NM_002087.4(GRN):c.421G>A (p.Val141Ile) rs63749853 0.00002
NM_002087.4(GRN):c.1145del (p.Thr382fs) rs63750805 0.00001
NM_002087.4(GRN):c.1241G>T (p.Gly414Val) rs63750920 0.00001
NM_002087.4(GRN):c.1409C>T (p.Pro470Leu) rs63750007 0.00001
NM_002087.4(GRN):c.1425C>T (p.Cys475=) rs63751104 0.00001
NM_002087.4(GRN):c.1477C>T (p.Arg493Ter) rs63751294 0.00001
NM_002087.4(GRN):c.2T>C (p.Met1Thr) rs63751006 0.00001
NM_002087.4(GRN):c.473G>A (p.Cys158Tyr) rs63750163 0.00001
NM_002087.4(GRN):c.804G>A (p.Thr268=) rs63750229 0.00001
NM_002087.3(GRN):c.1144dup (p.Thr382Asnfs) rs63749905
NM_002087.4(GRN):c.-8+3A>T rs63751020
NM_002087.4(GRN):c.-8+5G>C rs63750313
NM_002087.4(GRN):c.1009C>T (p.Gln337Ter) rs63751406
NM_002087.4(GRN):c.102del (p.Gly35fs) rs63751073
NM_002087.4(GRN):c.1095_1096del (p.Pro365_Cys366insTer) rs63749988
NM_002087.4(GRN):c.1157G>A (p.Trp386Ter) rs63751213
NM_002087.4(GRN):c.1201C>T (p.Gln401Ter) rs63750118
NM_002087.4(GRN):c.1231_1232del (p.Val411fs) rs63750351
NM_002087.4(GRN):c.1231_1232dup (p.Val411_Ala412insTer) rs63750351
NM_002087.4(GRN):c.1252C>T (p.Arg418Ter) rs63751180
NM_002087.4(GRN):c.138+1G>A rs63749844
NM_002087.4(GRN):c.1395dup (p.Cys466fs) rs63749951
NM_002087.4(GRN):c.1402C>T (p.Gln468Ter) rs63749908
NM_002087.4(GRN):c.1422C>T (p.Cys474=) rs63751470
NM_002087.4(GRN):c.154del (p.Thr52fs) rs63751092
NM_002087.4(GRN):c.158T>C (p.Leu53Pro) rs63750481
NM_002087.4(GRN):c.1623G>C (p.Trp541Cys) rs63751060
NM_002087.4(GRN):c.1666C>T (p.Arg556Cys) rs63750116
NM_002087.4(GRN):c.234_235del (p.Gly79fs) rs63750373
NM_002087.4(GRN):c.243del (p.Ser82fs) rs63751193
NM_002087.4(GRN):c.264G>A (p.Glu88=) rs63751166
NM_002087.4(GRN):c.26C>A (p.Ala9Asp) rs63751243
NM_002087.4(GRN):c.313T>C (p.Cys105Arg) rs63750441
NM_002087.4(GRN):c.317G>A (p.Ser106Asn) rs63750202
NM_002087.4(GRN):c.328C>T (p.Arg110Ter) rs63750411
NM_002087.4(GRN):c.361del (p.Val121fs) rs63749940
NM_002087.4(GRN):c.373C>T (p.Gln125Ter) rs63750077
NM_002087.4(GRN):c.380_381del (p.Pro127fs) rs63750405
NM_002087.4(GRN):c.384_387del (p.Gln130fs) rs63750768
NM_002087.4(GRN):c.388_391del (p.Gln130fs) rs63749801
NM_002087.4(GRN):c.3G>A (p.Met1Ile) rs63750331
NM_002087.4(GRN):c.463-1G>A rs63750536
NM_002087.4(GRN):c.468_474del (p.Cys157fs) rs63750247
NM_002087.4(GRN):c.63_64insC (p.Asp22fs) rs63750981
NM_002087.4(GRN):c.658A>T (p.Thr220Ser) rs63750683
NM_002087.4(GRN):c.675_676del (p.Ser226fs) rs63751085
NM_002087.4(GRN):c.759_760del (p.Cys253_Asp254delinsTer) rs63751035
NM_002087.4(GRN):c.773G>A (p.Ser258Asn) rs63751000
NM_002087.4(GRN):c.781C>A (p.Leu261Ile) rs63750435
NM_002087.4(GRN):c.813_816del (p.Thr272fs) rs63749877
NM_002087.4(GRN):c.835_835+1insCTGA rs63750976
NM_002087.4(GRN):c.836-1G>C rs63751296
NM_002087.4(GRN):c.87_90dup (p.Cys31fs) rs63751057
NM_002087.4(GRN):c.909del (p.Trp304fs) rs63750366
NM_002087.4(GRN):c.910_911insTG (p.Trp304fs) rs63751239
NM_002087.4(GRN):c.911G>A (p.Trp304Ter) rs63751177
NM_002087.4(GRN):c.933+1G>A rs63750707
NM_002087.4(GRN):c.942C>A (p.Cys314Ter) rs63750926
NM_002087.4(GRN):c.996G>A (p.Lys332=) rs63750785
NM_002087.4(GRN):c.998del (p.Gly333fs) rs63750873
NM_002087.4(GRN):c.99C>T (p.Asp33=) rs63750742

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