ClinVar Miner

List of variants in gene GRN reported as pathogenic for GRN-related frontotemporal lobar degeneration with Tdp43 inclusions; Neuronal ceroid lipofuscinosis 11

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 58
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_002087.4(GRN):c.1010_1011del (p.Gln337fs) rs1598364961 0.00001
NM_002087.4(GRN):c.1145del (p.Thr382fs) rs63750805 0.00001
NM_002087.4(GRN):c.1477C>T (p.Arg493Ter) rs63751294 0.00001
NC_000017.10:g.(?_42426434)_(42430018_?)del
NM_002087.3(GRN):c.1144dup (p.Thr382Asnfs) rs63749905
NM_002087.4(GRN):c.1009C>T (p.Gln337Ter) rs63751406
NM_002087.4(GRN):c.1072C>T (p.Gln358Ter) rs1555611293
NM_002087.4(GRN):c.1153del (p.Glu385fs) rs2143342203
NM_002087.4(GRN):c.1158G>A (p.Trp386Ter) rs2044779598
NM_002087.4(GRN):c.1166_1167del (p.Cys389fs)
NM_002087.4(GRN):c.1179+1G>C rs2510057446
NM_002087.4(GRN):c.1179+3A>G rs2510057451
NM_002087.4(GRN):c.118_121dup (p.Cys41Ter) rs2510054302
NM_002087.4(GRN):c.1216C>T (p.Gln406Ter) rs2143344360
NM_002087.4(GRN):c.1227del (p.Cys410fs) rs2510057852
NM_002087.4(GRN):c.1252C>T (p.Arg418Ter) rs63751180
NM_002087.4(GRN):c.128_129insCC (p.Pro44fs) rs2510054318
NM_002087.4(GRN):c.1317_1318del (p.Asp441fs) rs2510057977
NM_002087.4(GRN):c.138+1G>A rs63749844
NM_002087.4(GRN):c.1414-1G>T
NM_002087.4(GRN):c.1414-2A>G rs1555611412
NM_002087.4(GRN):c.1458C>A (p.Tyr486Ter)
NM_002087.4(GRN):c.1492_1495del (p.Glu498fs) rs2510058297
NM_002087.4(GRN):c.180dup (p.Cys61fs) rs2510054484
NM_002087.4(GRN):c.1A>G (p.Met1Val) rs746037872
NM_002087.4(GRN):c.234_235del (p.Gly79fs) rs63750373
NM_002087.4(GRN):c.264+1del rs2510054566
NM_002087.4(GRN):c.265-2del rs2510054676
NM_002087.4(GRN):c.26C>A (p.Ala9Asp) rs63751243
NM_002087.4(GRN):c.295_308del (p.Cys99fs) rs2510054721
NM_002087.4(GRN):c.299del (p.Pro100fs) rs2048353899
NM_002087.4(GRN):c.2T>C (p.Met1Thr) rs63751006
NM_002087.4(GRN):c.328C>T (p.Arg110Ter) rs63750411
NM_002087.4(GRN):c.349+1G>C rs1598363083
NM_002087.4(GRN):c.383_386del (p.Asp128fs) rs2048359069
NM_002087.4(GRN):c.388C>T (p.Gln130Ter) rs2510055303
NM_002087.4(GRN):c.388_391del (p.Gln130fs) rs63749801
NM_002087.4(GRN):c.39dup (p.Leu14fs) rs2143325096
NM_002087.4(GRN):c.468_474del (p.Cys157fs) rs63750247
NM_002087.4(GRN):c.472_496dup (p.Pro166delinsLeuTer) rs2510055566
NM_002087.4(GRN):c.592_593del (p.Arg198fs) rs1555611136
NM_002087.4(GRN):c.5G>A (p.Trp2Ter) rs2510054161
NM_002087.4(GRN):c.614C>A (p.Ser205Ter) rs777211749
NM_002087.4(GRN):c.657del (p.Thr220fs)
NM_002087.4(GRN):c.675_676del (p.Ser226fs) rs63751085
NM_002087.4(GRN):c.6G>A (p.Trp2Ter) rs1555610855
NM_002087.4(GRN):c.768_769dup (p.Gln257fs) rs1567887004
NM_002087.4(GRN):c.774dup (p.Lys259Ter)
NM_002087.4(GRN):c.775_778del (p.Lys259fs) rs2143337849
NM_002087.4(GRN):c.784_787del (p.Ser262fs) rs2510056456
NM_002087.4(GRN):c.80dup (p.Val28fs) rs1392550887
NM_002087.4(GRN):c.813_816del (p.Thr272fs) rs63749877
NM_002087.4(GRN):c.836-1G>C rs63751296
NM_002087.4(GRN):c.87dup (p.Cys30fs) rs794729672
NM_002087.4(GRN):c.898C>T (p.Gln300Ter) rs1555611253
NM_002087.4(GRN):c.910_911dup (p.Trp304fs) rs750312986
NM_002087.4(GRN):c.911G>A (p.Trp304Ter) rs63751177
NM_002087.4(GRN):c.991C>T (p.Gln331Ter) rs1567887496

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.