ClinVar Miner

List of variants in gene PRKG1 reported as benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 67
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_006258.4(PRKG1):c.1001+223G>A rs7097336 0.99847
NM_006258.4(PRKG1):c.1313+194T>C rs1194516 0.89799
NM_006258.4(PRKG1):c.762+113C>T rs10823860 0.75789
NM_006258.4(PRKG1):c.762+256C>A rs7083138 0.75786
NM_006258.4(PRKG1):c.762+146G>A rs7081919 0.75582
NM_006258.4(PRKG1):c.1076+31C>A rs10824173 0.74535
NM_006258.4(PRKG1):c.1710-252G>A rs7916242 0.61859
NM_006258.4(PRKG1):c.*253_*254insG rs5784918 0.48078
NM_006258.4(PRKG1):c.1962+29G>A rs10762675 0.47979
NM_006258.4(PRKG1):c.1173+239A>G rs10824300 0.46905
NM_006258.4(PRKG1):c.840+62C>T rs12778630 0.38605
NM_006258.4(PRKG1):c.763-296A>G rs1904008 0.38426
NM_006258.4(PRKG1):c.763-291A>C rs1904009 0.38422
NM_006258.4(PRKG1):c.936-216C>T rs34582712 0.33197
NM_006258.4(PRKG1):c.762+274G>T rs34873454 0.27250
NM_006258.4(PRKG1):c.*157C>T rs1881597 0.26778
NM_006258.4(PRKG1):c.762+132A>G rs11000040 0.20928
NM_006258.4(PRKG1):c.936-61A>T rs17642863 0.16867
NM_006258.4(PRKG1):c.1001+206T>C rs58118931 0.15673
NM_006258.4(PRKG1):c.1896-149G>A rs41281544 0.14100
NM_006258.4(PRKG1):c.936-295C>A rs77138124 0.12074
NM_006258.4(PRKG1):c.1896-263G>A rs16928983 0.11275
NM_001098512.3(PRKG1):c.267-79022C>T rs12264657 0.09404
NM_006258.4(PRKG1):c.1314-195C>T rs16928725 0.07297
NM_006258.4(PRKG1):c.1002-65C>T rs73344945 0.05135
NM_006258.4(PRKG1):c.1895+170A>G rs11001464 0.04558
NM_006258.4(PRKG1):c.935+262C>T rs17560996 0.03825
NM_006258.4(PRKG1):c.936-170G>T rs16927140 0.03308
NM_006258.4(PRKG1):c.1076+125A>C rs7897308 0.03249
NM_006258.4(PRKG1):c.1076+114G>C rs7908413 0.03248
NM_006258.4(PRKG1):c.1173+214C>A rs79543394 0.03148
NM_006258.4(PRKG1):c.1173+215T>A rs77530078 0.03146
NM_006258.4(PRKG1):c.312-170del rs75959880 0.03074
NM_006258.4(PRKG1):c.1174-217T>C rs74135384 0.02747
NM_006258.4(PRKG1):c.762+104A>T rs74135025 0.02506
NM_006258.4(PRKG1):c.1403+28A>G rs76977136 0.02474
NM_006258.4(PRKG1):c.1709+178G>A rs16928850 0.02385
NM_001098512.3(PRKG1):c.-359del rs201938144 0.02272
NM_006258.4(PRKG1):c.936-70T>C rs115286711 0.01937
NM_006258.4(PRKG1):c.593-192A>C rs16913410 0.01680
NM_006258.4(PRKG1):c.1963-151A>G rs9664313 0.01665
NM_006258.4(PRKG1):c.1071A>G (p.Lys357=) rs75650199 0.00097
GRCh37/hg19 10q21.1(chr10:53204509-53211991)x1
GRCh37/hg19 10q21.1(chr10:53269467-53318238)x1
GRCh37/hg19 10q21.1(chr10:53699753-53701052)x1
GRCh37/hg19 10q21.1(chr10:53825576-53983258)x3
GRCh37/hg19 10q21.1(chr10:54012974-54017651)x1
GRCh37/hg19 10q21.1(chr10:54016062-54019620)x0
GRCh37/hg19 10q21.1(chr10:54016062-54024195)x3
GRCh37/hg19 10q21.1(chr10:54016062-54028464)x1
GRCh37/hg19 10q21.1(chr10:54016099-54019620)x1
NC_000010.11:g.50990877del rs111693383
NM_001098512.3(PRKG1):c.-474C>T rs2248908
NM_001098512.3(PRKG1):c.-49_-48insTGC rs35361017
NM_001098512.3(PRKG1):c.-68GCC[12] rs79957958
NM_001098512.3(PRKG1):c.-68GCC[15] rs79957958
NM_001098512.3(PRKG1):c.-68GCC[8] rs79957958
NM_006258.4(PRKG1):c.1076+19_1076+20insTGGCCTT rs146504019
NM_006258.4(PRKG1):c.1076+22785T>C
NM_006258.4(PRKG1):c.1174-84G>T rs10454466
NM_006258.4(PRKG1):c.1545+27G>T rs7912782
NM_006258.4(PRKG1):c.312-170G>T rs3740292
NM_006258.4(PRKG1):c.478+163_478+166del rs142371458
NM_006258.4(PRKG1):c.699-118del rs34697221
NM_006258.4(PRKG1):c.699-118dup rs34697221
NM_006258.4(PRKG1):c.762+1165_762+1166insATATATATATATATATTTTTT
NM_006258.4(PRKG1):c.762+1165_762+1166insATATATATATATATTTTTT

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.