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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 49

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HGVS	dbSNP	gnomAD frequency
NM_002087.4(GRN):c.359C>A (p.Ser120Tyr)	rs63750043	0.00076
NM_002087.3(GRN):c.-45C>G	rs563336550	0.00057
NM_002087.4(GRN):c.393C>G (p.Phe131Leu)	rs149180605	0.00052
NM_002087.4(GRN):c.1253G>A (p.Arg418Gln)	rs63751100	0.00022
NM_002087.3(GRN):c.-203G>C	rs555738837	0.00010
NM_002087.4(GRN):c.1555G>A (p.Val519Met)	rs141111290	0.00010
NM_002087.4(GRN):c.415T>C (p.Cys139Arg)	rs763841075	0.00010
NM_002087.4(GRN):c.53C>T (p.Thr18Met)	rs199572314	0.00009
NM_002087.3(GRN):c.-100A>G	rs956983853	0.00008
NM_002087.4(GRN):c.229G>A (p.Val77Ile)	rs148531161	0.00008
NM_002087.4(GRN):c.1562G>A (p.Cys521Tyr)	rs553119528	0.00006
NM_002087.4(GRN):c.361G>A (p.Val121Met)	rs780731069	0.00006
NM_002087.4(GRN):c.442G>A (p.Gly148Arg)	rs375343686	0.00006
NM_002087.4(GRN):c.102C>T (p.Pro34=)	rs63751074	0.00005
NM_002087.4(GRN):c.128G>A (p.Arg43His)	rs766068311	0.00005
NM_002087.4(GRN):c.1540G>A (p.Val514Met)	rs142926942	0.00005
NM_002087.4(GRN):c.803C>T (p.Thr268Met)	rs202006119	0.00005
NM_002087.4(GRN):c.1193C>T (p.Ser398Leu)	rs148213321	0.00004
NM_002087.4(GRN):c.1112G>C (p.Ser371Thr)	rs149023078	0.00003
NM_002087.4(GRN):c.103G>A (p.Gly35Arg)	rs533451404	0.00002
NM_002087.4(GRN):c.1373C>T (p.Pro458Leu)	rs63750537	0.00002
NM_002087.4(GRN):c.157C>G (p.Leu53Val)	rs906652114	0.00002
NM_002087.4(GRN):c.238A>T (p.Thr80Ser)	rs1022228740	0.00002
NM_002087.4(GRN):c.836-3C>T	rs771907059	0.00002
NM_002087.4(GRN):c.1288C>G (p.Pro430Ala)	rs200645022	0.00001
NM_002087.4(GRN):c.1352C>T (p.Pro451Leu)	rs752428000	0.00001
NM_002087.4(GRN):c.1448C>T (p.Pro483Leu)	rs774128685	0.00001
NM_002087.4(GRN):c.22G>A (p.Val8Met)	rs774367010	0.00001
NM_002087.4(GRN):c.254C>T (p.Pro85Leu)	rs1275075189	0.00001
NM_002087.4(GRN):c.280G>A (p.Asp94Asn)	rs375678079	0.00001
NM_002087.4(GRN):c.928A>C (p.Thr310Pro)	rs969767392	0.00001
NM_002087.4(GRN):c.1015C>G (p.Pro339Ala)
NM_002087.4(GRN):c.1036_1038del (p.Glu346del)	rs751373342
NM_002087.4(GRN):c.1097G>A (p.Cys366Tyr)	rs878886923
NM_002087.4(GRN):c.1330T>C (p.Cys444Arg)
NM_002087.4(GRN):c.1407G>A (p.Leu469=)	rs779394553
NM_002087.4(GRN):c.1585_1587del (p.Asp529del)
NM_002087.4(GRN):c.1626C>T (p.Ala542=)	rs386352314
NM_002087.4(GRN):c.1636T>C (p.Tyr546His)	rs2143349053
NM_002087.4(GRN):c.1644+1G>A	rs2143349147
NM_002087.4(GRN):c.1672_1673delinsGA (p.Cys558Asp)	rs2143350279
NM_002087.4(GRN):c.1691G>A (p.Arg564His)	rs971443926
NM_002087.4(GRN):c.293G>A (p.Cys98Tyr)
NM_002087.4(GRN):c.332C>T (p.Ser111Phe)	rs1354832051
NM_002087.4(GRN):c.349+6G>A	rs1567885891
NM_002087.4(GRN):c.406T>G (p.Phe136Val)
NM_002087.4(GRN):c.413C>T (p.Thr138Met)
NM_002087.4(GRN):c.796G>C (p.Ala266Pro)	rs747362041
NM_002087.4(GRN):c.837G>A (p.Val279=)

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