ClinVar Miner

List of variants in gene GRIP1 reported as uncertain significance for auditory system disease

Included ClinVar conditions (549):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 74
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HGVS dbSNP
NM_001366722.1(GRIP1):c.*1019C>T
NM_001366722.1(GRIP1):c.*1149A>G
NM_001366722.1(GRIP1):c.*1216G>T
NM_001366722.1(GRIP1):c.*1261dup rs35499444
NM_001366722.1(GRIP1):c.*1262T>A rs886049791
NM_001366722.1(GRIP1):c.*1287A>T rs544816589
NM_001366722.1(GRIP1):c.*1328G>A rs886049790
NM_001366722.1(GRIP1):c.*1388_*1390dup rs886049789
NM_001366722.1(GRIP1):c.*138C>T rs191549204
NM_001366722.1(GRIP1):c.*1422_*1426del rs886049788
NM_001366722.1(GRIP1):c.*1495_*1497dup rs553937765
NM_001366722.1(GRIP1):c.*1511G>A
NM_001366722.1(GRIP1):c.*1548_*1551dup rs886049787
NM_001366722.1(GRIP1):c.*1559dup rs886049786
NM_001366722.1(GRIP1):c.*228C>A
NM_001366722.1(GRIP1):c.*235G>T rs886049796
NM_001366722.1(GRIP1):c.*417G>A rs886049795
NM_001366722.1(GRIP1):c.*4C>T
NM_001366722.1(GRIP1):c.*611T>C
NM_001366722.1(GRIP1):c.*617G>A
NM_001366722.1(GRIP1):c.*667C>T
NM_001366722.1(GRIP1):c.*679dup rs367709432
NM_001366722.1(GRIP1):c.*716T>C rs531925092
NM_001366722.1(GRIP1):c.*723_*725dup rs886049794
NM_001366722.1(GRIP1):c.*735_*738dup rs551666983
NM_001366722.1(GRIP1):c.*752_*754TAT[3] rs148302164
NM_001366722.1(GRIP1):c.*753_*757del rs886049793
NM_001366722.1(GRIP1):c.*821T>G rs867272684
NM_001366722.1(GRIP1):c.*832G>C
NM_001366722.1(GRIP1):c.*85_*87dup rs553542220
NM_001366722.1(GRIP1):c.*915T>C rs886049792
NM_001366722.1(GRIP1):c.*930T>A rs138773990
NM_001366722.1(GRIP1):c.*93A>G
NM_001366722.1(GRIP1):c.*99G>A
NM_001366722.1(GRIP1):c.-158G>A rs559798312
NM_001366722.1(GRIP1):c.-165A>C rs566069611
NM_001366722.1(GRIP1):c.-172A>G rs188800373
NM_001366722.1(GRIP1):c.1269G>A (p.Gly423=)
NM_001366722.1(GRIP1):c.1381T>A (p.Leu461Met)
NM_001366722.1(GRIP1):c.1428G>A (p.Thr476=) rs202009431
NM_001366722.1(GRIP1):c.1444G>A (p.Gly482Arg) rs771823092
NM_001366722.1(GRIP1):c.1471G>A (p.Val491Met)
NM_001366722.1(GRIP1):c.1583A>G (p.Asn528Ser) rs374486330
NM_001366722.1(GRIP1):c.160G>A (p.Val54Ile) rs199768740
NM_001366722.1(GRIP1):c.1688-6T>C rs111776176
NM_001366722.1(GRIP1):c.1756A>C (p.Ile586Leu) rs189438534
NM_001366722.1(GRIP1):c.1794C>A (p.Asp598Glu)
NM_001366722.1(GRIP1):c.1801G>A (p.Val601Ile) rs199936956
NM_001366722.1(GRIP1):c.1880A>G (p.Asp627Gly)
NM_001366722.1(GRIP1):c.2361G>A (p.Lys787=) rs886049797
NM_001366722.1(GRIP1):c.236G>A (p.Arg79Lys)
NM_001366722.1(GRIP1):c.2394G>A (p.Thr798=)
NM_001366722.1(GRIP1):c.240A>G (p.Val80=) rs886049799
NM_001366722.1(GRIP1):c.2423C>T (p.Ser808Leu)
NM_001366722.1(GRIP1):c.2558G>A (p.Arg853Gln) rs760273176
NM_001366722.1(GRIP1):c.270T>C (p.Ala90=) rs867711989
NM_001366722.1(GRIP1):c.2793G>A (p.Ser931=) rs371224677
NM_001366722.1(GRIP1):c.2814T>C (p.Asn938=)
NM_001366722.1(GRIP1):c.2849G>A (p.Arg950Gln)
NM_001366722.1(GRIP1):c.2870G>A (p.Arg957His) rs202030145
NM_001366722.1(GRIP1):c.2885C>T (p.Pro962Leu) rs540468070
NM_001366722.1(GRIP1):c.3048T>C (p.Phe1016=) rs372970620
NM_001366722.1(GRIP1):c.3199G>C (p.Val1067Leu)
NM_001366722.1(GRIP1):c.3222C>T (p.Ser1074=)
NM_001366722.1(GRIP1):c.3223G>A (p.Gly1075Arg)
NM_001366722.1(GRIP1):c.3304T>A (p.Trp1102Arg)
NM_001366722.1(GRIP1):c.3332A>G (p.Gln1111Arg)
NM_001366722.1(GRIP1):c.345C>T (p.Asp115=) rs760613522
NM_001366722.1(GRIP1):c.553G>A (p.Val185Ile) rs754804786
NM_001366722.1(GRIP1):c.730G>A (p.Val244Met)
NM_001366722.1(GRIP1):c.817T>C (p.Cys273Arg) rs201673783
NM_001366722.1(GRIP1):c.820A>G (p.Asn274Asp)
NM_001366722.1(GRIP1):c.872+7A>G rs886049798
NM_001366722.1(GRIP1):c.92A>G (p.Lys31Arg)

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