ClinVar Miner

List of variants in gene GRIP1 reported as uncertain significance for abdominal and pelvic region disorder

Included ClinVar conditions (961):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 73
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HGVS dbSNP
NM_021150.4(GRIP1):c.*1019C>T
NM_021150.4(GRIP1):c.*1149A>G
NM_021150.4(GRIP1):c.*1216G>T
NM_021150.4(GRIP1):c.*1261dup rs35499444
NM_021150.4(GRIP1):c.*1262T>A rs886049791
NM_021150.4(GRIP1):c.*1287A>T rs544816589
NM_021150.4(GRIP1):c.*1328G>A rs886049790
NM_021150.4(GRIP1):c.*1388_*1390dup rs886049789
NM_021150.4(GRIP1):c.*138C>T rs191549204
NM_021150.4(GRIP1):c.*1422_*1426del rs886049788
NM_021150.4(GRIP1):c.*1495_*1497dup rs553937765
NM_021150.4(GRIP1):c.*1511G>A
NM_021150.4(GRIP1):c.*1548_*1551dup rs886049787
NM_021150.4(GRIP1):c.*1559dup rs886049786
NM_021150.4(GRIP1):c.*228C>A
NM_021150.4(GRIP1):c.*235G>T rs886049796
NM_021150.4(GRIP1):c.*417G>A rs886049795
NM_021150.4(GRIP1):c.*4C>T
NM_021150.4(GRIP1):c.*611T>C
NM_021150.4(GRIP1):c.*617G>A
NM_021150.4(GRIP1):c.*667C>T
NM_021150.4(GRIP1):c.*679dup rs367709432
NM_021150.4(GRIP1):c.*716T>C rs531925092
NM_021150.4(GRIP1):c.*723_*725dup rs886049794
NM_021150.4(GRIP1):c.*735_*738dup rs551666983
NM_021150.4(GRIP1):c.*752_*754TAT[3] rs148302164
NM_021150.4(GRIP1):c.*753_*757del rs886049793
NM_021150.4(GRIP1):c.*821T>G rs867272684
NM_021150.4(GRIP1):c.*832G>C
NM_021150.4(GRIP1):c.*85_*87dup rs553542220
NM_021150.4(GRIP1):c.*915T>C rs886049792
NM_021150.4(GRIP1):c.*930T>A rs138773990
NM_021150.4(GRIP1):c.*93A>G
NM_021150.4(GRIP1):c.*99G>A
NM_021150.4(GRIP1):c.-158G>A rs559798312
NM_021150.4(GRIP1):c.-165A>C rs566069611
NM_021150.4(GRIP1):c.-172A>G rs188800373
NM_021150.4(GRIP1):c.1113G>A (p.Gly371=)
NM_021150.4(GRIP1):c.1225T>A (p.Leu409Met)
NM_021150.4(GRIP1):c.1272G>A (p.Thr424=)
NM_021150.4(GRIP1):c.1288G>A (p.Gly430Arg) rs771823092
NM_021150.4(GRIP1):c.1315G>A (p.Val439Met)
NM_021150.4(GRIP1):c.1427A>G (p.Asn476Ser) rs374486330
NM_021150.4(GRIP1):c.1532-6T>C
NM_021150.4(GRIP1):c.1600A>C (p.Ile534Leu) rs189438534
NM_021150.4(GRIP1):c.160G>A (p.Val54Ile) rs199768740
NM_021150.4(GRIP1):c.1638C>A (p.Asp546Glu)
NM_021150.4(GRIP1):c.1645G>A (p.Val549Ile) rs199936956
NM_021150.4(GRIP1):c.1724A>G (p.Asp575Gly)
NM_021150.4(GRIP1):c.2205G>A (p.Lys735=) rs886049797
NM_021150.4(GRIP1):c.2238G>A (p.Thr746=)
NM_021150.4(GRIP1):c.236G>A (p.Arg79Lys)
NM_021150.4(GRIP1):c.2402G>A (p.Arg801Gln) rs760273176
NM_021150.4(GRIP1):c.240A>G (p.Val80=) rs886049799
NM_021150.4(GRIP1):c.2637G>A (p.Ser879=) rs371224677
NM_021150.4(GRIP1):c.2658T>C (p.Asn886=)
NM_021150.4(GRIP1):c.2693G>A (p.Arg898Gln)
NM_021150.4(GRIP1):c.270T>C (p.Ala90=) rs867711989
NM_021150.4(GRIP1):c.2714G>A (p.Arg905His) rs202030145
NM_021150.4(GRIP1):c.2729C>T (p.Pro910Leu) rs540468070
NM_021150.4(GRIP1):c.2892T>C (p.Phe964=) rs372970620
NM_021150.4(GRIP1):c.3043G>C (p.Val1015Leu)
NM_021150.4(GRIP1):c.3066C>T (p.Ser1022=)
NM_021150.4(GRIP1):c.3067G>A (p.Gly1023Arg)
NM_021150.4(GRIP1):c.3148T>A (p.Trp1050Arg)
NM_021150.4(GRIP1):c.3176A>G (p.Gln1059Arg)
NM_021150.4(GRIP1):c.345C>T (p.Asp115=) rs760613522
NM_021150.4(GRIP1):c.553G>A (p.Val185Ile) rs754804786
NM_021150.4(GRIP1):c.730G>A (p.Val244Met)
NM_021150.4(GRIP1):c.817T>C (p.Cys273Arg) rs201673783
NM_021150.4(GRIP1):c.820A>G (p.Asn274Asp)
NM_021150.4(GRIP1):c.872+7A>G rs886049798
NM_021150.4(GRIP1):c.92A>G (p.Lys31Arg)

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