ClinVar Miner

List of variants in gene GPC3 reported as benign for abdominal and pelvic region disorder

Included ClinVar conditions (913):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 32
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HGVS dbSNP
NM_001164617.2(GPC3):c.1236-8T>C rs182950534
NM_001164617.2(GPC3):c.1354G>A (p.Val452Met) rs11539789
NM_001164617.2(GPC3):c.204G>A (p.Lys68=) rs61754632
NM_004484.3(GPC3):c.1032+9C>T rs200782847
NM_004484.3(GPC3):c.1232G>T (p.Ser411Ile) rs139206747
NM_004484.3(GPC3):c.1254C>T (p.Asn418=) rs150766741
NM_004484.3(GPC3):c.1287G>A (p.Val429=) rs756598026
NM_004484.3(GPC3):c.1426A>G (p.Met476Val) rs200265913
NM_004484.3(GPC3):c.1500T>C (p.Asp500=) rs2314298
NM_004484.3(GPC3):c.1574-7_1574-4del rs751413609
NM_004484.3(GPC3):c.1626A>G (p.Ala542=) rs61754631
NM_004484.3(GPC3):c.1631C>T (p.Pro544Leu) rs375606908
NM_004484.3(GPC3):c.1632G>A (p.Pro544=) rs766482434
NM_004484.3(GPC3):c.1641C>T (p.Asn547=) rs772217919
NM_004484.3(GPC3):c.1680C>T (p.Ser560=) rs748480657
NM_004484.3(GPC3):c.168C>G (p.Pro56=) rs188592483
NM_004484.3(GPC3):c.1716G>C (p.Val572=) rs779688123
NM_004484.3(GPC3):c.172C>T (p.Pro58Ser) rs147231796
NM_004484.3(GPC3):c.358C>T (p.Arg120Cys) rs587778392
NM_004484.3(GPC3):c.359G>A (p.Arg120His) rs148021273
NM_004484.3(GPC3):c.384C>T (p.Ala128=) rs761541528
NM_004484.3(GPC3):c.459T>G (p.Ser153=) rs775459305
NM_004484.3(GPC3):c.485A>G (p.Asn162Ser) rs780431445
NM_004484.3(GPC3):c.648G>C (p.Met216Ile) rs752516966
NM_004484.3(GPC3):c.660C>T (p.Ser220=) rs138450923
NM_004484.3(GPC3):c.79_81CCG[6] (p.Pro31dup) rs749104500
NM_004484.3(GPC3):c.826G>A (p.Gly276Ser) rs141100113
NM_004484.3(GPC3):c.876T>C (p.Ile292=) rs61754633
NM_004484.3(GPC3):c.889A>G (p.Arg297Gly) rs148951753
NM_004484.3(GPC3):c.897C>T (p.Tyr299=) rs200421668
NM_004484.3(GPC3):c.972T>C (p.Phe324=) rs183678432
NM_004484.3(GPC3):c.995A>G (p.Gln332Arg) rs78696048

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