ClinVar Miner

List of variants in gene PRICKLE1 reported as likely benign for not provided

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Gene type:
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Total variants: 22
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HGVS dbSNP
NM_153026.3(PRICKLE1):c.-48-137G>T rs113411095
NM_153026.3(PRICKLE1):c.-48-204G>A rs74781866
NM_153026.3(PRICKLE1):c.108C>G (p.Val36=) rs147268650
NM_153026.3(PRICKLE1):c.108C>T (p.Val36=) rs147268650
NM_153026.3(PRICKLE1):c.133-5del rs1009731020
NM_153026.3(PRICKLE1):c.133-75G>T rs77568691
NM_153026.3(PRICKLE1):c.1440G>C (p.Leu480=) rs367822804
NM_153026.3(PRICKLE1):c.1470C>A (p.Gly490=) rs1213762995
NM_153026.3(PRICKLE1):c.1623A>T (p.Ala541=) rs776141626
NM_153026.3(PRICKLE1):c.1629C>A (p.Ser543=) rs748556304
NM_153026.3(PRICKLE1):c.1639+8_1639+20del rs1488350369
NM_153026.3(PRICKLE1):c.1640-256C>G rs114719652
NM_153026.3(PRICKLE1):c.2439G>A (p.Arg813=) rs138524511
NM_153026.3(PRICKLE1):c.246+230C>T rs111539888
NM_153026.3(PRICKLE1):c.247-207A>T rs7952738
NM_153026.3(PRICKLE1):c.2475C>G (p.Gly825=) rs1593099130
NM_153026.3(PRICKLE1):c.444T>G (p.Gly148=) rs1060504780
NM_153026.3(PRICKLE1):c.447G>A (p.Val149=) rs561240990
NM_153026.3(PRICKLE1):c.588+61A>T rs114395641
NM_153026.3(PRICKLE1):c.776-258C>G rs73273967
NM_153026.3(PRICKLE1):c.819C>T (p.His273=) rs763656364
NM_153026.3(PRICKLE1):c.915G>A (p.Thr305=) rs150052192

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