ClinVar Miner

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

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Gene type:
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Total variants: 19
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HGVS dbSNP
NM_022041.3(GAN):c.1272C>T (p.Tyr424=) rs1386745649
NM_022041.3(GAN):c.1287C>G (p.Gly429=) rs563049431
NM_022041.3(GAN):c.1287C>T (p.Gly429=) rs563049431
NM_022041.3(GAN):c.1373+9C>T rs1597407148
NM_022041.3(GAN):c.1503-7T>C rs1387006177
NM_022041.3(GAN):c.1629C>T (p.Tyr543=) rs772065469
NM_022041.3(GAN):c.1684C>G (p.Pro562Ala) rs79901179
NM_022041.3(GAN):c.1686A>C (p.Pro562=) rs1306397594
NM_022041.3(GAN):c.1689C>T (p.Ser563=) rs375075356
NM_022041.3(GAN):c.1716C>G (p.Ala572=) rs1434797669
NM_022041.3(GAN):c.255G>A (p.Glu85=) rs911350150
NM_022041.3(GAN):c.283-10A>G rs759028377
NM_022041.3(GAN):c.283-40G>T rs117009369
NM_022041.3(GAN):c.634-6C>T rs199874705
NM_022041.3(GAN):c.756G>T (p.Pro252=) rs138585506
NM_022041.3(GAN):c.819G>A (p.Glu273=) rs987754331
NM_022041.3(GAN):c.873G>A (p.Ala291=) rs749264810
NM_022041.4(GAN):c.1416G>A (p.Val472=)
NM_022041.4(GAN):c.334C>T (p.Leu112=)

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