ClinVar Miner

List of variants in gene PSAT1 reported as likely benign

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Gene type:
ClinVar version:
Total variants: 20
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HGVS dbSNP
NM_058179.4(PSAT1):c.*592A>C rs115361057
NM_058179.4(PSAT1):c.*865C>G rs529821810
NM_058179.4(PSAT1):c.1008-11G>T rs200199574
NM_058179.4(PSAT1):c.270C>G (p.Leu90=) rs775726256
NM_058179.4(PSAT1):c.367A>G (p.Ile123Val) rs116577685
NM_058179.4(PSAT1):c.369C>T (p.Ile123=) rs762328288
NM_058179.4(PSAT1):c.393T>C (p.Tyr131=) rs370268538
NM_058179.4(PSAT1):c.456C>T (p.Cys152=)
NM_058179.4(PSAT1):c.468G>A (p.Thr156=) rs200962308
NM_058179.4(PSAT1):c.546G>A (p.Leu182=) rs772396082
NM_058179.4(PSAT1):c.571-4T>A rs539694042
NM_058179.4(PSAT1):c.792C>T (p.Ala264=) rs371935677
NM_058179.4(PSAT1):c.795G>A (p.Ala265=) rs184256039
NM_058179.4(PSAT1):c.813C>T (p.Ser271=) rs747711253
NM_058179.4(PSAT1):c.831A>G (p.Thr277=) rs1462773959
NM_058179.4(PSAT1):c.869+9A>G rs368990190
NM_058179.4(PSAT1):c.870-4T>C rs775923430
NM_058179.4(PSAT1):c.884C>G (p.Pro295Arg) rs148080212
NM_058179.4(PSAT1):c.90A>G (p.Leu30=) rs1587632398
NM_058179.4(PSAT1):c.916C>T (p.Arg306Cys) rs113824905

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