ClinVar Miner

List of variants in gene APOA1 studied for abdominal and pelvic region disorder

Included ClinVar conditions (961):
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Total variants: 28
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HGVS dbSNP
APOA1, 12-BP DEL AND 2-BP INS
NM_000039.2(APOA1):c.*19C>G rs187335584
NM_000039.2(APOA1):c.-11G>A rs199729971
NM_000039.2(APOA1):c.116C>T (p.Ala39Val) rs746314593
NM_000039.2(APOA1):c.168G>A (p.Gln56=) rs760886281
NM_000039.2(APOA1):c.181G>A (p.Ala61Thr) rs12718465
NM_000039.2(APOA1):c.284T>A (p.Phe95Tyr) rs138407155
NM_000039.2(APOA1):c.28G>A (p.Val10Met) rs750125257
NM_000039.2(APOA1):c.388_390AAG[1] (p.Lys131del)
NM_000039.2(APOA1):c.41C>T (p.Thr14Met) rs778560581
NM_000039.2(APOA1):c.454G>A (p.Glu152Lys) rs574061789
NM_000039.2(APOA1):c.480G>T (p.Glu160Asp) rs769548576
NM_000039.2(APOA1):c.498C>A (p.Ser166Arg) rs757899657
NM_000039.2(APOA1):c.562G>T (p.Ala188Ser) rs140770089
NM_000039.2(APOA1):c.593T>C (p.Leu198Ser) rs121912729
NM_000039.2(APOA1):c.595G>C (p.Ala199Pro) rs121912730
NM_000039.2(APOA1):c.732C>G (p.Pro244=) rs5080
NM_000039.2(APOA1):c.9T>C (p.Ala3=) rs141383703
NM_000039.3(APOA1):c.*17C>T
NM_000039.3(APOA1):c.-29G>A
NM_000039.3(APOA1):c.127G>C (p.Val43Leu)
NM_000039.3(APOA1):c.178T>G (p.Ser60Ala)
NM_000039.3(APOA1):c.447G>A (p.Glu149=)
NM_000039.3(APOA1):c.625G>A (p.Gly209Ser)
NM_000039.3(APOA1):c.677C>T (p.Thr226Met)
NM_000039.3(APOA1):c.705C>G (p.Leu235=)
NM_001318021.1(APOA1):c.-108T>C rs121912726
NM_001318021.1(APOA1):c.-77T>G rs121912724

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