ClinVar Miner

List of variants in gene TSC2 reported as uncertain significance by Fulgent Genetics,Fulgent Genetics

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Total variants: 16
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HGVS dbSNP
NM_000548.5(TSC2):c.1033C>T (p.Leu345Phe) rs397515146
NM_000548.5(TSC2):c.1373G>A (p.Arg458Gln) rs878854077
NM_000548.5(TSC2):c.1622C>G (p.Pro541Arg) rs752953762
NM_000548.5(TSC2):c.1678G>A (p.Val560Met) rs141631268
NM_000548.5(TSC2):c.1774A>G (p.Ser592Gly) rs910068556
NM_000548.5(TSC2):c.1870G>A (p.Asp624Asn) rs1334081822
NM_000548.5(TSC2):c.2015C>T (p.Pro672Leu) rs768864353
NM_000548.5(TSC2):c.2023G>T (p.Ala675Ser) rs764840082
NM_000548.5(TSC2):c.2252G>A (p.Arg751Gln) rs749593050
NM_000548.5(TSC2):c.3226G>A (p.Gly1076Arg) rs747910305
NM_000548.5(TSC2):c.3380G>A (p.Arg1127Gln) rs746197874
NM_000548.5(TSC2):c.3551C>T (p.Ala1184Val) rs1060500939
NM_000548.5(TSC2):c.3956A>T (p.Asp1319Val) rs45517322
NM_000548.5(TSC2):c.4063A>G (p.Arg1355Gly) rs1555513911
NM_000548.5(TSC2):c.501G>C (p.Trp167Cys) rs755728007
NM_000548.5(TSC2):c.560A>G (p.Asn187Ser) rs45505405

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