ClinVar Miner

List of variants in gene TJP2 reported as likely benign by Invitae

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Total variants: 21
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HGVS dbSNP
NM_004817.4(TJP2):c.1005G>A (p.Thr335=) rs140444730
NM_004817.4(TJP2):c.1473C>A (p.Ala491=) rs138509345
NM_004817.4(TJP2):c.1713C>A (p.Ala571=) rs376280878
NM_004817.4(TJP2):c.1877C>G (p.Thr626Ser) rs149911553
NM_004817.4(TJP2):c.2384C>T (p.Pro795Leu) rs139867659
NM_004817.4(TJP2):c.2493G>A (p.Thr831=) rs944668173
NM_004817.4(TJP2):c.2553A>C (p.Ala851=) rs763701380
NM_004817.4(TJP2):c.258C>T (p.Val86=) rs530810462
NM_004817.4(TJP2):c.2636A>G (p.Gln879Arg) rs75450131
NM_004817.4(TJP2):c.2832G>A (p.Pro944=) rs191634088
NM_004817.4(TJP2):c.2859G>T (p.Ser953=) rs369972534
NM_004817.4(TJP2):c.2937C>T (p.Ser979=) rs138333815
NM_004817.4(TJP2):c.303A>G (p.Ala101=) rs756808587
NM_004817.4(TJP2):c.334G>A (p.Ala112Thr) rs144396411
NM_004817.4(TJP2):c.3372G>A (p.Thr1124=) rs745427593
NM_004817.4(TJP2):c.3450T>C (p.Tyr1150=) rs779575464
NM_004817.4(TJP2):c.395C>G (p.Pro132Arg) rs141496493
NM_004817.4(TJP2):c.61-6A>T rs200415824
NM_004817.4(TJP2):c.705G>T (p.Arg235=) rs750625862
NM_004817.4(TJP2):c.908C>T (p.Pro303Leu) rs199641113
NM_004817.4(TJP2):c.911G>A (p.Gly304Glu) rs200222645

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