ClinVar Miner

List of variants in gene TJP2 reported as likely benign by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

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Total variants: 17
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HGVS dbSNP
NM_004817.4(TJP2):c.1521-7A>C rs373242928
NM_004817.4(TJP2):c.185C>T (p.Thr62Met) rs138241615
NM_004817.4(TJP2):c.1877C>G (p.Thr626Ser) rs149911553
NM_004817.4(TJP2):c.2720T>C (p.Met907Thr) rs149659876
NM_004817.4(TJP2):c.2819C>T (p.Pro940Leu) rs199852211
NM_004817.4(TJP2):c.2859G>T (p.Ser953=) rs369972534
NM_004817.4(TJP2):c.2865G>A (p.Pro955=) rs727503480
NM_004817.4(TJP2):c.2880+19C>T rs200384355
NM_004817.4(TJP2):c.2880+72G>A rs397516632
NM_004817.4(TJP2):c.2970A>G (p.Ala990=) rs727503481
NM_004817.4(TJP2):c.2992-8C>T rs143965233
NM_004817.4(TJP2):c.3063C>T (p.Ala1021=) rs367977493
NM_004817.4(TJP2):c.3190G>T (p.Val1064Leu) rs199892018
NM_004817.4(TJP2):c.3407+3A>G rs727505291
NM_004817.4(TJP2):c.3407+7G>A rs369322645
NM_004817.4(TJP2):c.698G>A (p.Arg233Gln) rs150883816
NM_004817.4(TJP2):c.918C>T (p.Ile306=) rs374523970

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