ClinVar Miner

List of variants in gene TJP2 reported as likely benign for not specified

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Total variants: 31
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HGVS dbSNP
NM_001170414.2(TJP2):c.116C>T (p.Thr39Met) rs138241615
NM_004817.3(TJP2):c.-26G>A rs147729271
NM_004817.3(TJP2):c.1005G>A (p.Thr335=) rs140444730
NM_004817.3(TJP2):c.239+14delC rs764370644
NM_004817.3(TJP2):c.2970A>G (p.Ala990=) rs727503481
NM_004817.3(TJP2):c.2992-8C>T rs143965233
NM_004817.3(TJP2):c.3063C>T (p.Ala1021=) rs367977493
NM_004817.3(TJP2):c.3190G>T (p.Val1064Leu) rs199892018
NM_004817.3(TJP2):c.3225C>T (p.Pro1075=) rs146241989
NM_004817.4(TJP2):c.1057-17A>G rs41277895
NM_004817.4(TJP2):c.1091C>T (p.Thr364Met) rs77321498
NM_004817.4(TJP2):c.1521-7A>C rs373242928
NM_004817.4(TJP2):c.1877C>G (p.Thr626Ser) rs149911553
NM_004817.4(TJP2):c.2646G>A (p.Ala882=) rs11788754
NM_004817.4(TJP2):c.2691C>T (p.Pro897=) rs149969431
NM_004817.4(TJP2):c.2720T>C (p.Met907Thr) rs149659876
NM_004817.4(TJP2):c.2778C>T (p.Asp926=) rs140442228
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.297G>A (p.Ser99=) rs72709079
NM_004817.4(TJP2):c.3372G>A (p.Thr1124=) rs745427593
NM_004817.4(TJP2):c.3407+3A>G rs727505291
NM_004817.4(TJP2):c.3407+7G>A rs369322645
NM_004817.4(TJP2):c.3495G>A (p.Glu1165=) rs111595785
NM_004817.4(TJP2):c.61-6A>T rs200415824
NM_004817.4(TJP2):c.698G>A (p.Arg233Gln) rs150883816
NM_004817.4(TJP2):c.887G>A (p.Ser296Asn) rs376434139
NM_004817.4(TJP2):c.918C>T (p.Ile306=) rs374523970

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