ClinVar Miner

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

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Gene type:
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Total variants: 16
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HGVS dbSNP
NM_004817.4(TJP2):c.-26G>A rs147729271
NM_004817.4(TJP2):c.1005G>A (p.Thr335=) rs140444730
NM_004817.4(TJP2):c.1091C>T (p.Thr364Met) rs77321498
NM_004817.4(TJP2):c.1557C>T (p.Asp519=) rs1461192304
NM_004817.4(TJP2):c.1780+78G>C rs78326540
NM_004817.4(TJP2):c.2040G>A (p.Gly680=) rs111723895
NM_004817.4(TJP2):c.2646G>A (p.Ala882=) rs11788754
NM_004817.4(TJP2):c.2778C>T (p.Asp926=) rs140442228
NM_004817.4(TJP2):c.297G>A (p.Ser99=) rs72709079
NM_004817.4(TJP2):c.2992-8C>T rs143965233
NM_004817.4(TJP2):c.3190G>T (p.Val1064Leu) rs199892018
NM_004817.4(TJP2):c.3225C>T (p.Pro1075=) rs146241989
NM_004817.4(TJP2):c.3342T>C (p.His1114=) rs61753629
NM_004817.4(TJP2):c.3495G>A (p.Glu1165=) rs111595785
NM_004817.4(TJP2):c.61-7A>G rs755087942
NM_004817.4(TJP2):c.698G>A (p.Arg233Gln) rs150883816

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