ClinVar Miner

List of variants in gene TJP2 reported as benign for not provided

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Total variants: 27
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HGVS dbSNP
GRCh37/hg19 9q21.11(chr9:71741320-71746253)x0
NM_004817.4(TJP2):c.1056+73C>A rs17062682
NM_004817.4(TJP2):c.1063G>C (p.Gly355Arg) rs78681604
NM_004817.4(TJP2):c.1091C>T (p.Thr364Met) rs77321498
NM_004817.4(TJP2):c.1350C>T (p.Ser450=) rs17062723
NM_004817.4(TJP2):c.1478G>A (p.Arg493Lys) rs41277901
NM_004817.4(TJP2):c.185C>T (p.Thr62Met) rs138241615
NM_004817.4(TJP2):c.1917C>T (p.Asp639=) rs12340440
NM_004817.4(TJP2):c.2004G>A (p.Met668Ile) rs34774441
NM_004817.4(TJP2):c.2040G>A (p.Gly680=) rs111723895
NM_004817.4(TJP2):c.2131T>C (p.Ser711Pro) rs35797487
NM_004817.4(TJP2):c.2137A>G (p.Ser713Gly) rs116545275
NM_004817.4(TJP2):c.2367A>G (p.Ala789=) rs75668442
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.2751C>T (p.Arg917=) rs184519036
NM_004817.4(TJP2):c.2778C>T (p.Asp926=) rs140442228
NM_004817.4(TJP2):c.2810T>C (p.Leu937Pro) rs28556975
NM_004817.4(TJP2):c.297G>A (p.Ser99=) rs72709079
NM_004817.4(TJP2):c.2992-8C>T rs143965233
NM_004817.4(TJP2):c.3407+45A>G rs41277913
NM_004817.4(TJP2):c.342+12G>T rs7027812
NM_004817.4(TJP2):c.3495G>A (p.Glu1165=) rs111595785
NM_004817.4(TJP2):c.60+39CGTGAG[3] rs59568063
NM_004817.4(TJP2):c.61-7344G>C rs73450853
NM_004817.4(TJP2):c.644G>A (p.Arg215His) rs201977617
NM_004817.4(TJP2):c.698G>A (p.Arg233Gln) rs150883816

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