ClinVar Miner

List of variants in gene SH3TC2 reported as benign by GeneDx

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Gene type:
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Total variants: 31
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HGVS dbSNP
NM_024577.3(SH3TC2):c.1002-119G>A rs11168081
NM_024577.3(SH3TC2):c.1135+197T>G rs2304034
NM_024577.3(SH3TC2):c.1350G>A (p.Pro450=) rs17722227
NM_024577.3(SH3TC2):c.1473C>T (p.Phe491=) rs144016931
NM_024577.3(SH3TC2):c.1842C>T (p.Asp614=) rs138411915
NM_024577.3(SH3TC2):c.2087A>G (p.His696Arg) rs17109261
NM_024577.3(SH3TC2):c.2322C>T (p.Asp774=) rs17795193
NM_024577.3(SH3TC2):c.2868A>G (p.Leu956=) rs115507662
NM_024577.3(SH3TC2):c.2872+37A>G rs17722209
NM_024577.3(SH3TC2):c.3053+103G>A rs10075404
NM_024577.3(SH3TC2):c.3054-241G>A rs55732303
NM_024577.3(SH3TC2):c.3054-65T>C rs11954893
NM_024577.3(SH3TC2):c.3205-138G>A rs77231639
NM_024577.3(SH3TC2):c.3294C>T (p.Thr1098=) rs193067884
NM_024577.3(SH3TC2):c.3327+225C>G rs1025475
NM_024577.3(SH3TC2):c.3327+70C>T rs1025476
NM_024577.3(SH3TC2):c.3328-315G>A rs1036191
NM_024577.3(SH3TC2):c.3594A>G (p.Pro1198=) rs6871030
NM_024577.3(SH3TC2):c.3795G>C (p.Leu1265=) rs144873879
NM_024577.3(SH3TC2):c.3834G>A (p.Ala1278=) rs117804174
NM_024577.3(SH3TC2):c.386-195T>C rs407696
NM_024577.3(SH3TC2):c.477T>A (p.Ser159=) rs77574155
NM_024577.3(SH3TC2):c.512G>A (p.Gly171Glu) rs17722293
NM_024577.3(SH3TC2):c.52+237G>A rs62380066
NM_024577.3(SH3TC2):c.52+239C>T rs40522
NM_024577.3(SH3TC2):c.529+178C>T rs17795277
NM_024577.3(SH3TC2):c.53-161C>T rs36077
NM_024577.3(SH3TC2):c.53-258G>T rs36076
NM_024577.3(SH3TC2):c.645C>T (p.Ser215=) rs80227512
NM_024577.3(SH3TC2):c.894C>T (p.Ile298=) rs779808918
NM_024577.4(SH3TC2):c.385+4_385+8del rs148930563

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