ClinVar Miner

List of variants in gene SH3TC2 reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 70
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HGVS dbSNP gnomAD frequency
NM_024577.4(SH3TC2):c.1002-119G>A rs11168081 0.99465
NM_024577.4(SH3TC2):c.53-258G>T rs36076 0.98442
NM_024577.4(SH3TC2):c.1587T>G (p.Arg529=) rs1432794 0.97933
NM_024577.4(SH3TC2):c.*3136G>A rs1019927 0.97931
NM_024577.4(SH3TC2):c.*15823T>C rs4562031 0.77381
NM_024577.4(SH3TC2):c.*16020A>C rs4543254 0.57641
NM_024577.4(SH3TC2):c.*11390A>G rs3213854 0.52790
NM_024577.4(SH3TC2):c.*3077C>T rs1045942 0.52772
NM_024577.4(SH3TC2):c.*5490G>A rs1432795 0.52698
NM_024577.4(SH3TC2):c.53-161C>T rs36077 0.52142
NM_024577.4(SH3TC2):c.386-195T>C rs407696 0.49879
NM_024577.4(SH3TC2):c.*14766T>A rs891919 0.49105
NM_024577.4(SH3TC2):c.1194T>C (p.Gly398=) rs1432793 0.48793
NM_024577.4(SH3TC2):c.3327+70C>T rs1025476 0.40788
NM_024577.4(SH3TC2):c.3328-315G>A rs1036191 0.39980
NM_024577.4(SH3TC2):c.*3196T>C rs3763022 0.34686
NM_024577.4(SH3TC2):c.52+239C>T rs40522 0.25014
NM_024577.4(SH3TC2):c.*8111A>C rs17109205 0.24306
NM_024577.4(SH3TC2):c.3053+103G>A rs10075404 0.24239
NM_024577.4(SH3TC2):c.*1909G>T rs998304 0.23360
NM_024577.4(SH3TC2):c.*1639T>C rs1007400 0.23355
NM_024577.4(SH3TC2):c.*5799C>T rs17109208 0.23286
NM_024577.4(SH3TC2):c.3054-65T>C rs11954893 0.23238
NM_024577.4(SH3TC2):c.3054-241G>A rs55732303 0.22879
NM_024577.4(SH3TC2):c.*14856C>A rs891920 0.22858
NM_024577.4(SH3TC2):c.*2956C>T rs3763020 0.22548
NM_024577.4(SH3TC2):c.1402G>T (p.Ala468Ser) rs6875902 0.22262
NM_024577.4(SH3TC2):c.3676-94C>A rs1432799 0.21366
NM_024577.4(SH3TC2):c.*6436G>T rs11168079 0.19789
NM_024577.4(SH3TC2):c.3054-268A>G rs1549907 0.16559
NM_024577.4(SH3TC2):c.2872+37A>G rs17722209 0.16479
NM_024577.4(SH3TC2):c.*6692A>G rs11168078 0.16452
NM_024577.4(SH3TC2):c.*14621G>T rs17795097 0.16395
NM_024577.4(SH3TC2):c.3205-340A>G rs7704297 0.16102
NM_024577.4(SH3TC2):c.1135+197T>G rs2304034 0.13526
NM_024577.4(SH3TC2):c.52+237G>A rs62380066 0.12451
NM_024577.4(SH3TC2):c.529+178C>T rs17795277 0.12117
NM_024577.4(SH3TC2):c.*10968G>A rs13166730 0.11562
NM_024577.4(SH3TC2):c.*19519G>A rs10039839 0.07821
NM_024577.4(SH3TC2):c.3676-269G>C rs1124473 0.07784
NM_024577.4(SH3TC2):c.*11852G>T rs13359285 0.07778
NM_024577.4(SH3TC2):c.3676-251T>C rs79910173 0.04322
NM_024577.4(SH3TC2):c.*1935T>C rs6883926 0.04318
NM_024577.4(SH3TC2):c.3205-138G>A rs77231639 0.04206
NM_024577.4(SH3TC2):c.*1944_*1946del rs35447358 0.03577
NM_024577.4(SH3TC2):c.*1940_*1941insT rs35713276 0.03576
NM_024577.4(SH3TC2):c.*21472A>G rs59731646 0.03434
NM_024577.4(SH3TC2):c.2235T>G (p.Ala745=) rs78120278 0.03339
NM_024577.4(SH3TC2):c.3472G>A (p.Val1158Ile) rs55853803 0.02130
NM_024577.4(SH3TC2):c.2872+9G>A rs76488338 0.01755
NM_024577.4(SH3TC2):c.*10864G>A rs189701174 0.00853
NM_024577.4(SH3TC2):c.645C>T (p.Ser215=) rs80227512 0.00587
NM_024577.4(SH3TC2):c.2087A>G (p.His696Arg) rs17109261 0.00521
NM_024577.4(SH3TC2):c.2691C>G (p.Asn897Lys) rs73795753 0.00494
NM_024577.4(SH3TC2):c.2913C>T (p.Ser971=) rs13436308 0.00462
NM_024577.4(SH3TC2):c.3362C>T (p.Ala1121Val) rs115577291 0.00390
NM_024577.4(SH3TC2):c.558C>T (p.Ser186=) rs141289653 0.00290
NM_024577.4(SH3TC2):c.3834G>A (p.Ala1278=) rs117804174 0.00133
NM_024577.4(SH3TC2):c.*39A>C rs76579569 0.00127
NM_024577.4(SH3TC2):c.2322C>T (p.Asp774=) rs17795193 0.00125
NM_024577.4(SH3TC2):c.1299G>A (p.Ser433=) rs140904010 0.00108
NM_024577.4(SH3TC2):c.1482C>T (p.Leu494=) rs200665714 0.00056
NM_024577.4(SH3TC2):c.188G>A (p.Arg63Lys) rs747938069 0.00010
NM_024577.4(SH3TC2):c.*10051ACCA[12] rs57301725
NM_024577.4(SH3TC2):c.*10051ACCA[13] rs57301725
NM_024577.4(SH3TC2):c.*10051ACCA[14] rs57301725
NM_024577.4(SH3TC2):c.*19406A>T rs72835351
NM_024577.4(SH3TC2):c.3327+225C>G rs1025475
NM_024577.4(SH3TC2):c.3594A>C (p.Pro1198=) rs6871030
NM_024577.4(SH3TC2):c.3676-98C>G rs76014357

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