ClinVar Miner

List of variants in gene SQSTM1 reported as likely benign for not provided

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Total variants: 44
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HGVS dbSNP gnomAD frequency
NM_003900.5(SQSTM1):c.673+237T>G rs79838921 0.02131
NM_003900.5(SQSTM1):c.822G>C (p.Glu274Asp) rs55793208 0.01529
NM_003900.5(SQSTM1):c.969+35G>A rs7735805 0.01470
NM_001142298.2(SQSTM1):c.-47-2346C>T rs116436326 0.01414
NM_003900.5(SQSTM1):c.754+134C>T rs56225166 0.01191
NM_001142298.2(SQSTM1):c.-47-2240G>A rs73351637 0.01117
NM_001142298.2(SQSTM1):c.-47-2160G>C rs576610830 0.00967
NM_003900.5(SQSTM1):c.961C>T (p.Arg321Cys) rs140226523 0.00943
NM_003900.5(SQSTM1):c.673+287C>T rs13358321 0.00842
NM_003900.5(SQSTM1):c.1165+251G>A rs114698136 0.00841
NM_003900.5(SQSTM1):c.*83G>A rs155790 0.00589
NM_003900.5(SQSTM1):c.673+127A>G rs143955370 0.00478
NM_003900.5(SQSTM1):c.970-104C>T rs189727708 0.00437
NM_003900.5(SQSTM1):c.984G>A (p.Ser328=) rs146164139 0.00374
NM_003900.5(SQSTM1):c.712A>G (p.Lys238Glu) rs11548633 0.00229
NM_003900.5(SQSTM1):c.1108T>C (p.Ser370Pro) rs143956614 0.00222
NM_003900.5(SQSTM1):c.350C>T (p.Ala117Val) rs147810437 0.00126
NM_003900.5(SQSTM1):c.888G>A (p.Pro296=) rs148984239 0.00073
NM_003900.5(SQSTM1):c.924G>A (p.Ala308=) rs139482113 0.00063
NM_003900.5(SQSTM1):c.1245G>A (p.Arg415=) rs148278350 0.00057
NM_003900.5(SQSTM1):c.98C>T (p.Ala33Val) rs200396166 0.00054
NM_003900.5(SQSTM1):c.1176G>A (p.Pro392=) rs75700262 0.00052
NM_003900.5(SQSTM1):c.1278G>A (p.Ala426=) rs143977783 0.00036
NM_003900.5(SQSTM1):c.513C>G (p.Pro171=) rs199931327 0.00019
NM_003900.5(SQSTM1):c.1038G>A (p.Val346=) rs150470670 0.00018
NM_003900.5(SQSTM1):c.1272C>T (p.Ile424=) rs374985304 0.00011
NM_003900.5(SQSTM1):c.1088G>A (p.Gly363Glu) rs375495050 0.00006
NM_003900.5(SQSTM1):c.1314G>A (p.Pro438=) rs182058393 0.00004
NM_003900.5(SQSTM1):c.540G>A (p.Ser180=) rs370203737 0.00004
NM_003900.5(SQSTM1):c.570C>T (p.His190=) rs758110159 0.00004
NM_003900.5(SQSTM1):c.1230C>T (p.Gly410=) rs766437927 0.00001
NM_003900.5(SQSTM1):c.384C>T (p.Cys128=) rs768088721 0.00001
NM_003900.5(SQSTM1):c.755-7C>T rs781389243 0.00001
NM_003900.5(SQSTM1):c.810C>T (p.Pro270=) rs1280918343 0.00001
NM_001142298.2(SQSTM1):c.-47-2192T>C rs534068817
NM_001142298.2(SQSTM1):c.-47-2236del rs199685457
NM_003900.4(SQSTM1):c.-35G>C rs189132632
NM_003900.5(SQSTM1):c.1119A>G (p.Gly373=) rs756626155
NM_003900.5(SQSTM1):c.302-269C>T rs113510309
NM_003900.5(SQSTM1):c.302-96C>T rs113087413
NM_003900.5(SQSTM1):c.532-4C>T rs763029496
NM_003900.5(SQSTM1):c.754+213C>A rs116597749
NM_003900.5(SQSTM1):c.835GAG[1] (p.Glu280del) rs752009611
NM_003900.5(SQSTM1):c.921G>C (p.Leu307=) rs952471580

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