ClinVar Miner

List of variants in gene SERPINB6 reported as likely benign for not provided

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Gene type:
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Total variants: 58
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HGVS dbSNP gnomAD frequency
NM_004568.6(SERPINB6):c.-11+107C>A rs576470382 0.01482
NM_004568.6(SERPINB6):c.-11+2722A>G rs3799196 0.01458
NM_004568.6(SERPINB6):c.-11+2315G>A rs72842026 0.01300
NM_004568.6(SERPINB6):c.-11+2751C>G rs116433001 0.01179
NM_004568.6(SERPINB6):c.312+298G>C rs79588648 0.01003
NM_004568.6(SERPINB6):c.313-279C>T rs146672242 0.01002
NM_004568.6(SERPINB6):c.574-286G>A rs113727991 0.00678
NM_004568.6(SERPINB6):c.-11+341G>A rs535386898 0.00605
NM_004568.6(SERPINB6):c.-11+2389T>G rs114362420 0.00597
NM_004568.6(SERPINB6):c.312+321G>T rs6909276 0.00240
NM_004568.6(SERPINB6):c.313-278G>A rs188632022 0.00122
NM_004568.6(SERPINB6):c.708C>T (p.Asp236=) rs144895010 0.00114
NM_004568.6(SERPINB6):c.100A>G (p.Met34Val) rs145538358 0.00081
NM_004568.6(SERPINB6):c.750C>T (p.Tyr250=) rs35617833 0.00070
NM_004568.6(SERPINB6):c.-10-31T>G rs375365980 0.00059
NM_004568.6(SERPINB6):c.121G>A (p.Val41Ile) rs140220538 0.00057
NM_004568.6(SERPINB6):c.314C>A (p.Ser105Tyr) rs148530934 0.00051
NM_004568.6(SERPINB6):c.996C>T (p.Ala332=) rs147792064 0.00036
NM_004568.6(SERPINB6):c.470C>T (p.Pro157Leu) rs141773281 0.00031
NM_004568.6(SERPINB6):c.424A>G (p.Thr142Ala) rs200861589 0.00026
NM_004568.6(SERPINB6):c.430+3G>A rs201080069 0.00021
NM_004568.6(SERPINB6):c.1050C>T (p.Cys350=) rs201048748 0.00019
NM_004568.6(SERPINB6):c.69C>T (p.Asn23=) rs148849865 0.00019
NM_004568.6(SERPINB6):c.12C>T (p.Leu4=) rs144857274 0.00018
NM_004568.6(SERPINB6):c.313-5C>G rs370994947 0.00018
NM_004568.6(SERPINB6):c.1110C>T (p.Cys370=) rs3188238 0.00007
NM_004568.6(SERPINB6):c.1092C>A (p.Thr364=) rs182270252 0.00006
NM_004568.6(SERPINB6):c.379G>A (p.Val127Ile) rs146252067 0.00006
NM_004568.6(SERPINB6):c.759C>T (p.Phe253=) rs201678985 0.00006
NM_004568.6(SERPINB6):c.18A>G (p.Glu6=) rs727505182 0.00005
NM_004568.6(SERPINB6):c.816G>A (p.Pro272=) rs151200580 0.00005
NM_004568.6(SERPINB6):c.313-15C>T rs190603417 0.00003
NM_004568.6(SERPINB6):c.1053C>T (p.Ala351=) rs748178838 0.00001
NM_004568.6(SERPINB6):c.165+20A>G rs370144516 0.00001
NM_004568.6(SERPINB6):c.313-19G>A rs1770231357 0.00001
NM_004568.6(SERPINB6):c.495T>C (p.Asn165=) rs776581052 0.00001
NM_004568.6(SERPINB6):c.-11+789_-11+792dup rs70995402
NM_004568.6(SERPINB6):c.-11+809G>T rs78441152
NM_004568.6(SERPINB6):c.1044C>T (p.Arg348=)
NM_004568.6(SERPINB6):c.132G>T (p.Gly44=) rs756760483
NM_004568.6(SERPINB6):c.165+183dup rs145725840
NM_004568.6(SERPINB6):c.165+226_165+228del rs533075608
NM_004568.6(SERPINB6):c.166-5T>A
NM_004568.6(SERPINB6):c.189C>T (p.Gly63=)
NM_004568.6(SERPINB6):c.252G>T (p.Thr84=)
NM_004568.6(SERPINB6):c.312+10A>C
NM_004568.6(SERPINB6):c.312+15C>T rs1770356286
NM_004568.6(SERPINB6):c.312+319_312+320insTG rs752569542
NM_004568.6(SERPINB6):c.363T>C (p.Leu121=) rs267600931
NM_004568.6(SERPINB6):c.375C>T (p.Ser125=)
NM_004568.6(SERPINB6):c.441G>A (p.Ala147=) rs201913568
NM_004568.6(SERPINB6):c.450C>G (p.Leu150=)
NM_004568.6(SERPINB6):c.543C>T (p.Asn181=)
NM_004568.6(SERPINB6):c.573+118del rs200683625
NM_004568.6(SERPINB6):c.573+16T>C
NM_004568.6(SERPINB6):c.705G>C (p.Pro235=) rs111416638
NM_004568.6(SERPINB6):c.771G>A (p.Thr257=)
NM_004568.6(SERPINB6):c.867G>A (p.Leu289=)

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