ClinVar Miner

List of variants in gene SBF2 reported as uncertain significance for not provided

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Total variants: 31
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HGVS dbSNP
NM_030962.3(SBF2):c.1159T>C (p.Phe387Leu) rs1247599264
NM_030962.3(SBF2):c.1327G>C (p.Val443Leu) rs765958389
NM_030962.3(SBF2):c.1420T>C (p.Phe474Leu) rs794727133
NM_030962.3(SBF2):c.1424A>G (p.Gln475Arg) rs199894823
NM_030962.3(SBF2):c.1509A>G (p.Glu503=) rs143773975
NM_030962.3(SBF2):c.1804A>G (p.Ile602Val) rs751375939
NM_030962.3(SBF2):c.257A>G (p.Tyr86Cys) rs745669920
NM_030962.3(SBF2):c.304G>T (p.Gly102Cys) rs879253916
NM_030962.3(SBF2):c.3574A>G (p.Thr1192Ala) rs761285334
NM_030962.3(SBF2):c.3754A>T (p.Ser1252Cys) rs139967004
NM_030962.3(SBF2):c.3824G>A (p.Arg1275His) rs150028248
NM_030962.3(SBF2):c.3831C>G (p.Ile1277Met) rs139522696
NM_030962.3(SBF2):c.3865C>T (p.Arg1289Trp) rs145107442
NM_030962.3(SBF2):c.3866G>A (p.Arg1289Gln) rs757836523
NM_030962.3(SBF2):c.4070T>C (p.Met1357Thr) rs1554907847
NM_030962.3(SBF2):c.4156C>G (p.Leu1386Val) rs771436343
NM_030962.3(SBF2):c.4522C>T (p.Arg1508Cys) rs141108330
NM_030962.3(SBF2):c.4563A>T (p.Leu1521Phe) rs148988271
NM_030962.3(SBF2):c.463C>A (p.Leu155Ile) rs1057524731
NM_030962.3(SBF2):c.4666T>C (p.Phe1556Leu) rs189911105
NM_030962.3(SBF2):c.4699-9C>A rs376668219
NM_030962.3(SBF2):c.4760C>G (p.Thr1587Ser) rs1554900597
NM_030962.3(SBF2):c.4799C>G (p.Thr1600Ser) rs183468503
NM_030962.3(SBF2):c.479G>T (p.Cys160Phe) rs1214507322
NM_030962.3(SBF2):c.5014_5016del (p.Lys1672del) rs750958357
NM_030962.3(SBF2):c.5017_5019GAA[1] (p.Glu1674del) rs572571832
NM_030962.3(SBF2):c.5054C>G (p.Ser1685Trp) rs148468522
NM_030962.3(SBF2):c.5058A>T (p.Arg1686Ser) rs146230559
NM_030962.3(SBF2):c.766C>A (p.Pro256Thr) rs879253987
NM_030962.3(SBF2):c.861+5G>C rs879253963
NM_030962.3(SBF2):c.87G>C (p.Gln29His) rs751336040

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