ClinVar Miner

List of variants reported as uncertain significance for Saethre-Chotzen syndrome

Included ClinVar conditions (6):
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ClinVar version:
Total variants: 122
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HGVS dbSNP gnomAD frequency
NM_000474.4(TWIST1):c.94G>A (p.Gly32Ser) rs878852992 0.00102
NM_000474.4(TWIST1):c.277A>G (p.Ser93Gly) rs925811677 0.00039
NM_000141.5(FGFR2):c.-165G>A rs886046766 0.00029
NM_000141.5(FGFR2):c.*921G>A rs185617859 0.00027
NM_000141.5(FGFR2):c.-173G>A rs540975865 0.00019
NM_000141.5(FGFR2):c.-622G>A rs886046768 0.00014
NM_000141.5(FGFR2):c.2426T>C (p.Leu809Pro) rs368003279 0.00011
NM_000141.5(FGFR2):c.289G>A (p.Ala97Thr) rs372430349 0.00011
NM_000141.5(FGFR2):c.989G>A (p.Arg330Gln) rs199757302 0.00011
NM_000141.5(FGFR2):c.-237C>A rs1013618217 0.00010
NM_000141.5(FGFR2):c.182G>A (p.Arg61His) rs199575491 0.00007
NM_000141.5(FGFR2):c.-371C>T rs527570655 0.00006
NM_000141.5(FGFR2):c.201C>T (p.Ala67=) rs200386134 0.00006
NM_000474.4(TWIST1):c.152G>T (p.Gly51Val) rs1305059157 0.00006
NM_000141.5(FGFR2):c.*736dup rs886046762 0.00005
NM_000141.5(FGFR2):c.16C>T (p.Arg6Cys) rs141724446 0.00005
NM_000141.5(FGFR2):c.780C>T (p.Ala260=) rs778288494 0.00005
NM_000141.5(FGFR2):c.*874A>G rs55723405 0.00004
NM_000141.5(FGFR2):c.-535G>C rs886046767 0.00004
NM_000141.5(FGFR2):c.*1126T>C rs370106008 0.00003
NM_000141.5(FGFR2):c.*1489C>T rs886046757 0.00003
NM_000141.5(FGFR2):c.*463A>G rs373313930 0.00003
NM_000141.5(FGFR2):c.*730G>C rs549293047 0.00003
NM_000141.5(FGFR2):c.-206C>A rs1238787517 0.00003
NM_000141.5(FGFR2):c.362T>C (p.Met121Thr) rs748322657 0.00003
NM_000141.5(FGFR2):c.772C>T (p.Leu258Phe) rs747171741 0.00003
NM_000141.4(FGFR2):c.*1539C>A rs1194799333 0.00002
NM_000141.5(FGFR2):c.1085C>T (p.Ala362Val) rs757846343 0.00002
NM_000141.5(FGFR2):c.1238C>T (p.Pro413Leu) rs372348666 0.00002
NM_000141.5(FGFR2):c.1328C>T (p.Pro443Leu) rs757125418 0.00002
NM_000141.5(FGFR2):c.1348C>T (p.Arg450Cys) rs536181987 0.00002
NM_000141.5(FGFR2):c.1561+6C>T rs781352732 0.00002
NM_000141.5(FGFR2):c.*1369C>T rs886046759 0.00001
NM_000141.5(FGFR2):c.*497T>C rs3135827 0.00001
NM_000141.5(FGFR2):c.-128G>A rs547739869 0.00001
NM_000141.5(FGFR2):c.-129C>T rs886046765 0.00001
NM_000141.5(FGFR2):c.-196G>A rs1457119353 0.00001
NM_000141.5(FGFR2):c.1167C>G (p.Ala389=) rs757648006 0.00001
NM_000141.5(FGFR2):c.1240G>A (p.Ala414Thr) rs769880096 0.00001
NM_000141.5(FGFR2):c.138A>C (p.Gln46His) rs748117555 0.00001
NM_000141.5(FGFR2):c.1562-11A>G rs41293744 0.00001
NM_000141.5(FGFR2):c.1562A>G (p.Asp521Gly) rs55689343 0.00001
NM_000141.5(FGFR2):c.1985A>G (p.Asn662Ser) rs962103382 0.00001
NM_000141.5(FGFR2):c.204C>T (p.Ala68=) rs747982371 0.00001
NM_000141.5(FGFR2):c.2077A>G (p.Met693Val) rs774682374 0.00001
NM_000141.5(FGFR2):c.788C>T (p.Pro263Leu) rs779326224 0.00001
NM_000141.5(FGFR2):c.910G>A (p.Asp304Asn) rs370877537 0.00001
NM_000474.4(TWIST1):c.134G>A (p.Ser45Asn) rs2522202 0.00001
NM_000474.4(TWIST1):c.250G>A (p.Gly84Ser) rs1310233431 0.00001
NM_000474.4(TWIST1):c.316C>G (p.Leu106Val) rs1230428800 0.00001
NM_000474.4(TWIST1):c.70C>G (p.Pro24Ala) rs559821440 0.00001
NM_000141.5(FGFR2):c.*1070T>C rs886046761
NM_000141.5(FGFR2):c.*1240A>C rs1403038230
NM_000141.5(FGFR2):c.*1283C>G rs1844298421
NM_000141.5(FGFR2):c.*1287A>C rs886046760
NM_000141.5(FGFR2):c.*1402T>C rs886046758
NM_000141.5(FGFR2):c.*256G>A rs763095219
NM_000141.5(FGFR2):c.-108C>T rs540720034
NM_000141.5(FGFR2):c.-17G>C rs766629665
NM_000141.5(FGFR2):c.-590G>C rs1221108798
NM_000141.5(FGFR2):c.-603C>T rs1863754113
NM_000141.5(FGFR2):c.1085-6A>G rs2134232051
NM_000141.5(FGFR2):c.1093A>C (p.Arg365=) rs1849564914
NM_000141.5(FGFR2):c.110-22TC[3] rs773932794
NM_000141.5(FGFR2):c.1179A>T (p.Val393=) rs886046763
NM_000141.5(FGFR2):c.1485G>T (p.Val495=) rs1362401352
NM_000141.5(FGFR2):c.1539C>A (p.Thr513=) rs74160617
NM_000141.5(FGFR2):c.1562-9_1562-7delinsAA rs2133978031
NM_000141.5(FGFR2):c.1735C>T (p.Arg579Trp) rs1564875549
NM_000141.5(FGFR2):c.2045A>G (p.His682Arg) rs1845557012
NM_000141.5(FGFR2):c.2444_2445del (p.Ile815fs) rs771208561
NM_000141.5(FGFR2):c.287G>A (p.Gly96Asp) rs1277734487
NM_000141.5(FGFR2):c.351T>C (p.Thr117=) rs886046764
NM_000141.5(FGFR2):c.625-8C>T rs1853240523
NM_000141.5(FGFR2):c.714G>A (p.Gly238=) rs1276387170
NM_000141.5(FGFR2):c.781G>A (p.Gly261Arg) rs2134317947
NM_000141.5(FGFR2):c.877C>T (p.His293Tyr) rs748526473
NM_000141.5(FGFR2):c.91A>T (p.Thr31Ser) rs1863017903
NM_000474.4(TWIST1):c.110G>A (p.Arg37His)
NM_000474.4(TWIST1):c.142G>A (p.Gly48Ser)
NM_000474.4(TWIST1):c.161G>T (p.Gly54Val) rs1788590971
NM_000474.4(TWIST1):c.185GCG[3] (p.Gly63_Asp64insGly)
NM_000474.4(TWIST1):c.203G>A (p.Ser68Asn) rs1051003265
NM_000474.4(TWIST1):c.203G>T (p.Ser68Ile)
NM_000474.4(TWIST1):c.241_264dup (p.Gly88_Gly89insCysGlyGlyGlyGlyGlyAlaGly)
NM_000474.4(TWIST1):c.245GCG[7] (p.Gly85_Gly86dup) rs754552080
NM_000474.4(TWIST1):c.253_276dup (p.Gly85_Gly92dup) rs544465774
NM_000474.4(TWIST1):c.256_276del (p.Gly86_Gly92del) rs544465774
NM_000474.4(TWIST1):c.259_276dup (p.Gly92_Ser93insAlaGlyGlyGlyGlyGly)
NM_000474.4(TWIST1):c.262GGC[6] (p.Gly92dup) rs750238627
NM_000474.4(TWIST1):c.273_293dup (p.Gly92_Gly98dup) rs1554442039
NM_000474.4(TWIST1):c.276_293del (p.Ser94_Ser99del) rs772470139
NM_000474.4(TWIST1):c.276_293dup (p.Ser99_Pro100insSerSerGlyGlyGlySer)
NM_000474.4(TWIST1):c.277AGC[5] (p.Ser95_Gly96insSerSer)
NM_000474.4(TWIST1):c.27_35dup (p.Pro12_Ala13insValSerPro)
NM_000474.4(TWIST1):c.328C>G (p.Arg110Gly)
NM_000474.4(TWIST1):c.328C>T (p.Arg110Trp) rs1585617188
NM_000474.4(TWIST1):c.341A>C (p.Asn114Thr) rs1554442021
NM_000474.4(TWIST1):c.359G>A (p.Arg120His)
NM_000474.4(TWIST1):c.361A>C (p.Thr121Pro) rs1788582586
NM_000474.4(TWIST1):c.367T>C (p.Ser123Pro) rs1554442008
NM_000474.4(TWIST1):c.375C>G (p.Asn125Lys)
NM_000474.4(TWIST1):c.388G>C (p.Ala130Pro)
NM_000474.4(TWIST1):c.395_415del (p.Arg132_Leu138del) rs1554441992
NM_000474.4(TWIST1):c.405C>G (p.Ile135Met) rs757121861
NM_000474.4(TWIST1):c.406C>A (p.Pro136Thr) rs1585616989
NM_000474.4(TWIST1):c.406C>G (p.Pro136Ala)
NM_000474.4(TWIST1):c.421G>A (p.Asp141Asn)
NM_000474.4(TWIST1):c.437T>C (p.Ile146Thr) rs1788580225
NM_000474.4(TWIST1):c.437T>G (p.Ile146Ser) rs1788580225
NM_000474.4(TWIST1):c.455C>A (p.Ala152Glu) rs1554441982
NM_000474.4(TWIST1):c.476T>C (p.Leu159Pro) rs1585616825
NM_000474.4(TWIST1):c.484del (p.Val162fs) rs1788579060
NM_000474.4(TWIST1):c.487C>T (p.Leu163Phe) rs867957820
NM_000474.4(TWIST1):c.488T>C (p.Leu163Pro)
NM_000474.4(TWIST1):c.508T>A (p.Ser170Thr)
NM_000474.4(TWIST1):c.510dup (p.Lys171fs) rs2115396517
NM_000474.4(TWIST1):c.518del (p.Ala173fs) rs2115396502
NM_000474.4(TWIST1):c.530_537dup (p.His180fs) rs2115396467
NM_000474.4(TWIST1):c.560T>C (p.Phe187Ser) rs1554441944
NM_000474.4(TWIST1):c.565G>A (p.Val189Ile)
NM_000474.4(TWIST1):c.94G>C (p.Gly32Arg)

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