ClinVar Miner

List of variants reported as uncertain significance for Melanoma, cutaneous malignant, susceptibility to, 1 by Baylor Genetics

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Total variants: 92
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HGVS dbSNP gnomAD frequency
NM_000455.5(STK11):c.613G>A (p.Ala205Thr) rs730881981 0.00004
NM_000455.5(STK11):c.1015C>G (p.Pro339Ala) rs769644352 0.00001
NM_000455.5(STK11):c.1016C>T (p.Pro339Leu) rs567896256 0.00001
NM_000455.5(STK11):c.1114G>A (p.Val372Ile) rs2080821529 0.00001
NM_000455.5(STK11):c.115C>T (p.Arg39Cys) rs876658779 0.00001
NM_000455.5(STK11):c.1197G>T (p.Gln399His) rs1436178098 0.00001
NM_000455.5(STK11):c.1213A>T (p.Arg405Trp) rs376718324 0.00001
NM_000455.5(STK11):c.1235A>G (p.Asn412Ser) rs786201309 0.00001
NM_000455.5(STK11):c.1262G>A (p.Ser421Asn) rs1253803683 0.00001
NM_000455.5(STK11):c.151A>C (p.Met51Leu) rs730881986 0.00001
NM_000455.5(STK11):c.299A>G (p.Gln100Arg) rs1060499957 0.00001
NM_000455.5(STK11):c.310A>T (p.Arg104Trp) rs587782783 0.00001
NM_000455.5(STK11):c.358G>A (p.Glu120Lys) rs775595174 0.00001
NM_000455.5(STK11):c.49C>G (p.Leu17Val) rs780581573 0.00001
NM_000455.5(STK11):c.577T>G (p.Ser193Ala) rs1064794883 0.00001
NM_000455.5(STK11):c.5A>C (p.Glu2Ala) rs1159551738 0.00001
NM_000455.5(STK11):c.605A>G (p.His202Arg) rs1206092648 0.00001
NM_000455.5(STK11):c.61G>A (p.Gly21Ser) rs1064793751 0.00001
NM_000455.5(STK11):c.71C>T (p.Thr24Met) rs770503805 0.00001
NM_000455.5(STK11):c.818C>T (p.Ala273Val) rs761164605 0.00001
NM_000455.5(STK11):c.929G>A (p.Arg310Gln) rs1555739158 0.00001
NM_000455.5(STK11):c.971C>T (p.Pro324Leu) rs367807476 0.00001
NM_000455.5(STK11):c.976C>A (p.Pro326Thr) rs771632414 0.00001
NM_000455.5(STK11):c.1016C>G (p.Pro339Arg) rs567896256
NM_000455.5(STK11):c.1027G>T (p.Asp343Tyr)
NM_000455.5(STK11):c.1037_1042del (p.Gly346_Ala347del) rs1060499969
NM_000455.5(STK11):c.1051G>A (p.Glu351Lys) rs746460823
NM_000455.5(STK11):c.1067T>C (p.Ile356Thr)
NM_000455.5(STK11):c.1075G>A (p.Asp359Asn) rs1060499967
NM_000455.5(STK11):c.1078A>T (p.Ile360Phe)
NM_000455.5(STK11):c.1088C>A (p.Thr363Asn) rs587778695
NM_000455.5(STK11):c.10G>T (p.Val4Leu) rs767300470
NM_000455.5(STK11):c.1105C>T (p.Pro369Ser) rs758887235
NM_000455.5(STK11):c.1108G>A (p.Gly370Arg) rs747655835
NM_000455.5(STK11):c.113C>G (p.Pro38Arg) rs1568690036
NM_000455.5(STK11):c.1168G>T (p.Val390Leu)
NM_000455.5(STK11):c.1178A>G (p.Asn393Ser) rs1060499965
NM_000455.5(STK11):c.1180G>C (p.Gly394Arg) rs768780695
NM_000455.5(STK11):c.1186G>C (p.Glu396Gln) rs763314442
NM_000455.5(STK11):c.1192_1193delinsTT (p.Ala398Leu) rs1599932256
NM_000455.5(STK11):c.1202G>A (p.Ser401Asn) rs587782291
NM_000455.5(STK11):c.1217C>G (p.Ala406Gly) rs748202003
NM_000455.5(STK11):c.1226G>T (p.Arg409Leu) rs587782364
NM_000455.5(STK11):c.1229C>A (p.Ala410Asp) rs372329880
NM_000455.5(STK11):c.1237C>T (p.Pro413Ser) rs1386678110
NM_000455.5(STK11):c.1243C>G (p.Arg415Gly) rs864622448
NM_000455.5(STK11):c.1244G>A (p.Arg415His) rs775978755
NM_000455.5(STK11):c.125G>A (p.Arg42Gln) rs148830698
NM_000455.5(STK11):c.1261_1262inv (p.Ser421Leu)
NM_000455.5(STK11):c.1273C>T (p.Arg425Cys) rs754853898
NM_000455.5(STK11):c.1274G>C (p.Arg425Pro) rs730881992
NM_000455.5(STK11):c.1276C>G (p.Arg426Gly) rs587782687
NM_000455.5(STK11):c.1282T>A (p.Ser428Thr) rs1064793938
NM_000455.5(STK11):c.1282T>C (p.Ser428Pro)
NM_000455.5(STK11):c.128C>T (p.Ala43Val) rs1555734967
NM_000455.5(STK11):c.1295A>G (p.Gln432Arg)
NM_000455.5(STK11):c.133C>G (p.Leu45Val) rs1568690121
NM_000455.5(STK11):c.229G>A (p.Val77Ile) rs1167680274
NM_000455.5(STK11):c.235A>G (p.Ile79Val)
NM_000455.5(STK11):c.238C>G (p.Leu80Val) rs1131690927
NM_000455.5(STK11):c.241AAG[3] (p.Lys84del) rs587782056
NM_000455.5(STK11):c.26T>A (p.Leu9Gln) rs764154797
NM_000455.5(STK11):c.31A>G (p.Met11Val) rs753834428
NM_000455.5(STK11):c.344A>C (p.Asp115Ala)
NM_000455.5(STK11):c.350T>C (p.Leu117Ser) rs1296728798
NM_000455.5(STK11):c.358G>C (p.Glu120Gln) rs775595174
NM_000455.5(STK11):c.463G>A (p.Gly155Arg) rs763353991
NM_000455.5(STK11):c.463G>C (p.Gly155Arg) rs763353991
NM_000455.5(STK11):c.54G>A (p.Met18Ile) rs755436889
NM_000455.5(STK11):c.622G>A (p.Asp208Asn) rs1555738372
NM_000455.5(STK11):c.625A>C (p.Thr209Pro) rs1555738373
NM_000455.5(STK11):c.64A>G (p.Met22Val) rs1174992777
NM_000455.5(STK11):c.676A>G (p.Asn226Asp)
NM_000455.5(STK11):c.692_694del (p.Phe231del)
NM_000455.5(STK11):c.704A>C (p.Lys235Thr) rs587780010
NM_000455.5(STK11):c.712A>G (p.Ile238Val)
NM_000455.5(STK11):c.719C>T (p.Ser240Leu) rs730881976
NM_000455.5(STK11):c.721G>A (p.Ala241Thr) rs587780721
NM_000455.5(STK11):c.799A>G (p.Ile267Val) rs1568709259
NM_000455.5(STK11):c.7G>A (p.Val3Met) rs906049559
NM_000455.5(STK11):c.838C>A (p.Pro280Thr)
NM_000455.5(STK11):c.842C>G (p.Pro281Arg) rs121913322
NM_000455.5(STK11):c.880C>T (p.Pro294Ser)
NM_000455.5(STK11):c.884C>G (p.Ala295Gly)
NM_000455.5(STK11):c.888G>T (p.Lys296Asn) rs1555738868
NM_000455.5(STK11):c.921-112G>T
NM_000455.5(STK11):c.921-113G>T
NM_000455.5(STK11):c.92C>T (p.Ser31Phe)
NM_000455.5(STK11):c.936A>C (p.Lys312Asn)
NM_000455.5(STK11):c.95C>T (p.Thr32Ile)
NM_000455.5(STK11):c.969_971del (p.Pro324del) rs876660268
NM_000455.5(STK11):c.977C>T (p.Pro326Leu) rs587781474

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