ClinVar Miner

List of variants reported as uncertain significance for Charcot-Marie-Tooth disease X-linked dominant 1 by Inherited Neuropathy Consortium Ii, University Of Miami

Included ClinVar conditions (1):
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ClinVar version:
Total variants: 88
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HGVS dbSNP gnomAD frequency
NM_000166.6(GJB1):c.110del (p.Val37fs) rs1602348754
NM_000166.6(GJB1):c.116del (p.Ala39fs) rs1602348779
NM_000166.6(GJB1):c.124_125del (p.Ser42fs) rs1602348794
NM_000166.6(GJB1):c.132G>A (p.Trp44Ter) rs879253935
NM_000166.6(GJB1):c.141_143dup (p.Lys48dup) rs1602348833
NM_000166.6(GJB1):c.155del (p.Ile52fs) rs1602348856
NM_000166.6(GJB1):c.179G>A (p.Cys60Tyr) rs1555937082
NM_000166.6(GJB1):c.187G>A (p.Val63Ile) rs116840818
NM_000166.6(GJB1):c.195T>G (p.Tyr65Ter) rs1602348907
NM_000166.6(GJB1):c.196_198del (p.Asp66del) rs1602348913
NM_000166.6(GJB1):c.208_209delinsTT (p.Pro70Phe) rs1602348930
NM_000166.6(GJB1):c.210dup (p.Ile71fs) rs1602348918
NM_000166.6(GJB1):c.217del (p.His73fs) rs1602348937
NM_000166.6(GJB1):c.225del (p.Leu76fs) rs116840820
NM_000166.6(GJB1):c.231G>A (p.Trp77Ter) rs879254096
NM_000166.6(GJB1):c.238C>T (p.Gln80Ter) rs1602348981
NM_000166.6(GJB1):c.248_257del (p.Leu83fs) rs1602349000
NM_000166.6(GJB1):c.273_274del (p.Ala92fs) rs1602349061
NM_000166.6(GJB1):c.275_276del (p.Ala92fs) rs1602349065
NM_000166.6(GJB1):c.277_278del (p.Met93fs) rs1602349068
NM_000166.6(GJB1):c.295C>T (p.Gln99Ter) rs1602349121
NM_000166.6(GJB1):c.304G>T (p.Glu102Ter) rs1602349143
NM_000166.6(GJB1):c.304_306del (p.Glu102del) rs1555937135
NM_000166.6(GJB1):c.313del (p.Met105fs) rs1602349163
NM_000166.6(GJB1):c.324dup (p.Glu109Ter) rs1555937143
NM_000166.6(GJB1):c.332_349del (p.His111_His116del) rs1602349197
NM_000166.6(GJB1):c.338_345delinsTGGC (p.Asp113fs) rs1602349208
NM_000166.6(GJB1):c.355G>T (p.Glu119Ter) rs1602349226
NM_000166.6(GJB1):c.358_360del (p.Val120del) rs1602349233
NM_000166.6(GJB1):c.371del (p.Lys124fs) rs1602349248
NM_000166.6(GJB1):c.383C>A (p.Ser128Ter) rs1602349272
NM_000166.6(GJB1):c.383C>G (p.Ser128Ter) rs1602349272
NM_000166.6(GJB1):c.394_395del (p.Trp132fs) rs1555937168
NM_000166.6(GJB1):c.396G>A (p.Trp132Ter) rs1602349293
NM_000166.6(GJB1):c.397del (p.Trp133fs) rs1602349299
NM_000166.6(GJB1):c.399G>A (p.Trp133Ter) rs1602349302
NM_000166.6(GJB1):c.410del (p.Ile137fs) rs1602349316
NM_000166.6(GJB1):c.424del (p.Arg142fs) rs1602349328
NM_000166.6(GJB1):c.429GTT[1] (p.Leu144del) rs1602349339
NM_000166.6(GJB1):c.42_43insT (p.Arg15fs) rs1602348598
NM_000166.6(GJB1):c.436_437delinsAT (p.Glu146Met) rs1602349347
NM_000166.6(GJB1):c.439del (p.Ala147fs) rs1602349352
NM_000166.6(GJB1):c.43del (p.Arg15fs) rs1602348594
NM_000166.6(GJB1):c.44_45delinsTT (p.Arg15Leu) rs1602348605
NM_000166.6(GJB1):c.454del (p.Val152fs) rs1602349383
NM_000166.6(GJB1):c.459_460del (p.Phe153fs) rs1602349393
NM_000166.6(GJB1):c.474del (p.Gly159fs) rs1602349441
NM_000166.6(GJB1):c.484dup (p.Met162fs) rs1602349460
NM_000166.6(GJB1):c.498_502del (p.Lys167fs) rs1602349473
NM_000166.6(GJB1):c.524dup (p.Asn175fs) rs1569215346
NM_000166.6(GJB1):c.533_536dup (p.Cys179Ter) rs1602349585
NM_000166.6(GJB1):c.553_555del (p.Thr185del) rs1602349648
NM_000166.6(GJB1):c.556G>T (p.Glu186Ter) rs116840821
NM_000166.6(GJB1):c.571dup (p.Thr191fs) rs1602349676
NM_000166.6(GJB1):c.573_574insTCA (p.Thr191_Val192insSer) rs1602349684
NM_000166.6(GJB1):c.576del (p.Phe193fs) rs1602349692
NM_000166.6(GJB1):c.59T>A (p.Ile20Asn) rs1569215025
NM_000166.6(GJB1):c.606del (p.Ile203fs) rs1602349746
NM_000166.6(GJB1):c.617dup (p.Ala207fs) rs1602349763
NM_000166.6(GJB1):c.61G>A (p.Gly21Ser) rs1602348633
NM_000166.6(GJB1):c.622del (p.Glu208fs) rs2147946914
NM_000166.6(GJB1):c.625GTG[1] (p.Val210del) rs1602349772
NM_000166.6(GJB1):c.629_632del (p.Val210fs) rs1602349779
NM_000166.6(GJB1):c.62del (p.Gly21fs) rs1602348638
NM_000166.6(GJB1):c.633C>A (p.Tyr211Ter) rs1569215443
NM_000166.6(GJB1):c.634del (p.Leu212fs) rs1602349791
NM_000166.6(GJB1):c.641_642delinsAT (p.Ile214Asn) rs1602349807
NM_000166.6(GJB1):c.64C>T (p.Arg22Ter) rs1555937020
NM_000166.6(GJB1):c.651T>A (p.Cys217Ter) rs1602349821
NM_000166.6(GJB1):c.658C>T (p.Arg220Ter) rs104894814
NM_000166.6(GJB1):c.65G>A (p.Arg22Gln) rs1060501002
NM_000166.6(GJB1):c.761dup (p.Gln255fs) rs1602349920
NM_000166.6(GJB1):c.772del (p.Ser258fs) rs1602349940
NM_000166.6(GJB1):c.775del (p.Ser258_Leu259insTer) rs1602349948
NM_000166.6(GJB1):c.77C>A (p.Ser26Ter) rs587777876
NM_000166.6(GJB1):c.77del (p.Ser26fs) rs1602348679
NM_000166.6(GJB1):c.785_786del (p.Ile262fs) rs1602349962
NM_000166.6(GJB1):c.793_821del (p.Arg264_Arg265insTer) rs1602349984
NM_000166.6(GJB1):c.800del (p.Pro267fs) rs1602350003
NM_000166.6(GJB1):c.822del (p.Glu275fs) rs1602350029
NM_000166.6(GJB1):c.842C>A (p.Ser281Ter) rs866253945
NM_000166.6(GJB1):c.844dup (p.Ala282fs) rs1602350062
NM_000166.6(GJB1):c.849C>A (p.Cys283Ter) rs748676943
NM_000166.6(GJB1):c.84del (p.Phe29fs) rs1602348695
NM_000166.6(GJB1):c.851G>C (p.Ter284Ser)
NM_000166.6(GJB1):c.852A>G (p.Ter284Trp)
NM_000166.6(GJB1):c.89T>C (p.Ile30Thr) rs104894817
NM_000166.6(GJB1):c.8G>A (p.Trp3Ter) rs1555936989

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