ClinVar Miner

List of variants reported as benign for Dyskeratosis congenita by Illumina Clinical Services Laboratory,Illumina

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ClinVar version:
Total variants: 36
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HGVS dbSNP
NM_025099.6(CTC1):c.*1041A>G rs148405704
NM_025099.6(CTC1):c.*1200T>C
NM_025099.6(CTC1):c.*1450G>A
NM_025099.6(CTC1):c.*1474G>A rs78517666
NM_025099.6(CTC1):c.*1668G>A
NM_025099.6(CTC1):c.*1807G>T rs3027251
NM_025099.6(CTC1):c.*1844G>A rs3027252
NM_025099.6(CTC1):c.*1960C>G rs11650309
NM_025099.6(CTC1):c.*2006T>C
NM_025099.6(CTC1):c.*2087A>G rs75503577
NM_025099.6(CTC1):c.*2338T>C rs8078338
NM_025099.6(CTC1):c.*275G>A rs3027246
NM_025099.6(CTC1):c.*2848A>C
NM_025099.6(CTC1):c.*3231A>G rs139845972
NM_025099.6(CTC1):c.*43C>T rs3027245
NM_025099.6(CTC1):c.*631T>G rs3027247
NM_025099.6(CTC1):c.1241G>C (p.Gly414Ala) rs62624978
NM_025099.6(CTC1):c.1307G>A (p.Arg436His) rs75790638
NM_025099.6(CTC1):c.1383G>A (p.Gln461=) rs145192682
NM_025099.6(CTC1):c.1617+11G>A
NM_025099.6(CTC1):c.1795C>T (p.Pro599Ser) rs183556317
NM_025099.6(CTC1):c.197+15C>T
NM_025099.6(CTC1):c.2160C>T (p.Thr720=) rs3027235
NM_025099.6(CTC1):c.2162G>C (p.Gly721Ala) rs62620189
NM_025099.6(CTC1):c.2353G>A (p.Glu785Lys) rs201561504
NM_025099.6(CTC1):c.2386-13T>G rs3027237
NM_025099.6(CTC1):c.2458A>G (p.Ile820Val) rs3027238
NM_025099.6(CTC1):c.248G>C (p.Ser83Thr) rs78870822
NM_025099.6(CTC1):c.2973T>C (p.Tyr991=) rs62637613
NM_025099.6(CTC1):c.3013A>G (p.Ile1005Val) rs3826543
NM_025099.6(CTC1):c.3591C>G (p.Ser1197=) rs115990839
NM_025099.6(CTC1):c.366A>G (p.Ala122=) rs73244859
NM_025099.6(CTC1):c.435+3= rs6503093
NM_025099.6(CTC1):c.477G>T (p.Leu159=) rs200658590
NM_025099.6(CTC1):c.695G>A (p.Arg232Gln) rs201592575
NM_025099.6(CTC1):c.990C>T (p.Asp330=) rs74506939

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