ClinVar Miner

List of variants reported as uncertain significance for dilated cardiomyopathy 1D by Fulgent Genetics, Fulgent Genetics

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 25
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HGVS dbSNP gnomAD frequency
NM_001276345.2(TNNT2):c.862C>T (p.Arg288Cys) rs121964857 0.00044
NM_001276345.2(TNNT2):c.692T>C (p.Ile231Thr) rs45520032 0.00015
NM_001276345.2(TNNT2):c.762G>T (p.Glu254Asp) rs45466197 0.00007
NM_001276345.2(TNNT2):c.863G>A (p.Arg288His) rs397516484 0.00005
NM_001276345.2(TNNT2):c.887G>A (p.Arg296His) rs141121678 0.00005
NM_001276345.2(TNNT2):c.248A>G (p.Asn83Ser) rs397516450 0.00004
NM_001276345.2(TNNT2):c.810+5G>A rs730881113 0.00004
NM_001276345.2(TNNT2):c.617G>A (p.Arg206Gln) rs371047521 0.00003
NM_001276345.2(TNNT2):c.110C>G (p.Ala37Gly) rs776406819 0.00002
NM_001276345.2(TNNT2):c.260C>T (p.Pro87Leu) rs144900708 0.00002
NM_001276345.2(TNNT2):c.411C>T (p.Ile137=) rs727504322 0.00001
NM_001276345.2(TNNT2):c.473G>A (p.Arg158Gln) rs730881102 0.00001
NM_001276345.2(TNNT2):c.601-1G>A rs483352835 0.00001
NM_001276345.2(TNNT2):c.613G>A (p.Glu205Lys) rs150008205 0.00001
NM_001276345.2(TNNT2):c.659A>T (p.Lys220Met) rs190805300 0.00001
NM_001276345.2(TNNT2):c.677G>A (p.Arg226Lys) rs1205564576 0.00001
NM_001276345.2(TNNT2):c.775G>A (p.Asp259Asn) rs141805127 0.00001
NM_001276345.2(TNNT2):c.163G>T (p.Glu55Ter) rs730881120
NM_001276345.2(TNNT2):c.282_283del (p.Arg94fs) rs1259701355
NM_001276345.2(TNNT2):c.286G>A (p.Asp96Asn) rs1553282768
NM_001276345.2(TNNT2):c.313A>G (p.Met105Val) rs397516458
NM_001276345.2(TNNT2):c.427G>C (p.Glu143Gln) rs1316344347
NM_001276345.2(TNNT2):c.806A>G (p.Tyr269Cys) rs1553280112
NM_001276345.2(TNNT2):c.812T>G (p.Ile271Ser) rs371384395
NM_001276345.2(TNNT2):c.865G>A (p.Gly289Arg) rs757664792

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