ClinVar Miner

List of variants studied for non-syndromic polydactyly by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

Included ClinVar conditions (43):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 11
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HGVS dbSNP gnomAD frequency
NM_000168.6(GLI3):c.2374C>T (p.Arg792Ter) rs121917714
NM_000168.6(GLI3):c.438C>G (p.Tyr146Ter) rs151222023
NM_001759.4(CCND2):c.559C>G (p.Leu187Val)
NM_001759.4(CCND2):c.808A>T (p.Lys270Ter) rs587777619
NM_001759.4(CCND2):c.838A>C (p.Thr280Pro)
NM_005027.4(PIK3R2):c.1117G>A (p.Gly373Arg) rs587776934
NM_005465.7(AKT3):c.1393C>T (p.Arg465Trp) rs587776935
NM_006486.3(FBLN1):c.1949G>A (p.Arg650His)
NM_152558.5(IQCE):c.1493G>A (p.Trp498Ter)
NM_152558.5(IQCE):c.1540del (p.Cys514fs)
NM_152558.5(IQCE):c.895_904del (p.Val301fs) rs773701437

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