ClinVar Miner

List of variants in gene combination FANCL, VRK2 reported as uncertain significance for DNA repair disease

Included ClinVar conditions (97):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 22
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HGVS dbSNP
NM_001114636.1(FANCL):c.791-10dupT rs374236117
NM_001130483.2(VRK2):c.41-31_41-28del rs748896681
NM_018062.3(FANCL):c.*165A>G rs866675905
NM_018062.3(FANCL):c.*296C>T rs201610023
NM_018062.3(FANCL):c.*333A>G rs147811379
NM_018062.3(FANCL):c.1007_1009del (p.Ile336_Cys337delinsSer) rs747253294
NM_018062.3(FANCL):c.1052G>A (p.Ser351Asn)
NM_018062.3(FANCL):c.1067T>G (p.Phe356Cys) rs773869051
NM_018062.3(FANCL):c.1088G>A (p.Ser363Asn)
NM_018062.3(FANCL):c.1096_1099dup (p.Thr367fs) rs759217526
NM_018062.3(FANCL):c.692G>A (p.Gly231Asp) rs1558737546
NM_018062.3(FANCL):c.706A>G (p.Ile236Val) rs762904548
NM_018062.3(FANCL):c.755T>G (p.Phe252Cys) rs139801716
NM_018062.3(FANCL):c.846A>T (p.Gln282His) rs535158133
NM_018062.3(FANCL):c.863T>C (p.Leu288Ser)
NM_018062.3(FANCL):c.881C>T (p.Ala294Val)
NM_018062.3(FANCL):c.884G>A (p.Arg295His) rs375526911
NM_018062.3(FANCL):c.904-9_904-7delCTT rs757041554
NM_018062.3(FANCL):c.932dup (p.Tyr311Ter) rs529201454
NM_018062.3(FANCL):c.949G>A (p.Gly317Ser) rs1060501896
NM_018062.3(FANCL):c.967G>T (p.Val323Leu) rs763057392
NM_018062.3(FANCL):c.969G>A (p.Val323=) rs200819615

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