ClinVar Miner

List of variants reported as uncertain significance for Epstein-Barr virus-related tumor

Included ClinVar conditions (9):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 11
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HGVS dbSNP gnomAD frequency
NM_000245.4(MET):c.2975C>T (p.Thr992Ile) rs56391007 0.00911
NM_000142.5(FGFR3):c.1181C>T (p.Thr394Met) rs747694886 0.00006
NM_000546.6(TP53):c.460G>A (p.Gly154Ser) rs137852789 0.00004
NM_000546.6(TP53):c.466C>T (p.Arg156Cys) rs563378859 0.00002
NM_000546.6(TP53):c.1000G>C (p.Gly334Arg) rs730882028 0.00001
NM_000546.6(TP53):c.461G>A (p.Gly154Asp) rs762846821 0.00001
NM_000546.6(TP53):c.760A>G (p.Ile254Val) rs746601313 0.00001
NM_007294.4(BRCA1):c.2885A>G (p.Glu962Gly) rs780367532 0.00001
NM_000546.6(TP53):c.677G>C (p.Gly226Ala) rs970212462
NM_002467.6(MYC):c.77A>G (p.Asn26Ser) rs4645959
NM_004985.5(KRAS):c.436G>A (p.Ala146Thr) rs121913527

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