ClinVar Miner

List of variants reported as likely benign for obsolete accelerated tumor formation, susceptibility to

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 56
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HGVS dbSNP gnomAD frequency
NM_002392.6(MDM2):c.1002T>C (p.Asn334=) rs199812774 0.00025
NM_002392.6(MDM2):c.359-15T>C rs779115220 0.00009
NM_002392.6(MDM2):c.777T>C (p.Ser259=) rs200318538 0.00009
NM_002392.6(MDM2):c.366G>A (p.Ser122=) rs376611439 0.00006
NM_002392.6(MDM2):c.919-11T>C rs184787147 0.00006
NM_002392.6(MDM2):c.524-3C>T rs778675786 0.00004
NM_002392.6(MDM2):c.450A>G (p.Glu150=) rs201591724 0.00003
NM_002392.6(MDM2):c.1365C>T (p.Cys455=) rs751275422 0.00002
NM_002392.6(MDM2):c.162T>C (p.Tyr54=) rs997464909 0.00002
NM_002392.6(MDM2):c.99+13del rs764486650 0.00002
NM_002392.6(MDM2):c.175-13A>G rs895182813 0.00001
NM_002392.6(MDM2):c.243A>G (p.Val81=) rs775062825 0.00001
NM_002392.6(MDM2):c.264A>G (p.Leu88=) rs760587938 0.00001
NM_002392.6(MDM2):c.447G>A (p.Gln149=) rs754627845 0.00001
NM_002392.6(MDM2):c.524-8A>G rs373328180 0.00001
NM_002392.6(MDM2):c.100-5T>G
NM_002392.6(MDM2):c.1011T>A (p.Pro337=)
NM_002392.6(MDM2):c.1179A>G (p.Gln393=)
NM_002392.6(MDM2):c.1248T>C (p.Asp416=)
NM_002392.6(MDM2):c.1368T>C (p.Ile456=)
NM_002392.6(MDM2):c.1485T>C (p.Tyr495=)
NM_002392.6(MDM2):c.1491C>T (p.Pro497=) rs757161769
NM_002392.6(MDM2):c.15-11T>C
NM_002392.6(MDM2):c.156C>T (p.Asp52=)
NM_002392.6(MDM2):c.175-15A>T
NM_002392.6(MDM2):c.175-18A>G
NM_002392.6(MDM2):c.175-7A>G rs2136121322
NM_002392.6(MDM2):c.234A>G (p.Gln78=)
NM_002392.6(MDM2):c.279C>T (p.Gly93=)
NM_002392.6(MDM2):c.309-5A>C rs763094430
NM_002392.6(MDM2):c.309-5A>G
NM_002392.6(MDM2):c.359-4T>G
NM_002392.6(MDM2):c.359-8TC[2]
NM_002392.6(MDM2):c.372A>G (p.Ser124=)
NM_002392.6(MDM2):c.393C>T (p.Asn131=)
NM_002392.6(MDM2):c.524-18T>G
NM_002392.6(MDM2):c.615G>C (p.Leu205=)
NM_002392.6(MDM2):c.672G>A (p.Thr224=)
NM_002392.6(MDM2):c.684+19G>A
NM_002392.6(MDM2):c.684+20T>C
NM_002392.6(MDM2):c.685-18A>T
NM_002392.6(MDM2):c.685-20A>T
NM_002392.6(MDM2):c.724T>C (p.Leu242=) rs1375531162
NM_002392.6(MDM2):c.783C>T (p.Asp261=)
NM_002392.6(MDM2):c.792T>C (p.Asp264=)
NM_002392.6(MDM2):c.816A>G (p.Gln272=) rs1192262800
NM_002392.6(MDM2):c.840+14T>C
NM_002392.6(MDM2):c.840+6dup
NM_002392.6(MDM2):c.841-16G>T
NM_002392.6(MDM2):c.858G>T (p.Val286=)
NM_002392.6(MDM2):c.864G>A (p.Gln288=)
NM_002392.6(MDM2):c.960C>G (p.Pro320=) rs373214952
NM_002392.6(MDM2):c.99+14T>G
NM_002392.6(MDM2):c.99+17C>T
NM_002392.6(MDM2):c.99+7_99+14del rs751949064
NM_002392.6(MDM2):c.99+8T>C

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