ClinVar for MedGen (Select 482320) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3017156	NM_002392.6(MDM2):c.652A>G (p.Ser218Gly)	MDM2 (S163G +2 more)	Single nucleotide variant (missense variant +1 more)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 3003842	NM_002392.6(MDM2):c.840+14T>C	MDM2	Single nucleotide variant (intron variant)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 2989658	NM_002392.6(MDM2):c.685-3del	MDM2	Deletion (intron variant)	Accelerated tumor formation, susceptibility to	GBenign
Select item 2979968	NM_002392.6(MDM2):c.100-5T>G	MDM2	Single nucleotide variant (intron variant)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 2920098	NM_002392.6(MDM2):c.1284_1287del (p.Glu429fs)	MDM2 (E374fs +5 more)	Deletion (frameshift variant)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 2909970	NM_002392.6(MDM2):c.443T>C (p.Leu148Pro)	MDM2 (L142P +1 more)	Single nucleotide variant (missense variant +1 more)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 2908949	NM_002392.6(MDM2):c.15-11T>C	MDM2, LOC126861563	Single nucleotide variant (intron variant)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 2907543	NM_002392.6(MDM2):c.178C>G (p.Leu60Val)	MDM2 (L54V +1 more)	Single nucleotide variant (missense variant +1 more)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 2905053	NM_002392.6(MDM2):c.50A>G (p.Asp17Gly)	LOC126861563, MDM2 (D17G +1 more)	Single nucleotide variant (missense variant)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 2898326	NM_002392.6(MDM2):c.1368T>C (p.Ile456=)	MDM2	Single nucleotide variant (synonymous variant)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 2864679	NM_002392.6(MDM2):c.1179A>G (p.Gln393=)	MDM2	Single nucleotide variant (synonymous variant)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 2859179	NM_002392.6(MDM2):c.815A>G (p.Gln272Arg)	MDM2 (Q217R +3 more)	Single nucleotide variant (missense variant +1 more)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 2851580	NM_002392.6(MDM2):c.279C>T (p.Gly93=)	MDM2	Single nucleotide variant (synonymous variant +1 more)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 2851134	NM_002392.6(MDM2):c.980G>C (p.Arg327Thr)	MDM2 (R272T +5 more)	Single nucleotide variant (missense variant)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 2849234	NM_002392.6(MDM2):c.309-5A>G	MDM2	Single nucleotide variant (intron variant)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 2847356	NM_002392.6(MDM2):c.582T>A (p.Ser194Arg)	MDM2 (S188R +2 more)	Single nucleotide variant (missense variant +1 more)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 2845861	NM_002392.6(MDM2):c.175-18A>G	MDM2	Single nucleotide variant (intron variant)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 2842828	NM_002392.6(MDM2):c.524-2A>G	MDM2	Single nucleotide variant (splice acceptor variant +1 more)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 2842827	NM_002392.6(MDM2):c.524-18T>G	MDM2	Single nucleotide variant (intron variant)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 2835232	NM_002392.6(MDM2):c.56C>T (p.Ala19Val)	LOC126861563, MDM2 (A13V +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2815165	NM_002392.6(MDM2):c.1103G>A (p.Cys368Tyr)	MDM2 (C192Y +5 more)	Single nucleotide variant (missense variant)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 2789656	NM_002392.6(MDM2):c.672G>A (p.Thr224=)	MDM2	Single nucleotide variant (synonymous variant +1 more)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 2776101	NM_002392.6(MDM2):c.783C>T (p.Asp261=)	MDM2	Single nucleotide variant (synonymous variant +1 more)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 2754667	NM_002392.6(MDM2):c.858G>T (p.Val286=)	MDM2	Single nucleotide variant (synonymous variant +1 more)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 2733344	NM_002392.6(MDM2):c.992T>G (p.Leu331Arg)	MDM2 (L278R +5 more)	Single nucleotide variant (missense variant)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 2733057	NM_002392.6(MDM2):c.156C>T (p.Asp52=)	MDM2	Single nucleotide variant (synonymous variant)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 2727921	NM_002392.6(MDM2):c.1485T>C (p.Tyr495=)	MDM2	Single nucleotide variant (synonymous variant)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 2723519	NM_002392.6(MDM2):c.1309C>T (p.Pro437Ser)	MDM2 (P235S +5 more)	Single nucleotide variant (missense variant)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 2721952	NM_002392.6(MDM2):c.1405A>T (p.Thr469Ser)	MDM2 (T463S +5 more)	Single nucleotide variant (missense variant)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 2720273	NM_002392.6(MDM2):c.377C>T (p.Thr126Ile)	MDM2 (T120I +1 more)	Single nucleotide variant (missense variant +1 more)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 2717687	NM_002392.6(MDM2):c.685-18A>T	MDM2	Single nucleotide variant (intron variant)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 2717686	NM_002392.6(MDM2):c.685-20A>T	MDM2	Single nucleotide variant (intron variant)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 2713641	NM_002392.6(MDM2):c.1150A>T (p.Asn384Tyr)	MDM2 (N208Y +5 more)	Single nucleotide variant (missense variant)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 2712337	NM_002392.6(MDM2):c.864G>A (p.Gln288=)	MDM2	Single nucleotide variant (synonymous variant +1 more)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 2707346	NM_002392.6(MDM2):c.792T>C (p.Asp264=)	MDM2	Single nucleotide variant (synonymous variant +1 more)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 2415997	NM_002392.6(MDM2):c.999G>T (p.Glu333Asp)	MDM2 (E131D +5 more)	Single nucleotide variant (missense variant)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 2194542	NM_002392.6(MDM2):c.1190G>A (p.Ser397Asn)	MDM2 (S342N +5 more)	Single nucleotide variant (missense variant)	Accelerated tumor formation, susceptibility to +1 more	GUncertain significance
Select item 2185408	NM_002392.6(MDM2):c.910T>C (p.Ser304Pro)	MDM2 (S298P +4 more)	Single nucleotide variant (missense variant +1 more)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 2181570	NM_002392.6(MDM2):c.694G>T (p.Ala232Ser)	MDM2 (A177S +3 more)	Single nucleotide variant (missense variant)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 2179863	NM_002392.6(MDM2):c.421C>G (p.Gln141Glu)	MDM2 (Q141E +1 more)	Single nucleotide variant (missense variant +1 more)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 2176080	NM_002392.6(MDM2):c.99+17C>T	LOC126861563, MDM2	Single nucleotide variant (intron variant)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 2170024	NM_002392.6(MDM2):c.1161A>C (p.Lys387Asn)	MDM2 (K387N +5 more)	Single nucleotide variant (missense variant)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 2168876	NM_002392.6(MDM2):c.615G>C (p.Leu205=)	MDM2	Single nucleotide variant (synonymous variant +1 more)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 2165333	NM_002392.6(MDM2):c.431T>C (p.Leu144Pro)	MDM2 (L144P +1 more)	Single nucleotide variant (missense variant +1 more)	Accelerated tumor formation, susceptibility to +1 more	GConflicting classifications of pathogenicity
Select item 2164923	NM_002392.6(MDM2):c.613C>G (p.Leu205Val)	MDM2 (L199V +2 more)	Single nucleotide variant (missense variant +1 more)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 2163429	NM_002392.6(MDM2):c.234A>G (p.Gln78=)	MDM2	Single nucleotide variant (synonymous variant +1 more)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 2156229	NM_002392.6(MDM2):c.1248T>C (p.Asp416=)	MDM2	Single nucleotide variant (synonymous variant)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 2155387	NM_002392.6(MDM2):c.99+8T>C	LOC126861563, MDM2	Single nucleotide variant (intron variant)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 2143363	NM_002392.6(MDM2):c.1202C>T (p.Ser401Phe)	MDM2 (S199F +5 more)	Single nucleotide variant (missense variant)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 2141608	NM_002392.6(MDM2):c.684+19G>A	MDM2	Single nucleotide variant (intron variant)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 2134944	NM_002392.6(MDM2):c.88C>A (p.Gln30Lys)	LOC126861563, MDM2 (Q30K +1 more)	Single nucleotide variant (missense variant)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 2123088	NM_002392.6(MDM2):c.305A>G (p.His102Arg)	MDM2 (H102R +1 more)	Single nucleotide variant (missense variant +1 more)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 2109271	NM_002392.6(MDM2):c.1011T>A (p.Pro337=)	MDM2	Single nucleotide variant (synonymous variant)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 2088438	NM_002392.6(MDM2):c.385A>C (p.Ser129Arg)	MDM2 (S129R +1 more)	Single nucleotide variant (missense variant +1 more)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 2075508	NM_002392.6(MDM2):c.372A>G (p.Ser124=)	MDM2	Single nucleotide variant (synonymous variant +1 more)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 2067479	NM_002392.6(MDM2):c.1191T>G (p.Ser397Arg)	MDM2 (S195R +5 more)	Single nucleotide variant (missense variant)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 2067239	NM_002392.6(MDM2):c.643A>G (p.Arg215Gly)	MDM2 (R160G +2 more)	Single nucleotide variant (missense variant +1 more)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 2062095	NM_002392.6(MDM2):c.840+6dup	MDM2	Duplication (intron variant)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 2056831	NM_002392.6(MDM2):c.14+5T>G	LOC126861563, MDM2	Single nucleotide variant (intron variant)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 2055577	NM_002392.6(MDM2):c.1304G>A (p.Ser435Asn)	MDM2 (S259N +5 more)	Single nucleotide variant (missense variant)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 2052780	NM_002392.6(MDM2):c.359-8TC[2]	MDM2	Microsatellite (intron variant)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 2047388	NM_002392.6(MDM2):c.403C>T (p.Leu135Phe)	MDM2 (L129F +1 more)	Single nucleotide variant (missense variant +1 more)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 2041198	NM_002392.6(MDM2):c.175-15A>T	MDM2	Single nucleotide variant (intron variant)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 2037810	NM_002392.6(MDM2):c.359-4T>G	MDM2	Single nucleotide variant (intron variant)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 2032377	NM_002392.6(MDM2):c.841-16G>T	MDM2	Single nucleotide variant (intron variant)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 2015499	NM_002392.6(MDM2):c.1030A>G (p.Lys344Glu)	MDM2 (K142E +5 more)	Single nucleotide variant (missense variant)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 1993941	NM_002392.6(MDM2):c.1079A>G (p.Glu360Gly)	MDM2 (E305G +5 more)	Single nucleotide variant (missense variant)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 1982252	NM_002392.6(MDM2):c.99+14T>G	LOC126861563, MDM2	Single nucleotide variant (intron variant)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 1982251	NM_002392.6(MDM2):c.99+12del	LOC126861563, MDM2	Deletion (intron variant)	Accelerated tumor formation, susceptibility to	GBenign
Select item 1961369	NM_002392.6(MDM2):c.1301C>G (p.Ser434Cys)	MDM2 (S434C +5 more)	Single nucleotide variant (missense variant)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 1938361	NM_002392.6(MDM2):c.398G>A (p.Cys133Tyr)	MDM2 (C133Y +1 more)	Single nucleotide variant (missense variant +1 more)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 1934140	NM_002392.6(MDM2):c.1114A>G (p.Ile372Val)	MDM2 (I170V +5 more)	Single nucleotide variant (missense variant)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 1930017	NM_002392.6(MDM2):c.589C>T (p.Leu197Phe)	MDM2 (L191F +2 more)	Single nucleotide variant (missense variant +1 more)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 1924439	NM_002392.6(MDM2):c.174+18A>G	MDM2	Single nucleotide variant (intron variant)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 1917952	NM_002392.6(MDM2):c.684+20T>C	MDM2	Single nucleotide variant (intron variant)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 1916784	NM_002392.6(MDM2):c.393C>T (p.Asn131=)	MDM2	Single nucleotide variant (synonymous variant +1 more)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 1674900	NM_002392.6(MDM2):c.840+14del	MDM2	Deletion (intron variant)	Accelerated tumor formation, susceptibility to	GBenign
Select item 1670037	NM_002392.6(MDM2):c.15-9del	MDM2, LOC126861563	Deletion (intron variant)	Accelerated tumor formation, susceptibility to	GBenign
Select item 1644981	NM_002392.6(MDM2):c.15-9dup	LOC126861563, MDM2	Duplication (intron variant)	Accelerated tumor formation, susceptibility to	GBenign
Select item 1637178	NM_002392.6(MDM2):c.99+7_99+14del	LOC126861563, MDM2	Deletion (intron variant)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 1635742	NM_002392.6(MDM2):c.1491C>T (p.Pro497=)	MDM2	Single nucleotide variant (synonymous variant)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 1631003	NM_002392.6(MDM2):c.243A>G (p.Val81=)	MDM2	Single nucleotide variant (synonymous variant +1 more)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 1624296	NM_002392.6(MDM2):c.919-11T>C	MDM2	Single nucleotide variant (intron variant)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 1599971	NM_002392.6(MDM2):c.918+15A>T	MDM2	Single nucleotide variant (intron variant)	Accelerated tumor formation, susceptibility to	GBenign
Select item 1597128	NM_002392.6(MDM2):c.359-15T>C	MDM2	Single nucleotide variant (intron variant)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 1596961	NM_002392.6(MDM2):c.816A>G (p.Gln272=)	MDM2	Single nucleotide variant (synonymous variant +1 more)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 1584716	NM_002392.6(MDM2):c.162T>C (p.Tyr54=)	MDM2	Single nucleotide variant (synonymous variant)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 1570835	NM_002392.6(MDM2):c.524-8A>G	MDM2	Single nucleotide variant (intron variant)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 1570222	NM_002392.6(MDM2):c.309-5A>C	MDM2	Single nucleotide variant (intron variant)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 1569761	NM_002392.6(MDM2):c.1365C>T (p.Cys455=)	MDM2	Single nucleotide variant (synonymous variant)	Accelerated tumor formation, susceptibility to +1 more	GLikely benign
Select item 1553638	NM_002392.6(MDM2):c.99+13del	LOC126861563, MDM2	Deletion (intron variant)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 1551851	NM_002392.6(MDM2):c.175-13A>G	MDM2	Single nucleotide variant (intron variant)	Accelerated tumor formation, susceptibility to	GLikely benign
Select item 1511133	NM_002392.6(MDM2):c.46A>G (p.Thr16Ala)	LOC126861563, MDM2 (T10A +1 more)	Single nucleotide variant (missense variant)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 1507206	NM_002392.6(MDM2):c.1237A>G (p.Ser413Gly)	MDM2 (S360G +5 more)	Single nucleotide variant (missense variant)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 1504296	NM_002392.6(MDM2):c.818A>C (p.Glu273Ala)	MDM2 (E267A +3 more)	Single nucleotide variant (missense variant +1 more)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 1501438	NM_002392.6(MDM2):c.212G>A (p.Arg71Gln)	MDM2 (R65Q +1 more)	Single nucleotide variant (missense variant +1 more)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 1482898	NM_002392.6(MDM2):c.536A>G (p.Asp179Gly)	MDM2 (D179G +2 more)	Single nucleotide variant (missense variant +1 more)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 1471228	NM_002392.6(MDM2):c.886T>G (p.Ser296Ala)	MDM2 (S290A +4 more)	Single nucleotide variant (missense variant +1 more)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 1466586	NM_002392.6(MDM2):c.913T>G (p.Leu305Val)	MDM2 (L250V +4 more)	Single nucleotide variant (missense variant +1 more)	Accelerated tumor formation, susceptibility to	GUncertain significance
Select item 1448253	NM_002392.6(MDM2):c.1289A>T (p.Glu430Val)	MDM2 (E424V +5 more)	Single nucleotide variant (missense variant)	Accelerated tumor formation, susceptibility to	GUncertain significance

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