ClinVar for MedGen (Select 766) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3245627	NC_000007.13:g.(?_116380991)_(116385169_?)del	MET	Deletion	Renal cell carcinoma	GUncertain significance
Select item 3245626	NC_000007.13:g.(?_116380896)_(116436178_?)dup	MET	Duplication	Renal cell carcinoma	GUncertain significance
Select item 3245625	NC_000007.13:g.(?_116339139)_(116381089_?)dup	MET	Duplication	Renal cell carcinoma	GUncertain significance
Select item 3245623	NC_000007.13:g.(?_116165117)_(116340358_?)dup	CAV1, MET	Duplication	Renal cell carcinoma	GUncertain significance
Select item 3245622	NC_000007.13:g.(?_116339139)_(116340358_?)del	MET	Deletion	Renal cell carcinoma	GUncertain significance
Select item 3021000	NM_000245.4(MET):c.2619A>G (p.Glu873=)	MET	Single nucleotide variant (synonymous variant)	Renal cell carcinoma	GUncertain significance
Select item 3020736	NM_000245.4(MET):c.1897C>T (p.His633Tyr)	MET (H633Y +1 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma	GUncertain significance
Select item 3020210	NM_000245.4(MET):c.1392+6T>C	MET	Single nucleotide variant (intron variant)	Renal cell carcinoma	GUncertain significance
Select item 3020206	NM_000245.4(MET):c.3150T>C (p.Thr1050=)	MET	Single nucleotide variant (synonymous variant)	Renal cell carcinoma	GLikely benign
Select item 3019890	NM_000245.4(MET):c.1108G>A (p.Val370Ile)	MET (V370I)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 3018827	NM_000245.4(MET):c.608C>A (p.Ser203Tyr)	MET (S203Y)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 3017419	NM_000245.4(MET):c.1944_1945delinsGC (p.Tyr649His)	MET (Y219H +1 more)	Indel (missense variant)	Renal cell carcinoma	GUncertain significance
Select item 3017018	NM_000245.4(MET):c.3028+3A>G	MET	Single nucleotide variant (intron variant)	Renal cell carcinoma	GUncertain significance
Select item 3016612	NM_000245.4(MET):c.2921_2946del (p.Arg974fs)	MET (R544fs +2 more)	Deletion (frameshift variant)	Renal cell carcinoma	GUncertain significance
Select item 3015202	NM_000245.4(MET):c.1484C>T (p.Thr495Ile)	MET (T495I +1 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma	GUncertain significance
Select item 3013733	NM_000245.4(MET):c.767A>G (p.Asn256Ser)	MET (N256S)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 3013605	NM_000245.4(MET):c.568G>A (p.Asp190Asn)	MET (D190N)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 3013357	NM_000245.4(MET):c.861A>G (p.Gly287=)	MET	Single nucleotide variant (synonymous variant +1 more)	Renal cell carcinoma	GLikely benign
Select item 3013280	NM_000245.4(MET):c.2583+11C>G	MET	Single nucleotide variant (intron variant)	Renal cell carcinoma	GLikely benign
Select item 3012713	NM_000245.4(MET):c.1527+18G>A	MET	Single nucleotide variant (intron variant)	Renal cell carcinoma	GLikely benign
Select item 3012649	NM_000245.4(MET):c.1226G>A (p.Cys409Tyr)	MET (C409Y)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 3011851	NM_000245.4(MET):c.2354A>T (p.Asn785Ile)	MET (N355I +2 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma	GUncertain significance
Select item 3011592	NM_000245.4(MET):c.3138A>G (p.Leu1046=)	MET	Single nucleotide variant (synonymous variant)	Renal cell carcinoma	GLikely benign
Select item 3009352	NM_000245.4(MET):c.2823A>G (p.Ile941Met)	MET (I511M +2 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma	GUncertain significance
Select item 3009349	NM_000245.4(MET):c.3936-11T>G	MET	Single nucleotide variant (intron variant)	Renal cell carcinoma	GLikely benign
Select item 3009164	NM_000245.4(MET):c.3382G>A (p.Gly1128Arg)	MET (G1146R +2 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma	GUncertain significance
Select item 3006238	NM_000245.4(MET):c.275A>G (p.His92Arg)	MET (H92R)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 3005924	NM_000245.4(MET):c.2225C>T (p.Pro742Leu)	MET (P742L +1 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma	GUncertain significance
Select item 3005484	NM_000245.4(MET):c.1717G>A (p.Ala573Thr)	MET (A573T +1 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma	GUncertain significance
Select item 3003190	NM_000245.4(MET):c.665C>G (p.Thr222Arg)	MET (T222R)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 3002227	NM_000245.4(MET):c.2265-66C>T	MET	Single nucleotide variant (intron variant)	Renal cell carcinoma	GLikely benign
Select item 3001624	NM_000245.4(MET):c.4048G>A (p.Val1350Ile)	MET (V1350I +2 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma	GUncertain significance
Select item 3000723	NM_000245.4(MET):c.1201-8T>C	MET	Single nucleotide variant (intron variant)	Renal cell carcinoma	GLikely benign
Select item 2999961	NM_000245.4(MET):c.3798+12G>A	MET	Single nucleotide variant (intron variant)	Renal cell carcinoma	GLikely benign
Select item 2999755	NM_000245.4(MET):c.2622G>C (p.Val874=)	MET	Single nucleotide variant (synonymous variant)	Renal cell carcinoma	GLikely benign
Select item 2998979	NM_000245.4(MET):c.2731-18T>G	MET	Single nucleotide variant (intron variant)	Renal cell carcinoma	GLikely benign
Select item 2998950	NM_000245.4(MET):c.365T>C (p.Val122Ala)	MET (V122A)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 2998578	NM_000245.4(MET):c.3340+6T>A	MET	Single nucleotide variant (intron variant)	Renal cell carcinoma	GUncertain significance
Select item 2996213	NM_000245.4(MET):c.2007G>T (p.Met669Ile)	MET (M239I +1 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma	GUncertain significance
Select item 2996185	NM_000245.4(MET):c.1702-17C>T	MET	Single nucleotide variant (intron variant)	Renal cell carcinoma	GLikely benign
Select item 2995641	NM_000245.4(MET):c.2395A>G (p.Ile799Val)	MET (I799V +2 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma	GUncertain significance
Select item 2995352	NM_000245.4(MET):c.1039G>T (p.Ala347Ser)	MET (A347S)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 2994199	NM_000245.4(MET):c.505C>T (p.Pro169Ser)	MET (P169S)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 2992242	NM_000245.4(MET):c.1966-7C>A	MET	Single nucleotide variant (intron variant)	Renal cell carcinoma	GLikely benign
Select item 2989927	NM_000245.4(MET):c.2640G>C (p.Lys880Asn)	MET (K880N +2 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma	GUncertain significance
Select item 2986655	NM_000245.4(MET):c.3500A>G (p.Asn1167Ser)	MET (N1185S +2 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma	GUncertain significance
Select item 2984447	NM_000245.4(MET):c.1201-7A>T	MET	Single nucleotide variant (intron variant)	Renal cell carcinoma	GLikely benign
Select item 2984276	NM_000245.4(MET):c.3143A>G (p.Gln1048Arg)	MET (Q1066R +2 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma	GUncertain significance
Select item 2977695	NM_000245.4(MET):c.373T>A (p.Tyr125Asn)	MET (Y125N)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 2975095	NM_000245.4(MET):c.2809G>A (p.Gly937Ser)	MET (G507S +2 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma	GUncertain significance
Select item 2974654	NM_000245.4(MET):c.2265-60T>A	MET	Single nucleotide variant (intron variant)	Renal cell carcinoma	GLikely benign
Select item 2974519	NM_000245.4(MET):c.3633-18T>C	MET	Single nucleotide variant (intron variant)	Renal cell carcinoma	GLikely benign
Select item 2974061	NM_000245.4(MET):c.2906T>C (p.Val969Ala)	MET (V539A +2 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma	GUncertain significance
Select item 2973911	NM_000245.4(MET):c.3784A>G (p.Thr1262Ala)	MET (T1262A +2 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma	GUncertain significance
Select item 2973654	NM_000245.4(MET):c.2902T>C (p.Leu968=)	MET	Single nucleotide variant (synonymous variant)	Renal cell carcinoma	GLikely benign
Select item 2973370	NM_000245.4(MET):c.3799-19C>G	MET	Single nucleotide variant (intron variant)	Renal cell carcinoma	GLikely benign
Select item 2970941	NM_000245.4(MET):c.2101A>C (p.Ser701Arg)	MET (S271R +1 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma +1 more	GUncertain significance
Select item 2970863	NM_000245.4(MET):c.3234G>A (p.Val1078=)	MET	Single nucleotide variant (synonymous variant)	Renal cell carcinoma	GLikely benign
Select item 2970862	NM_000245.4(MET):c.954G>A (p.Gln318=)	MET	Single nucleotide variant (synonymous variant +1 more)	Renal cell carcinoma	GLikely benign
Select item 2968845	NM_000245.4(MET):c.2078G>A (p.Gly693Asp)	MET (G693D +1 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma	GUncertain significance
Select item 2968165	NM_000245.4(MET):c.2265-25T>G	MET (V765G)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 2963760	NM_000245.4(MET):c.3184C>T (p.Leu1062=)	MET	Single nucleotide variant (synonymous variant)	Renal cell carcinoma	GLikely benign
Select item 2963202	NM_000245.4(MET):c.911G>A (p.Arg304Lys)	MET (R304K)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 2962629	NM_000245.4(MET):c.1175C>A (p.Pro392His)	MET (P392H)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 2960996	NM_000245.4(MET):c.2499C>T (p.Leu833=)	MET	Single nucleotide variant (synonymous variant)	Renal cell carcinoma	GLikely benign
Select item 2960251	NM_000245.4(MET):c.1682G>C (p.Cys561Ser)	MET (C561S +1 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma	GUncertain significance
Select item 2957122	NM_000245.4(MET):c.1445A>G (p.Asp482Gly)	MET (D482G +1 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma	GUncertain significance
Select item 2956031	NM_000245.4(MET):c.572G>T (p.Arg191Leu)	MET (R191L)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 2920571	NM_000245.4(MET):c.24dup (p.Pro9fs)	MET (P9fs)	Duplication (frameshift variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 2919540	NM_000245.4(MET):c.2487A>T (p.Lys829Asn)	MET (K847N +2 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma	GUncertain significance
Select item 2919100	NM_000245.4(MET):c.17T>G (p.Val6Gly)	MET (V6G)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 2918853	NM_000245.4(MET):c.4112C>T (p.Ser1371Leu)	MET (S941L +2 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma	GUncertain significance
Select item 2917506	NM_000245.4(MET):c.1965+11T>C	MET	Single nucleotide variant (intron variant)	Renal cell carcinoma	GLikely benign
Select item 2914976	NM_000245.4(MET):c.3651A>G (p.Thr1217=)	MET	Single nucleotide variant (synonymous variant)	Renal cell carcinoma	GLikely benign
Select item 2914708	NM_000245.4(MET):c.3972C>G (p.Ala1324=)	MET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 2913869	NM_000245.4(MET):c.3522+18C>T	MET	Single nucleotide variant (intron variant)	Renal cell carcinoma	GLikely benign
Select item 2912428	NM_000245.4(MET):c.3295G>A (p.Asp1099Asn)	MET (D1117N +2 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma	GUncertain significance
Select item 2912111	NM_000245.4(MET):c.3799-11del	MET	Deletion (intron variant)	Renal cell carcinoma	GLikely benign
Select item 2911184	NM_000245.4(MET):c.1636G>C (p.Val546Leu)	MET (V116L +1 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma	GUncertain significance
Select item 2911113	NM_000245.4(MET):c.1701+15C>T	MET	Single nucleotide variant (intron variant)	Renal cell carcinoma	GLikely benign
Select item 2910909	NM_000245.4(MET):c.2137G>A (p.Ala713Thr)	MET (A713T +1 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma	GUncertain significance
Select item 2910021	NM_000245.4(MET):c.4027A>G (p.Thr1343Ala)	MET (T1361A +2 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma	GUncertain significance
Select item 2909718	NM_000245.4(MET):c.1392+3A>G	MET	Single nucleotide variant (intron variant)	Renal cell carcinoma	GUncertain significance
Select item 2909603	NM_000245.4(MET):c.3935+7_3935+8insCCT	MET	Insertion (intron variant)	Renal cell carcinoma	GLikely benign
Select item 2907157	NM_000245.4(MET):c.37G>C (p.Val13Leu)	MET (V13L)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 2904934	NM_000245.4(MET):c.528G>A (p.Val176=)	MET	Single nucleotide variant (synonymous variant +1 more)	Renal cell carcinoma	GLikely benign
Select item 2904772	NM_000245.4(MET):c.2110A>T (p.Asn704Tyr)	MET (N274Y +1 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma	GUncertain significance
Select item 2903179	NM_000245.4(MET):c.586T>C (p.Phe196Leu)	MET (F196L)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 2902341	NM_000245.4(MET):c.3704A>G (p.Tyr1235Cys)	MET (Y1253C +2 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma	GUncertain significance
Select item 2901955	NM_000245.4(MET):c.262C>A (p.Pro88Thr)	MET (P88T)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 2901952	NM_000245.4(MET):c.2265-29A>G	MET (I764V)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 2900746	NM_000245.4(MET):c.3871G>C (p.Asp1291His)	MET (D1291H +2 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma	GUncertain significance
Select item 2900470	NM_000245.4(MET):c.3783C>G (p.Thr1261=)	MET	Single nucleotide variant (synonymous variant)	Renal cell carcinoma	GLikely benign
Select item 2899857	NM_000245.4(MET):c.2264+15C>T	MET	Single nucleotide variant (intron variant)	Renal cell carcinoma	GLikely benign
Select item 2897481	NM_000245.4(MET):c.537C>G (p.Ala179=)	MET	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 2891999	NM_000245.4(MET):c.538C>T (p.Leu180=)	MET	Single nucleotide variant (synonymous variant +1 more)	Renal cell carcinoma	GLikely benign
Select item 2890573	NM_000245.4(MET):c.985C>G (p.Leu329Val)	MET (L329V)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma	GUncertain significance
Select item 2890481	NM_000245.4(MET):c.1875A>T (p.Thr625=)	MET	Single nucleotide variant (synonymous variant)	Renal cell carcinoma	GLikely benign
Select item 2888966	NM_000245.4(MET):c.3687G>A (p.Met1229Ile)	MET (M1229I +2 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma	GUncertain significance
Select item 2887839	NM_000245.4(MET):c.2918C>G (p.Ala973Gly)	MET (A543G +2 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma	GUncertain significance

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