RET[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2785488	NM_020975.6(RET):c.34C>T (p.Arg12Cys)	RET (R12C)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2	GUncertain significance
Select item 1352051	NM_020975.6(RET):c.34C>G (p.Arg12Gly)	RET (R12G)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1510726	NM_020975.6(RET):c.35G>A (p.Arg12His)	RET (R12H)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2	GUncertain significance
Select item 824772	NM_020975.6(RET):c.43_51dup (p.Leu19_Pro20insLeuLeuLeu)	RET	Duplication (inframe_indel +1 more)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 3022887	NM_020975.6(RET):c.43_48dup (p.Leu19_Pro20insLeuLeu)	RET	Duplication (inframe_indel +1 more)	Multiple endocrine neoplasia, type 2	GUncertain significance
Select item 943957	NM_020975.6(RET):c.40_41insGGTTGC (p.Leu13_Leu14insArgLeu)	RET	Insertion (inframe_indel +1 more)	Multiple endocrine neoplasia, type 2	GUncertain significance
Select item 580433	NM_020975.6(RET):c.43_51del (p.Leu17_Leu19del)	RET	Deletion (inframe_indel +1 more)	Multiple endocrine neoplasia, type 2 +1 more	GConflicting classifications of pathogenicity
Select item 1932474	NM_020975.6(RET):c.39G>C (p.Leu13=)	RET	Single nucleotide variant (synonymous variant)	Multiple endocrine neoplasia, type 2	GLikely benign
Select item 1736876	NM_020975.6(RET):c.39G>A (p.Leu13=)	RET	Single nucleotide variant (synonymous variant)	Multiple endocrine neoplasia, type 2 +1 more	GLikely benign
Select item 1737851	NM_020975.6(RET):c.41_43delinsGGTTGCTGC (p.Leu13_Leu14insArgLeu)	RET	Indel (inframe_indel +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1472013	NM_020975.6(RET):c.41T>C (p.Leu14Pro)	RET (L14P)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +1 more	GUncertain significance
Select item 1388329	NM_020975.6(RET):c.43_44insGGC (p.Leu14_Leu15insTrp)	RET	Insertion (inframe_indel +1 more)	Multiple endocrine neoplasia, type 2	GUncertain significance
Select item 1367349	NM_020975.6(RET):c.44TGC[7] (p.Leu19_Pro20insLeuLeu)	RET	Microsatellite (inframe_indel +1 more)	Multiple endocrine neoplasia, type 2 +1 more	GConflicting classifications of pathogenicity
Select item 1112203	NM_020975.6(RET):c.43T>C (p.Leu15=)	RET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 648453	NM_020975.6(RET):c.44TGC[6] (p.Leu19_Pro20insLeu)	RET	Microsatellite (inframe_indel +1 more)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 216728	NM_020975.6(RET):c.44TGC[8] (p.Leu19_Pro20insLeuLeuLeu)	RET	Microsatellite (inframe_indel +1 more)	Multiple endocrine neoplasia type 2A +8 more	GConflicting classifications of pathogenicity
Select item 2454134	NM_020975.6(RET):c.44TGC[2] (p.Leu17_Leu19del)	RET	Microsatellite (inframe_indel +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 1741794	NM_020975.6(RET):c.45dup (p.Leu16fs)	RET (L16fs)	Duplication (frameshift variant)	Hereditary cancer-predisposing syndrome	GPathogenic
Select item 1427613	NM_020975.6(RET):c.44T>C (p.Leu15Ser)	RET (L15S)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2	GUncertain significance
Select item 835920	NM_020975.6(RET):c.44TGC[3] (p.Leu18_Leu19del)	RET	Microsatellite (inframe_indel +1 more)	Multiple endocrine neoplasia, type 2 +1 more	GConflicting classifications of pathogenicity
Select item 543749	NM_020975.6(RET):c.44TGC[4] (p.Leu19del)	RET (L19del)	Microsatellite (inframe_indel +1 more)	Multiple endocrine neoplasia, type 2 +2 more	GConflicting classifications of pathogenicity
Select item 233052	NM_020975.6(RET):c.45G>A (p.Leu15=)	RET	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 3227559	NM_020975.6(RET):c.46C>G (p.Leu16Val)	RET (L16V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 477376	NM_020975.6(RET):c.46C>T (p.Leu16=)	RET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 572655	NM_020975.6(RET):c.47T>A (p.Leu16Gln)	RET (L16Q)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +2 more	GUncertain significance
Select item 1743969	NM_020975.6(RET):c.48G>A (p.Leu16=)	RET	Single nucleotide variant (synonymous variant)	Multiple endocrine neoplasia, type 2 +1 more	GLikely benign
Select item 1744661	NM_020975.6(RET):c.49C>A (p.Leu17Met)	RET (L17M)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 762646	NM_020975.6(RET):c.49C>T (p.Leu17=)	RET	Single nucleotide variant (synonymous variant)	Multiple endocrine neoplasia, type 2 +2 more	GLikely benign
Select item 1039584	NM_020975.6(RET):c.50T>C (p.Leu17Pro)	RET (L17P)	Single nucleotide variant (missense variant)	Family history of cancer +2 more	GUncertain significance
Select item 241364	NM_020975.6(RET):c.57_65dup (p.Leu22_Gly23insProLeuLeu)	RET	Duplication (inframe_indel +1 more)	Multiple endocrine neoplasia, type 2 +1 more	GUncertain significance
Select item 3227561	NM_020975.6(RET):c.51G>C (p.Leu17=)	RET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 760678	NM_020975.6(RET):c.51G>A (p.Leu17=)	RET	Single nucleotide variant (synonymous variant)	Multiple endocrine neoplasia, type 2 +1 more	GLikely benign
Select item 1090285	NM_020975.6(RET):c.52C>T (p.Leu18=)	RET	Single nucleotide variant (synonymous variant)	Multiple endocrine neoplasia, type 2	GLikely benign
Select item 1480994	NM_020975.6(RET):c.53T>C (p.Leu18Pro)	RET (L18P)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1747958	NM_020975.6(RET):c.54G>A (p.Leu18=)	RET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 1748549	NM_020975.6(RET):c.55C>A (p.Leu19Met)	RET (L19M)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 2107657	NM_020975.6(RET):c.56T>C (p.Leu19Pro)	RET (L19P)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +1 more	GUncertain significance
Select item 423618	NM_020975.6(RET):c.59_61dup (p.Pro20_Leu21insPro)	RET	Duplication (inframe_indel +1 more)	Multiple endocrine neoplasia, type 2 +2 more	GUncertain significance
Select item 3344343	NM_020975.6(RET):c.57G>T (p.Leu19=)	RET	Single nucleotide variant (synonymous variant)	RET-related disorder	GLikely benign
Select item 755049	NM_020975.6(RET):c.57G>C (p.Leu19=)	RET	Single nucleotide variant (synonymous variant)	Multiple endocrine neoplasia, type 2 +1 more	GLikely benign
Select item 543729	NM_020975.6(RET):c.58C>T (p.Pro20Ser)	RET (P20S)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1448380	NM_020975.6(RET):c.59C>T (p.Pro20Leu)	RET (P20L)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2	GUncertain significance
Select item 965788	NM_020975.6(RET):c.59C>G (p.Pro20Arg)	RET (P20R)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +1 more	GUncertain significance
Select item 952569	NM_020975.6(RET):c.59C>A (p.Pro20Gln)	RET (P20Q)	Single nucleotide variant (missense variant)	Hirschsprung disease, susceptibility to, 1 +7 more	GUncertain significance
Select item 3313745	NM_020975.6(RET):c.60G>T (p.Pro20=)	RET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 1608560	NM_020975.6(RET):c.60G>A (p.Pro20=)	RET	Single nucleotide variant (synonymous variant)	Multiple endocrine neoplasia, type 2	GLikely benign
Select item 1548581	NM_020975.6(RET):c.60G>C (p.Pro20=)	RET	Single nucleotide variant (synonymous variant)	Multiple endocrine neoplasia, type 2	GLikely benign
Select item 946053	NM_020975.6(RET):c.60_65del (p.Leu21_Leu22del)	RET	Deletion (inframe_indel +1 more)	Multiple endocrine neoplasia, type 2	GUncertain significance
Select item 1085791	NM_020975.6(RET):c.61C>T (p.Leu21=)	RET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 2084198	NM_020975.6(RET):c.63_64delinsCT (p.Leu21_Leu22=)	RET	Indel (synonymous variant)	Multiple endocrine neoplasia, type 2	GLikely benign
Select item 1134102	NM_020975.6(RET):c.63G>A (p.Leu21=)	RET	Single nucleotide variant (synonymous variant)	Multiple endocrine neoplasia, type 2 +1 more	GLikely benign
Select item 3075550	NM_020975.6(RET):c.67G>A (p.Gly23Ser)	RET (G23S)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2	GUncertain significance
Select item 1755516	NM_020975.6(RET):c.67G>C (p.Gly23Arg)	RET (G23R)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 950776	NM_020975.6(RET):c.68G>T (p.Gly23Val)	RET (G23V)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +1 more	GUncertain significance
Select item 486342	NM_020975.6(RET):c.68G>A (p.Gly23Asp)	RET (G23D)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +1 more	GUncertain significance
Select item 1386322	NM_020975.6(RET):c.69C>T (p.Gly23=)	RET	Single nucleotide variant (synonymous variant)	Multiple endocrine neoplasia, type 2	GUncertain significance
Select item 1140737	NM_020975.6(RET):c.69C>G (p.Gly23=)	RET	Single nucleotide variant (synonymous variant)	Multiple endocrine neoplasia, type 2 +1 more	GLikely benign
Select item 1757154	NM_020975.6(RET):c.70A>G (p.Lys24Glu)	RET (K24E)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 1758176	NM_020975.6(RET):c.72A>G (p.Lys24=)	RET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 2809347	NM_020975.6(RET):c.73+3G>A	RET	Single nucleotide variant (intron variant)	Multiple endocrine neoplasia, type 2	GUncertain significance
Select item 2918367	NM_020975.6(RET):c.73+9dup	RET	Duplication (intron variant)	Multiple endocrine neoplasia, type 2	GLikely benign
Select item 1656664	NM_020975.6(RET):c.73+8C>T	RET	Single nucleotide variant (intron variant)	Multiple endocrine neoplasia, type 2	GLikely benign
Select item 1108933	NM_020975.6(RET):c.73+8C>G	RET	Single nucleotide variant (intron variant)	Multiple endocrine neoplasia, type 2	GLikely benign
Select item 792378	NM_020975.6(RET):c.73+9del	RET	Deletion (intron variant)	Multiple endocrine neoplasia, type 2	GLikely benign
Select item 543783	NM_020975.6(RET):c.73+9T>G	RET	Single nucleotide variant (intron variant)	Multiple endocrine neoplasia, type 2	GLikely benign
Select item 1141262	NM_020975.6(RET):c.73+10G>A	RET	Single nucleotide variant (intron variant)	Multiple endocrine neoplasia, type 2	GLikely benign
Select item 413478	NM_020975.6(RET):c.73+10G>C	RET	Single nucleotide variant (intron variant)	Multiple endocrine neoplasia, type 2	GLikely benign
Select item 2086153	NM_020975.6(RET):c.73+11C>T	RET	Single nucleotide variant (intron variant)	Multiple endocrine neoplasia, type 2	GLikely benign
Select item 1661705	NM_020975.6(RET):c.73+12C>A	RET	Single nucleotide variant (intron variant)	Multiple endocrine neoplasia, type 2	GLikely benign
Select item 2072250	NM_020975.6(RET):c.73+13G>A	RET	Single nucleotide variant (intron variant)	Multiple endocrine neoplasia, type 2	GLikely benign
Select item 1947605	NM_020975.6(RET):c.73+13G>T	RET	Single nucleotide variant (intron variant)	Multiple endocrine neoplasia, type 2	GLikely benign
Select item 1996446	NM_020975.6(RET):c.73+14G>A	RET	Single nucleotide variant (intron variant)	Multiple endocrine neoplasia, type 2	GLikely benign
Select item 2817141	NM_020975.6(RET):c.73+15C>G	RET	Single nucleotide variant (intron variant)	Multiple endocrine neoplasia, type 2	GLikely benign
Select item 2713646	NM_020975.6(RET):c.73+15C>T	RET	Single nucleotide variant (intron variant)	Multiple endocrine neoplasia, type 2	GLikely benign
Select item 2916695	NM_020975.6(RET):c.73+16C>T	RET	Single nucleotide variant (intron variant)	Multiple endocrine neoplasia, type 2	GLikely benign
Select item 2904935	NM_020975.6(RET):c.73+16C>A	RET	Single nucleotide variant (intron variant)	Multiple endocrine neoplasia, type 2	GLikely benign
Select item 1592544	NM_020975.6(RET):c.73+17G>T	RET	Single nucleotide variant (intron variant)	Multiple endocrine neoplasia, type 2 +5 more	GLikely benign
Select item 2073740	NM_020975.6(RET):c.73+18C>T	RET	Single nucleotide variant (intron variant)	Multiple endocrine neoplasia, type 2	GLikely benign
Select item 2723664	NM_020975.6(RET):c.73+19C>G	RET	Single nucleotide variant (intron variant)	Multiple endocrine neoplasia, type 2	GLikely benign
Select item 1229273	NM_020975.6(RET):c.73+53G>A	RET	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 676894	NM_020975.6(RET):c.73+104C>T	RET	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1293631	NM_020975.6(RET):c.73+171_73+172del	RET	Deletion (intron variant)	not provided	GBenign
Select item 1286547	NM_020975.6(RET):c.73+173_73+174insCGGGCGGCG	RET	Microsatellite (intron variant)	not provided	GBenign
Select item 1242123	NM_020975.6(RET):c.73+172A>C	RET	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1216709	NM_020975.6(RET):c.73+188G>A	RET	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 677842	NM_020975.6(RET):c.74-158G>T	RET	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 677050	NM_020975.6(RET):c.74-126G>T	RET	Single nucleotide variant (intron variant)	Multiple endocrine neoplasia, type 2 +1 more	GBenign
Select item 1280354	NM_020975.6(RET):c.74-57dup	RET	Duplication (intron variant)	not provided	GBenign
Select item 1181790	NM_020975.6(RET):c.74-58_74-57dup	RET	Duplication (intron variant)	not provided	GLikely benign
Select item 1258537	NM_020975.6(RET):c.74-57del	RET	Deletion (intron variant)	not provided	GBenign
Select item 802567	NM_020975.6(RET):c.74-50G>T	RET	Single nucleotide variant (intron variant)	Multiple endocrine neoplasia type 2A	GBenign
Select item 1998468	NM_020975.6(RET):c.74-20C>T	RET	Single nucleotide variant (intron variant)	Multiple endocrine neoplasia, type 2	GLikely benign
Select item 1626009	NM_020975.6(RET):c.74-12_74-5del	RET	Deletion (intron variant)	Multiple endocrine neoplasia, type 2	GLikely benign
Select item 2785464	NM_020975.6(RET):c.74-18C>T	RET	Single nucleotide variant (intron variant)	Multiple endocrine neoplasia, type 2	GLikely benign
Select item 2882220	NM_020975.6(RET):c.74-17T>G	RET	Single nucleotide variant (intron variant)	Multiple endocrine neoplasia, type 2	GLikely benign
Select item 1653287	NM_020975.6(RET):c.74-11_74-10dup	RET	Duplication (intron variant)	Multiple endocrine neoplasia, type 2	GLikely benign
Select item 653522	NC_000010.11:g.(?_43100449)_(43102639_?)del	RET	Deletion	Multiple endocrine neoplasia, type 2	GLikely pathogenic
Select item 764947	NM_020975.6(RET):c.74-7C>T	RET	Single nucleotide variant (intron variant)	Multiple endocrine neoplasia, type 2	GLikely benign
Select item 477386	NM_020975.6(RET):c.74-5C>T	RET	Single nucleotide variant (intron variant)	Multiple endocrine neoplasia, type 2 +1 more	GConflicting classifications of pathogenicity
Select item 1499429	NM_020975.6(RET):c.74-2A>T	RET	Single nucleotide variant (splice acceptor variant +1 more)	Multiple endocrine neoplasia, type 2	GLikely pathogenic

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