ClinVar for Gene (Select 5979) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3227576	NM_020975.6(RET):c.968C>T (p.Thr323Ile)	RET (T227I +3 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227575	NM_020975.6(RET):c.955C>T (p.Leu319Phe)	RET (L223F +3 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227574	NM_020975.6(RET):c.877G>A (p.Val293Met)	RET (V197M +3 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227572	NM_020975.6(RET):c.827T>G (p.Val276Gly)	RET (V180G +3 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227571	NM_020975.6(RET):c.806C>T (p.Ala269Val)	RET (A15V +3 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227570	NM_020975.6(RET):c.801C>T (p.Asp267=)	RET	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3227569	NM_020975.6(RET):c.763A>G (p.Met255Val)	RET (M159V +3 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227568	NM_020975.6(RET):c.756G>C (p.Glu252Asp)	RET (E156D +2 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3227567	NM_020975.6(RET):c.736C>G (p.His246Asp)	RET (H150D +2 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3227566	NM_020975.6(RET):c.709T>G (p.Tyr237Asp)	RET (Y141D +2 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227565	NM_020975.6(RET):c.653C>T (p.Pro218Leu)	RET (P122L +2 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3227564	NM_020975.6(RET):c.633T>G (p.Gly211=)	RET	Single nucleotide variant (synonymous variant +2 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3227563	NM_020975.6(RET):c.605T>C (p.Val202Ala)	RET (V159A +1 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227562	NM_020975.6(RET):c.538C>G (p.Arg180Gly)	RET (R137G +1 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	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 3227560	NM_020975.6(RET):c.492G>C (p.Glu164Asp)	RET (E121D +1 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	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 3227558	NM_020975.6(RET):c.375C>G (p.Val125=)	RET	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3227557	NM_020975.6(RET):c.3324A>C (p.Leu1108Phe)	RET (L1012F +13 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3227556	NM_020975.6(RET):c.3300G>T (p.Met1100Ile)	RET (M1100I +13 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227555	NM_020975.6(RET):c.3294C>G (p.Asn1098Lys)	RET (N1002K +13 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227554	NM_020975.6(RET):c.3280dup (p.Ser1094fs)	RET (S1049fs +13 more)	Duplication (frameshift variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227553	NM_020975.6(RET):c.3247A>T (p.Thr1083Ser)	RET (T1038S +13 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227552	NM_020975.6(RET):c.3245del (p.Gly1082fs)	RET (G1037fs +13 more)	Deletion (frameshift variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227551	NM_020975.6(RET):c.3210T>C (p.Pro1070=)	RET	Single nucleotide variant (synonymous variant +2 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3227550	NM_020975.6(RET):c.3098T>C (p.Leu1033Pro)	RET (L1033P +17 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227549	NM_020975.6(RET):c.3079C>T (p.Leu1027=)	RET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3227548	NM_020975.6(RET):c.2953C>A (p.Leu985Met)	RET (L502M +17 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227547	NM_020975.6(RET):c.2919A>G (p.Pro973=)	RET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3227546	NM_020975.6(RET):c.2905C>A (p.Arg969=)	RET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3227545	NM_020975.6(RET):c.2880C>G (p.Leu960=)	RET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3227544	NM_020975.6(RET):c.2875C>A (p.Arg959=)	RET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3227543	NM_020975.6(RET):c.2859T>C (p.Pro953=)	RET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3227542	NM_020975.6(RET):c.2829G>A (p.Glu943=)	RET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3227541	NM_020975.6(RET):c.2783A>G (p.Tyr928Cys)	RET (Y445C +17 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227540	NM_020975.6(RET):c.275C>G (p.Thr92Ser)	RET (T92S)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227539	NM_020975.6(RET):c.2735G>A (p.Arg912Gln)	RET (R658Q +16 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227538	NM_020975.6(RET):c.2731G>T (p.Gly911Cys)	RET (G428C +17 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227537	NM_020975.6(RET):c.2659A>C (p.Lys887Gln)	RET (K404Q +17 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227536	NM_020975.6(RET):c.2603T>G (p.Met868Arg)	RET (M385R +17 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227535	NM_020975.6(RET):c.2600A>C (p.Glu867Ala)	RET (E384A +17 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227534	NM_020975.6(RET):c.2580G>T (p.Gln860His)	RET (Q377H +17 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227533	NM_020975.6(RET):c.2577A>G (p.Ser859=)	RET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3227532	NM_020975.6(RET):c.2513T>A (p.Leu838Gln)	RET (L355Q +17 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227531	NM_020975.6(RET):c.2509T>C (p.Ser837Pro)	RET (S354P +17 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227530	NM_020975.6(RET):c.2465_2470delinsGGG (p.Val822_Pro824delinsGlyAla)	RET	Indel (inframe_indel)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227529	NM_020975.6(RET):c.2453A>G (p.Glu818Gly)	RET (E335G +17 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227528	NM_020975.6(RET):c.2445C>G (p.Phe815Leu)	RET (F332L +17 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227527	NM_020975.6(RET):c.2417A>T (p.Tyr806Phe)	RET (Y323F +17 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227525	NM_020975.6(RET):c.2370_2371delinsTC (p.Leu790_Tyr791delinsPheHis)	RET	Indel (missense variant)	Hereditary cancer-predisposing syndrome	GLikely pathogenic
Select item 3227524	NM_020975.6(RET):c.2240A>G (p.Lys747Arg)	RET (K264R +17 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227523	NM_020975.6(RET):c.2177T>C (p.Leu726Pro)	RET (L243P +17 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227522	NM_020975.6(RET):c.2132T>A (p.Ile711Asn)	RET (I228N +17 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227521	NM_020975.6(RET):c.2053G>T (p.Val685Phe)	RET (V202F +17 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227520	NM_020975.6(RET):c.2051C>G (p.Pro684Arg)	RET (P201R +17 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227519	NM_020975.6(RET):c.2025C>A (p.Thr675=)	RET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3227518	NM_020975.6(RET):c.1981C>T (p.His661Tyr)	RET (H178Y +14 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227517	NM_020975.6(RET):c.1911G>A (p.Val637=)	RET	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3227516	NM_020975.6(RET):c.1855T>C (p.Phe619Leu)	RET (F136L +12 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227515	NM_020975.6(RET):c.1686C>G (p.Thr562=)	RET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227514	NM_020975.6(RET):c.1683C>T (p.Ser561=)	RET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3227513	NM_020975.6(RET):c.1637G>A (p.Gly546Glu)	RET (G151E +12 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227512	NM_020975.6(RET):c.1600C>T (p.Leu534=)	RET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3227511	NM_020975.6(RET):c.1575G>A (p.Arg525=)	RET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3227510	NM_020975.6(RET):c.155A>C (p.Tyr52Ser)	RET (Y52S)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227509	NM_020975.6(RET):c.1532A>G (p.Glu511Gly)	RET (E116G +12 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227508	NM_020975.6(RET):c.1497G>T (p.Gln499His)	RET (Q169H +8 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227507	NM_020975.6(RET):c.1359G>A (p.Gly453=)	RET	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3227506	NM_020975.6(RET):c.1356A>C (p.Leu452=)	RET	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3227505	NM_020975.6(RET):c.1348A>C (p.Ser450Arg)	RET (S120R +8 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227504	NM_020975.6(RET):c.1299C>T (p.Phe433=)	RET	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3227503	NM_020975.6(RET):c.1244G>A (p.Arg415Lys)	RET (R161K +6 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227502	NM_020975.6(RET):c.1226C>T (p.Ser409Phe)	RET (S155F +6 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227501	NM_020975.6(RET):c.1204C>T (p.Leu402=)	RET	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3227500	NM_020975.6(RET):c.104C>T (p.Ala35Val)	RET (A35V)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3227499	NM_020975.6(RET):c.1022A>C (p.Gln341Pro)	RET (Q245P +3 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3076059	NM_020975.6(RET):c.1296= (p.Ala432=)	RET	Variation (synonymous variant +2 more)	not specified	GBenign
Select item 3076011	NM_020975.6(RET):c.1860C>A (p.Cys620Ter)	RET (C137* +12 more)	Single nucleotide variant (nonsense +1 more)	Aganglionic megacolon	GPathogenic
Select item 3075553	NM_020975.6(RET):c.3149G>T (p.Arg1050Leu)	RET (R1005L +17 more)	Single nucleotide variant (missense variant +1 more)	Multiple endocrine neoplasia, type 2	GUncertain significance
Select item 3075552	NM_020975.6(RET):c.3064A>G (p.Thr1022Ala)	RET (T1022A +17 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2	GUncertain significance
Select item 3075551	NM_020975.6(RET):c.2452G>C (p.Glu818Gln)	RET (E335Q +17 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2	GUncertain significance
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 3075400	NM_020975.6(RET):c.1437C>G (p.Ala479=)	RET	Single nucleotide variant (synonymous variant +1 more)	Multiple endocrine neoplasia, type 2	GLikely benign
Select item 3075356	NM_020975.6(RET):c.3090C>A (p.Asp1030Glu)	RET (D1030E +17 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2	GUncertain significance
Select item 3075316	NM_020975.6(RET):c.3079C>A (p.Leu1027Met)	RET (L1027M +17 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2	GUncertain significance
Select item 3074979	NM_020975.6(RET):c.2802-3C>T	RET	Single nucleotide variant (intron variant)	Multiple endocrine neoplasia, type 2	GLikely benign
Select item 3074853	NM_020975.6(RET):c.-4G>T	LOC106736614, RET	Single nucleotide variant (5 prime UTR variant)	Multiple endocrine neoplasia, type 2	GUncertain significance
Select item 3074605	NM_020975.6(RET):c.1160G>C (p.Gly387Ala)	RET (G133A +6 more)	Single nucleotide variant (intron variant +1 more)	Multiple endocrine neoplasia, type 2	GUncertain significance
Select item 3074602	NM_020975.6(RET):c.3230T>C (p.Leu1077Pro)	RET (L1032P +13 more)	Single nucleotide variant (missense variant +2 more)	Multiple endocrine neoplasia, type 2	GUncertain significance
Select item 3074499	NM_020975.6(RET):c.1197G>C (p.Pro399=)	RET	Single nucleotide variant (intron variant +1 more)	Multiple endocrine neoplasia, type 2	GLikely benign
Select item 3074492	NM_020975.6(RET):c.1259C>T (p.Ala420Val)	RET (A166V +6 more)	Single nucleotide variant (missense variant +1 more)	Multiple endocrine neoplasia, type 2	GUncertain significance
Select item 3074393	NM_020975.6(RET):c.807G>C (p.Ala269=)	RET	Single nucleotide variant (intron variant +1 more)	Multiple endocrine neoplasia, type 2	GLikely benign
Select item 3074392	NM_020975.6(RET):c.808C>A (p.Pro270Thr)	RET (P16T +3 more)	Single nucleotide variant (intron variant +1 more)	Multiple endocrine neoplasia, type 2	GUncertain significance
Select item 3074327	NM_020975.6(RET):c.2501A>C (p.Asn834Thr)	RET (N351T +17 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2	GUncertain significance
Select item 3074143	NM_020975.6(RET):c.2217C>G (p.Val739=)	RET	Single nucleotide variant (synonymous variant)	Multiple endocrine neoplasia, type 2	GLikely benign
Select item 3074062	NM_020975.6(RET):c.458C>A (p.Ser153Tyr)	RET (S153Y)	Single nucleotide variant (missense variant +1 more)	Multiple endocrine neoplasia, type 2	GUncertain significance
Select item 3074030	NM_020975.6(RET):c.2161C>G (p.Arg721Gly)	RET (R238G +17 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2	GUncertain significance
Select item 3073934	NM_020975.6(RET):c.1517G>C (p.Gly506Ala)	RET (G176A +8 more)	Single nucleotide variant (missense variant +1 more)	Multiple endocrine neoplasia, type 2 +1 more	GUncertain significance
Select item 3073914	NM_020975.6(RET):c.2543T>G (p.Met848Arg)	RET (M365R +17 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2	GUncertain significance
Select item 3073559	NM_020975.6(RET):c.626-12C>T	RET	Single nucleotide variant (intron variant +1 more)	Multiple endocrine neoplasia, type 2	GLikely benign

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