"Ambry Genetics"[submitter] AND "RET"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1756637	NM_020975.6(RET):c.-7_-4del	LOC106736614, RET	Deletion (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 2447524	NM_020975.6(RET):c.2_7dup (p.Ala2_Lys3insMetAla)	LOC106736614, RET	Duplication (inframe_indel +2 more)	Multiple endocrine neoplasia, type 2 +1 more	GConflicting classifications of pathogenicity
Select item 1751015	NM_020975.6(RET):c.-5G>C	LOC106736614, RET	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 825359	NM_020975.6(RET):c.-4G>A	LOC106736614, RET	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1736907	NM_020975.6(RET):c.-3G>A	LOC106736614, RET	Single nucleotide variant (5 prime UTR variant)	Multiple endocrine neoplasia, type 2 +1 more	GUncertain significance
Select item 229201	NM_020975.6(RET):c.-2C>A	LOC106736614, RET	Single nucleotide variant (5 prime UTR variant)	Hirschsprung disease, susceptibility to, 1 +7 more	GConflicting classifications of pathogenicity
Select item 1784210	NM_020975.6(RET):c.-1G>A	LOC106736614, RET	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1020843	NM_020975.6(RET):c.5_28dup (p.Ala9_Gly10insAlaLysAlaThrSerGlyAlaAla)	LOC106736614, RET	Duplication (inframe_indel +2 more)	not specified +2 more	GUncertain significance
Select item 2914324	NM_020975.6(RET):c.5C>A (p.Ala2Glu)	LOC106736614, RET (A2E)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 767548	NM_020975.6(RET):c.6G>A (p.Ala2=)	LOC106736614, RET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 584566	NM_020975.6(RET):c.7A>G (p.Lys3Glu)	LOC106736614, RET (K3E)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +1 more	GUncertain significance
Select item 1023866	NM_020975.6(RET):c.10G>A (p.Ala4Thr)	LOC106736614, RET (A4T)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1771753	NM_020975.6(RET):c.13A>G (p.Thr5Ala)	LOC106736614, RET (T5A)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1486379	NM_020975.6(RET):c.14C>T (p.Thr5Met)	LOC106736614, RET (T5M)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +1 more	GUncertain significance
Select item 1776161	NM_020975.6(RET):c.15G>T (p.Thr5=)	LOC106736614, RET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 819613	NM_020975.6(RET):c.15G>C (p.Thr5=)	LOC106736614, RET	Single nucleotide variant (synonymous variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 1782267	NM_020975.6(RET):c.18C>G (p.Ser6=)	LOC106736614, RET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 1782262	NM_020975.6(RET):c.18C>A (p.Ser6=)	LOC106736614, RET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 477331	NM_020975.6(RET):c.18C>T (p.Ser6=)	LOC106736614, RET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 1001221	NM_020975.6(RET):c.19G>A (p.Gly7Ser)	LOC106736614, RET (G7S)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +1 more	GUncertain significance
Select item 486313	NM_020975.6(RET):c.20G>A (p.Gly7Asp)	LOC106736614, RET (G7D)	Single nucleotide variant (missense variant)	not provided +7 more	GUncertain significance
Select item 2568372	NM_020975.6(RET):c.21T>C (p.Gly7=)	LOC106736614, RET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3313699	NM_020975.6(RET):c.22G>A (p.Ala8Thr)	LOC106736614, RET (A8T)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 842268	NM_020975.6(RET):c.22G>T (p.Ala8Ser)	LOC106736614, RET (A8S)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +1 more	GUncertain significance
Select item 1790712	NM_020975.6(RET):c.23C>T (p.Ala8Val)	LOC106736614, RET (A8V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1792215	NM_020975.6(RET):c.24C>T (p.Ala8=)	LOC106736614, RET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 1796199	NM_020975.6(RET):c.27G>C (p.Ala9=)	LOC106736614, RET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 1796194	NM_020975.6(RET):c.27G>A (p.Ala9=)	LOC106736614, RET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 1061842	NM_020975.6(RET):c.35_55dup (p.Leu18_Leu19insArgLeuLeuLeuLeuLeuLeu)	LOC106736614, RET	Duplication (inframe_indel +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1053894	NM_020975.6(RET):c.35_52dup (p.Leu17_Leu18insArgLeuLeuLeuLeuLeu)	LOC106736614, RET	Duplication (inframe_indel +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1035794	NM_020975.6(RET):c.29G>A (p.Gly10Glu)	LOC106736614, RET (G10E)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 477365	NM_020975.6(RET):c.30G>A (p.Gly10=)	LOC106736614, RET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 486316	NM_020975.6(RET):c.31C>A (p.Leu11Met)	LOC106736614, RET (L11M)	Single nucleotide variant (missense variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 477368	NM_020975.6(RET):c.31C>T (p.Leu11=)	LOC106736614, RET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +6 more	GLikely benign
Select item 136117	NM_020975.6(RET):c.31C>G (p.Leu11Val)	LOC106736614, RET (L11V)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +1 more	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 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 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 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 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 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 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)	Hereditary cancer-predisposing syndrome +1 more	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 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 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 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 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 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 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 477386	NM_020975.6(RET):c.74-5C>T	RET	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 1964452	NM_020975.6(RET):c.76G>A (p.Ala26Thr)	RET (A26T)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 3016033	NM_020975.6(RET):c.77C>T (p.Ala26Val)	RET (A26V)	Single nucleotide variant (missense variant +1 more)	Multiple endocrine neoplasia, type 2 +2 more	GUncertain significance
Select item 1593575	NM_020975.6(RET):c.78A>T (p.Ala26=)	RET	Single nucleotide variant (synonymous variant +1 more)	Multiple endocrine neoplasia, type 2 +1 more	GLikely benign
Select item 413462	NM_020975.6(RET):c.79T>C (p.Leu27=)	RET	Single nucleotide variant (synonymous variant +1 more)	Multiple endocrine neoplasia, type 2 +7 more	GLikely benign
Select item 477388	NM_020975.6(RET):c.81G>A (p.Leu27=)	RET	Single nucleotide variant (synonymous variant +1 more)	not provided +7 more	GLikely benign
Select item 651895	NM_020975.6(RET):c.82G>A (p.Gly28Ser)	RET (G28S)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +7 more	GConflicting classifications of pathogenicity
Select item 765499	NM_020975.6(RET):c.87C>G (p.Leu29=)	RET	Single nucleotide variant (synonymous variant +1 more)	Multiple endocrine neoplasia, type 2 +1 more	GLikely benign
Select item 1378130	NM_020975.6(RET):c.89A>G (p.Tyr30Cys)	RET (Y30C)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +1 more	GUncertain significance
Select item 762105	NM_020975.6(RET):c.90C>T (p.Tyr30=)	RET	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 543774	NM_020975.6(RET):c.96G>A (p.Ser32=)	RET	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +6 more	GLikely benign
Select item 951605	NM_020975.6(RET):c.100G>T (p.Asp34Tyr)	RET (D34Y)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1392266	NM_020975.6(RET):c.101A>G (p.Asp34Gly)	RET (D34G)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
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 2561470	NM_020975.6(RET):c.104C>G (p.Ala35Gly)	RET (A35G)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 2703074	NM_020975.6(RET):c.108C>T (p.Tyr36=)	RET	Single nucleotide variant (synonymous variant +1 more)	Multiple endocrine neoplasia, type 2 +1 more	GLikely benign
Select item 477304	NM_020975.6(RET):c.109T>C (p.Trp37Arg)	RET (W37R)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 647519	NM_020975.6(RET):c.113A>T (p.Glu38Val)	RET (E38V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1159316	NM_020975.6(RET):c.114G>A (p.Glu38=)	RET	Single nucleotide variant (synonymous variant +1 more)	Multiple endocrine neoplasia, type 2 +1 more	GLikely benign
Select item 699886	NM_020975.6(RET):c.118C>T (p.Leu40=)	RET	Single nucleotide variant (synonymous variant +1 more)	Multiple endocrine neoplasia, type 2 +1 more	GLikely benign
Select item 1755119	NM_020975.6(RET):c.122A>T (p.Tyr41Phe)	RET (Y41F)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1951525	NM_020975.6(RET):c.129C>G (p.Asp43Glu)	RET (D43E)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 818716	NM_020975.6(RET):c.129C>A (p.Asp43Glu)	RET (D43E)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +1 more	GUncertain significance

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