"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "RET"[ge - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 477374	NM_020975.6(RET):c.-37G>C	LOC106736614, RET	Single nucleotide variant (5 prime UTR variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 662839	NC_000010.10:g.(?_43572697)_(43623727_?)dup	LOC110121502, LOC130003705 +8 more	Duplication	Multiple endocrine neoplasia, type 2	GUncertain significance
Select item 477299	NC_000010.10:g.(?_43572701)_(43623723_?)dup	LOC130003709, LOC130003710 +8 more	Duplication	Multiple endocrine neoplasia, type 2	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 2733287	NM_020975.6(RET):c.6G>T (p.Ala2=)	LOC106736614, RET	Single nucleotide variant (synonymous variant)	Multiple endocrine neoplasia, type 2	GLikely benign
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)	Hereditary cancer-predisposing syndrome +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 860225	NM_020975.6(RET):c.11C>T (p.Ala4Val)	LOC106736614, RET (A4V)	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 840153	NM_020975.6(RET):c.14C>G (p.Thr5Arg)	LOC106736614, RET (T5R)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2	GUncertain significance
Select item 1962949	NM_020975.6(RET):c.15G>A (p.Thr5=)	LOC106736614, RET	Single nucleotide variant (synonymous variant)	Multiple endocrine neoplasia, type 2	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 1011760	NM_020975.6(RET):c.16T>C (p.Ser6Pro)	LOC106736614, RET (S6P)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +1 more	GUncertain significance
Select item 655125	NM_020975.6(RET):c.16T>G (p.Ser6Ala)	LOC106736614, RET (S6A)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2	GUncertain significance
Select item 477331	NM_020975.6(RET):c.18C>T (p.Ser6=)	LOC106736614, RET	Single nucleotide variant (synonymous variant)	Multiple endocrine neoplasia, type 2 +2 more	GConflicting classifications of pathogenicity
Select item 2717904	NM_020975.6(RET):c.19G>C (p.Gly7Arg)	LOC106736614, RET (G7R)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2	GUncertain significance
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 1406841	NM_020975.6(RET):c.20G>T (p.Gly7Val)	LOC106736614, RET (G7V)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2	GUncertain significance
Select item 486313	NM_020975.6(RET):c.20G>A (p.Gly7Asp)	LOC106736614, RET (G7D)	Single nucleotide variant (missense variant)	Hirschsprung disease, susceptibility to, 1 +7 more	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 2713355	NM_020975.6(RET):c.28G>A (p.Gly10Arg)	LOC106736614, RET (G10R)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2	GUncertain significance
Select item 1426573	NM_020975.6(RET):c.29G>C (p.Gly10Ala)	LOC106736614, RET (G10A)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +1 more	GUncertain significance
Select item 1061842	NM_020975.6(RET):c.35_55dup (p.Leu18_Leu19insArgLeuLeuLeuLeuLeuLeu)	LOC106736614, RET	Duplication (inframe_indel +1 more)	Multiple endocrine neoplasia, type 2 +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 936337	NM_020975.6(RET):c.29G>T (p.Gly10Val)	LOC106736614, RET (G10V)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2	GUncertain significance
Select item 662154	NM_020975.6(RET):c.30G>T (p.Gly10=)	LOC106736614, RET	Single nucleotide variant (synonymous variant)	Multiple endocrine neoplasia, type 2 +1 more	GConflicting classifications of pathogenicity
Select item 477365	NM_020975.6(RET):c.30G>A (p.Gly10=)	LOC106736614, RET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 486316	NM_020975.6(RET):c.31C>A (p.Leu11Met)	LOC106736614, RET (L11M)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +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 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 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)	Multiple endocrine neoplasia, type 2 +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 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 2A +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 477376	NM_020975.6(RET):c.46C>T (p.Leu16=)	RET	Single nucleotide variant (synonymous variant)	Multiple endocrine neoplasia, type 2 +1 more	GLikely benign
Select item 572655	NM_020975.6(RET):c.47T>A (p.Leu16Gln)	RET (L16Q)	Single nucleotide variant (missense variant)	Hirschsprung disease, susceptibility to, 1 +3 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 762646	NM_020975.6(RET):c.49C>T (p.Leu17=)	RET	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 1039584	NM_020975.6(RET):c.50T>C (p.Leu17Pro)	RET (L17P)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +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 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 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 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 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)	Hereditary cancer-predisposing syndrome +7 more	GUncertain significance
Select item 1608560	NM_020975.6(RET):c.60G>A (p.Pro20=)	RET	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	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 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 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 13952	NM_020975.6(RET):c.73+9277T>C	LOC110121502, MCS+9.7 +1 more	Single nucleotide variant (intron variant)	Multiple endocrine neoplasia, type 2 +3 more	GBenign; risk factor

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