"GeneDx"[submitter] AND "RET"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1186865	NC_000010.11:g.43076732C>A	LOC106736614, RET	Single nucleotide variant	not provided	GLikely benign
Select item 1250759	NC_000010.11:g.43076848G>A	LOC106736614, RET	Single nucleotide variant	not provided	GBenign
Select item 1195506	NC_000010.11:g.43076978C>T	LOC106736614, RET	Single nucleotide variant	not provided	GLikely benign
Select item 1189242	NC_000010.11:g.43077033C>T	LOC106736614, RET	Single nucleotide variant	not provided	GLikely benign
Select item 368898	NM_020630.5(RET):c.-200A>G	LOC106736614, RET	Single nucleotide variant	Renal hypodysplasia/aplasia 1 +4 more	GBenign
Select item 368899	NM_020975.5(RET):c.-196C>A	LOC106736614, RET	Single nucleotide variant	Renal hypodysplasia/aplasia 1 +4 more	GBenign/Likely benign
Select item 1225708	NM_020975.6(RET):c.-68C>T	LOC106736614, RET	Single nucleotide variant (5 prime UTR variant)	not provided	GBenign
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 1321691	NM_020975.6(RET):c.-6C>T	LOC106736614, RET	Single nucleotide variant (5 prime UTR variant)	not provided	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 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 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 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 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 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 1290350	NM_020975.6(RET):c.73+9189C>A	LOC110121502, MCS+9.7 +1 more	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1254248	NM_020975.6(RET):c.73+9189C>T	LOC110121502, MCS+9.7 +1 more	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 378478	NM_020975.6(RET):c.73+9201C>T	LOC110121502, MCS+9.7 +1 more	Single nucleotide variant (intron variant)	not specified	GBenign
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
Select item 1229701	NM_020975.6(RET):c.73+9331A>G	LOC110121502, MCS+9.7 +1 more	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1189903	NM_020975.6(RET):c.73+9385_73+9395del	LOC110121502, MCS+9.7 +1 more	Deletion (intron variant)	Multiple endocrine neoplasia, type 2 +1 more	GBenign/Likely benign
Select item 695195	NM_020975.6(RET):c.73+9494A>C	LOC110121502, MCS+9.7 +1 more	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
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 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 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 405538	NM_020975.6(RET):c.134C>T (p.Ala45Val)	RET (A45V)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +8 more	GUncertain significance
Select item 13940	NM_020975.6(RET):c.135= (p.Ala45=)	RET	Single nucleotide variant (synonymous variant +2 more)	Multiple endocrine neoplasia, type 2 +2 more	GBenign
Select item 819219	NM_020975.6(RET):c.143C>T (p.Thr48Met)	RET (T48M)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 215905	NM_020975.6(RET):c.144G>A (p.Thr48=)	RET	Single nucleotide variant (synonymous variant +1 more)	not provided +7 more	GLikely benign
Select item 1406391	NM_020975.6(RET):c.161A>G (p.His54Arg)	RET (H54R)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 36723	NM_020975.6(RET):c.166C>A (p.Leu56Met)	RET (L56M)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +8 more	GConflicting classifications of pathogenicity
Select item 423343	NM_020975.6(RET):c.175G>A (p.Ala59Thr)	RET (A59T)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +3 more	GConflicting classifications of pathogenicity
Select item 1449642	NM_020975.6(RET):c.179C>T (p.Pro60Leu)	RET (P60L)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 477338	NM_020975.6(RET):c.204G>T (p.Leu68=)	RET	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
Select item 569870	NM_020975.6(RET):c.224C>T (p.Thr75Met)	RET (T75M)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 184368	NM_020975.6(RET):c.225G>A (p.Thr75=)	RET	Single nucleotide variant (synonymous variant +1 more)	Multiple endocrine neoplasia type 2B +8 more	GConflicting classifications of pathogenicity
Select item 477344	NM_020975.6(RET):c.230G>A (p.Arg77His)	RET (R77H)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +2 more	GConflicting classifications of pathogenicity
Select item 405541	NM_020975.6(RET):c.235C>T (p.Arg79Trp)	RET (R79W)	Single nucleotide variant (missense variant)	not provided +6 more	GConflicting classifications of pathogenicity
Select item 477345	NM_020975.6(RET):c.236G>A (p.Arg79Gln)	RET (R79Q)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia type 2B +7 more	GConflicting classifications of pathogenicity
Select item 188305	NM_020975.6(RET):c.262A>G (p.Ile88Val)	RET (I88V)	Single nucleotide variant (missense variant)	not provided +5 more	GConflicting classifications of pathogenicity
Select item 1389003	NM_020975.6(RET):c.265C>A (p.Gln89Lys)	RET (Q89K)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +2 more	GUncertain significance
Select item 1493320	NM_020975.6(RET):c.274A>G (p.Thr92Ala)	RET (T92A)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +2 more	GUncertain significance
Select item 1063665	NM_020975.6(RET):c.319G>A (p.Glu107Lys)	RET (E107K)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +1 more	GUncertain significance
Select item 136120	NM_020975.6(RET):c.335G>A (p.Arg112His)	RET (R112H)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 95996	NM_020975.6(RET):c.337+9G>A	RET	Single nucleotide variant (intron variant)	not provided +9 more	GBenign/Likely benign
Select item 299887	NM_020975.6(RET):c.337+12G>A	RET	Single nucleotide variant (intron variant)	Multiple endocrine neoplasia, type 2 +9 more	GBenign/Likely benign
Select item 677056	NM_020975.6(RET):c.337+137G>T	RET	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1189719	NM_020975.6(RET):c.337+196G>A	RET	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 676895	NM_020975.6(RET):c.337+247C>T	RET	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1223741	NM_020975.6(RET):c.337+258G>T	RET	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 676909	NM_020975.6(RET):c.338-201C>G	RET	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1254437	NM_020975.6(RET):c.338-174_338-162del	RET	Deletion (intron variant)	not provided	GLikely benign
Select item 1293633	NM_020975.6(RET):c.338-106G>A	RET	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 13947	NM_020975.6(RET):c.341G>A (p.Arg114His)	RET (R114H)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +8 more	GBenign/Likely benign
Select item 373412	NM_020975.6(RET):c.361G>A (p.Val121Ile)	RET (V121I)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +2 more	GConflicting classifications of pathogenicity
Select item 95997	NM_020975.6(RET):c.375C>A (p.Val125=)	RET	Single nucleotide variant (synonymous variant +1 more)	Renal hypodysplasia/aplasia 1 +8 more	GBenign/Likely benign
Select item 141671	NM_020975.6(RET):c.405C>T (p.Gly135=)	RET	Single nucleotide variant (synonymous variant +1 more)	RET-related disorder +4 more	GConflicting classifications of pathogenicity
Select item 216727	NM_020975.6(RET):c.406G>A (p.Glu136Lys)	RET (E136K)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +8 more	GConflicting classifications of pathogenicity
Select item 216729	NM_020975.6(RET):c.431G>A (p.Arg144His)	RET (R144H)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia type 2A +7 more	GUncertain significance
Select item 2916120	NM_020975.6(RET):c.443_445del (p.Ser148del)	RET (S148del)	Deletion (inframe_indel +2 more)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 1016306	NM_020975.6(RET):c.445TTC[1] (p.Phe150del)	RET (F150del)	Microsatellite (inframe_indel +1 more)	Hirschsprung disease, susceptibility to, 1 +7 more	GUncertain significance
Select item 1502247	NM_020975.6(RET):c.451A>G (p.Asn151Asp)	RET (N151D)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 486321	NM_020975.6(RET):c.452A>G (p.Asn151Ser)	RET (N151S)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +7 more	GConflicting classifications of pathogenicity
Select item 215531	NM_020975.6(RET):c.468C>T (p.Ala156=)	RET	Single nucleotide variant (synonymous variant +1 more)	not provided +8 more	GBenign/Likely benign
Select item 486343	NM_020975.6(RET):c.478C>T (p.Leu160Phe)	RET (L160F +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 1480894	NM_020975.6(RET):c.485C>A (p.Pro162His)	RET (P162H +1 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +2 more	GUncertain significance
Select item 477377	NM_020975.6(RET):c.487C>A (p.Arg163=)	RET	Single nucleotide variant (synonymous variant +1 more)	not provided +6 more	GConflicting classifications of pathogenicity
Select item 2574749	NM_020975.6(RET):c.488G>T (p.Arg163Leu)	RET (R120L +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2497782	NM_020975.6(RET):c.499T>G (p.Phe167Val)	RET (F124V +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 41844	NM_020975.6(RET):c.509C>T (p.Thr170Ile)	RET (T170I +1 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia type 2A +4 more	GUncertain significance
Select item 641521	NM_020975.6(RET):c.523C>G (p.Arg175Gly)	RET (R175G +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 381592	NM_020975.6(RET):c.523C>T (p.Arg175Cys)	RET (R175C +1 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +2 more	GUncertain significance
Select item 405526	NM_020975.6(RET):c.529C>T (p.Arg177Trp)	RET (R177W +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 405549	NM_020975.6(RET):c.530G>A (p.Arg177Gln)	RET (R177Q +1 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +3 more	GConflicting classifications of pathogenicity
Select item 505008	NM_020975.6(RET):c.544C>A (p.Pro182Thr)	RET (P182T +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 2568329	NM_020975.6(RET):c.545C>T (p.Pro182Leu)	RET (P139L +1 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 136121	NM_020975.6(RET):c.597C>T (p.Asn199=)	RET	Single nucleotide variant (synonymous variant +1 more)	Pheochromocytoma +7 more	GConflicting classifications of pathogenicity
Select item 560871	NM_020975.6(RET):c.602G>C (p.Ser201Thr)	RET (S201T +1 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +7 more	GConflicting classifications of pathogenicity
Select item 184536	NM_020975.6(RET):c.604G>A (p.Val202Met)	RET (V202M +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +9 more	GUncertain significance
Select item 677057	NM_020975.6(RET):c.625+118A>G	RET	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 679372	NM_020975.6(RET):c.625+139C>T	RET	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1216495	NM_020975.6(RET):c.626-189_626-180del	RET	Deletion (intron variant)	not provided	GLikely benign
Select item 1208843	NM_020975.6(RET):c.626-151G>A	RET	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GLikely benign
Select item 1175432	NM_020975.6(RET):c.626-72_626-71del	RET	Deletion (intron variant +1 more)	not provided	GBenign
Select item 405554	NM_020975.6(RET):c.628G>A (p.Glu210Lys)	RET (E210K +2 more)	Single nucleotide variant (missense variant)	Pheochromocytoma +7 more	GUncertain significance
Select item 405525	NM_020975.6(RET):c.650C>A (p.Ala217Asp)	RET (A217D +2 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +8 more	GUncertain significance
Select item 1754100	NM_020975.6(RET):c.653C>G (p.Pro218Arg)	RET (P175R +2 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +2 more	GUncertain significance
Select item 220254	NM_020975.6(RET):c.654G>A (p.Pro218=)	RET	Single nucleotide variant (synonymous variant +2 more)	Multiple endocrine neoplasia +7 more	GBenign/Likely benign
Select item 1011103	NM_020975.6(RET):c.664G>A (p.Glu222Lys)	RET (E222K +2 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +2 more	GUncertain significance
Select item 1755230	NM_020975.6(RET):c.674C>T (p.Thr225Met)	RET (T225M +2 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +2 more	GUncertain significance

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