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

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 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 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 864094	NM_020975.6(RET):c.178C>T (p.Pro60Ser)	RET (P60S)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +6 more	GUncertain significance
Select item 997535	NM_020975.6(RET):c.199C>G (p.Arg67Gly)	RET (R67G)	Single nucleotide variant (missense variant)	Hirschsprung disease, susceptibility to, 1	GUncertain significance
Select item 477335	NM_020975.6(RET):c.199C>T (p.Arg67Cys)	RET (R67C)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +6 more	GUncertain significance
Select item 570756	NM_020975.6(RET):c.266A>G (p.Gln89Arg)	RET (Q89R)	Single nucleotide variant (missense variant)	Hirschsprung disease, susceptibility to, 1 +2 more	GUncertain significance
Select item 216726	NM_020975.6(RET):c.334C>T (p.Arg112Cys)	RET (R112C)	Single nucleotide variant (missense variant)	Renal hypodysplasia/aplasia 1 +7 more	GUncertain significance
Select item 543735	NM_020975.6(RET):c.350C>A (p.Pro117His)	RET (P117H)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +6 more	GUncertain significance
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 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 477375	NM_020975.6(RET):c.464C>A (p.Pro155Gln)	RET (P155Q)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 2138848	NM_020975.6(RET):c.485C>G (p.Pro162Arg)	RET (P162R +1 more)	Single nucleotide variant (missense variant)	Hirschsprung disease, susceptibility to, 1 +2 more	GUncertain significance
Select item 992568	NM_020975.6(RET):c.487C>T (p.Arg163Trp)	RET (R163W +1 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +2 more	GUncertain significance
Select item 3240303	NM_020975.6(RET):c.518C>T (p.Ser173Phe)	RET (S130F +1 more)	Single nucleotide variant (missense variant +1 more)	Hirschsprung disease, susceptibility to, 1	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 161360	NM_020975.6(RET):c.539G>A (p.Arg180Gln)	RET (R180Q +1 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +6 more	GConflicting classifications of pathogenicity
Select item 188067	NM_020975.6(RET):c.548G>A (p.Gly183Asp)	RET (G183D +1 more)	Single nucleotide variant (missense variant)	Hirschsprung disease, susceptibility to, 1 +6 more	GUncertain significance
Select item 1748837	NM_020975.6(RET):c.564C>A (p.Phe188Leu)	RET (F145L +1 more)	Single nucleotide variant (missense variant)	Hirschsprung disease, susceptibility to, 1 +2 more	GUncertain significance
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 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 826412	NM_020975.6(RET):c.644G>A (p.Arg215His)	RET (R215H +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 2973642	NM_020975.6(RET):c.647G>A (p.Cys216Tyr)	RET (C120Y +2 more)	Single nucleotide variant (missense variant +2 more)	Multiple endocrine neoplasia, type 2 +1 more	GUncertain significance
Select item 1450795	NM_020975.6(RET):c.657C>G (p.Asp219Glu)	RET (D219E +2 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +2 more	GUncertain significance
Select item 968066	NM_020975.6(RET):c.677G>C (p.Arg226Pro)	RET (R226P +2 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia type 2A +6 more	GUncertain significance
Select item 662310	NM_020975.6(RET):c.701G>A (p.Arg234Gln)	RET (R234Q +2 more)	Single nucleotide variant (missense variant)	Pheochromocytoma +7 more	GConflicting classifications of pathogenicity
Select item 2678316	NM_020975.6(RET):c.712G>C (p.Glu238Gln)	RET (E142Q +2 more)	Single nucleotide variant (missense variant +2 more)	Hirschsprung disease, susceptibility to, 1	GUncertain significance
Select item 477383	NM_020975.6(RET):c.718G>C (p.Val240Leu)	RET (V240L +2 more)	Single nucleotide variant (missense variant)	Renal hypodysplasia/aplasia 1 +5 more	GConflicting classifications of pathogenicity
Select item 486315	NM_020975.6(RET):c.736C>A (p.His246Asn)	RET (H246N +2 more)	Single nucleotide variant (missense variant)	Hirschsprung disease, susceptibility to, 1 +7 more	GConflicting classifications of pathogenicity
Select item 2678318	NM_020975.6(RET):c.737A>T (p.His246Leu)	RET (H150L +2 more)	Single nucleotide variant (missense variant +2 more)	Hirschsprung disease, susceptibility to, 1	GUncertain significance
Select item 136124	NM_020975.6(RET):c.757G>A (p.Val253Met)	RET (V253M +2 more)	Single nucleotide variant (missense variant)	Hirschsprung disease, susceptibility to, 1 +2 more	GConflicting classifications of pathogenicity
Select item 1759791	NM_020975.6(RET):c.760G>T (p.Val254Leu)	RET (V211L +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 543748	NM_020975.6(RET):c.796G>A (p.Asp266Asn)	RET (D266N +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +2 more	GUncertain significance
Select item 576885	NM_020975.6(RET):c.826G>T (p.Val276Phe)	RET (V276F +3 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 2061872	NM_020975.6(RET):c.830A>G (p.Asp277Gly)	RET (D23G +3 more)	Single nucleotide variant (missense variant)	Hirschsprung disease, susceptibility to, 1 +1 more	GUncertain significance
Select item 1763538	NM_020975.6(RET):c.847G>C (p.Val283Leu)	RET (V29L +3 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1765018	NM_020975.6(RET):c.889C>T (p.Arg297Cys)	RET (R254C +3 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 486328	NM_020975.6(RET):c.920C>T (p.Ser307Leu)	RET (S307L +3 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 477391	NM_020975.6(RET):c.943A>C (p.Thr315Pro)	RET (T315P +3 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 578566	NM_020975.6(RET):c.950C>T (p.Thr317Met)	RET (T317M +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +3 more	GUncertain significance
Select item 24881	NM_020975.6(RET):c.961G>A (p.Gly321Arg)	RET (G67R +2 more)	Single nucleotide variant (missense variant)	not provided +7 more	GConflicting classifications of pathogenicity
Select item 188078	NM_020975.6(RET):c.972G>C (p.Trp324Cys)	RET (W324C +3 more)	Single nucleotide variant (missense variant)	not provided +8 more	GConflicting classifications of pathogenicity
Select item 477393	NM_020975.6(RET):c.973G>A (p.Ala325Thr)	RET (A325T +3 more)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 216731	NM_020975.6(RET):c.977A>G (p.Gln326Arg)	RET (Q326R +3 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +7 more	GUncertain significance
Select item 2678315	NM_020975.6(RET):c.983C>T (p.Thr328Ile)	RET (T232I +3 more)	Single nucleotide variant (missense variant +1 more)	Hirschsprung disease, susceptibility to, 1	GUncertain significance
Select item 657732	NM_020975.6(RET):c.1008C>G (p.Asn336Lys)	RET (N336K +3 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 432780	NM_020975.6(RET):c.1009G>A (p.Glu337Lys)	RET (E337K +3 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 38594	NM_020975.6(RET):c.1013C>T (p.Thr338Ile)	RET (T338I +3 more)	Single nucleotide variant (missense variant)	not provided +5 more	GConflicting classifications of pathogenicity
Select item 838975	NM_020975.6(RET):c.1030G>A (p.Gly344Ser)	RET (G344S +3 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 822070	NM_020975.6(RET):c.1039G>A (p.Val347Met)	RET (V347M +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +2 more	GUncertain significance
Select item 219791	NM_020975.6(RET):c.1052T>A (p.Val351Glu)	RET (V351E +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia type 2A +4 more	GConflicting classifications of pathogenicity
Select item 666109	NM_020975.6(RET):c.1063A>G (p.Arg355Gly)	RET (R101G +3 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +3 more	GConflicting classifications of pathogenicity
Select item 543747	NM_020975.6(RET):c.1079G>A (p.Arg360Gln)	RET (R360Q +6 more)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 548864	NM_020975.6(RET):c.1083C>A (p.Asn361Lys)	RET (N361K +6 more)	Single nucleotide variant (missense variant)	not provided +6 more	GUncertain significance
Select item 477303	NM_020975.6(RET):c.1090A>G (p.Ile364Val)	RET (I364V +6 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 567350	NM_020975.6(RET):c.1094C>T (p.Ser365Leu)	RET (S365L +6 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 486314	NM_020975.6(RET):c.1102C>T (p.Arg368Cys)	RET (R368C +6 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +7 more	GConflicting classifications of pathogenicity
Select item 216712	NM_020975.6(RET):c.1103G>A (p.Arg368His)	RET (R368H +6 more)	Single nucleotide variant (missense variant)	Hirschsprung disease, susceptibility to, 1 +7 more	GUncertain significance
Select item 220574	NM_020975.6(RET):c.1124T>A (p.Leu375Gln)	RET (L375Q +6 more)	Single nucleotide variant (missense variant)	Congenital central hypoventilation +4 more	GConflicting classifications of pathogenicity
Select item 405529	NM_020975.6(RET):c.1151C>G (p.Pro384Arg)	RET (P384R +6 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +8 more	GUncertain significance
Select item 405539	NM_020975.6(RET):c.1165C>T (p.Leu389Phe)	RET (L389F +6 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +5 more	GConflicting classifications of pathogenicity
Select item 372081	NM_020975.6(RET):c.1187C>T (p.Ser396Leu)	RET (S396L +6 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +5 more	GUncertain significance
Select item 224354	NM_020975.6(RET):c.1201A>T (p.Ser401Cys)	RET (S401C +6 more)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 1327060	NM_020975.6(RET):c.1232C>G (p.Ser411Cys)	RET (S157C +6 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +2 more	GUncertain significance
Select item 219872	NM_020975.6(RET):c.1253G>A (p.Arg418Gln)	RET (R418Q +6 more)	Single nucleotide variant (missense variant)	Hirschsprung disease, susceptibility to, 1 +7 more	GConflicting classifications of pathogenicity
Select item 220306	NM_020975.6(RET):c.1264-5C>G	RET	Single nucleotide variant (intron variant)	Multiple endocrine neoplasia, type 2 +1 more	GConflicting classifications of pathogenicity
Select item 570796	NM_020975.6(RET):c.1277G>A (p.Cys426Tyr)	RET (C426Y +8 more)	Single nucleotide variant (missense variant)	Hirschsprung disease, susceptibility to, 1 +4 more	GUncertain significance
Select item 664592	NM_020975.6(RET):c.1282G>A (p.Glu428Lys)	RET (E428K +8 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 1769192	NM_020975.6(RET):c.1295C>T (p.Ala432Val)	RET (A102V +8 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia type 2A +4 more	GUncertain significance
Select item 2678319	NM_020975.6(RET):c.1303G>A (p.Gly435Ser)	RET (G105S +8 more)	Single nucleotide variant (missense variant +1 more)	Multiple endocrine neoplasia, type 2 +1 more	GUncertain significance
Select item 136098	NM_020975.6(RET):c.1344C>G (p.Asn448Lys)	RET (N448K +8 more)	Single nucleotide variant (missense variant)	Hirschsprung disease, susceptibility to, 1 +8 more	GConflicting classifications of pathogenicity
Select item 187665	NM_020975.6(RET):c.1352C>T (p.Thr451Met)	RET (T451M +8 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 405546	NM_020975.6(RET):c.1375G>A (p.Glu459Lys)	RET (E459K +8 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +6 more	GUncertain significance
Select item 432998	NM_020975.6(RET):c.1399G>C (p.Val467Leu)	RET (V467L +8 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia type 2A +7 more	GUncertain significance
Select item 1461344	NM_020975.6(RET):c.1412A>C (p.Lys471Thr)	RET (K217T +8 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +1 more	GUncertain significance
Select item 299892	NM_020975.6(RET):c.1420C>T (p.Arg474Trp)	RET (R474W +8 more)	Single nucleotide variant (missense variant)	Pheochromocytoma +8 more	GConflicting classifications of pathogenicity
Select item 572175	NM_020975.6(RET):c.1423C>T (p.Arg475Trp)	RET (R475W +8 more)	Single nucleotide variant (missense variant)	Familial medullary thyroid carcinoma +7 more	GUncertain significance
Select item 135188	NM_020975.6(RET):c.1424G>A (p.Arg475Gln)	RET (R475Q +8 more)	Single nucleotide variant (missense variant)	Hirschsprung disease, susceptibility to, 1 +4 more	GUncertain significance
Select item 845362	NM_020975.6(RET):c.1440A>T (p.Glu480Asp)	RET (E226D +8 more)	Single nucleotide variant (missense variant)	Hirschsprung disease, susceptibility to, 1 +2 more	GUncertain significance
Select item 405534	NM_020975.6(RET):c.1448A>G (p.Tyr483Cys)	RET (Y483C +8 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +7 more	GUncertain significance
Select item 486306	NM_020975.6(RET):c.1493C>T (p.Ala498Val)	RET (A498V +8 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +7 more	GUncertain significance
Select item 477319	NM_020975.6(RET):c.1567A>C (p.Lys523Gln)	RET (K523Q +12 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 571739	NM_020975.6(RET):c.1573C>G (p.Arg525Gly)	RET (R525G +12 more)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 1775944	NM_020975.6(RET):c.1592G>A (p.Cys531Tyr)	RET (C277Y +12 more)	Single nucleotide variant (missense variant)	Hirschsprung disease, susceptibility to, 1 +1 more	GUncertain significance
Select item 24887	NM_020975.6(RET):c.1597G>A (p.Gly533Ser)	RET (G279S +11 more)	Single nucleotide variant (missense variant)	not provided +8 more	GConflicting classifications of pathogenicity
Select item 877094	NM_020975.6(RET):c.1601T>C (p.Leu534Pro)	RET (L534P +12 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +5 more	GUncertain significance
Select item 1312671	NM_020975.6(RET):c.1633C>A (p.Gln545Lys)	RET (Q291K +12 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +2 more	GUncertain significance
Select item 136102	NM_020975.6(RET):c.1642G>A (p.Gly548Ser)	RET (G548S +12 more)	Single nucleotide variant (missense variant)	Hirschsprung disease, susceptibility to, 1 +7 more	GConflicting classifications of pathogenicity
Select item 220113	NM_020975.6(RET):c.1678C>T (p.Pro560Ser)	RET (P560S +12 more)	Single nucleotide variant (missense variant)	Hirschsprung disease, susceptibility to, 1 +3 more	GConflicting classifications of pathogenicity
Select item 665308	NM_020975.6(RET):c.1681A>C (p.Ser561Arg)	RET (S561R +12 more)	Single nucleotide variant (missense variant)	Hirschsprung disease, susceptibility to, 1 +2 more	GUncertain significance
Select item 477325	NM_020975.6(RET):c.1756C>T (p.Leu586Phe)	RET (L586F +12 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +2 more	GUncertain significance
Select item 966506	NM_020975.6(RET):c.1783G>A (p.Glu595Lys)	RET (E595K +12 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +2 more	GUncertain significance
Select item 3240304	NM_020975.6(RET):c.1820G>A (p.Gly607Asp)	RET (G124D +12 more)	Single nucleotide variant (missense variant +1 more)	Hirschsprung disease, susceptibility to, 1	GUncertain significance
Select item 13933	NM_020975.6(RET):c.1826G>A (p.Cys609Tyr)	RET (C609Y +12 more)	Single nucleotide variant (missense variant)	Familial medullary thyroid carcinoma +5 more	GPathogenic
Select item 24913	NM_020975.6(RET):c.1891G>A (p.Asp631Asn)	RET (D631N +14 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +8 more	GConflicting classifications of pathogenicity
Select item 549831	NM_020975.6(RET):c.1893C>A (p.Asp631Glu)	RET (D631E +14 more)	Single nucleotide variant (missense variant)	not specified +3 more	GUncertain significance

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