List of variants in gene RET reported as likely benign for Multiple endocrine neoplasia, type 2b

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 33

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.1336G>C (p.Gly446Arg)	rs115423919	0.00238
NM_020975.6(RET):c.337+12G>A	rs200468424	0.00198
NM_020975.6(RET):c.2372A>T (p.Tyr791Phe)	rs77724903	0.00178
NM_020975.6(RET):c.1197G>A (p.Pro399=)	rs148371113	0.00108
NM_020975.6(RET):c.225G>A (p.Thr75=)	rs151267865	0.00052
NM_020975.6(RET):c.337+34C>T	rs368088467	0.00022
NM_020975.6(RET):c.1017G>A (p.Ser339=)	rs369810881	0.00014
NM_020975.6(RET):c.1437C>T (p.Ala479=)	rs576806356	0.00011
NM_020975.6(RET):c.1522+35C>T	rs377130948	0.00011
NM_020975.6(RET):c.1879+17C>T	rs369920430	0.00010
NM_020975.6(RET):c.3243T>C (p.Asp1081=)	rs144192900	0.00010
NM_020975.6(RET):c.1530C>T (p.Ala510=)	rs553492964	0.00009
NM_020975.6(RET):c.2136+15G>A	rs751183869	0.00009
NM_020975.6(RET):c.1879+13C>T	rs375573788	0.00008
NM_020975.6(RET):c.1182C>T (p.Asn394=)	rs376465385	0.00007
NM_020975.6(RET):c.2409C>T (p.Ile803=)	rs535051804	0.00006
NM_020975.6(RET):c.337+29G>A	rs578158807	0.00005
NM_020975.6(RET):c.693C>T (p.Arg231=)	rs576806329	0.00004
NM_020975.6(RET):c.1013C>T (p.Thr338Ile)	rs377767433	0.00003
NM_020975.6(RET):c.2298G>A (p.Pro766=)	rs140658743	0.00003
NM_020975.6(RET):c.582G>A (p.Gln194=)	rs368116579	0.00003
NM_020975.6(RET):c.1095G>A (p.Ser365=)	rs201992974	0.00002
NM_020975.6(RET):c.1264-4C>T	rs587780806	0.00002
NM_020975.6(RET):c.2226G>A (p.Thr742=)	rs762876946	0.00002
NM_020975.6(RET):c.1539G>A (p.Ala513=)	rs761430718	0.00001
NM_020975.6(RET):c.1648+24G>A	rs1057517640	0.00001
NM_020975.6(RET):c.1908G>A (p.Thr636=)	rs886038663	0.00001
NM_020975.6(RET):c.3057G>A (p.Ala1019=)	rs369579749	0.00001
NM_020975.6(RET):c.322A>C (p.Lys108Gln)	rs567877611	0.00001
NM_020975.6(RET):c.1866C>T (p.Pro622=)	rs201979255
NM_020975.6(RET):c.2554A>G (p.Ile852Val)	rs561276725
NM_020975.6(RET):c.3040-11C>G	rs1057517646
NM_020975.6(RET):c.951G>A (p.Thr317=)	rs375812189

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