List of variants in gene RET reported as uncertain significance by Mendelics

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: 42

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.1531G>A (p.Glu511Lys)	rs201553718	0.00018
NM_020975.6(RET):c.1642G>A (p.Gly548Ser)	rs374461212	0.00011
NM_020975.6(RET):c.961G>A (p.Gly321Arg)	rs377767388	0.00009
NM_020975.6(RET):c.2081G>A (p.Arg694Gln)	rs141185224	0.00008
NM_020975.6(RET):c.1597G>A (p.Gly533Ser)	rs75873440	0.00006
NM_020975.6(RET):c.2116G>A (p.Val706Met)	rs137855422	0.00006
NM_020975.6(RET):c.2527G>A (p.Glu843Lys)	rs755837568	0.00006
NM_020975.6(RET):c.452A>G (p.Asn151Ser)	rs150261092	0.00005
NM_020975.6(RET):c.1423C>T (p.Arg475Trp)	rs746512075	0.00004
NM_020975.6(RET):c.1438G>A (p.Glu480Lys)	rs537874538	0.00004
NM_020975.6(RET):c.2371T>A (p.Tyr791Asn)	rs377767417	0.00004
NM_020975.6(RET):c.2931C>G (p.Ser977Arg)	rs375414982	0.00004
NM_020975.6(RET):c.1013C>T (p.Thr338Ile)	rs377767433	0.00003
NM_020975.6(RET):c.134C>T (p.Ala45Val)	rs763526874	0.00002
NM_020975.6(RET):c.973G>A (p.Ala325Thr)	rs779719517	0.00002
NM_020975.6(RET):c.1183G>C (p.Val395Leu)	rs1452469572	0.00001
NM_020975.6(RET):c.1448A>G (p.Tyr483Cys)	rs752322996	0.00001
NM_020975.6(RET):c.1462A>T (p.Thr488Ser)	rs753733901	0.00001
NM_020975.6(RET):c.1760-3C>T	rs587781734	0.00001
NM_020975.6(RET):c.1907C>T (p.Thr636Met)	rs1035958105	0.00001
NM_020975.6(RET):c.2129A>G (p.Lys710Arg)	rs774983492	0.00001
NM_020975.6(RET):c.2234A>T (p.His745Leu)	rs534094626	0.00001
NM_020975.6(RET):c.3052C>T (p.Leu1018Phe)	rs766330880	0.00001
NM_020975.6(RET):c.3091G>A (p.Asp1031Asn)	rs200989078	0.00001
NM_020975.6(RET):c.3314C>T (p.Ala1105Val)	rs532862288	0.00001
NM_020975.6(RET):c.652C>T (p.Pro218Ser)	rs1009392744	0.00001
NM_020975.6(RET):c.1064-4G>T	rs1837849469
NM_020975.6(RET):c.1377G>T (p.Glu459Asp)	rs1564494424
NM_020975.6(RET):c.1466A>T (p.Asp489Val)	rs923351888
NM_020975.6(RET):c.1467C>A (p.Asp489Glu)	rs372648203
NM_020975.6(RET):c.1567A>C (p.Lys523Gln)	rs766278774
NM_020975.6(RET):c.1876C>A (p.Gln626Lys)	rs1255575160
NM_020975.6(RET):c.2090T>C (p.Leu697Pro)	rs1293039001
NM_020975.6(RET):c.2330A>G (p.Asn777Ser)	rs377767415
NM_020975.6(RET):c.2348A>C (p.Asn783Thr)	rs587778656
NM_020975.6(RET):c.2432C>G (p.Ser811Cys)	rs587778657
NM_020975.6(RET):c.2531G>A (p.Arg844Gln)	rs55947360
NM_020975.6(RET):c.2834T>C (p.Val945Ala)	rs1408196943
NM_020975.6(RET):c.3182T>C (p.Leu1061Pro)	rs536486113
NM_020975.6(RET):c.428C>T (p.Ala143Val)	rs1564490082
NM_020975.6(RET):c.44TGC[8] (p.Leu19_Pro20insLeuLeuLeu)	rs768132465
NM_020975.6(RET):c.938G>T (p.Arg313Leu)	rs77702891

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