List of variants in gene RET reported as benign by Ambry Genetics

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: 48

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.1296A>G (p.Ala432=)	rs1800860	0.74268
NM_020975.6(RET):c.337+9G>A	rs2435351	0.20641
NM_020975.6(RET):c.2712C>G (p.Ser904=)	rs1800863	0.17043
NM_020975.6(RET):c.2071G>A (p.Gly691Ser)	rs1799939	0.16640
NM_020975.6(RET):c.2508C>T (p.Ser836=)	rs1800862	0.03791
NM_020975.6(RET):c.1264-5C>T	rs9282835	0.02749
NM_020975.6(RET):c.2944C>T (p.Arg982Cys)	rs17158558	0.01567
NM_020975.6(RET):c.375C>A (p.Val125=)	rs1800859	0.00877
NM_020975.6(RET):c.166C>A (p.Leu56Met)	rs145633958	0.00310
NM_020975.6(RET):c.1336G>C (p.Gly446Arg)	rs115423919	0.00238
NM_020975.6(RET):c.1465G>A (p.Asp489Asn)	rs9282834	0.00068
NM_020975.6(RET):c.833C>A (p.Thr278Asn)	rs35118262	0.00056
NM_020975.6(RET):c.1354C>A (p.Leu452Ile)	rs151148041	0.00043
NM_020975.6(RET):c.200G>A (p.Arg67His)	rs192489011	0.00036
NM_020975.6(RET):c.341G>A (p.Arg114His)	rs76397662	0.00029
NM_020975.6(RET):c.874G>A (p.Val292Met)	rs34682185	0.00023
NM_020975.6(RET):c.2522C>T (p.Pro841Leu)	rs149891333	0.00015
NM_020975.6(RET):c.398G>A (p.Arg133His)	rs138265837	0.00012
NM_020975.6(RET):c.2611G>A (p.Val871Ile)	rs145170911	0.00008
NM_020975.6(RET):c.1942G>A (p.Val648Ile)	rs77711105	0.00007
NM_020975.6(RET):c.82G>A (p.Gly28Ser)	rs779905135	0.00007
NM_020975.6(RET):c.1150C>G (p.Pro384Ala)	rs536298339	0.00006
NM_020975.6(RET):c.1649-4G>A	rs369769303	0.00006
NM_020975.6(RET):c.2116G>A (p.Val706Met)	rs137855422	0.00006
NM_020975.6(RET):c.1363G>A (p.Val455Ile)	rs145966037	0.00005
NM_020975.6(RET):c.2001A>T (p.Pro667=)	rs563316790	0.00004
NM_020975.6(RET):c.2290G>A (p.Ala764Thr)	rs748799148	0.00004
NM_020975.6(RET):c.1867G>A (p.Glu623Lys)	rs377767402	0.00003
NM_020975.6(RET):c.2285-4T>G	rs376601566	0.00003
NM_020975.6(RET):c.270G>A (p.Glu90=)	rs755967110	0.00003
NM_020975.6(RET):c.626-4G>A	rs775956924	0.00003
NM_020975.6(RET):c.1253G>A (p.Arg418Gln)	rs371731991	0.00002
NM_020975.6(RET):c.1264-4C>T	rs587780806	0.00002
NM_020975.6(RET):c.2488G>A (p.Gly830Arg)	rs200127630	0.00002
NM_020975.6(RET):c.304G>A (p.Asp102Asn)	rs201244749	0.00002
NM_020975.6(RET):c.3200C>T (p.Pro1067Leu)	rs760625882	0.00002
NM_020975.6(RET):c.488G>A (p.Arg163Gln)	rs149403911	0.00002
NM_020975.6(RET):c.1618A>G (p.Arg540Gly)	rs543376293	0.00001
NM_020975.6(RET):c.2005A>G (p.Ile669Val)	rs776986585	0.00001
NM_020975.6(RET):c.2246G>C (p.Arg749Thr)	rs34288963	0.00001
NM_020975.6(RET):c.235C>T (p.Arg79Trp)	rs537523906	0.00001
NM_020975.6(RET):c.322A>C (p.Lys108Gln)	rs567877611	0.00001
NM_020975.6(RET):c.1840GAG[2] (p.Glu616del)	rs377767399
NM_020975.6(RET):c.2030G>A (p.Arg677Gln)	rs536038262
NM_020975.6(RET):c.2531G>A (p.Arg844Gln)	rs55947360
NM_020975.6(RET):c.2554A>G (p.Ile852Val)	rs561276725
NM_020975.6(RET):c.624G>T (p.Glu208Asp)	rs781750106
NM_020975.6(RET):c.960C>T (p.Pro320=)	rs756761746

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