List of variants in gene RET reported as likely benign by Color Diagnostics, LLC DBA Color Health

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: 31

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.166C>A (p.Leu56Met)	rs145633958	0.00310
NM_020975.6(RET):c.1124T>A (p.Leu375Gln)	rs142338976	0.00066
NM_020975.6(RET):c.262A>G (p.Ile88Val)	rs141679950	0.00056
NM_020975.6(RET):c.225G>A (p.Thr75=)	rs151267865	0.00052
NM_020975.6(RET):c.3112A>G (p.Thr1038Ala)	rs201740483	0.00047
NM_020975.6(RET):c.1946C>T (p.Ser649Leu)	rs148935214	0.00039
NM_020975.6(RET):c.1050C>T (p.Thr350=)	rs142188675	0.00029
NM_020975.6(RET):c.2673G>A (p.Ser891=)	rs201620214	0.00027
NM_020975.6(RET):c.1118C>T (p.Ala373Val)	rs546866208	0.00017
NM_020975.6(RET):c.1017G>A (p.Ser339=)	rs369810881	0.00014
NM_020975.6(RET):c.1701C>T (p.Asp567=)	rs201209972	0.00014
NM_020975.6(RET):c.1893C>T (p.Asp631=)	rs55846256	0.00013
NM_020975.6(RET):c.2988G>A (p.Pro996=)	rs145798106	0.00013
NM_020975.6(RET):c.597C>T (p.Asn199=)	rs55810667	0.00012
NM_020975.6(RET):c.3243T>C (p.Asp1081=)	rs144192900	0.00010
NM_020975.6(RET):c.1182C>T (p.Asn394=)	rs376465385	0.00009
NM_020975.6(RET):c.175G>A (p.Ala59Thr)	rs376565365	0.00006
NM_020975.6(RET):c.2427C>T (p.Tyr809=)	rs577929869	0.00005
NM_020975.6(RET):c.1064-6C>T	rs768878280	0.00004
NM_020975.6(RET):c.603C>T (p.Ser201=)	rs780120451	0.00004
NM_020975.6(RET):c.693C>T (p.Arg231=)	rs576806329	0.00004
NM_020975.6(RET):c.2358T>C (p.His786=)	rs758715544	0.00003
NM_020975.6(RET):c.1941C>T (p.Ile647=)	rs75225191	0.00002
NM_020975.6(RET):c.1161C>T (p.Gly387=)	rs763967472	0.00001
NM_020975.6(RET):c.1515G>A (p.Glu505=)	rs924204743	0.00001
NM_020975.6(RET):c.1890C>T (p.Cys630=)	rs781145070	0.00001
NM_020975.6(RET):c.2784C>T (p.Tyr928=)	rs779594537	0.00001
NM_020975.6(RET):c.333C>G (p.Val111=)	rs772779267	0.00001
NM_020975.6(RET):c.621G>A (p.Leu207=)	rs1343290853
NM_020975.6(RET):c.624G>T (p.Glu208Asp)	rs781750106
NM_020975.6(RET):c.828C>G (p.Val276=)	rs876660380

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