ClinVar Miner

List of variants in gene RET reported as not provided

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Gene type:
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Total variants: 29
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HGVS dbSNP
NM_020630.4(RET):c.1049C>T (p.Thr350Ile) rs587778660
NM_020630.4(RET):c.135G= (p.Ala45=) rs1800858
NM_020630.4(RET):c.1424G>A (p.Arg475Gln) rs138624658
NM_020630.4(RET):c.200G>A (p.Arg67His) rs192489011
NM_020630.4(RET):c.3116C>A (p.Pro1039Gln) rs79853121
NM_020630.4(RET):c.488G>A (p.Arg163Gln) rs149403911
NM_020630.5(RET):c.135A= (p.Ala45=) rs1800858
NM_020630.5(RET):c.874G>A (p.Val292Met) rs34682185
NM_020975.4(RET):c.1157C>T (p.Ala386Val) rs115272158
NM_020975.4(RET):c.1296A>G (p.Ala432=) rs1800860
NM_020975.4(RET):c.1336G>C (p.Gly446Arg) rs115423919
NM_020975.4(RET):c.1465G>A (p.Asp489Asn) rs9282834
NM_020975.4(RET):c.1573C>T (p.Arg525Trp) rs545625150
NM_020975.4(RET):c.166C>A (p.Leu56Met) rs145633958
NM_020975.4(RET):c.1826G>A (p.Cys609Tyr) rs77939446
NM_020975.4(RET):c.1896_1897delGCinsCG (p.Glu632_Leu633delinsAspVal) rs267607009
NM_020975.4(RET):c.1946C>T (p.Ser649Leu) rs148935214
NM_020975.4(RET):c.2071G>A (p.Gly691Ser) rs1799939
NM_020975.4(RET):c.2261C>T (p.Thr754Met) rs181856591
NM_020975.4(RET):c.2348A>C (p.Asn783Thr) rs587778656
NM_020975.4(RET):c.2875C>T (p.Arg959Trp) rs587778658
NM_020975.4(RET):c.2944C>T (p.Arg982Cys) rs17158558
NM_020975.4(RET):c.304G>A (p.Asp102Asn) rs201244749
NM_020975.4(RET):c.3185A>G (p.Tyr1062Cys) rs587778659
NM_020975.4(RET):c.337+9G>A rs2435351
NM_020975.4(RET):c.341G>A (p.Arg114His) rs76397662
NM_020975.4(RET):c.833C>A (p.Thr278Asn) rs35118262
NM_020975.5(RET):c.2432C>G (p.Ser811Cys) rs587778657
NM_020975.6(RET):c.1438G>A (p.Glu480Lys) rs537874538

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