ClinVar Miner

List of variants in gene RET reported by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 105
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HGVS dbSNP gnomAD frequency
NM_020975.6(RET):c.2944C>T (p.Arg982Cys) rs17158558 0.01651
NM_020975.6(RET):c.375C>A (p.Val125=) rs1800859 0.00877
NM_020975.6(RET):c.2137-744A>G rs564936051 0.00606
NM_020975.6(RET):c.2137-384C>T rs189038012 0.00494
NM_020975.6(RET):c.2284+46G>C rs147601354 0.00420
NM_020975.6(RET):c.166C>A (p.Leu56Met) rs145633958 0.00310
NM_020975.6(RET):c.337+12G>A rs200468424 0.00198
NM_020975.6(RET):c.2136+437T>C rs181457644 0.00189
NM_020975.6(RET):c.2372A>T (p.Tyr791Phe) rs77724903 0.00178
NM_020975.6(RET):c.*1130A>G rs572936041 0.00129
NM_020975.6(RET):c.2136+272G>A rs768973064 0.00120
NM_020975.6(RET):c.2136+151G>A rs528995550 0.00109
NM_020975.6(RET):c.2137-396G>A rs568899039 0.00082
NM_020975.6(RET):c.1119G>A (p.Ala373=) rs113931414 0.00078
NM_020975.6(RET):c.*1430A>G rs775114955 0.00057
NM_020975.6(RET):c.833C>A (p.Thr278Asn) rs35118262 0.00056
NM_020975.6(RET):c.625+143C>T rs539080572 0.00051
NM_020975.6(RET):c.2136+763G>A rs555731175 0.00046
NM_020975.6(RET):c.1946C>T (p.Ser649Leu) rs148935214 0.00039
NM_020975.6(RET):c.2037C>T (p.Pro679=) rs55862116 0.00039
NM_020975.6(RET):c.341G>A (p.Arg114His) rs76397662 0.00039
NM_020975.6(RET):c.2137-251A>G rs991923171 0.00034
NM_020975.6(RET):c.1158G>A (p.Ala386=) rs373540097 0.00030
NM_020975.6(RET):c.2673G>A (p.Ser891=) rs201620214 0.00027
NM_020975.6(RET):c.785T>C (p.Val262Ala) rs139790943 0.00025
NM_020975.6(RET):c.2137-794T>C rs780700885 0.00024
NM_020975.6(RET):c.874G>A (p.Val292Met) rs34682185 0.00023
NM_020975.6(RET):c.2410G>A (p.Val804Met) rs79658334 0.00022
NM_020975.6(RET):c.1879+355G>A rs534767762 0.00021
NM_020975.6(RET):c.2052G>A (p.Pro684=) rs145122337 0.00019
NM_020975.6(RET):c.1531G>A (p.Glu511Lys) rs201553718 0.00018
NM_020975.6(RET):c.1017G>A (p.Ser339=) rs369810881 0.00014
NM_020975.6(RET):c.1063+9G>A rs765463636 0.00014
NM_020975.6(RET):c.1699G>A (p.Asp567Asn) rs147219360 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.1437C>T (p.Ala479=) rs576806356 0.00011
NM_020975.6(RET):c.1522+35C>T rs377130948 0.00011
NM_020975.6(RET):c.2556C>G (p.Ile852Met) rs377767426 0.00011
NM_020975.6(RET):c.957C>A (p.Leu319=) rs149926238 0.00011
NM_020975.6(RET):c.961G>A (p.Gly321Arg) rs377767388 0.00009
NM_020975.6(RET):c.1894G>A (p.Glu632Lys) rs377767407 0.00006
NM_020975.6(RET):c.1649-4G>A rs369769303 0.00005
NM_020975.6(RET):c.2393-9C>T rs567543719 0.00005
NM_020975.6(RET):c.2418C>T (p.Tyr806=) rs553418132 0.00005
NM_020975.6(RET):c.2268C>T (p.Ala756=) rs370791179 0.00004
NM_020975.6(RET):c.2298G>A (p.Pro766=) rs140658743 0.00004
NM_020975.6(RET):c.693C>T (p.Arg231=) rs576806329 0.00004
NM_020975.6(RET):c.79T>C (p.Leu27=) rs377160777 0.00004
NM_020975.6(RET):c.1908G>A (p.Thr636=) rs886038663 0.00003
NM_020975.6(RET):c.2392+19T>C rs778745375 0.00003
NM_020975.6(RET):c.335G>A (p.Arg112His) rs587780814 0.00003
NM_020975.6(RET):c.582G>A (p.Gln194=) rs368116579 0.00003
NM_020975.6(RET):c.1188G>A (p.Ser396=) rs758510657 0.00002
NM_020975.6(RET):c.1264-4C>T rs587780806 0.00002
NM_020975.6(RET):c.1326G>A (p.Leu442=) rs746055866 0.00002
NM_020975.6(RET):c.144G>A (p.Thr48=) rs759872307 0.00002
NM_020975.6(RET):c.1941C>T (p.Ile647=) rs75225191 0.00002
NM_020975.6(RET):c.825C>T (p.Gly275=) rs150797149 0.00002
NM_020975.6(RET):c.1029C>T (p.Asn343=) rs764668178 0.00001
NM_020975.6(RET):c.1221C>T (p.Thr407=) rs1222385123 0.00001
NM_020975.6(RET):c.1305C>T (p.Gly435=) rs749093977 0.00001
NM_020975.6(RET):c.1374C>T (p.Ala458=) rs190750926 0.00001
NM_020975.6(RET):c.1386G>A (p.Ser462=) rs587780807 0.00001
NM_020975.6(RET):c.1464C>T (p.Thr488=) rs921948385 0.00001
NM_020975.6(RET):c.159C>T (p.Val53=) rs753523209 0.00001
NM_020975.6(RET):c.1782C>T (p.His594=) rs863224426 0.00001
NM_020975.6(RET):c.1890C>T (p.Cys630=) rs781145070 0.00001
NM_020975.6(RET):c.1926C>G (p.Val642=) rs766962871 0.00001
NM_020975.6(RET):c.2370G>T (p.Leu790Phe) rs75030001 0.00001
NM_020975.6(RET):c.2679C>T (p.Phe893=) rs768188546 0.00001
NM_020975.6(RET):c.2832C>T (p.Ile944=) rs755606269 0.00001
NM_020975.6(RET):c.3057G>A (p.Ala1019=) rs369579749 0.00001
NM_020975.6(RET):c.3117G>A (p.Pro1039=) rs775773414 0.00001
NM_020975.6(RET):c.432C>T (p.Arg144=) rs756999107 0.00001
NM_020975.6(RET):c.628G>A (p.Glu210Lys) rs1060500762 0.00001
NM_020975.6(RET):c.*1046G>C rs143948954
NM_020975.6(RET):c.*500C>T rs564665995
NM_020975.6(RET):c.1215C>T (p.Pro405=) rs748588678
NM_020975.6(RET):c.1494C>T (p.Ala498=)
NM_020975.6(RET):c.1521A>G (p.Ser507=) rs876660561
NM_020975.6(RET):c.1521A>T (p.Ser507=) rs876660561
NM_020975.6(RET):c.1598G>C (p.Gly533Ala)
NM_020975.6(RET):c.1826G>T (p.Cys609Phe) rs77939446
NM_020975.6(RET):c.2136+509G>T rs146344379
NM_020975.6(RET):c.2137-166G>A rs529847759
NM_020975.6(RET):c.2284+54C>A rs566375223
NM_020975.6(RET):c.2304G>C (p.Glu768Asp) rs78014899
NM_020975.6(RET):c.2410G>C (p.Val804Leu) rs79658334
NM_020975.6(RET):c.2450G>T (p.Arg817Leu) rs1345166214
NM_020975.6(RET):c.2523G>T (p.Pro841=) rs56195026
NM_020975.6(RET):c.2531G>A (p.Arg844Gln) rs55947360
NM_020975.6(RET):c.2566T>C (p.Trp856Arg) rs1838163811
NM_020975.6(RET):c.2832C>G (p.Ile944Met) rs755606269
NM_020975.6(RET):c.3056C>T (p.Ala1019Val) rs1371891301
NM_020975.6(RET):c.3339T>C (p.Asp1113=) rs1198032104
NM_020975.6(RET):c.49C>T (p.Leu17=) rs1328756940
NM_020975.6(RET):c.625+23C>G
NM_020975.6(RET):c.723C>A (p.Ala241=) rs544252468
NM_020975.6(RET):c.810C>T (p.Pro270=) rs1160403666
NM_020975.6(RET):c.921A>G (p.Ser307=) rs748294306
NM_020975.6(RET):c.936G>A (p.Arg312=) rs1837778702
NM_020975.6(RET):c.952C>T (p.Leu318=) rs1235573033

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