ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 59
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HGVS dbSNP gnomAD frequency
NM_020975.6(RET):c.2137-744A>G rs564936051 0.00606
NM_020975.6(RET):c.166C>A (p.Leu56Met) rs145633958 0.00310
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.2136+272G>A rs768973064 0.00121
NM_020975.6(RET):c.*1130A>G rs572936041 0.00112
NM_020975.6(RET):c.2137-396G>A rs568899039 0.00083
NM_020975.6(RET):c.1119G>A (p.Ala373=) rs113931414 0.00079
NM_020975.6(RET):c.*1430A>G rs775114955 0.00053
NM_020975.6(RET):c.1946C>T (p.Ser649Leu) rs148935214 0.00039
NM_020975.6(RET):c.1158G>A (p.Ala386=) rs373540097 0.00034
NM_020975.6(RET):c.341G>A (p.Arg114His) rs76397662 0.00029
NM_020975.6(RET):c.2673G>A (p.Ser891=) rs201620214 0.00027
NM_020975.6(RET):c.2137-794T>C rs780700885 0.00024
NM_020975.6(RET):c.785T>C (p.Val262Ala) rs139790943 0.00024
NM_020975.6(RET):c.2052G>A (p.Pro684=) rs145122337 0.00019
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.2988G>A (p.Pro996=) rs145798106 0.00014
NM_020975.6(RET):c.1893C>T (p.Asp631=) rs55846256 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.957C>A (p.Leu319=) rs149926238 0.00011
NM_020975.6(RET):c.2418C>T (p.Tyr806=) rs553418132 0.00005
NM_020975.6(RET):c.693C>T (p.Arg231=) rs576806329 0.00004
NM_020975.6(RET):c.2298G>A (p.Pro766=) rs140658743 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.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.1374C>T (p.Ala458=) rs190750926 0.00001
NM_020975.6(RET):c.1782C>T (p.His594=) rs863224426 0.00001
NM_020975.6(RET):c.1926C>G (p.Val642=) rs766962871 0.00001
NM_020975.6(RET):c.2268C>T (p.Ala756=) rs370791179 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.*500C>T
NM_020975.6(RET):c.1215C>T (p.Pro405=) rs748588678
NM_020975.6(RET):c.1521A>T (p.Ser507=) rs876660561
NM_020975.6(RET):c.1879+355G>A
NM_020975.6(RET):c.2136+151G>A
NM_020975.6(RET):c.2136+509G>T
NM_020975.6(RET):c.2136+763G>A
NM_020975.6(RET):c.2137-166G>A
NM_020975.6(RET):c.2137-251A>G
NM_020975.6(RET):c.2137-384C>T
NM_020975.6(RET):c.2284+54C>A rs566375223
NM_020975.6(RET):c.2523G>T (p.Pro841=) rs56195026
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.723C>A (p.Ala241=) rs544252468
NM_020975.6(RET):c.810C>T (p.Pro270=) rs1160403666
NM_020975.6(RET):c.936G>A (p.Arg312=) rs1837778702
NM_020975.6(RET):c.952C>T (p.Leu318=) rs1235573033

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