ClinVar Miner

List of variants in gene RET reported as uncertain significance for adrenal gland pheochromocytoma

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 77
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HGVS dbSNP
NM_020975.6(RET):c.*1020G>T rs886047004
NM_020975.6(RET):c.*1103C>T rs886047005
NM_020975.6(RET):c.*1109T>C rs886047006
NM_020975.6(RET):c.*1112A>G
NM_020975.6(RET):c.*1212C>T rs551902553
NM_020975.6(RET):c.*1233T>C rs886047007
NM_020975.6(RET):c.*1278del rs886047008
NM_020975.6(RET):c.*1337A>T rs886047009
NM_020975.6(RET):c.*1345G>T rs886047010
NM_020975.6(RET):c.*1430A>G
NM_020975.6(RET):c.*1489G>A rs535080963
NM_020975.6(RET):c.*1516C>T
NM_020975.6(RET):c.*1533A>G
NM_020975.6(RET):c.*159G>T
NM_020975.6(RET):c.*1646T>G rs886047011
NM_020975.6(RET):c.*1659T>C rs886047012
NM_020975.6(RET):c.*175C>G rs886046990
NM_020975.6(RET):c.*1797T>C rs886047013
NM_020975.6(RET):c.*1797T>G rs886047013
NM_020975.6(RET):c.*180G>A
NM_020975.6(RET):c.*1886T>G
NM_020975.6(RET):c.*1900C>A
NM_020975.6(RET):c.*358G>T rs886046991
NM_020975.6(RET):c.*368G>T rs756051983
NM_020975.6(RET):c.*446A>G rs886046992
NM_020975.6(RET):c.*453G>T rs886046993
NM_020975.6(RET):c.*500C>G
NM_020975.6(RET):c.*506G>T rs886046995
NM_020975.6(RET):c.*509A>G rs886046996
NM_020975.6(RET):c.*538G>T rs886046997
NM_020975.6(RET):c.*553G>T rs886046998
NM_020975.6(RET):c.*600delinsTT rs1588882236
NM_020975.6(RET):c.*749dup rs886047000
NM_020975.6(RET):c.*763C>T rs886047001
NM_020975.6(RET):c.*824G>T rs886047002
NM_020975.6(RET):c.*883G>A
NM_020975.6(RET):c.*935C>A rs886047003
NM_020975.6(RET):c.1062T>C (p.Tyr354=)
NM_020975.6(RET):c.1109T>A (p.Met370Lys) rs886046987
NM_020975.6(RET):c.1162G>A (p.Val388Ile) rs776223166
NM_020975.6(RET):c.1165C>T (p.Leu389Phe) rs895556824
NM_020975.6(RET):c.1264-8C>T rs769595884
NM_020975.6(RET):c.1326G>T (p.Leu442=)
NM_020975.6(RET):c.1420C>T (p.Arg474Trp) rs775842917
NM_020975.6(RET):c.1462A>T (p.Thr488Ser) rs753733901
NM_020975.6(RET):c.1597G>A (p.Gly533Ser) rs75873440
NM_020975.6(RET):c.1601T>C (p.Leu534Pro)
NM_020975.6(RET):c.1618A>G (p.Arg540Gly) rs543376293
NM_020975.6(RET):c.1649-4G>A rs369769303
NM_020975.6(RET):c.166C>A (p.Leu56Met) rs145633958
NM_020975.6(RET):c.1760-12G>A rs377767392
NM_020975.6(RET):c.1798C>T (p.Arg600Trp) rs745418960
NM_020975.6(RET):c.1879+14G>A rs532810255
NM_020975.6(RET):c.1880-5C>A
NM_020975.6(RET):c.1890C>T (p.Cys630=) rs781145070
NM_020975.6(RET):c.1946C>T (p.Ser649Leu) rs148935214
NM_020975.6(RET):c.2050C>T (p.Pro684Ser) rs141347316
NM_020975.6(RET):c.2129A>G (p.Lys710Arg) rs774983492
NM_020975.6(RET):c.2332G>A (p.Val778Ile) rs75686697
NM_020975.6(RET):c.2403C>T (p.Leu801=) rs1554819519
NM_020975.6(RET):c.2467G>A (p.Gly823Arg) rs138847998
NM_020975.6(RET):c.2523G>T (p.Pro841=) rs56195026
NM_020975.6(RET):c.2580G>A (p.Gln860=) rs886046988
NM_020975.6(RET):c.2847A>G (p.Gly949=) rs886046989
NM_020975.6(RET):c.2876G>A (p.Arg959Gln) rs745650861
NM_020975.6(RET):c.2939+7G>A rs374565577
NM_020975.6(RET):c.2982A>C (p.Lys994Asn) rs199718928
NM_020975.6(RET):c.3052C>T (p.Leu1018Phe) rs766330880
NM_020975.6(RET):c.334C>T (p.Arg112Cys) rs762626209
NM_020975.6(RET):c.432C>T (p.Arg144=) rs756999107
NM_020975.6(RET):c.484C>T (p.Pro162Ser) rs1564490122
NM_020975.6(RET):c.596A>G (p.Asn199Ser) rs886046986
NM_020975.6(RET):c.603C>T (p.Ser201=) rs780120451
NM_020975.6(RET):c.628G>A (p.Glu210Lys) rs1060500762
NM_020975.6(RET):c.693C>T (p.Arg231=) rs576806329
NM_020975.6(RET):c.867+4C>G
NM_020975.6(RET):c.972G>C (p.Trp324Cys) rs758298916

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