ClinVar Miner

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

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 47
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HGVS dbSNP
NM_020975.6(RET):c.*1046G>C
NM_020975.6(RET):c.*1116T>C rs2435355
NM_020975.6(RET):c.*1130A>G rs572936041
NM_020975.6(RET):c.*1326T>C
NM_020975.6(RET):c.*1348G>A rs149252070
NM_020975.6(RET):c.*1506G>A rs2742241
NM_020975.6(RET):c.*1558A>C rs142572876
NM_020975.6(RET):c.*1583G>A rs192065891
NM_020975.6(RET):c.*1591G>A rs76759170
NM_020975.6(RET):c.*1599G>A rs145954635
NM_020975.6(RET):c.*1644G>C rs117119161
NM_020975.6(RET):c.*1812C>A
NM_020975.6(RET):c.*1870C>T rs146771196
NM_020975.6(RET):c.*29C>A
NM_020975.6(RET):c.*330A>G rs141460872
NM_020975.6(RET):c.*388G>A rs3026782
NM_020975.6(RET):c.*492G>C
NM_020975.6(RET):c.*576G>A rs185408658
NM_020975.6(RET):c.*95C>T rs17028
NM_020975.6(RET):c.1119G>A (p.Ala373=) rs113931414
NM_020975.6(RET):c.1158G>A (p.Ala386=) rs373540097
NM_020975.6(RET):c.1296A>G (p.Ala432=) rs1800860
NM_020975.6(RET):c.1336G>C (p.Gly446Arg) rs115423919
NM_020975.6(RET):c.1523-7C>T rs567967877
NM_020975.6(RET):c.1699G>A (p.Asp567Asn) rs147219360
NM_020975.6(RET):c.1879+13C>T rs375573788
NM_020975.6(RET):c.2037C>T (p.Pro679=) rs55862116
NM_020975.6(RET):c.2052G>A (p.Pro684=) rs145122337
NM_020975.6(RET):c.2081G>A (p.Arg694Gln) rs141185224
NM_020975.6(RET):c.220G>A (p.Gly74Ser) rs764938319
NM_020975.6(RET):c.225G>A (p.Thr75=) rs151267865
NM_020975.6(RET):c.235C>T (p.Arg79Trp) rs537523906
NM_020975.6(RET):c.2393-14C>T rs144269978
NM_020975.6(RET):c.2418C>T (p.Tyr806=) rs553418132
NM_020975.6(RET):c.2538C>T (p.Leu846=) rs201816539
NM_020975.6(RET):c.2712C>G (p.Ser904=) rs1800863
NM_020975.6(RET):c.2976G>A (p.Pro992=) rs528823385
NM_020975.6(RET):c.2988G>A (p.Pro996=) rs145798106
NM_020975.6(RET):c.3188-9C>T rs551159582
NM_020975.6(RET):c.3243T>C (p.Asp1081=) rs144192900
NM_020975.6(RET):c.341G>A (p.Arg114His) rs76397662
NM_020975.6(RET):c.375C>A (p.Val125=) rs1800859
NM_020975.6(RET):c.487C>A (p.Arg163=) rs371153966
NM_020975.6(RET):c.566G>A (p.Arg189His) rs753707182
NM_020975.6(RET):c.597C>T (p.Asn199=) rs55810667
NM_020975.6(RET):c.654G>A (p.Pro218=) rs137928436
NM_020975.6(RET):c.833C>A (p.Thr278Asn) rs35118262

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