ClinVar Miner

List of variants reported as likely benign for endocrine gland neoplasm by KCCC/NGS Laboratory, Kuwait Cancer Control Center

Included ClinVar conditions (161):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 34
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HGVS dbSNP gnomAD frequency
NM_003000.3(SDHB):c.-37T>C rs143031690 0.00411
NM_004168.4(SDHA):c.313-19G>T rs185555941 0.00235
NM_024529.5(CDC73):c.-95G>A rs143969598 0.00133
NM_004168.4(SDHA):c.1368G>A (p.Ser456=) rs149875171 0.00117
NM_004168.4(SDHA):c.1002G>A (p.Ala334=) rs144252500 0.00075
NM_001370259.2(MEN1):c.18C>T (p.Ala6=) rs369348210 0.00039
NM_020975.6(RET):c.337+34C>T rs368088467 0.00022
NM_001370259.2(MEN1):c.762G>A (p.Leu254=) rs199909967 0.00018
NM_024529.5(CDC73):c.840G>A (p.Leu280=) rs10921320 0.00012
NM_003000.3(SDHB):c.113G>A (p.Arg38His) rs143058777 0.00010
NM_020975.6(RET):c.1879+17C>T rs369920430 0.00010
NM_004168.4(SDHA):c.1661G>A (p.Arg554Gln) rs376391115 0.00009
NM_020975.6(RET):c.2136+15G>A rs751183869 0.00009
NM_020975.6(RET):c.1879+13C>T rs375573788 0.00008
NM_001370259.2(MEN1):c.1071C>T (p.Asp357=) rs371964966 0.00003
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_004168.4(SDHA):c.1737C>T (p.Ile579=) rs201454617 0.00002
NM_001370259.2(MEN1):c.1392G>A (p.Ala464=) rs754445482 0.00001
NM_001370259.2(MEN1):c.303C>T (p.Val101=) rs1463347315 0.00001
NM_003000.3(SDHB):c.700C>T (p.Leu234=) rs201728852 0.00001
NM_004168.4(SDHA):c.1182C>T (p.Asp394=) rs377317558 0.00001
NM_004168.4(SDHA):c.1308C>T (p.Tyr436=) rs762494024 0.00001
NM_004168.4(SDHA):c.1323C>T (p.Ala441=) rs751561561 0.00001
NM_004168.4(SDHA):c.1410C>T (p.Ser470=) rs556476038 0.00001
NM_004168.4(SDHA):c.896-4G>A rs555881974 0.00001
NM_020975.6(RET):c.1539G>A (p.Ala513=) rs761430718 0.00001
NM_020975.6(RET):c.1908G>A (p.Thr636=) rs886038663 0.00001
NM_020975.6(RET):c.322A>C (p.Lys108Gln) rs567877611 0.00001
NM_024529.5(CDC73):c.1011C>T (p.Ala337=) rs372567546 0.00001
NM_001370259.2(MEN1):c.1410G>A (p.Pro470=) rs1060503795
NM_020975.6(RET):c.1866C>T (p.Pro622=) rs201979255
NM_020975.6(RET):c.2554A>G (p.Ile852Val) rs561276725
NM_020975.6(RET):c.951G>A (p.Thr317=) rs375812189

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