ClinVar Miner

List of variants reported as uncertain significance for adenocarcinoma by St. Jude Molecular Pathology, St. Jude Children's Research Hospital

Included ClinVar conditions (112):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 35
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HGVS dbSNP gnomAD frequency
NM_000245.4(MET):c.406G>A (p.Val136Ile) rs199701987 0.00058
NM_000245.4(MET):c.1412G>A (p.Gly471Glu) rs373312981 0.00016
NM_004360.5(CDH1):c.1568A>G (p.Tyr523Cys) rs553907248 0.00016
NM_000245.4(MET):c.1771C>T (p.Arg591Trp) rs45602940 0.00015
NM_000245.4(MET):c.2684C>T (p.Thr895Met) rs199502137 0.00011
NM_004360.5(CDH1):c.1241C>A (p.Thr414Asn) rs755571454 0.00006
NM_004360.5(CDH1):c.846G>A (p.Met282Ile) rs200932258 0.00006
NM_000245.4(MET):c.2674G>A (p.Val892Ile) rs761243391 0.00005
NM_004360.5(CDH1):c.1988A>G (p.Tyr663Cys) rs372182377 0.00005
NM_000245.4(MET):c.4016C>T (p.Ala1339Val) rs1453842331 0.00004
NM_004360.5(CDH1):c.1865A>G (p.Asn622Ser) rs147925149 0.00004
NM_000245.4(MET):c.3221G>A (p.Ser1074Asn) rs752641437 0.00003
NM_000245.4(MET):c.762A>C (p.Glu254Asp) rs760278126 0.00003
NM_000245.4(MET):c.2755G>A (p.Val919Ile) rs759522148 0.00002
NM_000245.4(MET):c.4011A>G (p.Ile1337Met) rs376418811 0.00002
NM_000245.4(MET):c.2914G>A (p.Asp972Asn) rs756031094 0.00001
NM_000245.4(MET):c.2974A>G (p.Thr992Ala) rs774433287 0.00001
NM_000245.4(MET):c.3997C>G (p.Leu1333Val) rs758738756 0.00001
NM_004360.5(CDH1):c.1351A>C (p.Ile451Leu) rs377416092 0.00001
NM_004360.5(CDH1):c.2201G>C (p.Arg734Thr) rs587781859 0.00001
NM_000245.4(MET):c.1507C>G (p.Leu503Val) rs1417433919
NM_000245.4(MET):c.1627G>A (p.Asp543Asn) rs763991073
NM_000245.4(MET):c.16G>T (p.Val6Leu) rs1395233386
NM_000245.4(MET):c.3352A>G (p.Ile1118Val) rs755234697
NM_000245.4(MET):c.3936-13_3936-10del rs745366999
NM_000245.4(MET):c.4118A>G (p.Asp1373Gly) rs773898036
NM_000245.4(MET):c.425A>G (p.Gln142Arg) rs768640780
NM_000455.5(STK11):c.397G>A (p.Val133Met) rs567769257
NM_004360.5(CDH1):c.1018A>T (p.Thr340Ser) rs116093741
NM_004360.5(CDH1):c.1181C>A (p.Thr394Asn) rs1332444039
NM_004360.5(CDH1):c.1566-8C>G rs587780114
NM_004360.5(CDH1):c.1928A>G (p.Asn643Ser) rs1567512606
NM_004360.5(CDH1):c.1955T>G (p.Leu652Trp) rs1567513174
NM_004360.5(CDH1):c.2351G>C (p.Arg784Pro) rs763203357
NM_024675.4(PALB2):c.2147A>G (p.Asn716Ser) rs148335539

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