ClinVar Miner

List of variants reported as benign for prostate cancer by KCCC/NGS Laboratory, Kuwait Cancer Control Center

Included ClinVar conditions (36):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 40
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HGVS dbSNP gnomAD frequency
NM_004360.5(CDH1):c.48+6C>T rs3743674 0.80384
NM_004360.5(CDH1):c.2076T>C (p.Ala692=) rs1801552 0.70379
NM_018127.7(ELAC2):c.1305-8T>C rs3760316 0.32355
NM_018127.7(ELAC2):c.297-11T>C rs58809197 0.27292
NM_018127.7(ELAC2):c.1218+15C>T rs55825263 0.26965
NM_018127.7(ELAC2):c.1304+17A>T rs55674356 0.26960
NM_006361.6(HOXB13):c.513T>C (p.Ser171=) rs9900627 0.11073
NM_004360.5(CDH1):c.1937-13T>C rs2276330 0.09635
NM_018127.7(ELAC2):c.1893A>G (p.Thr631=) rs17552022 0.08581
NM_018127.7(ELAC2):c.491-14T>C rs74556312 0.08556
NM_004360.5(CDH1):c.531+10G>C rs33963999 0.03907
NM_004360.5(CDH1):c.2253C>T (p.Asn751=) rs33964119 0.03869
NM_018127.7(ELAC2):c.798-20G>T rs77528900 0.03735
NM_004360.5(CDH1):c.48+5C>G rs77312180 0.03370
NM_018127.7(ELAC2):c.2130C>T (p.Ser710=) rs7217826 0.02093
NM_004360.5(CDH1):c.1896C>T (p.His632=) rs33969373 0.02054
NM_004360.5(CDH1):c.2634C>T (p.Gly878=) rs2229044 0.01638
NM_018127.7(ELAC2):c.1389C>T (p.Tyr463=) rs77972324 0.01451
NM_004360.5(CDH1):c.933C>G (p.Leu311=) rs35539711 0.00974
NM_004360.5(CDH1):c.-71C>G rs34033771 0.00927
NM_018127.7(ELAC2):c.1479G>C (p.Pro493=) rs140335642 0.00771
NM_018127.7(ELAC2):c.368-4T>A rs139778647 0.00657
NM_004360.5(CDH1):c.2439+22C>T rs34751606 0.00346
NM_004360.5(CDH1):c.833-16C>G rs33984587 0.00332
NM_004360.5(CDH1):c.1680G>C (p.Thr560=) rs35741240 0.00261
NM_004360.5(CDH1):c.324A>G (p.Arg108=) rs116542018 0.00255
NM_004360.5(CDH1):c.345G>A (p.Thr115=) rs1801023 0.00236
NM_018127.7(ELAC2):c.174G>A (p.Val58=) rs2286334 0.00196
NM_004360.5(CDH1):c.2292C>T (p.Asp764=) rs61747636 0.00159
NM_006361.6(HOXB13):c.735G>A (p.Lys245=) rs138675188 0.00147
NM_004360.5(CDH1):c.2440-6C>G rs139757930 0.00145
NM_004360.5(CDH1):c.1138-3C>T rs36103202 0.00042
NM_004360.5(CDH1):c.1239C>T (p.Tyr413=) rs36074916 0.00041
NM_004360.5(CDH1):c.303C>T (p.Tyr101=) rs150789339 0.00027
NM_006361.6(HOXB13):c.602-9G>A rs148901331 0.00022
NM_004360.5(CDH1):c.1773C>T (p.Asn591=) rs373719554 0.00001
NM_004360.5(CDH1):c.604G>A (p.Val202Ile) rs546716073 0.00001
NM_004360.5(CDH1):c.1308G>A (p.Leu436=) rs557551011
NM_006361.6(HOXB13):c.366C>T (p.Ser122=) rs8556
NM_018127.7(ELAC2):c.1560A>G (p.Thr520=) rs11545302

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