ClinVar Miner

List of variants in gene CNNM2 reported as likely benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 105
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HGVS dbSNP gnomAD frequency
NM_017649.5(CNNM2):c.1621+7408C>T rs143934882 0.01353
NM_017649.5(CNNM2):c.2419-53C>T rs115260652 0.01257
NM_017649.5(CNNM2):c.564C>T (p.Ser188=) rs117691462 0.00404
NM_017649.5(CNNM2):c.*52C>T rs367767821 0.00271
NM_017649.5(CNNM2):c.903C>T (p.Tyr301=) rs140279763 0.00044
NM_017649.5(CNNM2):c.1896A>G (p.Leu632=) rs114898118 0.00031
NM_017649.5(CNNM2):c.342G>T (p.Thr114=) rs375416482 0.00029
NM_017649.5(CNNM2):c.1515C>T (p.Pro505=) rs144140948 0.00026
NM_017649.5(CNNM2):c.1053T>G (p.Gly351=) rs112549758 0.00016
NM_017649.5(CNNM2):c.1243C>T (p.Leu415=) rs113308552 0.00016
NM_017649.5(CNNM2):c.804G>T (p.Leu268=) rs148386496 0.00013
NM_017649.5(CNNM2):c.1698C>T (p.Ile566=) rs371434890 0.00009
NM_017649.5(CNNM2):c.390G>C (p.Pro130=) rs534061178 0.00006
NM_017649.5(CNNM2):c.2400G>A (p.Ser800=) rs775113694 0.00005
NM_017649.5(CNNM2):c.609C>G (p.Gly203=) rs940090909 0.00005
NM_017649.5(CNNM2):c.1293G>A (p.Glu431=) rs202014868 0.00003
NM_017649.5(CNNM2):c.621C>T (p.Ser207=) rs767302259 0.00002
NM_017649.5(CNNM2):c.1002C>G (p.Leu334=) rs763530748 0.00001
NM_017649.5(CNNM2):c.1765+11T>C rs901937775 0.00001
NM_017649.5(CNNM2):c.1779G>A (p.Thr593=) rs780257259 0.00001
NM_017649.5(CNNM2):c.2073+8G>T rs1302420255 0.00001
NM_017649.5(CNNM2):c.2073+9A>T rs1348088944 0.00001
NM_017649.5(CNNM2):c.2121G>A (p.Ala707=) rs755761869 0.00001
NM_017649.5(CNNM2):c.2190C>T (p.Thr730=) rs1021927212 0.00001
NM_017649.5(CNNM2):c.2307C>T (p.Asp769=) rs751443884 0.00001
NM_017649.5(CNNM2):c.2322A>G (p.Thr774=) rs756002318 0.00001
NM_017649.5(CNNM2):c.237G>A (p.Leu79=) rs777820126 0.00001
NM_017649.5(CNNM2):c.2418+10G>A rs1464300541 0.00001
NM_017649.5(CNNM2):c.*150C>T
NM_017649.5(CNNM2):c.1011C>T (p.Ile337=)
NM_017649.5(CNNM2):c.1014C>T (p.Ala338=)
NM_017649.5(CNNM2):c.1026C>A (p.Leu342=)
NM_017649.5(CNNM2):c.1041C>T (p.Val347=) rs754630284
NM_017649.5(CNNM2):c.1074C>T (p.Ile358=)
NM_017649.5(CNNM2):c.1086C>T (p.Ala362=) rs1469518805
NM_017649.5(CNNM2):c.1206C>T (p.Gly402=)
NM_017649.5(CNNM2):c.120C>T (p.Ile40=) rs1845507943
NM_017649.5(CNNM2):c.1275C>T (p.Asn425=)
NM_017649.5(CNNM2):c.1305C>T (p.Ile435=)
NM_017649.5(CNNM2):c.1335G>A (p.Thr445=)
NM_017649.5(CNNM2):c.1359C>A (p.Leu453=)
NM_017649.5(CNNM2):c.138G>A (p.Gly46=)
NM_017649.5(CNNM2):c.1440C>T (p.Arg480=)
NM_017649.5(CNNM2):c.1461G>A (p.Glu487=)
NM_017649.5(CNNM2):c.1485G>A (p.Leu495=)
NM_017649.5(CNNM2):c.1485G>C (p.Leu495=)
NM_017649.5(CNNM2):c.153G>A (p.Leu51=)
NM_017649.5(CNNM2):c.1557C>T (p.Asn519=)
NM_017649.5(CNNM2):c.15C>T (p.Gly5=)
NM_017649.5(CNNM2):c.1621+18_1621+19del
NM_017649.5(CNNM2):c.1621+288del rs752188951
NM_017649.5(CNNM2):c.1621+7245A>G
NM_017649.5(CNNM2):c.1622-14T>C
NM_017649.5(CNNM2):c.1622-14T>G
NM_017649.5(CNNM2):c.1683T>C (p.Tyr561=)
NM_017649.5(CNNM2):c.1690C>T (p.Leu564=)
NM_017649.5(CNNM2):c.1692G>T (p.Leu564=)
NM_017649.5(CNNM2):c.1765+14T>A
NM_017649.5(CNNM2):c.1765+7A>G
NM_017649.5(CNNM2):c.1766-16T>C
NM_017649.5(CNNM2):c.1766-17_1766-15del
NM_017649.5(CNNM2):c.1766-9C>T
NM_017649.5(CNNM2):c.1779G>C (p.Thr593=)
NM_017649.5(CNNM2):c.1903+9A>G
NM_017649.5(CNNM2):c.2058C>T (p.Phe686=)
NM_017649.5(CNNM2):c.2074-10C>T
NM_017649.5(CNNM2):c.2074-20C>T rs2134359792
NM_017649.5(CNNM2):c.2124C>T (p.Ser708=)
NM_017649.5(CNNM2):c.2167+19C>G
NM_017649.5(CNNM2):c.2199C>T (p.Val733=) rs2134364622
NM_017649.5(CNNM2):c.2355G>A (p.Ser785=)
NM_017649.5(CNNM2):c.2355G>C (p.Ser785=) rs189582508
NM_017649.5(CNNM2):c.2385G>T (p.Ser795=) rs370749106
NM_017649.5(CNNM2):c.240G>A (p.Glu80=) rs1243294239
NM_017649.5(CNNM2):c.2418+9C>T
NM_017649.5(CNNM2):c.2419-5C>T
NM_017649.5(CNNM2):c.2421C>A (p.Ile807=)
NM_017649.5(CNNM2):c.2472C>G (p.Thr824=)
NM_017649.5(CNNM2):c.2496C>T (p.Asn832=)
NM_017649.5(CNNM2):c.2509T>C (p.Leu837=)
NM_017649.5(CNNM2):c.2529T>C (p.His843=)
NM_017649.5(CNNM2):c.2532C>T (p.Asp844=)
NM_017649.5(CNNM2):c.2583G>A (p.Thr861=)
NM_017649.5(CNNM2):c.258G>A (p.Ser86=)
NM_017649.5(CNNM2):c.2592G>A (p.Lys864=)
NM_017649.5(CNNM2):c.2619C>T (p.Gly873=)
NM_017649.5(CNNM2):c.273G>A (p.Gly91=)
NM_017649.5(CNNM2):c.285G>C (p.Val95=)
NM_017649.5(CNNM2):c.336C>T (p.Asn112=) rs1205111885
NM_017649.5(CNNM2):c.570C>T (p.Tyr190=)
NM_017649.5(CNNM2):c.594C>A (p.Pro198=)
NM_017649.5(CNNM2):c.600G>T (p.Leu200=) rs1590244122
NM_017649.5(CNNM2):c.603C>T (p.Gly201=)
NM_017649.5(CNNM2):c.630C>T (p.Gly210=)
NM_017649.5(CNNM2):c.657G>A (p.Gly219=)
NM_017649.5(CNNM2):c.678C>T (p.Pro226=)
NM_017649.5(CNNM2):c.753C>T (p.Phe251=) rs1590244475
NM_017649.5(CNNM2):c.757C>T (p.Leu253=)
NM_017649.5(CNNM2):c.762C>T (p.Pro254=)
NM_017649.5(CNNM2):c.829C>T (p.Leu277=)
NM_017649.5(CNNM2):c.888G>A (p.Glu296=)
NM_017649.5(CNNM2):c.927C>G (p.Arg309=)
NM_017649.5(CNNM2):c.95G>T (p.Ser32Ile)
NM_017649.5(CNNM2):c.96C>T (p.Ser32=)
NM_017649.5(CNNM2):c.975G>C (p.Leu325=) rs1590244875

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