ClinVar Miner

List of variants in gene CORO2B

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Total variants: 41
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HGVS dbSNP gnomAD frequency
NM_006091.5(CORO2B):c.581T>A (p.Leu194Gln) rs138122643 0.00253
NM_006091.5(CORO2B):c.186C>T (p.Gly62=) rs61747072 0.00131
NM_006091.5(CORO2B):c.540G>A (p.Thr180=) rs144633179 0.00027
NM_006091.5(CORO2B):c.199G>A (p.Val67Ile) rs749693049 0.00009
NM_006091.5(CORO2B):c.178G>A (p.Ala60Thr) rs140464148 0.00006
NM_006091.5(CORO2B):c.29C>T (p.Pro10Leu) rs371239183 0.00006
NM_006091.5(CORO2B):c.26G>A (p.Arg9His) rs370083446 0.00005
NM_006091.5(CORO2B):c.539C>T (p.Thr180Met) rs779907122 0.00005
NM_006091.5(CORO2B):c.707G>A (p.Arg236Gln) rs553808342 0.00004
NM_006091.5(CORO2B):c.152G>A (p.Arg51His) rs753693651 0.00003
NM_006091.5(CORO2B):c.305T>C (p.Ile102Thr) rs748810483 0.00003
NM_006091.5(CORO2B):c.371G>A (p.Arg124Gln) rs755169184 0.00003
NM_006091.5(CORO2B):c.932T>C (p.Met311Thr) rs754182653 0.00003
NM_006091.5(CORO2B):c.355G>A (p.Glu119Lys) rs758897752 0.00002
NM_006091.5(CORO2B):c.1076G>A (p.Arg359Gln) rs267604301 0.00001
NM_006091.5(CORO2B):c.1330C>T (p.Arg444Trp) rs781425248 0.00001
NM_006091.5(CORO2B):c.1385G>A (p.Arg462His) rs761554395 0.00001
NM_006091.5(CORO2B):c.1436A>T (p.Asn479Ile) rs562497372 0.00001
NM_006091.5(CORO2B):c.344G>T (p.Trp115Leu) rs760180049 0.00001
NM_006091.5(CORO2B):c.638G>A (p.Arg213His) rs1317954287 0.00001
NM_006091.5(CORO2B):c.1025A>G (p.Lys342Arg) rs758837711
NM_006091.5(CORO2B):c.1156G>C (p.Gly386Arg) rs2505073722
NM_006091.5(CORO2B):c.1159G>A (p.Gly387Ser) rs2505073724
NM_006091.5(CORO2B):c.1196A>G (p.Glu399Gly)
NM_006091.5(CORO2B):c.1202A>G (p.Tyr401Cys)
NM_006091.5(CORO2B):c.1254T>G (p.Ser418Arg)
NM_006091.5(CORO2B):c.1274A>G (p.Asp425Gly) rs2505074865
NM_006091.5(CORO2B):c.1319G>A (p.Arg440Gln)
NM_006091.5(CORO2B):c.1323G>A (p.Met441Ile)
NM_006091.5(CORO2B):c.1390C>T (p.Arg464Trp) rs146678597
NM_006091.5(CORO2B):c.1391G>A (p.Arg464Gln)
NM_006091.5(CORO2B):c.1429C>A (p.Pro477Thr) rs377512463
NM_006091.5(CORO2B):c.230A>C (p.Glu77Ala)
NM_006091.5(CORO2B):c.358G>T (p.Gly120Cys) rs1160224442
NM_006091.5(CORO2B):c.361G>A (p.Gly121Arg)
NM_006091.5(CORO2B):c.435G>T (p.Trp145Cys) rs1892898282
NM_006091.5(CORO2B):c.438C>A (p.His146Gln) rs1453150855
NM_006091.5(CORO2B):c.721G>C (p.Gly241Arg) rs2505060066
NM_006091.5(CORO2B):c.731G>C (p.Arg244Thr) rs2505060111
NM_006091.5(CORO2B):c.835G>T (p.Asp279Tyr) rs2505061621
NM_006091.5(CORO2B):c.96T>A (p.Asp32Glu) rs779692073

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