ClinVar Miner

List of variants in gene CDH23 reported as likely benign by PreventionGenetics, part of Exact Sciences

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Gene type:
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Total variants: 62
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HGVS dbSNP gnomAD frequency
NM_022124.6(CDH23):c.1449+76C>A rs41281304 0.00518
NM_022124.6(CDH23):c.2878G>A (p.Glu960Lys) rs111033458 0.00299
NM_022124.6(CDH23):c.6705C>T (p.Ile2235=) rs114827737 0.00203
NM_022124.6(CDH23):c.3010G>A (p.Val1004Met) rs79705488 0.00151
NM_022124.6(CDH23):c.2239C>T (p.Arg747Cys) rs200649500 0.00136
NM_022124.6(CDH23):c.2781C>T (p.Tyr927=) rs375102725 0.00123
NM_022124.6(CDH23):c.4287C>T (p.Pro1429=) rs377493327 0.00101
NM_022124.6(CDH23):c.2745C>T (p.Ile915=) rs183220886 0.00048
NM_022124.6(CDH23):c.4947G>A (p.Thr1649=) rs373046094 0.00047
NM_022124.6(CDH23):c.574G>C (p.Glu192Gln) rs199514829 0.00045
NM_022124.6(CDH23):c.4892C>T (p.Ala1631Val) rs370762269 0.00025
NM_022124.6(CDH23):c.9381-144C>A rs187068482 0.00025
NM_022124.6(CDH23):c.9438G>A (p.Ala3146=) rs200572025 0.00025
NM_022124.6(CDH23):c.2572G>A (p.Val858Ile) rs181275139 0.00023
NM_022124.6(CDH23):c.5236C>T (p.Arg1746Trp) rs201763918 0.00021
NM_022124.6(CDH23):c.6426A>G (p.Leu2142=) rs371932558 0.00017
NM_022124.6(CDH23):c.2891G>A (p.Arg964Gln) rs376560330 0.00014
NM_022124.6(CDH23):c.5985C>T (p.Tyr1995=) rs370762205 0.00014
NM_022124.6(CDH23):c.1227G>A (p.Ala409=) rs371212430 0.00011
NM_022124.6(CDH23):c.3186C>A (p.Thr1062=) rs201589645 0.00010
NM_022124.6(CDH23):c.9771A>C (p.Gly3257=) rs373249121 0.00010
NM_022124.6(CDH23):c.2854G>A (p.Glu952Lys) rs370554545 0.00009
NM_022124.6(CDH23):c.8499C>T (p.Arg2833=) rs397517358 0.00009
NM_022124.6(CDH23):c.8979+4C>T rs775540400 0.00009
NM_022124.6(CDH23):c.5442C>T (p.Ile1814=) rs373768157 0.00008
NM_022124.6(CDH23):c.856C>T (p.Leu286=) rs727502918 0.00008
NM_022124.6(CDH23):c.4773G>A (p.Pro1591=) rs376037961 0.00006
NM_022124.6(CDH23):c.6366C>T (p.Thr2122=) rs368440578 0.00006
NM_022124.6(CDH23):c.6911G>A (p.Arg2304Gln) rs201434373 0.00006
NM_022124.6(CDH23):c.2832C>T (p.Ser944=) rs775998990 0.00005
NM_022124.6(CDH23):c.330C>T (p.His110=) rs201232514 0.00005
NM_022124.6(CDH23):c.4854G>A (p.Thr1618=) rs376538879 0.00005
NM_022124.6(CDH23):c.2502C>T (p.Arg834=) rs55918133 0.00004
NM_022124.6(CDH23):c.4230C>T (p.Asp1410=) rs762720558 0.00004
NM_022124.6(CDH23):c.5713-9A>G rs397517343 0.00004
NM_022124.6(CDH23):c.5919C>T (p.Pro1973=) rs752519912 0.00004
NM_022124.6(CDH23):c.9198+10G>A rs758760731 0.00004
NM_022124.6(CDH23):c.2587+45C>T rs373980701 0.00003
NM_022124.6(CDH23):c.2790G>A (p.Pro930=) rs111033528 0.00003
NM_022124.6(CDH23):c.7077A>C (p.Thr2359=) rs191154178 0.00003
NM_022124.6(CDH23):c.2289+9G>A rs370927096 0.00002
NM_022124.6(CDH23):c.5790C>T (p.Asp1930=) rs572668890 0.00002
NM_022124.6(CDH23):c.9738+7G>A rs561629875 0.00002
NM_022124.6(CDH23):c.1695C>G (p.Ala565=) rs372380590 0.00001
NM_022124.6(CDH23):c.1698C>T (p.Tyr566=) rs373296547 0.00001
NM_022124.6(CDH23):c.4260C>T (p.Phe1420=) rs1839633496 0.00001
NM_022124.6(CDH23):c.777C>A (p.Thr259=) rs542798557 0.00001
NM_022124.6(CDH23):c.8290G>A (p.Val2764Met) rs556148352 0.00001
NM_022124.6(CDH23):c.8406C>T (p.Ile2802=) rs752125151 0.00001
NM_022124.6(CDH23):c.9108G>A (p.Glu3036=) rs768198017 0.00001
NM_022124.6(CDH23):c.9429C>T (p.Ala3143=) rs1000025762 0.00001
NM_022124.6(CDH23):c.9633+7C>T rs975152782 0.00001
NM_022124.6(CDH23):c.10036G>C (p.Glu3346Gln) rs562525508
NM_022124.6(CDH23):c.2193G>C (p.Thr731=) rs397517315
NM_022124.6(CDH23):c.2359_2382del (p.Leu787_Asp794del) rs886038668
NM_022124.6(CDH23):c.2664C>T (p.Pro888=) rs760919073
NM_022124.6(CDH23):c.2734-10T>C
NM_022124.6(CDH23):c.588G>A (p.Glu196=) rs886047129
NM_022124.6(CDH23):c.777C>T (p.Thr259=) rs542798557
NM_022124.6(CDH23):c.8308+4G>C rs751021859
NM_022124.6(CDH23):c.9381-150A>C
NM_022124.6(CDH23):c.9468G>C (p.Leu3156=)

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