List of variants in gene CDON reported as benign for congenital nervous system disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 101

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001378964.1(CDON):c.3662T>A (p.Ile1221Asn)	rs684535	0.74435
NM_001378964.1(CDON):c.223G>A (p.Val75Ile)	rs3740912	0.64193
NM_001378964.1(CDON):c.*2740T>C	rs2186754	0.49995
NM_001378964.1(CDON):c.*2830A>G	rs1065398	0.49008
NM_016952.4(CDON):c.*4135C>T	rs4937076	0.48573
NM_001378964.1(CDON):c.3294G>A (p.Thr1098=)	rs3740904	0.37090
NM_001378964.1(CDON):c.2037G>A (p.Ala679=)	rs516664	0.34680
NM_001378964.1(CDON):c.3165T>C (p.Asn1055=)	rs564214	0.32369
NM_001378964.1(CDON):c.3039C>T (p.Asn1013=)	rs684805	0.31531
NM_001378964.1(CDON):c.*3884T>G	rs13424	0.29239
NM_001378964.1(CDON):c.*4052C>T	rs3039	0.25442
NM_001378964.1(CDON):c.*140A>G	rs3737336	0.25130
NM_001378964.1(CDON):c.3549C>T (p.Val1183=)	rs2276061	0.25099
NM_001378964.1(CDON):c.*3490T>C	rs11220285	0.20329
NM_001378964.1(CDON):c.*3765C>T	rs1047070	0.20261
NM_001378964.1(CDON):c.2057C>T (p.Ala686Val)	rs12274923	0.16080
NM_001378964.1(CDON):c.350-13T>C	rs3740910	0.10340
NM_001378964.1(CDON):c.484G>A (p.Glu162Lys)	rs3740909	0.10334
NM_001378964.1(CDON):c.640+12G>A	rs4426144	0.10328
NM_001378964.1(CDON):c.*2379T>C	rs562083604	0.08788
NM_001378964.1(CDON):c.*1332T>G	rs77555036	0.06389
NM_001378964.1(CDON):c.*278T>C	rs73628538	0.05323
NM_001378964.1(CDON):c.*3862G>T	rs73019367	0.03885
NM_001378964.1(CDON):c.330T>C (p.Pro110=)	rs35131477	0.03518
NM_001378964.1(CDON):c.*3076T>A	rs73019370	0.02663
NM_001378964.1(CDON):c.3526G>A (p.Val1176Ile)	rs78304400	0.02598
NM_001378964.1(CDON):c.-57C>T	rs11829014	0.02582
NM_001378964.1(CDON):c.-51A>C	rs11822173	0.02579
NM_001378964.1(CDON):c.197A>G (p.Lys66Arg)	rs7122277	0.02566
NM_001378964.1(CDON):c.*4080G>A	rs79685272	0.02502
NM_001378964.1(CDON):c.*3830G>A	rs116746244	0.02483
NM_001378964.1(CDON):c.1851+14G>A	rs113328989	0.02329
NM_001378964.1(CDON):c.1603G>A (p.Ala535Thr)	rs76247998	0.02319
NM_001378964.1(CDON):c.*2734G>A	rs12294405	0.02212
NM_001378964.1(CDON):c.2623A>G (p.Ser875Gly)	rs115533243	0.02079
NM_001378964.1(CDON):c.*2097G>A	rs76179044	0.01826
NM_001378964.1(CDON):c.*2717C>T	rs12294553	0.01820
NM_001378964.1(CDON):c.1671G>A (p.Lys557=)	rs35884952	0.01761
NM_001378964.1(CDON):c.1296G>A (p.Pro432=)	rs11220313	0.01713
NM_001378964.1(CDON):c.1051C>G (p.Pro351Ala)	rs35665264	0.01595
NM_001378964.1(CDON):c.9G>A (p.Pro3=)	rs113593771	0.00955
NM_001378964.1(CDON):c.*3628C>G	rs140783947	0.00931
NM_001378964.1(CDON):c.*3514A>G	rs77815115	0.00819
NM_001378964.1(CDON):c.*1671G>A	rs7940762	0.00691
NM_001378964.1(CDON):c.*3424T>C	rs147791703	0.00689
NM_001378964.1(CDON):c.*3777G>A	rs74527873	0.00675
NM_001378964.1(CDON):c.3559C>T (p.Arg1187Cys)	rs150174788	0.00647
NM_001378964.1(CDON):c.2051C>G (p.Thr684Ser)	rs145983470	0.00624
NM_001378964.1(CDON):c.3588C>T (p.Asp1196=)	rs140895899	0.00553
NM_001378964.1(CDON):c.*1061T>C	rs114455813	0.00548
NM_001378964.1(CDON):c.*2992T>C	rs116579152	0.00490
NM_001378964.1(CDON):c.2392A>G (p.Ile798Val)	rs142919781	0.00466
NM_001378964.1(CDON):c.*3409T>G	rs141160538	0.00465
NM_001378964.1(CDON):c.*2749C>G	rs76176354	0.00408
NM_001378964.1(CDON):c.2923G>A (p.Val975Ile)	rs113921147	0.00303
NM_001378964.1(CDON):c.1818G>T (p.Leu606=)	rs147925363	0.00262
NM_001378964.1(CDON):c.*3141A>G	rs191432564	0.00257
NM_001378964.1(CDON):c.*696T>C	rs566390376	0.00243
NM_001378964.1(CDON):c.*12C>T	rs200595011	0.00242
NM_001378964.1(CDON):c.*167A>G	rs141225852	0.00231
NM_001378964.1(CDON):c.1500C>T (p.Cys500=)	rs142388716	0.00220
NM_001378964.1(CDON):c.1310G>A (p.Arg437His)	rs114866803	0.00203
NM_001378964.1(CDON):c.*916G>A	rs79576369	0.00202
NM_001378964.1(CDON):c.*2291T>C	rs192250689	0.00191
NM_001378964.1(CDON):c.*4000C>T	rs79719160	0.00162
NM_001378964.1(CDON):c.*2573G>A	rs115327518	0.00151
NM_001378964.1(CDON):c.2279G>A (p.Arg760Gln)	rs150587299	0.00139
NM_001378964.1(CDON):c.350-11A>G	rs199981607	0.00072
NM_001378964.1(CDON):c.2139T>C (p.Asp713=)	rs144874246	0.00066
NM_001378964.1(CDON):c.*2264C>T	rs185017679	0.00065
NM_001378964.1(CDON):c.*2024C>T	rs148239384	0.00059
NM_001378964.1(CDON):c.3726A>C (p.Thr1242=)	rs139588649	0.00046
NM_001378964.1(CDON):c.*864G>A	rs144806373	0.00045
NM_001378964.1(CDON):c.350-19G>A	rs189909997	0.00042
NM_001378964.1(CDON):c.2535A>G (p.Leu845=)	rs149843751	0.00041
NM_001378964.1(CDON):c.726G>A (p.Glu242=)	rs142667570	0.00040
NM_001378964.1(CDON):c.3631+9G>A	rs189386496	0.00039
NM_001378964.1(CDON):c.77-11T>C	rs200967203	0.00029
NM_001378964.1(CDON):c.1940C>T (p.Pro647Leu)	rs200961603	0.00021
NM_001378964.1(CDON):c.3459T>C (p.Ser1153=)	rs186048531	0.00010
NM_001378964.1(CDON):c.1414C>G (p.Pro472Ala)	rs750020763	0.00009
NM_001378964.1(CDON):c.3191G>A (p.Ser1064Asn)	rs113558382	0.00009
NM_001378964.1(CDON):c.*911T>C	rs369720108	0.00007
NM_001378964.1(CDON):c.*1307T>G	rs539481575	0.00004
NM_001378964.1(CDON):c.*589C>T	rs565527208	0.00004
NM_001378964.1(CDON):c.1977C>T (p.Ser659=)	rs563267429	0.00004
NM_001378964.1(CDON):c.*1016C>T	rs545234191	0.00001
NM_001378964.1(CDON):c.*601T>A	rs549303080	0.00001
NM_001378964.1(CDON):c.3156G>A (p.Lys1052=)	rs758026817	0.00001
NM_001378964.1(CDON):c.*1933A>G	rs2509616
NM_001378964.1(CDON):c.*2003C>G	rs73019373
NM_001378964.1(CDON):c.*2345T>A	rs58251767
NM_001378964.1(CDON):c.*2347T>C	rs58515733
NM_001378964.1(CDON):c.*871C>T	rs148777681
NM_001378964.1(CDON):c.*897T>C	rs563620294
NM_001378964.1(CDON):c.*983A>G	rs76724574
NM_001378964.1(CDON):c.1553-17TC[3]	rs762936563
NM_001378964.1(CDON):c.2286G>A (p.Arg762=)
NM_001378964.1(CDON):c.2362+49C>A	rs11220309
NM_001378964.1(CDON):c.244C>T (p.Leu82=)	rs552008016
NM_001378964.1(CDON):c.2868C>A (p.Thr956=)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.