ClinVar Miner

List of variants in gene CP reported as benign for central nervous system disorder

Included ClinVar conditions (2490):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 43
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HGVS dbSNP gnomAD frequency
NM_000096.4(CP):c.1632A>T (p.Glu544Asp) rs701753 0.86852
NM_000096.4(CP):c.2662-12T>C rs16861582 0.33387
NM_000096.4(CP):c.2286-15del rs143522213 0.30978
NM_000096.4(CP):c.1632= (p.Glu544=) rs701753 0.13148
NM_000096.4(CP):c.394+20C>T rs17847023 0.08668
NM_000096.4(CP):c.782-14C>T rs34067682 0.05131
NM_000096.4(CP):c.1950A>C (p.Gly650=) rs1053709 0.04222
NM_000096.4(CP):c.2554+17G>A rs35593818 0.02896
NM_000096.4(CP):c.1652C>T (p.Thr551Ile) rs61733458 0.02154
NM_000096.4(CP):c.1099C>T (p.Arg367Cys) rs34624984 0.01447
NM_000096.4(CP):c.1209-15T>A rs35465173 0.01446
NM_000096.4(CP):c.2378G>A (p.Arg793His) rs115552500 0.01239
NM_000096.4(CP):c.2286-12T>G rs183671127 0.01016
NM_000096.4(CP):c.669G>C (p.Val223=) rs35438054 0.00599
NM_000096.4(CP):c.1275T>C (p.Tyr425=) rs34237139 0.00484
NM_000096.4(CP):c.1349-13T>C rs17847017 0.00469
NM_000096.4(CP):c.1348+9T>C rs35272481 0.00465
NM_000096.4(CP):c.2525A>G (p.Glu842Gly) rs149858116 0.00437
NM_000096.4(CP):c.2522C>G (p.Thr841Arg) rs56033670 0.00435
NM_000096.4(CP):c.2878+12T>G rs35848147 0.00288
NM_000096.4(CP):c.394+19G>A rs188121726 0.00272
NM_000096.4(CP):c.1430C>T (p.Pro477Leu) rs35331711 0.00242
NM_000096.4(CP):c.993T>C (p.Pro331=) rs17847025 0.00213
NM_000096.4(CP):c.2793A>G (p.Leu931=) rs34987997 0.00186
NM_000096.4(CP):c.347C>A (p.Pro116His) rs73866999 0.00150
NM_000096.4(CP):c.2878+14T>C rs75520320 0.00063
NM_000096.4(CP):c.2554+18G>A rs201627704 0.00046
NM_000096.4(CP):c.2997C>T (p.His999=) rs147475926 0.00029
NM_000096.4(CP):c.981G>A (p.Val327=) rs144467178 0.00026
NM_000096.4(CP):c.457G>A (p.Glu153Lys) rs138646392 0.00016
NM_000096.4(CP):c.3006C>T (p.Ser1002=) rs199877380 0.00011
NM_000096.4(CP):c.2662-14T>C rs189155564 0.00004
NM_000096.4(CP):c.1038C>T (p.Ala346=) rs146895584 0.00003
NM_000096.4(CP):c.2611G>A (p.Asp871Asn) rs529607771 0.00001
NM_000096.4(CP):c.1209-11del rs748250466
NM_000096.4(CP):c.1209-11dup rs748250466
NM_000096.4(CP):c.2286-14dup rs561633350
NM_000096.4(CP):c.2286-15G>T rs34861155
NM_000096.4(CP):c.2286-15_2286-14del rs201677287
NM_000096.4(CP):c.2286-4del rs561633350
NM_000096.4(CP):c.2554+14C>G rs200965170
NM_000096.4(CP):c.2554+19dup
NM_000096.4(CP):c.694C>T (p.Leu232=)

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