ClinVar Miner

List of variants in gene CP reported as benign for anemia (disease)

Included ClinVar conditions (281):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 26
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NM_000096.4(CP):c.1099C>T (p.Arg367Cys) rs34624984
NM_000096.4(CP):c.1275T>C (p.Tyr425=) rs34237139
NM_000096.4(CP):c.1348+9T>C rs35272481
NM_000096.4(CP):c.1349-13T>C rs17847017
NM_000096.4(CP):c.1430C>T (p.Pro477Leu) rs35331711
NM_000096.4(CP):c.1632= (p.Glu544=) rs701753
NM_000096.4(CP):c.1652C>T (p.Thr551Ile) rs61733458
NM_000096.4(CP):c.1950A>C (p.Gly650=) rs1053709
NM_000096.4(CP):c.2286-12T>G rs183671127
NM_000096.4(CP):c.2286-15G>T rs34861155
NM_000096.4(CP):c.2286-15del rs143522213
NM_000096.4(CP):c.2378G>A (p.Arg793His) rs115552500
NM_000096.4(CP):c.2522C>G (p.Thr841Arg) rs56033670
NM_000096.4(CP):c.2525A>G (p.Glu842Gly) rs149858116
NM_000096.4(CP):c.2554+14C>G rs200965170
NM_000096.4(CP):c.2611G>A (p.Asp871Asn) rs529607771
NM_000096.4(CP):c.2662-12T>C rs16861582
NM_000096.4(CP):c.2793A>G (p.Leu931=) rs34987997
NM_000096.4(CP):c.2997C>T (p.His999=) rs147475926
NM_000096.4(CP):c.3006C>T (p.Ser1002=) rs199877380
NM_000096.4(CP):c.347C>A (p.Pro116His) rs73866999
NM_000096.4(CP):c.457G>A (p.Glu153Lys) rs138646392
NM_000096.4(CP):c.669G>C (p.Val223=) rs35438054
NM_000096.4(CP):c.782-14C>T rs34067682
NM_000096.4(CP):c.993T>C (p.Pro331=) rs17847025

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