ClinVar Miner

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

Included ClinVar conditions (258):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 14
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HGVS dbSNP
NM_000096.3(CP):c.1099C>T (p.Arg367Cys) rs34624984
NM_000096.3(CP):c.1209-15T>A rs35465173
NM_000096.3(CP):c.1293C>T (p.Ala431=) rs758930665
NM_000096.3(CP):c.1349-13T>C rs17847017
NM_000096.3(CP):c.1430C>T (p.Pro477Leu) rs35331711
NM_000096.3(CP):c.1652C>T (p.Thr551Ile) rs61733458
NM_000096.3(CP):c.1680C>T (p.Cys560=) rs1553761342
NM_000096.3(CP):c.1950A>C (p.Gly650=) rs1053709
NM_000096.3(CP):c.2286-12T>G rs183671127
NM_000096.3(CP):c.2286-15G>T rs34861155
NM_000096.3(CP):c.249T>C (p.Thr83=) rs138512757
NM_000096.3(CP):c.2793A>G (p.Leu931=) rs34987997
NM_000096.3(CP):c.782-14C>T rs34067682
NM_000096.3(CP):c.993T>C (p.Pro331=) rs17847025

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