ClinVar Miner

List of variants in gene PCARE reported as likely benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 21
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HGVS dbSNP
NM_001029883.3(PCARE):c.*1145G>A
NM_001029883.3(PCARE):c.*1601G>A rs72861029
NM_001029883.3(PCARE):c.*1704A>G rs72788189
NM_001029883.3(PCARE):c.*1742G>C
NM_001029883.3(PCARE):c.*1748C>T
NM_001029883.3(PCARE):c.*2209G>A rs77448535
NM_001029883.3(PCARE):c.*2293G>C rs1562394
NM_001029883.3(PCARE):c.*2300C>T rs115478100
NM_001029883.3(PCARE):c.*2584C>T rs79961309
NM_001029883.3(PCARE):c.*286G>T rs78759931
NM_001029883.3(PCARE):c.*3041A>G
NM_001029883.3(PCARE):c.*686A>T rs116550481
NM_001029883.3(PCARE):c.*778A>T
NM_001029883.3(PCARE):c.*983G>A rs74315958
NM_001029883.3(PCARE):c.1844T>A (p.Val615Asp) rs140776870
NM_001029883.3(PCARE):c.2864G>A (p.Arg955Gln) rs184249075
NM_001029883.3(PCARE):c.3447G>A (p.Pro1149=) rs200278694
NM_001029883.3(PCARE):c.3522C>T (p.Asp1174=) rs188815175
NM_001029883.3(PCARE):c.3669-2AGC[4]
NM_001029883.3(PCARE):c.366T>C (p.His122=) rs17007546
NM_001029883.3(PCARE):c.3739G>A (p.Gly1247Ser) rs187333111

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