ClinVar Miner

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

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 22
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HGVS dbSNP
NM_001101426.4(CRPPA):c.*1470T>G rs528279923
NM_001101426.4(CRPPA):c.*1855G>C rs111577730
NM_001101426.4(CRPPA):c.*2119C>A rs148625258
NM_001101426.4(CRPPA):c.*2155A>C
NM_001101426.4(CRPPA):c.*2197G>C rs371376395
NM_001101426.4(CRPPA):c.*2219_*2222GTAC[3] rs58170479
NM_001101426.4(CRPPA):c.*2226_*2229dup rs200404448
NM_001101426.4(CRPPA):c.*2304A>G rs547400634
NM_001101426.4(CRPPA):c.*2351C>T rs114572844
NM_001101426.4(CRPPA):c.*2368_*2373del rs72267760
NM_001101426.4(CRPPA):c.*2488G>A rs753515691
NM_001101426.4(CRPPA):c.*2493_*2494TA[2] rs72031454
NM_001101426.4(CRPPA):c.*2981C>T
NM_001101426.4(CRPPA):c.*3087G>A rs148322529
NM_001101426.4(CRPPA):c.*3254C>G rs185506130
NM_001101426.4(CRPPA):c.*3284A>G
NM_001101426.4(CRPPA):c.*3374C>T
NM_001101426.4(CRPPA):c.*73_*74TG[5] rs139003391
NM_001101426.4(CRPPA):c.32C>G (p.Pro11Arg) rs192925278
NM_001101426.4(CRPPA):c.346C>T (p.Arg116Cys) rs61744487
NM_001101426.4(CRPPA):c.685-25GTT[6] rs142647500
NM_001101426.4(CRPPA):c.836-9del rs3839757

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