ClinVar Miner

List of variants in gene CRPPA 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: 22
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HGVS dbSNP
NM_001101426.3(CRPPA):c.*1043C>G rs149771453
NM_001101426.3(CRPPA):c.*1099C>T rs141259768
NM_001101426.3(CRPPA):c.*1848C>T rs78791023
NM_001101426.3(CRPPA):c.*1849G>A rs60843615
NM_001101426.3(CRPPA):c.*2149A>C rs28569130
NM_001101426.3(CRPPA):c.*2181A>G rs183114712
NM_001101426.3(CRPPA):c.*2197G>C rs371376395
NM_001101426.3(CRPPA):c.*2223_*2226dupGTAC rs58170479
NM_001101426.3(CRPPA):c.*2226_*2229dupCATA rs200404448
NM_001101426.3(CRPPA):c.*2276T>C rs117664754
NM_001101426.3(CRPPA):c.*2351C>T rs114572844
NM_001101426.3(CRPPA):c.*2368T>G rs9691122
NM_001101426.3(CRPPA):c.*2368_*2373delTTATAT rs72267760
NM_001101426.3(CRPPA):c.*2497_*2498delTA rs72031454
NM_001101426.3(CRPPA):c.*321A>G rs7788119
NM_001101426.3(CRPPA):c.*34C>G rs16878689
NM_001101426.3(CRPPA):c.*791T>C rs17150159
NM_001101426.3(CRPPA):c.*79_*80dupTG rs139003391
NM_001101426.3(CRPPA):c.407C>T (p.Ala136Val) rs61734789
NM_001101426.3(CRPPA):c.685-13_685-11dupGTT rs142647500
NM_001101426.3(CRPPA):c.726A>G (p.Gln242=) rs61746966
NM_001101426.3(CRPPA):c.836-9delT rs3839757

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