List of variants in gene CRPPA reported as likely benign by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 44

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HGVS	dbSNP	gnomAD frequency
NM_001101426.4(CRPPA):c.934-210A>T	rs73684109	0.01242
NM_001101426.4(CRPPA):c.685-254T>C	rs73065181	0.01158
NM_001101426.4(CRPPA):c.933+207C>A	rs114323347	0.01137
NM_001101426.4(CRPPA):c.684+164G>C	rs74911987	0.01101
NM_001101426.4(CRPPA):c.1251+252G>A	rs28617534	0.00886
NM_001101426.4(CRPPA):c.685-78G>T	rs115870182	0.00773
NM_001101426.4(CRPPA):c.789+276C>T	rs77362308	0.00773
NM_001101426.4(CRPPA):c.836-83A>G	rs114980259	0.00688
NM_001101426.4(CRPPA):c.836-277C>G	rs57952940	0.00563
NM_001101426.4(CRPPA):c.1120-132G>T	rs147175902	0.00549
NM_001101426.4(CRPPA):c.*86A>G	rs16878685	0.00522
NM_001101426.4(CRPPA):c.535-218G>T	rs115455870	0.00416
NM_001101426.4(CRPPA):c.933+223C>T	rs184997230	0.00348
NM_001101426.4(CRPPA):c.535-295A>G	rs114960762	0.00309
NM_001101426.4(CRPPA):c.934-52T>G	rs149948893	0.00275
NM_001101426.4(CRPPA):c.1054C>A (p.Gln352Lys)	rs185594460	0.00151
NM_001101426.4(CRPPA):c.1059G>A (p.Lys353=)	rs181099904	0.00151
NM_001101426.4(CRPPA):c.790-14T>C	rs142414812	0.00123
NM_001101426.4(CRPPA):c.790-11C>T	rs141363557	0.00101
NM_001101426.4(CRPPA):c.1251+16A>T	rs187344556	0.00082
NM_001101426.4(CRPPA):c.222G>A (p.Arg74=)	rs769058832	0.00056
NM_001101426.4(CRPPA):c.999T>C (p.Asp333=)	rs376909665	0.00026
NM_001101426.4(CRPPA):c.684+12G>C	rs376232862	0.00019
NM_001101426.4(CRPPA):c.876A>G (p.Glu292=)	rs371300262	0.00019
NM_001101426.4(CRPPA):c.693C>A (p.Asp231Glu)	rs770257307	0.00016
NM_001101426.4(CRPPA):c.123G>C (p.Gly41=)	rs761842188	0.00011
NM_001101426.4(CRPPA):c.243A>G (p.Leu81=)	rs763209907	0.00011
NM_001101426.4(CRPPA):c.551G>A (p.Arg184Gln)	rs773739293	0.00007
NM_001101426.4(CRPPA):c.1170C>T (p.Asn390=)	rs760178734	0.00003
NM_001101426.4(CRPPA):c.933+3A>G	rs377582530	0.00003
NM_001101426.4(CRPPA):c.825G>A (p.Ser275=)	rs766874330	0.00002
NM_001101426.4(CRPPA):c.645A>G (p.Gln215=)	rs532057629	0.00001
NM_001101426.4(CRPPA):c.685-19del	rs778040240	0.00001
NM_001101426.4(CRPPA):c.1120-20C>G	rs758565814
NM_001101426.4(CRPPA):c.1120-291C>T	rs183379625
NM_001101426.4(CRPPA):c.1120-297C>G	rs11980781
NM_001101426.4(CRPPA):c.1338T>G (p.Gly446=)	rs1424229425
NM_001101426.4(CRPPA):c.261A>G (p.Val87=)	rs886044356
NM_001101426.4(CRPPA):c.360C>T (p.Val120=)	rs183141256
NM_001101426.4(CRPPA):c.535-132_535-129del	rs199607912
NM_001101426.4(CRPPA):c.535-173dup	rs376172562
NM_001101426.4(CRPPA):c.535-268T>A	rs75231577
NM_001101426.4(CRPPA):c.535-279dup	rs1303885278
NM_001101426.4(CRPPA):c.934-182_934-180del	rs144982982

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