Variants in gene CRPPA with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 11

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001101426.4(CRPPA):c.726A>G (p.Gln242=)	rs61746966	0.02927
NM_001101426.4(CRPPA):c.407C>T (p.Ala136Val)	rs61734789	0.02478
NM_001101426.4(CRPPA):c.947C>A (p.Thr316Lys)	rs114363936	0.00703
NM_001101426.4(CRPPA):c.346C>T (p.Arg116Cys)	rs61744487	0.00561
NM_001101426.4(CRPPA):c.*86A>G	rs16878685	0.00512
NM_001101426.4(CRPPA):c.1220T>C (p.Leu407Ser)	rs141625803	0.00164
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.*73TG[5]	rs139003391
NM_001101426.4(CRPPA):c.685-25GTT[6]	rs142647500
NM_001101426.4(CRPPA):c.836-9del	rs3839757

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.