List of variants in gene CRPPA reported as pathogenic for not provided

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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: 12

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HGVS	dbSNP	gnomAD frequency
NM_001101426.4(CRPPA):c.835+2T>C	rs773325665	0.00005
NM_001101426.4(CRPPA):c.643C>T (p.Gln215Ter)	rs370627877	0.00003
NM_001101426.4(CRPPA):c.550C>T (p.Arg184Ter)	rs370499190	0.00001
GRCh37/hg19 7p21.2(chr7:16369989-16486969)x1
NM_001101426.4(CRPPA):c.1030dup (p.Thr344fs)	rs1554300194
NM_001101426.4(CRPPA):c.1105GTT[3] (p.Val372del)	rs587777798
NM_001101426.4(CRPPA):c.1120-1G>T	rs397515396
NM_001101426.4(CRPPA):c.1123_1126del (p.His375fs)	rs1554291235
NM_001101426.4(CRPPA):c.1186G>T (p.Glu396Ter)	rs886042554
NM_001101426.4(CRPPA):c.1354T>C (p.Ter452Arg)	rs186882839
NM_001101426.4(CRPPA):c.258-1G>C	rs767978961
NM_001101426.4(CRPPA):c.802C>T (p.Arg268Ter)	rs368593151

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