List of variants in gene CRPPA reported by OMIM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_001101426.4(CRPPA):c.277_279del (p.Ile93del)	rs397515398	0.00005
NM_001101426.3(CRPPA):c.(535_684)+6399_(535_684)+14526del
NM_001101426.4(CRPPA):c.1105GTT[3] (p.Val372del)	rs587777798
NM_001101426.4(CRPPA):c.1120-1G>T	rs397515396
NM_001101426.4(CRPPA):c.256A>T (p.Arg86Ter)	rs397514548
NM_001101426.4(CRPPA):c.364G>C (p.Ala122Pro)	rs387907162
NM_001101426.4(CRPPA):c.466G>A (p.Asp156Asn)	rs397514547
NM_001101426.4(CRPPA):c.638T>G (p.Met213Arg)	rs397515408
NM_001101426.4(CRPPA):c.647C>A (p.Ala216Asp)	rs387907160
NM_001101426.4(CRPPA):c.713C>T (p.Thr238Ile)	rs397515409
NM_001101426.4(CRPPA):c.789+2T>G	rs397515397
NM_001101426.4(CRPPA):c.802C>T (p.Arg268Ter)	rs368593151
NM_001101426.4(CRPPA):c.832A>T (p.Lys278Ter)	rs387907161

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