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

Minimum submission review status:		Collection method:
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Gene type:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 26

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HGVS	dbSNP
NM_001101426.4(CRPPA):c.-21C>T	rs935897175
NM_001101426.4(CRPPA):c.1054C>A (p.Gln352Lys)	rs185594460
NM_001101426.4(CRPPA):c.1059G>A (p.Lys353=)	rs181099904
NM_001101426.4(CRPPA):c.1120-20C>G	rs758565814
NM_001101426.4(CRPPA):c.1120-291C>T	rs183379625
NM_001101426.4(CRPPA):c.1170C>T (p.Asn390=)	rs760178734
NM_001101426.4(CRPPA):c.123G>C (p.Gly41=)	rs761842188
NM_001101426.4(CRPPA):c.1251+16A>T	rs187344556
NM_001101426.4(CRPPA):c.1251+252G>A	rs28617534
NM_001101426.4(CRPPA):c.1338T>G (p.Gly446=)	rs1424229425
NM_001101426.4(CRPPA):c.222G>A (p.Arg74=)	rs769058832
NM_001101426.4(CRPPA):c.261A>G (p.Val87=)	rs886044356
NM_001101426.4(CRPPA):c.346C>T (p.Arg116Cys)	rs61744487
NM_001101426.4(CRPPA):c.52C>T (p.Leu18=)	rs886043287
NM_001101426.4(CRPPA):c.551G>A (p.Arg184Gln)	rs773739293
NM_001101426.4(CRPPA):c.645A>G (p.Gln215=)	rs532057629
NM_001101426.4(CRPPA):c.67G>T (p.Gly23Cys)	rs187484645
NM_001101426.4(CRPPA):c.684+12G>C	rs376232862
NM_001101426.4(CRPPA):c.685-19del	rs778040240
NM_001101426.4(CRPPA):c.789+276C>T	rs77362308
NM_001101426.4(CRPPA):c.790-11C>T	rs141363557
NM_001101426.4(CRPPA):c.790-14T>C	rs142414812
NM_001101426.4(CRPPA):c.825G>A (p.Ser275=)	rs766874330
NM_001101426.4(CRPPA):c.876A>G (p.Glu292=)	rs371300262
NM_001101426.4(CRPPA):c.933+3A>G	rs377582530
NM_001101426.4(CRPPA):c.999T>C (p.Asp333=)	rs376909665

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