List of variants in gene C19orf12 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_031448.6(C19orf12):c.391A>G (p.Lys131Glu)	rs146170087	0.00094
NM_031448.6(C19orf12):c.154G>C (p.Ala52Pro)	rs376103979	0.00013
NM_031448.6(C19orf12):c.-2C>T	rs397514477	0.00003
NM_031448.6(C19orf12):c.172G>A (p.Gly58Arg)	rs515726205	0.00001
NM_031448.6(C19orf12):c.215C>T (p.Pro72Leu)	rs201987973	0.00001
NM_001031726.4(C19orf12):c.164_166delGGG	rs398122409
NM_031448.6(C19orf12):c.171_181del (p.Gly58fs)	rs515726204
NM_031448.6(C19orf12):c.194_204del (p.Met65fs)	rs1599534394
NM_031448.6(C19orf12):c.205C>T (p.Gln69Ter)	rs1064797235
NM_031448.6(C19orf12):c.232_233del (p.Met78fs)	rs1599534276
NM_031448.6(C19orf12):c.303G>A (p.Trp101Ter)	rs1555714808
NM_031448.6(C19orf12):c.362T>A (p.Leu121Gln)	rs387907173

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