List of variants in gene IRF6 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: 18

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HGVS	dbSNP	gnomAD frequency
NM_006147.4(IRF6):c.1016G>T (p.Arg339Ile)	rs121434231
NM_006147.4(IRF6):c.1137G>A (p.Trp379Ter)	rs121434228
NM_006147.4(IRF6):c.1177C>T (p.Gln393Ter)	rs121434225
NM_006147.4(IRF6):c.1186C>T (p.Pro396Ser)	rs121434230
NM_006147.4(IRF6):c.1198C>T (p.Arg400Trp)	rs28942095
NM_006147.4(IRF6):c.1199G>A (p.Arg400Gln)	rs200166664
NM_006147.4(IRF6):c.1271C>T (p.Ser424Leu)	rs387906968
NM_006147.4(IRF6):c.1316T>C (p.Leu439Pro)	rs886038202
NM_006147.4(IRF6):c.134G>A (p.Arg45Gln)	rs121434229
NM_006147.4(IRF6):c.145C>T (p.Gln49Ter)	rs397515434
NM_006147.4(IRF6):c.16C>T (p.Arg6Cys)	rs28942094
NM_006147.4(IRF6):c.250C>T (p.Arg84Cys)	rs121434226
NM_006147.4(IRF6):c.251G>A (p.Arg84His)	rs121434227
NM_006147.4(IRF6):c.251G>T (p.Arg84Leu)	rs121434227
NM_006147.4(IRF6):c.274G>T (p.Glu92Ter)	rs121434224
NM_006147.4(IRF6):c.5C>T (p.Ala2Val)	rs28942093
NM_006147.4(IRF6):c.65T>C (p.Leu22Pro)	rs387906967
NM_006147.4(IRF6):c.870_888delinsA (p.Phe290_Asp296delinsLeu)	rs587776569

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