List of variants in gene ANKRD11 reported by Institute for Human Genetics, University Hospital Essen

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_013275.6(ANKRD11):c.1381_1384del (p.Glu461fs)	rs1597464953
NM_013275.6(ANKRD11):c.1711_1723del (p.Thr571fs)	rs2151763044
NM_013275.6(ANKRD11):c.1903_1907del (p.Lys635fs)	rs886041125
NM_013275.6(ANKRD11):c.1977C>A (p.Tyr659Ter)	rs749201074
NM_013275.6(ANKRD11):c.2398_2401del (p.Glu800fs)	rs797045027
NM_013275.6(ANKRD11):c.2408_2412del (p.Lys803fs)	rs886039902
NM_013275.6(ANKRD11):c.2692C>T (p.Arg898Ter)	rs780011005
NM_013275.6(ANKRD11):c.3591_3594del (p.Lys1198fs)	rs2151754276
NM_013275.6(ANKRD11):c.3888dup (p.Asn1297fs)	rs2151752804
NM_013275.6(ANKRD11):c.4087C>T (p.Arg1363Ter)	rs1364690005
NM_013275.6(ANKRD11):c.4218C>A (p.Tyr1406Ter)	rs764501022
NM_013275.6(ANKRD11):c.5123C>A (p.Ser1708Ter)	rs371204323
NM_013275.6(ANKRD11):c.7356dup (p.Lys2453fs)	rs2151729404
NM_013275.6(ANKRD11):c.7411_7422del (p.Thr2471_Gly2474del)	rs2151729118
NM_013275.6(ANKRD11):c.7470+2T>C	rs2151728875
NM_013275.6(ANKRD11):c.915del (p.Pro306fs)	rs2151766822

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