List of variants in gene ANKRD1 reported by Clinical Genetics, Academic Medical Center

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: 28

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HGVS	dbSNP	gnomAD frequency
NM_014391.3(ANKRD1):c.346-19T>A	rs10881854	0.05519
NM_014391.3(ANKRD1):c.346-15_346-14insA	rs60700562	0.04025
NM_014391.3(ANKRD1):c.346-15T>A	rs11595794	0.01808
NM_014391.3(ANKRD1):c.-17A>G	rs79341122	0.00753
NM_014391.3(ANKRD1):c.348G>A (p.Thr116=)	rs137914723	0.00748
NM_014391.3(ANKRD1):c.148G>C (p.Ala50Pro)	rs28730751	0.00387
NM_014391.3(ANKRD1):c.827C>T (p.Ala276Val)	rs35550482	0.00244
NM_014391.3(ANKRD1):c.319G>T (p.Val107Leu)	rs114435632	0.00240
NM_014391.3(ANKRD1):c.208-16C>T	rs79793575	0.00226
NM_014391.3(ANKRD1):c.208-15G>A	rs116511484	0.00184
NM_014391.3(ANKRD1):c.197G>A (p.Arg66Gln)	rs150797476	0.00092
NM_014391.3(ANKRD1):c.369G>A (p.Thr123=)	rs148979787	0.00069
NM_014391.3(ANKRD1):c.368C>T (p.Thr123Met)	rs145387010	0.00030
NM_014391.3(ANKRD1):c.652-10A>T	rs397517252	0.00023
NM_014391.3(ANKRD1):c.449A>T (p.Asp150Val)	rs150266349	0.00019
NM_014391.3(ANKRD1):c.750+17G>A	rs373898620	0.00009
NM_014391.3(ANKRD1):c.150C>G (p.Ala50=)	rs147484763	0.00006
NM_014391.3(ANKRD1):c.560C>T (p.Ser187Phe)	rs397517251	0.00001
NM_014391.3(ANKRD1):c.652-8T>C	rs753205311	0.00001
NM_014391.3(ANKRD1):c.710A>G (p.His237Arg)	rs145326465	0.00001
NM_014391.3(ANKRD1):c.196C>G (p.Arg66Gly)	rs397517249
NM_014391.3(ANKRD1):c.222dup (p.Leu75fs)	rs776659587
NM_014391.3(ANKRD1):c.346-16_346-15insATA	rs60923931
NM_014391.3(ANKRD1):c.346-17_346-10del	rs397517250
NM_014391.3(ANKRD1):c.346-19_346-14del	rs58762441
NM_014391.3(ANKRD1):c.346-19_346-18del	rs398014415
NM_014391.3(ANKRD1):c.346-43AT[13]	rs60406118
NM_014391.3(ANKRD1):c.3G>T (p.Met1Ile)	rs188706671

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