Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
16	g.89280737_89280739del	CA2576097314	ANKRD11	c.5805_5807del (p.Asp1935del) c.5608_5610del (n.5608_5610del) c.745-5546_745-5544del (n.745-5546_745-5544del) c.152-5546_152-5544del c.5703_5705del (p.Asp1901del) c.5508_5510del (p.Asp1836del) c.5676_5678del (p.Asp1892del)
16	g.89280739C>A	CA397152766	ANKRD11	c.5803G>T (p.Asp1935Tyr) c.5606G>T (n.5606G>T) c.745-5548G>T (n.745-5548G>T) c.152-5548G>T c.5701G>T (p.Asp1901Tyr) c.5506G>T (p.Asp1836Tyr) c.5674G>T (p.Asp1892Tyr)
16	g.89280739C>G	CA397152769	ANKRD11	c.5803G>C (p.Asp1935His) c.5606G>C (n.5606G>C) c.745-5548G>C (n.745-5548G>C) c.152-5548G>C c.5701G>C (p.Asp1901His) c.5506G>C (p.Asp1836His) c.5674G>C (p.Asp1892His)
16	g.89280739C>T	CA397152771	ANKRD11	c.5803G>A (p.Asp1935Asn) c.5606G>A (n.5606G>A) c.745-5548G>A (n.745-5548G>A) c.152-5548G>A c.5701G>A (p.Asp1901Asn) c.5506G>A (p.Asp1836Asn) c.5674G>A (p.Asp1892Asn)	gnomAD v4
16	g.89280740C>A	CA8241714	ANKRD11	c.5802G>T (p.Leu1934=) c.5605G>T (n.5605G>T) c.745-5549G>T (n.745-5549G>T) c.152-5549G>T c.5700G>T (p.Leu1900=) c.5505G>T (p.Leu1835=) c.5673G>T (p.Leu1891=)	dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16	g.89280740C=	CA2241587645	ANKRD11	c.5802G= (p.Leu1934=) c.5605G= (n.5605G=) c.745-5549G= (n.745-5549G=) c.152-5549G= c.5700G= (p.Leu1900=) c.5505G= (p.Leu1835=) c.5673G= (p.Leu1891=)
16	g.89280740C>G	CA497373452	ANKRD11	c.5802G>C (p.Leu1934=) c.5605G>C (n.5605G>C) c.745-5549G>C (n.745-5549G>C) c.152-5549G>C c.5700G>C (p.Leu1900=) c.5505G>C (p.Leu1835=) c.5673G>C (p.Leu1891=)
16	g.89280740C>T	CA8241715	ANKRD11	c.5802G>A (p.Leu1934=) c.5605G>A (n.5605G>A) c.745-5549G>A (n.745-5549G>A) c.152-5549G>A c.5700G>A (p.Leu1900=) c.5505G>A (p.Leu1835=) c.5673G>A (p.Leu1891=)	dbSNP ExAC gnomAD v2 gnomAD v4
16	g.89280741A=	CA2241587646	ANKRD11	c.5801T= (p.Leu1934=) c.5604T= (n.5604T=) c.745-5550T= (n.745-5550T=) c.152-5550T= c.5699T= (p.Leu1900=) c.5504T= (p.Leu1835=) c.5672T= (p.Leu1891=)
16	g.89280741A>C	CA397152778	ANKRD11	c.5801T>G (p.Leu1934Arg) c.5604T>G (n.5604T>G) c.745-5550T>G (n.745-5550T>G) c.152-5550T>G c.5699T>G (p.Leu1900Arg) c.5504T>G (p.Leu1835Arg) c.5672T>G (p.Leu1891Arg)
16	g.89280741A>G	CA397152775	ANKRD11	c.5801T>C (p.Leu1934Pro) c.5604T>C (n.5604T>C) c.745-5550T>C (n.745-5550T>C) c.152-5550T>C c.5699T>C (p.Leu1900Pro) c.5504T>C (p.Leu1835Pro) c.5672T>C (p.Leu1891Pro)	ClinVar dbSNP gnomAD v2 gnomAD v4
16	g.89280741A>T	CA397152776	ANKRD11	c.5801T>A (p.Leu1934Gln) c.5604T>A (n.5604T>A) c.745-5550T>A (n.745-5550T>A) c.152-5550T>A c.5699T>A (p.Leu1900Gln) c.5504T>A (p.Leu1835Gln) c.5672T>A (p.Leu1891Gln)
16	g.89280742G>A	CA497373454	ANKRD11	c.5800C>T (p.Leu1934=) c.5603C>T (n.5603C>T) c.745-5551C>T (n.745-5551C>T) c.152-5551C>T c.5698C>T (p.Leu1900=) c.5503C>T (p.Leu1835=) c.5671C>T (p.Leu1891=)	gnomAD v4
16	g.89280742G>C	CA397152781	ANKRD11	c.5800C>G (p.Leu1934Val) c.5603C>G (n.5603C>G) c.745-5551C>G (n.745-5551C>G) c.152-5551C>G c.5698C>G (p.Leu1900Val) c.5503C>G (p.Leu1835Val) c.5671C>G (p.Leu1891Val)
16	g.89280742G>T	CA397152783	ANKRD11	c.5800C>A (p.Leu1934Met) c.5603C>A (n.5603C>A) c.745-5551C>A (n.745-5551C>A) c.152-5551C>A c.5698C>A (p.Leu1900Met) c.5503C>A (p.Leu1835Met) c.5671C>A (p.Leu1891Met)	gnomAD v4
16	g.89280743C>A	CA497373456	ANKRD11	c.5799G>T (p.Pro1933=) c.5602G>T (n.5602G>T) c.745-5552G>T (n.745-5552G>T) c.152-5552G>T c.5697G>T (p.Pro1899=) c.5502G>T (p.Pro1834=) c.5670G>T (p.Pro1890=)	ClinVar dbSNP gnomAD v2 gnomAD v4
16	g.89280743C=	CA2241587647	ANKRD11	c.5799G= (p.Pro1933=) c.5602G= (n.5602G=) c.745-5552G= (n.745-5552G=) c.152-5552G= c.5697G= (p.Pro1899=) c.5502G= (p.Pro1834=) c.5670G= (p.Pro1890=)
16	g.89280743C>G	CA286511242	ANKRD11	c.5799G>C (p.Pro1933=) c.5602G>C (n.5602G>C) c.745-5552G>C (n.745-5552G>C) c.152-5552G>C c.5697G>C (p.Pro1899=) c.5502G>C (p.Pro1834=) c.5670G>C (p.Pro1890=)	dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16	g.89280743C>T	CA8241716	ANKRD11	c.5799G>A (p.Pro1933=) c.5602G>A (n.5602G>A) c.745-5552G>A (n.745-5552G>A) c.152-5552G>A c.5697G>A (p.Pro1899=) c.5502G>A (p.Pro1834=) c.5670G>A (p.Pro1890=)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16	g.89280744G>A	CA8241717	ANKRD11	c.5798C>T (p.Pro1933Leu) c.5601C>T (n.5601C>T) c.745-5553C>T (n.745-5553C>T) c.152-5553C>T c.5696C>T (p.Pro1899Leu) c.5501C>T (p.Pro1834Leu) c.5669C>T (p.Pro1890Leu)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16	g.89280744G>C	CA8241718	ANKRD11	c.5798C>G (p.Pro1933Arg) c.5601C>G (n.5601C>G) c.745-5553C>G (n.745-5553C>G) c.152-5553C>G c.5696C>G (p.Pro1899Arg) c.5501C>G (p.Pro1834Arg) c.5669C>G (p.Pro1890Arg)	dbSNP ExAC gnomAD v2 gnomAD v4
16	g.89280744G=	CA2241587648	ANKRD11	c.5798C= (p.Pro1933=) c.5601C= (n.5601C=) c.745-5553C= (n.745-5553C=) c.152-5553C= c.5696C= (p.Pro1899=) c.5501C= (p.Pro1834=) c.5669C= (p.Pro1890=)
16	g.89280744G>T	CA397152787	ANKRD11	c.5798C>A (p.Pro1933Gln) c.5601C>A (n.5601C>A) c.745-5553C>A (n.745-5553C>A) c.152-5553C>A c.5696C>A (p.Pro1899Gln) c.5501C>A (p.Pro1834Gln) c.5669C>A (p.Pro1890Gln)
16	g.89280745G>A	CA397152791	ANKRD11	c.5797C>T (p.Pro1933Ser) c.5600C>T (n.5600C>T) c.745-5554C>T (n.745-5554C>T) c.152-5554C>T c.5695C>T (p.Pro1899Ser) c.5500C>T (p.Pro1834Ser) c.5668C>T (p.Pro1890Ser)	dbSNP gnomAD v4
16	g.89280745G>C	CA397152793	ANKRD11	c.5797C>G (p.Pro1933Ala) c.5600C>G (n.5600C>G) c.745-5554C>G (n.745-5554C>G) c.152-5554C>G c.5695C>G (p.Pro1899Ala) c.5500C>G (p.Pro1834Ala) c.5668C>G (p.Pro1890Ala)
16	g.89280745G=	CA2241587649	ANKRD11	c.5797C= (p.Pro1933=) c.5600C= (n.5600C=) c.745-5554C= (n.745-5554C=) c.152-5554C= c.5695C= (p.Pro1899=) c.5500C= (p.Pro1834=) c.5668C= (p.Pro1890=)
16	g.89280745G>T	CA8241719	ANKRD11	c.5797C>A (p.Pro1933Thr) c.5600C>A (n.5600C>A) c.745-5554C>A (n.745-5554C>A) c.152-5554C>A c.5695C>A (p.Pro1899Thr) c.5500C>A (p.Pro1834Thr) c.5668C>A (p.Pro1890Thr)	dbSNP ExAC gnomAD v2 gnomAD v4
16	g.89280746C>A	CA397152800	ANKRD11	c.5796G>T (p.Glu1932Asp) c.5599G>T (n.5599G>T) c.745-5555G>T (n.745-5555G>T) c.152-5555G>T c.5694G>T (p.Glu1898Asp) c.5499G>T (p.Glu1833Asp) c.5667G>T (p.Glu1889Asp)
16	g.89280746C=	CA2241587650	ANKRD11	c.5796G= (p.Glu1932=) c.5599G= (n.5599G=) c.745-5555G= (n.745-5555G=) c.152-5555G= c.5694G= (p.Glu1898=) c.5499G= (p.Glu1833=) c.5667G= (p.Glu1889=)
16	g.89280746C>G	CA397152802	ANKRD11	c.5796G>C (p.Glu1932Asp) c.5599G>C (n.5599G>C) c.745-5555G>C (n.745-5555G>C) c.152-5555G>C c.5694G>C (p.Glu1898Asp) c.5499G>C (p.Glu1833Asp) c.5667G>C (p.Glu1889Asp)
16	g.89280746C>T	CA286511258	ANKRD11	c.5796G>A (p.Glu1932=) c.5599G>A (n.5599G>A) c.745-5555G>A (n.745-5555G>A) c.152-5555G>A c.5694G>A (p.Glu1898=) c.5499G>A (p.Glu1833=) c.5667G>A (p.Glu1889=)	dbSNP
16	g.89280747T>A	CA397152804	ANKRD11	c.5795A>T (p.Glu1932Val) c.5598A>T (n.5598A>T) c.745-5556A>T (n.745-5556A>T) c.152-5556A>T c.5693A>T (p.Glu1898Val) c.5498A>T (p.Glu1833Val) c.5666A>T (p.Glu1889Val)	ClinVar dbSNP gnomAD v3 gnomAD v4
16	g.89280747T>C	CA397152808	ANKRD11	c.5795A>G (p.Glu1932Gly) c.5598A>G (n.5598A>G) c.745-5556A>G (n.745-5556A>G) c.152-5556A>G c.5693A>G (p.Glu1898Gly) c.5498A>G (p.Glu1833Gly) c.5666A>G (p.Glu1889Gly)
16	g.89280747T>G	CA397152806	ANKRD11	c.5795A>C (p.Glu1932Ala) c.5598A>C (n.5598A>C) c.745-5556A>C (n.745-5556A>C) c.152-5556A>C c.5693A>C (p.Glu1898Ala) c.5498A>C (p.Glu1833Ala) c.5666A>C (p.Glu1889Ala)
16	g.89280747T=	CA2241587651	ANKRD11	c.5795A= (p.Glu1932=) c.5598A= (n.5598A=) c.745-5556A= (n.745-5556A=) c.152-5556A= c.5693A= (p.Glu1898=) c.5498A= (p.Glu1833=) c.5666A= (p.Glu1889=)
16	g.89280748C>A	CA397152810	ANKRD11	c.5794G>T (p.Glu1932Ter) c.5597G>T (n.5597G>T) c.745-5557G>T (n.745-5557G>T) c.152-5557G>T c.5692G>T (p.Glu1898Ter) c.5497G>T (p.Glu1833Ter) c.5665G>T (p.Glu1889Ter)
16	g.89280748C>G	CA397152815	ANKRD11	c.5794G>C (p.Glu1932Gln) c.5597G>C (n.5597G>C) c.745-5557G>C (n.745-5557G>C) c.152-5557G>C c.5692G>C (p.Glu1898Gln) c.5497G>C (p.Glu1833Gln) c.5665G>C (p.Glu1889Gln)
16	g.89280748C>T	CA397152813	ANKRD11	c.5794G>A (p.Glu1932Lys) c.5597G>A (n.5597G>A) c.745-5557G>A (n.745-5557G>A) c.152-5557G>A c.5692G>A (p.Glu1898Lys) c.5497G>A (p.Glu1833Lys) c.5665G>A (p.Glu1889Lys)
16	g.89280749C>A	CA497373460	ANKRD11	c.5793G>T (p.Leu1931=) c.5596G>T (n.5596G>T) c.745-5558G>T (n.745-5558G>T) c.152-5558G>T c.5691G>T (p.Leu1897=) c.5496G>T (p.Leu1832=) c.5664G>T (p.Leu1888=)
16	g.89280749C>G	CA497373467	ANKRD11	c.5793G>C (p.Leu1931=) c.5596G>C (n.5596G>C) c.745-5558G>C (n.745-5558G>C) c.152-5558G>C c.5691G>C (p.Leu1897=) c.5496G>C (p.Leu1832=) c.5664G>C (p.Leu1888=)
16	g.89280749C>T	CA497373465	ANKRD11	c.5793G>A (p.Leu1931=) c.5596G>A (n.5596G>A) c.745-5558G>A (n.745-5558G>A) c.152-5558G>A c.5691G>A (p.Leu1897=) c.5496G>A (p.Leu1832=) c.5664G>A (p.Leu1888=)
16	g.89280750A>C	CA397152817	ANKRD11	c.5792T>G (p.Leu1931Arg) c.5595T>G (n.5595T>G) c.745-5559T>G (n.745-5559T>G) c.152-5559T>G c.5690T>G (p.Leu1897Arg) c.5495T>G (p.Leu1832Arg) c.5663T>G (p.Leu1888Arg)	gnomAD v4
16	g.89280750A>G	CA397152823	ANKRD11	c.5792T>C (p.Leu1931Pro) c.5595T>C (n.5595T>C) c.745-5559T>C (n.745-5559T>C) c.152-5559T>C c.5690T>C (p.Leu1897Pro) c.5495T>C (p.Leu1832Pro) c.5663T>C (p.Leu1888Pro)
16	g.89280750A>T	CA397152825	ANKRD11	c.5792T>A (p.Leu1931Gln) c.5595T>A (n.5595T>A) c.745-5559T>A (n.745-5559T>A) c.152-5559T>A c.5690T>A (p.Leu1897Gln) c.5495T>A (p.Leu1832Gln) c.5663T>A (p.Leu1888Gln)
16	g.89280750_89280765delinsAGGTAGCTGGGCTCCG	CA2241587652	ANKRD11	c.5777_5792delinsCGGAGCCCAGCTACCT (p.Pro1926=) c.5580_5595delinsCGGAGCCCAGCTACCT (n.5580_5595delinsCGGAGCCCAGCTACCT) c.745-5574_745-5559delinsCGGAGCCCAGCTACCT (n.745-5574_745-5559delinsCGGAGCCCAGCTACCT) c.152-5574_152-5559delinsCGGAGCCCAGCTACCT c.5675_5690delinsCGGAGCCCAGCTACCT (p.Pro1892=) c.5480_5495delinsCGGAGCCCAGCTACCT (p.Pro1827=) c.5648_5663delinsCGGAGCCCAGCTACCT (p.Pro1883=)
16	g.89280751G>A	CA286511259	ANKRD11	c.5791C>T (p.Leu1931=) c.5594C>T (n.5594C>T) c.745-5560C>T (n.745-5560C>T) c.152-5560C>T c.5689C>T (p.Leu1897=) c.5494C>T (p.Leu1832=) c.5662C>T (p.Leu1888=)	dbSNP gnomAD v3 gnomAD v4
16	g.89280751G>C	CA397152826	ANKRD11	c.5791C>G (p.Leu1931Val) c.5594C>G (n.5594C>G) c.745-5560C>G (n.745-5560C>G) c.152-5560C>G c.5689C>G (p.Leu1897Val) c.5494C>G (p.Leu1832Val) c.5662C>G (p.Leu1888Val)	dbSNP gnomAD v2 gnomAD v4
16	g.89280751G=	CA2241587653	ANKRD11	c.5791C= (p.Leu1931=) c.5594C= (n.5594C=) c.745-5560C= (n.745-5560C=) c.152-5560C= c.5689C= (p.Leu1897=) c.5494C= (p.Leu1832=) c.5662C= (p.Leu1888=)
16	g.89280751G>T	CA397152829	ANKRD11	c.5791C>A (p.Leu1931Met) c.5594C>A (n.5594C>A) c.745-5560C>A (n.745-5560C>A) c.152-5560C>A c.5689C>A (p.Leu1897Met) c.5494C>A (p.Leu1832Met) c.5662C>A (p.Leu1888Met)
16	g.89280753_89280767del	CA8241720	ANKRD11	c.5777_5791del (p.Pro1926_Tyr1930del) c.5580_5594del (n.5580_5594del) c.745-5574_745-5560del (n.745-5574_745-5560del) c.152-5574_152-5560del c.5675_5689del (p.Pro1892_Tyr1896del) c.5480_5494del (p.Pro1827_Tyr1831del) c.5648_5662del (p.Pro1883_Tyr1887del)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16	g.89280752G>A	CA497373469	ANKRD11	c.5790C>T (p.Tyr1930=) c.5593C>T (n.5593C>T) c.745-5561C>T (n.745-5561C>T) c.152-5561C>T c.5688C>T (p.Tyr1896=) c.5493C>T (p.Tyr1831=) c.5661C>T (p.Tyr1887=)	gnomAD v4
16	g.89280752G>C	CA10603349	ANKRD11	c.5790C>G (p.Tyr1930Ter) c.5593C>G (n.5593C>G) c.745-5561C>G (n.745-5561C>G) c.152-5561C>G c.5688C>G (p.Tyr1896Ter) c.5493C>G (p.Tyr1831Ter) c.5661C>G (p.Tyr1887Ter)	ClinVar dbSNP
16	g.89280752G=	CA2241587654	ANKRD11	c.5790C= (p.Tyr1930=) c.5593C= (n.5593C=) c.745-5561C= (n.745-5561C=) c.152-5561C= c.5688C= (p.Tyr1896=) c.5493C= (p.Tyr1831=) c.5661C= (p.Tyr1887=)
16	g.89280752G>T	CA397152839	ANKRD11	c.5790C>A (p.Tyr1930Ter) c.5593C>A (n.5593C>A) c.745-5561C>A (n.745-5561C>A) c.152-5561C>A c.5688C>A (p.Tyr1896Ter) c.5493C>A (p.Tyr1831Ter) c.5661C>A (p.Tyr1887Ter)
16	g.89280753T>A	CA397152842	ANKRD11	c.5789A>T (p.Tyr1930Phe) c.5592A>T (n.5592A>T) c.745-5562A>T (n.745-5562A>T) c.152-5562A>T c.5687A>T (p.Tyr1896Phe) c.5492A>T (p.Tyr1831Phe) c.5660A>T (p.Tyr1887Phe)
16	g.89280753T>C	CA397152844	ANKRD11	c.5789A>G (p.Tyr1930Cys) c.5592A>G (n.5592A>G) c.745-5562A>G (n.745-5562A>G) c.152-5562A>G c.5687A>G (p.Tyr1896Cys) c.5492A>G (p.Tyr1831Cys) c.5660A>G (p.Tyr1887Cys)
16	g.89280753T>G	CA397152846	ANKRD11	c.5789A>C (p.Tyr1930Ser) c.5592A>C (n.5592A>C) c.745-5562A>C (n.745-5562A>C) c.152-5562A>C c.5687A>C (p.Tyr1896Ser) c.5492A>C (p.Tyr1831Ser) c.5660A>C (p.Tyr1887Ser)
16	g.89280754A>C	CA397152851	ANKRD11	c.5788T>G (p.Tyr1930Asp) c.5591T>G (n.5591T>G) c.745-5563T>G (n.745-5563T>G) c.152-5563T>G c.5686T>G (p.Tyr1896Asp) c.5491T>G (p.Tyr1831Asp) c.5659T>G (p.Tyr1887Asp)
16	g.89280754A>G	CA397152848	ANKRD11	c.5788T>C (p.Tyr1930His) c.5591T>C (n.5591T>C) c.745-5563T>C (n.745-5563T>C) c.152-5563T>C c.5686T>C (p.Tyr1896His) c.5491T>C (p.Tyr1831His) c.5659T>C (p.Tyr1887His)
16	g.89280754A>T	CA397152849	ANKRD11	c.5788T>A (p.Tyr1930Asn) c.5591T>A (n.5591T>A) c.745-5563T>A (n.745-5563T>A) c.152-5563T>A c.5686T>A (p.Tyr1896Asn) c.5491T>A (p.Tyr1831Asn) c.5659T>A (p.Tyr1887Asn)
16	g.89280755G>A	CA497373471	ANKRD11	c.5787C>T (p.Ser1929=) c.5590C>T (n.5590C>T) c.745-5564C>T (n.745-5564C>T) c.152-5564C>T c.5685C>T (p.Ser1895=) c.5490C>T (p.Ser1830=) c.5658C>T (p.Ser1886=)	dbSNP gnomAD v3 gnomAD v4
16	g.89280755G>C	CA397152853	ANKRD11	c.5787C>G (p.Ser1929Arg) c.5590C>G (n.5590C>G) c.745-5564C>G (n.745-5564C>G) c.152-5564C>G c.5685C>G (p.Ser1895Arg) c.5490C>G (p.Ser1830Arg) c.5658C>G (p.Ser1886Arg)	gnomAD v4
16	g.89280755G=	CA2241587655	ANKRD11	c.5787C= (p.Ser1929=) c.5590C= (n.5590C=) c.745-5564C= (n.745-5564C=) c.152-5564C= c.5685C= (p.Ser1895=) c.5490C= (p.Ser1830=) c.5658C= (p.Ser1886=)
16	g.89280755G>T	CA397152854	ANKRD11	c.5787C>A (p.Ser1929Arg) c.5590C>A (n.5590C>A) c.745-5564C>A (n.745-5564C>A) c.152-5564C>A c.5685C>A (p.Ser1895Arg) c.5490C>A (p.Ser1830Arg) c.5658C>A (p.Ser1886Arg)
16	g.89280756C>A	CA397152857	ANKRD11	c.5786G>T (p.Ser1929Ile) c.5589G>T (n.5589G>T) c.745-5565G>T (n.745-5565G>T) c.152-5565G>T c.5684G>T (p.Ser1895Ile) c.5489G>T (p.Ser1830Ile) c.5657G>T (p.Ser1886Ile)
16	g.89280756C=	CA2241587656	ANKRD11	c.5786G= (p.Ser1929=) c.5589G= (n.5589G=) c.745-5565G= (n.745-5565G=) c.152-5565G= c.5684G= (p.Ser1895=) c.5489G= (p.Ser1830=) c.5657G= (p.Ser1886=)
16	g.89280756C>G	CA397152859	ANKRD11	c.5786G>C (p.Ser1929Thr) c.5589G>C (n.5589G>C) c.745-5565G>C (n.745-5565G>C) c.152-5565G>C c.5684G>C (p.Ser1895Thr) c.5489G>C (p.Ser1830Thr) c.5657G>C (p.Ser1886Thr)
16	g.89280756C>T	CA397152860	ANKRD11	c.5786G>A (p.Ser1929Asn) c.5589G>A (n.5589G>A) c.745-5565G>A (n.745-5565G>A) c.152-5565G>A c.5684G>A (p.Ser1895Asn) c.5489G>A (p.Ser1830Asn) c.5657G>A (p.Ser1886Asn)	ClinVar dbSNP gnomAD v2 gnomAD v4
16	g.89280757T>A	CA397152861	ANKRD11	c.5785A>T (p.Ser1929Cys) c.5588A>T (n.5588A>T) c.745-5566A>T (n.745-5566A>T) c.152-5566A>T c.5683A>T (p.Ser1895Cys) c.5488A>T (p.Ser1830Cys) c.5656A>T (p.Ser1886Cys)
16	g.89280757T>C	CA397152862	ANKRD11	c.5785A>G (p.Ser1929Gly) c.5588A>G (n.5588A>G) c.745-5566A>G (n.745-5566A>G) c.152-5566A>G c.5683A>G (p.Ser1895Gly) c.5488A>G (p.Ser1830Gly) c.5656A>G (p.Ser1886Gly)
16	g.89280757T>G	CA397152864	ANKRD11	c.5785A>C (p.Ser1929Arg) c.5588A>C (n.5588A>C) c.745-5566A>C (n.745-5566A>C) c.152-5566A>C c.5683A>C (p.Ser1895Arg) c.5488A>C (p.Ser1830Arg) c.5656A>C (p.Ser1886Arg)
16	g.89280757_89280759del	CA2634942997	ANKRD11	c.5783_5785del (p.Pro1928_Ser1929delinsArg) c.5586_5588del (n.5586_5588del) c.745-5568_745-5566del (n.745-5568_745-5566del) c.152-5568_152-5566del c.5681_5683del (p.Pro1894_Ser1895delinsArg) c.5486_5488del (p.Pro1829_Ser1830delinsArg) c.5654_5656del (p.Pro1885_Ser1886delinsArg)	gnomAD v4
16	g.89280758G>A	CA497373475	ANKRD11	c.5784C>T (p.Pro1928=) c.5587C>T (n.5587C>T) c.745-5567C>T (n.745-5567C>T) c.152-5567C>T c.5682C>T (p.Pro1894=) c.5487C>T (p.Pro1829=) c.5655C>T (p.Pro1885=)
16	g.89280758G>C	CA497373476	ANKRD11	c.5784C>G (p.Pro1928=) c.5587C>G (n.5587C>G) c.745-5567C>G (n.745-5567C>G) c.152-5567C>G c.5682C>G (p.Pro1894=) c.5487C>G (p.Pro1829=) c.5655C>G (p.Pro1885=)
16	g.89280758G>T	CA497373473	ANKRD11	c.5784C>A (p.Pro1928=) c.5587C>A (n.5587C>A) c.745-5567C>A (n.745-5567C>A) c.152-5567C>A c.5682C>A (p.Pro1894=) c.5487C>A (p.Pro1829=) c.5655C>A (p.Pro1885=)
16	g.89280759G>A	CA8241721	ANKRD11	c.5783C>T (p.Pro1928Leu) c.5586C>T (n.5586C>T) c.745-5568C>T (n.745-5568C>T) c.152-5568C>T c.5681C>T (p.Pro1894Leu) c.5486C>T (p.Pro1829Leu) c.5654C>T (p.Pro1885Leu)	dbSNP ExAC gnomAD v2 gnomAD v4
16	g.89280759G>C	CA397152867	ANKRD11	c.5783C>G (p.Pro1928Arg) c.5586C>G (n.5586C>G) c.745-5568C>G (n.745-5568C>G) c.152-5568C>G c.5681C>G (p.Pro1894Arg) c.5486C>G (p.Pro1829Arg) c.5654C>G (p.Pro1885Arg)
16	g.89280759G=	CA2241587657	ANKRD11	c.5783C= (p.Pro1928=) c.5586C= (n.5586C=) c.745-5568C= (n.745-5568C=) c.152-5568C= c.5681C= (p.Pro1894=) c.5486C= (p.Pro1829=) c.5654C= (p.Pro1885=)
16	g.89280759G>T	CA397152869	ANKRD11	c.5783C>A (p.Pro1928His) c.5586C>A (n.5586C>A) c.745-5568C>A (n.745-5568C>A) c.152-5568C>A c.5681C>A (p.Pro1894His) c.5486C>A (p.Pro1829His) c.5654C>A (p.Pro1885His)
16	g.89280760G>A	CA397152872	ANKRD11	c.5782C>T (p.Pro1928Ser) c.5585C>T (n.5585C>T) c.745-5569C>T (n.745-5569C>T) c.152-5569C>T c.5680C>T (p.Pro1894Ser) c.5485C>T (p.Pro1829Ser) c.5653C>T (p.Pro1885Ser)	gnomAD v4
16	g.89280760G>C	CA397152874	ANKRD11	c.5782C>G (p.Pro1928Ala) c.5585C>G (n.5585C>G) c.745-5569C>G (n.745-5569C>G) c.152-5569C>G c.5680C>G (p.Pro1894Ala) c.5485C>G (p.Pro1829Ala) c.5653C>G (p.Pro1885Ala)	gnomAD v4
16	g.89280760G>T	CA397152871	ANKRD11	c.5782C>A (p.Pro1928Thr) c.5585C>A (n.5585C>A) c.745-5569C>A (n.745-5569C>A) c.152-5569C>A c.5680C>A (p.Pro1894Thr) c.5485C>A (p.Pro1829Thr) c.5653C>A (p.Pro1885Thr)
16	g.89280761C>A	CA397152876	ANKRD11	c.5781G>T (p.Glu1927Asp) c.5584G>T (n.5584G>T) c.745-5570G>T (n.745-5570G>T) c.152-5570G>T c.5679G>T (p.Glu1893Asp) c.5484G>T (p.Glu1828Asp) c.5652G>T (p.Glu1884Asp)
16	g.89280761C>G	CA397152878	ANKRD11	c.5781G>C (p.Glu1927Asp) c.5584G>C (n.5584G>C) c.745-5570G>C (n.745-5570G>C) c.152-5570G>C c.5679G>C (p.Glu1893Asp) c.5484G>C (p.Glu1828Asp) c.5652G>C (p.Glu1884Asp)	gnomAD v4
16	g.89280761C>T	CA497373478	ANKRD11	c.5781G>A (p.Glu1927=) c.5584G>A (n.5584G>A) c.745-5570G>A (n.745-5570G>A) c.152-5570G>A c.5679G>A (p.Glu1893=) c.5484G>A (p.Glu1828=) c.5652G>A (p.Glu1884=)	gnomAD v4
16	g.89280762T>A	CA397152880	ANKRD11	c.5780A>T (p.Glu1927Val) c.5583A>T (n.5583A>T) c.745-5571A>T (n.745-5571A>T) c.152-5571A>T c.5678A>T (p.Glu1893Val) c.5483A>T (p.Glu1828Val) c.5651A>T (p.Glu1884Val)
16	g.89280762T>C	CA397152882	ANKRD11	c.5780A>G (p.Glu1927Gly) c.5583A>G (n.5583A>G) c.745-5571A>G (n.745-5571A>G) c.152-5571A>G c.5678A>G (p.Glu1893Gly) c.5483A>G (p.Glu1828Gly) c.5651A>G (p.Glu1884Gly)
16	g.89280762T>G	CA397152884	ANKRD11	c.5780A>C (p.Glu1927Ala) c.5583A>C (n.5583A>C) c.745-5571A>C (n.745-5571A>C) c.152-5571A>C c.5678A>C (p.Glu1893Ala) c.5483A>C (p.Glu1828Ala) c.5651A>C (p.Glu1884Ala)
16	g.89280763C>A	CA397152887	ANKRD11	c.5779G>T (p.Glu1927Ter) c.5582G>T (n.5582G>T) c.745-5572G>T (n.745-5572G>T) c.152-5572G>T c.5677G>T (p.Glu1893Ter) c.5482G>T (p.Glu1828Ter) c.5650G>T (p.Glu1884Ter)
16	g.89280763C>G	CA397152888	ANKRD11	c.5779G>C (p.Glu1927Gln) c.5582G>C (n.5582G>C) c.745-5572G>C (n.745-5572G>C) c.152-5572G>C c.5677G>C (p.Glu1893Gln) c.5482G>C (p.Glu1828Gln) c.5650G>C (p.Glu1884Gln)	ClinVar gnomAD v4
16	g.89280763C>T	CA397152891	ANKRD11	c.5779G>A (p.Glu1927Lys) c.5582G>A (n.5582G>A) c.745-5572G>A (n.745-5572G>A) c.152-5572G>A c.5677G>A (p.Glu1893Lys) c.5482G>A (p.Glu1828Lys) c.5650G>A (p.Glu1884Lys)
16	g.89280764C>A	CA497373500	ANKRD11	c.5778G>T (p.Pro1926=) c.5581G>T (n.5581G>T) c.745-5573G>T (n.745-5573G>T) c.152-5573G>T c.5676G>T (p.Pro1892=) c.5481G>T (p.Pro1827=) c.5649G>T (p.Pro1883=)
16	g.89280764C=	CA2241587658	ANKRD11	c.5778G= (p.Pro1926=) c.5581G= (n.5581G=) c.745-5573G= (n.745-5573G=) c.152-5573G= c.5676G= (p.Pro1892=) c.5481G= (p.Pro1827=) c.5649G= (p.Pro1883=)
16	g.89280764C>G	CA497373501	ANKRD11	c.5778G>C (p.Pro1926=) c.5581G>C (n.5581G>C) c.745-5573G>C (n.745-5573G>C) c.152-5573G>C c.5676G>C (p.Pro1892=) c.5481G>C (p.Pro1827=) c.5649G>C (p.Pro1883=)
16	g.89280764C>T	CA8241722	ANKRD11	c.5778G>A (p.Pro1926=) c.5581G>A (n.5581G>A) c.745-5573G>A (n.745-5573G>A) c.152-5573G>A c.5676G>A (p.Pro1892=) c.5481G>A (p.Pro1827=) c.5649G>A (p.Pro1883=)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16	g.89280765G>A	CA8241723	ANKRD11	c.5777C>T (p.Pro1926Leu) c.5580C>T (n.5580C>T) c.745-5574C>T (n.745-5574C>T) c.152-5574C>T c.5675C>T (p.Pro1892Leu) c.5480C>T (p.Pro1827Leu) c.5648C>T (p.Pro1883Leu)	dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16	g.89280765G>C	CA397153070	ANKRD11	c.5777C>G (p.Pro1926Arg) c.5580C>G (n.5580C>G) c.745-5574C>G (n.745-5574C>G) c.152-5574C>G c.5675C>G (p.Pro1892Arg) c.5480C>G (p.Pro1827Arg) c.5648C>G (p.Pro1883Arg)	dbSNP gnomAD v3 gnomAD v4
16	g.89280765G=	CA2241587659	ANKRD11	c.5777C= (p.Pro1926=) c.5580C= (n.5580C=) c.745-5574C= (n.745-5574C=) c.152-5574C= c.5675C= (p.Pro1892=) c.5480C= (p.Pro1827=) c.5648C= (p.Pro1883=)
16	g.89280765G>T	CA397153071	ANKRD11	c.5777C>A (p.Pro1926Gln) c.5580C>A (n.5580C>A) c.745-5574C>A (n.745-5574C>A) c.152-5574C>A c.5675C>A (p.Pro1892Gln) c.5480C>A (p.Pro1827Gln) c.5648C>A (p.Pro1883Gln)
16	g.89280770dup	CA624452384	ANKRD11	c.5777dup (p.Glu1927GlyfsTer23) c.5580dup (n.5580dup) c.745-5574dup (n.745-5574dup) c.152-5574dup c.5675dup (p.Glu1893GlyfsTer23) c.5480dup (p.Glu1828GlyfsTer23) c.5648dup (p.Glu1884GlyfsTer23)	ClinVar dbSNP gnomAD v2 gnomAD v4
16	g.89280770del	CA2634943012	ANKRD11	c.5777del (p.Pro1926ArgfsTer?) c.5580del (n.5580del) c.745-5574del (n.745-5574del) c.152-5574del c.5675del (p.Pro1892ArgfsTer?) c.5480del (p.Pro1827ArgfsTer?) c.5648del (p.Pro1883ArgfsTer?)	gnomAD v4
16	g.89280766G>A	CA397153073	ANKRD11	c.5776C>T (p.Pro1926Ser) c.5579C>T (n.5579C>T) c.745-5575C>T (n.745-5575C>T) c.152-5575C>T c.5674C>T (p.Pro1892Ser) c.5479C>T (p.Pro1827Ser) c.5647C>T (p.Pro1883Ser)
16	g.89280766G>C	CA397153074	ANKRD11	c.5776C>G (p.Pro1926Ala) c.5579C>G (n.5579C>G) c.745-5575C>G (n.745-5575C>G) c.152-5575C>G c.5674C>G (p.Pro1892Ala) c.5479C>G (p.Pro1827Ala) c.5647C>G (p.Pro1883Ala)
16	g.89280766G>T	CA397153072	ANKRD11	c.5776C>A (p.Pro1926Thr) c.5579C>A (n.5579C>A) c.745-5575C>A (n.745-5575C>A) c.152-5575C>A c.5674C>A (p.Pro1892Thr) c.5479C>A (p.Pro1827Thr) c.5647C>A (p.Pro1883Thr)
16	g.89280767G>A	CA497373502	ANKRD11	c.5775C>T (p.Pro1925=) c.5578C>T (n.5578C>T) c.745-5576C>T (n.745-5576C>T) c.152-5576C>T c.5673C>T (p.Pro1891=) c.5478C>T (p.Pro1826=) c.5646C>T (p.Pro1882=)	dbSNP gnomAD v2 gnomAD v4
16	g.89280767G>C	CA497373503	ANKRD11	c.5775C>G (p.Pro1925=) c.5578C>G (n.5578C>G) c.745-5576C>G (n.745-5576C>G) c.152-5576C>G c.5673C>G (p.Pro1891=) c.5478C>G (p.Pro1826=) c.5646C>G (p.Pro1882=)
16	g.89280767G=	CA2241587660	ANKRD11	c.5775C= (p.Pro1925=) c.5578C= (n.5578C=) c.745-5576C= (n.745-5576C=) c.152-5576C= c.5673C= (p.Pro1891=) c.5478C= (p.Pro1826=) c.5646C= (p.Pro1882=)
16	g.89280767G>T	CA497373504	ANKRD11	c.5775C>A (p.Pro1925=) c.5578C>A (n.5578C>A) c.745-5576C>A (n.745-5576C>A) c.152-5576C>A c.5673C>A (p.Pro1891=) c.5478C>A (p.Pro1826=) c.5646C>A (p.Pro1882=)	dbSNP gnomAD v3 gnomAD v4
16	g.89280768G>A	CA397153075	ANKRD11	c.5774C>T (p.Pro1925Leu) c.5577C>T (n.5577C>T) c.745-5577C>T (n.745-5577C>T) c.152-5577C>T c.5672C>T (p.Pro1891Leu) c.5477C>T (p.Pro1826Leu) c.5645C>T (p.Pro1882Leu)
16	g.89280768G>C	CA397153076	ANKRD11	c.5774C>G (p.Pro1925Arg) c.5577C>G (n.5577C>G) c.745-5577C>G (n.745-5577C>G) c.152-5577C>G c.5672C>G (p.Pro1891Arg) c.5477C>G (p.Pro1826Arg) c.5645C>G (p.Pro1882Arg)	gnomAD v4
16	g.89280768G>T	CA397153077	ANKRD11	c.5774C>A (p.Pro1925His) c.5577C>A (n.5577C>A) c.745-5577C>A (n.745-5577C>A) c.152-5577C>A c.5672C>A (p.Pro1891His) c.5477C>A (p.Pro1826His) c.5645C>A (p.Pro1882His)
16	g.89280769G>A	CA8241725	ANKRD11	c.5773C>T (p.Pro1925Ser) c.5576C>T (n.5576C>T) c.745-5578C>T (n.745-5578C>T) c.152-5578C>T c.5671C>T (p.Pro1891Ser) c.5476C>T (p.Pro1826Ser) c.5644C>T (p.Pro1882Ser)	dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16	g.89280769G>C	CA397153078	ANKRD11	c.5773C>G (p.Pro1925Ala) c.5576C>G (n.5576C>G) c.745-5578C>G (n.745-5578C>G) c.152-5578C>G c.5671C>G (p.Pro1891Ala) c.5476C>G (p.Pro1826Ala) c.5644C>G (p.Pro1882Ala)	gnomAD v4
16	g.89280769G=	CA2241587661	ANKRD11	c.5773C= (p.Pro1925=) c.5576C= (n.5576C=) c.745-5578C= (n.745-5578C=) c.152-5578C= c.5671C= (p.Pro1891=) c.5476C= (p.Pro1826=) c.5644C= (p.Pro1882=)
16	g.89280769G>T	CA8241724	ANKRD11	c.5773C>A (p.Pro1925Thr) c.5576C>A (n.5576C>A) c.745-5578C>A (n.745-5578C>A) c.152-5578C>A c.5671C>A (p.Pro1891Thr) c.5476C>A (p.Pro1826Thr) c.5644C>A (p.Pro1882Thr)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16	g.89280770G>A	CA497373505	ANKRD11	c.5772C>T (p.Ile1924=) c.5575C>T (n.5575C>T) c.745-5579C>T (n.745-5579C>T) c.152-5579C>T c.5670C>T (p.Ile1890=) c.5475C>T (p.Ile1825=) c.5643C>T (p.Ile1881=)	gnomAD v4
16	g.89280770G>C	CA397153079	ANKRD11	c.5772C>G (p.Ile1924Met) c.5575C>G (n.5575C>G) c.745-5579C>G (n.745-5579C>G) c.152-5579C>G c.5670C>G (p.Ile1890Met) c.5475C>G (p.Ile1825Met) c.5643C>G (p.Ile1881Met)	gnomAD v4
16	g.89280770G>T	CA497373506	ANKRD11	c.5772C>A (p.Ile1924=) c.5575C>A (n.5575C>A) c.745-5579C>A (n.745-5579C>A) c.152-5579C>A c.5670C>A (p.Ile1890=) c.5475C>A (p.Ile1825=) c.5643C>A (p.Ile1881=)	gnomAD v4
16	g.89280771A>C	CA397153080	ANKRD11	c.5771T>G (p.Ile1924Ser) c.5574T>G (n.5574T>G) c.745-5580T>G (n.745-5580T>G) c.152-5580T>G c.5669T>G (p.Ile1890Ser) c.5474T>G (p.Ile1825Ser) c.5642T>G (p.Ile1881Ser)
16	g.89280771A>G	CA397153082	ANKRD11	c.5771T>C (p.Ile1924Thr) c.5574T>C (n.5574T>C) c.745-5580T>C (n.745-5580T>C) c.152-5580T>C c.5669T>C (p.Ile1890Thr) c.5474T>C (p.Ile1825Thr) c.5642T>C (p.Ile1881Thr)
16	g.89280771A>T	CA397153081	ANKRD11	c.5771T>A (p.Ile1924Asn) c.5574T>A (n.5574T>A) c.745-5580T>A (n.745-5580T>A) c.152-5580T>A c.5669T>A (p.Ile1890Asn) c.5474T>A (p.Ile1825Asn) c.5642T>A (p.Ile1881Asn)
16	g.89280772T>A	CA397153083	ANKRD11	c.5770A>T (p.Ile1924Phe) c.5573A>T (n.5573A>T) c.745-5581A>T (n.745-5581A>T) c.152-5581A>T c.5668A>T (p.Ile1890Phe) c.5473A>T (p.Ile1825Phe) c.5641A>T (p.Ile1881Phe)
16	g.89280772T>C	CA397153084	ANKRD11	c.5770A>G (p.Ile1924Val) c.5573A>G (n.5573A>G) c.745-5581A>G (n.745-5581A>G) c.152-5581A>G c.5668A>G (p.Ile1890Val) c.5473A>G (p.Ile1825Val) c.5641A>G (p.Ile1881Val)
16	g.89280772T>G	CA397153085	ANKRD11	c.5770A>C (p.Ile1924Leu) c.5573A>C (n.5573A>C) c.745-5581A>C (n.745-5581A>C) c.152-5581A>C c.5668A>C (p.Ile1890Leu) c.5473A>C (p.Ile1825Leu) c.5641A>C (p.Ile1881Leu)
16	g.89280773G>A	CA497373508	ANKRD11	c.5769C>T (p.Ile1923=) c.5572C>T (n.5572C>T) c.745-5582C>T (n.745-5582C>T) c.152-5582C>T c.5667C>T (p.Ile1889=) c.5472C>T (p.Ile1824=) c.5640C>T (p.Ile1880=)	gnomAD v4
16	g.89280773G>C	CA397153086	ANKRD11	c.5769C>G (p.Ile1923Met) c.5572C>G (n.5572C>G) c.745-5582C>G (n.745-5582C>G) c.152-5582C>G c.5667C>G (p.Ile1889Met) c.5472C>G (p.Ile1824Met) c.5640C>G (p.Ile1880Met)
16	g.89280773G>T	CA497373507	ANKRD11	c.5769C>A (p.Ile1923=) c.5572C>A (n.5572C>A) c.745-5582C>A (n.745-5582C>A) c.152-5582C>A c.5667C>A (p.Ile1889=) c.5472C>A (p.Ile1824=) c.5640C>A (p.Ile1880=)
16	g.89280774A>C	CA397153087	ANKRD11	c.5768T>G (p.Ile1923Ser) c.5571T>G (n.5571T>G) c.745-5583T>G (n.745-5583T>G) c.152-5583T>G c.5666T>G (p.Ile1889Ser) c.5471T>G (p.Ile1824Ser) c.5639T>G (p.Ile1880Ser)
16	g.89280774A>G	CA397153089	ANKRD11	c.5768T>C (p.Ile1923Thr) c.5571T>C (n.5571T>C) c.745-5583T>C (n.745-5583T>C) c.152-5583T>C c.5666T>C (p.Ile1889Thr) c.5471T>C (p.Ile1824Thr) c.5639T>C (p.Ile1880Thr)	gnomAD v4
16	g.89280774A>T	CA397153088	ANKRD11	c.5768T>A (p.Ile1923Asn) c.5571T>A (n.5571T>A) c.745-5583T>A (n.745-5583T>A) c.152-5583T>A c.5666T>A (p.Ile1889Asn) c.5471T>A (p.Ile1824Asn) c.5639T>A (p.Ile1880Asn)
16	g.89280775T>A	CA397153090	ANKRD11	c.5767A>T (p.Ile1923Phe) c.5570A>T (n.5570A>T) c.745-5584A>T (n.745-5584A>T) c.152-5584A>T c.5665A>T (p.Ile1889Phe) c.5470A>T (p.Ile1824Phe) c.5638A>T (p.Ile1880Phe)
16	g.89280775T>C	CA397153092	ANKRD11	c.5767A>G (p.Ile1923Val) c.5570A>G (n.5570A>G) c.745-5584A>G (n.745-5584A>G) c.152-5584A>G c.5665A>G (p.Ile1889Val) c.5470A>G (p.Ile1824Val) c.5638A>G (p.Ile1880Val)	gnomAD v4
16	g.89280775T>G	CA397153091	ANKRD11	c.5767A>C (p.Ile1923Leu) c.5570A>C (n.5570A>C) c.745-5584A>C (n.745-5584A>C) c.152-5584A>C c.5665A>C (p.Ile1889Leu) c.5470A>C (p.Ile1824Leu) c.5638A>C (p.Ile1880Leu)
16	g.89280776G>A	CA8241726	ANKRD11	c.5766C>T (p.Ala1922=) c.5569C>T (n.5569C>T) c.745-5585C>T (n.745-5585C>T) c.152-5585C>T c.5664C>T (p.Ala1888=) c.5469C>T (p.Ala1823=) c.5637C>T (p.Ala1879=)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16	g.89280776G>C	CA497373509	ANKRD11	c.5766C>G (p.Ala1922=) c.5569C>G (n.5569C>G) c.745-5585C>G (n.745-5585C>G) c.152-5585C>G c.5664C>G (p.Ala1888=) c.5469C>G (p.Ala1823=) c.5637C>G (p.Ala1879=)
16	g.89280776G=	CA2241587662	ANKRD11	c.5766C= (p.Ala1922=) c.5569C= (n.5569C=) c.745-5585C= (n.745-5585C=) c.152-5585C= c.5664C= (p.Ala1888=) c.5469C= (p.Ala1823=) c.5637C= (p.Ala1879=)
16	g.89280776G>T	CA497373510	ANKRD11	c.5766C>A (p.Ala1922=) c.5569C>A (n.5569C>A) c.745-5585C>A (n.745-5585C>A) c.152-5585C>A c.5664C>A (p.Ala1888=) c.5469C>A (p.Ala1823=) c.5637C>A (p.Ala1879=)
16	g.89280777_89280804del	CA2580092410	ANKRD11	c.5739_5766del (p.Glu1915SerfsTer?) c.5542_5569del (n.5542_5569del) c.745-5612_745-5585del (n.745-5612_745-5585del) c.152-5612_152-5585del c.5637_5664del (p.Glu1881SerfsTer?) c.5442_5469del (p.Glu1816SerfsTer?) c.5610_5637del (p.Glu1872SerfsTer?)	ClinVar
16	g.89280777G>A	CA397153095	ANKRD11	c.5765C>T (p.Ala1922Val) c.5568C>T (n.5568C>T) c.745-5586C>T (n.745-5586C>T) c.152-5586C>T c.5663C>T (p.Ala1888Val) c.5468C>T (p.Ala1823Val) c.5636C>T (p.Ala1879Val)
16	g.89280777G>C	CA397153093	ANKRD11	c.5765C>G (p.Ala1922Gly) c.5568C>G (n.5568C>G) c.745-5586C>G (n.745-5586C>G) c.152-5586C>G c.5663C>G (p.Ala1888Gly) c.5468C>G (p.Ala1823Gly) c.5636C>G (p.Ala1879Gly)
16	g.89280777G>T	CA397153094	ANKRD11	c.5765C>A (p.Ala1922Asp) c.5568C>A (n.5568C>A) c.745-5586C>A (n.745-5586C>A) c.152-5586C>A c.5663C>A (p.Ala1888Asp) c.5468C>A (p.Ala1823Asp) c.5636C>A (p.Ala1879Asp)
16	g.89280778C>A	CA397153096	ANKRD11	c.5764G>T (p.Ala1922Ser) c.5567G>T (n.5567G>T) c.745-5587G>T (n.745-5587G>T) c.152-5587G>T c.5662G>T (p.Ala1888Ser) c.5467G>T (p.Ala1823Ser) c.5635G>T (p.Ala1879Ser)
16	g.89280778C=	CA2241587663	ANKRD11	c.5764G= (p.Ala1922=) c.5567G= (n.5567G=) c.745-5587G= (n.745-5587G=) c.152-5587G= c.5662G= (p.Ala1888=) c.5467G= (p.Ala1823=) c.5635G= (p.Ala1879=)
16	g.89280778C>G	CA397153097	ANKRD11	c.5764G>C (p.Ala1922Pro) c.5567G>C (n.5567G>C) c.745-5587G>C (n.745-5587G>C) c.152-5587G>C c.5662G>C (p.Ala1888Pro) c.5467G>C (p.Ala1823Pro) c.5635G>C (p.Ala1879Pro)
16	g.89280778C>T	CA8241727	ANKRD11	c.5764G>A (p.Ala1922Thr) c.5567G>A (n.5567G>A) c.745-5587G>A (n.745-5587G>A) c.152-5587G>A c.5662G>A (p.Ala1888Thr) c.5467G>A (p.Ala1823Thr) c.5635G>A (p.Ala1879Thr)	dbSNP ExAC gnomAD v2 gnomAD v4
16	g.89280779G>A	CA8241728	ANKRD11	c.5763C>T (p.Ala1921=) c.5566C>T (n.5566C>T) c.745-5588C>T (n.745-5588C>T) c.152-5588C>T c.5661C>T (p.Ala1887=) c.5466C>T (p.Ala1822=) c.5634C>T (p.Ala1878=)	dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16	g.89280779G>C	CA497373512	ANKRD11	c.5763C>G (p.Ala1921=) c.5566C>G (n.5566C>G) c.745-5588C>G (n.745-5588C>G) c.152-5588C>G c.5661C>G (p.Ala1887=) c.5466C>G (p.Ala1822=) c.5634C>G (p.Ala1878=)
16	g.89280779G=	CA2241587664	ANKRD11	c.5763C= (p.Ala1921=) c.5566C= (n.5566C=) c.745-5588C= (n.745-5588C=) c.152-5588C= c.5661C= (p.Ala1887=) c.5466C= (p.Ala1822=) c.5634C= (p.Ala1878=)
16	g.89280779G>T	CA497373511	ANKRD11	c.5763C>A (p.Ala1921=) c.5566C>A (n.5566C>A) c.745-5588C>A (n.745-5588C>A) c.152-5588C>A c.5661C>A (p.Ala1887=) c.5466C>A (p.Ala1822=) c.5634C>A (p.Ala1878=)
16	g.89280780G>A	CA397153098	ANKRD11	c.5762C>T (p.Ala1921Val) c.5565C>T (n.5565C>T) c.745-5589C>T (n.745-5589C>T) c.152-5589C>T c.5660C>T (p.Ala1887Val) c.5465C>T (p.Ala1822Val) c.5633C>T (p.Ala1878Val)	dbSNP COSMIC
16	g.89280780G>C	CA397153099	ANKRD11	c.5762C>G (p.Ala1921Gly) c.5565C>G (n.5565C>G) c.745-5589C>G (n.745-5589C>G) c.152-5589C>G c.5660C>G (p.Ala1887Gly) c.5465C>G (p.Ala1822Gly) c.5633C>G (p.Ala1878Gly)
16	g.89280780G>T	CA397153100	ANKRD11	c.5762C>A (p.Ala1921Asp) c.5565C>A (n.5565C>A) c.745-5589C>A (n.745-5589C>A) c.152-5589C>A c.5660C>A (p.Ala1887Asp) c.5465C>A (p.Ala1822Asp) c.5633C>A (p.Ala1878Asp)
16	g.89280781C>A	CA397153101	ANKRD11	c.5761G>T (p.Ala1921Ser) c.5564G>T (n.5564G>T) c.745-5590G>T (n.745-5590G>T) c.152-5590G>T c.5659G>T (p.Ala1887Ser) c.5464G>T (p.Ala1822Ser) c.5632G>T (p.Ala1878Ser)
16	g.89280781C=	CA2241587665	ANKRD11	c.5761G= (p.Ala1921=) c.5564G= (n.5564G=) c.745-5590G= (n.745-5590G=) c.152-5590G= c.5659G= (p.Ala1887=) c.5464G= (p.Ala1822=) c.5632G= (p.Ala1878=)
16	g.89280781C>G	CA397153102	ANKRD11	c.5761G>C (p.Ala1921Pro) c.5564G>C (n.5564G>C) c.745-5590G>C (n.745-5590G>C) c.152-5590G>C c.5659G>C (p.Ala1887Pro) c.5464G>C (p.Ala1822Pro) c.5632G>C (p.Ala1878Pro)	dbSNP
16	g.89280781C>T	CA397153103	ANKRD11	c.5761G>A (p.Ala1921Thr) c.5564G>A (n.5564G>A) c.745-5590G>A (n.745-5590G>A) c.152-5590G>A c.5659G>A (p.Ala1887Thr) c.5464G>A (p.Ala1822Thr) c.5632G>A (p.Ala1878Thr)	dbSNP gnomAD v2 gnomAD v4
16	g.89280782C>A	CA497373513	ANKRD11	c.5760G>T (p.Thr1920=) c.5563G>T (n.5563G>T) c.745-5591G>T (n.745-5591G>T) c.152-5591G>T c.5658G>T (p.Thr1886=) c.5463G>T (p.Thr1821=) c.5631G>T (p.Thr1877=)
16	g.89280782C=	CA2241587666	ANKRD11	c.5760G= (p.Thr1920=) c.5563G= (n.5563G=) c.745-5591G= (n.745-5591G=) c.152-5591G= c.5658G= (p.Thr1886=) c.5463G= (p.Thr1821=) c.5631G= (p.Thr1877=)
16	g.89280782C>G	CA8241730	ANKRD11	c.5760G>C (p.Thr1920=) c.5563G>C (n.5563G>C) c.745-5591G>C (n.745-5591G>C) c.152-5591G>C c.5658G>C (p.Thr1886=) c.5463G>C (p.Thr1821=) c.5631G>C (p.Thr1877=)	dbSNP ExAC gnomAD v2
16	g.89280782C>T	CA8241729	ANKRD11	c.5760G>A (p.Thr1920=) c.5563G>A (n.5563G>A) c.745-5591G>A (n.745-5591G>A) c.152-5591G>A c.5658G>A (p.Thr1886=) c.5463G>A (p.Thr1821=) c.5631G>A (p.Thr1877=)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16	g.89280783G>A	CA397153104	ANKRD11	c.5759C>T (p.Thr1920Met) c.5562C>T (n.5562C>T) c.745-5592C>T (n.745-5592C>T) c.152-5592C>T c.5657C>T (p.Thr1886Met) c.5462C>T (p.Thr1821Met) c.5630C>T (p.Thr1877Met)	dbSNP gnomAD v4 COSMIC
16	g.89280783G>C	CA397153105	ANKRD11	c.5759C>G (p.Thr1920Arg) c.5562C>G (n.5562C>G) c.745-5592C>G (n.745-5592C>G) c.152-5592C>G c.5657C>G (p.Thr1886Arg) c.5462C>G (p.Thr1821Arg) c.5630C>G (p.Thr1877Arg)
16	g.89280783G=	CA2241587667	ANKRD11	c.5759C= (p.Thr1920=) c.5562C= (n.5562C=) c.745-5592C= (n.745-5592C=) c.152-5592C= c.5657C= (p.Thr1886=) c.5462C= (p.Thr1821=) c.5630C= (p.Thr1877=)
16	g.89280783G>T	CA397153106	ANKRD11	c.5759C>A (p.Thr1920Lys) c.5562C>A (n.5562C>A) c.745-5592C>A (n.745-5592C>A) c.152-5592C>A c.5657C>A (p.Thr1886Lys) c.5462C>A (p.Thr1821Lys) c.5630C>A (p.Thr1877Lys)
16	g.89280784T>A	CA397153107	ANKRD11	c.5758A>T (p.Thr1920Ser) c.5561A>T (n.5561A>T) c.745-5593A>T (n.745-5593A>T) c.152-5593A>T c.5656A>T (p.Thr1886Ser) c.5461A>T (p.Thr1821Ser) c.5629A>T (p.Thr1877Ser)
16	g.89280784T>C	CA397153108	ANKRD11	c.5758A>G (p.Thr1920Ala) c.5561A>G (n.5561A>G) c.745-5593A>G (n.745-5593A>G) c.152-5593A>G c.5656A>G (p.Thr1886Ala) c.5461A>G (p.Thr1821Ala) c.5629A>G (p.Thr1877Ala)
16	g.89280784T>G	CA397153109	ANKRD11	c.5758A>C (p.Thr1920Pro) c.5561A>C (n.5561A>C) c.745-5593A>C (n.745-5593A>C) c.152-5593A>C c.5656A>C (p.Thr1886Pro) c.5461A>C (p.Thr1821Pro) c.5629A>C (p.Thr1877Pro)	dbSNP
16	g.89280784T=	CA2241587668	ANKRD11	c.5758A= (p.Thr1920=) c.5561A= (n.5561A=) c.745-5593A= (n.745-5593A=) c.152-5593A= c.5656A= (p.Thr1886=) c.5461A= (p.Thr1821=) c.5629A= (p.Thr1877=)
16	g.89280785C>A	CA497373514	ANKRD11	c.5757G>T (p.Ala1919=) c.5560G>T (n.5560G>T) c.745-5594G>T (n.745-5594G>T) c.152-5594G>T c.5655G>T (p.Ala1885=) c.5460G>T (p.Ala1820=) c.5628G>T (p.Ala1876=)
16	g.89280785C=	CA2241587669	ANKRD11	c.5757G= (p.Ala1919=) c.5560G= (n.5560G=) c.745-5594G= (n.745-5594G=) c.152-5594G= c.5655G= (p.Ala1885=) c.5460G= (p.Ala1820=) c.5628G= (p.Ala1876=)
16	g.89280785C>G	CA497373515	ANKRD11	c.5757G>C (p.Ala1919=) c.5560G>C (n.5560G>C) c.745-5594G>C (n.745-5594G>C) c.152-5594G>C c.5655G>C (p.Ala1885=) c.5460G>C (p.Ala1820=) c.5628G>C (p.Ala1876=)
16	g.89280785C>T	CA8241731	ANKRD11	c.5757G>A (p.Ala1919=) c.5560G>A (n.5560G>A) c.745-5594G>A (n.745-5594G>A) c.152-5594G>A c.5655G>A (p.Ala1885=) c.5460G>A (p.Ala1820=) c.5628G>A (p.Ala1876=)	dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16	g.89280786G>A	CA397153110	ANKRD11	c.5756C>T (p.Ala1919Val) c.5559C>T (n.5559C>T) c.745-5595C>T (n.745-5595C>T) c.152-5595C>T c.5654C>T (p.Ala1885Val) c.5459C>T (p.Ala1820Val) c.5627C>T (p.Ala1876Val)	dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16	g.89280786G>C	CA8241732	ANKRD11	c.5756C>G (p.Ala1919Gly) c.5559C>G (n.5559C>G) c.745-5595C>G (n.745-5595C>G) c.152-5595C>G c.5654C>G (p.Ala1885Gly) c.5459C>G (p.Ala1820Gly) c.5627C>G (p.Ala1876Gly)	dbSNP ExAC gnomAD v2 gnomAD v4
16	g.89280786G=	CA2241587670	ANKRD11	c.5756C= (p.Ala1919=) c.5559C= (n.5559C=) c.745-5595C= (n.745-5595C=) c.152-5595C= c.5654C= (p.Ala1885=) c.5459C= (p.Ala1820=) c.5627C= (p.Ala1876=)
16	g.89280786G>T	CA397153111	ANKRD11	c.5756C>A (p.Ala1919Glu) c.5559C>A (n.5559C>A) c.745-5595C>A (n.745-5595C>A) c.152-5595C>A c.5654C>A (p.Ala1885Glu) c.5459C>A (p.Ala1820Glu) c.5627C>A (p.Ala1876Glu)
16	g.89280787C>A	CA8241733	ANKRD11	c.5755G>T (p.Ala1919Ser) c.5558G>T (n.5558G>T) c.745-5596G>T (n.745-5596G>T) c.152-5596G>T c.5653G>T (p.Ala1885Ser) c.5458G>T (p.Ala1820Ser) c.5626G>T (p.Ala1876Ser)	dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16	g.89280787C=	CA2241587671	ANKRD11	c.5755G= (p.Ala1919=) c.5558G= (n.5558G=) c.745-5596G= (n.745-5596G=) c.152-5596G= c.5653G= (p.Ala1885=) c.5458G= (p.Ala1820=) c.5626G= (p.Ala1876=)
16	g.89280787C>G	CA397153113	ANKRD11	c.5755G>C (p.Ala1919Pro) c.5558G>C (n.5558G>C) c.745-5596G>C (n.745-5596G>C) c.152-5596G>C c.5653G>C (p.Ala1885Pro) c.5458G>C (p.Ala1820Pro) c.5626G>C (p.Ala1876Pro)	gnomAD v4
16	g.89280787C>T	CA397153112	ANKRD11	c.5755G>A (p.Ala1919Thr) c.5558G>A (n.5558G>A) c.745-5596G>A (n.745-5596G>A) c.152-5596G>A c.5653G>A (p.Ala1885Thr) c.5458G>A (p.Ala1820Thr) c.5626G>A (p.Ala1876Thr)	dbSNP
16	g.89280788C>A	CA397153114	ANKRD11	c.5754G>T (p.Gln1918His) c.5557G>T (n.5557G>T) c.745-5597G>T (n.745-5597G>T) c.152-5597G>T c.5652G>T (p.Gln1884His) c.5457G>T (p.Gln1819His) c.5625G>T (p.Gln1875His)
16	g.89280788C>G	CA397153115	ANKRD11	c.5754G>C (p.Gln1918His) c.5557G>C (n.5557G>C) c.745-5597G>C (n.745-5597G>C) c.152-5597G>C c.5652G>C (p.Gln1884His) c.5457G>C (p.Gln1819His) c.5625G>C (p.Gln1875His)
16	g.89280788C>T	CA497373516	ANKRD11	c.5754G>A (p.Gln1918=) c.5557G>A (n.5557G>A) c.745-5597G>A (n.745-5597G>A) c.152-5597G>A c.5652G>A (p.Gln1884=) c.5457G>A (p.Gln1819=) c.5625G>A (p.Gln1875=)
16	g.89280789T>A	CA397153116	ANKRD11	c.5753A>T (p.Gln1918Leu) c.5556A>T (n.5556A>T) c.745-5598A>T (n.745-5598A>T) c.152-5598A>T c.5651A>T (p.Gln1884Leu) c.5456A>T (p.Gln1819Leu) c.5624A>T (p.Gln1875Leu)
16	g.89280789T>C	CA397153117	ANKRD11	c.5753A>G (p.Gln1918Arg) c.5556A>G (n.5556A>G) c.745-5598A>G (n.745-5598A>G) c.152-5598A>G c.5651A>G (p.Gln1884Arg) c.5456A>G (p.Gln1819Arg) c.5624A>G (p.Gln1875Arg)	dbSNP gnomAD v3 gnomAD v4
16	g.89280789T>G	CA397153118	ANKRD11	c.5753A>C (p.Gln1918Pro) c.5556A>C (n.5556A>C) c.745-5598A>C (n.745-5598A>C) c.152-5598A>C c.5651A>C (p.Gln1884Pro) c.5456A>C (p.Gln1819Pro) c.5624A>C (p.Gln1875Pro)
16	g.89280789T=	CA2241587672	ANKRD11	c.5753A= (p.Gln1918=) c.5556A= (n.5556A=) c.745-5598A= (n.745-5598A=) c.152-5598A= c.5651A= (p.Gln1884=) c.5456A= (p.Gln1819=) c.5624A= (p.Gln1875=)
16	g.89280790G>A	CA397153121	ANKRD11	c.5752C>T (p.Gln1918Ter) c.5555C>T (n.5555C>T) c.745-5599C>T (n.745-5599C>T) c.152-5599C>T c.5650C>T (p.Gln1884Ter) c.5455C>T (p.Gln1819Ter) c.5623C>T (p.Gln1875Ter)
16	g.89280790G>C	CA397153119	ANKRD11	c.5752C>G (p.Gln1918Glu) c.5555C>G (n.5555C>G) c.745-5599C>G (n.745-5599C>G) c.152-5599C>G c.5650C>G (p.Gln1884Glu) c.5455C>G (p.Gln1819Glu) c.5623C>G (p.Gln1875Glu)	gnomAD v4
16	g.89280790G>T	CA397153120	ANKRD11	c.5752C>A (p.Gln1918Lys) c.5555C>A (n.5555C>A) c.745-5599C>A (n.745-5599C>A) c.152-5599C>A c.5650C>A (p.Gln1884Lys) c.5455C>A (p.Gln1819Lys) c.5623C>A (p.Gln1875Lys)	COSMIC
16	g.89280791C>A	CA397153122	ANKRD11	c.5751G>T (p.Gln1917His) c.5554G>T (n.5554G>T) c.745-5600G>T (n.745-5600G>T) c.152-5600G>T c.5649G>T (p.Gln1883His) c.5454G>T (p.Gln1818His) c.5622G>T (p.Gln1874His)	gnomAD v4
16	g.89280791C>G	CA397153123	ANKRD11	c.5751G>C (p.Gln1917His) c.5554G>C (n.5554G>C) c.745-5600G>C (n.745-5600G>C) c.152-5600G>C c.5649G>C (p.Gln1883His) c.5454G>C (p.Gln1818His) c.5622G>C (p.Gln1874His)	gnomAD v4
16	g.89280791C>T	CA497373518	ANKRD11	c.5751G>A (p.Gln1917=) c.5554G>A (n.5554G>A) c.745-5600G>A (n.745-5600G>A) c.152-5600G>A c.5649G>A (p.Gln1883=) c.5454G>A (p.Gln1818=) c.5622G>A (p.Gln1874=)	gnomAD v4
16	g.89280792T>A	CA397153124	ANKRD11	c.5750A>T (p.Gln1917Leu) c.5553A>T (n.5553A>T) c.745-5601A>T (n.745-5601A>T) c.152-5601A>T c.5648A>T (p.Gln1883Leu) c.5453A>T (p.Gln1818Leu) c.5621A>T (p.Gln1874Leu)
16	g.89280792T>C	CA397153125	ANKRD11	c.5750A>G (p.Gln1917Arg) c.5553A>G (n.5553A>G) c.745-5601A>G (n.745-5601A>G) c.152-5601A>G c.5648A>G (p.Gln1883Arg) c.5453A>G (p.Gln1818Arg) c.5621A>G (p.Gln1874Arg)	gnomAD v4
16	g.89280792T>G	CA397153126	ANKRD11	c.5750A>C (p.Gln1917Pro) c.5553A>C (n.5553A>C) c.745-5601A>C (n.745-5601A>C) c.152-5601A>C c.5648A>C (p.Gln1883Pro) c.5453A>C (p.Gln1818Pro) c.5621A>C (p.Gln1874Pro)
16	g.89280793G>A	CA397153127	ANKRD11	c.5749C>T (p.Gln1917Ter) c.5552C>T (n.5552C>T) c.745-5602C>T (n.745-5602C>T) c.152-5602C>T c.5647C>T (p.Gln1883Ter) c.5452C>T (p.Gln1818Ter) c.5620C>T (p.Gln1874Ter)
16	g.89280793G>C	CA397153129	ANKRD11	c.5749C>G (p.Gln1917Glu) c.5552C>G (n.5552C>G) c.745-5602C>G (n.745-5602C>G) c.152-5602C>G c.5647C>G (p.Gln1883Glu) c.5452C>G (p.Gln1818Glu) c.5620C>G (p.Gln1874Glu)
16	g.89280793G>T	CA397153128	ANKRD11	c.5749C>A (p.Gln1917Lys) c.5552C>A (n.5552C>A) c.745-5602C>A (n.745-5602C>A) c.152-5602C>A c.5647C>A (p.Gln1883Lys) c.5452C>A (p.Gln1818Lys) c.5620C>A (p.Gln1874Lys)
16	g.89280794G>A	CA8241734	ANKRD11	c.5748C>T (p.Asp1916=) c.5551C>T (n.5551C>T) c.745-5603C>T (n.745-5603C>T) c.152-5603C>T c.5646C>T (p.Asp1882=) c.5451C>T (p.Asp1817=) c.5619C>T (p.Asp1873=)	dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16	g.89280794G>C	CA397153130	ANKRD11	c.5748C>G (p.Asp1916Glu) c.5551C>G (n.5551C>G) c.745-5603C>G (n.745-5603C>G) c.152-5603C>G c.5646C>G (p.Asp1882Glu) c.5451C>G (p.Asp1817Glu) c.5619C>G (p.Asp1873Glu)	gnomAD v4
16	g.89280794G=	CA2241587673	ANKRD11	c.5748C= (p.Asp1916=) c.5551C= (n.5551C=) c.745-5603C= (n.745-5603C=) c.152-5603C= c.5646C= (p.Asp1882=) c.5451C= (p.Asp1817=) c.5619C= (p.Asp1873=)
16	g.89280794G>T	CA397153131	ANKRD11	c.5748C>A (p.Asp1916Glu) c.5551C>A (n.5551C>A) c.745-5603C>A (n.745-5603C>A) c.152-5603C>A c.5646C>A (p.Asp1882Glu) c.5451C>A (p.Asp1817Glu) c.5619C>A (p.Asp1873Glu)
16	g.89280795T>A	CA397153132	ANKRD11	c.5747A>T (p.Asp1916Val) c.5550A>T (n.5550A>T) c.745-5604A>T (n.745-5604A>T) c.152-5604A>T c.5645A>T (p.Asp1882Val) c.5450A>T (p.Asp1817Val) c.5618A>T (p.Asp1873Val)
16	g.89280795T>C	CA397153133	ANKRD11	c.5747A>G (p.Asp1916Gly) c.5550A>G (n.5550A>G) c.745-5604A>G (n.745-5604A>G) c.152-5604A>G c.5645A>G (p.Asp1882Gly) c.5450A>G (p.Asp1817Gly) c.5618A>G (p.Asp1873Gly)
16	g.89280795T>G	CA397153134	ANKRD11	c.5747A>C (p.Asp1916Ala) c.5550A>C (n.5550A>C) c.745-5604A>C (n.745-5604A>C) c.152-5604A>C c.5645A>C (p.Asp1882Ala) c.5450A>C (p.Asp1817Ala) c.5618A>C (p.Asp1873Ala)	dbSNP
16	g.89280795T=	CA2241587674	ANKRD11	c.5747A= (p.Asp1916=) c.5550A= (n.5550A=) c.745-5604A= (n.745-5604A=) c.152-5604A= c.5645A= (p.Asp1882=) c.5450A= (p.Asp1817=) c.5618A= (p.Asp1873=)
16	g.89280796C>A	CA397153135	ANKRD11	c.5746G>T (p.Asp1916Tyr) c.5549G>T (n.5549G>T) c.745-5605G>T (n.745-5605G>T) c.152-5605G>T c.5644G>T (p.Asp1882Tyr) c.5449G>T (p.Asp1817Tyr) c.5617G>T (p.Asp1873Tyr)	gnomAD v4
16	g.89280796C=	CA2241587675	ANKRD11	c.5746G= (p.Asp1916=) c.5549G= (n.5549G=) c.745-5605G= (n.745-5605G=) c.152-5605G= c.5644G= (p.Asp1882=) c.5449G= (p.Asp1817=) c.5617G= (p.Asp1873=)
16	g.89280796C>G	CA397153136	ANKRD11	c.5746G>C (p.Asp1916His) c.5549G>C (n.5549G>C) c.745-5605G>C (n.745-5605G>C) c.152-5605G>C c.5644G>C (p.Asp1882His) c.5449G>C (p.Asp1817His) c.5617G>C (p.Asp1873His)
16	g.89280796C>T	CA397153137	ANKRD11	c.5746G>A (p.Asp1916Asn) c.5549G>A (n.5549G>A) c.745-5605G>A (n.745-5605G>A) c.152-5605G>A c.5644G>A (p.Asp1882Asn) c.5449G>A (p.Asp1817Asn) c.5617G>A (p.Asp1873Asn)	dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16	g.89280797C>A	CA397153138	ANKRD11	c.5745G>T (p.Glu1915Asp) c.5548G>T (n.5548G>T) c.745-5606G>T (n.745-5606G>T) c.152-5606G>T c.5643G>T (p.Glu1881Asp) c.5448G>T (p.Glu1816Asp) c.5616G>T (p.Glu1872Asp)
16	g.89280797C>G	CA397153139	ANKRD11	c.5745G>C (p.Glu1915Asp) c.5548G>C (n.5548G>C) c.745-5606G>C (n.745-5606G>C) c.152-5606G>C c.5643G>C (p.Glu1881Asp) c.5448G>C (p.Glu1816Asp) c.5616G>C (p.Glu1872Asp)
16	g.89280797C>T	CA497373523	ANKRD11	c.5745G>A (p.Glu1915=) c.5548G>A (n.5548G>A) c.745-5606G>A (n.745-5606G>A) c.152-5606G>A c.5643G>A (p.Glu1881=) c.5448G>A (p.Glu1816=) c.5616G>A (p.Glu1872=)	gnomAD v4
16	g.89280798T>A	CA397153141	ANKRD11	c.5744A>T (p.Glu1915Val) c.5547A>T (n.5547A>T) c.745-5607A>T (n.745-5607A>T) c.152-5607A>T c.5642A>T (p.Glu1881Val) c.5447A>T (p.Glu1816Val) c.5615A>T (p.Glu1872Val)
16	g.89280798T>C	CA397153142	ANKRD11	c.5744A>G (p.Glu1915Gly) c.5547A>G (n.5547A>G) c.745-5607A>G (n.745-5607A>G) c.152-5607A>G c.5642A>G (p.Glu1881Gly) c.5447A>G (p.Glu1816Gly) c.5615A>G (p.Glu1872Gly)
16	g.89280798T>G	CA397153140	ANKRD11	c.5744A>C (p.Glu1915Ala) c.5547A>C (n.5547A>C) c.745-5607A>C (n.745-5607A>C) c.152-5607A>C c.5642A>C (p.Glu1881Ala) c.5447A>C (p.Glu1816Ala) c.5615A>C (p.Glu1872Ala)
16	g.89280799C>A	CA397153143	ANKRD11	c.5743G>T (p.Glu1915Ter) c.5546G>T (n.5546G>T) c.745-5608G>T (n.745-5608G>T) c.152-5608G>T c.5641G>T (p.Glu1881Ter) c.5446G>T (p.Glu1816Ter) c.5614G>T (p.Glu1872Ter)
16	g.89280799C=	CA2241587676	ANKRD11	c.5743G= (p.Glu1915=) c.5546G= (n.5546G=) c.745-5608G= (n.745-5608G=) c.152-5608G= c.5641G= (p.Glu1881=) c.5446G= (p.Glu1816=) c.5614G= (p.Glu1872=)
16	g.89280799C>G	CA397153144	ANKRD11	c.5743G>C (p.Glu1915Gln) c.5546G>C (n.5546G>C) c.745-5608G>C (n.745-5608G>C) c.152-5608G>C c.5641G>C (p.Glu1881Gln) c.5446G>C (p.Glu1816Gln) c.5614G>C (p.Glu1872Gln)
16	g.89280799C>T	CA8241735	ANKRD11	c.5743G>A (p.Glu1915Lys) c.5546G>A (n.5546G>A) c.745-5608G>A (n.745-5608G>A) c.152-5608G>A c.5641G>A (p.Glu1881Lys) c.5446G>A (p.Glu1816Lys) c.5614G>A (p.Glu1872Lys)	dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16	g.89280800G>A	CA8241736	ANKRD11	c.5742C>T (p.Ser1914=) c.5545C>T (n.5545C>T) c.745-5609C>T (n.745-5609C>T) c.152-5609C>T c.5640C>T (p.Ser1880=) c.5445C>T (p.Ser1815=) c.5613C>T (p.Ser1871=)	dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16	g.89280800G>C	CA497373526	ANKRD11	c.5742C>G (p.Ser1914=) c.5545C>G (n.5545C>G) c.745-5609C>G (n.745-5609C>G) c.152-5609C>G c.5640C>G (p.Ser1880=) c.5445C>G (p.Ser1815=) c.5613C>G (p.Ser1871=)	gnomAD v4
16	g.89280800G=	CA2241587677	ANKRD11	c.5742C= (p.Ser1914=) c.5545C= (n.5545C=) c.745-5609C= (n.745-5609C=) c.152-5609C= c.5640C= (p.Ser1880=) c.5445C= (p.Ser1815=) c.5613C= (p.Ser1871=)
16	g.89280800G>T	CA497373525	ANKRD11	c.5742C>A (p.Ser1914=) c.5545C>A (n.5545C>A) c.745-5609C>A (n.745-5609C>A) c.152-5609C>A c.5640C>A (p.Ser1880=) c.5445C>A (p.Ser1815=) c.5613C>A (p.Ser1871=)
16	g.89280801G>A	CA397153145	ANKRD11	c.5741C>T (p.Ser1914Phe) c.5544C>T (n.5544C>T) c.745-5610C>T (n.745-5610C>T) c.152-5610C>T c.5639C>T (p.Ser1880Phe) c.5444C>T (p.Ser1815Phe) c.5612C>T (p.Ser1871Phe)	gnomAD v4
16	g.89280801G>C	CA397153146	ANKRD11	c.5741C>G (p.Ser1914Cys) c.5544C>G (n.5544C>G) c.745-5610C>G (n.745-5610C>G) c.152-5610C>G c.5639C>G (p.Ser1880Cys) c.5444C>G (p.Ser1815Cys) c.5612C>G (p.Ser1871Cys)
16	g.89280801G>T	CA397153147	ANKRD11	c.5741C>A (p.Ser1914Tyr) c.5544C>A (n.5544C>A) c.745-5610C>A (n.745-5610C>A) c.152-5610C>A c.5639C>A (p.Ser1880Tyr) c.5444C>A (p.Ser1815Tyr) c.5612C>A (p.Ser1871Tyr)
16	g.89280802A=	CA2241587678	ANKRD11	c.5740T= (p.Ser1914=) c.5543T= (n.5543T=) c.745-5611T= (n.745-5611T=) c.152-5611T= c.5638T= (p.Ser1880=) c.5443T= (p.Ser1815=) c.5611T= (p.Ser1871=)
16	g.89280802A>C	CA397153148	ANKRD11	c.5740T>G (p.Ser1914Ala) c.5543T>G (n.5543T>G) c.745-5611T>G (n.745-5611T>G) c.152-5611T>G c.5638T>G (p.Ser1880Ala) c.5443T>G (p.Ser1815Ala) c.5611T>G (p.Ser1871Ala)
16	g.89280802A>G	CA397153150	ANKRD11	c.5740T>C (p.Ser1914Pro) c.5543T>C (n.5543T>C) c.745-5611T>C (n.745-5611T>C) c.152-5611T>C c.5638T>C (p.Ser1880Pro) c.5443T>C (p.Ser1815Pro) c.5611T>C (p.Ser1871Pro)	dbSNP
16	g.89280802A>T	CA397153149	ANKRD11	c.5740T>A (p.Ser1914Thr) c.5543T>A (n.5543T>A) c.745-5611T>A (n.745-5611T>A) c.152-5611T>A c.5638T>A (p.Ser1880Thr) c.5443T>A (p.Ser1815Thr) c.5611T>A (p.Ser1871Thr)
16	g.89280803G>A	CA8241737	ANKRD11	c.5739C>T (p.Thr1913=) c.5542C>T (n.5542C>T) c.745-5612C>T (n.745-5612C>T) c.152-5612C>T c.5637C>T (p.Thr1879=) c.5442C>T (p.Thr1814=) c.5610C>T (p.Thr1870=)	dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16	g.89280803G>C	CA497373528	ANKRD11	c.5739C>G (p.Thr1913=) c.5542C>G (n.5542C>G) c.745-5612C>G (n.745-5612C>G) c.152-5612C>G c.5637C>G (p.Thr1879=) c.5442C>G (p.Thr1814=) c.5610C>G (p.Thr1870=)
16	g.89280803G=	CA2241587679	ANKRD11	c.5739C= (p.Thr1913=) c.5542C= (n.5542C=) c.745-5612C= (n.745-5612C=) c.152-5612C= c.5637C= (p.Thr1879=) c.5442C= (p.Thr1814=) c.5610C= (p.Thr1870=)
16	g.89280803G>T	CA497373529	ANKRD11	c.5739C>A (p.Thr1913=) c.5542C>A (n.5542C>A) c.745-5612C>A (n.745-5612C>A) c.152-5612C>A c.5637C>A (p.Thr1879=) c.5442C>A (p.Thr1814=) c.5610C>A (p.Thr1870=)
16	g.89280804G>A	CA397153151	ANKRD11	c.5738C>T (p.Thr1913Ile) c.5541C>T (n.5541C>T) c.745-5613C>T (n.745-5613C>T) c.152-5613C>T c.5636C>T (p.Thr1879Ile) c.5441C>T (p.Thr1814Ile) c.5609C>T (p.Thr1870Ile)	ClinVar dbSNP gnomAD v3 gnomAD v4
16	g.89280804G>C	CA397153152	ANKRD11	c.5738C>G (p.Thr1913Ser) c.5541C>G (n.5541C>G) c.745-5613C>G (n.745-5613C>G) c.152-5613C>G c.5636C>G (p.Thr1879Ser) c.5441C>G (p.Thr1814Ser) c.5609C>G (p.Thr1870Ser)
16	g.89280804G=	CA2241587680	ANKRD11	c.5738C= (p.Thr1913=) c.5541C= (n.5541C=) c.745-5613C= (n.745-5613C=) c.152-5613C= c.5636C= (p.Thr1879=) c.5441C= (p.Thr1814=) c.5609C= (p.Thr1870=)
16	g.89280804G>T	CA8241738	ANKRD11	c.5738C>A (p.Thr1913Asn) c.5541C>A (n.5541C>A) c.745-5613C>A (n.745-5613C>A) c.152-5613C>A c.5636C>A (p.Thr1879Asn) c.5441C>A (p.Thr1814Asn) c.5609C>A (p.Thr1870Asn)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16	g.89280805T>A	CA397153154	ANKRD11	c.5737A>T (p.Thr1913Ser) c.5540A>T (n.5540A>T) c.745-5614A>T (n.745-5614A>T) c.152-5614A>T c.5635A>T (p.Thr1879Ser) c.5440A>T (p.Thr1814Ser) c.5608A>T (p.Thr1870Ser)
16	g.89280805T>C	CA8241739	ANKRD11	c.5737A>G (p.Thr1913Ala) c.5540A>G (n.5540A>G) c.745-5614A>G (n.745-5614A>G) c.152-5614A>G c.5635A>G (p.Thr1879Ala) c.5440A>G (p.Thr1814Ala) c.5608A>G (p.Thr1870Ala)	dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16	g.89280805T>G	CA397153153	ANKRD11	c.5737A>C (p.Thr1913Pro) c.5540A>C (n.5540A>C) c.745-5614A>C (n.745-5614A>C) c.152-5614A>C c.5635A>C (p.Thr1879Pro) c.5440A>C (p.Thr1814Pro) c.5608A>C (p.Thr1870Pro)	dbSNP
16	g.89280805T=	CA2241587681	ANKRD11	c.5737A= (p.Thr1913=) c.5540A= (n.5540A=) c.745-5614A= (n.745-5614A=) c.152-5614A= c.5635A= (p.Thr1879=) c.5440A= (p.Thr1814=) c.5608A= (p.Thr1870=)
16	g.89280806G>A	CA497373534	ANKRD11	c.5736C>T (p.Asp1912=) c.5539C>T (n.5539C>T) c.745-5615C>T (n.745-5615C>T) c.152-5615C>T c.5634C>T (p.Asp1878=) c.5439C>T (p.Asp1813=) c.5607C>T (p.Asp1869=)	dbSNP gnomAD v4
16	g.89280806G>C	CA397153155	ANKRD11	c.5736C>G (p.Asp1912Glu) c.5539C>G (n.5539C>G) c.745-5615C>G (n.745-5615C>G) c.152-5615C>G c.5634C>G (p.Asp1878Glu) c.5439C>G (p.Asp1813Glu) c.5607C>G (p.Asp1869Glu)
16	g.89280806G=	CA2241587682	ANKRD11	c.5736C= (p.Asp1912=) c.5539C= (n.5539C=) c.745-5615C= (n.745-5615C=) c.152-5615C= c.5634C= (p.Asp1878=) c.5439C= (p.Asp1813=) c.5607C= (p.Asp1869=)
16	g.89280806G>T	CA8241740	ANKRD11	c.5736C>A (p.Asp1912Glu) c.5539C>A (n.5539C>A) c.745-5615C>A (n.745-5615C>A) c.152-5615C>A c.5634C>A (p.Asp1878Glu) c.5439C>A (p.Asp1813Glu) c.5607C>A (p.Asp1869Glu)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16	g.89280807T>A	CA397153156	ANKRD11	c.5735A>T (p.Asp1912Val) c.5538A>T (n.5538A>T) c.745-5616A>T (n.745-5616A>T) c.152-5616A>T c.5633A>T (p.Asp1878Val) c.5438A>T (p.Asp1813Val) c.5606A>T (p.Asp1869Val)
16	g.89280807T>C	CA397153157	ANKRD11	c.5735A>G (p.Asp1912Gly) c.5538A>G (n.5538A>G) c.745-5616A>G (n.745-5616A>G) c.152-5616A>G c.5633A>G (p.Asp1878Gly) c.5438A>G (p.Asp1813Gly) c.5606A>G (p.Asp1869Gly)	gnomAD v4
16	g.89280807T>G	CA397153158	ANKRD11	c.5735A>C (p.Asp1912Ala) c.5538A>C (n.5538A>C) c.745-5616A>C (n.745-5616A>C) c.152-5616A>C c.5633A>C (p.Asp1878Ala) c.5438A>C (p.Asp1813Ala) c.5606A>C (p.Asp1869Ala)
16	g.89280808C>A	CA397153159	ANKRD11	c.5734G>T (p.Asp1912Tyr) c.5537G>T (n.5537G>T) c.745-5617G>T (n.745-5617G>T) c.152-5617G>T c.5632G>T (p.Asp1878Tyr) c.5437G>T (p.Asp1813Tyr) c.5605G>T (p.Asp1869Tyr)
16	g.89280808C>G	CA397153160	ANKRD11	c.5734G>C (p.Asp1912His) c.5537G>C (n.5537G>C) c.745-5617G>C (n.745-5617G>C) c.152-5617G>C c.5632G>C (p.Asp1878His) c.5437G>C (p.Asp1813His) c.5605G>C (p.Asp1869His)
16	g.89280808C>T	CA397153161	ANKRD11	c.5734G>A (p.Asp1912Asn) c.5537G>A (n.5537G>A) c.745-5617G>A (n.745-5617G>A) c.152-5617G>A c.5632G>A (p.Asp1878Asn) c.5437G>A (p.Asp1813Asn) c.5605G>A (p.Asp1869Asn)
16	g.89280809C>A	CA497373536	ANKRD11	c.5733G>T (p.Leu1911=) c.5536G>T (n.5536G>T) c.745-5618G>T (n.745-5618G>T) c.152-5618G>T c.5631G>T (p.Leu1877=) c.5436G>T (p.Leu1812=) c.5604G>T (p.Leu1868=)
16	g.89280809C=	CA2241587683	ANKRD11	c.5733G= (p.Leu1911=) c.5536G= (n.5536G=) c.745-5618G= (n.745-5618G=) c.152-5618G= c.5631G= (p.Leu1877=) c.5436G= (p.Leu1812=) c.5604G= (p.Leu1868=)
16	g.89280809C>G	CA497373537	ANKRD11	c.5733G>C (p.Leu1911=) c.5536G>C (n.5536G>C) c.745-5618G>C (n.745-5618G>C) c.152-5618G>C c.5631G>C (p.Leu1877=) c.5436G>C (p.Leu1812=) c.5604G>C (p.Leu1868=)
16	g.89280809C>T	CA497373539	ANKRD11	c.5733G>A (p.Leu1911=) c.5536G>A (n.5536G>A) c.745-5618G>A (n.745-5618G>A) c.152-5618G>A c.5631G>A (p.Leu1877=) c.5436G>A (p.Leu1812=) c.5604G>A (p.Leu1868=)	dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16	g.89280810A=	CA2241587684	ANKRD11	c.5732T= (p.Leu1911=) c.5535T= (n.5535T=) c.745-5619T= (n.745-5619T=) c.152-5619T= c.5630T= (p.Leu1877=) c.5435T= (p.Leu1812=) c.5603T= (p.Leu1868=)
16	g.89280810A>C	CA397153162	ANKRD11	c.5732T>G (p.Leu1911Arg) c.5535T>G (n.5535T>G) c.745-5619T>G (n.745-5619T>G) c.152-5619T>G c.5630T>G (p.Leu1877Arg) c.5435T>G (p.Leu1812Arg) c.5603T>G (p.Leu1868Arg)	dbSNP gnomAD v4
16	g.89280810A>G	CA397153163	ANKRD11	c.5732T>C (p.Leu1911Pro) c.5535T>C (n.5535T>C) c.745-5619T>C (n.745-5619T>C) c.152-5619T>C c.5630T>C (p.Leu1877Pro) c.5435T>C (p.Leu1812Pro) c.5603T>C (p.Leu1868Pro)	dbSNP gnomAD v2 gnomAD v4
16	g.89280810A>T	CA286513469	ANKRD11	c.5732T>A (p.Leu1911Gln) c.5535T>A (n.5535T>A) c.745-5619T>A (n.745-5619T>A) c.152-5619T>A c.5630T>A (p.Leu1877Gln) c.5435T>A (p.Leu1812Gln) c.5603T>A (p.Leu1868Gln)	dbSNP gnomAD v2 gnomAD v4
16	g.89280811G>A	CA497373541	ANKRD11	c.5731C>T (p.Leu1911=) c.5534C>T (n.5534C>T) c.745-5620C>T (n.745-5620C>T) c.152-5620C>T c.5629C>T (p.Leu1877=) c.5434C>T (p.Leu1812=) c.5602C>T (p.Leu1868=)	dbSNP gnomAD v4
16	g.89280811G>C	CA397153164	ANKRD11	c.5731C>G (p.Leu1911Val) c.5534C>G (n.5534C>G) c.745-5620C>G (n.745-5620C>G) c.152-5620C>G c.5629C>G (p.Leu1877Val) c.5434C>G (p.Leu1812Val) c.5602C>G (p.Leu1868Val)
16	g.89280811G=	CA2241587685	ANKRD11	c.5731C= (p.Leu1911=) c.5534C= (n.5534C=) c.745-5620C= (n.745-5620C=) c.152-5620C= c.5629C= (p.Leu1877=) c.5434C= (p.Leu1812=) c.5602C= (p.Leu1868=)
16	g.89280811G>T	CA397153165	ANKRD11	c.5731C>A (p.Leu1911Met) c.5534C>A (n.5534C>A) c.745-5620C>A (n.745-5620C>A) c.152-5620C>A c.5629C>A (p.Leu1877Met) c.5434C>A (p.Leu1812Met) c.5602C>A (p.Leu1868Met)	gnomAD v4
16	g.89280812G>A	CA8241741	ANKRD11	c.5730C>T (p.Asp1910=) c.5533C>T (n.5533C>T) c.745-5621C>T (n.745-5621C>T) c.152-5621C>T c.5628C>T (p.Asp1876=) c.5433C>T (p.Asp1811=) c.5601C>T (p.Asp1867=)	dbSNP ExAC gnomAD v2 gnomAD v4
16	g.89280812G>C	CA397153166	ANKRD11	c.5730C>G (p.Asp1910Glu) c.5533C>G (n.5533C>G) c.745-5621C>G (n.745-5621C>G) c.152-5621C>G c.5628C>G (p.Asp1876Glu) c.5433C>G (p.Asp1811Glu) c.5601C>G (p.Asp1867Glu)
16	g.89280812G=	CA2241587686	ANKRD11	c.5730C= (p.Asp1910=) c.5533C= (n.5533C=) c.745-5621C= (n.745-5621C=) c.152-5621C= c.5628C= (p.Asp1876=) c.5433C= (p.Asp1811=) c.5601C= (p.Asp1867=)
16	g.89280812G>T	CA8241742	ANKRD11	c.5730C>A (p.Asp1910Glu) c.5533C>A (n.5533C>A) c.745-5621C>A (n.745-5621C>A) c.152-5621C>A c.5628C>A (p.Asp1876Glu) c.5433C>A (p.Asp1811Glu) c.5601C>A (p.Asp1867Glu)	dbSNP ExAC gnomAD v2 gnomAD v4
16	g.89280813T>A	CA397153167	ANKRD11	c.5729A>T (p.Asp1910Val) c.5532A>T (n.5532A>T) c.745-5622A>T (n.745-5622A>T) c.152-5622A>T c.5627A>T (p.Asp1876Val) c.5432A>T (p.Asp1811Val) c.5600A>T (p.Asp1867Val)
16	g.89280813T>C	CA397153168	ANKRD11	c.5729A>G (p.Asp1910Gly) c.5532A>G (n.5532A>G) c.745-5622A>G (n.745-5622A>G) c.152-5622A>G c.5627A>G (p.Asp1876Gly) c.5432A>G (p.Asp1811Gly) c.5600A>G (p.Asp1867Gly)	dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16	g.89280813T>G	CA397153169	ANKRD11	c.5729A>C (p.Asp1910Ala) c.5532A>C (n.5532A>C) c.745-5622A>C (n.745-5622A>C) c.152-5622A>C c.5627A>C (p.Asp1876Ala) c.5432A>C (p.Asp1811Ala) c.5600A>C (p.Asp1867Ala)	dbSNP
16	g.89280813T=	CA2241587687	ANKRD11	c.5729A= (p.Asp1910=) c.5532A= (n.5532A=) c.745-5622A= (n.745-5622A=) c.152-5622A= c.5627A= (p.Asp1876=) c.5432A= (p.Asp1811=) c.5600A= (p.Asp1867=)
16	g.89280814C>A	CA397153170	ANKRD11	c.5728G>T (p.Asp1910Tyr) c.5531G>T (n.5531G>T) c.745-5623G>T (n.745-5623G>T) c.152-5623G>T c.5626G>T (p.Asp1876Tyr) c.5431G>T (p.Asp1811Tyr) c.5599G>T (p.Asp1867Tyr)
16	g.89280814C>G	CA397153171	ANKRD11	c.5728G>C (p.Asp1910His) c.5531G>C (n.5531G>C) c.745-5623G>C (n.745-5623G>C) c.152-5623G>C c.5626G>C (p.Asp1876His) c.5431G>C (p.Asp1811His) c.5599G>C (p.Asp1867His)	gnomAD v4
16	g.89280814C>T	CA397153172	ANKRD11	c.5728G>A (p.Asp1910Asn) c.5531G>A (n.5531G>A) c.745-5623G>A (n.745-5623G>A) c.152-5623G>A c.5626G>A (p.Asp1876Asn) c.5431G>A (p.Asp1811Asn) c.5599G>A (p.Asp1867Asn)
16	g.89280815C>A	CA497373549	ANKRD11	c.5727G>T (p.Pro1909=) c.5530G>T (n.5530G>T) c.745-5624G>T (n.745-5624G>T) c.152-5624G>T c.5625G>T (p.Pro1875=) c.5430G>T (p.Pro1810=) c.5598G>T (p.Pro1866=)
16	g.89280815C=	CA2241587688	ANKRD11	c.5727G= (p.Pro1909=) c.5530G= (n.5530G=) c.745-5624G= (n.745-5624G=) c.152-5624G= c.5625G= (p.Pro1875=) c.5430G= (p.Pro1810=) c.5598G= (p.Pro1866=)
16	g.89280815C>G	CA497373551	ANKRD11	c.5727G>C (p.Pro1909=) c.5530G>C (n.5530G>C) c.745-5624G>C (n.745-5624G>C) c.152-5624G>C c.5625G>C (p.Pro1875=) c.5430G>C (p.Pro1810=) c.5598G>C (p.Pro1866=)
16	g.89280815C>T	CA497373547	ANKRD11	c.5727G>A (p.Pro1909=) c.5530G>A (n.5530G>A) c.745-5624G>A (n.745-5624G>A) c.152-5624G>A c.5625G>A (p.Pro1875=) c.5430G>A (p.Pro1810=) c.5598G>A (p.Pro1866=)	dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16	g.89280816G>A	CA8241743	ANKRD11	c.5726C>T (p.Pro1909Leu) c.5529C>T (n.5529C>T) c.745-5625C>T (n.745-5625C>T) c.152-5625C>T c.5624C>T (p.Pro1875Leu) c.5429C>T (p.Pro1810Leu) c.5597C>T (p.Pro1866Leu)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16	g.89280816G>C	CA397153173	ANKRD11	c.5726C>G (p.Pro1909Arg) c.5529C>G (n.5529C>G) c.745-5625C>G (n.745-5625C>G) c.152-5625C>G c.5624C>G (p.Pro1875Arg) c.5429C>G (p.Pro1810Arg) c.5597C>G (p.Pro1866Arg)
16	g.89280816G=	CA2241587689	ANKRD11	c.5726C= (p.Pro1909=) c.5529C= (n.5529C=) c.745-5625C= (n.745-5625C=) c.152-5625C= c.5624C= (p.Pro1875=) c.5429C= (p.Pro1810=) c.5597C= (p.Pro1866=)
16	g.89280816G>T	CA397153174	ANKRD11	c.5726C>A (p.Pro1909Gln) c.5529C>A (n.5529C>A) c.745-5625C>A (n.745-5625C>A) c.152-5625C>A c.5624C>A (p.Pro1875Gln) c.5429C>A (p.Pro1810Gln) c.5597C>A (p.Pro1866Gln)
16	g.89280820dup	CA2808088003	ANKRD11	c.5726dup (p.Asp1910GlyfsTer?) c.5529dup (n.5529dup) c.745-5625dup (n.745-5625dup) c.152-5625dup c.5624dup (p.Asp1876GlyfsTer?) c.5429dup (p.Asp1811GlyfsTer?) c.5597dup (p.Asp1867GlyfsTer?)
16	g.89280820del	CA2634943071	ANKRD11	c.5726del (p.Pro1909ArgfsTer?) c.5529del (n.5529del) c.745-5625del (n.745-5625del) c.152-5625del c.5624del (p.Pro1875ArgfsTer?) c.5429del (p.Pro1810ArgfsTer?) c.5597del (p.Pro1866ArgfsTer?)	gnomAD v4
16	g.89280817G>A	CA8241744	ANKRD11	c.5725C>T (p.Pro1909Ser) c.5528C>T (n.5528C>T) c.745-5626C>T (n.745-5626C>T) c.152-5626C>T c.5623C>T (p.Pro1875Ser) c.5428C>T (p.Pro1810Ser) c.5596C>T (p.Pro1866Ser)	dbSNP ExAC gnomAD v2 gnomAD v4
16	g.89280817G>C	CA397153175	ANKRD11	c.5725C>G (p.Pro1909Ala) c.5528C>G (n.5528C>G) c.745-5626C>G (n.745-5626C>G) c.152-5626C>G c.5623C>G (p.Pro1875Ala) c.5428C>G (p.Pro1810Ala) c.5596C>G (p.Pro1866Ala)
16	g.89280817G=	CA2241587690	ANKRD11	c.5725C= (p.Pro1909=) c.5528C= (n.5528C=) c.745-5626C= (n.745-5626C=) c.152-5626C= c.5623C= (p.Pro1875=) c.5428C= (p.Pro1810=) c.5596C= (p.Pro1866=)
16	g.89280817G>T	CA397153176	ANKRD11	c.5725C>A (p.Pro1909Thr) c.5528C>A (n.5528C>A) c.745-5626C>A (n.745-5626C>A) c.152-5626C>A c.5623C>A (p.Pro1875Thr) c.5428C>A (p.Pro1810Thr) c.5596C>A (p.Pro1866Thr)
16	g.89280818G>A	CA497373558	ANKRD11	c.5724C>T (p.Pro1908=) c.5527C>T (n.5527C>T) c.745-5627C>T (n.745-5627C>T) c.152-5627C>T c.5622C>T (p.Pro1874=) c.5427C>T (p.Pro1809=) c.5595C>T (p.Pro1865=)	ClinVar dbSNP gnomAD v4
16	g.89280818G>C	CA497373555	ANKRD11	c.5724C>G (p.Pro1908=) c.5527C>G (n.5527C>G) c.745-5627C>G (n.745-5627C>G) c.152-5627C>G c.5622C>G (p.Pro1874=) c.5427C>G (p.Pro1809=) c.5595C>G (p.Pro1865=)
16	g.89280818G=	CA2241587691	ANKRD11	c.5724C= (p.Pro1908=) c.5527C= (n.5527C=) c.745-5627C= (n.745-5627C=) c.152-5627C= c.5622C= (p.Pro1874=) c.5427C= (p.Pro1809=) c.5595C= (p.Pro1865=)
16	g.89280818G>T	CA497373557	ANKRD11	c.5724C>A (p.Pro1908=) c.5527C>A (n.5527C>A) c.745-5627C>A (n.745-5627C>A) c.152-5627C>A c.5622C>A (p.Pro1874=) c.5427C>A (p.Pro1809=) c.5595C>A (p.Pro1865=)
16	g.89280819G>A	CA8241745	ANKRD11	c.5723C>T (p.Pro1908Leu) c.5526C>T (n.5526C>T) c.745-5628C>T (n.745-5628C>T) c.152-5628C>T c.5621C>T (p.Pro1874Leu) c.5426C>T (p.Pro1809Leu) c.5594C>T (p.Pro1865Leu)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16	g.89280819G>C	CA397153178	ANKRD11	c.5723C>G (p.Pro1908Arg) c.5526C>G (n.5526C>G) c.745-5628C>G (n.745-5628C>G) c.152-5628C>G c.5621C>G (p.Pro1874Arg) c.5426C>G (p.Pro1809Arg) c.5594C>G (p.Pro1865Arg)
16	g.89280819G=	CA2241587692	ANKRD11	c.5723C= (p.Pro1908=) c.5526C= (n.5526C=) c.745-5628C= (n.745-5628C=) c.152-5628C= c.5621C= (p.Pro1874=) c.5426C= (p.Pro1809=) c.5594C= (p.Pro1865=)
16	g.89280819G>T	CA397153177	ANKRD11	c.5723C>A (p.Pro1908His) c.5526C>A (n.5526C>A) c.745-5628C>A (n.745-5628C>A) c.152-5628C>A c.5621C>A (p.Pro1874His) c.5426C>A (p.Pro1809His) c.5594C>A (p.Pro1865His)	gnomAD v4
16	g.89280820G>A	CA8241747	ANKRD11	c.5722C>T (p.Pro1908Ser) c.5525C>T (n.5525C>T) c.745-5629C>T (n.745-5629C>T) c.152-5629C>T c.5620C>T (p.Pro1874Ser) c.5425C>T (p.Pro1809Ser) c.5593C>T (p.Pro1865Ser)	dbSNP ExAC gnomAD v2 gnomAD v4
16	g.89280820G>C	CA397153179	ANKRD11	c.5722C>G (p.Pro1908Ala) c.5525C>G (n.5525C>G) c.745-5629C>G (n.745-5629C>G) c.152-5629C>G c.5620C>G (p.Pro1874Ala) c.5425C>G (p.Pro1809Ala) c.5593C>G (p.Pro1865Ala)	gnomAD v4
16	g.89280820G=	CA2241587693	ANKRD11	c.5722C= (p.Pro1908=) c.5525C= (n.5525C=) c.745-5629C= (n.745-5629C=) c.152-5629C= c.5620C= (p.Pro1874=) c.5425C= (p.Pro1809=) c.5593C= (p.Pro1865=)
16	g.89280820G>T	CA8241746	ANKRD11	c.5722C>A (p.Pro1908Thr) c.5525C>A (n.5525C>A) c.745-5629C>A (n.745-5629C>A) c.152-5629C>A c.5620C>A (p.Pro1874Thr) c.5425C>A (p.Pro1809Thr) c.5593C>A (p.Pro1865Thr)	dbSNP ExAC gnomAD v2 gnomAD v4
16	g.89280821A=	CA2241587694	ANKRD11	c.5721T= (p.Leu1907=) c.5524T= (n.5524T=) c.745-5630T= (n.745-5630T=) c.152-5630T= c.5619T= (p.Leu1873=) c.5424T= (p.Leu1808=) c.5592T= (p.Leu1864=)
16	g.89280821A>C	CA497373561	ANKRD11	c.5721T>G (p.Leu1907=) c.5524T>G (n.5524T>G) c.745-5630T>G (n.745-5630T>G) c.152-5630T>G c.5619T>G (p.Leu1873=) c.5424T>G (p.Leu1808=) c.5592T>G (p.Leu1864=)
16	g.89280821A>G	CA8241748	ANKRD11	c.5721T>C (p.Leu1907=) c.5524T>C (n.5524T>C) c.745-5630T>C (n.745-5630T>C) c.152-5630T>C c.5619T>C (p.Leu1873=) c.5424T>C (p.Leu1808=) c.5592T>C (p.Leu1864=)	dbSNP ExAC gnomAD v2 gnomAD v4
16	g.89280821A>T	CA497373560	ANKRD11	c.5721T>A (p.Leu1907=) c.5524T>A (n.5524T>A) c.745-5630T>A (n.745-5630T>A) c.152-5630T>A c.5619T>A (p.Leu1873=) c.5424T>A (p.Leu1808=) c.5592T>A (p.Leu1864=)
16	g.89280822A>C	CA397153180	ANKRD11	c.5720T>G (p.Leu1907Arg) c.5523T>G (n.5523T>G) c.745-5631T>G (n.745-5631T>G) c.152-5631T>G c.5618T>G (p.Leu1873Arg) c.5423T>G (p.Leu1808Arg) c.5591T>G (p.Leu1864Arg)
16	g.89280822A>G	CA397153181	ANKRD11	c.5720T>C (p.Leu1907Pro) c.5523T>C (n.5523T>C) c.745-5631T>C (n.745-5631T>C) c.152-5631T>C c.5618T>C (p.Leu1873Pro) c.5423T>C (p.Leu1808Pro) c.5591T>C (p.Leu1864Pro)	COSMIC
16	g.89280822A>T	CA397153182	ANKRD11	c.5720T>A (p.Leu1907His) c.5523T>A (n.5523T>A) c.745-5631T>A (n.745-5631T>A) c.152-5631T>A c.5618T>A (p.Leu1873His) c.5423T>A (p.Leu1808His) c.5591T>A (p.Leu1864His)
16	g.89280823G>A	CA397153183	ANKRD11	c.5719C>T (p.Leu1907Phe) c.5522C>T (n.5522C>T) c.745-5632C>T (n.745-5632C>T) c.152-5632C>T c.5617C>T (p.Leu1873Phe) c.5422C>T (p.Leu1808Phe) c.5590C>T (p.Leu1864Phe)	dbSNP gnomAD v2 gnomAD v4
16	g.89280823G>C	CA397153184	ANKRD11	c.5719C>G (p.Leu1907Val) c.5522C>G (n.5522C>G) c.745-5632C>G (n.745-5632C>G) c.152-5632C>G c.5617C>G (p.Leu1873Val) c.5422C>G (p.Leu1808Val) c.5590C>G (p.Leu1864Val)
16	g.89280823G=	CA2241587695	ANKRD11	c.5719C= (p.Leu1907=) c.5522C= (n.5522C=) c.745-5632C= (n.745-5632C=) c.152-5632C= c.5617C= (p.Leu1873=) c.5422C= (p.Leu1808=) c.5590C= (p.Leu1864=)
16	g.89280823G>T	CA286513510	ANKRD11	c.5719C>A (p.Leu1907Ile) c.5522C>A (n.5522C>A) c.745-5632C>A (n.745-5632C>A) c.152-5632C>A c.5617C>A (p.Leu1873Ile) c.5422C>A (p.Leu1808Ile) c.5590C>A (p.Leu1864Ile)	dbSNP gnomAD v4
16	g.89280824G>A	CA497373574	ANKRD11	c.5718C>T (p.Ala1906=) c.5521C>T (n.5521C>T) c.745-5633C>T (n.745-5633C>T) c.152-5633C>T c.5616C>T (p.Ala1872=) c.5421C>T (p.Ala1807=) c.5589C>T (p.Ala1863=)
16	g.89280824G>C	CA497373572	ANKRD11	c.5718C>G (p.Ala1906=) c.5521C>G (n.5521C>G) c.745-5633C>G (n.745-5633C>G) c.152-5633C>G c.5616C>G (p.Ala1872=) c.5421C>G (p.Ala1807=) c.5589C>G (p.Ala1863=)	gnomAD v4
16	g.89280824G>T	CA497373570	ANKRD11	c.5718C>A (p.Ala1906=) c.5521C>A (n.5521C>A) c.745-5633C>A (n.745-5633C>A) c.152-5633C>A c.5616C>A (p.Ala1872=) c.5421C>A (p.Ala1807=) c.5589C>A (p.Ala1863=)
16	g.89280825G>A	CA397153185	ANKRD11	c.5717C>T (p.Ala1906Val) c.5520C>T (n.5520C>T) c.745-5634C>T (n.745-5634C>T) c.152-5634C>T c.5615C>T (p.Ala1872Val) c.5420C>T (p.Ala1807Val) c.5588C>T (p.Ala1863Val)	gnomAD v4
16	g.89280825G>C	CA397153186	ANKRD11	c.5717C>G (p.Ala1906Gly) c.5520C>G (n.5520C>G) c.745-5634C>G (n.745-5634C>G) c.152-5634C>G c.5615C>G (p.Ala1872Gly) c.5420C>G (p.Ala1807Gly) c.5588C>G (p.Ala1863Gly)
16	g.89280825G>T	CA397153187	ANKRD11	c.5717C>A (p.Ala1906Asp) c.5520C>A (n.5520C>A) c.745-5634C>A (n.745-5634C>A) c.152-5634C>A c.5615C>A (p.Ala1872Asp) c.5420C>A (p.Ala1807Asp) c.5588C>A (p.Ala1863Asp)
16	g.89280826C>A	CA397153190	ANKRD11	c.5716G>T (p.Ala1906Ser) c.5519G>T (n.5519G>T) c.745-5635G>T (n.745-5635G>T) c.152-5635G>T c.5614G>T (p.Ala1872Ser) c.5419G>T (p.Ala1807Ser) c.5587G>T (p.Ala1863Ser)	gnomAD v4
16	g.89280826C=	CA2241587696	ANKRD11	c.5716G= (p.Ala1906=) c.5519G= (n.5519G=) c.745-5635G= (n.745-5635G=) c.152-5635G= c.5614G= (p.Ala1872=) c.5419G= (p.Ala1807=) c.5587G= (p.Ala1863=)
16	g.89280826C>G	CA397153189	ANKRD11	c.5716G>C (p.Ala1906Pro) c.5519G>C (n.5519G>C) c.745-5635G>C (n.745-5635G>C) c.152-5635G>C c.5614G>C (p.Ala1872Pro) c.5419G>C (p.Ala1807Pro) c.5587G>C (p.Ala1863Pro)	gnomAD v4
16	g.89280826C>T	CA397153188	ANKRD11	c.5716G>A (p.Ala1906Thr) c.5519G>A (n.5519G>A) c.745-5635G>A (n.745-5635G>A) c.152-5635G>A c.5614G>A (p.Ala1872Thr) c.5419G>A (p.Ala1807Thr) c.5587G>A (p.Ala1863Thr)	ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16	g.89280827C>A	CA497373582	ANKRD11	c.5715G>T (p.Gly1905=) c.5518G>T (n.5518G>T) c.745-5636G>T (n.745-5636G>T) c.152-5636G>T c.5613G>T (p.Gly1871=) c.5418G>T (p.Gly1806=) c.5586G>T (p.Gly1862=)	gnomAD v4
16	g.89280827C=	CA2241587697	ANKRD11	c.5715G= (p.Gly1905=) c.5518G= (n.5518G=) c.745-5636G= (n.745-5636G=) c.152-5636G= c.5613G= (p.Gly1871=) c.5418G= (p.Gly1806=) c.5586G= (p.Gly1862=)
16	g.89280827C>G	CA8241749	ANKRD11	c.5715G>C (p.Gly1905=) c.5518G>C (n.5518G>C) c.745-5636G>C (n.745-5636G>C) c.152-5636G>C c.5613G>C (p.Gly1871=) c.5418G>C (p.Gly1806=) c.5586G>C (p.Gly1862=)	dbSNP ExAC gnomAD v2
16	g.89280827C>T	CA497373579	ANKRD11	c.5715G>A (p.Gly1905=) c.5518G>A (n.5518G>A) c.745-5636G>A (n.745-5636G>A) c.152-5636G>A c.5613G>A (p.Gly1871=) c.5418G>A (p.Gly1806=) c.5586G>A (p.Gly1862=)	gnomAD v4
16	g.89280828C>A	CA397153191	ANKRD11	c.5714G>T (p.Gly1905Val) c.5517G>T (n.5517G>T) c.745-5637G>T (n.745-5637G>T) c.152-5637G>T c.5612G>T (p.Gly1871Val) c.5417G>T (p.Gly1806Val) c.5585G>T (p.Gly1862Val)	gnomAD v4
16	g.89280828C>G	CA397153193	ANKRD11	c.5714G>C (p.Gly1905Ala) c.5517G>C (n.5517G>C) c.745-5637G>C (n.745-5637G>C) c.152-5637G>C c.5612G>C (p.Gly1871Ala) c.5417G>C (p.Gly1806Ala) c.5585G>C (p.Gly1862Ala)
16	g.89280828C>T	CA397153192	ANKRD11	c.5714G>A (p.Gly1905Glu) c.5517G>A (n.5517G>A) c.745-5637G>A (n.745-5637G>A) c.152-5637G>A c.5612G>A (p.Gly1871Glu) c.5417G>A (p.Gly1806Glu) c.5585G>A (p.Gly1862Glu)	gnomAD v4
16	g.89280829C>A	CA397153194	ANKRD11	c.5713G>T (p.Gly1905Trp) c.5516G>T (n.5516G>T) c.745-5638G>T (n.745-5638G>T) c.152-5638G>T c.5611G>T (p.Gly1871Trp) c.5416G>T (p.Gly1806Trp) c.5584G>T (p.Gly1862Trp)	gnomAD v4
16	g.89280829C>G	CA397153196	ANKRD11	c.5713G>C (p.Gly1905Arg) c.5516G>C (n.5516G>C) c.745-5638G>C (n.745-5638G>C) c.152-5638G>C c.5611G>C (p.Gly1871Arg) c.5416G>C (p.Gly1806Arg) c.5584G>C (p.Gly1862Arg)	ClinVar
16	g.89280829C>T	CA397153195	ANKRD11	c.5713G>A (p.Gly1905Arg) c.5516G>A (n.5516G>A) c.745-5638G>A (n.745-5638G>A) c.152-5638G>A c.5611G>A (p.Gly1871Arg) c.5416G>A (p.Gly1806Arg) c.5584G>A (p.Gly1862Arg)
16	g.89280829_89280830insA	CA2695223940	ANKRD11	c.5712_5713insT (p.Gly1905TrpfsTer?) c.5515_5516insT (n.5515_5516insT) c.745-5639_745-5638insT (n.745-5639_745-5638insT) c.152-5639_152-5638insT c.5610_5611insT (p.Gly1871TrpfsTer?) c.5415_5416insT (p.Gly1806TrpfsTer?) c.5583_5584insT (p.Gly1862TrpfsTer?)
16	g.89280830T>A	CA397153197	ANKRD11	c.5712A>T (p.Glu1904Asp) c.5515A>T (n.5515A>T) c.745-5639A>T (n.745-5639A>T) c.152-5639A>T c.5610A>T (p.Glu1870Asp) c.5415A>T (p.Glu1805Asp) c.5583A>T (p.Glu1861Asp)
16	g.89280830T>C	CA497373586	ANKRD11	c.5712A>G (p.Glu1904=) c.5515A>G (n.5515A>G) c.745-5639A>G (n.745-5639A>G) c.152-5639A>G c.5610A>G (p.Glu1870=) c.5415A>G (p.Glu1805=) c.5583A>G (p.Glu1861=)
16	g.89280830T>G	CA397153198	ANKRD11	c.5712A>C (p.Glu1904Asp) c.5515A>C (n.5515A>C) c.745-5639A>C (n.745-5639A>C) c.152-5639A>C c.5610A>C (p.Glu1870Asp) c.5415A>C (p.Glu1805Asp) c.5583A>C (p.Glu1861Asp)	dbSNP gnomAD v2 gnomAD v4
16	g.89280830T=	CA2241587698	ANKRD11	c.5712A= (p.Glu1904=) c.5515A= (n.5515A=) c.745-5639A= (n.745-5639A=) c.152-5639A= c.5610A= (p.Glu1870=) c.5415A= (p.Glu1805=) c.5583A= (p.Glu1861=)
16	g.89280831T>A	CA397153199	ANKRD11	c.5711A>T (p.Glu1904Val) c.5514A>T (n.5514A>T) c.745-5640A>T (n.745-5640A>T) c.152-5640A>T c.5609A>T (p.Glu1870Val) c.5414A>T (p.Glu1805Val) c.5582A>T (p.Glu1861Val)
16	g.89280831T>C	CA397153201	ANKRD11	c.5711A>G (p.Glu1904Gly) c.5514A>G (n.5514A>G) c.745-5640A>G (n.745-5640A>G) c.152-5640A>G c.5609A>G (p.Glu1870Gly) c.5414A>G (p.Glu1805Gly) c.5582A>G (p.Glu1861Gly)	dbSNP gnomAD v4
16	g.89280831T>G	CA397153200	ANKRD11	c.5711A>C (p.Glu1904Ala) c.5514A>C (n.5514A>C) c.745-5640A>C (n.745-5640A>C) c.152-5640A>C c.5609A>C (p.Glu1870Ala) c.5414A>C (p.Glu1805Ala) c.5582A>C (p.Glu1861Ala)
16	g.89280831T=	CA2241587699	ANKRD11	c.5711A= (p.Glu1904=) c.5514A= (n.5514A=) c.745-5640A= (n.745-5640A=) c.152-5640A= c.5609A= (p.Glu1870=) c.5414A= (p.Glu1805=) c.5582A= (p.Glu1861=)
16	g.89280832C>A	CA397153202	ANKRD11	c.5710G>T (p.Glu1904Ter) c.5513G>T (n.5513G>T) c.745-5641G>T (n.745-5641G>T) c.152-5641G>T c.5608G>T (p.Glu1870Ter) c.5413G>T (p.Glu1805Ter) c.5581G>T (p.Glu1861Ter)	gnomAD v4
16	g.89280832C=	CA2241587700	ANKRD11	c.5710G= (p.Glu1904=) c.5513G= (n.5513G=) c.745-5641G= (n.745-5641G=) c.152-5641G= c.5608G= (p.Glu1870=) c.5413G= (p.Glu1805=) c.5581G= (p.Glu1861=)
16	g.89280832C>G	CA397153203	ANKRD11	c.5710G>C (p.Glu1904Gln) c.5513G>C (n.5513G>C) c.745-5641G>C (n.745-5641G>C) c.152-5641G>C c.5608G>C (p.Glu1870Gln) c.5413G>C (p.Glu1805Gln) c.5581G>C (p.Glu1861Gln)	gnomAD v4
16	g.89280832C>T	CA286513519	ANKRD11	c.5710G>A (p.Glu1904Lys) c.5513G>A (n.5513G>A) c.745-5641G>A (n.745-5641G>A) c.152-5641G>A c.5608G>A (p.Glu1870Lys) c.5413G>A (p.Glu1805Lys) c.5581G>A (p.Glu1861Lys)	dbSNP gnomAD v2 gnomAD v4
16	g.89280833G>A	CA497373594	ANKRD11	c.5709C>T (p.Leu1903=) c.5512C>T (n.5512C>T) c.745-5642C>T (n.745-5642C>T) c.152-5642C>T c.5607C>T (p.Leu1869=) c.5412C>T (p.Leu1804=) c.5580C>T (p.Leu1860=)	dbSNP gnomAD v4
16	g.89280833G>C	CA497373595	ANKRD11	c.5709C>G (p.Leu1903=) c.5512C>G (n.5512C>G) c.745-5642C>G (n.745-5642C>G) c.152-5642C>G c.5607C>G (p.Leu1869=) c.5412C>G (p.Leu1804=) c.5580C>G (p.Leu1860=)
16	g.89280833G=	CA2241587701	ANKRD11	c.5709C= (p.Leu1903=) c.5512C= (n.5512C=) c.745-5642C= (n.745-5642C=) c.152-5642C= c.5607C= (p.Leu1869=) c.5412C= (p.Leu1804=) c.5580C= (p.Leu1860=)
16	g.89280833G>T	CA497373596	ANKRD11	c.5709C>A (p.Leu1903=) c.5512C>A (n.5512C>A) c.745-5642C>A (n.745-5642C>A) c.152-5642C>A c.5607C>A (p.Leu1869=) c.5412C>A (p.Leu1804=) c.5580C>A (p.Leu1860=)
16	g.89280834A>C	CA397153204	ANKRD11	c.5708T>G (p.Leu1903Arg) c.5511T>G (n.5511T>G) c.745-5643T>G (n.745-5643T>G) c.152-5643T>G c.5606T>G (p.Leu1869Arg) c.5411T>G (p.Leu1804Arg) c.5579T>G (p.Leu1860Arg)
16	g.89280834A>G	CA397153206	ANKRD11	c.5708T>C (p.Leu1903Pro) c.5511T>C (n.5511T>C) c.745-5643T>C (n.745-5643T>C) c.152-5643T>C c.5606T>C (p.Leu1869Pro) c.5411T>C (p.Leu1804Pro) c.5579T>C (p.Leu1860Pro)
16	g.89280834A>T	CA397153205	ANKRD11	c.5708T>A (p.Leu1903His) c.5511T>A (n.5511T>A) c.745-5643T>A (n.745-5643T>A) c.152-5643T>A c.5606T>A (p.Leu1869His) c.5411T>A (p.Leu1804His) c.5579T>A (p.Leu1860His)
16	g.89280835G>A	CA397153207	ANKRD11	c.5707C>T (p.Leu1903Phe) c.5510C>T (n.5510C>T) c.745-5644C>T (n.745-5644C>T) c.152-5644C>T c.5605C>T (p.Leu1869Phe) c.5410C>T (p.Leu1804Phe) c.5578C>T (p.Leu1860Phe)	dbSNP gnomAD v2 gnomAD v4 COSMIC
16	g.89280835G>C	CA397153208	ANKRD11	c.5707C>G (p.Leu1903Val) c.5510C>G (n.5510C>G) c.745-5644C>G (n.745-5644C>G) c.152-5644C>G c.5605C>G (p.Leu1869Val) c.5410C>G (p.Leu1804Val) c.5578C>G (p.Leu1860Val)
16	g.89280835G=	CA2241587702	ANKRD11	c.5707C= (p.Leu1903=) c.5510C= (n.5510C=) c.745-5644C= (n.745-5644C=) c.152-5644C= c.5605C= (p.Leu1869=) c.5410C= (p.Leu1804=) c.5578C= (p.Leu1860=)
16	g.89280835G>T	CA397153209	ANKRD11	c.5707C>A (p.Leu1903Ile) c.5510C>A (n.5510C>A) c.745-5644C>A (n.745-5644C>A) c.152-5644C>A c.5605C>A (p.Leu1869Ile) c.5410C>A (p.Leu1804Ile) c.5578C>A (p.Leu1860Ile)
16	g.89280836G>A	CA497373601	ANKRD11	c.5706C>T (p.Ser1902=) c.5509C>T (n.5509C>T) c.745-5645C>T (n.745-5645C>T) c.152-5645C>T c.5604C>T (p.Ser1868=) c.5409C>T (p.Ser1803=) c.5577C>T (p.Ser1859=)	dbSNP gnomAD v4
16	g.89280836G>C	CA497373605	ANKRD11	c.5706C>G (p.Ser1902=) c.5509C>G (n.5509C>G) c.745-5645C>G (n.745-5645C>G) c.152-5645C>G c.5604C>G (p.Ser1868=) c.5409C>G (p.Ser1803=) c.5577C>G (p.Ser1859=)
16	g.89280836G=	CA2241587703	ANKRD11	c.5706C= (p.Ser1902=) c.5509C= (n.5509C=) c.745-5645C= (n.745-5645C=) c.152-5645C= c.5604C= (p.Ser1868=) c.5409C= (p.Ser1803=) c.5577C= (p.Ser1859=)
16	g.89280836G>T	CA497373606	ANKRD11	c.5706C>A (p.Ser1902=) c.5509C>A (n.5509C>A) c.745-5645C>A (n.745-5645C>A) c.152-5645C>A c.5604C>A (p.Ser1868=) c.5409C>A (p.Ser1803=) c.5577C>A (p.Ser1859=)
16	g.89280837G>A	CA397153210	ANKRD11	c.5705C>T (p.Ser1902Phe) c.5508C>T (n.5508C>T) c.745-5646C>T (n.745-5646C>T) c.152-5646C>T c.5603C>T (p.Ser1868Phe) c.5408C>T (p.Ser1803Phe) c.5576C>T (p.Ser1859Phe)
16	g.89280837G>C	CA397153211	ANKRD11	c.5705C>G (p.Ser1902Cys) c.5508C>G (n.5508C>G) c.745-5646C>G (n.745-5646C>G) c.152-5646C>G c.5603C>G (p.Ser1868Cys) c.5408C>G (p.Ser1803Cys) c.5576C>G (p.Ser1859Cys)
16	g.89280837G>T	CA397153212	ANKRD11	c.5705C>A (p.Ser1902Tyr) c.5508C>A (n.5508C>A) c.745-5646C>A (n.745-5646C>A) c.152-5646C>A c.5603C>A (p.Ser1868Tyr) c.5408C>A (p.Ser1803Tyr) c.5576C>A (p.Ser1859Tyr)
16	g.89280838A>C	CA397153213	ANKRD11	c.5704T>G (p.Ser1902Ala) c.5507T>G (n.5507T>G) c.745-5647T>G (n.745-5647T>G) c.152-5647T>G c.5602T>G (p.Ser1868Ala) c.5407T>G (p.Ser1803Ala) c.5575T>G (p.Ser1859Ala)
16	g.89280838A>G	CA397153214	ANKRD11	c.5704T>C (p.Ser1902Pro) c.5507T>C (n.5507T>C) c.745-5647T>C (n.745-5647T>C) c.152-5647T>C c.5602T>C (p.Ser1868Pro) c.5407T>C (p.Ser1803Pro) c.5575T>C (p.Ser1859Pro)
16	g.89280838A>T	CA397153215	ANKRD11	c.5704T>A (p.Ser1902Thr) c.5507T>A (n.5507T>A) c.745-5647T>A (n.745-5647T>A) c.152-5647T>A c.5602T>A (p.Ser1868Thr) c.5407T>A (p.Ser1803Thr) c.5575T>A (p.Ser1859Thr)
16	g.89280839A>C	CA497373616	ANKRD11	c.5703T>G (p.Pro1901=) c.5506T>G (n.5506T>G) c.745-5648T>G (n.745-5648T>G) c.152-5648T>G c.5601T>G (p.Pro1867=) c.5406T>G (p.Pro1802=) c.5574T>G (p.Pro1858=)
16	g.89280839A>G	CA497373618	ANKRD11	c.5703T>C (p.Pro1901=) c.5506T>C (n.5506T>C) c.745-5648T>C (n.745-5648T>C) c.152-5648T>C c.5601T>C (p.Pro1867=) c.5406T>C (p.Pro1802=) c.5574T>C (p.Pro1858=)	gnomAD v4
16	g.89280839A>T	CA497373620	ANKRD11	c.5703T>A (p.Pro1901=) c.5506T>A (n.5506T>A) c.745-5648T>A (n.745-5648T>A) c.152-5648T>A c.5601T>A (p.Pro1867=) c.5406T>A (p.Pro1802=) c.5574T>A (p.Pro1858=)

Number of alleles fetched