Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
3	g.138945277_138946050delinsGCGGCTGCAGCAGCTGCGGCTGCAGCCGCGGGCCCCGGTAGCCCTGGCGCGGCCGCTGTGGTCAAGGGGCTGGCGGGCCCGGCCGCCTCGTACGGGCCGTACACACGCGTGCAGAGCATGGCGCTGCCCCCCGGCGTAGTGAACTCGTACAATGGCCTGGGAGGCCCGCCGGCCGCACCCCCGCCTCCGCCGCACCCCCACCCGCATCCGCACGCACACCATCTGCACGCGGCCGCCGCACCGCCGCCTGCCCCACCGCACCACGGGGCCGCCGCGCCGCCGCCGGGCCAGCTCAGCCCTGCCAGCCCAGCCACCGCCGCGCCCCCGGCGCCCGCGCCCACCAGTGCGCCGGGCCTGCAGTTCGCTTGTGCCCGGCAGCCCGAGCTCGCCATGATGCATTGCTCTTACTGGGACCACGACAGCAAGACCGGCGCGCTGCATTCGCGCCTCGATCTCTGAGAGCCCACCGCATGCCGGTGCAGACGGATGCGAGGATGCAGGGACGCGCGACGCCGGCCCCGGTCGCAGCCGACGACGCCGCCGCCAGCCTGACCTCACACCCTCTGGGCCCGCCTCTGGAGCCAGCGCCCAGGGTCCCTCTGTGCTTTTTCGCTTTCCTAAGCTCCTGTCGCTCCTCTTTGTCCCCTCAGTTTATGTCCTCCTGTGCTCACCTCCCTGACCTCTGTGACCTTGCACTCCCCTGGCCTGAAGCTGCCTCTCTGCGCGCTTTCTACTGGGCTCGTCTCTTTCCGGAGCCCCAGCGTCTCCTGCCCA	CA2580068839	FOXL2	c.673_315delinsTGGGCAGGAGACGCTGGGGCTCCGGAAAGAGACGAGCCCAGTAGAAAGCGCGCAGAGAGGCAGCTTCAGGCCAGGGGAGTGCAAGGTCACAGAGGTCAGGGAGGTGAGCACAGGAGGACATAAACTGAGGGGACAAAGAGGAGCGACAGGAGCTTAGGAAAGCGAAAAAGCACAGAGGGACCCTGGGCGCTGGCTCCAGAGGCGGGCCCAGAGGGTGTGAGGTCAGGCTGGCGGCGGCGTCGTCGGCTGCGACCGGGGCCGGCGTCGCGCGTCCCTGCATCCTCGCATCCGTCTGCACCGGCATGCGGTGGGCTCTCAGAGATCGAGGCGCGAATGCAGCGCGCCGGTCTTGCTGTCGTGGTCCCAGTAAGAGCAATGCATCATGGCGAGCTCGGGCTGCCGGGCACAAGCGAACTGCAGGCCCGGCGCACTGGTGGGCGCGGGCGCCGGGGGCGCGGCGGTGGCTGGGCTGGCAGGGCTGAGCTGGCCCGGCGGCGGCGCGGCGGCCCCGTGGTGCGGTGGGGCAGGCGGCGGTGCGGCGGCCGCGTGCAGATGGTGTGCGTGCGGATGCGGGTGGGGGTGCGGCGGAGGCGGGGGTGCGGCCGGCGGGCCTCCCAGGCCATTGTACGAGTTCACTACGCCGGGGGGCAGCGCCATGCTCTGCACGCGTGTGTACGGCCCGTACGAGGCGGCCGGGCCCGCCAGCCCCTTGACCACAGCGGCCGCGCCAGGGCTACCGGGGCCCGCGGCTGCAGCCGCAGCTGCTGCAGCCGC (n.[c.673_315delinsTGGGCAGGAGACGCTGGGGCTCCGGAAAGAGACGAGCCCAGTAGAAAGCGCGCAGAGAGGCAGCTTCAGGCCAGGGGAGTGCAAGGTCACAGAGGTCAGGGAGGTGAGCACAGGAGGACATAAACTGAGGGGACAAAGAGGAGCGACAGGAGCTTAGGAAAGCGAAAAAGCACAGAGGGACCCTGGGCGCTGGCTCCAGAGGCGGGCCCAGAGGGTGTGAGGTCAGGCTGGCGGCGGCGTCGTCGGCTGCGACCGGGGCCGGCGTCGCGCGTCCCTGCATCCTCGCATCCGTCTGCACCGGCATGCGGTGGGCTCTCAGAGATCGAGGCGCGAATGCAGCGCGCCGGTCTTGCTGTCGTGGTCCCAGTAAGAGCAATGCATCATGGCGAGCTCGGGCTGCCGGGCACAAGCGAACTGCAGGCCCGGCGCACTGGTGGGCGCGGGCGCCGGGGGCGCGGCGGTGGCTGGGCTGGCAGGGCTGAGCTGGCCCGGCGGCGGCGCGGCGGCCCCGTGGTGCGGTGGGGCAGGCGGCGGTGCGGCGGCCGCGTGCAGATGGTGTGCGTGCGGATGCGGGTGGGGGTGCGGCGGAGGCGGGGGTGCGGCCGGCGGGCCTCCCAGGCCATTGTACGAGTTCACTACGCCGGGGGGCAGCGCCATGCTCTGCACGCGTGTGTACGGCCCGTACGAGGCGGCCGGGCCCGCCAGCCCCTTGACCACAGCGGCCGCGCCAGGGCTACCGGGGCCCGCGGCTGCAGCCGCAGCTGCTGCAGCCGC;Ala225TrpfsTer41])	ClinVar
3	g.138945883_138945972del	CA2667925573	FOXL2	c.759_848del (p.Ser254_Ala283del)	gnomAD v4
3	g.138945934del	CA2667925811	FOXL2	c.789del (p.Ser263ArgfsTer8)	gnomAD v4
3	g.138945934G>A	CA436094005	FOXL2	c.789C>T (p.Ser263=)	gnomAD v4
3	g.138945934G>C	CA354703578	FOXL2	c.789C>G (p.Ser263Arg)	gnomAD v4
3	g.138945934G>T	CA354703588	FOXL2	c.789C>A (p.Ser263Arg)	ClinVar dbSNP gnomAD v4
3	g.138945935C>A	CA354703591	FOXL2	c.788G>T (p.Ser263Ile)	gnomAD v4
3	g.138945935C>G	CA354703592	FOXL2	c.788G>C (p.Ser263Thr)	gnomAD v4
3	g.138945935C>T	CA354703593	FOXL2	c.788G>A (p.Ser263Asn)	dbSNP gnomAD v4
3	g.138945936T>A	CA354703594	FOXL2	c.787A>T (p.Ser263Cys)	gnomAD v4
3	g.138945936T>C	CA354703596	FOXL2	c.787A>G (p.Ser263Gly)	gnomAD v4
3	g.138945936T>G	CA354703598	FOXL2	c.787A>C (p.Ser263Arg)	dbSNP gnomAD v3 gnomAD v4
3	g.138945936T=	CA1405402243	FOXL2	c.787A= (p.Ser263=)
3	g.138945937C>A	CA354703600	FOXL2	c.786G>T (p.Gln262His)	gnomAD v4
3	g.138945937C>G	CA354703609	FOXL2	c.786G>C (p.Gln262His)
3	g.138945937C>T	CA436094008	FOXL2	c.786G>A (p.Gln262=)	gnomAD v4
3	g.138945938T>A	CA354703613	FOXL2	c.785A>T (p.Gln262Leu)	gnomAD v4
3	g.138945938T>C	CA354703615	FOXL2	c.785A>G (p.Gln262Arg)	gnomAD v4
3	g.138945938T>G	CA354703617	FOXL2	c.785A>C (p.Gln262Pro)
3	g.138945939G>A	CA354703620	FOXL2	c.784C>T (p.Gln262Ter)	ClinVar dbSNP gnomAD v4
3	g.138945939G>C	CA354703623	FOXL2	c.784C>G (p.Gln262Glu)
3	g.138945939G=	CA1405402244	FOXL2	c.784C= (p.Gln262=)
3	g.138945939G>T	CA354703624	FOXL2	c.784C>A (p.Gln262Lys)	gnomAD v4
3	g.138945940C>A	CA436094011	FOXL2	c.783G>T (p.Val261=)	gnomAD v4
3	g.138945940C>G	CA436094012	FOXL2	c.783G>C (p.Val261=)	gnomAD v4
3	g.138945940C>T	CA436094014	FOXL2	c.783G>A (p.Val261=)	gnomAD v4
3	g.138945941A>C	CA354703633	FOXL2	c.782T>G (p.Val261Gly)
3	g.138945941A>G	CA354703635	FOXL2	c.782T>C (p.Val261Ala)	gnomAD v4
3	g.138945941A>T	CA354703636	FOXL2	c.782T>A (p.Val261Glu)	gnomAD v4
3	g.138945942C>A	CA354703639	FOXL2	c.781G>T (p.Val261Leu)	gnomAD v4
3	g.138945942C>G	CA354703642	FOXL2	c.781G>C (p.Val261Leu)	gnomAD v4
3	g.138945942C>T	CA354703644	FOXL2	c.781G>A (p.Val261Met)	gnomAD v4
3	g.138945943G>A	CA436094018	FOXL2	c.780C>T (p.Arg260=)	gnomAD v4
3	g.138945943G>C	CA436094019	FOXL2	c.780C>G (p.Arg260=)
3	g.138945943G>T	CA436094022	FOXL2	c.780C>A (p.Arg260=)	gnomAD v4
3	g.138945944C>A	CA354703653	FOXL2	c.779G>T (p.Arg260Leu)	gnomAD v4
3	g.138945944C=	CA1405402245	FOXL2	c.779G= (p.Arg260=)
3	g.138945944C>G	CA354703655	FOXL2	c.779G>C (p.Arg260Pro)
3	g.138945944C>T	CA354703649	FOXL2	c.779G>A (p.Arg260His)	dbSNP gnomAD v4
3	g.138945945G>A	CA354703658	FOXL2	c.778C>T (p.Arg260Cys)	gnomAD v4
3	g.138945945G>C	CA354703660	FOXL2	c.778C>G (p.Arg260Gly)	dbSNP gnomAD v4
3	g.138945945G=	CA1405402246	FOXL2	c.778C= (p.Arg260=)
3	g.138945945G>T	CA354703663	FOXL2	c.778C>A (p.Arg260Ser)	dbSNP gnomAD v4
3	g.138945947_138945950del	CA2580615980	FOXL2	c.775_778del (p.Thr259AlafsTer11)	ClinVar dbSNP
3	g.138945946T>A	CA2639726	FOXL2	c.777A>T (p.Thr259=)	dbSNP ExAC gnomAD v2 gnomAD v4
3	g.138945946T>C	CA436094027	FOXL2	c.777A>G (p.Thr259=)	gnomAD v4
3	g.138945946T>G	CA436094028	FOXL2	c.777A>C (p.Thr259=)
3	g.138945946T=	CA1405402247	FOXL2	c.777A= (p.Thr259=)
3	g.138945946dup	CA10654866	FOXL2	c.777dup (p.Arg260ThrfsTer?)	ClinVar dbSNP
3	g.138945947G>A	CA354703669	FOXL2	c.776C>T (p.Thr259Ile)	gnomAD v4

Number of alleles fetched