Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.1610446_1613897delCA891843163FOXC1c.1_*1790del (n.[c.1_*1790del;Met1=])
c.1_3452del (n.[c.1_3452del;Met1=])
ClinVar
6g.1610685_1610729delCA2695205854FOXC1c.240_284del (p.Tyr81_Pro95del)
6g.1610700_1610701delinsTTCA2695205857FOXC1c.255_256delinsTT (p.Leu86Phe)
6g.1610701_1610712delCA2573140134FOXC1c.256_267del (p.Leu86_Met89del)
ClinVar dbSNP
6g.1610701C>ACA362558414FOXC1c.256C>A (p.Leu86Ile)
6g.1610701C=CA1605822456FOXC1c.256C= (p.Leu86=)
6g.1610701C>GCA362558415FOXC1c.256C>G (p.Leu86Val)
6g.1610701C>TCA10588416FOXC1c.256C>T (p.Leu86Phe)
ClinVar dbSNP
6g.1610702T>ACA362558417FOXC1c.257T>A (p.Leu86His)
6g.1610702T>CCA362558418FOXC1c.257T>C (p.Leu86Pro)
6g.1610702T>GCA362558416FOXC1c.257T>G (p.Leu86Arg)
ClinVar
6g.1610702_1610703insTACA645541563FOXC1c.257_258insTA (p.Ile87ThrfsTer16)
COSMIC
6g.1610703C>ACA448393251FOXC1c.258C>A (p.Leu86=)
COSMIC
6g.1610703C=CA1605822457FOXC1c.258C= (p.Leu86=)
6g.1610703C>GCA448393252FOXC1c.258C>G (p.Leu86=)
6g.1610703C>TCA448393253FOXC1c.258C>T (p.Leu86=)
dbSNP gnomAD v4
6g.1610704A>CCA362558419FOXC1c.259A>C (p.Ile87Leu)
6g.1610704A>GCA362558421FOXC1c.259A>G (p.Ile87Val)
gnomAD v4
6g.1610704A>TCA362558420FOXC1c.259A>T (p.Ile87Phe)
6g.1610705T>ACA362558422FOXC1c.260T>A (p.Ile87Asn)
6g.1610705T>CCA362558424FOXC1c.260T>C (p.Ile87Thr)
6g.1610705T>GCA362558423FOXC1c.260T>G (p.Ile87Ser)
6g.1610706C>ACA448393259FOXC1c.261C>A (p.Ile87=)
6g.1610706C=CA1605822458FOXC1c.261C= (p.Ile87=)
6g.1610706C>GCA119641FOXC1c.261C>G (p.Ile87Met)
ClinVar dbSNP
6g.1610706C>TCA448393258FOXC1c.261C>T (p.Ile87=)
ClinVar gnomAD v4
6g.1610707A=CA1605822459FOXC1c.262A= (p.Thr88=)
6g.1610707A>CCA362558425FOXC1c.262A>C (p.Thr88Pro)
ClinVar dbSNP
6g.1610707A>GCA362558426FOXC1c.262A>G (p.Thr88Ala)
6g.1610707A>TCA362558427FOXC1c.262A>T (p.Thr88Ser)
6g.1610708C>ACA362558428FOXC1c.263C>A (p.Thr88Asn)
6g.1610708C=CA1605822460FOXC1c.263C= (p.Thr88=)
6g.1610708C>GCA362558429FOXC1c.263C>G (p.Thr88Ser)
6g.1610708C>TCA234027FOXC1c.263C>T (p.Thr88Ile)
ClinVar dbSNP
6g.1610709dupCA2497029025FOXC1c.264dup (p.Met89HisfsTer?)
6g.1610709C>ACA448393263FOXC1c.264C>A (p.Thr88=)
6g.1610709C=CA1605822461FOXC1c.264C= (p.Thr88=)
6g.1610709C>GCA448393265FOXC1c.264C>G (p.Thr88=)
gnomAD v4
6g.1610709C>TCA448393267FOXC1c.264C>T (p.Thr88=)
ClinVar dbSNP gnomAD v4
6g.1610710A>CCA362558430FOXC1c.265A>C (p.Met89Leu)
6g.1610710A>GCA362558431FOXC1c.265A>G (p.Met89Val)
gnomAD v4
6g.1610710A>TCA362558432FOXC1c.265A>T (p.Met89Leu)
6g.1610711T>ACA362558435FOXC1c.266T>A (p.Met89Lys)
6g.1610711T>CCA362558433FOXC1c.266T>C (p.Met89Thr)
6g.1610711T>GCA362558434FOXC1c.266T>G (p.Met89Arg)
6g.1610712G>ACA362558436FOXC1c.267G>A (p.Met89Ile)
gnomAD v4
6g.1610712G>CCA362558437FOXC1c.267G>C (p.Met89Ile)
6g.1610712G>TCA362558438FOXC1c.267G>T (p.Met89Ile)
6g.1610713G>ACA16044261FOXC1c.268G>A (p.Ala90Thr)
ClinVar dbSNP
6g.1610713G>CCA362558439FOXC1c.268G>C (p.Ala90Pro)

Number of alleles fetched