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.1610701_1610712delCA2573140134FOXC1c.256_267del (p.Leu86_Met89del)
ClinVar dbSNP
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)
6g.1610713G=CA1605822462FOXC1c.268G= (p.Ala90=)
6g.1610713G>TCA362558440FOXC1c.268G>T (p.Ala90Ser)
gnomAD v4
6g.1610714C>ACA16044262FOXC1c.269C>A (p.Ala90Asp)
ClinVar dbSNP
6g.1610714C=CA1605822463FOXC1c.269C= (p.Ala90=)
6g.1610714C>GCA362558441FOXC1c.269C>G (p.Ala90Gly)
6g.1610714C>TCA362558442FOXC1c.269C>T (p.Ala90Val)
ClinVar
6g.1610715C>ACA448393275FOXC1c.270C>A (p.Ala90=)
6g.1610715C=CA1605822464FOXC1c.270C= (p.Ala90=)
6g.1610715C>GCA3614728FOXC1c.270C>G (p.Ala90=)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.1610715C>TCA448393277FOXC1c.270C>T (p.Ala90=)
dbSNP gnomAD v2 gnomAD v4
6g.1610716A>CCA362558444FOXC1c.271A>C (p.Ile91Leu)
6g.1610716A>GCA362558445FOXC1c.271A>G (p.Ile91Val)
6g.1610716A>TCA362558443FOXC1c.271A>T (p.Ile91Phe)
6g.1610717T>ACA362558446FOXC1c.272T>A (p.Ile91Asn)
6g.1610717T>CCA362558447FOXC1c.272T>C (p.Ile91Thr)
6g.1610717T>GCA362558448FOXC1c.272T>G (p.Ile91Ser)
6g.1610718C>ACA448393278FOXC1c.273C>A (p.Ile91=)
6g.1610718C>GCA362558449FOXC1c.273C>G (p.Ile91Met)
6g.1610718C>TCA448393280FOXC1c.273C>T (p.Ile91=)
6g.1610719C>ACA362558450FOXC1c.274C>A (p.Gln92Lys)
gnomAD v4
6g.1610719C>GCA362558451FOXC1c.274C>G (p.Gln92Glu)
gnomAD v4
6g.1610719C>TCA362558452FOXC1c.274C>T (p.Gln92Ter)
ClinVar
6g.1610720A>CCA362558453FOXC1c.275A>C (p.Gln92Pro)
ClinVar dbSNP

Number of alleles fetched