Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.60509172_60510205delCA915948932C14orf39,SIX6c.-227_572+235del
c.-144+5194_-144+6227del (n.-144+5194_-144+6227del)
ClinVar
14g.60509891A=CA2140829079C14orf39,SIX6c.493A= (p.Thr165=)
c.-144+5504T= (n.-144+5504T=)
14g.60509891A>CCA390087419C14orf39,SIX6c.493A>C (p.Thr165Pro)
c.-144+5504T>G (n.-144+5504T>G)
14g.60509891A>GCA214925C14orf39,SIX6c.493A>G (p.Thr165Ala)
c.-144+5504T>C (n.-144+5504T>C)
ClinVar dbSNP
14g.60509891A>TCA390087421C14orf39,SIX6c.493A>T (p.Thr165Ser)
c.-144+5504T>A (n.-144+5504T>A)
14g.60509892C>ACA390087423C14orf39,SIX6c.494C>A (p.Thr165Asn)
c.-144+5503G>T (n.-144+5503G>T)
14g.60509892C>GCA390087426C14orf39,SIX6c.494C>G (p.Thr165Ser)
c.-144+5503G>C (n.-144+5503G>C)
14g.60509892C>TCA390087425C14orf39,SIX6c.494C>T (p.Thr165Ile)
c.-144+5503G>A (n.-144+5503G>A)
gnomAD v4
14g.60509893C>ACA486814145C14orf39,SIX6c.495C>A (p.Thr165=)
c.-144+5502G>T (n.-144+5502G>T)
14g.60509893C=CA2140829084C14orf39,SIX6c.495C= (p.Thr165=)
c.-144+5502G= (n.-144+5502G=)
14g.60509893C>GCA486814146C14orf39,SIX6c.495C>G (p.Thr165=)
c.-144+5502G>C (n.-144+5502G>C)
14g.60509893C>TCA7212600C14orf39,SIX6c.495C>T (p.Thr165=)
c.-144+5502G>A (n.-144+5502G>A)
dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
14g.60509894G>ACA7212601C14orf39,SIX6c.496G>A (p.Gly166Arg)
c.-144+5501C>T (n.-144+5501C>T)
dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
14g.60509894G>CCA390087429C14orf39,SIX6c.496G>C (p.Gly166Arg)
c.-144+5501C>G (n.-144+5501C>G)
dbSNP gnomAD v2 gnomAD v4
14g.60509894G=CA2140829089C14orf39,SIX6c.496G= (p.Gly166=)
c.-144+5501C= (n.-144+5501C=)
14g.60509894G>TCA390087430C14orf39,SIX6c.496G>T (p.Gly166Ter)
c.-144+5501C>A (n.-144+5501C>A)
14g.60509895G>ACA390087432C14orf39,SIX6c.497G>A (p.Gly166Glu)
c.-144+5500C>T (n.-144+5500C>T)
14g.60509895G>CCA390087435C14orf39,SIX6c.497G>C (p.Gly166Ala)
c.-144+5500C>G (n.-144+5500C>G)
14g.60509895G>TCA390087433C14orf39,SIX6c.497G>T (p.Gly166Val)
c.-144+5500C>A (n.-144+5500C>A)
14g.60509896A>CCA486814147C14orf39,SIX6c.498A>C (p.Gly166=)
c.-144+5499T>G (n.-144+5499T>G)
14g.60509896A>GCA486814148C14orf39,SIX6c.498A>G (p.Gly166=)
c.-144+5499T>C (n.-144+5499T>C)
14g.60509896A>TCA486814149C14orf39,SIX6c.498A>T (p.Gly166=)
c.-144+5499T>A (n.-144+5499T>A)
14g.60509897C>ACA390087437C14orf39,SIX6c.499C>A (p.Leu167Met)
c.-144+5498G>T (n.-144+5498G>T)
gnomAD v4
14g.60509897C>GCA390087438C14orf39,SIX6c.499C>G (p.Leu167Val)
c.-144+5498G>C (n.-144+5498G>C)
14g.60509897C>TCA486814150C14orf39,SIX6c.499C>T (p.Leu167=)
c.-144+5498G>A (n.-144+5498G>A)
14g.60509898T>ACA390087440C14orf39,SIX6c.500T>A (p.Leu167Gln)
c.-144+5497A>T (n.-144+5497A>T)
gnomAD v4
14g.60509898T>CCA390087441C14orf39,SIX6c.500T>C (p.Leu167Pro)
c.-144+5497A>G (n.-144+5497A>G)
14g.60509898T>GCA390087443C14orf39,SIX6c.500T>G (p.Leu167Arg)
c.-144+5497A>C (n.-144+5497A>C)
14g.60509899G>ACA486814151C14orf39,SIX6c.501G>A (p.Leu167=)
c.-144+5496C>T (n.-144+5496C>T)
gnomAD v4
14g.60509899G>CCA486814152C14orf39,SIX6c.501G>C (p.Leu167=)
c.-144+5496C>G (n.-144+5496C>G)
14g.60509899G>TCA486814153C14orf39,SIX6c.501G>T (p.Leu167=)
c.-144+5496C>A (n.-144+5496C>A)
14g.60509900A=CA2140829095C14orf39,SIX6c.502A= (p.Thr168=)
c.-144+5495T= (n.-144+5495T=)
14g.60509900A>CCA390087445C14orf39,SIX6c.502A>C (p.Thr168Pro)
c.-144+5495T>G (n.-144+5495T>G)
14g.60509900A>GCA262195816C14orf39,SIX6c.502A>G (p.Thr168Ala)
c.-144+5495T>C (n.-144+5495T>C)
dbSNP gnomAD v4
14g.60509900A>TCA390087447C14orf39,SIX6c.502A>T (p.Thr168Ser)
c.-144+5495T>A (n.-144+5495T>A)
14g.60509901C>ACA390087449C14orf39,SIX6c.503C>A (p.Thr168Asn)
c.-144+5494G>T (n.-144+5494G>T)
dbSNP gnomAD v4
14g.60509901C=CA2140829101C14orf39,SIX6c.503C= (p.Thr168=)
c.-144+5494G= (n.-144+5494G=)
14g.60509901C>GCA390087451C14orf39,SIX6c.503C>G (p.Thr168Ser)
c.-144+5494G>C (n.-144+5494G>C)
14g.60509901C>TCA390087452C14orf39,SIX6c.503C>T (p.Thr168Ile)
c.-144+5494G>A (n.-144+5494G>A)
ClinVar dbSNP
14g.60509904dupCA2575582719C14orf39,SIX6c.506dup (p.Thr170TyrfsTer?)
c.-144+5494dup (n.-144+5494dup)
14g.60509902C>ACA486814155C14orf39,SIX6c.504C>A (p.Thr168=)
c.-144+5493G>T (n.-144+5493G>T)
14g.60509902C>GCA486814156C14orf39,SIX6c.504C>G (p.Thr168=)
c.-144+5493G>C (n.-144+5493G>C)
14g.60509902C>TCA486814154C14orf39,SIX6c.504C>T (p.Thr168=)
c.-144+5493G>A (n.-144+5493G>A)
gnomAD v4
14g.60509903C>ACA390087454C14orf39,SIX6c.505C>A (p.Pro169Thr)
c.-144+5492G>T (n.-144+5492G>T)
gnomAD v4
14g.60509903C>GCA390087457C14orf39,SIX6c.505C>G (p.Pro169Ala)
c.-144+5492G>C (n.-144+5492G>C)
14g.60509903C>TCA390087455C14orf39,SIX6c.505C>T (p.Pro169Ser)
c.-144+5492G>A (n.-144+5492G>A)
14g.60509904C>ACA390087458C14orf39,SIX6c.506C>A (p.Pro169His)
c.-144+5491G>T (n.-144+5491G>T)
14g.60509904C=CA2140829102C14orf39,SIX6c.506C= (p.Pro169=)
c.-144+5491G= (n.-144+5491G=)
14g.60509904C>GCA390087460C14orf39,SIX6c.506C>G (p.Pro169Arg)
c.-144+5491G>C (n.-144+5491G>C)
14g.60509904C>TCA7212602C14orf39,SIX6c.506C>T (p.Pro169Leu)
c.-144+5491G>A (n.-144+5491G>A)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched