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.60509791G>ACA486973673C14orf39,SIX6c.393G>A (p.Lys131=)
c.-144+5604C>T (n.-144+5604C>T)
dbSNP gnomAD v4
14g.60509791G>CCA390087028C14orf39,SIX6c.393G>C (p.Lys131Asn)
c.-144+5604C>G (n.-144+5604C>G)
14g.60509791G=CA2140828725C14orf39,SIX6c.393G= (p.Lys131=)
c.-144+5604C= (n.-144+5604C=)
14g.60509791G>TCA390087030C14orf39,SIX6c.393G>T (p.Lys131Asn)
c.-144+5604C>A (n.-144+5604C>A)
14g.60509792A=CA2140828737C14orf39,SIX6c.394A= (p.Thr132=)
c.-144+5603T= (n.-144+5603T=)
14g.60509792A>CCA390087032C14orf39,SIX6c.394A>C (p.Thr132Pro)
c.-144+5603T>G (n.-144+5603T>G)
14g.60509792A>GCA262195812C14orf39,SIX6c.394A>G (p.Thr132Ala)
c.-144+5603T>C (n.-144+5603T>C)
dbSNP
14g.60509792A>TCA390087034C14orf39,SIX6c.394A>T (p.Thr132Ser)
c.-144+5603T>A (n.-144+5603T>A)
dbSNP gnomAD v2 gnomAD v4
14g.60509793C>ACA390087036C14orf39,SIX6c.395C>A (p.Thr132Lys)
c.-144+5602G>T (n.-144+5602G>T)
14g.60509793C>GCA390087038C14orf39,SIX6c.395C>G (p.Thr132Arg)
c.-144+5602G>C (n.-144+5602G>C)
14g.60509793C>TCA390087039C14orf39,SIX6c.395C>T (p.Thr132Ile)
c.-144+5602G>A (n.-144+5602G>A)
14g.60509794A>CCA486973679C14orf39,SIX6c.396A>C (p.Thr132=)
c.-144+5601T>G (n.-144+5601T>G)
14g.60509794A>GCA486973680C14orf39,SIX6c.396A>G (p.Thr132=)
c.-144+5601T>C (n.-144+5601T>C)
14g.60509794A>TCA486973681C14orf39,SIX6c.396A>T (p.Thr132=)
c.-144+5601T>A (n.-144+5601T>A)
14g.60509795C>ACA390087044C14orf39,SIX6c.397C>A (p.His133Asn)
c.-144+5600G>T (n.-144+5600G>T)
gnomAD v4
14g.60509795C=CA2140828743C14orf39,SIX6c.397C= (p.His133=)
c.-144+5600G= (n.-144+5600G=)
14g.60509795C>GCA7212588C14orf39,SIX6c.397C>G (p.His133Asp)
c.-144+5600G>C (n.-144+5600G>C)
dbSNP ExAC gnomAD v2 gnomAD v4
14g.60509795C>TCA390087042C14orf39,SIX6c.397C>T (p.His133Tyr)
c.-144+5600G>A (n.-144+5600G>A)
14g.60509796A=CA2140828746C14orf39,SIX6c.398A= (p.His133=)
c.-144+5599T= (n.-144+5599T=)
14g.60509796A>CCA390087049C14orf39,SIX6c.398A>C (p.His133Pro)
c.-144+5599T>G (n.-144+5599T>G)
dbSNP gnomAD v3 gnomAD v4
14g.60509796A>GCA390087046C14orf39,SIX6c.398A>G (p.His133Arg)
c.-144+5599T>C (n.-144+5599T>C)
14g.60509796A>TCA390087048C14orf39,SIX6c.398A>T (p.His133Leu)
c.-144+5599T>A (n.-144+5599T>A)
14g.60509797C>ACA390087051C14orf39,SIX6c.399C>A (p.His133Gln)
c.-144+5598G>T (n.-144+5598G>T)
14g.60509797C>GCA390087053C14orf39,SIX6c.399C>G (p.His133Gln)
c.-144+5598G>C (n.-144+5598G>C)
14g.60509797C>TCA486973685C14orf39,SIX6c.399C>T (p.His133=)
c.-144+5598G>A (n.-144+5598G>A)
14g.60509798T>ACA390087056C14orf39,SIX6c.400T>A (p.Cys134Ser)
c.-144+5597A>T (n.-144+5597A>T)
14g.60509798T>CCA390087058C14orf39,SIX6c.400T>C (p.Cys134Arg)
c.-144+5597A>G (n.-144+5597A>G)
gnomAD v4
14g.60509798T>GCA390087059C14orf39,SIX6c.400T>G (p.Cys134Gly)
c.-144+5597A>C (n.-144+5597A>C)
14g.60509799G>ACA390087062C14orf39,SIX6c.401G>A (p.Cys134Tyr)
c.-144+5596C>T (n.-144+5596C>T)
dbSNP
14g.60509799G>CCA390087063C14orf39,SIX6c.401G>C (p.Cys134Ser)
c.-144+5596C>G (n.-144+5596C>G)
14g.60509799G=CA2140828759C14orf39,SIX6c.401G= (p.Cys134=)
c.-144+5596C= (n.-144+5596C=)
14g.60509799G>TCA390087065C14orf39,SIX6c.401G>T (p.Cys134Phe)
c.-144+5596C>A (n.-144+5596C>A)
14g.60509800C>ACA390087067C14orf39,SIX6c.402C>A (p.Cys134Ter)
c.-144+5595G>T (n.-144+5595G>T)
14g.60509800C>GCA390087069C14orf39,SIX6c.402C>G (p.Cys134Trp)
c.-144+5595G>C (n.-144+5595G>C)
14g.60509800C>TCA486973689C14orf39,SIX6c.402C>T (p.Cys134=)
c.-144+5595G>A (n.-144+5595G>A)
14g.60509801T>ACA390087074C14orf39,SIX6c.403T>A (p.Phe135Ile)
c.-144+5594A>T (n.-144+5594A>T)
14g.60509801T>CCA390087072C14orf39,SIX6c.403T>C (p.Phe135Leu)
c.-144+5594A>G (n.-144+5594A>G)
14g.60509801T>GCA390087070C14orf39,SIX6c.403T>G (p.Phe135Val)
c.-144+5594A>C (n.-144+5594A>C)
14g.60509802T>ACA390087076C14orf39,SIX6c.404T>A (p.Phe135Tyr)
c.-144+5593A>T (n.-144+5593A>T)
14g.60509802T>CCA390087077C14orf39,SIX6c.404T>C (p.Phe135Ser)
c.-144+5593A>G (n.-144+5593A>G)
14g.60509802T>GCA390087079C14orf39,SIX6c.404T>G (p.Phe135Cys)
c.-144+5593A>C (n.-144+5593A>C)
14g.60509803C>ACA390087081C14orf39,SIX6c.405C>A (p.Phe135Leu)
c.-144+5592G>T (n.-144+5592G>T)
14g.60509803C>GCA390087082C14orf39,SIX6c.405C>G (p.Phe135Leu)
c.-144+5592G>C (n.-144+5592G>C)
14g.60509803C>TCA486973690C14orf39,SIX6c.405C>T (p.Phe135=)
c.-144+5592G>A (n.-144+5592G>A)
gnomAD v4
14g.60509804A>CCA390087085C14orf39,SIX6c.406A>C (p.Lys136Gln)
c.-144+5591T>G (n.-144+5591T>G)
14g.60509804A>GCA390087086C14orf39,SIX6c.406A>G (p.Lys136Glu)
c.-144+5591T>C (n.-144+5591T>C)
14g.60509804A>TCA390087088C14orf39,SIX6c.406A>T (p.Lys136Ter)
c.-144+5591T>A (n.-144+5591T>A)
14g.60509805A>CCA390087090C14orf39,SIX6c.407A>C (p.Lys136Thr)
c.-144+5590T>G (n.-144+5590T>G)
ClinVar
14g.60509805A>GCA390087091C14orf39,SIX6c.407A>G (p.Lys136Arg)
c.-144+5590T>C (n.-144+5590T>C)

Number of alleles fetched