Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.149978306A>CCA447402567SLC26A2n.886A>C
c.654A>C (p.Ala218=)
c.327A>C (p.Ala109=)
5g.149978306A>GCA447402569SLC26A2n.886A>G
c.654A>G (p.Ala218=)
c.327A>G (p.Ala109=)
5g.149978306A>TCA447402570SLC26A2n.886A>T
c.654A>T (p.Ala218=)
c.327A>T (p.Ala109=)
5g.149978307A=CA1590737493SLC26A2n.887A=
c.655A= (p.Ile219=)
c.328A= (p.Ile110=)
5g.149978307A>CCA361705456SLC26A2n.887A>C
c.655A>C (p.Ile219Leu)
c.328A>C (p.Ile110Leu)
5g.149978307A>GCA3505288SLC26A2n.887A>G
c.655A>G (p.Ile219Val)
c.328A>G (p.Ile110Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.149978307A>TCA361705455SLC26A2n.887A>T
c.655A>T (p.Ile219Phe)
c.328A>T (p.Ile110Phe)
5g.149978308T>ACA361705457SLC26A2n.888T>A
c.656T>A (p.Ile219Asn)
c.329T>A (p.Ile110Asn)
5g.149978308T>CCA361705458SLC26A2n.888T>C
c.656T>C (p.Ile219Thr)
c.329T>C (p.Ile110Thr)
5g.149978308T>GCA361705459SLC26A2n.888T>G
c.656T>G (p.Ile219Ser)
c.329T>G (p.Ile110Ser)
5g.149978309T>ACA447402573SLC26A2n.889T>A
c.657T>A (p.Ile219=)
c.330T>A (p.Ile110=)
5g.149978309T>CCA447402575SLC26A2n.889T>C
c.657T>C (p.Ile219=)
c.330T>C (p.Ile110=)
 COSMIC
5g.149978309T>GCA361705460SLC26A2n.889T>G
c.657T>G (p.Ile219Met)
c.330T>G (p.Ile110Met)
5g.149978309_149978312dupCA2675943471SLC26A2n.889_892dup
c.657_660dup (p.Val221TyrfsTer?)
c.330_333dup (p.Val112TyrfsTer27)
 gnomAD v4
5g.149978310A=CA1590737494SLC26A2n.890A=
c.658A= (p.Met220=)
c.331A= (p.Met111=)
5g.149978310A>CCA361705461SLC26A2n.890A>C
c.658A>C (p.Met220Leu)
c.331A>C (p.Met111Leu)
5g.149978310A>GCA129082739SLC26A2n.890A>G
c.658A>G (p.Met220Val)
c.331A>G (p.Met111Val)
 dbSNP gnomAD v3 gnomAD v4
5g.149978310A>TCA361705462SLC26A2n.890A>T
c.658A>T (p.Met220Leu)
c.331A>T (p.Met111Leu)
5g.149978311T>ACA361705463SLC26A2n.891T>A
c.659T>A (p.Met220Lys)
c.332T>A (p.Met111Lys)
5g.149978311T>CCA361705464SLC26A2n.891T>C
c.659T>C (p.Met220Thr)
c.332T>C (p.Met111Thr)
5g.149978311T>GCA361705465SLC26A2n.891T>G
c.659T>G (p.Met220Arg)
c.332T>G (p.Met111Arg)
5g.149978312G>ACA361705468SLC26A2n.892G>A
c.660G>A (p.Met220Ile)
c.333G>A (p.Met111Ile)
5g.149978312G>CCA361705467SLC26A2n.892G>C
c.660G>C (p.Met220Ile)
c.333G>C (p.Met111Ile)
5g.149978312G>TCA361705466SLC26A2n.892G>T
c.660G>T (p.Met220Ile)
c.333G>T (p.Met111Ile)
5g.149978313G>ACA129082741SLC26A2n.893G>A
c.661G>A (p.Val221Ile)
c.334G>A (p.Val112Ile)
 dbSNP gnomAD v3 gnomAD v4
5g.149978313G>CCA361705469SLC26A2n.893G>C
c.661G>C (p.Val221Leu)
c.334G>C (p.Val112Leu)
5g.149978313G=CA1590737495SLC26A2n.893G=
c.661G= (p.Val221=)
c.334G= (p.Val112=)
5g.149978313G>TCA361705470SLC26A2n.893G>T
c.661G>T (p.Val221Phe)
c.334G>T (p.Val112Phe)
 dbSNP gnomAD v3 gnomAD v4
5g.149978314T>ACA361705471SLC26A2n.894T>A
c.662T>A (p.Val221Asp)
c.335T>A (p.Val112Asp)
5g.149978314T>CCA361705472SLC26A2n.894T>C
c.662T>C (p.Val221Ala)
c.335T>C (p.Val112Ala)
5g.149978314T>GCA361705473SLC26A2n.894T>G
c.662T>G (p.Val221Gly)
c.335T>G (p.Val112Gly)
5g.149978315T>ACA447402582SLC26A2n.895T>A
c.663T>A (p.Val221=)
c.336T>A (p.Val112=)
5g.149978315T>CCA447402584SLC26A2n.895T>C
c.663T>C (p.Val221=)
c.336T>C (p.Val112=)
5g.149978315T>GCA447402585SLC26A2n.895T>G
c.663T>G (p.Val221=)
c.336T>G (p.Val112=)
5g.149978316G>ACA361705474SLC26A2n.896G>A
c.664G>A (p.Gly222Ser)
c.337G>A (p.Gly113Ser)
5g.149978316G>CCA361705475SLC26A2n.896G>C
c.664G>C (p.Gly222Arg)
c.337G>C (p.Gly113Arg)
5g.149978316G>TCA361705476SLC26A2n.896G>T
c.664G>T (p.Gly222Cys)
c.337G>T (p.Gly113Cys)
5g.149978317G>ACA361705477SLC26A2n.897G>A
c.665G>A (p.Gly222Asp)
c.338G>A (p.Gly113Asp)
5g.149978317G>CCA361705478SLC26A2n.897G>C
c.665G>C (p.Gly222Ala)
c.338G>C (p.Gly113Ala)
5g.149978317G>TCA361705479SLC26A2n.897G>T
c.665G>T (p.Gly222Val)
c.338G>T (p.Gly113Val)
5g.149978318C>ACA447402588SLC26A2n.898C>A
c.666C>A (p.Gly222=)
c.339C>A (p.Gly113=)
5g.149978318C>GCA447402589SLC26A2n.898C>G
c.666C>G (p.Gly222=)
c.339C>G (p.Gly113=)
5g.149978318C>TCA447402590SLC26A2n.898C>T
c.666C>T (p.Gly222=)
c.339C>T (p.Gly113=)
5g.149978319A>CCA361705482SLC26A2n.899A>C
c.667A>C (p.Ser223Arg)
c.340A>C (p.Ser114Arg)
 COSMIC
5g.149978319A>GCA361705480SLC26A2n.899A>G
c.667A>G (p.Ser223Gly)
c.340A>G (p.Ser114Gly)
5g.149978319A>TCA361705481SLC26A2n.899A>T
c.667A>T (p.Ser223Cys)
c.340A>T (p.Ser114Cys)
5g.149978320G>ACA3505289SLC26A2n.900G>A
c.668G>A (p.Ser223Asn)
c.341G>A (p.Ser114Asn)
 dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
5g.149978320G>CCA361705483SLC26A2n.900G>C
c.668G>C (p.Ser223Thr)
c.341G>C (p.Ser114Thr)
5g.149978320G=CA1590737496SLC26A2n.900G=
c.668G= (p.Ser223=)
c.341G= (p.Ser114=)
5g.149978320G>TCA361705484SLC26A2n.900G>T
c.668G>T (p.Ser223Ile)
c.341G>T (p.Ser114Ile)
5g.149978321C>ACA361705485SLC26A2n.901C>A
c.669C>A (p.Ser223Arg)
c.342C>A (p.Ser114Arg)
5g.149978321C=CA1590737497SLC26A2n.901C=
c.669C= (p.Ser223=)
c.342C= (p.Ser114=)
5g.149978321C>GCA361705486SLC26A2n.901C>G
c.669C>G (p.Ser223Arg)
c.342C>G (p.Ser114Arg)
 dbSNP gnomAD v2 gnomAD v4
5g.149978321C>TCA447402595SLC26A2n.901C>T
c.669C>T (p.Ser223=)
c.342C>T (p.Ser114=)
5g.149978322A>CCA361705487SLC26A2n.902A>C
c.670A>C (p.Thr224Pro)
c.343A>C (p.Thr115Pro)
5g.149978322A>GCA361705488SLC26A2n.902A>G
c.670A>G (p.Thr224Ala)
c.343A>G (p.Thr115Ala)
5g.149978322A>TCA361705489SLC26A2n.902A>T
c.670A>T (p.Thr224Ser)
c.343A>T (p.Thr115Ser)
5g.149978323C>ACA361705490SLC26A2n.903C>A
c.671C>A (p.Thr224Asn)
c.344C>A (p.Thr115Asn)
5g.149978323C>GCA361705491SLC26A2n.903C>G
c.671C>G (p.Thr224Ser)
c.344C>G (p.Thr115Ser)
5g.149978323C>TCA361705492SLC26A2n.903C>T
c.671C>T (p.Thr224Ile)
c.344C>T (p.Thr115Ile)
5g.149978324T>ACA447402599SLC26A2n.904T>A
c.672T>A (p.Thr224=)
c.345T>A (p.Thr115=)
5g.149978324T>CCA447402600SLC26A2n.904T>C
c.672T>C (p.Thr224=)
c.345T>C (p.Thr115=)
 ClinVar dbSNP
5g.149978324T>GCA447402601SLC26A2n.904T>G
c.672T>G (p.Thr224=)
c.345T>G (p.Thr115=)
5g.149978324T=CA1590737498SLC26A2n.904T=
c.672T= (p.Thr224=)
c.345T= (p.Thr115=)
5g.149978325G>ACA361705494SLC26A2n.905G>A
c.673G>A (p.Val225Ile)
c.346G>A (p.Val116Ile)
 dbSNP
5g.149978325G>CCA361705495SLC26A2n.905G>C
c.673G>C (p.Val225Leu)
c.346G>C (p.Val116Leu)
5g.149978325G=CA1590737499SLC26A2n.905G=
c.673G= (p.Val225=)
c.346G= (p.Val116=)
5g.149978325G>TCA361705493SLC26A2n.905G>T
c.673G>T (p.Val225Leu)
c.346G>T (p.Val116Leu)
5g.149978326T>ACA361705498SLC26A2n.906T>A
c.674T>A (p.Val225Glu)
c.347T>A (p.Val116Glu)
5g.149978326T>CCA361705496SLC26A2n.906T>C
c.674T>C (p.Val225Ala)
c.347T>C (p.Val116Ala)
5g.149978326T>GCA361705497SLC26A2n.906T>G
c.674T>G (p.Val225Gly)
c.347T>G (p.Val116Gly)
5g.149978327A>CCA447402606SLC26A2n.907A>C
c.675A>C (p.Val225=)
c.348A>C (p.Val116=)
5g.149978327A>GCA447402607SLC26A2n.907A>G
c.675A>G (p.Val225=)
c.348A>G (p.Val116=)
5g.149978327A>TCA447402608SLC26A2n.907A>T
c.675A>T (p.Val225=)
c.348A>T (p.Val116=)
5g.149978328A>CCA361705499SLC26A2n.908A>C
c.676A>C (p.Thr226Pro)
c.349A>C (p.Thr117Pro)
5g.149978328A>GCA361705500SLC26A2n.908A>G
c.676A>G (p.Thr226Ala)
c.349A>G (p.Thr117Ala)
5g.149978328A>TCA361705501SLC26A2n.908A>T
c.676A>T (p.Thr226Ser)
c.349A>T (p.Thr117Ser)
5g.149978329C>ACA361705502SLC26A2n.909C>A
c.677C>A (p.Thr226Asn)
c.350C>A (p.Thr117Asn)
5g.149978329C>GCA361705503SLC26A2n.909C>G
c.677C>G (p.Thr226Ser)
c.350C>G (p.Thr117Ser)
5g.149978329C>TCA361705504SLC26A2n.909C>T
c.677C>T (p.Thr226Ile)
c.350C>T (p.Thr117Ile)
 gnomAD v4
5g.149978330C>ACA447402614SLC26A2n.910C>A
c.678C>A (p.Thr226=)
c.351C>A (p.Thr117=)
 ClinVar dbSNP
5g.149978330C=CA1590737500SLC26A2n.910C=
c.678C= (p.Thr226=)
c.351C= (p.Thr117=)
5g.149978330C>GCA129082758SLC26A2n.910C>G
c.678C>G (p.Thr226=)
c.351C>G (p.Thr117=)
 dbSNP gnomAD v4
5g.149978330C>TCA447402617SLC26A2n.910C>T
c.678C>T (p.Thr226=)
c.351C>T (p.Thr117=)
 gnomAD v4
5g.149978331T>ACA361705505SLC26A2n.911T>A
c.679T>A (p.Phe227Ile)
c.352T>A (p.Phe118Ile)
5g.149978331T>CCA361705506SLC26A2n.911T>C
c.679T>C (p.Phe227Leu)
c.352T>C (p.Phe118Leu)
5g.149978331T>GCA361705507SLC26A2n.911T>G
c.679T>G (p.Phe227Val)
c.352T>G (p.Phe118Val)
5g.149978332T>ACA361705510SLC26A2n.912T>A
c.680T>A (p.Phe227Tyr)
c.353T>A (p.Phe118Tyr)
5g.149978332T>CCA361705509SLC26A2n.912T>C
c.680T>C (p.Phe227Ser)
c.353T>C (p.Phe118Ser)
5g.149978332T>GCA361705508SLC26A2n.912T>G
c.680T>G (p.Phe227Cys)
c.353T>G (p.Phe118Cys)
5g.149978333_149978335dupCA2675943472SLC26A2n.913_915dup
c.681_683dup (p.Ile228_Ala229insIle)
c.354_356dup (p.Ile119_Ala120insIle)
 gnomAD v4
5g.149978333T>ACA361705511SLC26A2n.913T>A
c.681T>A (p.Phe227Leu)
c.354T>A (p.Phe118Leu)
5g.149978333T>CCA447402624SLC26A2n.913T>C
c.681T>C (p.Phe227=)
c.354T>C (p.Phe118=)
 gnomAD v4
5g.149978333T>GCA361705512SLC26A2n.913T>G
c.681T>G (p.Phe227Leu)
c.354T>G (p.Phe118Leu)
5g.149978334A>CCA361705513SLC26A2n.914A>C
c.682A>C (p.Ile228Leu)
c.355A>C (p.Ile119Leu)
5g.149978334A>GCA361705514SLC26A2n.914A>G
c.682A>G (p.Ile228Val)
c.355A>G (p.Ile119Val)
5g.149978334A>TCA361705515SLC26A2n.914A>T
c.682A>T (p.Ile228Leu)
c.355A>T (p.Ile119Leu)
5g.149978335T>ACA361705516SLC26A2n.915T>A
c.683T>A (p.Ile228Lys)
c.356T>A (p.Ile119Lys)
5g.149978335T>CCA361705517SLC26A2n.915T>C
c.683T>C (p.Ile228Thr)
c.356T>C (p.Ile119Thr)
5g.149978335T>GCA361705518SLC26A2n.915T>G
c.683T>G (p.Ile228Arg)
c.356T>G (p.Ile119Arg)
5g.149978336A>CCA447402626SLC26A2n.916A>C
c.684A>C (p.Ile228=)
c.357A>C (p.Ile119=)
5g.149978336A>GCA361705519SLC26A2n.916A>G
c.684A>G (p.Ile228Met)
c.357A>G (p.Ile119Met)
5g.149978336A>TCA447402628SLC26A2n.916A>T
c.684A>T (p.Ile228=)
c.357A>T (p.Ile119=)
5g.149978337G>ACA361705520SLC26A2n.917G>A
c.685G>A (p.Ala229Thr)
c.358G>A (p.Ala120Thr)
 COSMIC
5g.149978337G>CCA361705521SLC26A2n.917G>C
c.685G>C (p.Ala229Pro)
c.358G>C (p.Ala120Pro)
5g.149978337G>TCA361705522SLC26A2n.917G>T
c.685G>T (p.Ala229Ser)
c.358G>T (p.Ala120Ser)
5g.149978338C>ACA361705524SLC26A2n.918C>A
c.686C>A (p.Ala229Asp)
c.359C>A (p.Ala120Asp)
 gnomAD v4
5g.149978338C>GCA361705525SLC26A2n.918C>G
c.686C>G (p.Ala229Gly)
c.359C>G (p.Ala120Gly)
5g.149978338C>TCA361705523SLC26A2n.918C>T
c.686C>T (p.Ala229Val)
c.359C>T (p.Ala120Val)
5g.149978339T>ACA447402631SLC26A2n.919T>A
c.687T>A (p.Ala229=)
c.360T>A (p.Ala120=)
5g.149978339T>CCA447402632SLC26A2n.919T>C
c.687T>C (p.Ala229=)
c.360T>C (p.Ala120=)
5g.149978339T>GCA447402630SLC26A2n.919T>G
c.687T>G (p.Ala229=)
c.360T>G (p.Ala120=)
 ClinVar
5g.149978340G>ACA361705526SLC26A2n.920G>A
c.688G>A (p.Gly230Arg)
c.361G>A (p.Gly121Arg)
 gnomAD v4 COSMIC
5g.149978340G>CCA361705527SLC26A2n.920G>C
c.688G>C (p.Gly230Arg)
c.361G>C (p.Gly121Arg)
5g.149978340G>TCA361705528SLC26A2n.920G>T
c.688G>T (p.Gly230Ter)
c.361G>T (p.Gly121Ter)
5g.149978341G>ACA361705529SLC26A2n.921G>A
c.689G>A (p.Gly230Glu)
c.362G>A (p.Gly121Glu)
5g.149978341G>CCA361705530SLC26A2n.921G>C
c.689G>C (p.Gly230Ala)
c.362G>C (p.Gly121Ala)
5g.149978341G>TCA361705531SLC26A2n.921G>T
c.689G>T (p.Gly230Val)
c.362G>T (p.Gly121Val)
 gnomAD v4
5g.149978342A>CCA447402634SLC26A2n.922A>C
c.690A>C (p.Gly230=)
c.363A>C (p.Gly121=)
5g.149978342A>GCA447402636SLC26A2n.922A>G
c.690A>G (p.Gly230=)
c.363A>G (p.Gly121=)
5g.149978342A>TCA447402635SLC26A2n.922A>T
c.690A>T (p.Gly230=)
c.363A>T (p.Gly121=)
5g.149978343G>ACA3505290SLC26A2n.923G>A
c.691G>A (p.Val231Ile)
c.364G>A (p.Val122Ile)
 dbSNP ExAC gnomAD v2 gnomAD v4
5g.149978343G>CCA361705532SLC26A2n.923G>C
c.691G>C (p.Val231Leu)
c.364G>C (p.Val122Leu)
5g.149978343G=CA1590737502SLC26A2n.923G=
c.691G= (p.Val231=)
c.364G= (p.Val122=)
5g.149978343G>TCA361705533SLC26A2n.923G>T
c.691G>T (p.Val231Phe)
c.364G>T (p.Val122Phe)
5g.149978343_149978344delinsGTCA1590737501SLC26A2n.923_924delinsGT
c.691_692delinsGT (p.Val231=)
c.364_365delinsGT (p.Val122=)
5g.149978344T>ACA361705534SLC26A2n.924T>A
c.692T>A (p.Val231Asp)
c.365T>A (p.Val122Asp)
5g.149978344T>CCA361705535SLC26A2n.924T>C
c.692T>C (p.Val231Ala)
c.365T>C (p.Val122Ala)
5g.149978344T>GCA361705536SLC26A2n.924T>G
c.692T>G (p.Val231Gly)
c.365T>G (p.Val122Gly)
5g.149978346delCA3505291SLC26A2n.926del
c.694del (p.Tyr232IlefsTer3)
c.367del (p.Tyr123IlefsTer?)
 dbSNP ExAC gnomAD v2
5g.149978345T>ACA447402649SLC26A2n.925T>A
c.693T>A (p.Val231=)
c.366T>A (p.Val122=)
5g.149978345T>CCA447402646SLC26A2n.925T>C
c.693T>C (p.Val231=)
c.366T>C (p.Val122=)
5g.149978345T>GCA447402647SLC26A2n.925T>G
c.693T>G (p.Val231=)
c.366T>G (p.Val122=)
5g.149978346T>ACA361705537SLC26A2n.926T>A
c.694T>A (p.Tyr232Asn)
c.367T>A (p.Tyr123Asn)
5g.149978346T>CCA361705539SLC26A2n.926T>C
c.694T>C (p.Tyr232His)
c.367T>C (p.Tyr123His)
5g.149978346T>GCA361705538SLC26A2n.926T>G
c.694T>G (p.Tyr232Asp)
c.367T>G (p.Tyr123Asp)
 dbSNP gnomAD v4
5g.149978346T=CA1590737503SLC26A2n.926T=
c.694T= (p.Tyr232=)
c.367T= (p.Tyr123=)
5g.149978347A=CA1590737504SLC26A2n.927A=
c.695A= (p.Tyr232=)
c.368A= (p.Tyr123=)
5g.149978347A>CCA361705540SLC26A2n.927A>C
c.695A>C (p.Tyr232Ser)
c.368A>C (p.Tyr123Ser)
5g.149978347A>GCA361705541SLC26A2n.927A>G
c.695A>G (p.Tyr232Cys)
c.368A>G (p.Tyr123Cys)
 ClinVar dbSNP gnomAD v4
5g.149978347A>TCA3505292SLC26A2n.927A>T
c.695A>T (p.Tyr232Phe)
c.368A>T (p.Tyr123Phe)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.149978347dupCA2740094133SLC26A2n.927dup
c.695dup (p.Tyr232Ter)
c.368dup (p.Tyr123Ter)
 ClinVar
5g.149978348T>ACA361705542SLC26A2n.928T>A
c.696T>A (p.Tyr232Ter)
c.369T>A (p.Tyr123Ter)
5g.149978348T>CCA129082765SLC26A2n.928T>C
c.696T>C (p.Tyr232=)
c.369T>C (p.Tyr123=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
5g.149978348T>GCA361705543SLC26A2n.928T>G
c.696T>G (p.Tyr232Ter)
c.369T>G (p.Tyr123Ter)
5g.149978348T=CA1590737505SLC26A2n.928T=
c.696T= (p.Tyr232=)
c.369T= (p.Tyr123=)
5g.149978349C>ACA361705544SLC26A2n.929C>A
c.697C>A (p.Gln233Lys)
c.370C>A (p.Gln124Lys)
5g.149978349C=CA1590737506SLC26A2n.929C=
c.697C= (p.Gln233=)
c.370C= (p.Gln124=)
5g.149978349C>GCA361705545SLC26A2n.929C>G
c.697C>G (p.Gln233Glu)
c.370C>G (p.Gln124Glu)
 gnomAD v4
5g.149978349C>TCA361705546SLC26A2n.929C>T
c.697C>T (p.Gln233Ter)
c.370C>T (p.Gln124Ter)
 ClinVar dbSNP gnomAD v2 gnomAD v4
5g.149978350A>CCA361705547SLC26A2n.930A>C
c.698A>C (p.Gln233Pro)
c.371A>C (p.Gln124Pro)
5g.149978350A>GCA361705548SLC26A2n.930A>G
c.698A>G (p.Gln233Arg)
c.371A>G (p.Gln124Arg)
 gnomAD v4 COSMIC
5g.149978350A>TCA361705549SLC26A2n.930A>T
c.698A>T (p.Gln233Leu)
c.371A>T (p.Gln124Leu)
5g.149978351G>ACA447402662SLC26A2n.931G>A
c.699G>A (p.Gln233=)
c.372G>A (p.Gln124=)
5g.149978351G>CCA361705550SLC26A2n.931G>C
c.699G>C (p.Gln233His)
c.372G>C (p.Gln124His)
 dbSNP
5g.149978351G=CA1590737507SLC26A2n.931G=
c.699G= (p.Gln233=)
c.372G= (p.Gln124=)
5g.149978351G>TCA361705551SLC26A2n.931G>T
c.699G>T (p.Gln233His)
c.372G>T (p.Gln124His)
5g.149978352G>ACA361705553SLC26A2n.932G>A
c.699+1G>A (n.699+1G>A)
c.372+1G>A (n.372+1G>A)
5g.149978352G>CCA361705554SLC26A2n.932G>C
c.699+1G>C (n.699+1G>C)
c.372+1G>C (n.372+1G>C)
5g.149978352G>TCA361705552SLC26A2n.932G>T
c.699+1G>T (n.699+1G>T)
c.372+1G>T (n.372+1G>T)
 gnomAD v4
5g.149978353T>ACA361705555SLC26A2n.933T>A
c.699+2T>A (n.699+2T>A)
c.372+2T>A (n.372+2T>A)
5g.149978353T>CCA16040989SLC26A2n.933T>C
c.699+2T>C (n.699+2T>C)
c.372+2T>C (n.372+2T>C)
 ClinVar dbSNP
5g.149978353T>GCA361705556SLC26A2n.933T>G
c.699+2T>G (n.699+2T>G)
c.372+2T>G (n.372+2T>G)
5g.149978353T=CA1590737508SLC26A2n.933T=
c.699+2T= (n.699+2T=)
c.372+2T= (n.372+2T=)
5g.149978354A=CA1590737509SLC26A2n.934A=
c.699+3A= (n.699+3A=)
c.372+3A= (n.372+3A=)
5g.149978354A>CCA3505293SLC26A2n.934A>C
c.699+3A>C (n.699+3A>C)
c.372+3A>C (n.372+3A>C)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
5g.149978354A>TCA2675943473SLC26A2n.934A>T
c.699+3A>T (n.699+3A>T)
c.372+3A>T (n.372+3A>T)
 gnomAD v4
5g.149978356G>TCA2675943474SLC26A2n.936G>T
c.699+5G>T (n.699+5G>T)
c.372+5G>T (n.372+5G>T)
 gnomAD v4
5g.149978357C>TCA2675943475SLC26A2n.937C>T
c.699+6C>T (n.699+6C>T)
c.372+6C>T (n.372+6C>T)
 gnomAD v4
5g.149978359G>ACA3505294SLC26A2n.939G>A
c.699+8G>A (n.699+8G>A)
c.372+8G>A (n.372+8G>A)
 dbSNP ExAC gnomAD v2 gnomAD v4
5g.149978359G=CA1590737510SLC26A2n.939G=
c.699+8G= (n.699+8G=)
c.372+8G= (n.372+8G=)
5g.149978359G>TCA2675943476SLC26A2n.939G>T
c.699+8G>T (n.699+8G>T)
c.372+8G>T (n.372+8G>T)
 gnomAD v4
5g.149978360C>ACA563955681SLC26A2n.940C>A
c.699+9C>A (n.699+9C>A)
c.372+9C>A (n.372+9C>A)
 dbSNP gnomAD v2 gnomAD v4
5g.149978360C=CA1590737511SLC26A2n.940C=
c.699+9C= (n.699+9C=)
c.372+9C= (n.372+9C=)
5g.149978361A>CCA2675943477SLC26A2n.941A>C
c.699+10A>C (n.699+10A>C)
c.372+10A>C (n.372+10A>C)
 gnomAD v4
5g.149978364_149978393dupCA3505295SLC26A2n.944_973dup
c.699+13_699+42dup (n.699+13_699+42dup)
c.372+13_372+42dup (n.372+13_372+42dup)
 dbSNP ExAC gnomAD v2 gnomAD v4
5g.149978362A=CA1590737512SLC26A2n.942A=
c.699+11A= (n.699+11A=)
c.372+11A= (n.372+11A=)
5g.149978362A>GCA3505296SLC26A2n.942A>G
c.699+11A>G (n.699+11A>G)
c.372+11A>G (n.372+11A>G)
 dbSNP ExAC gnomAD v2 gnomAD v4
5g.149978364G>ACA2675943478SLC26A2n.944G>A
c.699+13G>A (n.699+13G>A)
c.372+13G>A (n.372+13G>A)
 gnomAD v4
5g.149978364G=CA1590737513SLC26A2n.944G=
c.699+13G= (n.699+13G=)
c.372+13G= (n.372+13G=)
5g.149978364G>TCA10623448SLC26A2n.944G>T
c.699+13G>T (n.699+13G>T)
c.372+13G>T (n.372+13G>T)
 ClinVar dbSNP gnomAD v4
5g.149978365A>GCA2675943479SLC26A2n.945A>G
c.699+14A>G (n.699+14A>G)
c.372+14A>G (n.372+14A>G)
 gnomAD v4
5g.149978366A=CA1590737514SLC26A2n.946A=
c.699+15A= (n.699+15A=)
c.372+15A= (n.372+15A=)
5g.149978366A>GCA1590737515SLC26A2n.946A>G
c.699+15A>G (n.699+15A>G)
c.372+15A>G (n.372+15A>G)
 ClinVar dbSNP gnomAD v3 gnomAD v4
5g.149978368C>ACA2675943480SLC26A2n.948C>A
c.699+17C>A (n.699+17C>A)
c.372+17C>A (n.372+17C>A)
 gnomAD v4
5g.149978368C>TCA2578449456SLC26A2n.948C>T
c.699+17C>T (n.699+17C>T)
c.372+17C>T (n.372+17C>T)
 ClinVar
5g.149978369A>GCA2675943481SLC26A2n.949A>G
c.699+18A>G (n.699+18A>G)
c.372+18A>G (n.372+18A>G)
 gnomAD v4
5g.149978370A=CA1590737516SLC26A2n.950A=
c.699+19A= (n.699+19A=)
c.372+19A= (n.372+19A=)
5g.149978370A>GCA1590737517SLC26A2n.950A>G
c.699+19A>G (n.699+19A>G)
c.372+19A>G (n.372+19A>G)
 dbSNP
5g.149978371T>CCA3505297SLC26A2n.951T>C
c.699+20T>C (n.699+20T>C)
c.372+20T>C (n.372+20T>C)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.149978371T=CA1590737518SLC26A2n.951T=
c.699+20T= (n.699+20T=)
c.372+20T= (n.372+20T=)
5g.149978371_149978376delCA2675943482SLC26A2n.951_956del
c.699+20_699+25del (n.699+20_699+25del)
c.372+20_372+25del (n.372+20_372+25del)
 gnomAD v4
5g.149978372T>ACA1590737520SLC26A2n.952T>A
c.699+21T>A (n.699+21T>A)
c.372+21T>A (n.372+21T>A)
 dbSNP
5g.149978372T=CA1590737519SLC26A2n.952T=
c.699+21T= (n.699+21T=)
c.372+21T= (n.372+21T=)
5g.149978373G>CCA1082857729SLC26A2n.953G>C
c.699+22G>C (n.699+22G>C)
c.372+22G>C (n.372+22G>C)
 dbSNP gnomAD v3 gnomAD v4
5g.149978373G=CA1590737521SLC26A2n.953G=
c.699+22G= (n.699+22G=)
c.372+22G= (n.372+22G=)
5g.149978373G>TCA2675943483SLC26A2n.953G>T
c.699+22G>T (n.699+22G>T)
c.372+22G>T (n.372+22G>T)
 gnomAD v4
5g.149978374G>ACA2675943484SLC26A2n.954G>A
c.699+23G>A (n.699+23G>A)
c.372+23G>A (n.372+23G>A)
 gnomAD v4
5g.149978374G>TCA2675943485SLC26A2n.954G>T
c.699+23G>T (n.699+23G>T)
c.372+23G>T (n.372+23G>T)
 gnomAD v4
5g.149978375T>ACA563955682SLC26A2n.955T>A
c.699+24T>A (n.699+24T>A)
c.372+24T>A (n.372+24T>A)
 dbSNP gnomAD v2 gnomAD v4
5g.149978375T>CCA129082793SLC26A2n.955T>C
c.699+24T>C (n.699+24T>C)
c.372+24T>C (n.372+24T>C)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
5g.149978375T=CA1590737522SLC26A2n.955T=
c.699+24T= (n.699+24T=)
c.372+24T= (n.372+24T=)
5g.149978377A=CA1590737523SLC26A2n.957A=
c.699+26A= (n.699+26A=)
c.372+26A= (n.372+26A=)
5g.149978377A>GCA563955683SLC26A2n.957A>G
c.699+26A>G (n.699+26A>G)
c.372+26A>G (n.372+26A>G)
 dbSNP gnomAD v2 gnomAD v4
5g.149978379_149978382delCA2675943486SLC26A2n.959_962del
c.699+28_699+31del (n.699+28_699+31del)
c.372+28_372+31del (n.372+28_372+31del)
 gnomAD v4
5g.149978381C>ACA2675943487SLC26A2n.961C>A
c.699+30C>A (n.699+30C>A)
c.372+30C>A (n.372+30C>A)
 gnomAD v4
5g.149978382T>ACA2578449457SLC26A2n.962T>A
c.699+31T>A (n.699+31T>A)
c.372+31T>A (n.372+31T>A)
5g.149978382T>CCA3505298SLC26A2n.962T>C
c.699+31T>C (n.699+31T>C)
c.372+31T>C (n.372+31T>C)
 dbSNP ExAC gnomAD v2 gnomAD v4
5g.149978382T=CA1590737524SLC26A2n.962T=
c.699+31T= (n.699+31T=)
c.372+31T= (n.372+31T=)
5g.149978383A>GCA2675943488SLC26A2n.963A>G
c.699+32A>G (n.699+32A>G)
c.372+32A>G (n.372+32A>G)
 gnomAD v4
5g.149978384G>ACA2675943489SLC26A2n.964G>A
c.699+33G>A (n.699+33G>A)
c.372+33G>A (n.372+33G>A)
 gnomAD v4
5g.149978385A>CCA2740693912SLC26A2n.965A>C
c.699+34A>C (n.699+34A>C)
c.372+34A>C (n.372+34A>C)
5g.149978386A=CA1590737525SLC26A2n.966A=
c.699+35A= (n.699+35A=)
c.372+35A= (n.372+35A=)
5g.149978386A>GCA3505299SLC26A2n.966A>G
c.699+35A>G (n.699+35A>G)
c.372+35A>G (n.372+35A>G)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.149978387A>TCA2578449458SLC26A2n.967A>T
c.699+36A>T (n.699+36A>T)
c.372+36A>T (n.372+36A>T)
5g.149978389_149978392delCA2675943490SLC26A2n.969_972del
c.699+38_699+41del (n.699+38_699+41del)
c.372+38_372+41del (n.372+38_372+41del)
 gnomAD v4
5g.149978390T>ACA2675943491SLC26A2n.970T>A
c.699+39T>A (n.699+39T>A)
c.372+39T>A (n.372+39T>A)
 gnomAD v4
5g.149978392A=CA1590737526SLC26A2n.972A=
c.699+41A= (n.699+41A=)
c.372+41A= (n.372+41A=)
5g.149978392A>CCA563955684SLC26A2n.972A>C
c.699+41A>C (n.699+41A>C)
c.372+41A>C (n.372+41A>C)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
5g.149978393T>ACA2578449459SLC26A2n.973T>A
c.699+42T>A (n.699+42T>A)
c.372+42T>A (n.372+42T>A)
5g.149978393T>CCA1590737528SLC26A2n.973T>C
c.699+42T>C (n.699+42T>C)
c.372+42T>C (n.372+42T>C)
 dbSNP
5g.149978393T=CA1590737527SLC26A2n.973T=
c.699+42T= (n.699+42T=)
c.372+42T= (n.372+42T=)
5g.149978394C>ACA2578449460SLC26A2n.974C>A
c.699+43C>A (n.699+43C>A)
c.372+43C>A (n.372+43C>A)
 gnomAD v4
5g.149978394C=CA1590737529SLC26A2n.974C=
c.699+43C= (n.699+43C=)
c.372+43C= (n.372+43C=)
5g.149978394C>GCA3505301SLC26A2n.974C>G
c.699+43C>G (n.699+43C>G)
c.372+43C>G (n.372+43C>G)
 dbSNP ExAC gnomAD v2 gnomAD v4
5g.149978394C>TCA3505300SLC26A2n.974C>T
c.699+43C>T (n.699+43C>T)
c.372+43C>T (n.372+43C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.149978396A=CA1590737530SLC26A2n.976A=
c.699+45A= (n.699+45A=)
c.372+45A= (n.372+45A=)
5g.149978396A>GCA1590737531SLC26A2n.976A>G
c.699+45A>G (n.699+45A>G)
c.372+45A>G (n.372+45A>G)
 dbSNP gnomAD v4
5g.149978397G>ACA2578449461SLC26A2n.977G>A
c.699+46G>A (n.699+46G>A)
c.372+46G>A (n.372+46G>A)
5g.149978397G>CCA1082857737SLC26A2n.977G>C
c.699+46G>C (n.699+46G>C)
c.372+46G>C (n.372+46G>C)
 dbSNP gnomAD v3 gnomAD v4
5g.149978397G=CA1590737532SLC26A2n.977G=
c.699+46G= (n.699+46G=)
c.372+46G= (n.372+46G=)
5g.149978398T>ACA2675943492SLC26A2n.978T>A
c.699+47T>A (n.699+47T>A)
c.372+47T>A (n.372+47T>A)
 gnomAD v4
5g.149978400C>ACA2675943493SLC26A2n.980C>A
c.699+49C>A (n.699+49C>A)
c.372+49C>A (n.372+49C>A)
 gnomAD v4
5g.149978400C>TCA2740693913SLC26A2n.980C>T
c.699+49C>T (n.699+49C>T)
c.372+49C>T (n.372+49C>T)
5g.149978401A=CA1590737533SLC26A2n.981A=
c.699+50A= (n.699+50A=)
c.372+50A= (n.372+50A=)
5g.149978401A>GCA3505302SLC26A2n.981A>G
c.699+50A>G (n.699+50A>G)
c.372+50A>G (n.372+50A>G)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.149978402T>ACA2675943494SLC26A2n.982T>A
c.699+51T>A (n.699+51T>A)
c.372+51T>A (n.372+51T>A)
 gnomAD v4
5g.149978402T>CCA2675943495SLC26A2n.982T>C
c.699+51T>C (n.699+51T>C)
c.372+51T>C (n.372+51T>C)
 gnomAD v4
5g.149978403G>ACA2768879997SLC26A2n.983G>A
c.699+52G>A (n.699+52G>A)
c.372+52G>A (n.372+52G>A)
5g.149978403G>TCA2675943496SLC26A2n.983G>T
c.699+52G>T (n.699+52G>T)
c.372+52G>T (n.372+52G>T)
 gnomAD v4
5g.149978404A>CCA2546515385SLC26A2n.984A>C
c.699+53A>C (n.699+53A>C)
c.372+53A>C (n.372+53A>C)
 gnomAD v4
5g.149978404A>GCA2675943497SLC26A2n.984A>G
c.699+53A>G (n.699+53A>G)
c.372+53A>G (n.372+53A>G)
 gnomAD v4
5g.149978404A>TCA2675943498SLC26A2n.984A>T
c.699+53A>T (n.699+53A>T)
c.372+53A>T (n.372+53A>T)
 gnomAD v4
5g.149978406A>GCA2578449462SLC26A2n.986A>G
c.699+55A>G (n.699+55A>G)
c.372+55A>G (n.372+55A>G)

Number of alleles fetched