Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.69035907T>ACA373527656FXNc.125T>A (p.Leu42Gln)
c.123T>A
gnomAD v4
9g.69035907T>CCA373527657FXNc.125T>C (p.Leu42Pro)
c.123T>C
gnomAD v4
9g.69035907T>GCA193369082FXNc.125T>G (p.Leu42Arg)
c.123T>G
ClinVar dbSNP gnomAD v4
9g.69035907T=CA1854034991FXNc.125T= (p.Leu42=)
c.123T=
9g.69035908G>ACA465233196FXNc.126G>A (p.Leu42=)
c.124G>A
gnomAD v4
9g.69035908G>CCA465233195FXNc.126G>C (p.Leu42=)
c.124G>C
9g.69035908G>TCA465233194FXNc.126G>T (p.Leu42=)
c.124G>T
gnomAD v4
9g.69035909C>ACA373527669FXNc.127C>A (p.Arg43Ser)
c.125C>A
gnomAD v4
9g.69035909C=CA1854034992FXNc.127C= (p.Arg43=)
c.125C=
9g.69035909C>GCA373527666FXNc.127C>G (p.Arg43Gly)
c.125C>G
9g.69035909C>TCA373527661FXNc.127C>T (p.Arg43Cys)
c.125C>T
dbSNP gnomAD v2 gnomAD v4
9g.69035912_69035936dupCA2690187681FXNc.130_154dup (p.Pro52HisfsTer?)
c.130_154dup (p.Pro52HisfsTer14)
c.128_152dup
c.130_154dup (p.Pro52HisfsTer15)
gnomAD v4
9g.69035910G>ACA5072644FXNc.128G>A (p.Arg43His)
c.126G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.69035910G>CCA373527674FXNc.128G>C (p.Arg43Pro)
c.126G>C
ClinVar dbSNP gnomAD v3 gnomAD v4
9g.69035910G=CA1854034993FXNc.128G= (p.Arg43=)
c.126G=
9g.69035910G>TCA373527676FXNc.128G>T (p.Arg43Leu)
c.126G>T
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.69035911C>ACA465233199FXNc.129C>A (p.Arg43=)
c.127C>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.69035911C=CA1854034994FXNc.129C= (p.Arg43=)
c.127C=
9g.69035911C>GCA465233198FXNc.129C>G (p.Arg43=)
c.127C>G
gnomAD v4
9g.69035911C>TCA465233197FXNc.129C>T (p.Arg43=)
c.127C>T
9g.69035912A=CA1854034995FXNc.130A= (p.Thr44=)
c.128A=
9g.69035912A>CCA373527679FXNc.130A>C (p.Thr44Pro)
c.128A>C
dbSNP gnomAD v2 gnomAD v4
9g.69035912A>GCA373527682FXNc.130A>G (p.Thr44Ala)
c.128A>G
9g.69035912A>TCA373527683FXNc.130A>T (p.Thr44Ser)
c.128A>T
gnomAD v4
9g.69035913C>ACA193369109FXNc.131C>A (p.Thr44Asn)
c.129C>A
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.69035913C=CA1854034996FXNc.131C= (p.Thr44=)
c.129C=
9g.69035913C>GCA373527689FXNc.131C>G (p.Thr44Ser)
c.129C>G
gnomAD v4
9g.69035913C>TCA373527687FXNc.131C>T (p.Thr44Ile)
c.129C>T
dbSNP
9g.69035914C>ACA465233201FXNc.132C>A (p.Thr44=)
c.130C>A
dbSNP gnomAD v4
9g.69035914C=CA1854034997FXNc.132C= (p.Thr44=)
c.130C=
9g.69035914C>GCA465233200FXNc.132C>G (p.Thr44=)
c.130C>G
gnomAD v4
9g.69035914C>TCA465233202FXNc.132C>T (p.Thr44=)
c.130C>T
dbSNP gnomAD v4
9g.69035918_69035928dupCA16622137FXNc.136_146dup (p.Cys50SerfsTer30)
c.136_146dup (p.Cys50SerfsTer21)
c.134_144dup
c.136_146dup (p.Cys50SerfsTer?)
9g.69035915G>ACA5072645FXNc.133G>A (p.Asp45Asn)
c.131G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.69035915G>CCA373527692FXNc.133G>C (p.Asp45His)
c.131G>C
dbSNP gnomAD v3 gnomAD v4
9g.69035915G=CA1854034998FXNc.133G= (p.Asp45=)
c.131G=
9g.69035915G>TCA373527694FXNc.133G>T (p.Asp45Tyr)
c.131G>T
gnomAD v4
9g.69035916A>CCA373527696FXNc.134A>C (p.Asp45Ala)
c.132A>C
9g.69035916A>GCA373527697FXNc.134A>G (p.Asp45Gly)
c.132A>G
dbSNP gnomAD v4
9g.69035916A>TCA373527699FXNc.134A>T (p.Asp45Val)
c.132A>T
9g.69035917C>ACA373527701FXNc.135C>A (p.Asp45Glu)
c.133C>A
gnomAD v4
9g.69035917C>GCA373527703FXNc.135C>G (p.Asp45Glu)
c.133C>G
9g.69035917C>TCA465233203FXNc.135C>T (p.Asp45=)
c.133C>T
gnomAD v4
9g.69035918A=CA1854034999FXNc.136A= (p.Ile46=)
c.134A=
9g.69035918A>CCA373527705FXNc.136A>C (p.Ile46Leu)
c.134A>C
9g.69035918A>GCA373527707FXNc.136A>G (p.Ile46Val)
c.134A>G
dbSNP gnomAD v3 gnomAD v4
9g.69035918A>TCA373527709FXNc.136A>T (p.Ile46Phe)
c.134A>T
gnomAD v4
9g.69035919T>ACA373527711FXNc.137T>A (p.Ile46Asn)
c.135T>A
dbSNP
9g.69035919T>CCA373527715FXNc.137T>C (p.Ile46Thr)
c.135T>C
dbSNP
9g.69035919T>GCA373527712FXNc.137T>G (p.Ile46Ser)
c.135T>G
dbSNP gnomAD v4

Number of alleles fetched