Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.63785042C>ACA657704480ARHGEF9c.30+74G>T (p.=)
n.99+74G>T
c.-118+10474G>T (p.=)
c.-132+74G>T (p.=)
c.-195+74G>T (p.=)
COSMIC
Xg.63785043G>ACA877128946ARHGEF9c.30+73C>T (p.=)
n.99+73C>T
c.-118+10473C>T (p.=)
c.-132+73C>T (p.=)
c.-195+73C>T (p.=)
Xg.63785043G>CCA330346012ARHGEF9c.30+73C>G (p.=)
n.99+73C>G
c.-118+10473C>G (p.=)
c.-132+73C>G (p.=)
c.-195+73C>G (p.=)
dbSNP
Xg.63785044T>CCA642213079ARHGEF9c.30+72A>G (p.=)
n.99+72A>G
c.-118+10472A>G (p.=)
c.-132+72A>G (p.=)
c.-195+72A>G (p.=)
gnomAD
Xg.63785071delCA642213080ARHGEF9c.30+49del (p.=)
n.99+49del
c.-118+10449del (p.=)
c.-132+49del (p.=)
c.-195+49del (p.=)
dbSNP gnomAD
Xg.63785070G>ACA642213081ARHGEF9c.30+46C>T (p.=)
n.99+46C>T
c.-118+10446C>T (p.=)
c.-132+46C>T (p.=)
c.-195+46C>T (p.=)
gnomAD
Xg.63785071G>ACA10432024ARHGEF9c.30+45C>T (p.=)
n.99+45C>T
c.-118+10445C>T (p.=)
c.-132+45C>T (p.=)
c.-195+45C>T (p.=)
dbSNP ExAC gnomAD
Xg.63785072A>GCA642213082ARHGEF9c.30+44T>C (p.=)
n.99+44T>C
c.-118+10444T>C (p.=)
c.-132+44T>C (p.=)
c.-195+44T>C (p.=)
gnomAD
Xg.63785073C>ACA330346013ARHGEF9c.30+43G>T (p.=)
n.99+43G>T
c.-118+10443G>T (p.=)
c.-132+43G>T (p.=)
c.-195+43G>T (p.=)
dbSNP
Xg.63785073C>TCA642213083ARHGEF9c.30+43G>A (p.=)
n.99+43G>A
c.-118+10443G>A (p.=)
c.-132+43G>A (p.=)
c.-195+43G>A (p.=)
gnomAD
Xg.63785079G>ACA1133627547ARHGEF9c.30+37C>T (p.=)
n.99+37C>T
c.-118+10437C>T (p.=)
c.-132+37C>T (p.=)
c.-195+37C>T (p.=)
Xg.63785092G>ACA642213084ARHGEF9c.30+24C>T (p.=)
n.99+24C>T
c.-118+10424C>T (p.=)
c.-132+24C>T (p.=)
c.-195+24C>T (p.=)
gnomAD
Xg.63785096C>TCA642213085ARHGEF9c.30+20G>A (p.=)
n.99+20G>A
c.-118+10420G>A (p.=)
c.-132+20G>A (p.=)
c.-195+20G>A (p.=)
gnomAD
Xg.63785101G>ACA877128976ARHGEF9c.30+15C>T (p.=)
n.99+15C>T
c.-118+10415C>T (p.=)
c.-132+15C>T (p.=)
c.-195+15C>T (p.=)
Xg.63785106A>GCA642213086ARHGEF9c.30+10T>C (p.=)
n.99+10T>C
c.-118+10410T>C (p.=)
c.-132+10T>C (p.=)
c.-195+10T>C (p.=)
gnomAD
Xg.63785109C>ACA877128979ARHGEF9c.30+7G>T (p.=)
n.99+7G>T
c.-118+10407G>T (p.=)
c.-132+7G>T (p.=)
c.-195+7G>T (p.=)
Xg.63785114A>CCA413405816ARHGEF9c.30+2T>G (p.=)
n.99+2T>G
c.-118+10402T>G (p.=)
c.-132+2T>G (p.=)
c.-195+2T>G (p.=)
Xg.63785114A>GCA413405818ARHGEF9c.30+2T>C (p.=)
n.99+2T>C
c.-118+10402T>C (p.=)
c.-132+2T>C (p.=)
c.-195+2T>C (p.=)
Xg.63785114A>TCA413405817ARHGEF9c.30+2T>A (p.=)
n.99+2T>A
c.-118+10402T>A (p.=)
c.-132+2T>A (p.=)
c.-195+2T>A (p.=)
Xg.63785115C>ACA413405819ARHGEF9c.30+1G>T (p.=)
n.99+1G>T
c.-118+10401G>T (p.=)
c.-132+1G>T (p.=)
c.-195+1G>T (p.=)
Xg.63785115C>GCA413405820ARHGEF9c.30+1G>C (p.=)
n.99+1G>C
c.-118+10401G>C (p.=)
c.-132+1G>C (p.=)
c.-195+1G>C (p.=)
Xg.63785115C>TCA413405821ARHGEF9c.30+1G>A (p.=)
n.99+1G>A
c.-118+10401G>A (p.=)
c.-132+1G>A (p.=)
c.-195+1G>A (p.=)
Xg.63785116C>ACA413405822ARHGEF9c.30G>T (p.Met10Ile)
n.99G>T
c.-118+10400G>T (p.=)
c.-132G>T (p.=)
c.-195G>T (p.=)
Xg.63785116C>GCA413405823ARHGEF9c.30G>C (p.Met10Ile)
n.99G>C
c.-118+10400G>C (p.=)
c.-132G>C (p.=)
c.-195G>C (p.=)
Xg.63785116C>TCA413405824ARHGEF9c.30G>A (p.Met10Ile)
n.99G>A
c.-118+10400G>A (p.=)
c.-132G>A (p.=)
c.-195G>A (p.=)
Xg.63785117A>CCA413405825ARHGEF9c.29T>G (p.Met10Arg)
n.98T>G
c.-118+10399T>G (p.=)
c.-133T>G (p.=)
c.-196T>G (p.=)
Xg.63785117A>GCA413405826ARHGEF9c.29T>C (p.Met10Thr)
n.98T>C
c.-118+10399T>C (p.=)
c.-133T>C (p.=)
c.-196T>C (p.=)
ClinVar gnomAD
Xg.63785117A>TCA413405827ARHGEF9c.29T>A (p.Met10Lys)
n.98T>A
c.-118+10399T>A (p.=)
c.-133T>A (p.=)
c.-196T>A (p.=)
Xg.63785118T>ACA413405828ARHGEF9c.28A>T (p.Met10Leu)
n.97A>T
c.-118+10398A>T (p.=)
c.-134A>T (p.=)
c.-197A>T (p.=)
Xg.63785118T>CCA413405829ARHGEF9c.28A>G (p.Met10Val)
n.97A>G
c.-118+10398A>G (p.=)
c.-134A>G (p.=)
c.-197A>G (p.=)
Xg.63785118T>GCA413405830ARHGEF9c.28A>C (p.Met10Leu)
n.97A>C
c.-118+10398A>C (p.=)
c.-134A>C (p.=)
c.-197A>C (p.=)
Xg.63785119T>ACA516873536ARHGEF9c.27A>T (p.Gly9=)
n.96A>T
c.-118+10397A>T (p.=)
c.-135A>T (p.=)
c.-198A>T (p.=)
Xg.63785119T>CCA516873535ARHGEF9c.27A>G (p.Gly9=)
n.96A>G
c.-118+10397A>G (p.=)
c.-135A>G (p.=)
c.-198A>G (p.=)
Xg.63785119T>GCA516873539ARHGEF9c.27A>C (p.Gly9=)
n.96A>C
c.-118+10397A>C (p.=)
c.-135A>C (p.=)
c.-198A>C (p.=)
Xg.63785120C>ACA413405831ARHGEF9c.26G>T (p.Gly9Val)
n.95G>T
c.-118+10396G>T (p.=)
c.-136G>T (p.=)
c.-199G>T (p.=)
Xg.63785120C>GCA413405833ARHGEF9c.26G>C (p.Gly9Ala)
n.95G>C
c.-118+10396G>C (p.=)
c.-136G>C (p.=)
c.-199G>C (p.=)
Xg.63785120C>TCA413405832ARHGEF9c.26G>A (p.Gly9Glu)
n.95G>A
c.-118+10396G>A (p.=)
c.-136G>A (p.=)
c.-199G>A (p.=)
COSMIC
Xg.63785121C>ACA413405834ARHGEF9c.25G>T (p.Gly9Ter)
n.94G>T
c.-118+10395G>T (p.=)
c.-137G>T (p.=)
c.-200G>T (p.=)
Xg.63785121C>GCA413405835ARHGEF9c.25G>C (p.Gly9Arg)
n.94G>C
c.-118+10395G>C (p.=)
c.-137G>C (p.=)
c.-200G>C (p.=)
Xg.63785121C>TCA413405836ARHGEF9c.25G>A (p.Gly9Arg)
n.94G>A
c.-118+10395G>A (p.=)
c.-137G>A (p.=)
c.-200G>A (p.=)
Xg.63785122C>ACA516873556ARHGEF9c.24G>T (p.Ser8=)
n.93G>T
c.-118+10394G>T (p.=)
c.-138G>T (p.=)
c.-201G>T (p.=)
Xg.63785122C>GCA516873559ARHGEF9c.24G>C (p.Ser8=)
n.93G>C
c.-118+10394G>C (p.=)
c.-138G>C (p.=)
c.-201G>C (p.=)
Xg.63785122C>TCA516873561ARHGEF9c.24G>A (p.Ser8=)
n.93G>A
c.-118+10394G>A (p.=)
c.-138G>A (p.=)
c.-201G>A (p.=)
ClinVar gnomAD
Xg.63785123G>ACA413405837ARHGEF9c.23C>T (p.Ser8Leu)
n.92C>T
c.-118+10393C>T (p.=)
c.-139C>T (p.=)
c.-202C>T (p.=)
Xg.63785123G>CCA413405838ARHGEF9c.23C>G (p.Ser8Trp)
n.92C>G
c.-118+10393C>G (p.=)
c.-139C>G (p.=)
c.-202C>G (p.=)
Xg.63785123G>TCA413405839ARHGEF9c.23C>A (p.Ser8Ter)
n.92C>A
c.-118+10393C>A (p.=)
c.-139C>A (p.=)
c.-202C>A (p.=)
Xg.63785124A>CCA413405840ARHGEF9c.22T>G (p.Ser8Ala)
n.91T>G
c.-118+10392T>G (p.=)
c.-140T>G (p.=)
c.-203T>G (p.=)
Xg.63785124A>GCA413405841ARHGEF9c.22T>C (p.Ser8Pro)
n.91T>C
c.-118+10392T>C (p.=)
c.-140T>C (p.=)
c.-203T>C (p.=)
Xg.63785124A>TCA413405842ARHGEF9c.22T>A (p.Ser8Thr)
n.91T>A
c.-118+10392T>A (p.=)
c.-140T>A (p.=)
c.-203T>A (p.=)
Xg.63785125T>ACA516873569ARHGEF9c.21A>T (p.Gly7=)
n.90A>T
c.-118+10391A>T (p.=)
c.-141A>T (p.=)
c.-204A>T (p.=)

Number of alleles fetched