Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.51915303_51915357delCA2739272048ACVRL1c.581_635del (p.Ser194Ter)
c.851_905del (p.Ser284Ter)
c.329_383del (p.Ser110Ter)
c.893_947del (p.Ser298Ter)
c.62_116del (p.Ser21Ter)
ClinVar
12g.51915314T>ACA384900591ACVRL1c.592T>A (p.Phe198Ile)
c.862T>A (p.Phe288Ile)
c.340T>A (p.Phe114Ile)
c.904T>A (p.Phe302Ile)
c.73T>A (p.Phe25Ile)
12g.51915314T>CCA384900592ACVRL1c.592T>C (p.Phe198Leu)
c.862T>C (p.Phe288Leu)
c.340T>C (p.Phe114Leu)
c.904T>C (p.Phe302Leu)
c.73T>C (p.Phe25Leu)
12g.51915314T>GCA384900594ACVRL1c.592T>G (p.Phe198Val)
c.862T>G (p.Phe288Val)
c.340T>G (p.Phe114Val)
c.904T>G (p.Phe302Val)
c.73T>G (p.Phe25Val)
12g.51915316dupCA913184985ACVRL1c.594dup (p.Leu199SerfsTer?)
c.864dup (p.Leu289SerfsTer?)
c.342dup (p.Leu115SerfsTer?)
c.906dup (p.Leu303SerfsTer?)
c.75dup (p.Leu26SerfsTer?)
ClinVar
12g.51915315T>ACA384900595ACVRL1c.593T>A (p.Phe198Tyr)
c.863T>A (p.Phe288Tyr)
c.341T>A (p.Phe114Tyr)
c.905T>A (p.Phe302Tyr)
c.74T>A (p.Phe25Tyr)
12g.51915315T>CCA384900597ACVRL1c.593T>C (p.Phe198Ser)
c.863T>C (p.Phe288Ser)
c.341T>C (p.Phe114Ser)
c.905T>C (p.Phe302Ser)
c.74T>C (p.Phe25Ser)
ClinVar dbSNP
12g.51915315T>GCA384900598ACVRL1c.593T>G (p.Phe198Cys)
c.863T>G (p.Phe288Cys)
c.341T>G (p.Phe114Cys)
c.905T>G (p.Phe302Cys)
c.74T>G (p.Phe25Cys)
12g.51915315T=CA2036269457ACVRL1c.593T= (p.Phe198=)
c.863T= (p.Phe288=)
c.341T= (p.Phe114=)
c.905T= (p.Phe302=)
c.74T= (p.Phe25=)
12g.51915316T>ACA384900600ACVRL1c.594T>A (p.Phe198Leu)
c.864T>A (p.Phe288Leu)
c.342T>A (p.Phe114Leu)
c.906T>A (p.Phe302Leu)
c.75T>A (p.Phe25Leu)
12g.51915316T>CCA480063177ACVRL1c.594T>C (p.Phe198=)
c.864T>C (p.Phe288=)
c.342T>C (p.Phe114=)
c.906T>C (p.Phe302=)
c.75T>C (p.Phe25=)
12g.51915316T>GCA384900601ACVRL1c.594T>G (p.Phe198Leu)
c.864T>G (p.Phe288Leu)
c.342T>G (p.Phe114Leu)
c.906T>G (p.Phe302Leu)
c.75T>G (p.Phe25Leu)
12g.51915317C>ACA384900603ACVRL1c.595C>A (p.Leu199Met)
c.865C>A (p.Leu289Met)
c.343C>A (p.Leu115Met)
c.907C>A (p.Leu303Met)
c.76C>A (p.Leu26Met)
12g.51915317C>GCA384900604ACVRL1c.595C>G (p.Leu199Val)
c.865C>G (p.Leu289Val)
c.343C>G (p.Leu115Val)
c.907C>G (p.Leu303Val)
c.76C>G (p.Leu26Val)
12g.51915317C>TCA480063178ACVRL1c.595C>T (p.Leu199=)
c.865C>T (p.Leu289=)
c.343C>T (p.Leu115=)
c.907C>T (p.Leu303=)
c.76C>T (p.Leu26=)
12g.51915318T>ACA384900606ACVRL1c.596T>A (p.Leu199Gln)
c.866T>A (p.Leu289Gln)
c.344T>A (p.Leu115Gln)
c.908T>A (p.Leu303Gln)
c.77T>A (p.Leu26Gln)
12g.51915318T>CCA384900608ACVRL1c.596T>C (p.Leu199Pro)
c.866T>C (p.Leu289Pro)
c.344T>C (p.Leu115Pro)
c.908T>C (p.Leu303Pro)
c.77T>C (p.Leu26Pro)
ClinVar
12g.51915318T>GCA384900609ACVRL1c.596T>G (p.Leu199Arg)
c.866T>G (p.Leu289Arg)
c.344T>G (p.Leu115Arg)
c.908T>G (p.Leu303Arg)
c.77T>G (p.Leu26Arg)
12g.51915318dupCA2695216743ACVRL1c.596dup (p.Gln200AlafsTer?)
c.866dup (p.Gln290AlafsTer?)
c.344dup (p.Gln116AlafsTer?)
c.908dup (p.Gln304AlafsTer?)
c.77dup (p.Gln27AlafsTer?)
12g.51915319delCA645594553ACVRL1c.597del (p.Gln200ArgfsTer11)
c.867del (p.Gln290ArgfsTer11)
c.345del (p.Gln116ArgfsTer11)
c.909del (p.Gln304ArgfsTer11)
c.78del (p.Gln27ArgfsTer11)
COSMIC COSMIC
12g.51915319G>ACA480063179ACVRL1c.597G>A (p.Leu199=)
c.867G>A (p.Leu289=)
c.345G>A (p.Leu115=)
c.909G>A (p.Leu303=)
c.78G>A (p.Leu26=)
12g.51915319G>CCA480063180ACVRL1c.597G>C (p.Leu199=)
c.867G>C (p.Leu289=)
c.345G>C (p.Leu115=)
c.909G>C (p.Leu303=)
c.78G>C (p.Leu26=)
gnomAD v4
12g.51915319G>TCA480063181ACVRL1c.597G>T (p.Leu199=)
c.867G>T (p.Leu289=)
c.345G>T (p.Leu115=)
c.909G>T (p.Leu303=)
c.78G>T (p.Leu26=)
12g.51915320C>ACA384900614ACVRL1c.598C>A (p.Gln200Lys)
c.868C>A (p.Gln290Lys)
c.346C>A (p.Gln116Lys)
c.910C>A (p.Gln304Lys)
c.79C>A (p.Gln27Lys)
12g.51915320C>GCA384900615ACVRL1c.598C>G (p.Gln200Glu)
c.868C>G (p.Gln290Glu)
c.346C>G (p.Gln116Glu)
c.910C>G (p.Gln304Glu)
c.79C>G (p.Gln27Glu)
12g.51915320C>TCA384900611ACVRL1c.598C>T (p.Gln200Ter)
c.868C>T (p.Gln290Ter)
c.346C>T (p.Gln116Ter)
c.910C>T (p.Gln304Ter)
c.79C>T (p.Gln27Ter)
ClinVar dbSNP
12g.51915320_51915322delinsCAGCA2036269458ACVRL1c.598_600delinsCAG (p.Gln200=)
c.868_870delinsCAG (p.Gln290=)
c.346_348delinsCAG (p.Gln116=)
c.910_912delinsCAG (p.Gln304=)
c.79_81delinsCAG (p.Gln27=)
12g.51915321A>CCA384900617ACVRL1c.599A>C (p.Gln200Pro)
c.869A>C (p.Gln290Pro)
c.347A>C (p.Gln116Pro)
c.911A>C (p.Gln304Pro)
c.80A>C (p.Gln27Pro)
12g.51915321A>GCA384900618ACVRL1c.599A>G (p.Gln200Arg)
c.869A>G (p.Gln290Arg)
c.347A>G (p.Gln116Arg)
c.911A>G (p.Gln304Arg)
c.80A>G (p.Gln27Arg)
12g.51915321A>TCA384900619ACVRL1c.599A>T (p.Gln200Leu)
c.869A>T (p.Gln290Leu)
c.347A>T (p.Gln116Leu)
c.911A>T (p.Gln304Leu)
c.80A>T (p.Gln27Leu)
12g.51915321_51915322delinsAGCA2036269459ACVRL1c.599_600delinsAG (p.Gln200=)
c.869_870delinsAG (p.Gln290=)
c.347_348delinsAG (p.Gln116=)
c.911_912delinsAG (p.Gln304=)
c.80_81delinsAG (p.Gln27=)
12g.51915324_51915325delCA915948523ACVRL1c.602_603del (p.Arg201ThrfsTer?)
c.872_873del (p.Arg291ThrfsTer?)
c.350_351del (p.Arg117ThrfsTer?)
c.914_915del (p.Arg305ThrfsTer?)
c.83_84del (p.Arg28ThrfsTer?)
ClinVar dbSNP
12g.51915322delCA913190986ACVRL1c.600del (p.Arg201AspfsTer10)
c.870del (p.Arg291AspfsTer10)
c.348del (p.Arg117AspfsTer10)
c.912del (p.Arg305AspfsTer10)
c.81del (p.Arg28AspfsTer10)
ClinVar dbSNP
12g.51915322G>ACA480063182ACVRL1c.600G>A (p.Gln200=)
c.870G>A (p.Gln290=)
c.348G>A (p.Gln116=)
c.912G>A (p.Gln304=)
c.81G>A (p.Gln27=)
dbSNP gnomAD v3 gnomAD v4
12g.51915322G>CCA384900620ACVRL1c.600G>C (p.Gln200His)
c.870G>C (p.Gln290His)
c.348G>C (p.Gln116His)
c.912G>C (p.Gln304His)
c.81G>C (p.Gln27His)
12g.51915322G=CA2036269460ACVRL1c.600G= (p.Gln200=)
c.870G= (p.Gln290=)
c.348G= (p.Gln116=)
c.912G= (p.Gln304=)
c.81G= (p.Gln27=)
12g.51915322G>TCA384900621ACVRL1c.600G>T (p.Gln200His)
c.870G>T (p.Gln290His)
c.348G>T (p.Gln116His)
c.912G>T (p.Gln304His)
c.81G>T (p.Gln27His)
12g.51915323A=CA2036269461ACVRL1c.601A= (p.Arg201=)
c.871A= (p.Arg291=)
c.349A= (p.Arg117=)
c.913A= (p.Arg305=)
c.82A= (p.Arg28=)
12g.51915323A>CCA480063183ACVRL1c.601A>C (p.Arg201=)
c.871A>C (p.Arg291=)
c.349A>C (p.Arg117=)
c.913A>C (p.Arg305=)
c.82A>C (p.Arg28=)
12g.51915323A>GCA236364040ACVRL1c.601A>G (p.Arg201Gly)
c.871A>G (p.Arg291Gly)
c.349A>G (p.Arg117Gly)
c.913A>G (p.Arg305Gly)
c.82A>G (p.Arg28Gly)
dbSNP
12g.51915323A>TCA384900623ACVRL1c.601A>T (p.Arg201Ter)
c.871A>T (p.Arg291Ter)
c.349A>T (p.Arg117Ter)
c.913A>T (p.Arg305Ter)
c.82A>T (p.Arg28Ter)
ClinVar dbSNP
12g.51915324G>ACA384900625ACVRL1c.602G>A (p.Arg201Lys)
c.872G>A (p.Arg291Lys)
c.350G>A (p.Arg117Lys)
c.914G>A (p.Arg305Lys)
c.83G>A (p.Arg28Lys)
12g.51915324G>CCA384900630ACVRL1c.602G>C (p.Arg201Thr)
c.872G>C (p.Arg291Thr)
c.350G>C (p.Arg117Thr)
c.914G>C (p.Arg305Thr)
c.83G>C (p.Arg28Thr)
gnomAD v4
12g.51915324G>TCA384900633ACVRL1c.602G>T (p.Arg201Ile)
c.872G>T (p.Arg291Ile)
c.350G>T (p.Arg117Ile)
c.914G>T (p.Arg305Ile)
c.83G>T (p.Arg28Ile)
12g.51915325A=CA2036269462ACVRL1c.603A= (p.Arg201=)
c.873A= (p.Arg291=)
c.351A= (p.Arg117=)
c.915A= (p.Arg305=)
c.84A= (p.Arg28=)
12g.51915325A>CCA384900634ACVRL1c.603A>C (p.Arg201Ser)
c.873A>C (p.Arg291Ser)
c.351A>C (p.Arg117Ser)
c.915A>C (p.Arg305Ser)
c.84A>C (p.Arg28Ser)
12g.51915325A>GCA480063184ACVRL1c.603A>G (p.Arg201=)
c.873A>G (p.Arg291=)
c.351A>G (p.Arg117=)
c.915A>G (p.Arg305=)
c.84A>G (p.Arg28=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.51915325A>TCA384900635ACVRL1c.603A>T (p.Arg201Ser)
c.873A>T (p.Arg291Ser)
c.351A>T (p.Arg117Ser)
c.915A>T (p.Arg305Ser)
c.84A>T (p.Arg28Ser)
12g.51915326delCA2695216744ACVRL1c.604del (p.Gln202ArgfsTer9)
c.874del (p.Gln292ArgfsTer9)
c.352del (p.Gln118ArgfsTer9)
c.916del (p.Gln306ArgfsTer9)
c.85del (p.Gln29ArgfsTer9)
12g.51915326C>ACA384900639ACVRL1c.604C>A (p.Gln202Lys)
c.874C>A (p.Gln292Lys)
c.352C>A (p.Gln118Lys)
c.916C>A (p.Gln306Lys)
c.85C>A (p.Gln29Lys)

Number of alleles fetched