Chr Mutation (hg38) CAid Gene Transcript Linkouts
18g.23560272C>ACA401780960NPC1c.840G>T (p.Leu280Phe)
n.754G>T
c.71G>T
c.375G>T (p.Leu125Phe)
18g.23560272C>GCA401780963NPC1c.840G>C (p.Leu280Phe)
n.754G>C
c.71G>C
c.375G>C (p.Leu125Phe)
18g.23560272C>TCA503522007NPC1c.840G>A (p.Leu280=)
n.754G>A
c.71G>A
c.375G>A (p.Leu125=)
18g.23560272_23560273delinsCACA2290175678NPC1c.839_840delinsTG (p.Leu280=)
n.753_754delinsTG
c.70_71delinsTG
c.374_375delinsTG (p.Leu125=)
18g.23560273A>CCA401780973NPC1c.839T>G (p.Leu280Trp)
n.753T>G
c.70T>G
c.374T>G (p.Leu125Trp)
18g.23560273A>GCA401780967NPC1c.839T>C (p.Leu280Ser)
n.753T>C
c.70T>C
c.374T>C (p.Leu125Ser)
18g.23560273A>TCA401780970NPC1c.839T>A (p.Leu280Ter)
n.753T>A
c.70T>A
c.374T>A (p.Leu125Ter)
18g.23560277delCA16043698NPC1c.839del (p.Leu280CysfsTer30)
n.753del
c.70del
c.374del (p.Leu125CysfsTer30)
ClinVar dbSNP
18g.23560274A>CCA401780976NPC1c.838T>G (p.Leu280Val)
n.752T>G
c.69T>G
c.373T>G (p.Leu125Val)
18g.23560274A>GCA503522009NPC1c.838T>C (p.Leu280=)
n.752T>C
c.69T>C
c.373T>C (p.Leu125=)
18g.23560274A>TCA401780978NPC1c.838T>A (p.Leu280Met)
n.752T>A
c.69T>A
c.373T>A (p.Leu125Met)
18g.23560275A=CA2290175679NPC1c.837T= (p.Phe279=)
n.751T=
c.68T=
c.372T= (p.Phe124=)
18g.23560275A>CCA401780981NPC1c.837T>G (p.Phe279Leu)
n.751T>G
c.68T>G
c.372T>G (p.Phe124Leu)
18g.23560275A>GCA503522010NPC1c.837T>C (p.Phe279=)
n.751T>C
c.68T>C
c.372T>C (p.Phe124=)
dbSNP gnomAD v3 gnomAD v4
18g.23560275A>TCA401780983NPC1c.837T>A (p.Phe279Leu)
n.751T>A
c.68T>A
c.372T>A (p.Phe124Leu)
18g.23560276A>CCA401780986NPC1c.836T>G (p.Phe279Cys)
n.750T>G
c.67T>G
c.371T>G (p.Phe124Cys)
18g.23560276A>GCA401780988NPC1c.836T>C (p.Phe279Ser)
n.750T>C
c.67T>C
c.371T>C (p.Phe124Ser)
18g.23560276A>TCA401780989NPC1c.836T>A (p.Phe279Tyr)
n.750T>A
c.67T>A
c.371T>A (p.Phe124Tyr)
18g.23560277A>CCA401780992NPC1c.835T>G (p.Phe279Val)
n.749T>G
c.66T>G
c.370T>G (p.Phe124Val)
18g.23560277A>GCA401780994NPC1c.835T>C (p.Phe279Leu)
n.749T>C
c.66T>C
c.370T>C (p.Phe124Leu)
18g.23560277A>TCA401780996NPC1c.835T>A (p.Phe279Ile)
n.749T>A
c.66T>A
c.370T>A (p.Phe124Ile)
18g.23560278C>ACA503522049NPC1c.834G>T (p.Ala278=)
n.748G>T
c.65G>T
c.369G>T (p.Ala123=)
18g.23560278C=CA2290175680NPC1c.834G= (p.Ala278=)
n.748G=
c.65G=
c.369G= (p.Ala123=)
18g.23560278C>GCA503522051NPC1c.834G>C (p.Ala278=)
n.748G>C
c.65G>C
c.369G>C (p.Ala123=)
18g.23560278C>TCA8913630NPC1c.834G>A (p.Ala278=)
n.748G>A
c.65G>A
c.369G>A (p.Ala123=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
18g.23560279G>ACA8913631NPC1c.833C>T (p.Ala278Val)
n.747C>T
c.64C>T
c.368C>T (p.Ala123Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.23560279G>CCA401781002NPC1c.833C>G (p.Ala278Gly)
n.747C>G
c.64C>G
c.368C>G (p.Ala123Gly)
18g.23560279G=CA2290175681NPC1c.833C= (p.Ala278=)
n.747C=
c.64C=
c.368C= (p.Ala123=)
18g.23560279G>TCA8913632NPC1c.833C>A (p.Ala278Glu)
n.747C>A
c.64C>A
c.368C>A (p.Ala123Glu)
dbSNP ExAC gnomAD v2 gnomAD v4
18g.23560280C>ACA401781011NPC1c.832G>T (p.Ala278Ser)
n.746G>T
c.63G>T
c.367G>T (p.Ala123Ser)
18g.23560280C>GCA401781013NPC1c.832G>C (p.Ala278Pro)
n.746G>C
c.63G>C
c.367G>C (p.Ala123Pro)
18g.23560280C>TCA401781015NPC1c.832G>A (p.Ala278Thr)
n.746G>A
c.63G>A
c.367G>A (p.Ala123Thr)
gnomAD v4
18g.23560281dupCA297074601NPC1c.832dup (p.Ala278GlyfsTer30)
n.746dup
c.63dup
c.367dup (p.Ala123GlyfsTer30)
dbSNP
18g.23560281C>ACA401781017NPC1c.831G>T (p.Met277Ile)
n.745G>T
c.62G>T
c.366G>T (p.Met122Ile)
18g.23560281C>GCA401781020NPC1c.831G>C (p.Met277Ile)
n.745G>C
c.62G>C
c.366G>C (p.Met122Ile)
gnomAD v4
18g.23560281C>TCA401781022NPC1c.831G>A (p.Met277Ile)
n.745G>A
c.62G>A
c.366G>A (p.Met122Ile)
18g.23560282delCA2641271867NPC1c.830del (p.Met277ArgfsTer?)
n.744del
c.61del
c.365del (p.Met122ArgfsTer?)
gnomAD v4
18g.23560282A>CCA401781025NPC1c.830T>G (p.Met277Arg)
n.744T>G
c.61T>G
c.365T>G (p.Met122Arg)
18g.23560282A>GCA401781026NPC1c.830T>C (p.Met277Thr)
n.744T>C
c.61T>C
c.365T>C (p.Met122Thr)
18g.23560282A>TCA401781028NPC1c.830T>A (p.Met277Lys)
n.744T>A
c.61T>A
c.365T>A (p.Met122Lys)
18g.23560283T>ACA401781034NPC1c.829A>T (p.Met277Leu)
n.743A>T
c.60A>T
c.364A>T (p.Met122Leu)
18g.23560283T>CCA8913633NPC1c.829A>G (p.Met277Val)
n.743A>G
c.60A>G
c.364A>G (p.Met122Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.23560283T>GCA401781032NPC1c.829A>C (p.Met277Leu)
n.743A>C
c.60A>C
c.364A>C (p.Met122Leu)
gnomAD v4
18g.23560283T=CA2290175682NPC1c.829A= (p.Met277=)
n.743A=
c.60A=
c.364A= (p.Met122=)
18g.23560284G>ACA503522057NPC1c.828C>T (p.Tyr276=)
n.742C>T
c.59C>T
c.363C>T (p.Tyr121=)
ClinVar dbSNP COSMIC COSMIC
18g.23560284G>CCA401781036NPC1c.828C>G (p.Tyr276Ter)
n.742C>G
c.59C>G
c.363C>G (p.Tyr121Ter)
18g.23560284G>TCA401781039NPC1c.828C>A (p.Tyr276Ter)
n.742C>A
c.59C>A
c.363C>A (p.Tyr121Ter)
18g.23560285T>ACA401781042NPC1c.827A>T (p.Tyr276Phe)
n.741A>T
c.58A>T
c.362A>T (p.Tyr121Phe)
18g.23560285T>CCA401781044NPC1c.827A>G (p.Tyr276Cys)
n.741A>G
c.58A>G
c.362A>G (p.Tyr121Cys)
18g.23560285T>GCA401781045NPC1c.827A>C (p.Tyr276Ser)
n.741A>C
c.58A>C
c.362A>C (p.Tyr121Ser)

Number of alleles fetched