Chr Mutation (hg38) CAid Gene Transcript Linkouts
18g.23539422G>ACA503322568NPC1c.2844C>T (p.Asp948=)
c.1922C>T
n.477C>T
c.2895C>T (p.Asp965=)
c.2430C>T (p.Asp810=)
ClinVar
18g.23539422G>CCA401792508NPC1c.2844C>G (p.Asp948Glu)
c.1922C>G
n.477C>G
c.2895C>G (p.Asp965Glu)
c.2430C>G (p.Asp810Glu)
ClinVar
18g.23539422G>TCA401792509NPC1c.2844C>A (p.Asp948Glu)
c.1922C>A
n.477C>A
c.2895C>A (p.Asp965Glu)
c.2430C>A (p.Asp810Glu)
18g.23539423T>ACA401792510NPC1c.2843A>T (p.Asp948Val)
c.1921A>T
n.476A>T
c.2894A>T (p.Asp965Val)
c.2429A>T (p.Asp810Val)
18g.23539423T>CCA401792511NPC1c.2843A>G (p.Asp948Gly)
c.1921A>G
n.476A>G
c.2894A>G (p.Asp965Gly)
c.2429A>G (p.Asp810Gly)
18g.23539423T>GCA401792512NPC1c.2843A>C (p.Asp948Ala)
c.1921A>C
n.476A>C
c.2894A>C (p.Asp965Ala)
c.2429A>C (p.Asp810Ala)
18g.23539424C>ACA401792515NPC1c.2842G>T (p.Asp948Tyr)
c.1920G>T
n.475G>T
c.2893G>T (p.Asp965Tyr)
c.2428G>T (p.Asp810Tyr)
gnomAD v4
18g.23539424C=CA2290165744NPC1c.2842G= (p.Asp948=)
c.1920G=
n.475G=
c.2893G= (p.Asp965=)
c.2428G= (p.Asp810=)
18g.23539424C>GCA401792514NPC1c.2842G>C (p.Asp948His)
c.1920G>C
n.475G>C
c.2893G>C (p.Asp965His)
c.2428G>C (p.Asp810His)
gnomAD v4
18g.23539424C>TCA401792513NPC1c.2842G>A (p.Asp948Asn)
c.1920G>A
n.475G>A
c.2893G>A (p.Asp965Asn)
c.2428G>A (p.Asp810Asn)
ClinVar dbSNP gnomAD v2 gnomAD v4
18g.23539425G>ACA8912944NPC1c.2841C>T (p.Phe947=)
c.1919C>T
n.474C>T
c.2892C>T (p.Phe964=)
c.2427C>T (p.Phe809=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
18g.23539425G>CCA401792516NPC1c.2841C>G (p.Phe947Leu)
c.1919C>G
n.474C>G
c.2892C>G (p.Phe964Leu)
c.2427C>G (p.Phe809Leu)
gnomAD v4
18g.23539425G=CA2290165745NPC1c.2841C= (p.Phe947=)
c.1919C=
n.474C=
c.2892C= (p.Phe964=)
c.2427C= (p.Phe809=)
18g.23539425G>TCA401792517NPC1c.2841C>A (p.Phe947Leu)
c.1919C>A
n.474C>A
c.2892C>A (p.Phe964Leu)
c.2427C>A (p.Phe809Leu)
18g.23539426A=CA2290165746NPC1c.2840T= (p.Phe947=)
c.1918T=
n.473T=
c.2891T= (p.Phe964=)
c.2426T= (p.Phe809=)
18g.23539426A>CCA401792518NPC1c.2840T>G (p.Phe947Cys)
c.1918T>G
n.473T>G
c.2891T>G (p.Phe964Cys)
c.2426T>G (p.Phe809Cys)
18g.23539426A>GCA401792519NPC1c.2840T>C (p.Phe947Ser)
c.1918T>C
n.473T>C
c.2891T>C (p.Phe964Ser)
c.2426T>C (p.Phe809Ser)
dbSNP gnomAD v2 gnomAD v4
18g.23539426A>TCA401792520NPC1c.2840T>A (p.Phe947Tyr)
c.1918T>A
n.473T>A
c.2891T>A (p.Phe964Tyr)
c.2426T>A (p.Phe809Tyr)
18g.23539427A>CCA401792521NPC1c.2839T>G (p.Phe947Val)
c.1917T>G
n.472T>G
c.2890T>G (p.Phe964Val)
c.2425T>G (p.Phe809Val)
18g.23539427A>GCA401792522NPC1c.2839T>C (p.Phe947Leu)
c.1917T>C
n.472T>C
c.2890T>C (p.Phe964Leu)
c.2425T>C (p.Phe809Leu)
18g.23539427A>TCA401792523NPC1c.2839T>A (p.Phe947Ile)
c.1917T>A
n.472T>A
c.2890T>A (p.Phe964Ile)
c.2425T>A (p.Phe809Ile)
18g.23539428A>CCA401792524NPC1c.2838T>G (p.Tyr946Ter)
c.1916T>G
n.471T>G
c.2889T>G (p.Tyr963Ter)
c.2424T>G (p.Tyr808Ter)
18g.23539428A>GCA503322569NPC1c.2838T>C (p.Tyr946=)
c.1916T>C
n.471T>C
c.2889T>C (p.Tyr963=)
c.2424T>C (p.Tyr808=)
18g.23539428A>TCA401792525NPC1c.2838T>A (p.Tyr946Ter)
c.1916T>A
n.471T>A
c.2889T>A (p.Tyr963Ter)
c.2424T>A (p.Tyr808Ter)
18g.23539429T>ACA401792528NPC1c.2837A>T (p.Tyr946Phe)
c.1915A>T
n.470A>T
c.2888A>T (p.Tyr963Phe)
c.2423A>T (p.Tyr808Phe)
18g.23539429T>CCA401792527NPC1c.2837A>G (p.Tyr946Cys)
c.1915A>G
n.470A>G
c.2888A>G (p.Tyr963Cys)
c.2423A>G (p.Tyr808Cys)
18g.23539429T>GCA401792526NPC1c.2837A>C (p.Tyr946Ser)
c.1915A>C
n.470A>C
c.2888A>C (p.Tyr963Ser)
c.2423A>C (p.Tyr808Ser)
18g.23539430A>CCA401792529NPC1c.2836T>G (p.Tyr946Asp)
c.1914T>G
n.469T>G
c.2887T>G (p.Tyr963Asp)
c.2422T>G (p.Tyr808Asp)
18g.23539430A>GCA401792531NPC1c.2836T>C (p.Tyr946His)
c.1914T>C
n.469T>C
c.2887T>C (p.Tyr963His)
c.2422T>C (p.Tyr808His)
gnomAD v4
18g.23539430A>TCA401792530NPC1c.2836T>A (p.Tyr946Asn)
c.1914T>A
n.469T>A
c.2887T>A (p.Tyr963Asn)
c.2422T>A (p.Tyr808Asn)
ClinVar
18g.23539431A>CCA401792532NPC1c.2835T>G (p.Asp945Glu)
c.1913T>G
n.468T>G
c.2886T>G (p.Asp962Glu)
c.2421T>G (p.Asp807Glu)
18g.23539431A>GCA503322570NPC1c.2835T>C (p.Asp945=)
c.1913T>C
n.468T>C
c.2886T>C (p.Asp962=)
c.2421T>C (p.Asp807=)
ClinVar
18g.23539431A>TCA401792533NPC1c.2835T>A (p.Asp945Glu)
c.1913T>A
n.468T>A
c.2886T>A (p.Asp962Glu)
c.2421T>A (p.Asp807Glu)
18g.23539432T>ACA401792534NPC1c.2834A>T (p.Asp945Val)
c.1912A>T
n.467A>T
c.2885A>T (p.Asp962Val)
c.2420A>T (p.Asp807Val)
18g.23539432T>CCA401792535NPC1c.2834A>G (p.Asp945Gly)
c.1912A>G
n.467A>G
c.2885A>G (p.Asp962Gly)
c.2420A>G (p.Asp807Gly)
18g.23539432T>GCA401792536NPC1c.2834A>C (p.Asp945Ala)
c.1912A>C
n.467A>C
c.2885A>C (p.Asp962Ala)
c.2420A>C (p.Asp807Ala)
18g.23539433C>ACA401792537NPC1c.2833G>T (p.Asp945Tyr)
c.1911G>T
n.466G>T
c.2884G>T (p.Asp962Tyr)
c.2419G>T (p.Asp807Tyr)
gnomAD v4 COSMIC
18g.23539433C=CA2290165747NPC1c.2833G= (p.Asp945=)
c.1911G=
n.466G=
c.2884G= (p.Asp962=)
c.2419G= (p.Asp807=)
18g.23539433C>GCA401792538NPC1c.2833G>C (p.Asp945His)
c.1911G>C
n.466G>C
c.2884G>C (p.Asp962His)
c.2419G>C (p.Asp807His)
18g.23539433C>TCA401792539NPC1c.2833G>A (p.Asp945Asn)
c.1911G>A
n.466G>A
c.2884G>A (p.Asp962Asn)
c.2419G>A (p.Asp807Asn)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
18g.23539434G>ACA8912945NPC1c.2832C>T (p.Asp944=)
c.1910C>T
n.465C>T
c.2883C>T (p.Asp961=)
c.2418C>T (p.Asp806=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.23539434G>CCA401792540NPC1c.2832C>G (p.Asp944Glu)
c.1910C>G
n.465C>G
c.2883C>G (p.Asp961Glu)
c.2418C>G (p.Asp806Glu)
18g.23539434G=CA2290165748NPC1c.2832C= (p.Asp944=)
c.1910C=
n.465C=
c.2883C= (p.Asp961=)
c.2418C= (p.Asp806=)
18g.23539434G>TCA401792541NPC1c.2832C>A (p.Asp944Glu)
c.1910C>A
n.465C>A
c.2883C>A (p.Asp961Glu)
c.2418C>A (p.Asp806Glu)
18g.23539435T>ACA401792544NPC1c.2831A>T (p.Asp944Val)
c.1909A>T
n.464A>T
c.2882A>T (p.Asp961Val)
c.2417A>T (p.Asp806Val)
18g.23539435T>CCA401792542NPC1c.2831A>G (p.Asp944Gly)
c.1909A>G
n.464A>G
c.2882A>G (p.Asp961Gly)
c.2417A>G (p.Asp806Gly)
18g.23539435T>GCA401792543NPC1c.2831A>C (p.Asp944Ala)
c.1909A>C
n.464A>C
c.2882A>C (p.Asp961Ala)
c.2417A>C (p.Asp806Ala)
18g.23539436C>ACA401792545NPC1c.2830G>T (p.Asp944Tyr)
c.1908G>T
n.463G>T
c.2881G>T (p.Asp961Tyr)
c.2416G>T (p.Asp806Tyr)
18g.23539436C=CA2290165749NPC1c.2830G= (p.Asp944=)
c.1908G=
n.463G=
c.2881G= (p.Asp961=)
c.2416G= (p.Asp806=)
18g.23539436C>GCA401792546NPC1c.2830G>C (p.Asp944His)
c.1908G>C
n.463G>C
c.2881G>C (p.Asp961His)
c.2416G>C (p.Asp806His)

Number of alleles fetched