Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.40363432C>ACA384413188LRRK2c.7059C>A (p.Asn2353Lys)
c.856C>A
c.*5968C>A (n.*5968C>A)
c.2833C>A
c.849C>A
c.2504C>A (n.2504C>A)
c.4146C>A
c.2226C>A (n.2226C>A)
c.2516C>A
c.6804C>A (p.Asn2268Lys)
n.3043C>A
c.2742C>A (p.Asn914Lys)
n.266C>A
c.4355C>A
n.3740C>A
c.5856C>A (p.Asn1952Lys)
n.485-8605G>T
c.3975C>A (p.Asn1325Lys)
c.3321C>A (p.Asn1107Lys)
12g.40363432C=CA2031025771LRRK2c.7059C= (p.Asn2353=)
c.856C=
c.*5968C= (n.*5968C=)
c.2833C=
c.849C=
c.2504C= (n.2504C=)
c.4146C=
c.2226C= (n.2226C=)
c.2516C=
c.6804C= (p.Asn2268=)
n.3043C=
c.2742C= (p.Asn914=)
n.266C=
c.4355C=
n.3740C=
c.5856C= (p.Asn1952=)
n.485-8605G=
c.3975C= (p.Asn1325=)
c.3321C= (p.Asn1107=)
12g.40363432C>GCA384413191LRRK2c.7059C>G (p.Asn2353Lys)
c.856C>G
c.*5968C>G (n.*5968C>G)
c.2833C>G
c.849C>G
c.2504C>G (n.2504C>G)
c.4146C>G
c.2226C>G (n.2226C>G)
c.2516C>G
c.6804C>G (p.Asn2268Lys)
n.3043C>G
c.2742C>G (p.Asn914Lys)
n.266C>G
c.4355C>G
n.3740C>G
c.5856C>G (p.Asn1952Lys)
n.485-8605G>C
c.3975C>G (p.Asn1325Lys)
c.3321C>G (p.Asn1107Lys)
12g.40363432C>TCA6514842LRRK2c.7059C>T (p.Asn2353=)
c.856C>T
c.*5968C>T (n.*5968C>T)
c.2833C>T
c.849C>T
c.2504C>T (n.2504C>T)
c.4146C>T
c.2226C>T (n.2226C>T)
c.2516C>T
c.6804C>T (p.Asn2268=)
n.3043C>T
c.2742C>T (p.Asn914=)
n.266C>T
c.4355C>T
n.3740C>T
c.5856C>T (p.Asn1952=)
n.485-8605G>A
c.3975C>T (p.Asn1325=)
c.3321C>T (p.Asn1107=)
dbSNP ExAC gnomAD v2
12g.40363433A=CA2031025774LRRK2c.7060A= (p.Ile2354=)
c.857A=
c.*5969A= (n.*5969A=)
c.2834A=
c.850A=
c.2505A= (n.2505A=)
c.4147A=
c.2227A= (n.2227A=)
c.2517A=
c.6805A= (p.Ile2269=)
n.3044A=
c.2743A= (p.Ile915=)
n.267A=
c.4356A=
n.3741A=
c.5857A= (p.Ile1953=)
n.485-8606T=
c.3976A= (p.Ile1326=)
c.3322A= (p.Ile1108=)
12g.40363433A>CCA384413196LRRK2c.7060A>C (p.Ile2354Leu)
c.857A>C
c.*5969A>C (n.*5969A>C)
c.2834A>C
c.850A>C
c.2505A>C (n.2505A>C)
c.4147A>C
c.2227A>C (n.2227A>C)
c.2517A>C
c.6805A>C (p.Ile2269Leu)
n.3044A>C
c.2743A>C (p.Ile915Leu)
n.267A>C
c.4356A>C
n.3741A>C
c.5857A>C (p.Ile1953Leu)
n.485-8606T>G
c.3976A>C (p.Ile1326Leu)
c.3322A>C (p.Ile1108Leu)
12g.40363433A>GCA384413198LRRK2c.7060A>G (p.Ile2354Val)
c.857A>G
c.*5969A>G (n.*5969A>G)
c.2834A>G
c.850A>G
c.2505A>G (n.2505A>G)
c.4147A>G
c.2227A>G (n.2227A>G)
c.2517A>G
c.6805A>G (p.Ile2269Val)
n.3044A>G
c.2743A>G (p.Ile915Val)
n.267A>G
c.4356A>G
n.3741A>G
c.5857A>G (p.Ile1953Val)
n.485-8606T>C
c.3976A>G (p.Ile1326Val)
c.3322A>G (p.Ile1108Val)
dbSNP gnomAD v3 gnomAD v4
12g.40363433A>TCA384413200LRRK2c.7060A>T (p.Ile2354Phe)
c.857A>T
c.*5969A>T (n.*5969A>T)
c.2834A>T
c.850A>T
c.2505A>T (n.2505A>T)
c.4147A>T
c.2227A>T (n.2227A>T)
c.2517A>T
c.6805A>T (p.Ile2269Phe)
n.3044A>T
c.2743A>T (p.Ile915Phe)
n.267A>T
c.4356A>T
n.3741A>T
c.5857A>T (p.Ile1953Phe)
n.485-8606T>A
c.3976A>T (p.Ile1326Phe)
c.3322A>T (p.Ile1108Phe)
12g.40363434T>ACA384413204LRRK2c.7061T>A (p.Ile2354Asn)
c.858T>A
c.*5970T>A (n.*5970T>A)
c.2835T>A
c.851T>A
c.2506T>A (n.2506T>A)
c.4148T>A
c.2228T>A (n.2228T>A)
c.2518T>A
c.6806T>A (p.Ile2269Asn)
n.3045T>A
c.2744T>A (p.Ile915Asn)
n.268T>A
c.4357T>A
n.3742T>A
c.5858T>A (p.Ile1953Asn)
n.485-8607A>T
c.3977T>A (p.Ile1326Asn)
c.3323T>A (p.Ile1108Asn)
gnomAD v4
12g.40363434T>CCA384413206LRRK2c.7061T>C (p.Ile2354Thr)
c.858T>C
c.*5970T>C (n.*5970T>C)
c.2835T>C
c.851T>C
c.2506T>C (n.2506T>C)
c.4148T>C
c.2228T>C (n.2228T>C)
c.2518T>C
c.6806T>C (p.Ile2269Thr)
n.3045T>C
c.2744T>C (p.Ile915Thr)
n.268T>C
c.4357T>C
n.3742T>C
c.5858T>C (p.Ile1953Thr)
n.485-8607A>G
c.3977T>C (p.Ile1326Thr)
c.3323T>C (p.Ile1108Thr)
12g.40363434T>GCA384413209LRRK2c.7061T>G (p.Ile2354Ser)
c.858T>G
c.*5970T>G (n.*5970T>G)
c.2835T>G
c.851T>G
c.2506T>G (n.2506T>G)
c.4148T>G
c.2228T>G (n.2228T>G)
c.2518T>G
c.6806T>G (p.Ile2269Ser)
n.3045T>G
c.2744T>G (p.Ile915Ser)
n.268T>G
c.4357T>G
n.3742T>G
c.5858T>G (p.Ile1953Ser)
n.485-8607A>C
c.3977T>G (p.Ile1326Ser)
c.3323T>G (p.Ile1108Ser)
12g.40363435C>ACA479247239LRRK2c.7062C>A (p.Ile2354=)
c.859C>A
c.*5971C>A (n.*5971C>A)
c.2836C>A
c.852C>A
c.2507C>A (n.2507C>A)
c.4149C>A
c.2229C>A (n.2229C>A)
c.2519C>A
c.6807C>A (p.Ile2269=)
n.3046C>A
c.2745C>A (p.Ile915=)
n.269C>A
c.4358C>A
n.3743C>A
c.5859C>A (p.Ile1953=)
n.485-8608G>T
c.3978C>A (p.Ile1326=)
c.3324C>A (p.Ile1108=)
gnomAD v4
12g.40363435C=CA2031025778LRRK2c.7062C= (p.Ile2354=)
c.859C=
c.*5971C= (n.*5971C=)
c.2836C=
c.852C=
c.2507C= (n.2507C=)
c.4149C=
c.2229C= (n.2229C=)
c.2519C=
c.6807C= (p.Ile2269=)
n.3046C=
c.2745C= (p.Ile915=)
n.269C=
c.4358C=
n.3743C=
c.5859C= (p.Ile1953=)
n.485-8608G=
c.3978C= (p.Ile1326=)
c.3324C= (p.Ile1108=)
12g.40363435C>GCA384413214LRRK2c.7062C>G (p.Ile2354Met)
c.859C>G
c.*5971C>G (n.*5971C>G)
c.2836C>G
c.852C>G
c.2507C>G (n.2507C>G)
c.4149C>G
c.2229C>G (n.2229C>G)
c.2519C>G
c.6807C>G (p.Ile2269Met)
n.3046C>G
c.2745C>G (p.Ile915Met)
n.269C>G
c.4358C>G
n.3743C>G
c.5859C>G (p.Ile1953Met)
n.485-8608G>C
c.3978C>G (p.Ile1326Met)
c.3324C>G (p.Ile1108Met)
12g.40363435C>TCA6514843LRRK2c.7062C>T (p.Ile2354=)
c.859C>T
c.*5971C>T (n.*5971C>T)
c.2836C>T
c.852C>T
c.2507C>T (n.2507C>T)
c.4149C>T
c.2229C>T (n.2229C>T)
c.2519C>T
c.6807C>T (p.Ile2269=)
n.3046C>T
c.2745C>T (p.Ile915=)
n.269C>T
c.4358C>T
n.3743C>T
c.5859C>T (p.Ile1953=)
n.485-8608G>A
c.3978C>T (p.Ile1326=)
c.3324C>T (p.Ile1108=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.40363436A=CA2031025783LRRK2c.7063A= (p.Ile2355=)
c.860A=
c.*5972A= (n.*5972A=)
c.2837A=
c.853A=
c.2508A= (n.2508A=)
c.4150A=
c.2230A= (n.2230A=)
c.2520A=
c.6808A= (p.Ile2270=)
n.3047A=
c.2746A= (p.Ile916=)
n.270A=
c.4359A=
n.3744A=
c.5860A= (p.Ile1954=)
n.485-8609T=
c.3979A= (p.Ile1327=)
c.3325A= (p.Ile1109=)
12g.40363436A>CCA384413215LRRK2c.7063A>C (p.Ile2355Leu)
c.860A>C
c.*5972A>C (n.*5972A>C)
c.2837A>C
c.853A>C
c.2508A>C (n.2508A>C)
c.4150A>C
c.2230A>C (n.2230A>C)
c.2520A>C
c.6808A>C (p.Ile2270Leu)
n.3047A>C
c.2746A>C (p.Ile916Leu)
n.270A>C
c.4359A>C
n.3744A>C
c.5860A>C (p.Ile1954Leu)
n.485-8609T>G
c.3979A>C (p.Ile1327Leu)
c.3325A>C (p.Ile1109Leu)
dbSNP gnomAD v3 gnomAD v4
12g.40363436A>GCA6514844LRRK2c.7063A>G (p.Ile2355Val)
c.860A>G
c.*5972A>G (n.*5972A>G)
c.2837A>G
c.853A>G
c.2508A>G (n.2508A>G)
c.4150A>G
c.2230A>G (n.2230A>G)
c.2520A>G
c.6808A>G (p.Ile2270Val)
n.3047A>G
c.2746A>G (p.Ile916Val)
n.270A>G
c.4359A>G
n.3744A>G
c.5860A>G (p.Ile1954Val)
n.485-8609T>C
c.3979A>G (p.Ile1327Val)
c.3325A>G (p.Ile1109Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.40363436A>TCA384413218LRRK2c.7063A>T (p.Ile2355Leu)
c.860A>T
c.*5972A>T (n.*5972A>T)
c.2837A>T
c.853A>T
c.2508A>T (n.2508A>T)
c.4150A>T
c.2230A>T (n.2230A>T)
c.2520A>T
c.6808A>T (p.Ile2270Leu)
n.3047A>T
c.2746A>T (p.Ile916Leu)
n.270A>T
c.4359A>T
n.3744A>T
c.5860A>T (p.Ile1954Leu)
n.485-8609T>A
c.3979A>T (p.Ile1327Leu)
c.3325A>T (p.Ile1109Leu)
12g.40363437T>ACA384413222LRRK2c.7064T>A (p.Ile2355Lys)
c.861T>A
c.*5973T>A (n.*5973T>A)
c.2838T>A
c.854T>A
c.2509T>A (n.2509T>A)
c.4151T>A
c.2231T>A (n.2231T>A)
c.2521T>A
c.6809T>A (p.Ile2270Lys)
n.3048T>A
c.2747T>A (p.Ile916Lys)
n.271T>A
c.4360T>A
n.3745T>A
c.5861T>A (p.Ile1954Lys)
n.485-8610A>T
c.3980T>A (p.Ile1327Lys)
c.3326T>A (p.Ile1109Lys)
gnomAD v4
12g.40363437T>CCA384413225LRRK2c.7064T>C (p.Ile2355Thr)
c.861T>C
c.*5973T>C (n.*5973T>C)
c.2838T>C
c.854T>C
c.2509T>C (n.2509T>C)
c.4151T>C
c.2231T>C (n.2231T>C)
c.2521T>C
c.6809T>C (p.Ile2270Thr)
n.3048T>C
c.2747T>C (p.Ile916Thr)
n.271T>C
c.4360T>C
n.3745T>C
c.5861T>C (p.Ile1954Thr)
n.485-8610A>G
c.3980T>C (p.Ile1327Thr)
c.3326T>C (p.Ile1109Thr)
dbSNP gnomAD v3 gnomAD v4
12g.40363437T>GCA384413227LRRK2c.7064T>G (p.Ile2355Arg)
c.861T>G
c.*5973T>G (n.*5973T>G)
c.2838T>G
c.854T>G
c.2509T>G (n.2509T>G)
c.4151T>G
c.2231T>G (n.2231T>G)
c.2521T>G
c.6809T>G (p.Ile2270Arg)
n.3048T>G
c.2747T>G (p.Ile916Arg)
n.271T>G
c.4360T>G
n.3745T>G
c.5861T>G (p.Ile1954Arg)
n.485-8610A>C
c.3980T>G (p.Ile1327Arg)
c.3326T>G (p.Ile1109Arg)
12g.40363437T=CA2031025792LRRK2c.7064T= (p.Ile2355=)
c.861T=
c.*5973T= (n.*5973T=)
c.2838T=
c.854T=
c.2509T= (n.2509T=)
c.4151T=
c.2231T= (n.2231T=)
c.2521T=
c.6809T= (p.Ile2270=)
n.3048T=
c.2747T= (p.Ile916=)
n.271T=
c.4360T=
n.3745T=
c.5861T= (p.Ile1954=)
n.485-8610A=
c.3980T= (p.Ile1327=)
c.3326T= (p.Ile1109=)
12g.40363438A=CA2031025799LRRK2c.7065A= (p.Ile2355=)
c.862A=
c.*5974A= (n.*5974A=)
c.2839A=
c.855A=
c.2510A= (n.2510A=)
c.4152A=
c.2232A= (n.2232A=)
c.2522A=
c.6810A= (p.Ile2270=)
n.3049A=
c.2748A= (p.Ile916=)
n.272A=
c.4361A=
n.3746A=
c.5862A= (p.Ile1954=)
n.485-8611T=
c.3981A= (p.Ile1327=)
c.3327A= (p.Ile1109=)
12g.40363438A>CCA479247250LRRK2c.7065A>C (p.Ile2355=)
c.862A>C
c.*5974A>C (n.*5974A>C)
c.2839A>C
c.855A>C
c.2510A>C (n.2510A>C)
c.4152A>C
c.2232A>C (n.2232A>C)
c.2522A>C
c.6810A>C (p.Ile2270=)
n.3049A>C
c.2748A>C (p.Ile916=)
n.272A>C
c.4361A>C
n.3746A>C
c.5862A>C (p.Ile1954=)
n.485-8611T>G
c.3981A>C (p.Ile1327=)
c.3327A>C (p.Ile1109=)
12g.40363438A>GCA384413230LRRK2c.7065A>G (p.Ile2355Met)
c.862A>G
c.*5974A>G (n.*5974A>G)
c.2839A>G
c.855A>G
c.2510A>G (n.2510A>G)
c.4152A>G
c.2232A>G (n.2232A>G)
c.2522A>G
c.6810A>G (p.Ile2270Met)
n.3049A>G
c.2748A>G (p.Ile916Met)
n.272A>G
c.4361A>G
n.3746A>G
c.5862A>G (p.Ile1954Met)
n.485-8611T>C
c.3981A>G (p.Ile1327Met)
c.3327A>G (p.Ile1109Met)
ClinVar dbSNP gnomAD v2 gnomAD v4
12g.40363438A>TCA479247251LRRK2c.7065A>T (p.Ile2355=)
c.862A>T
c.*5974A>T (n.*5974A>T)
c.2839A>T
c.855A>T
c.2510A>T (n.2510A>T)
c.4152A>T
c.2232A>T (n.2232A>T)
c.2522A>T
c.6810A>T (p.Ile2270=)
n.3049A>T
c.2748A>T (p.Ile916=)
n.272A>T
c.4361A>T
n.3746A>T
c.5862A>T (p.Ile1954=)
n.485-8611T>A
c.3981A>T (p.Ile1327=)
c.3327A>T (p.Ile1109=)
12g.40363438_40363440delinsAACCA2031025800LRRK2c.7065_7067delinsAAC (p.Ile2355=)
c.862_864delinsAAC
c.*5974_*5976delinsAAC (n.*5974_*5976delinsAAC)
c.2839_2841delinsAAC
c.855_857delinsAAC
c.2510_2512delinsAAC (n.2510_2512delinsAAC)
c.4152_4154delinsAAC
c.2232_2234delinsAAC (n.2232_2234delinsAAC)
c.2522_2524delinsAAC
c.6810_6812delinsAAC (p.Ile2270=)
n.3049_3051delinsAAC
c.2748_2750delinsAAC (p.Ile916=)
n.272_274delinsAAC
c.4361_4363delinsAAC
n.3746_3748delinsAAC
c.5862_5864delinsAAC (p.Ile1954=)
n.485-8613_485-8611delinsGTT
c.3981_3983delinsAAC (p.Ile1327=)
c.3327_3329delinsAAC (p.Ile1109=)
12g.40363439A=CA2031025806LRRK2c.7066A= (p.Thr2356=)
c.863A=
c.*5975A= (n.*5975A=)
c.2840A=
c.856A=
c.2511A= (n.2511A=)
c.4153A=
c.2233A= (n.2233A=)
c.2523A=
c.6811A= (p.Thr2271=)
n.3050A=
c.2749A= (p.Thr917=)
n.273A=
c.4362A=
n.3747A=
c.5863A= (p.Thr1955=)
n.485-8612T=
c.3982A= (p.Thr1328=)
c.3328A= (p.Thr1110=)
12g.40363439A>CCA384413233LRRK2c.7066A>C (p.Thr2356Pro)
c.863A>C
c.*5975A>C (n.*5975A>C)
c.2840A>C
c.856A>C
c.2511A>C (n.2511A>C)
c.4153A>C
c.2233A>C (n.2233A>C)
c.2523A>C
c.6811A>C (p.Thr2271Pro)
n.3050A>C
c.2749A>C (p.Thr917Pro)
n.273A>C
c.4362A>C
n.3747A>C
c.5863A>C (p.Thr1955Pro)
n.485-8612T>G
c.3982A>C (p.Thr1328Pro)
c.3328A>C (p.Thr1110Pro)
12g.40363439A>GCA384413236LRRK2c.7066A>G (p.Thr2356Ala)
c.863A>G
c.*5975A>G (n.*5975A>G)
c.2840A>G
c.856A>G
c.2511A>G (n.2511A>G)
c.4153A>G
c.2233A>G (n.2233A>G)
c.2523A>G
c.6811A>G (p.Thr2271Ala)
n.3050A>G
c.2749A>G (p.Thr917Ala)
n.273A>G
c.4362A>G
n.3747A>G
c.5863A>G (p.Thr1955Ala)
n.485-8612T>C
c.3982A>G (p.Thr1328Ala)
c.3328A>G (p.Thr1110Ala)
12g.40363439A>TCA384413235LRRK2c.7066A>T (p.Thr2356Ser)
c.863A>T
c.*5975A>T (n.*5975A>T)
c.2840A>T
c.856A>T
c.2511A>T (n.2511A>T)
c.4153A>T
c.2233A>T (n.2233A>T)
c.2523A>T
c.6811A>T (p.Thr2271Ser)
n.3050A>T
c.2749A>T (p.Thr917Ser)
n.273A>T
c.4362A>T
n.3747A>T
c.5863A>T (p.Thr1955Ser)
n.485-8612T>A
c.3982A>T (p.Thr1328Ser)
c.3328A>T (p.Thr1110Ser)
12g.40363440_40363441delCA919070288LRRK2c.7067_7068del (p.Thr2356SerfsTer11)
c.864_865del
c.*5976_*5977del (n.*5976_*5977del)
c.2841_2842del
c.857_858del
c.2512_2513del (n.2512_2513del)
c.4154_4155del
c.2234_2235del (n.2234_2235del)
c.2524_2525del
c.6812_6813del (p.Thr2271SerfsTer11)
n.3051_3052del
c.2750_2751del (p.Thr917SerfsTer11)
n.274_275del
c.4363_4364del
n.3748_3749del
c.5864_5865del (p.Thr1955SerfsTer11)
n.485-8613_485-8612del
c.3983_3984del (p.Thr1328SerfsTer11)
c.3329_3330del (p.Thr1110SerfsTer11)
dbSNP
12g.40363439_40363440insACCA688734216LRRK2c.7066_7067insAC (p.Thr2356AsnfsTer5)
c.863_864insAC
c.*5975_*5976insAC (n.*5975_*5976insAC)
c.2840_2841insAC
c.856_857insAC
c.2511_2512insAC (n.2511_2512insAC)
c.4153_4154insAC
c.2233_2234insAC (n.2233_2234insAC)
c.2523_2524insAC
c.6811_6812insAC (p.Thr2271AsnfsTer5)
n.3050_3051insAC
c.2749_2750insAC (p.Thr917AsnfsTer5)
n.273_274insAC
c.4362_4363insAC
n.3747_3748insAC
c.5863_5864insAC (p.Thr1955AsnfsTer5)
n.485-8613_485-8612insGT
c.3982_3983insAC (p.Thr1328AsnfsTer5)
c.3328_3329insAC (p.Thr1110AsnfsTer5)
12g.40363439_40363440insGTCA235359569LRRK2c.7066_7067insGT (p.Thr2356SerfsTer5)
c.863_864insGT
c.*5975_*5976insGT (n.*5975_*5976insGT)
c.2840_2841insGT
c.856_857insGT
c.2511_2512insGT (n.2511_2512insGT)
c.4153_4154insGT
c.2233_2234insGT (n.2233_2234insGT)
c.2523_2524insGT
c.6811_6812insGT (p.Thr2271SerfsTer5)
n.3050_3051insGT
c.2749_2750insGT (p.Thr917SerfsTer5)
n.273_274insGT
c.4362_4363insGT
n.3747_3748insGT
c.5863_5864insGT (p.Thr1955SerfsTer5)
n.485-8613_485-8612insAC
c.3982_3983insGT (p.Thr1328SerfsTer5)
c.3328_3329insGT (p.Thr1110SerfsTer5)
dbSNP
12g.40363440C>ACA384413238LRRK2c.7067C>A (p.Thr2356Lys)
c.864C>A
c.*5976C>A (n.*5976C>A)
c.2841C>A
c.857C>A
c.2512C>A (n.2512C>A)
c.4154C>A
c.2234C>A (n.2234C>A)
c.2524C>A
c.6812C>A (p.Thr2271Lys)
n.3051C>A
c.2750C>A (p.Thr917Lys)
n.274C>A
c.4363C>A
n.3748C>A
c.5864C>A (p.Thr1955Lys)
n.485-8613G>T
c.3983C>A (p.Thr1328Lys)
c.3329C>A (p.Thr1110Lys)
12g.40363440C=CA2031025822LRRK2c.7067C= (p.Thr2356=)
c.864C=
c.*5976C= (n.*5976C=)
c.2841C=
c.857C=
c.2512C= (n.2512C=)
c.4154C=
c.2234C= (n.2234C=)
c.2524C=
c.6812C= (p.Thr2271=)
n.3051C=
c.2750C= (p.Thr917=)
n.274C=
c.4363C=
n.3748C=
c.5864C= (p.Thr1955=)
n.485-8613G=
c.3983C= (p.Thr1328=)
c.3329C= (p.Thr1110=)
12g.40363440C>GCA384413239LRRK2c.7067C>G (p.Thr2356Arg)
c.864C>G
c.*5976C>G (n.*5976C>G)
c.2841C>G
c.857C>G
c.2512C>G (n.2512C>G)
c.4154C>G
c.2234C>G (n.2234C>G)
c.2524C>G
c.6812C>G (p.Thr2271Arg)
n.3051C>G
c.2750C>G (p.Thr917Arg)
n.274C>G
c.4363C>G
n.3748C>G
c.5864C>G (p.Thr1955Arg)
n.485-8613G>C
c.3983C>G (p.Thr1328Arg)
c.3329C>G (p.Thr1110Arg)
12g.40363440C>TCA343673LRRK2c.7067C>T (p.Thr2356Ile)
c.864C>T
c.*5976C>T (n.*5976C>T)
c.2841C>T
c.857C>T
c.2512C>T (n.2512C>T)
c.4154C>T
c.2234C>T (n.2234C>T)
c.2524C>T
c.6812C>T (p.Thr2271Ile)
n.3051C>T
c.2750C>T (p.Thr917Ile)
n.274C>T
c.4363C>T
n.3748C>T
c.5864C>T (p.Thr1955Ile)
n.485-8613G>A
c.3983C>T (p.Thr1328Ile)
c.3329C>T (p.Thr1110Ile)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.40363441A>CCA479247258LRRK2c.7068A>C (p.Thr2356=)
c.865A>C
c.*5977A>C (n.*5977A>C)
c.2842A>C
c.858A>C
c.2513A>C (n.2513A>C)
c.4155A>C
c.2235A>C (n.2235A>C)
c.2525A>C
c.6813A>C (p.Thr2271=)
n.3052A>C
c.2751A>C (p.Thr917=)
n.275A>C
c.4364A>C
n.3749A>C
c.5865A>C (p.Thr1955=)
n.485-8614T>G
c.3984A>C (p.Thr1328=)
c.3330A>C (p.Thr1110=)
12g.40363441A>GCA479247259LRRK2c.7068A>G (p.Thr2356=)
c.865A>G
c.*5977A>G (n.*5977A>G)
c.2842A>G
c.858A>G
c.2513A>G (n.2513A>G)
c.4155A>G
c.2235A>G (n.2235A>G)
c.2525A>G
c.6813A>G (p.Thr2271=)
n.3052A>G
c.2751A>G (p.Thr917=)
n.275A>G
c.4364A>G
n.3749A>G
c.5865A>G (p.Thr1955=)
n.485-8614T>C
c.3984A>G (p.Thr1328=)
c.3330A>G (p.Thr1110=)
12g.40363441A>TCA479247260LRRK2c.7068A>T (p.Thr2356=)
c.865A>T
c.*5977A>T (n.*5977A>T)
c.2842A>T
c.858A>T
c.2513A>T (n.2513A>T)
c.4155A>T
c.2235A>T (n.2235A>T)
c.2525A>T
c.6813A>T (p.Thr2271=)
n.3052A>T
c.2751A>T (p.Thr917=)
n.275A>T
c.4364A>T
n.3749A>T
c.5865A>T (p.Thr1955=)
n.485-8614T>A
c.3984A>T (p.Thr1328=)
c.3330A>T (p.Thr1110=)
ClinVar
12g.40363442G>ACA6514845LRRK2c.7069G>A (p.Val2357Met)
c.866G>A
c.*5978G>A (n.*5978G>A)
c.2843G>A
c.859G>A
c.2514G>A (n.2514G>A)
c.4156G>A
c.2236G>A (n.2236G>A)
c.2526G>A
c.6814G>A (p.Val2272Met)
n.3053G>A
c.2752G>A (p.Val918Met)
n.276G>A
c.4365G>A
n.3750G>A
c.5866G>A (p.Val1956Met)
n.485-8615C>T
c.3985G>A (p.Val1329Met)
c.3331G>A (p.Val1111Met)
dbSNP ExAC gnomAD v2 gnomAD v4
12g.40363442G>CCA384413242LRRK2c.7069G>C (p.Val2357Leu)
c.866G>C
c.*5978G>C (n.*5978G>C)
c.2843G>C
c.859G>C
c.2514G>C (n.2514G>C)
c.4156G>C
c.2236G>C (n.2236G>C)
c.2526G>C
c.6814G>C (p.Val2272Leu)
n.3053G>C
c.2752G>C (p.Val918Leu)
n.276G>C
c.4365G>C
n.3750G>C
c.5866G>C (p.Val1956Leu)
n.485-8615C>G
c.3985G>C (p.Val1329Leu)
c.3331G>C (p.Val1111Leu)
ClinVar
12g.40363442G=CA2031025836LRRK2c.7069G= (p.Val2357=)
c.866G=
c.*5978G= (n.*5978G=)
c.2843G=
c.859G=
c.2514G= (n.2514G=)
c.4156G=
c.2236G= (n.2236G=)
c.2526G=
c.6814G= (p.Val2272=)
n.3053G=
c.2752G= (p.Val918=)
n.276G=
c.4365G=
n.3750G=
c.5866G= (p.Val1956=)
n.485-8615C=
c.3985G= (p.Val1329=)
c.3331G= (p.Val1111=)
12g.40363442G>TCA384413241LRRK2c.7069G>T (p.Val2357Leu)
c.866G>T
c.*5978G>T (n.*5978G>T)
c.2843G>T
c.859G>T
c.2514G>T (n.2514G>T)
c.4156G>T
c.2236G>T (n.2236G>T)
c.2526G>T
c.6814G>T (p.Val2272Leu)
n.3053G>T
c.2752G>T (p.Val918Leu)
n.276G>T
c.4365G>T
n.3750G>T
c.5866G>T (p.Val1956Leu)
n.485-8615C>A
c.3985G>T (p.Val1329Leu)
c.3331G>T (p.Val1111Leu)
gnomAD v4
12g.40363443T>ACA384413243LRRK2c.7070T>A (p.Val2357Glu)
c.867T>A
c.*5979T>A (n.*5979T>A)
c.2844T>A
c.860T>A
c.2515T>A (n.2515T>A)
c.4157T>A
c.2237T>A (n.2237T>A)
c.2527T>A
c.6815T>A (p.Val2272Glu)
n.3054T>A
c.2753T>A (p.Val918Glu)
n.277T>A
c.4366T>A
n.3751T>A
c.5867T>A (p.Val1956Glu)
n.485-8616A>T
c.3986T>A (p.Val1329Glu)
c.3332T>A (p.Val1111Glu)
12g.40363443T>CCA6514846LRRK2c.7070T>C (p.Val2357Ala)
c.867T>C
c.*5979T>C (n.*5979T>C)
c.2844T>C
c.860T>C
c.2515T>C (n.2515T>C)
c.4157T>C
c.2237T>C (n.2237T>C)
c.2527T>C
c.6815T>C (p.Val2272Ala)
n.3054T>C
c.2753T>C (p.Val918Ala)
n.277T>C
c.4366T>C
n.3751T>C
c.5867T>C (p.Val1956Ala)
n.485-8616A>G
c.3986T>C (p.Val1329Ala)
c.3332T>C (p.Val1111Ala)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.40363443T>GCA384413245LRRK2c.7070T>G (p.Val2357Gly)
c.867T>G
c.*5979T>G (n.*5979T>G)
c.2844T>G
c.860T>G
c.2515T>G (n.2515T>G)
c.4157T>G
c.2237T>G (n.2237T>G)
c.2527T>G
c.6815T>G (p.Val2272Gly)
n.3054T>G
c.2753T>G (p.Val918Gly)
n.277T>G
c.4366T>G
n.3751T>G
c.5867T>G (p.Val1956Gly)
n.485-8616A>C
c.3986T>G (p.Val1329Gly)
c.3332T>G (p.Val1111Gly)
12g.40363443T=CA2031025838LRRK2c.7070T= (p.Val2357=)
c.867T=
c.*5979T= (n.*5979T=)
c.2844T=
c.860T=
c.2515T= (n.2515T=)
c.4157T=
c.2237T= (n.2237T=)
c.2527T=
c.6815T= (p.Val2272=)
n.3054T=
c.2753T= (p.Val918=)
n.277T=
c.4366T=
n.3751T=
c.5867T= (p.Val1956=)
n.485-8616A=
c.3986T= (p.Val1329=)
c.3332T= (p.Val1111=)

Number of alleles fetched