Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.40298281_40298282delinsTACA2030982777LRRK2c.3135_3136delinsTA (p.Asn1045=)
c.*2044_*2045delinsTA (n.*2044_*2045delinsTA)
c.2880_2881delinsTA (p.Asn960=)
c.179_180delinsTA
c.1932_1933delinsTA (p.Asn644=)
c.51_52delinsTA (p.Asn17=)
n.3377_3378delinsTA
12g.40298282A>CCA384414154LRRK2c.3136A>C (p.Lys1046Gln)
c.*2045A>C (n.*2045A>C)
c.2881A>C (p.Lys961Gln)
c.180A>C
c.1933A>C (p.Lys645Gln)
c.52A>C (p.Lys18Gln)
n.3378A>C
12g.40298282A>GCA384414156LRRK2c.3136A>G (p.Lys1046Glu)
c.*2045A>G (n.*2045A>G)
c.2881A>G (p.Lys961Glu)
c.180A>G
c.1933A>G (p.Lys645Glu)
c.52A>G (p.Lys18Glu)
n.3378A>G
12g.40298282A>TCA384414158LRRK2c.3136A>T (p.Lys1046Ter)
c.*2045A>T (n.*2045A>T)
c.2881A>T (p.Lys961Ter)
c.180A>T
c.1933A>T (p.Lys645Ter)
c.52A>T (p.Lys18Ter)
n.3378A>T
12g.40298284delCA604810345LRRK2c.3138del (p.Lys1046AsnfsTer10)
c.*2047del (n.*2047del)
c.2883del (p.Lys961AsnfsTer10)
c.182del
c.1935del (p.Lys645AsnfsTer10)
c.54del (p.Lys18AsnfsTer10)
n.3380del
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.40298283A=CA2030982778LRRK2c.3137A= (p.Lys1046=)
c.*2046A= (n.*2046A=)
c.2882A= (p.Lys961=)
c.181A=
c.1934A= (p.Lys645=)
c.53A= (p.Lys18=)
n.3379A=
12g.40298283A>CCA384414161LRRK2c.3137A>C (p.Lys1046Thr)
c.*2046A>C (n.*2046A>C)
c.2882A>C (p.Lys961Thr)
c.181A>C
c.1934A>C (p.Lys645Thr)
c.53A>C (p.Lys18Thr)
n.3379A>C
ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC
12g.40298283A>GCA384414164LRRK2c.3137A>G (p.Lys1046Arg)
c.*2046A>G (n.*2046A>G)
c.2882A>G (p.Lys961Arg)
c.181A>G
c.1934A>G (p.Lys645Arg)
c.53A>G (p.Lys18Arg)
n.3379A>G
12g.40298283A>TCA384414165LRRK2c.3137A>T (p.Lys1046Ile)
c.*2046A>T (n.*2046A>T)
c.2882A>T (p.Lys961Ile)
c.181A>T
c.1934A>T (p.Lys645Ile)
c.53A>T (p.Lys18Ile)
n.3379A>T
12g.40298284A>CCA384414168LRRK2c.3138A>C (p.Lys1046Asn)
c.*2047A>C (n.*2047A>C)
c.2883A>C (p.Lys961Asn)
c.182A>C
c.1935A>C (p.Lys645Asn)
c.54A>C (p.Lys18Asn)
n.3380A>C
12g.40298284A>GCA479391122LRRK2c.3138A>G (p.Lys1046=)
c.*2047A>G (n.*2047A>G)
c.2883A>G (p.Lys961=)
c.182A>G
c.1935A>G (p.Lys645=)
c.54A>G (p.Lys18=)
n.3380A>G
gnomAD v4
12g.40298284A>TCA384414169LRRK2c.3138A>T (p.Lys1046Asn)
c.*2047A>T (n.*2047A>T)
c.2883A>T (p.Lys961Asn)
c.182A>T
c.1935A>T (p.Lys645Asn)
c.54A>T (p.Lys18Asn)
n.3380A>T
ClinVar gnomAD v4
12g.40298285T>ACA384414175LRRK2c.3139T>A (p.Phe1047Ile)
c.*2048T>A (n.*2048T>A)
c.2884T>A (p.Phe962Ile)
c.183T>A
c.1936T>A (p.Phe646Ile)
c.55T>A (p.Phe19Ile)
n.3381T>A
12g.40298285T>CCA384414173LRRK2c.3139T>C (p.Phe1047Leu)
c.*2048T>C (n.*2048T>C)
c.2884T>C (p.Phe962Leu)
c.183T>C
c.1936T>C (p.Phe646Leu)
c.55T>C (p.Phe19Leu)
n.3381T>C
12g.40298285T>GCA384414172LRRK2c.3139T>G (p.Phe1047Val)
c.*2048T>G (n.*2048T>G)
c.2884T>G (p.Phe962Val)
c.183T>G
c.1936T>G (p.Phe646Val)
c.55T>G (p.Phe19Val)
n.3381T>G
dbSNP
12g.40298285T=CA2030982779LRRK2c.3139T= (p.Phe1047=)
c.*2048T= (n.*2048T=)
c.2884T= (p.Phe962=)
c.183T=
c.1936T= (p.Phe646=)
c.55T= (p.Phe19=)
n.3381T=
12g.40298286T>ACA384414179LRRK2c.3140T>A (p.Phe1047Tyr)
c.*2049T>A (n.*2049T>A)
c.2885T>A (p.Phe962Tyr)
c.184T>A
c.1937T>A (p.Phe646Tyr)
c.56T>A (p.Phe19Tyr)
n.3382T>A
12g.40298286T>CCA384414177LRRK2c.3140T>C (p.Phe1047Ser)
c.*2049T>C (n.*2049T>C)
c.2885T>C (p.Phe962Ser)
c.184T>C
c.1937T>C (p.Phe646Ser)
c.56T>C (p.Phe19Ser)
n.3382T>C
12g.40298286T>GCA384414178LRRK2c.3140T>G (p.Phe1047Cys)
c.*2049T>G (n.*2049T>G)
c.2885T>G (p.Phe962Cys)
c.184T>G
c.1937T>G (p.Phe646Cys)
c.56T>G (p.Phe19Cys)
n.3382T>G
12g.40298287T>ACA384414181LRRK2c.3141T>A (p.Phe1047Leu)
c.*2050T>A (n.*2050T>A)
c.2886T>A (p.Phe962Leu)
c.185T>A
c.1938T>A (p.Phe646Leu)
c.57T>A (p.Phe19Leu)
n.3383T>A
12g.40298287T>CCA479391124LRRK2c.3141T>C (p.Phe1047=)
c.*2050T>C (n.*2050T>C)
c.2886T>C (p.Phe962=)
c.185T>C
c.1938T>C (p.Phe646=)
c.57T>C (p.Phe19=)
n.3383T>C
12g.40298287T>GCA384414183LRRK2c.3141T>G (p.Phe1047Leu)
c.*2050T>G (n.*2050T>G)
c.2886T>G (p.Phe962Leu)
c.185T>G
c.1938T>G (p.Phe646Leu)
c.57T>G (p.Phe19Leu)
n.3383T>G
12g.40298288A>CCA384414186LRRK2c.3142A>C (p.Thr1048Pro)
c.*2051A>C (n.*2051A>C)
c.2887A>C (p.Thr963Pro)
c.186A>C
c.1939A>C (p.Thr647Pro)
c.58A>C (p.Thr20Pro)
n.3384A>C
12g.40298288A>GCA384414188LRRK2c.3142A>G (p.Thr1048Ala)
c.*2051A>G (n.*2051A>G)
c.2887A>G (p.Thr963Ala)
c.186A>G
c.1939A>G (p.Thr647Ala)
c.58A>G (p.Thr20Ala)
n.3384A>G
gnomAD v4
12g.40298288A>TCA384414190LRRK2c.3142A>T (p.Thr1048Ser)
c.*2051A>T (n.*2051A>T)
c.2887A>T (p.Thr963Ser)
c.186A>T
c.1939A>T (p.Thr647Ser)
c.58A>T (p.Thr20Ser)
n.3384A>T
gnomAD v4
12g.40298289C>ACA384414192LRRK2c.3143C>A (p.Thr1048Lys)
c.*2052C>A (n.*2052C>A)
c.2888C>A (p.Thr963Lys)
c.187C>A
c.1940C>A (p.Thr647Lys)
c.59C>A (p.Thr20Lys)
n.3385C>A
12g.40298289C>GCA384414195LRRK2c.3143C>G (p.Thr1048Arg)
c.*2052C>G (n.*2052C>G)
c.2888C>G (p.Thr963Arg)
c.187C>G
c.1940C>G (p.Thr647Arg)
c.59C>G (p.Thr20Arg)
n.3385C>G
COSMIC COSMIC
12g.40298289C>TCA384414198LRRK2c.3143C>T (p.Thr1048Ile)
c.*2052C>T (n.*2052C>T)
c.2888C>T (p.Thr963Ile)
c.187C>T
c.1940C>T (p.Thr647Ile)
c.59C>T (p.Thr20Ile)
n.3385C>T
ClinVar gnomAD v4
12g.40298290A>CCA479391128LRRK2c.3144A>C (p.Thr1048=)
c.*2053A>C (n.*2053A>C)
c.2889A>C (p.Thr963=)
c.188A>C
c.1941A>C (p.Thr647=)
c.60A>C (p.Thr20=)
n.3386A>C
12g.40298290A>GCA479391129LRRK2c.3144A>G (p.Thr1048=)
c.*2053A>G (n.*2053A>G)
c.2889A>G (p.Thr963=)
c.188A>G
c.1941A>G (p.Thr647=)
c.60A>G (p.Thr20=)
n.3386A>G
12g.40298290A>TCA479391130LRRK2c.3144A>T (p.Thr1048=)
c.*2053A>T (n.*2053A>T)
c.2889A>T (p.Thr963=)
c.188A>T
c.1941A>T (p.Thr647=)
c.60A>T (p.Thr20=)
n.3386A>T
12g.40298291T>ACA384414200LRRK2c.3145T>A (p.Ser1049Thr)
c.*2054T>A (n.*2054T>A)
c.2890T>A (p.Ser964Thr)
c.189T>A
c.1942T>A (p.Ser648Thr)
c.61T>A (p.Ser21Thr)
n.3387T>A
12g.40298291T>CCA384414202LRRK2c.3145T>C (p.Ser1049Pro)
c.*2054T>C (n.*2054T>C)
c.2890T>C (p.Ser964Pro)
c.189T>C
c.1942T>C (p.Ser648Pro)
c.61T>C (p.Ser21Pro)
n.3387T>C
12g.40298291T>GCA384414204LRRK2c.3145T>G (p.Ser1049Ala)
c.*2054T>G (n.*2054T>G)
c.2890T>G (p.Ser964Ala)
c.189T>G
c.1942T>G (p.Ser648Ala)
c.61T>G (p.Ser21Ala)
n.3387T>G
12g.40298292C>ACA384414211LRRK2c.3146C>A (p.Ser1049Ter)
c.*2055C>A (n.*2055C>A)
c.2891C>A (p.Ser964Ter)
c.190C>A
c.1943C>A (p.Ser648Ter)
c.62C>A (p.Ser21Ter)
n.3388C>A
COSMIC COSMIC
12g.40298292C>GCA384414207LRRK2c.3146C>G (p.Ser1049Ter)
c.*2055C>G (n.*2055C>G)
c.2891C>G (p.Ser964Ter)
c.190C>G
c.1943C>G (p.Ser648Ter)
c.62C>G (p.Ser21Ter)
n.3388C>G
12g.40298292C>TCA384414209LRRK2c.3146C>T (p.Ser1049Leu)
c.*2055C>T (n.*2055C>T)
c.2891C>T (p.Ser964Leu)
c.190C>T
c.1943C>T (p.Ser648Leu)
c.62C>T (p.Ser21Leu)
n.3388C>T
gnomAD v4
12g.40298293A=CA2030982780LRRK2c.3147A= (p.Ser1049=)
c.*2056A= (n.*2056A=)
c.2892A= (p.Ser964=)
c.191A=
c.1944A= (p.Ser648=)
c.63A= (p.Ser21=)
n.3389A=
12g.40298293A>CCA479391131LRRK2c.3147A>C (p.Ser1049=)
c.*2056A>C (n.*2056A>C)
c.2892A>C (p.Ser964=)
c.191A>C
c.1944A>C (p.Ser648=)
c.63A>C (p.Ser21=)
n.3389A>C
12g.40298293A>GCA479391132LRRK2c.3147A>G (p.Ser1049=)
c.*2056A>G (n.*2056A>G)
c.2892A>G (p.Ser964=)
c.191A>G
c.1944A>G (p.Ser648=)
c.63A>G (p.Ser21=)
n.3389A>G
ClinVar
12g.40298293A>TCA6513848LRRK2c.3147A>T (p.Ser1049=)
c.*2056A>T (n.*2056A>T)
c.2892A>T (p.Ser964=)
c.191A>T
c.1944A>T (p.Ser648=)
c.63A>T (p.Ser21=)
n.3389A>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.40298294T>ACA384414216LRRK2c.3148T>A (p.Phe1050Ile)
c.*2057T>A (n.*2057T>A)
c.2893T>A (p.Phe965Ile)
c.192T>A
c.1945T>A (p.Phe649Ile)
c.64T>A (p.Phe22Ile)
n.3390T>A
12g.40298294T>CCA384414218LRRK2c.3148T>C (p.Phe1050Leu)
c.*2057T>C (n.*2057T>C)
c.2893T>C (p.Phe965Leu)
c.192T>C
c.1945T>C (p.Phe649Leu)
c.64T>C (p.Phe22Leu)
n.3390T>C
gnomAD v4
12g.40298294T>GCA384414221LRRK2c.3148T>G (p.Phe1050Val)
c.*2057T>G (n.*2057T>G)
c.2893T>G (p.Phe965Val)
c.192T>G
c.1945T>G (p.Phe649Val)
c.64T>G (p.Phe22Val)
n.3390T>G
12g.40298295T>ACA384414223LRRK2c.3149T>A (p.Phe1050Tyr)
c.*2058T>A (n.*2058T>A)
c.2894T>A (p.Phe965Tyr)
c.193T>A
c.1946T>A (p.Phe649Tyr)
c.65T>A (p.Phe22Tyr)
n.3391T>A
12g.40298295T>CCA384414224LRRK2c.3149T>C (p.Phe1050Ser)
c.*2058T>C (n.*2058T>C)
c.2894T>C (p.Phe965Ser)
c.193T>C
c.1946T>C (p.Phe649Ser)
c.65T>C (p.Phe22Ser)
n.3391T>C
12g.40298295T>GCA384414225LRRK2c.3149T>G (p.Phe1050Cys)
c.*2058T>G (n.*2058T>G)
c.2894T>G (p.Phe965Cys)
c.193T>G
c.1946T>G (p.Phe649Cys)
c.65T>G (p.Phe22Cys)
n.3391T>G
12g.40298296T>ACA384414228LRRK2c.3150T>A (p.Phe1050Leu)
c.*2059T>A (n.*2059T>A)
c.2895T>A (p.Phe965Leu)
c.194T>A
c.1947T>A (p.Phe649Leu)
c.66T>A (p.Phe22Leu)
n.3392T>A
12g.40298296T>CCA6513849LRRK2c.3150T>C (p.Phe1050=)
c.*2059T>C (n.*2059T>C)
c.2895T>C (p.Phe965=)
c.194T>C
c.1947T>C (p.Phe649=)
c.66T>C (p.Phe22=)
n.3392T>C
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
12g.40298296T>GCA384414238LRRK2c.3150T>G (p.Phe1050Leu)
c.*2059T>G (n.*2059T>G)
c.2895T>G (p.Phe965Leu)
c.194T>G
c.1947T>G (p.Phe649Leu)
c.66T>G (p.Phe22Leu)
n.3392T>G

Number of alleles fetched