Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.40340400G>ACA339926LRRK2c.6055G>A (p.Gly2019Ser)
c.4852G>A (p.Gly1618Ser)
c.2971G>A (p.Gly991Ser)
c.2317G>A (p.Gly773Ser)
n.3351G>A
n.2736G>A
ClinVar dbSNP ExAC gnomAD
12g.40340400G>CCA384403979LRRK2c.6055G>C (p.Gly2019Arg)
c.4852G>C (p.Gly1618Arg)
c.2971G>C (p.Gly991Arg)
c.2317G>C (p.Gly773Arg)
n.3351G>C
n.2736G>C
12g.40340400G>TCA384403980LRRK2c.6055G>T (p.Gly2019Cys)
c.4852G>T (p.Gly1618Cys)
c.2971G>T (p.Gly991Cys)
c.2317G>T (p.Gly773Cys)
n.3351G>T
n.2736G>T
12g.40340401G>ACA384403981LRRK2c.6056G>A (p.Gly2019Asp)
c.4853G>A (p.Gly1618Asp)
c.2972G>A (p.Gly991Asp)
c.2318G>A (p.Gly773Asp)
n.3352G>A
n.2737G>A
COSMIC COSMIC
12g.40340401G>CCA384403984LRRK2c.6056G>C (p.Gly2019Ala)
c.4853G>C (p.Gly1618Ala)
c.2972G>C (p.Gly991Ala)
c.2318G>C (p.Gly773Ala)
n.3352G>C
n.2737G>C
12g.40340401G>TCA384403982LRRK2c.6056G>T (p.Gly2019Val)
c.4853G>T (p.Gly1618Val)
c.2972G>T (p.Gly991Val)
c.2318G>T (p.Gly773Val)
n.3352G>T
n.2737G>T
12g.40340402C>ACA479238735LRRK2c.6057C>A (p.Gly2019=)
c.4854C>A (p.Gly1618=)
c.2973C>A (p.Gly991=)
c.2319C>A (p.Gly773=)
n.3353C>A
n.2738C>A
12g.40340402C>GCA479238737LRRK2c.6057C>G (p.Gly2019=)
c.4854C>G (p.Gly1618=)
c.2973C>G (p.Gly991=)
c.2319C>G (p.Gly773=)
n.3353C>G
n.2738C>G
12g.40340402C>TCA479238733LRRK2c.6057C>T (p.Gly2019=)
c.4854C>T (p.Gly1618=)
c.2973C>T (p.Gly991=)
c.2319C>T (p.Gly773=)
n.3353C>T
n.2738C>T
12g.40340403A>CCA384403985LRRK2c.6058A>C (p.Ile2020Leu)
c.4855A>C (p.Ile1619Leu)
c.2974A>C (p.Ile992Leu)
c.2320A>C (p.Ile774Leu)
n.3354A>C
n.2739A>C
12g.40340403A>GCA384403987LRRK2c.6058A>G (p.Ile2020Val)
c.4855A>G (p.Ile1619Val)
c.2974A>G (p.Ile992Val)
c.2320A>G (p.Ile774Val)
n.3354A>G
n.2739A>G
12g.40340403A>TCA384403989LRRK2c.6058A>T (p.Ile2020Phe)
c.4855A>T (p.Ile1619Phe)
c.2974A>T (p.Ile992Phe)
c.2320A>T (p.Ile774Phe)
n.3354A>T
n.2739A>T
12g.40340404T>ACA384403991LRRK2c.6059T>A (p.Ile2020Asn)
c.4856T>A (p.Ile1619Asn)
c.2975T>A (p.Ile992Asn)
c.2321T>A (p.Ile774Asn)
n.3355T>A
n.2740T>A
12g.40340404T>CCA339928LRRK2c.6059T>C (p.Ile2020Thr)
c.4856T>C (p.Ile1619Thr)
c.2975T>C (p.Ile992Thr)
c.2321T>C (p.Ile774Thr)
n.3355T>C
n.2740T>C
ClinVar dbSNP
12g.40340404T>GCA384403993LRRK2c.6059T>G (p.Ile2020Ser)
c.4856T>G (p.Ile1619Ser)
c.2975T>G (p.Ile992Ser)
c.2321T>G (p.Ile774Ser)
n.3355T>G
n.2740T>G
12g.40340405T>ACA479238746LRRK2c.6060T>A (p.Ile2020=)
c.4857T>A (p.Ile1619=)
c.2976T>A (p.Ile992=)
c.2322T>A (p.Ile774=)
n.3356T>A
n.2741T>A
12g.40340405T>CCA479238743LRRK2c.6060T>C (p.Ile2020=)
c.4857T>C (p.Ile1619=)
c.2976T>C (p.Ile992=)
c.2322T>C (p.Ile774=)
n.3356T>C
n.2741T>C
12g.40340405T>GCA384403995LRRK2c.6060T>G (p.Ile2020Met)
c.4857T>G (p.Ile1619Met)
c.2976T>G (p.Ile992Met)
c.2322T>G (p.Ile774Met)
n.3356T>G
n.2741T>G
12g.40340406G>ACA384403997LRRK2c.6061G>A (p.Ala2021Thr)
c.4858G>A (p.Ala1620Thr)
c.2977G>A (p.Ala993Thr)
c.2323G>A (p.Ala775Thr)
n.3357G>A
n.2742G>A
12g.40340406G>CCA384403998LRRK2c.6061G>C (p.Ala2021Pro)
c.4858G>C (p.Ala1620Pro)
c.2977G>C (p.Ala993Pro)
c.2323G>C (p.Ala775Pro)
n.3357G>C
n.2742G>C
12g.40340406G>TCA384403999LRRK2c.6061G>T (p.Ala2021Ser)
c.4858G>T (p.Ala1620Ser)
c.2977G>T (p.Ala993Ser)
c.2323G>T (p.Ala775Ser)
n.3357G>T
n.2742G>T
12g.40340407C>ACA384404000LRRK2c.6062C>A (p.Ala2021Asp)
c.4859C>A (p.Ala1620Asp)
c.2978C>A (p.Ala993Asp)
c.2324C>A (p.Ala775Asp)
n.3358C>A
n.2743C>A
12g.40340407C>GCA384404001LRRK2c.6062C>G (p.Ala2021Gly)
c.4859C>G (p.Ala1620Gly)
c.2978C>G (p.Ala993Gly)
c.2324C>G (p.Ala775Gly)
n.3358C>G
n.2743C>G
12g.40340407C>TCA384404003LRRK2c.6062C>T (p.Ala2021Val)
c.4859C>T (p.Ala1620Val)
c.2978C>T (p.Ala993Val)
c.2324C>T (p.Ala775Val)
n.3358C>T
n.2743C>T
12g.40340408T>ACA479238749LRRK2c.6063T>A (p.Ala2021=)
c.4860T>A (p.Ala1620=)
c.2979T>A (p.Ala993=)
c.2325T>A (p.Ala775=)
n.3359T>A
n.2744T>A
12g.40340408T>CCA479238752LRRK2c.6063T>C (p.Ala2021=)
c.4860T>C (p.Ala1620=)
c.2979T>C (p.Ala993=)
c.2325T>C (p.Ala775=)
n.3359T>C
n.2744T>C
12g.40340408T>GCA479238751LRRK2c.6063T>G (p.Ala2021=)
c.4860T>G (p.Ala1620=)
c.2979T>G (p.Ala993=)
c.2325T>G (p.Ala775=)
n.3359T>G
n.2744T>G
12g.40340409C>ACA384404006LRRK2c.6064C>A (p.Gln2022Lys)
c.4861C>A (p.Gln1621Lys)
c.2980C>A (p.Gln994Lys)
c.2326C>A (p.Gln776Lys)
n.3360C>A
n.2745C>A
12g.40340409C>GCA384404008LRRK2c.6064C>G (p.Gln2022Glu)
c.4861C>G (p.Gln1621Glu)
c.2980C>G (p.Gln994Glu)
c.2326C>G (p.Gln776Glu)
n.3360C>G
n.2745C>G
12g.40340409C>TCA384404005LRRK2c.6064C>T (p.Gln2022Ter)
c.4861C>T (p.Gln1621Ter)
c.2980C>T (p.Gln994Ter)
c.2326C>T (p.Gln776Ter)
n.3360C>T
n.2745C>T
12g.40340410A>CCA384404012LRRK2c.6065A>C (p.Gln2022Pro)
c.4862A>C (p.Gln1621Pro)
c.2981A>C (p.Gln994Pro)
c.2327A>C (p.Gln776Pro)
n.3361A>C
n.2746A>C
12g.40340410A>GCA384404011LRRK2c.6065A>G (p.Gln2022Arg)
c.4862A>G (p.Gln1621Arg)
c.2981A>G (p.Gln994Arg)
c.2327A>G (p.Gln776Arg)
n.3361A>G
n.2746A>G
12g.40340410A>TCA384404013LRRK2c.6065A>T (p.Gln2022Leu)
c.4862A>T (p.Gln1621Leu)
c.2981A>T (p.Gln994Leu)
c.2327A>T (p.Gln776Leu)
n.3361A>T
n.2746A>T
12g.40340411G>ACA6514596LRRK2c.6066G>A (p.Gln2022=)
c.4863G>A (p.Gln1621=)
c.2982G>A (p.Gln994=)
c.2328G>A (p.Gln776=)
n.3362G>A
n.2747G>A
ClinVar dbSNP ExAC gnomAD
12g.40340411G>CCA384404016LRRK2c.6066G>C (p.Gln2022His)
c.4863G>C (p.Gln1621His)
c.2982G>C (p.Gln994His)
c.2328G>C (p.Gln776His)
n.3362G>C
n.2747G>C
12g.40340411G>TCA384404018LRRK2c.6066G>T (p.Gln2022His)
c.4863G>T (p.Gln1621His)
c.2982G>T (p.Gln994His)
c.2328G>T (p.Gln776His)
n.3362G>T
n.2747G>T
12g.40340412T>ACA384404021LRRK2c.6067T>A (p.Tyr2023Asn)
c.4864T>A (p.Tyr1622Asn)
c.2983T>A (p.Tyr995Asn)
c.2329T>A (p.Tyr777Asn)
n.3363T>A
n.2748T>A
12g.40340412T>CCA384404022LRRK2c.6067T>C (p.Tyr2023His)
c.4864T>C (p.Tyr1622His)
c.2983T>C (p.Tyr995His)
c.2329T>C (p.Tyr777His)
n.3363T>C
n.2748T>C
12g.40340412T>GCA384404023LRRK2c.6067T>G (p.Tyr2023Asp)
c.4864T>G (p.Tyr1622Asp)
c.2983T>G (p.Tyr995Asp)
c.2329T>G (p.Tyr777Asp)
n.3363T>G
n.2748T>G
12g.40340413A>CCA384404024LRRK2c.6068A>C (p.Tyr2023Ser)
c.4865A>C (p.Tyr1622Ser)
c.2984A>C (p.Tyr995Ser)
c.2330A>C (p.Tyr777Ser)
n.3364A>C
n.2749A>C
12g.40340413A>GCA384404025LRRK2c.6068A>G (p.Tyr2023Cys)
c.4865A>G (p.Tyr1622Cys)
c.2984A>G (p.Tyr995Cys)
c.2330A>G (p.Tyr777Cys)
n.3364A>G
n.2749A>G
COSMIC COSMIC
12g.40340413A>TCA384404026LRRK2c.6068A>T (p.Tyr2023Phe)
c.4865A>T (p.Tyr1622Phe)
c.2984A>T (p.Tyr995Phe)
c.2330A>T (p.Tyr777Phe)
n.3364A>T
n.2749A>T
12g.40340414C>ACA384404027LRRK2c.6069C>A (p.Tyr2023Ter)
c.4866C>A (p.Tyr1622Ter)
c.2985C>A (p.Tyr995Ter)
c.2331C>A (p.Tyr777Ter)
n.3365C>A
n.2750C>A
12g.40340414C>GCA384404028LRRK2c.6069C>G (p.Tyr2023Ter)
c.4866C>G (p.Tyr1622Ter)
c.2985C>G (p.Tyr995Ter)
c.2331C>G (p.Tyr777Ter)
n.3365C>G
n.2750C>G
12g.40340414C>TCA479238766LRRK2c.6069C>T (p.Tyr2023=)
c.4866C>T (p.Tyr1622=)
c.2985C>T (p.Tyr995=)
c.2331C>T (p.Tyr777=)
n.3365C>T
n.2750C>T
12g.40340415T>ACA384404032LRRK2c.6070T>A (p.Cys2024Ser)
c.4867T>A (p.Cys1623Ser)
c.2986T>A (p.Cys996Ser)
c.2332T>A (p.Cys778Ser)
n.3366T>A
n.2751T>A
12g.40340415T>CCA384404030LRRK2c.6070T>C (p.Cys2024Arg)
c.4867T>C (p.Cys1623Arg)
c.2986T>C (p.Cys996Arg)
c.2332T>C (p.Cys778Arg)
n.3366T>C
n.2751T>C
12g.40340415T>GCA384404029LRRK2c.6070T>G (p.Cys2024Gly)
c.4867T>G (p.Cys1623Gly)
c.2986T>G (p.Cys996Gly)
c.2332T>G (p.Cys778Gly)
n.3366T>G
n.2751T>G
12g.40340416G>ACA384404034LRRK2c.6071G>A (p.Cys2024Tyr)
c.4868G>A (p.Cys1623Tyr)
c.2987G>A (p.Cys996Tyr)
c.2333G>A (p.Cys778Tyr)
n.3367G>A
n.2752G>A
COSMIC COSMIC
12g.40340416G>CCA384404036LRRK2c.6071G>C (p.Cys2024Ser)
c.4868G>C (p.Cys1623Ser)
c.2987G>C (p.Cys996Ser)
c.2333G>C (p.Cys778Ser)
n.3367G>C
n.2752G>C

Number of alleles fetched