Chr Mutation (hg38) CAid Gene Transcript Linkouts
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
12g.40340416G>TCA6514597LRRK2c.6071G>T (p.Cys2024Phe)
c.4868G>T (p.Cys1623Phe)
c.2987G>T (p.Cys996Phe)
c.2333G>T (p.Cys778Phe)
n.3367G>T
n.2752G>T
dbSNP ExAC gnomAD
12g.40340417C>ACA384404038LRRK2c.6072C>A (p.Cys2024Ter)
c.4869C>A (p.Cys1623Ter)
c.2988C>A (p.Cys996Ter)
c.2334C>A (p.Cys778Ter)
n.3368C>A
n.2753C>A
12g.40340417C>GCA384404040LRRK2c.6072C>G (p.Cys2024Trp)
c.4869C>G (p.Cys1623Trp)
c.2988C>G (p.Cys996Trp)
c.2334C>G (p.Cys778Trp)
n.3368C>G
n.2753C>G
12g.40340417C>TCA479238776LRRK2c.6072C>T (p.Cys2024=)
c.4869C>T (p.Cys1623=)
c.2988C>T (p.Cys996=)
c.2334C>T (p.Cys778=)
n.3368C>T
n.2753C>T
12g.40340418T>ACA384404042LRRK2c.6073T>A (p.Cys2025Ser)
c.4870T>A (p.Cys1624Ser)
c.2989T>A (p.Cys997Ser)
c.2335T>A (p.Cys779Ser)
n.3369T>A
n.2754T>A
12g.40340418T>CCA384404044LRRK2c.6073T>C (p.Cys2025Arg)
c.4870T>C (p.Cys1624Arg)
c.2989T>C (p.Cys997Arg)
c.2335T>C (p.Cys779Arg)
n.3369T>C
n.2754T>C
12g.40340418T>GCA384404045LRRK2c.6073T>G (p.Cys2025Gly)
c.4870T>G (p.Cys1624Gly)
c.2989T>G (p.Cys997Gly)
c.2335T>G (p.Cys779Gly)
n.3369T>G
n.2754T>G
12g.40340419G>ACA384404047LRRK2c.6074G>A (p.Cys2025Tyr)
c.4871G>A (p.Cys1624Tyr)
c.2990G>A (p.Cys997Tyr)
c.2336G>A (p.Cys779Tyr)
n.3370G>A
n.2755G>A
12g.40340419G>CCA384404049LRRK2c.6074G>C (p.Cys2025Ser)
c.4871G>C (p.Cys1624Ser)
c.2990G>C (p.Cys997Ser)
c.2336G>C (p.Cys779Ser)
n.3370G>C
n.2755G>C
12g.40340419G>TCA384404050LRRK2c.6074G>T (p.Cys2025Phe)
c.4871G>T (p.Cys1624Phe)
c.2990G>T (p.Cys997Phe)
c.2336G>T (p.Cys779Phe)
n.3370G>T
n.2755G>T
12g.40340420T>ACA384404058LRRK2c.6075T>A (p.Cys2025Ter)
c.4872T>A (p.Cys1624Ter)
c.2991T>A (p.Cys997Ter)
c.2337T>A (p.Cys779Ter)
n.3371T>A
n.2756T>A
12g.40340420T>CCA479238784LRRK2c.6075T>C (p.Cys2025=)
c.4872T>C (p.Cys1624=)
c.2991T>C (p.Cys997=)
c.2337T>C (p.Cys779=)
n.3371T>C
n.2756T>C
12g.40340420T>GCA384404060LRRK2c.6075T>G (p.Cys2025Trp)
c.4872T>G (p.Cys1624Trp)
c.2991T>G (p.Cys997Trp)
c.2337T>G (p.Cys779Trp)
n.3371T>G
n.2756T>G
12g.40340421A>CCA479238787LRRK2c.6076A>C (p.Arg2026=)
c.4873A>C (p.Arg1625=)
c.2992A>C (p.Arg998=)
c.2338A>C (p.Arg780=)
n.3372A>C
n.2757A>C
12g.40340421A>GCA384404062LRRK2c.6076A>G (p.Arg2026Gly)
c.4873A>G (p.Arg1625Gly)
c.2992A>G (p.Arg998Gly)
c.2338A>G (p.Arg780Gly)
n.3372A>G
n.2757A>G
12g.40340421A>TCA384404069LRRK2c.6076A>T (p.Arg2026Ter)
c.4873A>T (p.Arg1625Ter)
c.2992A>T (p.Arg998Ter)
c.2338A>T (p.Arg780Ter)
n.3372A>T
n.2757A>T
12g.40340422G>ACA384404072LRRK2c.6077G>A (p.Arg2026Lys)
c.4874G>A (p.Arg1625Lys)
c.2993G>A (p.Arg998Lys)
c.2339G>A (p.Arg780Lys)
n.3373G>A
n.2758G>A
COSMIC COSMIC
12g.40340422G>CCA384404074LRRK2c.6077G>C (p.Arg2026Thr)
c.4874G>C (p.Arg1625Thr)
c.2993G>C (p.Arg998Thr)
c.2339G>C (p.Arg780Thr)
n.3373G>C
n.2758G>C
12g.40340422G>TCA384404076LRRK2c.6077G>T (p.Arg2026Ile)
c.4874G>T (p.Arg1625Ile)
c.2993G>T (p.Arg998Ile)
c.2339G>T (p.Arg780Ile)
n.3373G>T
n.2758G>T
12g.40340423A>CCA384404078LRRK2c.6078A>C (p.Arg2026Ser)
c.4875A>C (p.Arg1625Ser)
c.2994A>C (p.Arg998Ser)
c.2340A>C (p.Arg780Ser)
n.3374A>C
n.2759A>C
12g.40340423A>GCA479238793LRRK2c.6078A>G (p.Arg2026=)
c.4875A>G (p.Arg1625=)
c.2994A>G (p.Arg998=)
c.2340A>G (p.Arg780=)
n.3374A>G
n.2759A>G

Number of alleles fetched