Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.189000730_189007456delCA913190215COL3A1c.2185-667_3157-44del
c.2284-667_3256-44del
c.2284-667_2528-598del
ClinVar
2g.189001289_189008107delCA913190216COL3A1c.2185-108_3391del
c.2284-108_3490del
c.2284-108_2581del
ClinVar
2g.189001505_189006012delCA913189729COL3A1c.2239-31_2941-194del
c.2338-31_3040-194del
c.2338-31_2528-2042del
ClinVar
2g.189003975T>ACA2662310060COL3A1c.2563-7T>A (n.2563-7T>A)
c.2662-7T>A (n.2662-7T>A)
c.2527+939T>A (n.2527+939T>A)
gnomAD v4
2g.189003976T>CCA2573134198COL3A1c.2563-6T>C (n.2563-6T>C)
c.2662-6T>C (n.2662-6T>C)
c.2527+940T>C (n.2527+940T>C)
ClinVar dbSNP
2g.189003977T>GCA2577185817COL3A1c.2563-5T>G (n.2563-5T>G)
c.2662-5T>G (n.2662-5T>G)
c.2527+941T>G (n.2527+941T>G)
2g.189003978G>ACA2662310061COL3A1c.2563-4G>A (n.2563-4G>A)
c.2662-4G>A (n.2662-4G>A)
c.2527+942G>A (n.2527+942G>A)
ClinVar gnomAD v4
2g.189003978G>TCA2662310062COL3A1c.2563-4G>T (n.2563-4G>T)
c.2662-4G>T (n.2662-4G>T)
c.2527+942G>T (n.2527+942G>T)
gnomAD v4
2g.189003979T>CCA2662310063COL3A1c.2563-3T>C (n.2563-3T>C)
c.2662-3T>C (n.2662-3T>C)
c.2527+943T>C (n.2527+943T>C)
gnomAD v4
2g.189003980A>CCA349843650COL3A1c.2563-2A>C (n.2563-2A>C)
c.2662-2A>C (n.2662-2A>C)
c.2527+944A>C (n.2527+944A>C)
2g.189003980A>GCA349843651COL3A1c.2563-2A>G (n.2563-2A>G)
c.2662-2A>G (n.2662-2A>G)
c.2527+944A>G (n.2527+944A>G)
2g.189003980A>TCA349843652COL3A1c.2563-2A>T (n.2563-2A>T)
c.2662-2A>T (n.2662-2A>T)
c.2527+944A>T (n.2527+944A>T)
2g.189003981G>ACA349843654COL3A1c.2563-1G>A (n.2563-1G>A)
c.2662-1G>A (n.2662-1G>A)
c.2527+945G>A (n.2527+945G>A)
2g.189003981G>CCA349843656COL3A1c.2563-1G>C (n.2563-1G>C)
c.2662-1G>C (n.2662-1G>C)
c.2527+945G>C (n.2527+945G>C)
2g.189003981G>TCA349843658COL3A1c.2563-1G>T (n.2563-1G>T)
c.2662-1G>T (n.2662-1G>T)
c.2527+945G>T (n.2527+945G>T)
2g.189003982G>ACA349843660COL3A1c.2563G>A (p.Gly855Ser)
c.2662G>A (p.Gly888Ser)
c.2527+946G>A (n.2527+946G>A)
2g.189003982G>CCA349843661COL3A1c.2563G>C (p.Gly855Arg)
c.2662G>C (p.Gly888Arg)
c.2527+946G>C (n.2527+946G>C)
2g.189003982G>TCA349843663COL3A1c.2563G>T (p.Gly855Cys)
c.2662G>T (p.Gly888Cys)
c.2527+946G>T (n.2527+946G>T)
2g.189003983G>ACA349843664COL3A1c.2564G>A (p.Gly855Asp)
c.2663G>A (p.Gly888Asp)
c.2527+947G>A (n.2527+947G>A)
2g.189003983G>CCA349843667COL3A1c.2564G>C (p.Gly855Ala)
c.2663G>C (p.Gly888Ala)
c.2527+947G>C (n.2527+947G>C)
2g.189003983G>TCA349843668COL3A1c.2564G>T (p.Gly855Val)
c.2663G>T (p.Gly888Val)
c.2527+947G>T (n.2527+947G>T)
2g.189003984T>ACA430311840COL3A1c.2565T>A (p.Gly855=)
c.2664T>A (p.Gly888=)
c.2527+948T>A (n.2527+948T>A)
2g.189003984T>CCA430311839COL3A1c.2565T>C (p.Gly855=)
c.2664T>C (p.Gly888=)
c.2527+948T>C (n.2527+948T>C)
2g.189003984T>GCA430311838COL3A1c.2565T>G (p.Gly855=)
c.2664T>G (p.Gly888=)
c.2527+948T>G (n.2527+948T>G)
2g.189003985A=CA1315403010COL3A1c.2566A= (p.Asn856=)
c.2665A= (p.Asn889=)
c.2527+949A= (n.2527+949A=)
2g.189003985A>CCA349843675COL3A1c.2566A>C (p.Asn856His)
c.2665A>C (p.Asn889His)
c.2527+949A>C (n.2527+949A>C)
2g.189003985A>GCA349843671COL3A1c.2566A>G (p.Asn856Asp)
c.2665A>G (p.Asn889Asp)
c.2527+949A>G (n.2527+949A>G)
2g.189003985A>TCA005577COL3A1c.2566A>T (p.Asn856Tyr)
c.2665A>T (p.Asn889Tyr)
c.2527+949A>T (n.2527+949A>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.189003986A=CA1315403011COL3A1c.2567A= (p.Asn856=)
c.2666A= (p.Asn889=)
c.2527+950A= (n.2527+950A=)
2g.189003986A>CCA349843677COL3A1c.2567A>C (p.Asn856Thr)
c.2666A>C (p.Asn889Thr)
c.2527+950A>C (n.2527+950A>C)
dbSNP
2g.189003986A>GCA349843679COL3A1c.2567A>G (p.Asn856Ser)
c.2666A>G (p.Asn889Ser)
c.2527+950A>G (n.2527+950A>G)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.189003986A>TCA349843681COL3A1c.2567A>T (p.Asn856Ile)
c.2666A>T (p.Asn889Ile)
c.2527+950A>T (n.2527+950A>T)
2g.189003987C>ACA075533COL3A1c.2568C>A (p.Asn856Lys)
c.2667C>A (p.Asn889Lys)
c.2527+951C>A (n.2527+951C>A)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.189003987C=CA1315403012COL3A1c.2568C= (p.Asn856=)
c.2667C= (p.Asn889=)
c.2527+951C= (n.2527+951C=)
2g.189003987C>GCA349843684COL3A1c.2568C>G (p.Asn856Lys)
c.2667C>G (p.Asn889Lys)
c.2527+951C>G (n.2527+951C>G)
2g.189003987C>TCA430311841COL3A1c.2568C>T (p.Asn856=)
c.2667C>T (p.Asn889=)
c.2527+951C>T (n.2527+951C>T)
2g.189003988C>ACA349843690COL3A1c.2569C>A (p.Pro857Thr)
c.2668C>A (p.Pro890Thr)
c.2527+952C>A (n.2527+952C>A)
gnomAD v4
2g.189003988C=CA1315403013COL3A1c.2569C= (p.Pro857=)
c.2668C= (p.Pro890=)
c.2527+952C= (n.2527+952C=)
2g.189003988C>GCA349843687COL3A1c.2569C>G (p.Pro857Ala)
c.2668C>G (p.Pro890Ala)
c.2527+952C>G (n.2527+952C>G)
ClinVar dbSNP gnomAD v4
2g.189003988C>TCA005585COL3A1c.2569C>T (p.Pro857Ser)
c.2668C>T (p.Pro890Ser)
c.2527+952C>T (n.2527+952C>T)
ClinVar dbSNP
2g.189003989C>ACA349843692COL3A1c.2570C>A (p.Pro857Gln)
c.2669C>A (p.Pro890Gln)
c.2527+953C>A (n.2527+953C>A)
gnomAD v3 gnomAD v4
2g.189003989C=CA1315403014COL3A1c.2570C= (p.Pro857=)
c.2669C= (p.Pro890=)
c.2527+953C= (n.2527+953C=)
2g.189003989C>GCA075537COL3A1c.2570C>G (p.Pro857Arg)
c.2669C>G (p.Pro890Arg)
c.2527+953C>G (n.2527+953C>G)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.189003989C>TCA62557275COL3A1c.2570C>T (p.Pro857Leu)
c.2669C>T (p.Pro890Leu)
c.2527+953C>T (n.2527+953C>T)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.189003990A>CCA430311844COL3A1c.2571A>C (p.Pro857=)
c.2670A>C (p.Pro890=)
c.2527+954A>C (n.2527+954A>C)
2g.189003990A>GCA430311846COL3A1c.2571A>G (p.Pro857=)
c.2670A>G (p.Pro890=)
c.2527+954A>G (n.2527+954A>G)
2g.189003990A>TCA430311845COL3A1c.2571A>T (p.Pro857=)
c.2670A>T (p.Pro890=)
c.2527+954A>T (n.2527+954A>T)
2g.189003991G>ACA349843697COL3A1c.2572G>A (p.Gly858Arg)
c.2671G>A (p.Gly891Arg)
c.2527+955G>A (n.2527+955G>A)
ClinVar
2g.189003991G>CCA349843699COL3A1c.2572G>C (p.Gly858Arg)
c.2671G>C (p.Gly891Arg)
c.2527+955G>C (n.2527+955G>C)
2g.189003991G>TCA349843701COL3A1c.2572G>T (p.Gly858Ter)
c.2671G>T (p.Gly891Ter)
c.2527+955G>T (n.2527+955G>T)
2g.189003992G>ACA349843708COL3A1c.2573G>A (p.Gly858Glu)
c.2672G>A (p.Gly891Glu)
c.2527+956G>A (n.2527+956G>A)
ClinVar dbSNP
2g.189003992G>CCA349843703COL3A1c.2573G>C (p.Gly858Ala)
c.2672G>C (p.Gly891Ala)
c.2527+956G>C (n.2527+956G>C)
2g.189003992G=CA1315403015COL3A1c.2573G= (p.Gly858=)
c.2672G= (p.Gly891=)
c.2527+956G= (n.2527+956G=)
2g.189003992G>TCA349843706COL3A1c.2573G>T (p.Gly858Val)
c.2672G>T (p.Gly891Val)
c.2527+956G>T (n.2527+956G>T)
2g.189003993A>CCA430311849COL3A1c.2574A>C (p.Gly858=)
c.2673A>C (p.Gly891=)
c.2527+957A>C (n.2527+957A>C)
2g.189003993A>GCA430311850COL3A1c.2574A>G (p.Gly858=)
c.2673A>G (p.Gly891=)
c.2527+957A>G (n.2527+957A>G)
2g.189003993A>TCA430311851COL3A1c.2574A>T (p.Gly858=)
c.2673A>T (p.Gly891=)
c.2527+957A>T (n.2527+957A>T)
2g.189003994C>ACA349843710COL3A1c.2575C>A (p.Pro859Thr)
c.2674C>A (p.Pro892Thr)
c.2527+958C>A (n.2527+958C>A)
2g.189003994C>GCA349843712COL3A1c.2575C>G (p.Pro859Ala)
c.2674C>G (p.Pro892Ala)
c.2527+958C>G (n.2527+958C>G)
2g.189003994C>TCA349843714COL3A1c.2575C>T (p.Pro859Ser)
c.2674C>T (p.Pro892Ser)
c.2527+958C>T (n.2527+958C>T)
COSMIC
2g.189003995C>ACA349843717COL3A1c.2576C>A (p.Pro859His)
c.2675C>A (p.Pro892His)
c.2527+959C>A (n.2527+959C>A)
gnomAD v4
2g.189003995C=CA1315403016COL3A1c.2576C= (p.Pro859=)
c.2675C= (p.Pro892=)
c.2527+959C= (n.2527+959C=)
2g.189003995C>GCA349843718COL3A1c.2576C>G (p.Pro859Arg)
c.2675C>G (p.Pro892Arg)
c.2527+959C>G (n.2527+959C>G)
2g.189003995C>TCA349843720COL3A1c.2576C>T (p.Pro859Leu)
c.2675C>T (p.Pro892Leu)
c.2527+959C>T (n.2527+959C>T)
ClinVar dbSNP gnomAD v4 COSMIC
2g.189003996C>ACA430311857COL3A1c.2577C>A (p.Pro859=)
c.2676C>A (p.Pro892=)
c.2527+960C>A (n.2527+960C>A)
2g.189003996C>GCA430311858COL3A1c.2577C>G (p.Pro859=)
c.2676C>G (p.Pro892=)
c.2527+960C>G (n.2527+960C>G)
2g.189003996C>TCA430311859COL3A1c.2577C>T (p.Pro859=)
c.2676C>T (p.Pro892=)
c.2527+960C>T (n.2527+960C>T)
2g.189003997C>ACA349843723COL3A1c.2578C>A (p.Pro860Thr)
c.2677C>A (p.Pro893Thr)
c.2527+961C>A (n.2527+961C>A)
2g.189003997C>GCA349843724COL3A1c.2578C>G (p.Pro860Ala)
c.2677C>G (p.Pro893Ala)
c.2527+961C>G (n.2527+961C>G)
2g.189003997C>TCA349843725COL3A1c.2578C>T (p.Pro860Ser)
c.2677C>T (p.Pro893Ser)
c.2527+961C>T (n.2527+961C>T)
gnomAD v4
2g.189003998C>ACA349843728COL3A1c.2579C>A (p.Pro860Gln)
c.2678C>A (p.Pro893Gln)
c.2527+962C>A (n.2527+962C>A)
2g.189003998C=CA1315403017COL3A1c.2579C= (p.Pro860=)
c.2678C= (p.Pro893=)
c.2527+962C= (n.2527+962C=)
2g.189003998C>GCA349843730COL3A1c.2579C>G (p.Pro860Arg)
c.2678C>G (p.Pro893Arg)
c.2527+962C>G (n.2527+962C>G)
ClinVar dbSNP gnomAD v4
2g.189003998C>TCA349843732COL3A1c.2579C>T (p.Pro860Leu)
c.2678C>T (p.Pro893Leu)
c.2527+962C>T (n.2527+962C>T)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
2g.189003999A>CCA430311863COL3A1c.2580A>C (p.Pro860=)
c.2679A>C (p.Pro893=)
c.2527+963A>C (n.2527+963A>C)
2g.189003999A>GCA430311865COL3A1c.2580A>G (p.Pro860=)
c.2679A>G (p.Pro893=)
c.2527+963A>G (n.2527+963A>G)
2g.189003999A>TCA430311866COL3A1c.2580A>T (p.Pro860=)
c.2679A>T (p.Pro893=)
c.2527+963A>T (n.2527+963A>T)
2g.189004000G>ACA349843735COL3A1c.2581G>A (p.Gly861Ser)
c.2680G>A (p.Gly894Ser)
c.2527+964G>A (n.2527+964G>A)
2g.189004000G>CCA349843737COL3A1c.2581G>C (p.Gly861Arg)
c.2680G>C (p.Gly894Arg)
c.2527+964G>C (n.2527+964G>C)
2g.189004000G>TCA349843736COL3A1c.2581G>T (p.Gly861Cys)
c.2680G>T (p.Gly894Cys)
c.2527+964G>T (n.2527+964G>T)
2g.189004001G>ACA349843740COL3A1c.2582G>A (p.Gly861Asp)
c.2681G>A (p.Gly894Asp)
c.2527+965G>A (n.2527+965G>A)
2g.189004001G>CCA005598COL3A1c.2582G>C (p.Gly861Ala)
c.2681G>C (p.Gly894Ala)
c.2527+965G>C (n.2527+965G>C)
ClinVar dbSNP gnomAD v4 COSMIC
2g.189004001G=CA1315403018COL3A1c.2582G= (p.Gly861=)
c.2681G= (p.Gly894=)
c.2527+965G= (n.2527+965G=)
2g.189004001G>TCA349843742COL3A1c.2582G>T (p.Gly861Val)
c.2681G>T (p.Gly894Val)
c.2527+965G>T (n.2527+965G>T)
2g.189004002T>ACA430311868COL3A1c.2583T>A (p.Gly861=)
c.2682T>A (p.Gly894=)
c.2527+966T>A (n.2527+966T>A)
2g.189004002T>CCA430311869COL3A1c.2583T>C (p.Gly861=)
c.2682T>C (p.Gly894=)
c.2527+966T>C (n.2527+966T>C)
gnomAD v4
2g.189004002T>GCA430311870COL3A1c.2583T>G (p.Gly861=)
c.2682T>G (p.Gly894=)
c.2527+966T>G (n.2527+966T>G)
2g.189004003C>ACA349843746COL3A1c.2584C>A (p.Pro862Thr)
c.2683C>A (p.Pro895Thr)
c.2527+967C>A (n.2527+967C>A)
2g.189004003C>GCA349843748COL3A1c.2584C>G (p.Pro862Ala)
c.2683C>G (p.Pro895Ala)
c.2527+967C>G (n.2527+967C>G)
2g.189004003C>TCA349843750COL3A1c.2584C>T (p.Pro862Ser)
c.2683C>T (p.Pro895Ser)
c.2527+967C>T (n.2527+967C>T)
2g.189004005delCA2662310064COL3A1c.2586del (p.Ser863AlafsTer?)
c.2685del (p.Ser896AlafsTer?)
c.2527+969del (n.2527+969del)
gnomAD v4
2g.189004004C>ACA349843753COL3A1c.2585C>A (p.Pro862His)
c.2684C>A (p.Pro895His)
c.2527+968C>A (n.2527+968C>A)
2g.189004004C=CA1315403019COL3A1c.2585C= (p.Pro862=)
c.2684C= (p.Pro895=)
c.2527+968C= (n.2527+968C=)
2g.189004004C>GCA349843755COL3A1c.2585C>G (p.Pro862Arg)
c.2684C>G (p.Pro895Arg)
c.2527+968C>G (n.2527+968C>G)
2g.189004004C>TCA349843757COL3A1c.2585C>T (p.Pro862Leu)
c.2684C>T (p.Pro895Leu)
c.2527+968C>T (n.2527+968C>T)
dbSNP gnomAD v2
2g.189004005C>ACA430311872COL3A1c.2586C>A (p.Pro862=)
c.2685C>A (p.Pro895=)
c.2527+969C>A (n.2527+969C>A)
2g.189004005C>GCA430311873COL3A1c.2586C>G (p.Pro862=)
c.2685C>G (p.Pro895=)
c.2527+969C>G (n.2527+969C>G)
2g.189004005C>TCA430311874COL3A1c.2586C>T (p.Pro862=)
c.2685C>T (p.Pro895=)
c.2527+969C>T (n.2527+969C>T)
ClinVar gnomAD v4
2g.189004006A>CCA349843760COL3A1c.2587A>C (p.Ser863Arg)
c.2686A>C (p.Ser896Arg)
c.2527+970A>C (n.2527+970A>C)
2g.189004006A>GCA349843761COL3A1c.2587A>G (p.Ser863Gly)
c.2686A>G (p.Ser896Gly)
c.2527+970A>G (n.2527+970A>G)
2g.189004006A>TCA349843762COL3A1c.2587A>T (p.Ser863Cys)
c.2686A>T (p.Ser896Cys)
c.2527+970A>T (n.2527+970A>T)
2g.189004007G>ACA349843766COL3A1c.2588G>A (p.Ser863Asn)
c.2687G>A (p.Ser896Asn)
c.2527+971G>A (n.2527+971G>A)
dbSNP gnomAD v3 gnomAD v4
2g.189004007G>CCA349843768COL3A1c.2588G>C (p.Ser863Thr)
c.2687G>C (p.Ser896Thr)
c.2527+971G>C (n.2527+971G>C)
2g.189004007G=CA1315403020COL3A1c.2588G= (p.Ser863=)
c.2687G= (p.Ser896=)
c.2527+971G= (n.2527+971G=)
2g.189004007G>TCA349843769COL3A1c.2588G>T (p.Ser863Ile)
c.2687G>T (p.Ser896Ile)
c.2527+971G>T (n.2527+971G>T)
2g.189004008C>ACA349843773COL3A1c.2589C>A (p.Ser863Arg)
c.2688C>A (p.Ser896Arg)
c.2527+972C>A (n.2527+972C>A)
dbSNP COSMIC
2g.189004008C=CA1315403021COL3A1c.2589C= (p.Ser863=)
c.2688C= (p.Ser896=)
c.2527+972C= (n.2527+972C=)
2g.189004008C>GCA349843776COL3A1c.2589C>G (p.Ser863Arg)
c.2688C>G (p.Ser896Arg)
c.2527+972C>G (n.2527+972C>G)
COSMIC
2g.189004008C>TCA62557291COL3A1c.2589C>T (p.Ser863=)
c.2688C>T (p.Ser896=)
c.2527+972C>T (n.2527+972C>T)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.189004009G>ACA005604COL3A1c.2590G>A (p.Gly864Ser)
c.2689G>A (p.Gly897Ser)
c.2527+973G>A (n.2527+973G>A)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.189004009G>CCA349843780COL3A1c.2590G>C (p.Gly864Arg)
c.2689G>C (p.Gly897Arg)
c.2527+973G>C (n.2527+973G>C)
2g.189004009G=CA1315403022COL3A1c.2590G= (p.Gly864=)
c.2689G= (p.Gly897=)
c.2527+973G= (n.2527+973G=)
2g.189004009G>TCA349843781COL3A1c.2590G>T (p.Gly864Cys)
c.2689G>T (p.Gly897Cys)
c.2527+973G>T (n.2527+973G>T)
2g.189004010G>ACA349843784COL3A1c.2591G>A (p.Gly864Asp)
c.2690G>A (p.Gly897Asp)
c.2527+974G>A (n.2527+974G>A)
ClinVar dbSNP
2g.189004010G>CCA349843785COL3A1c.2591G>C (p.Gly864Ala)
c.2690G>C (p.Gly897Ala)
c.2527+974G>C (n.2527+974G>C)
gnomAD v4
2g.189004010G=CA1315403023COL3A1c.2591G= (p.Gly864=)
c.2690G= (p.Gly897=)
c.2527+974G= (n.2527+974G=)
2g.189004010G>TCA349843787COL3A1c.2591G>T (p.Gly864Val)
c.2690G>T (p.Gly897Val)
c.2527+974G>T (n.2527+974G>T)
2g.189004011T>ACA430311880COL3A1c.2592T>A (p.Gly864=)
c.2691T>A (p.Gly897=)
c.2527+975T>A (n.2527+975T>A)
2g.189004011T>CCA430311878COL3A1c.2592T>C (p.Gly864=)
c.2691T>C (p.Gly897=)
c.2527+975T>C (n.2527+975T>C)
2g.189004011T>GCA430311877COL3A1c.2592T>G (p.Gly864=)
c.2691T>G (p.Gly897=)
c.2527+975T>G (n.2527+975T>G)
2g.189004012T>ACA349843790COL3A1c.2593T>A (p.Ser865Thr)
c.2692T>A (p.Ser898Thr)
c.2527+976T>A (n.2527+976T>A)
2g.189004012T>CCA349843792COL3A1c.2593T>C (p.Ser865Pro)
c.2692T>C (p.Ser898Pro)
c.2527+976T>C (n.2527+976T>C)
gnomAD v4
2g.189004012T>GCA349843794COL3A1c.2593T>G (p.Ser865Ala)
c.2692T>G (p.Ser898Ala)
c.2527+976T>G (n.2527+976T>G)
2g.189004013C>ACA349843797COL3A1c.2594C>A (p.Ser865Tyr)
c.2693C>A (p.Ser898Tyr)
c.2527+977C>A (n.2527+977C>A)
2g.189004013C>GCA349843798COL3A1c.2594C>G (p.Ser865Cys)
c.2693C>G (p.Ser898Cys)
c.2527+977C>G (n.2527+977C>G)
2g.189004013C>TCA349843796COL3A1c.2594C>T (p.Ser865Phe)
c.2693C>T (p.Ser898Phe)
c.2527+977C>T (n.2527+977C>T)
2g.189004014T>ACA430311882COL3A1c.2595T>A (p.Ser865=)
c.2694T>A (p.Ser898=)
c.2527+978T>A (n.2527+978T>A)
2g.189004014T>CCA430311883COL3A1c.2595T>C (p.Ser865=)
c.2694T>C (p.Ser898=)
c.2527+978T>C (n.2527+978T>C)
gnomAD v4
2g.189004014T>GCA430311885COL3A1c.2595T>G (p.Ser865=)
c.2694T>G (p.Ser898=)
c.2527+978T>G (n.2527+978T>G)
2g.189004015C>ACA349843800COL3A1c.2596C>A (p.Pro866Thr)
c.2695C>A (p.Pro899Thr)
c.2527+979C>A (n.2527+979C>A)
2g.189004015C>GCA349843802COL3A1c.2596C>G (p.Pro866Ala)
c.2695C>G (p.Pro899Ala)
c.2527+979C>G (n.2527+979C>G)
2g.189004015C>TCA349843804COL3A1c.2596C>T (p.Pro866Ser)
c.2695C>T (p.Pro899Ser)
c.2527+979C>T (n.2527+979C>T)
2g.189004016C>ACA349843805COL3A1c.2597C>A (p.Pro866Gln)
c.2696C>A (p.Pro899Gln)
c.2527+980C>A (n.2527+980C>A)
2g.189004016C>GCA349843807COL3A1c.2597C>G (p.Pro866Arg)
c.2696C>G (p.Pro899Arg)
c.2527+980C>G (n.2527+980C>G)
2g.189004016C>TCA349843809COL3A1c.2597C>T (p.Pro866Leu)
c.2696C>T (p.Pro899Leu)
c.2527+980C>T (n.2527+980C>T)
gnomAD v4
2g.189004017A>CCA430311887COL3A1c.2598A>C (p.Pro866=)
c.2697A>C (p.Pro899=)
c.2527+981A>C (n.2527+981A>C)
2g.189004017A>GCA430311888COL3A1c.2598A>G (p.Pro866=)
c.2697A>G (p.Pro899=)
c.2527+981A>G (n.2527+981A>G)
2g.189004017A>TCA430311889COL3A1c.2598A>T (p.Pro866=)
c.2697A>T (p.Pro899=)
c.2527+981A>T (n.2527+981A>T)
2g.189004018G>ACA349843812COL3A1c.2599G>A (p.Gly867Ser)
c.2698G>A (p.Gly900Ser)
c.2527+982G>A (n.2527+982G>A)
2g.189004018G>CCA349843814COL3A1c.2599G>C (p.Gly867Arg)
c.2698G>C (p.Gly900Arg)
c.2527+982G>C (n.2527+982G>C)
2g.189004018G>TCA349843815COL3A1c.2599G>T (p.Gly867Cys)
c.2698G>T (p.Gly900Cys)
c.2527+982G>T (n.2527+982G>T)
2g.189004019G>ACA005611COL3A1c.2600G>A (p.Gly867Asp)
c.2699G>A (p.Gly900Asp)
c.2527+983G>A (n.2527+983G>A)
ClinVar dbSNP
2g.189004019G>CCA349843819COL3A1c.2600G>C (p.Gly867Ala)
c.2699G>C (p.Gly900Ala)
c.2527+983G>C (n.2527+983G>C)
gnomAD v4
2g.189004019G=CA1315403024COL3A1c.2600G= (p.Gly867=)
c.2699G= (p.Gly900=)
c.2527+983G= (n.2527+983G=)
2g.189004019G>TCA349843821COL3A1c.2600G>T (p.Gly867Val)
c.2699G>T (p.Gly900Val)
c.2527+983G>T (n.2527+983G>T)
2g.189004020C>ACA430311894COL3A1c.2601C>A (p.Gly867=)
c.2700C>A (p.Gly900=)
c.2527+984C>A (n.2527+984C>A)
2g.189004020C=CA1315403025COL3A1c.2601C= (p.Gly867=)
c.2700C= (p.Gly900=)
c.2527+984C= (n.2527+984C=)
2g.189004020C>GCA430311896COL3A1c.2601C>G (p.Gly867=)
c.2700C>G (p.Gly900=)
c.2527+984C>G (n.2527+984C>G)
dbSNP gnomAD v3 gnomAD v4
2g.189004020C>TCA005619COL3A1c.2601C>T (p.Gly867=)
c.2700C>T (p.Gly900=)
c.2527+984C>T (n.2527+984C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.189004021A>CCA349843828COL3A1c.2602A>C (p.Lys868Gln)
c.2701A>C (p.Lys901Gln)
c.2527+985A>C (n.2527+985A>C)
2g.189004021A>GCA349843826COL3A1c.2602A>G (p.Lys868Glu)
c.2701A>G (p.Lys901Glu)
c.2527+985A>G (n.2527+985A>G)
2g.189004021A>TCA349843824COL3A1c.2602A>T (p.Lys868Ter)
c.2701A>T (p.Lys901Ter)
c.2527+985A>T (n.2527+985A>T)
2g.189004022A=CA1315403026COL3A1c.2603A= (p.Lys868=)
c.2702A= (p.Lys901=)
c.2527+986A= (n.2527+986A=)
2g.189004022A>CCA349843831COL3A1c.2603A>C (p.Lys868Thr)
c.2702A>C (p.Lys901Thr)
c.2527+986A>C (n.2527+986A>C)
2g.189004022A>GCA62557344COL3A1c.2603A>G (p.Lys868Arg)
c.2702A>G (p.Lys901Arg)
c.2527+986A>G (n.2527+986A>G)
dbSNP gnomAD v3 gnomAD v4
2g.189004022A>TCA349843834COL3A1c.2603A>T (p.Lys868Met)
c.2702A>T (p.Lys901Met)
c.2527+986A>T (n.2527+986A>T)
COSMIC
2g.189004023G>ACA430311903COL3A1c.2604G>A (p.Lys868=)
c.2703G>A (p.Lys901=)
c.2527+987G>A (n.2527+987G>A)
COSMIC
2g.189004023G>CCA349843837COL3A1c.2604G>C (p.Lys868Asn)
c.2703G>C (p.Lys901Asn)
c.2527+987G>C (n.2527+987G>C)
2g.189004023G>TCA349843838COL3A1c.2604G>T (p.Lys868Asn)
c.2703G>T (p.Lys901Asn)
c.2527+987G>T (n.2527+987G>T)
2g.189004024G>ACA349843841COL3A1c.2605G>A (p.Asp869Asn)
c.2704G>A (p.Asp902Asn)
c.2527+988G>A (n.2527+988G>A)
2g.189004024G>CCA349843843COL3A1c.2605G>C (p.Asp869His)
c.2704G>C (p.Asp902His)
c.2527+988G>C (n.2527+988G>C)
gnomAD v4
2g.189004024G>TCA349843844COL3A1c.2605G>T (p.Asp869Tyr)
c.2704G>T (p.Asp902Tyr)
c.2527+988G>T (n.2527+988G>T)
2g.189004025A>CCA349843848COL3A1c.2606A>C (p.Asp869Ala)
c.2705A>C (p.Asp902Ala)
c.2527+989A>C (n.2527+989A>C)
2g.189004025A>GCA349843849COL3A1c.2606A>G (p.Asp869Gly)
c.2705A>G (p.Asp902Gly)
c.2527+989A>G (n.2527+989A>G)
2g.189004025A>TCA349843852COL3A1c.2606A>T (p.Asp869Val)
c.2705A>T (p.Asp902Val)
c.2527+989A>T (n.2527+989A>T)
2g.189004026T>ACA349843854COL3A1c.2607T>A (p.Asp869Glu)
c.2706T>A (p.Asp902Glu)
c.2527+990T>A (n.2527+990T>A)
2g.189004026T>CCA430311905COL3A1c.2607T>C (p.Asp869=)
c.2706T>C (p.Asp902=)
c.2527+990T>C (n.2527+990T>C)
2g.189004026T>GCA349843856COL3A1c.2607T>G (p.Asp869Glu)
c.2706T>G (p.Asp902Glu)
c.2527+990T>G (n.2527+990T>G)
2g.189004027G>ACA349843861COL3A1c.2608G>A (p.Gly870Arg)
c.2707G>A (p.Gly903Arg)
c.2527+991G>A (n.2527+991G>A)
2g.189004027G>CCA349843863COL3A1c.2608G>C (p.Gly870Arg)
c.2707G>C (p.Gly903Arg)
c.2527+991G>C (n.2527+991G>C)
2g.189004027G>TCA349843859COL3A1c.2608G>T (p.Gly870Trp)
c.2707G>T (p.Gly903Trp)
c.2527+991G>T (n.2527+991G>T)
2g.189004028G>ACA005626COL3A1c.2609G>A (p.Gly870Glu)
c.2708G>A (p.Gly903Glu)
c.2527+992G>A (n.2527+992G>A)
ClinVar dbSNP
2g.189004028G>CCA349843865COL3A1c.2609G>C (p.Gly870Ala)
c.2708G>C (p.Gly903Ala)
c.2527+992G>C (n.2527+992G>C)
2g.189004028G=CA1315403027COL3A1c.2609G= (p.Gly870=)
c.2708G= (p.Gly903=)
c.2527+992G= (n.2527+992G=)
2g.189004028G>TCA349843868COL3A1c.2609G>T (p.Gly870Val)
c.2708G>T (p.Gly903Val)
c.2527+992G>T (n.2527+992G>T)
2g.189004029G>ACA16603973COL3A1c.2610G>A (p.Gly870=)
c.2709G>A (p.Gly903=)
c.2527+993G>A (n.2527+993G>A)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.189004029G>CCA430311910COL3A1c.2610G>C (p.Gly870=)
c.2709G>C (p.Gly903=)
c.2527+993G>C (n.2527+993G>C)
2g.189004029G=CA1315403028COL3A1c.2610G= (p.Gly870=)
c.2709G= (p.Gly903=)
c.2527+993G= (n.2527+993G=)
2g.189004029G>TCA430311911COL3A1c.2610G>T (p.Gly870=)
c.2709G>T (p.Gly903=)
c.2527+993G>T (n.2527+993G>T)
gnomAD v4
2g.189004030C>ACA62557346COL3A1c.2611C>A (p.Pro871Thr)
c.2710C>A (p.Pro904Thr)
c.2527+994C>A (n.2527+994C>A)
dbSNP gnomAD v2 gnomAD v4
2g.189004030C=CA1315403029COL3A1c.2611C= (p.Pro871=)
c.2710C= (p.Pro904=)
c.2527+994C= (n.2527+994C=)
2g.189004030C>GCA349843873COL3A1c.2611C>G (p.Pro871Ala)
c.2710C>G (p.Pro904Ala)
c.2527+994C>G (n.2527+994C>G)
2g.189004030C>TCA349843874COL3A1c.2611C>T (p.Pro871Ser)
c.2710C>T (p.Pro904Ser)
c.2527+994C>T (n.2527+994C>T)
2g.189004034dupCA430311919COL3A1c.2615dup (p.Gly873ArgfsTer5)
c.2714dup (p.Gly906ArgfsTer5)
c.2527+998dup (n.2527+998dup)
COSMIC
2g.189004031C>ACA349843878COL3A1c.2612C>A (p.Pro871His)
c.2711C>A (p.Pro904His)
c.2527+995C>A (n.2527+995C>A)
2g.189004031C>GCA349843879COL3A1c.2612C>G (p.Pro871Arg)
c.2711C>G (p.Pro904Arg)
c.2527+995C>G (n.2527+995C>G)
2g.189004031C>TCA349843881COL3A1c.2612C>T (p.Pro871Leu)
c.2711C>T (p.Pro904Leu)
c.2527+995C>T (n.2527+995C>T)
ClinVar gnomAD v4
2g.189004032C>ACA430311921COL3A1c.2613C>A (p.Pro871=)
c.2712C>A (p.Pro904=)
c.2527+996C>A (n.2527+996C>A)
2g.189004032C=CA1315403030COL3A1c.2613C= (p.Pro871=)
c.2712C= (p.Pro904=)
c.2527+996C= (n.2527+996C=)
2g.189004032C>GCA430311920COL3A1c.2613C>G (p.Pro871=)
c.2712C>G (p.Pro904=)
c.2527+996C>G (n.2527+996C>G)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.189004032C>TCA075550COL3A1c.2613C>T (p.Pro871=)
c.2712C>T (p.Pro904=)
c.2527+996C>T (n.2527+996C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.189004033C>ACA349843884COL3A1c.2614C>A (p.Pro872Thr)
c.2713C>A (p.Pro905Thr)
c.2527+997C>A (n.2527+997C>A)
2g.189004033C=CA1315403031COL3A1c.2614C= (p.Pro872=)
c.2713C= (p.Pro905=)
c.2527+997C= (n.2527+997C=)
2g.189004033C>GCA62557352COL3A1c.2614C>G (p.Pro872Ala)
c.2713C>G (p.Pro905Ala)
c.2527+997C>G (n.2527+997C>G)
dbSNP
2g.189004033C>TCA349843887COL3A1c.2614C>T (p.Pro872Ser)
c.2713C>T (p.Pro905Ser)
c.2527+997C>T (n.2527+997C>T)
ClinVar dbSNP COSMIC
2g.189004034C>ACA349843888COL3A1c.2615C>A (p.Pro872Gln)
c.2714C>A (p.Pro905Gln)
c.2527+998C>A (n.2527+998C>A)
2g.189004034C=CA1315403032COL3A1c.2615C= (p.Pro872=)
c.2714C= (p.Pro905=)
c.2527+998C= (n.2527+998C=)
2g.189004034C>GCA349843890COL3A1c.2615C>G (p.Pro872Arg)
c.2714C>G (p.Pro905Arg)
c.2527+998C>G (n.2527+998C>G)
2g.189004034C>TCA10612164COL3A1c.2615C>T (p.Pro872Leu)
c.2714C>T (p.Pro905Leu)
c.2527+998C>T (n.2527+998C>T)
ClinVar dbSNP
2g.189004035A>CCA430311924COL3A1c.2616A>C (p.Pro872=)
c.2715A>C (p.Pro905=)
c.2527+999A>C (n.2527+999A>C)
2g.189004035A>GCA430311925COL3A1c.2616A>G (p.Pro872=)
c.2715A>G (p.Pro905=)
c.2527+999A>G (n.2527+999A>G)
2g.189004035A>TCA430311926COL3A1c.2616A>T (p.Pro872=)
c.2715A>T (p.Pro905=)
c.2527+999A>T (n.2527+999A>T)
2g.189004036G>ACA349843898COL3A1c.2617G>A (p.Gly873Ser)
c.2716G>A (p.Gly906Ser)
c.2527+1000G>A (n.2527+1000G>A)
ClinVar dbSNP
2g.189004036G>CCA349843894COL3A1c.2617G>C (p.Gly873Arg)
c.2716G>C (p.Gly906Arg)
c.2527+1000G>C (n.2527+1000G>C)
ClinVar
2g.189004036G=CA1315403033COL3A1c.2617G= (p.Gly873=)
c.2716G= (p.Gly906=)
c.2527+1000G= (n.2527+1000G=)
2g.189004036G>TCA349843896COL3A1c.2617G>T (p.Gly873Cys)
c.2716G>T (p.Gly906Cys)
c.2527+1000G>T (n.2527+1000G>T)
2g.189004037G>ACA349843900COL3A1c.2618G>A (p.Gly873Asp)
c.2717G>A (p.Gly906Asp)
c.2527+1001G>A (n.2527+1001G>A)
ClinVar
2g.189004037G>CCA349843903COL3A1c.2618G>C (p.Gly873Ala)
c.2717G>C (p.Gly906Ala)
c.2527+1001G>C (n.2527+1001G>C)
2g.189004037G>TCA349843905COL3A1c.2618G>T (p.Gly873Val)
c.2717G>T (p.Gly906Val)
c.2527+1001G>T (n.2527+1001G>T)
COSMIC
2g.189004038T>ACA430311928COL3A1c.2619T>A (p.Gly873=)
c.2718T>A (p.Gly906=)
c.2527+1002T>A (n.2527+1002T>A)
2g.189004038T>CCA075553COL3A1c.2619T>C (p.Gly873=)
c.2718T>C (p.Gly906=)
c.2527+1002T>C (n.2527+1002T>C)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.189004038T>GCA430311929COL3A1c.2619T>G (p.Gly873=)
c.2718T>G (p.Gly906=)
c.2527+1002T>G (n.2527+1002T>G)
2g.189004038T=CA1315403034COL3A1c.2619T= (p.Gly873=)
c.2718T= (p.Gly906=)
c.2527+1002T= (n.2527+1002T=)
2g.189004039C>ACA349843909COL3A1c.2620C>A (p.Pro874Thr)
c.2719C>A (p.Pro907Thr)
c.2527+1003C>A (n.2527+1003C>A)
2g.189004039C>GCA349843910COL3A1c.2620C>G (p.Pro874Ala)
c.2719C>G (p.Pro907Ala)
c.2527+1003C>G (n.2527+1003C>G)
2g.189004039C>TCA349843912COL3A1c.2620C>T (p.Pro874Ser)
c.2719C>T (p.Pro907Ser)
c.2527+1003C>T (n.2527+1003C>T)
COSMIC
2g.189004040C>ACA349843915COL3A1c.2621C>A (p.Pro874His)
c.2720C>A (p.Pro907His)
c.2527+1004C>A (n.2527+1004C>A)
2g.189004040C=CA1315403035COL3A1c.2621C= (p.Pro874=)
c.2720C= (p.Pro907=)
c.2527+1004C= (n.2527+1004C=)
2g.189004040C>GCA349843917COL3A1c.2621C>G (p.Pro874Arg)
c.2720C>G (p.Pro907Arg)
c.2527+1004C>G (n.2527+1004C>G)
2g.189004040C>TCA349843919COL3A1c.2621C>T (p.Pro874Leu)
c.2720C>T (p.Pro907Leu)
c.2527+1004C>T (n.2527+1004C>T)
ClinVar dbSNP
2g.189004041T>ACA430311936COL3A1c.2622T>A (p.Pro874=)
c.2721T>A (p.Pro907=)
c.2527+1005T>A (n.2527+1005T>A)
2g.189004041T>CCA430311937COL3A1c.2622T>C (p.Pro874=)
c.2721T>C (p.Pro907=)
c.2527+1005T>C (n.2527+1005T>C)
2g.189004041T>GCA430311938COL3A1c.2622T>G (p.Pro874=)
c.2721T>G (p.Pro907=)
c.2527+1005T>G (n.2527+1005T>G)
2g.189004042G>ACA62557376COL3A1c.2623G>A (p.Ala875Thr)
c.2722G>A (p.Ala908Thr)
c.2527+1006G>A (n.2527+1006G>A)
dbSNP gnomAD v4
2g.189004042G>CCA349843923COL3A1c.2623G>C (p.Ala875Pro)
c.2722G>C (p.Ala908Pro)
c.2527+1006G>C (n.2527+1006G>C)
2g.189004042G=CA1315403036COL3A1c.2623G= (p.Ala875=)
c.2722G= (p.Ala908=)
c.2527+1006G= (n.2527+1006G=)
2g.189004042G>TCA349843925COL3A1c.2623G>T (p.Ala875Ser)
c.2722G>T (p.Ala908Ser)
c.2527+1006G>T (n.2527+1006G>T)
2g.189004043C>ACA349843928COL3A1c.2624C>A (p.Ala875Glu)
c.2723C>A (p.Ala908Glu)
c.2527+1007C>A (n.2527+1007C>A)
gnomAD v4
2g.189004043C=CA1315403037COL3A1c.2624C= (p.Ala875=)
c.2723C= (p.Ala908=)
c.2527+1007C= (n.2527+1007C=)
2g.189004043C>GCA075557COL3A1c.2624C>G (p.Ala875Gly)
c.2723C>G (p.Ala908Gly)
c.2527+1007C>G (n.2527+1007C>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.189004043C>TCA075559COL3A1c.2624C>T (p.Ala875Val)
c.2723C>T (p.Ala908Val)
c.2527+1007C>T (n.2527+1007C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
2g.189004044G>ACA075564COL3A1c.2625G>A (p.Ala875=)
c.2724G>A (p.Ala908=)
c.2527+1008G>A (n.2527+1008G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.189004044G>CCA430311943COL3A1c.2625G>C (p.Ala875=)
c.2724G>C (p.Ala908=)
c.2527+1008G>C (n.2527+1008G>C)
2g.189004044G=CA1315403038COL3A1c.2625G= (p.Ala875=)
c.2724G= (p.Ala908=)
c.2527+1008G= (n.2527+1008G=)
2g.189004044G>TCA430311944COL3A1c.2625G>T (p.Ala875=)
c.2724G>T (p.Ala908=)
c.2527+1008G>T (n.2527+1008G>T)
gnomAD v4
2g.189004046delCA430311947COL3A1c.2627del (p.Gly876ValfsTer?)
c.2726del (p.Gly909ValfsTer?)
c.2527+1010del (n.2527+1010del)
COSMIC
2g.189004045G>ACA349843935COL3A1c.2626G>A (p.Gly876Ser)
c.2725G>A (p.Gly909Ser)
c.2527+1009G>A (n.2527+1009G>A)
2g.189004045G>CCA349843937COL3A1c.2626G>C (p.Gly876Arg)
c.2725G>C (p.Gly909Arg)
c.2527+1009G>C (n.2527+1009G>C)
2g.189004045G>TCA349843939COL3A1c.2626G>T (p.Gly876Cys)
c.2725G>T (p.Gly909Cys)
c.2527+1009G>T (n.2527+1009G>T)
2g.189004046G>ACA349843941COL3A1c.2627G>A (p.Gly876Asp)
c.2726G>A (p.Gly909Asp)
c.2527+1010G>A (n.2527+1010G>A)
ClinVar dbSNP COSMIC
2g.189004046G>CCA349843943COL3A1c.2627G>C (p.Gly876Ala)
c.2726G>C (p.Gly909Ala)
c.2527+1010G>C (n.2527+1010G>C)
2g.189004046G=CA1315403039COL3A1c.2627G= (p.Gly876=)
c.2726G= (p.Gly909=)
c.2527+1010G= (n.2527+1010G=)
2g.189004046G>TCA005632COL3A1c.2627G>T (p.Gly876Val)
c.2726G>T (p.Gly909Val)
c.2527+1010G>T (n.2527+1010G>T)
ClinVar dbSNP
2g.189004047T>ACA430311951COL3A1c.2628T>A (p.Gly876=)
c.2727T>A (p.Gly909=)
c.2527+1011T>A (n.2527+1011T>A)
2g.189004047T>CCA430311950COL3A1c.2628T>C (p.Gly876=)
c.2727T>C (p.Gly909=)
c.2527+1011T>C (n.2527+1011T>C)
2g.189004047T>GCA430311949COL3A1c.2628T>G (p.Gly876=)
c.2727T>G (p.Gly909=)
c.2527+1011T>G (n.2527+1011T>G)
2g.189004048A>CCA349843947COL3A1c.2629A>C (p.Asn877His)
c.2728A>C (p.Asn910His)
c.2527+1012A>C (n.2527+1012A>C)
2g.189004048A>GCA349843948COL3A1c.2629A>G (p.Asn877Asp)
c.2728A>G (p.Asn910Asp)
c.2527+1012A>G (n.2527+1012A>G)
2g.189004048A>TCA349843949COL3A1c.2629A>T (p.Asn877Tyr)
c.2728A>T (p.Asn910Tyr)
c.2527+1012A>T (n.2527+1012A>T)
2g.189004049A>CCA349843952COL3A1c.2630A>C (p.Asn877Thr)
c.2729A>C (p.Asn910Thr)
c.2527+1013A>C (n.2527+1013A>C)
2g.189004049A>GCA349843953COL3A1c.2630A>G (p.Asn877Ser)
c.2729A>G (p.Asn910Ser)
c.2527+1013A>G (n.2527+1013A>G)
gnomAD v4
2g.189004049A>TCA349843955COL3A1c.2630A>T (p.Asn877Ile)
c.2729A>T (p.Asn910Ile)
c.2527+1013A>T (n.2527+1013A>T)
2g.189004050C>ACA349843960COL3A1c.2631C>A (p.Asn877Lys)
c.2730C>A (p.Asn910Lys)
c.2527+1014C>A (n.2527+1014C>A)
2g.189004050C>GCA349843957COL3A1c.2631C>G (p.Asn877Lys)
c.2730C>G (p.Asn910Lys)
c.2527+1014C>G (n.2527+1014C>G)
2g.189004050C>TCA430311958COL3A1c.2631C>T (p.Asn877=)
c.2730C>T (p.Asn910=)
c.2527+1014C>T (n.2527+1014C>T)
2g.189004051A=CA1315403040COL3A1c.2632A= (p.Thr878=)
c.2731A= (p.Thr911=)
c.2527+1015A= (n.2527+1015A=)
2g.189004051A>CCA349843962COL3A1c.2632A>C (p.Thr878Pro)
c.2731A>C (p.Thr911Pro)
c.2527+1015A>C (n.2527+1015A>C)
2g.189004051A>GCA349843963COL3A1c.2632A>G (p.Thr878Ala)
c.2731A>G (p.Thr911Ala)
c.2527+1015A>G (n.2527+1015A>G)
gnomAD v4
2g.189004051A>TCA349843965COL3A1c.2632A>T (p.Thr878Ser)
c.2731A>T (p.Thr911Ser)
c.2527+1015A>T (n.2527+1015A>T)
dbSNP
2g.189004052C>ACA349843967COL3A1c.2633C>A (p.Thr878Asn)
c.2732C>A (p.Thr911Asn)
c.2527+1016C>A (n.2527+1016C>A)
2g.189004052C=CA1315403041COL3A1c.2633C= (p.Thr878=)
c.2732C= (p.Thr911=)
c.2527+1016C= (n.2527+1016C=)
2g.189004052C>GCA075568COL3A1c.2633C>G (p.Thr878Ser)
c.2732C>G (p.Thr911Ser)
c.2527+1016C>G (n.2527+1016C>G)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.189004052C>TCA349843970COL3A1c.2633C>T (p.Thr878Ile)
c.2732C>T (p.Thr911Ile)
c.2527+1016C>T (n.2527+1016C>T)
dbSNP gnomAD v2 gnomAD v4
2g.189004053T>ACA430311960COL3A1c.2634T>A (p.Thr878=)
c.2733T>A (p.Thr911=)
c.2527+1017T>A (n.2527+1017T>A)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.189004053T>CCA075571COL3A1c.2634T>C (p.Thr878=)
c.2733T>C (p.Thr911=)
c.2527+1017T>C (n.2527+1017T>C)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.189004053T>GCA430311963COL3A1c.2634T>G (p.Thr878=)
c.2733T>G (p.Thr911=)
c.2527+1017T>G (n.2527+1017T>G)
2g.189004053T=CA1315403042COL3A1c.2634T= (p.Thr878=)
c.2733T= (p.Thr911=)
c.2527+1017T= (n.2527+1017T=)
2g.189004054G>ACA349843974COL3A1c.2635G>A (p.Gly879Ser)
c.2734G>A (p.Gly912Ser)
c.2527+1018G>A (n.2527+1018G>A)
ClinVar dbSNP
2g.189004054G>CCA349843976COL3A1c.2635G>C (p.Gly879Arg)
c.2734G>C (p.Gly912Arg)
c.2527+1018G>C (n.2527+1018G>C)
2g.189004054G>TCA349843978COL3A1c.2635G>T (p.Gly879Cys)
c.2734G>T (p.Gly912Cys)
c.2527+1018G>T (n.2527+1018G>T)
2g.189004055G>ACA005640COL3A1c.2636G>A (p.Gly879Asp)
c.2735G>A (p.Gly912Asp)
c.2527+1019G>A (n.2527+1019G>A)
ClinVar dbSNP gnomAD v4
2g.189004055G>CCA349843982COL3A1c.2636G>C (p.Gly879Ala)
c.2735G>C (p.Gly912Ala)
c.2527+1019G>C (n.2527+1019G>C)
2g.189004055G=CA1315403043COL3A1c.2636G= (p.Gly879=)
c.2735G= (p.Gly912=)
c.2527+1019G= (n.2527+1019G=)
2g.189004055G>TCA349843984COL3A1c.2636G>T (p.Gly879Val)
c.2735G>T (p.Gly912Val)
c.2527+1019G>T (n.2527+1019G>T)
2g.189004056T>ACA430311968COL3A1c.2637T>A (p.Gly879=)
c.2736T>A (p.Gly912=)
c.2527+1020T>A (n.2527+1020T>A)
2g.189004056T>CCA430311969COL3A1c.2637T>C (p.Gly879=)
c.2736T>C (p.Gly912=)
c.2527+1020T>C (n.2527+1020T>C)
dbSNP gnomAD v2 gnomAD v4
2g.189004056T>GCA430311970COL3A1c.2637T>G (p.Gly879=)
c.2736T>G (p.Gly912=)
c.2527+1020T>G (n.2527+1020T>G)
gnomAD v4
2g.189004056T=CA1315403044COL3A1c.2637T= (p.Gly879=)
c.2736T= (p.Gly912=)
c.2527+1020T= (n.2527+1020T=)
2g.189004057G>ACA349843991COL3A1c.2638G>A (p.Ala880Thr)
c.2737G>A (p.Ala913Thr)
c.2527+1021G>A (n.2527+1021G>A)
2g.189004057G>CCA349843988COL3A1c.2638G>C (p.Ala880Pro)
c.2737G>C (p.Ala913Pro)
c.2527+1021G>C (n.2527+1021G>C)
ClinVar
2g.189004057G>TCA349843990COL3A1c.2638G>T (p.Ala880Ser)
c.2737G>T (p.Ala913Ser)
c.2527+1021G>T (n.2527+1021G>T)
2g.189004058C>ACA349843995COL3A1c.2639C>A (p.Ala880Asp)
c.2738C>A (p.Ala913Asp)
c.2527+1022C>A (n.2527+1022C>A)
COSMIC
2g.189004058C>GCA349843999COL3A1c.2639C>G (p.Ala880Gly)
c.2738C>G (p.Ala913Gly)
c.2527+1022C>G (n.2527+1022C>G)
2g.189004058C>TCA349843996COL3A1c.2639C>T (p.Ala880Val)
c.2738C>T (p.Ala913Val)
c.2527+1022C>T (n.2527+1022C>T)
2g.189004059T>ACA430311974COL3A1c.2640T>A (p.Ala880=)
c.2739T>A (p.Ala913=)
c.2527+1023T>A (n.2527+1023T>A)
2g.189004059T>CCA430311975COL3A1c.2640T>C (p.Ala880=)
c.2739T>C (p.Ala913=)
c.2527+1023T>C (n.2527+1023T>C)
dbSNP gnomAD v2 gnomAD v4
2g.189004059T>GCA430311976COL3A1c.2640T>G (p.Ala880=)
c.2739T>G (p.Ala913=)
c.2527+1023T>G (n.2527+1023T>G)
2g.189004059T=CA1315403045COL3A1c.2640T= (p.Ala880=)
c.2739T= (p.Ala913=)
c.2527+1023T= (n.2527+1023T=)
2g.189004060C>ACA349844000COL3A1c.2641C>A (p.Pro881Thr)
c.2740C>A (p.Pro914Thr)
c.2527+1024C>A (n.2527+1024C>A)
COSMIC
2g.189004060C>GCA349844003COL3A1c.2641C>G (p.Pro881Ala)
c.2740C>G (p.Pro914Ala)
c.2527+1024C>G (n.2527+1024C>G)
2g.189004060C>TCA349844005COL3A1c.2641C>T (p.Pro881Ser)
c.2740C>T (p.Pro914Ser)
c.2527+1024C>T (n.2527+1024C>T)
gnomAD v4 COSMIC
2g.189004061C>ACA349844006COL3A1c.2642C>A (p.Pro881His)
c.2741C>A (p.Pro914His)
c.2527+1025C>A (n.2527+1025C>A)
2g.189004061C>GCA349844008COL3A1c.2642C>G (p.Pro881Arg)
c.2741C>G (p.Pro914Arg)
c.2527+1025C>G (n.2527+1025C>G)
2g.189004061C>TCA349844011COL3A1c.2642C>T (p.Pro881Leu)
c.2741C>T (p.Pro914Leu)
c.2527+1025C>T (n.2527+1025C>T)
2g.189004062T>ACA430311980COL3A1c.2643T>A (p.Pro881=)
c.2742T>A (p.Pro914=)
c.2527+1026T>A (n.2527+1026T>A)
2g.189004062T>CCA430311981COL3A1c.2643T>C (p.Pro881=)
c.2742T>C (p.Pro914=)
c.2527+1026T>C (n.2527+1026T>C)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.189004062T>GCA430311982COL3A1c.2643T>G (p.Pro881=)
c.2742T>G (p.Pro914=)
c.2527+1026T>G (n.2527+1026T>G)
2g.189004062T=CA1315403046COL3A1c.2643T= (p.Pro881=)
c.2742T= (p.Pro914=)
c.2527+1026T= (n.2527+1026T=)
2g.189004063G>ACA349844013COL3A1c.2644G>A (p.Gly882Ser)
c.2743G>A (p.Gly915Ser)
c.2527+1027G>A (n.2527+1027G>A)
ClinVar dbSNP
2g.189004063G>CCA349844015COL3A1c.2644G>C (p.Gly882Arg)
c.2743G>C (p.Gly915Arg)
c.2527+1027G>C (n.2527+1027G>C)
2g.189004063G>TCA349844017COL3A1c.2644G>T (p.Gly882Cys)
c.2743G>T (p.Gly915Cys)
c.2527+1027G>T (n.2527+1027G>T)
2g.189004064G>ACA349844020COL3A1c.2645G>A (p.Gly882Asp)
c.2744G>A (p.Gly915Asp)
c.2527+1028G>A (n.2527+1028G>A)
2g.189004064G>CCA349844022COL3A1c.2645G>C (p.Gly882Ala)
c.2744G>C (p.Gly915Ala)
c.2527+1028G>C (n.2527+1028G>C)
2g.189004064G>TCA349844023COL3A1c.2645G>T (p.Gly882Val)
c.2744G>T (p.Gly915Val)
c.2527+1028G>T (n.2527+1028G>T)
2g.189004065C>ACA075574COL3A1c.2646C>A (p.Gly882=)
c.2745C>A (p.Gly915=)
c.2527+1029C>A (n.2527+1029C>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.189004065C=CA1315403047COL3A1c.2646C= (p.Gly882=)
c.2745C= (p.Gly915=)
c.2527+1029C= (n.2527+1029C=)
2g.189004065C>GCA430311985COL3A1c.2646C>G (p.Gly882=)
c.2745C>G (p.Gly915=)
c.2527+1029C>G (n.2527+1029C>G)
2g.189004065C>TCA075577COL3A1c.2646C>T (p.Gly882=)
c.2745C>T (p.Gly915=)
c.2527+1029C>T (n.2527+1029C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.189004066A=CA1315403048COL3A1c.2647A= (p.Ser883=)
c.2746A= (p.Ser916=)
c.2527+1030A= (n.2527+1030A=)
2g.189004066A>CCA349844025COL3A1c.2647A>C (p.Ser883Arg)
c.2746A>C (p.Ser916Arg)
c.2527+1030A>C (n.2527+1030A>C)
2g.189004066A>GCA349844027COL3A1c.2647A>G (p.Ser883Gly)
c.2746A>G (p.Ser916Gly)
c.2527+1030A>G (n.2527+1030A>G)
dbSNP
2g.189004066A>TCA349844028COL3A1c.2647A>T (p.Ser883Cys)
c.2746A>T (p.Ser916Cys)
c.2527+1030A>T (n.2527+1030A>T)
2g.189004067G>ACA349844031COL3A1c.2648G>A (p.Ser883Asn)
c.2747G>A (p.Ser916Asn)
c.2527+1031G>A (n.2527+1031G>A)
gnomAD v4
2g.189004067G>CCA349844032COL3A1c.2648G>C (p.Ser883Thr)
c.2747G>C (p.Ser916Thr)
c.2527+1031G>C (n.2527+1031G>C)
dbSNP gnomAD v3 gnomAD v4
2g.189004067G=CA1315403049COL3A1c.2648G= (p.Ser883=)
c.2747G= (p.Ser916=)
c.2527+1031G= (n.2527+1031G=)
2g.189004067G>TCA349844034COL3A1c.2648G>T (p.Ser883Ile)
c.2747G>T (p.Ser916Ile)
c.2527+1031G>T (n.2527+1031G>T)
2g.189004068C>ACA349844038COL3A1c.2649C>A (p.Ser883Arg)
c.2748C>A (p.Ser916Arg)
c.2527+1032C>A (n.2527+1032C>A)
2g.189004068C>GCA349844036COL3A1c.2649C>G (p.Ser883Arg)
c.2748C>G (p.Ser916Arg)
c.2527+1032C>G (n.2527+1032C>G)
2g.189004068C>TCA430311993COL3A1c.2649C>T (p.Ser883=)
c.2748C>T (p.Ser916=)
c.2527+1032C>T (n.2527+1032C>T)
2g.189004069C>ACA62557413COL3A1c.2650C>A (p.Pro884Thr)
c.2749C>A (p.Pro917Thr)
c.2527+1033C>A (n.2527+1033C>A)
dbSNP
2g.189004069C=CA1315403050COL3A1c.2650C= (p.Pro884=)
c.2749C= (p.Pro917=)
c.2527+1033C= (n.2527+1033C=)
2g.189004069C>GCA349844040COL3A1c.2650C>G (p.Pro884Ala)
c.2749C>G (p.Pro917Ala)
c.2527+1033C>G (n.2527+1033C>G)
2g.189004069C>TCA349844042COL3A1c.2650C>T (p.Pro884Ser)
c.2749C>T (p.Pro917Ser)
c.2527+1033C>T (n.2527+1033C>T)
ClinVar dbSNP gnomAD v4
2g.189004070C>ACA349844045COL3A1c.2651C>A (p.Pro884His)
c.2750C>A (p.Pro917His)
c.2527+1034C>A (n.2527+1034C>A)
2g.189004070C>GCA349844047COL3A1c.2651C>G (p.Pro884Arg)
c.2750C>G (p.Pro917Arg)
c.2527+1034C>G (n.2527+1034C>G)
2g.189004070C>TCA349844048COL3A1c.2651C>T (p.Pro884Leu)
c.2750C>T (p.Pro917Leu)
c.2527+1034C>T (n.2527+1034C>T)
2g.189004071T>ACA430312001COL3A1c.2652T>A (p.Pro884=)
c.2751T>A (p.Pro917=)
c.2527+1035T>A (n.2527+1035T>A)
2g.189004071T>CCA430312000COL3A1c.2652T>C (p.Pro884=)
c.2751T>C (p.Pro917=)
c.2527+1035T>C (n.2527+1035T>C)
2g.189004071T>GCA430311998COL3A1c.2652T>G (p.Pro884=)
c.2751T>G (p.Pro917=)
c.2527+1035T>G (n.2527+1035T>G)
2g.189004072G>ACA349844050COL3A1c.2653G>A (p.Gly885Arg)
c.2752G>A (p.Gly918Arg)
c.2527+1036G>A (n.2527+1036G>A)
ClinVar dbSNP
2g.189004072G>CCA349844054COL3A1c.2653G>C (p.Gly885Arg)
c.2752G>C (p.Gly918Arg)
c.2527+1036G>C (n.2527+1036G>C)
2g.189004072G=CA1315403051COL3A1c.2653G= (p.Gly885=)
c.2752G= (p.Gly918=)
c.2527+1036G= (n.2527+1036G=)
2g.189004072G>TCA349844052COL3A1c.2653G>T (p.Gly885Ter)
c.2752G>T (p.Gly918Ter)
c.2527+1036G>T (n.2527+1036G>T)

Number of alleles fetched