Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.50198433_50199305delinsACA2573131850COL1A1c.392_543delinsT
17g.50199236_50199252delCA2695226552COL1A1c.449_465del (p.Pro150ArgfsTer13)
17g.50199244_50199315delCA2638681625COL1A1c.392_463del (p.Arg131_Gly154del)
gnomAD v4
17g.50199238_50199239delinsAGCA2263920593COL1A1c.458_459delinsCT (p.Pro153=)
17g.50199238_50199256delinsAGGGGGTCCGGGAGGTCCGCA2263920594COL1A1c.441_459delinsCGGACCTCCCGGACCCCCT (p.Pro147=)
17g.50199239G>ACA400227274COL1A1c.458C>T (p.Pro153Leu)
gnomAD v4
17g.50199239G>CCA400227276COL1A1c.458C>G (p.Pro153Arg)
17g.50199239G>TCA400227275COL1A1c.458C>A (p.Pro153His)
gnomAD v4
17g.50199243dupCA645293910COL1A1c.458dup (p.Gly154TrpfsTer15)
ClinVar dbSNP
17g.50199243delCA915950624COL1A1c.458del (p.Pro153LeufsTer?)
ClinVar dbSNP gnomAD v4
17g.50199250_50199267dupCA2638681687COL1A1c.441_458dup (p.Pro153_Gly154insGlyProProGlyProPro)
ClinVar gnomAD v4
17g.50199250_50199267delCA500852144COL1A1c.441_458del (p.Gly148_Pro153del)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.50199251_50199277delCA2573154235COL1A1c.432_458del (p.Gly145_Pro153del)
ClinVar dbSNP gnomAD v4
17g.50199240G>ACA400227277COL1A1c.457C>T (p.Pro153Ser)
ClinVar gnomAD v4
17g.50199240G>CCA400227278COL1A1c.457C>G (p.Pro153Ala)
gnomAD v4
17g.50199240G>TCA400227280COL1A1c.457C>A (p.Pro153Thr)
gnomAD v4
17g.50199241G>ACA500852145COL1A1c.456C>T (p.Pro152=)
gnomAD v4
17g.50199241G>CCA500852146COL1A1c.456C>G (p.Pro152=)
17g.50199241G>TCA500852147COL1A1c.456C>A (p.Pro152=)
gnomAD v4
17g.50199241_50199250delinsGGGTCCGGGACA2263920596COL1A1c.447_456delinsTCCCGGACCC (p.Pro149=)
17g.50199242G>ACA400227281COL1A1c.455C>T (p.Pro152Leu)
gnomAD v4
17g.50199242G>CCA400227282COL1A1c.455C>G (p.Pro152Arg)
gnomAD v4
17g.50199242G=CA2263920597COL1A1c.455C= (p.Pro152=)
17g.50199242G>TCA400227283COL1A1c.455C>A (p.Pro152His)
dbSNP gnomAD v3 gnomAD v4
17g.50199258_50199259insAGGTCCGGGAGGTCCGGGCA626486269COL1A1c.455_456insTCCCGGACCTCCCGGACC (p.Pro152_Pro153insProGlyProProGlyPro)
ClinVar dbSNP gnomAD v2 gnomAD v4
17g.50199250_50199258dupCA2576317756COL1A1c.447_455dup (p.Pro152_Pro153insProGlyPro)
gnomAD v4
17g.50199250_50199258delCA626486268COL1A1c.447_455del (p.Pro150_Pro152del)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.50199243G>ACA400227285COL1A1c.454C>T (p.Pro152Ser)
17g.50199243G>CCA400227286COL1A1c.454C>G (p.Pro152Ala)
17g.50199243G=CA2263920598COL1A1c.454C= (p.Pro152=)
17g.50199243G>TCA400227288COL1A1c.454C>A (p.Pro152Thr)
ClinVar dbSNP gnomAD v2 gnomAD v4
17g.50199244T>ACA500852148COL1A1c.453A>T (p.Gly151=)
dbSNP gnomAD v2 gnomAD v4
17g.50199244T>CCA500852149COL1A1c.453A>G (p.Gly151=)
17g.50199244T>GCA500852150COL1A1c.453A>C (p.Gly151=)
17g.50199244T=CA2263920599COL1A1c.453A= (p.Gly151=)
17g.50199245C>ACA400227289COL1A1c.452G>T (p.Gly151Val)
gnomAD v4
17g.50199245C=CA2263920600COL1A1c.452G= (p.Gly151=)
17g.50199245C>GCA400227291COL1A1c.452G>C (p.Gly151Ala)
17g.50199245C>TCA291550346COL1A1c.452G>A (p.Gly151Glu)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.50199246dupCA2573050781COL1A1c.452dup (p.Pro152ThrfsTer17)
ClinVar dbSNP
17g.50199246C>ACA400227294COL1A1c.451G>T (p.Gly151Ter)
gnomAD v4
17g.50199246C>GCA400227292COL1A1c.451G>C (p.Gly151Arg)
17g.50199246C>TCA400227293COL1A1c.451G>A (p.Gly151Arg)
ClinVar
17g.50199247G>ACA500852151COL1A1c.450C>T (p.Pro150=)
gnomAD v4
17g.50199247G>CCA500852152COL1A1c.450C>G (p.Pro150=)
gnomAD v4
17g.50199247G>TCA500852153COL1A1c.450C>A (p.Pro150=)
gnomAD v4
17g.50199248G>ACA400227295COL1A1c.449C>T (p.Pro150Leu)
ClinVar gnomAD v4
17g.50199248G>CCA400227297COL1A1c.449C>G (p.Pro150Arg)
17g.50199248G>TCA400227298COL1A1c.449C>A (p.Pro150His)
gnomAD v4
17g.50199249G>ACA400227300COL1A1c.448C>T (p.Pro150Ser)
gnomAD v4
17g.50199249G>CCA400227301COL1A1c.448C>G (p.Pro150Ala)
gnomAD v4
17g.50199249G>TCA400227302COL1A1c.448C>A (p.Pro150Thr)
17g.50199250A=CA2263920602COL1A1c.447T= (p.Pro149=)
17g.50199250A>CCA500852154COL1A1c.447T>G (p.Pro149=)
17g.50199250A>GCA500852155COL1A1c.447T>C (p.Pro149=)
dbSNP gnomAD v2 gnomAD v4
17g.50199250A>TCA500852156COL1A1c.447T>A (p.Pro149=)
17g.50199250_50199259delinsAGGTCCGGGGCA2263920601COL1A1c.438_447delinsCCCCGGACCT (p.Pro146=)
17g.50199251G>ACA400227307COL1A1c.446C>T (p.Pro149Leu)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.50199251G>CCA400227304COL1A1c.446C>G (p.Pro149Arg)
17g.50199251G=CA2263920603COL1A1c.446C= (p.Pro149=)
17g.50199251G>TCA400227305COL1A1c.446C>A (p.Pro149His)
17g.50199268_50199276dupCA8645700COL1A1c.438_446dup (p.Pro149_Pro150insProGlyPro)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.50199268_50199276delCA626486271COL1A1c.438_446del (p.Pro147_Pro149del)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.50199259_50199276delCA2638681844COL1A1c.429_446del (p.Pro144_Pro149del)
gnomAD v4
17g.50199252G>ACA400227309COL1A1c.445C>T (p.Pro149Ser)
dbSNP gnomAD v2 gnomAD v4
17g.50199252G>CCA400227311COL1A1c.445C>G (p.Pro149Ala)
17g.50199252G=CA2263920604COL1A1c.445C= (p.Pro149=)
17g.50199252G>TCA400227312COL1A1c.445C>A (p.Pro149Thr)
gnomAD v4
17g.50199253T>ACA500852159COL1A1c.444A>T (p.Gly148=)
17g.50199253T>CCA500852158COL1A1c.444A>G (p.Gly148=)
17g.50199253T>GCA500852157COL1A1c.444A>C (p.Gly148=)
17g.50199254C>ACA400227313COL1A1c.443G>T (p.Gly148Val)
17g.50199254C>GCA400227315COL1A1c.443G>C (p.Gly148Ala)
17g.50199254C>TCA400227317COL1A1c.443G>A (p.Gly148Glu)
17g.50199255dupCA2739291025COL1A1c.443dup (p.Pro149ThrfsTer20)
17g.50199255C>ACA400227318COL1A1c.442G>T (p.Gly148Ter)
gnomAD v4
17g.50199255C>GCA400227321COL1A1c.442G>C (p.Gly148Arg)
17g.50199255C>TCA400227320COL1A1c.442G>A (p.Gly148Arg)
gnomAD v4
17g.50199255_50199256delinsCGCA2263920605COL1A1c.441_442delinsCG (p.Pro147=)
17g.50199256G>ACA500852160COL1A1c.441C>T (p.Pro147=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.50199256G>CCA500852161COL1A1c.441C>G (p.Pro147=)
dbSNP gnomAD v2 gnomAD v4
17g.50199256G=CA2263920606COL1A1c.441C= (p.Pro147=)
17g.50199256G>TCA500852162COL1A1c.441C>A (p.Pro147=)
gnomAD v4
17g.50199256delinsTGACA2695226553COL1A1c.441delinsTCA (p.Gly148GlnfsTer?)
17g.50199261dupCA2638681886COL1A1c.441dup (p.Gly148ArgfsTer21)
gnomAD v4
17g.50199261delCA626486275COL1A1c.441del (p.Gly148AspfsTer?)
ClinVar dbSNP gnomAD v2 gnomAD v4
17g.50199257G>ACA400227323COL1A1c.440C>T (p.Pro147Leu)
17g.50199257G>CCA400227324COL1A1c.440C>G (p.Pro147Arg)
dbSNP
17g.50199257G=CA2263920607COL1A1c.440C= (p.Pro147=)
17g.50199257G>TCA400227326COL1A1c.440C>A (p.Pro147His)
gnomAD v4
17g.50199258G>ACA400227327COL1A1c.439C>T (p.Pro147Ser)
ClinVar gnomAD v4
17g.50199258G>CCA400227329COL1A1c.439C>G (p.Pro147Ala)
gnomAD v4
17g.50199258G>TCA400227330COL1A1c.439C>A (p.Pro147Thr)
17g.50199259G>ACA291550373COL1A1c.438C>T (p.Pro146=)
dbSNP gnomAD v4
17g.50199259G>CCA500852163COL1A1c.438C>G (p.Pro146=)
17g.50199259G=CA2263920608COL1A1c.438C= (p.Pro146=)
17g.50199259G>TCA500852164COL1A1c.438C>A (p.Pro146=)
gnomAD v4
17g.50199260G>ACA400227332COL1A1c.437C>T (p.Pro146Leu)
gnomAD v4
17g.50199260G>CCA400227334COL1A1c.437C>G (p.Pro146Arg)
17g.50199260G>TCA400227335COL1A1c.437C>A (p.Pro146His)
gnomAD v4
17g.50199261G>ACA8645702COL1A1c.436C>T (p.Pro146Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.50199261G>CCA400227337COL1A1c.436C>G (p.Pro146Ala)
ClinVar dbSNP gnomAD v4
17g.50199261G=CA2263920609COL1A1c.436C= (p.Pro146=)
17g.50199261G>TCA8645701COL1A1c.436C>A (p.Pro146Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.50199262T>ACA500852165COL1A1c.435A>T (p.Gly145=)
17g.50199262T>CCA500852166COL1A1c.435A>G (p.Gly145=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.50199262T>GCA500852167COL1A1c.435A>C (p.Gly145=)
17g.50199262T=CA2263920610COL1A1c.435A= (p.Gly145=)
17g.50199263C>ACA400227340COL1A1c.434G>T (p.Gly145Val)
17g.50199263C>GCA400227338COL1A1c.434G>C (p.Gly145Ala)
17g.50199263C>TCA400227339COL1A1c.434G>A (p.Gly145Glu)
17g.50199263_50199264insGCA2695226554COL1A1c.433_434insC (p.Gly145AlafsTer24)
17g.50199264C>ACA400227341COL1A1c.433G>T (p.Gly145Ter)
gnomAD v4
17g.50199264C=CA2263920612COL1A1c.433G= (p.Gly145=)
17g.50199264C>GCA400227342COL1A1c.433G>C (p.Gly145Arg)
17g.50199264C>TCA400227343COL1A1c.433G>A (p.Gly145Arg)
ClinVar dbSNP gnomAD v4
17g.50199264_50199265delinsCGCA2263920611COL1A1c.432_433delinsCG (p.Pro144=)
17g.50199264_50199274delinsACA2739291026COL1A1c.423_433delinsT (p.Gly142AspfsTer?)
17g.50199265G>ACA500852170COL1A1c.432C>T (p.Pro144=)
ClinVar dbSNP gnomAD v2 gnomAD v4
17g.50199265G>CCA500852169COL1A1c.432C>G (p.Pro144=)
dbSNP gnomAD v4
17g.50199265G=CA2263920613COL1A1c.432C= (p.Pro144=)
17g.50199265G>TCA500852168COL1A1c.432C>A (p.Pro144=)
gnomAD v4
17g.50199270dupCA645293911COL1A1c.432dup (p.Gly145ArgfsTer24)
ClinVar dbSNP gnomAD v4
17g.50199270delCA291550378COL1A1c.432del (p.Gly145AspfsTer?)
ClinVar dbSNP gnomAD v2 gnomAD v4
17g.50199266G>ACA400227344COL1A1c.431C>T (p.Pro144Leu)
gnomAD v4
17g.50199266G>CCA400227345COL1A1c.431C>G (p.Pro144Arg)
gnomAD v4
17g.50199266G>TCA400227346COL1A1c.431C>A (p.Pro144His)
gnomAD v4
17g.50199267G>ACA291550395COL1A1c.430C>T (p.Pro144Ser)
ClinVar dbSNP gnomAD v3 gnomAD v4
17g.50199267G>CCA400227347COL1A1c.430C>G (p.Pro144Ala)
gnomAD v4
17g.50199267G=CA2263920614COL1A1c.430C= (p.Pro144=)
17g.50199267G>TCA400227348COL1A1c.430C>A (p.Pro144Thr)
gnomAD v4
17g.50199268G>ACA500852171COL1A1c.429C>T (p.Pro143=)
ClinVar gnomAD v4
17g.50199268G>CCA500852173COL1A1c.429C>G (p.Pro143=)
17g.50199268G>TCA500852172COL1A1c.429C>A (p.Pro143=)
gnomAD v4
17g.50199269G>ACA400227349COL1A1c.428C>T (p.Pro143Leu)
dbSNP gnomAD v2 gnomAD v4
17g.50199269G>CCA400227350COL1A1c.428C>G (p.Pro143Arg)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.50199269G=CA2263920615COL1A1c.428C= (p.Pro143=)
17g.50199269G>TCA291550399COL1A1c.428C>A (p.Pro143His)
dbSNP gnomAD v4
17g.50199270G>ACA291550400COL1A1c.427C>T (p.Pro143Ser)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.50199270G>CCA400227351COL1A1c.427C>G (p.Pro143Ala)
dbSNP gnomAD v3 gnomAD v4
17g.50199270G=CA2263920616COL1A1c.427C= (p.Pro143=)
17g.50199270G>TCA400227352COL1A1c.427C>A (p.Pro143Thr)
gnomAD v4
17g.50199271T>ACA500852176COL1A1c.426A>T (p.Gly142=)
17g.50199271T>CCA500852175COL1A1c.426A>G (p.Gly142=)
gnomAD v4
17g.50199271T>GCA500852174COL1A1c.426A>C (p.Gly142=)
17g.50199272C>ACA400227353COL1A1c.425G>T (p.Gly142Val)
gnomAD v4
17g.50199272C>GCA400227354COL1A1c.425G>C (p.Gly142Ala)
17g.50199272C>TCA400227355COL1A1c.425G>A (p.Gly142Glu)
gnomAD v4
17g.50199273C>ACA400227356COL1A1c.424G>T (p.Gly142Ter)
gnomAD v4
17g.50199273C=CA2263920617COL1A1c.424G= (p.Gly142=)
17g.50199273C>GCA400227357COL1A1c.424G>C (p.Gly142Arg)
17g.50199273C>TCA400227358COL1A1c.424G>A (p.Gly142Arg)
ClinVar dbSNP gnomAD v4
17g.50199274G>ACA500852177COL1A1c.423C>T (p.Pro141=)
dbSNP gnomAD v2 gnomAD v4
17g.50199274G>CCA500852179COL1A1c.423C>G (p.Pro141=)
17g.50199274G=CA2263920618COL1A1c.423C= (p.Pro141=)
17g.50199274G>TCA500852178COL1A1c.423C>A (p.Pro141=)
17g.50199276delCA2580094384COL1A1c.423del (p.Gly142AspfsTer?)
ClinVar
17g.50199275G>ACA400227360COL1A1c.422C>T (p.Pro141Leu)
gnomAD v4
17g.50199275G>CCA400227362COL1A1c.422C>G (p.Pro141Arg)
17g.50199275G>TCA400227363COL1A1c.422C>A (p.Pro141His)
17g.50199276G>ACA400227365COL1A1c.421C>T (p.Pro141Ser)
dbSNP gnomAD v2 gnomAD v4
17g.50199276G>CCA400227366COL1A1c.421C>G (p.Pro141Ala)
17g.50199276G=CA2263920619COL1A1c.421C= (p.Pro141=)
17g.50199276G>TCA400227368COL1A1c.421C>A (p.Pro141Thr)
17g.50199277A>CCA500852180COL1A1c.420T>G (p.Leu140=)
17g.50199277A>GCA500852181COL1A1c.420T>C (p.Leu140=)
17g.50199277A>TCA500852182COL1A1c.420T>A (p.Leu140=)
17g.50199277_50199278delinsAACA2263920620COL1A1c.419_420delinsTT (p.Leu140=)
17g.50199277_50199278delinsGGCA658656725COL1A1c.419_420delinsCC (p.Leu140Pro)
ClinVar dbSNP
17g.50199278A>CCA400227371COL1A1c.419T>G (p.Leu140Arg)
n.640T>G
17g.50199278A>GCA400227374COL1A1c.419T>C (p.Leu140Pro)
n.640T>C
17g.50199278A>TCA400227372COL1A1c.419T>A (p.Leu140His)
n.640T>A
17g.50199278_50199281delCA2695226555COL1A1c.416_419del (p.Gly139ValfsTer?)
n.637_640del
17g.50199279G>ACA400227377COL1A1c.418C>T (p.Leu140Phe)
n.639C>T
dbSNP gnomAD v2 gnomAD v4
17g.50199279G>CCA400227380COL1A1c.418C>G (p.Leu140Val)
n.639C>G
dbSNP gnomAD v3 gnomAD v4
17g.50199279G=CA2263920621COL1A1c.418C= (p.Leu140=)
n.639C=
17g.50199279G>TCA400227379COL1A1c.418C>A (p.Leu140Ile)
n.639C>A
gnomAD v4
17g.50199280T>ACA500852183COL1A1c.417A>T (p.Gly139=)
n.638A>T
17g.50199280T>CCA500852184COL1A1c.417A>G (p.Gly139=)
n.638A>G
17g.50199280T>GCA500852185COL1A1c.417A>C (p.Gly139=)
n.638A>C
17g.50199281C>ACA400227382COL1A1c.416G>T (p.Gly139Val)
n.637G>T
gnomAD v4
17g.50199281C>GCA400227384COL1A1c.416G>C (p.Gly139Ala)
n.637G>C
17g.50199281C>TCA400227386COL1A1c.416G>A (p.Gly139Glu)
n.637G>A
gnomAD v4
17g.50199282delCA2576317757COL1A1c.416del (p.Gly139AspfsTer?)
n.637del
17g.50199282C>ACA400227388COL1A1c.415G>T (p.Gly139Ter)
n.636G>T
ClinVar gnomAD v4
17g.50199282C>GCA400227390COL1A1c.415G>C (p.Gly139Arg)
n.636G>C
17g.50199282C>TCA400227392COL1A1c.415G>A (p.Gly139Arg)
n.636G>A
17g.50199283A>CCA500852186COL1A1c.414T>G (p.Pro138=)
n.635T>G
ClinVar dbSNP
17g.50199283A>GCA500852187COL1A1c.414T>C (p.Pro138=)
n.635T>C
gnomAD v4
17g.50199283A>TCA500852188COL1A1c.414T>A (p.Pro138=)
n.635T>A
17g.50199284G>ACA400227395COL1A1c.413C>T (p.Pro138Leu)
n.634C>T
dbSNP
17g.50199284G>CCA400227396COL1A1c.413C>G (p.Pro138Arg)
n.634C>G
gnomAD v4
17g.50199284G=CA2263920622COL1A1c.413C= (p.Pro138=)
n.634C=
17g.50199284G>TCA400227397COL1A1c.413C>A (p.Pro138His)
n.634C>A
gnomAD v4 COSMIC
17g.50199285_50199288delCA2695226556COL1A1c.410_413del (p.Gln137LeufsTer?)
n.631_634del
17g.50199285G>ACA400227399COL1A1c.412C>T (p.Pro138Ser)
n.633C>T
17g.50199285G>CCA400227400COL1A1c.412C>G (p.Pro138Ala)
n.633C>G
17g.50199285G>TCA400227402COL1A1c.412C>A (p.Pro138Thr)
n.633C>A
gnomAD v4
17g.50199286C>ACA400227404COL1A1c.411G>T (p.Gln137His)
n.632G>T
gnomAD v4
17g.50199286C>GCA400227405COL1A1c.411G>C (p.Gln137His)
n.632G>C
gnomAD v4
17g.50199286C>TCA500852189COL1A1c.411G>A (p.Gln137=)
n.632G>A
ClinVar gnomAD v4
17g.50199287T>ACA400227407COL1A1c.410A>T (p.Gln137Leu)
n.631A>T
gnomAD v4
17g.50199287T>CCA400227409COL1A1c.410A>G (p.Gln137Arg)
n.631A>G
gnomAD v4
17g.50199287T>GCA400227411COL1A1c.410A>C (p.Gln137Pro)
n.631A>C
17g.50199288G>ACA400227413COL1A1c.409C>T (p.Gln137Ter)
n.630C>T
ClinVar gnomAD v4
17g.50199288G>CCA400227415COL1A1c.409C>G (p.Gln137Glu)
n.630C>G
17g.50199288G>TCA400227417COL1A1c.409C>A (p.Gln137Lys)
n.630C>A
gnomAD v4
17g.50199289T>ACA500852190COL1A1c.408A>T (p.Gly136=)
n.629A>T
c.462A>T (p.Gly154=)
gnomAD v4
17g.50199289T>CCA8645703COL1A1c.408A>G (p.Gly136=)
n.629A>G
c.462A>G (p.Gly154=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.50199289T>GCA500852191COL1A1c.408A>C (p.Gly136=)
n.629A>C
c.462A>C (p.Gly154=)
17g.50199289T=CA2263920623COL1A1c.408A= (p.Gly136=)
n.629A=
c.462A= (p.Gly154=)
17g.50199290C>ACA400227421COL1A1c.407G>T (p.Gly136Val)
n.628G>T
c.461G>T (p.Gly154Val)
gnomAD v4
17g.50199290C>GCA400227422COL1A1c.407G>C (p.Gly136Ala)
n.628G>C
c.461G>C (p.Gly154Ala)
17g.50199290C>TCA400227423COL1A1c.407G>A (p.Gly136Glu)
n.628G>A
c.461G>A (p.Gly154Glu)
gnomAD v4 COSMIC
17g.50199291dupCA2695226557COL1A1c.407dup (p.Gln137ThrfsTer?)
n.628dup
c.461dup (p.Gly154=)
17g.50199291C>ACA400227426COL1A1c.406G>T (p.Gly136Ter)
n.627G>T
c.460G>T (p.Gly154Ter)
gnomAD v4
17g.50199291C>GCA400227428COL1A1c.406G>C (p.Gly136Arg)
n.627G>C
c.460G>C (p.Gly154Arg)
17g.50199291C>TCA400227429COL1A1c.406G>A (p.Gly136Arg)
n.627G>A
c.460G>A (p.Gly154Arg)
17g.50199292A>CCA500852192COL1A1c.405T>G (p.Pro135=)
n.626T>G
c.459T>G (p.Pro153=)
17g.50199292A>GCA500852193COL1A1c.405T>C (p.Pro135=)
n.626T>C
c.459T>C (p.Pro153=)
ClinVar gnomAD v4
17g.50199292A>TCA500852194COL1A1c.405T>A (p.Pro135=)
n.626T>A
c.459T>A (p.Pro153=)
17g.50199293G>ACA400227433COL1A1c.404C>T (p.Pro135Leu)
n.625C>T
c.458C>T (p.Pro153Leu)
17g.50199293G>CCA400227435COL1A1c.404C>G (p.Pro135Arg)
n.625C>G
c.458C>G (p.Pro153Arg)
ClinVar dbSNP
17g.50199293G>TCA400227434COL1A1c.404C>A (p.Pro135His)
n.625C>A
c.458C>A (p.Pro153His)
gnomAD v4
17g.50199294G>ACA400227437COL1A1c.403C>T (p.Pro135Ser)
n.624C>T
c.457C>T (p.Pro153Ser)
17g.50199294G>CCA400227439COL1A1c.403C>G (p.Pro135Ala)
n.624C>G
c.457C>G (p.Pro153Ala)
17g.50199294G>TCA400227440COL1A1c.403C>A (p.Pro135Thr)
n.624C>A
c.457C>A (p.Pro153Thr)
17g.50199295G>ACA500852195COL1A1c.402C>T (p.Ile134=)
n.623C>T
c.456C>T (p.Ile152=)
dbSNP gnomAD v3 gnomAD v4
17g.50199295G>CCA400227441COL1A1c.402C>G (p.Ile134Met)
n.623C>G
c.456C>G (p.Ile152Met)
dbSNP gnomAD v3 gnomAD v4
17g.50199295G=CA2263920624COL1A1c.402C= (p.Ile134=)
n.623C=
c.456C= (p.Ile152=)
17g.50199295G>TCA500852196COL1A1c.402C>A (p.Ile134=)
n.623C>A
c.456C>A (p.Ile152=)
gnomAD v4
17g.50199296A=CA2263920625COL1A1c.401T= (p.Ile134=)
n.622T=
c.455T= (p.Ile152=)
17g.50199296A>CCA400227442COL1A1c.401T>G (p.Ile134Ser)
n.622T>G
c.455T>G (p.Ile152Ser)
17g.50199296A>GCA400227443COL1A1c.401T>C (p.Ile134Thr)
n.622T>C
c.455T>C (p.Ile152Thr)
gnomAD v4
17g.50199296A>TCA8645704COL1A1c.401T>A (p.Ile134Asn)
n.622T>A
c.455T>A (p.Ile152Asn)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.50199296dupCA2580094386COL1A1c.401dup (p.Gly136TrpfsTer?)
n.622dup
c.455dup (p.Gly154TrpfsTer?)
ClinVar
17g.50199297T>ACA400227445COL1A1c.400A>T (p.Ile134Phe)
n.621A>T
c.454A>T (p.Ile152Phe)
17g.50199297T>CCA400227446COL1A1c.400A>G (p.Ile134Val)
n.621A>G
c.454A>G (p.Ile152Val)
17g.50199297T>GCA400227447COL1A1c.400A>C (p.Ile134Leu)
n.621A>C
c.454A>C (p.Ile152Leu)
17g.50199297dupCA1139665715COL1A1c.400dup (p.Ile134AsnfsTer?)
n.621dup
c.454dup (p.Ile152AsnfsTer?)
17g.50199297_50199306delinsTGCCATCTCGCA2263920626COL1A1c.391_400delinsCGAGATGGCA (p.Arg131=)
n.612_621delinsCGAGATGGCA
c.445_454delinsCGAGATGGCA (p.Arg149=)
17g.50199298G>ACA8645705COL1A1c.399C>T (p.Gly133=)
n.620C>T
c.453C>T (p.Gly151=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.50199298G>CCA500852197COL1A1c.399C>G (p.Gly133=)
n.620C>G
c.453C>G (p.Gly151=)
17g.50199298G=CA2263920628COL1A1c.399C= (p.Gly133=)
n.620C=
c.453C= (p.Gly151=)
17g.50199298G>TCA500852198COL1A1c.399C>A (p.Gly133=)
n.620C>A
c.453C>A (p.Gly151=)
gnomAD v4
17g.50199302_50199310delCA2263920627COL1A1c.391_399del (p.Arg131_Gly133del)
n.612_620del
c.445_453del (p.Arg149_Gly151del)
dbSNP
17g.50199299C>ACA400227454COL1A1c.398G>T (p.Gly133Val)
n.619G>T
c.452G>T (p.Gly151Val)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.50199299C=CA2263920629COL1A1c.398G= (p.Gly133=)
n.619G=
c.452G= (p.Gly151=)
17g.50199299C>GCA400227452COL1A1c.398G>C (p.Gly133Ala)
n.619G>C
c.452G>C (p.Gly151Ala)
17g.50199299C>TCA400227450COL1A1c.398G>A (p.Gly133Asp)
n.619G>A
c.452G>A (p.Gly151Asp)
gnomAD v4
17g.50199300C>ACA400227456COL1A1c.397G>T (p.Gly133Cys)
n.618G>T
c.451G>T (p.Gly151Cys)
17g.50199300C>GCA400227458COL1A1c.397G>C (p.Gly133Arg)
n.618G>C
c.451G>C (p.Gly151Arg)
17g.50199300C>TCA400227460COL1A1c.397G>A (p.Gly133Ser)
n.618G>A
c.451G>A (p.Gly151Ser)
17g.50199301A>CCA400227462COL1A1c.396T>G (p.Asp132Glu)
n.617T>G
c.450T>G (p.Asp150Glu)
17g.50199301A>GCA500852199COL1A1c.396T>C (p.Asp132=)
n.617T>C
c.450T>C (p.Asp150=)
ClinVar
17g.50199301A>TCA400227464COL1A1c.396T>A (p.Asp132Glu)
n.617T>A
c.450T>A (p.Asp150Glu)
17g.50199302T>ACA400227466COL1A1c.395A>T (p.Asp132Val)
n.616A>T
c.449A>T (p.Asp150Val)
gnomAD v4
17g.50199302T>CCA8645706COL1A1c.395A>G (p.Asp132Gly)
n.616A>G
c.449A>G (p.Asp150Gly)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.50199302T>GCA400227468COL1A1c.395A>C (p.Asp132Ala)
n.616A>C
c.449A>C (p.Asp150Ala)
17g.50199302T=CA2263920630COL1A1c.395A= (p.Asp132=)
n.616A=
c.449A= (p.Asp150=)
17g.50199304_50199305delCA2580612658COL1A1c.394_395del (p.Asp132TrpfsTer?)
n.615_616del
c.448_449del (p.Asp150TrpfsTer?)
ClinVar dbSNP
17g.50199303C>ACA400227471COL1A1c.394G>T (p.Asp132Tyr)
n.615G>T
c.448G>T (p.Asp150Tyr)
gnomAD v4
17g.50199303C>GCA400227473COL1A1c.394G>C (p.Asp132His)
n.615G>C
c.448G>C (p.Asp150His)
gnomAD v4
17g.50199303C>TCA400227474COL1A1c.394G>A (p.Asp132Asn)
n.615G>A
c.448G>A (p.Asp150Asn)
gnomAD v4
17g.50199304T>ACA8645707COL1A1c.393A>T (p.Arg131=)
n.614A>T
c.447A>T (p.Arg149=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.50199304T>CCA500852200COL1A1c.393A>G (p.Arg131=)
n.614A>G
c.447A>G (p.Arg149=)
gnomAD v4
17g.50199304T>GCA500852201COL1A1c.393A>C (p.Arg131=)
n.614A>C
c.447A>C (p.Arg149=)
17g.50199304T=CA2263920631COL1A1c.393A= (p.Arg131=)
n.614A=
c.447A= (p.Arg149=)
17g.50199305C>ACA400227480COL1A1c.392G>T (p.Arg131Leu)
n.613G>T
c.446G>T (p.Arg149Leu)
gnomAD v4
17g.50199305C=CA2263920632COL1A1c.392G= (p.Arg131=)
n.613G=
c.446G= (p.Arg149=)
17g.50199305C>GCA400227477COL1A1c.392G>C (p.Arg131Pro)
n.613G>C
c.446G>C (p.Arg149Pro)
dbSNP gnomAD v2 gnomAD v4
17g.50199305C>TCA400227479COL1A1c.392G>A (p.Arg131Gln)
n.613G>A
c.446G>A (p.Arg149Gln)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.50199306G>ACA400227482COL1A1c.391C>T (p.Arg131Ter)
n.612C>T
c.445C>T (p.Arg149Ter)
ClinVar dbSNP gnomAD v4
17g.50199306G>CCA400227483COL1A1c.391C>G (p.Arg131Gly)
n.612C>G
c.445C>G (p.Arg149Gly)
gnomAD v4
17g.50199306G=CA2263920633COL1A1c.391C= (p.Arg131=)
n.612C=
c.445C= (p.Arg149=)
17g.50199306G>TCA8645708COL1A1c.391C>A (p.Arg131=)
n.612C>A
c.445C>A (p.Arg149=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.50199306_50199307insTCA2695226558COL1A1c.390_391insA (p.Arg131ThrfsTer?)
n.611_612insA
c.444_445insA (p.Arg149ThrfsTer?)
17g.50199307G>ACA500852202COL1A1c.390C>T (p.Gly130=)
n.611C>T
c.444C>T (p.Gly148=)
gnomAD v4
17g.50199307G>CCA500852203COL1A1c.390C>G (p.Gly130=)
n.611C>G
c.444C>G (p.Gly148=)
17g.50199307G=CA2263920634COL1A1c.390C= (p.Gly130=)
n.611C=
c.444C= (p.Gly148=)
17g.50199307G>TCA500852204COL1A1c.390C>A (p.Gly130=)
n.611C>A
c.444C>A (p.Gly148=)
dbSNP gnomAD v4
17g.50199307_50199308insTCA291550411COL1A1c.389_390insA (p.Arg131ProfsTer?)
n.610_611insA
c.443_444insA (p.Arg149ProfsTer?)
dbSNP
17g.50199308C>ACA400227487COL1A1c.389G>T (p.Gly130Val)
n.610G>T
c.443G>T (p.Gly148Val)
gnomAD v4
17g.50199308C>GCA400227489COL1A1c.389G>C (p.Gly130Ala)
n.610G>C
c.443G>C (p.Gly148Ala)
17g.50199308C>TCA400227485COL1A1c.389G>A (p.Gly130Asp)
n.610G>A
c.443G>A (p.Gly148Asp)
17g.50199309C>ACA400227495COL1A1c.388G>T (p.Gly130Cys)
n.609G>T
c.442G>T (p.Gly148Cys)
ClinVar dbSNP
17g.50199309C=CA2263920635COL1A1c.388G= (p.Gly130=)
n.609G=
c.442G= (p.Gly148=)
17g.50199309C>GCA400227492COL1A1c.388G>C (p.Gly130Arg)
n.609G>C
c.442G>C (p.Gly148Arg)
17g.50199309C>TCA400227493COL1A1c.388G>A (p.Gly130Ser)
n.609G>A
c.442G>A (p.Gly148Ser)
17g.50199309_50199310delinsCACA2263920636COL1A1c.387_388delinsTG (p.Pro129=)
n.608_609delinsTG
c.441_442delinsTG (p.Pro147=)
17g.50199310delCA658656726COL1A1c.387del (p.Gly130AlafsTer?)
n.608del
c.441del (p.Gly148AlafsTer?)
ClinVar dbSNP
17g.50199310A>CCA500852206COL1A1c.387T>G (p.Pro129=)
n.608T>G
c.441T>G (p.Pro147=)
17g.50199310A>GCA500852205COL1A1c.387T>C (p.Pro129=)
n.608T>C
c.441T>C (p.Pro147=)
ClinVar gnomAD v4
17g.50199310A>TCA500852207COL1A1c.387T>A (p.Pro129=)
n.608T>A
c.441T>A (p.Pro147=)
17g.50199310_50199311delinsAGCA2263920637COL1A1c.386_387delinsCT (p.Pro129=)
n.607_608delinsCT
c.440_441delinsCT (p.Pro147=)
17g.50199311G>ACA400227497COL1A1c.386C>T (p.Pro129Leu)
n.607C>T
c.440C>T (p.Pro147Leu)
17g.50199311G>CCA400227499COL1A1c.386C>G (p.Pro129Arg)
n.607C>G
c.440C>G (p.Pro147Arg)
17g.50199311G=CA2263920638COL1A1c.386C= (p.Pro129=)
n.607C=
c.440C= (p.Pro147=)
17g.50199311G>TCA291550413COL1A1c.386C>A (p.Pro129His)
n.607C>A
c.440C>A (p.Pro147His)
dbSNP gnomAD v4
17g.50199316dupCA645509528COL1A1c.386dup (p.Gly130TrpfsTer?)
n.607dup
c.440dup (p.Gly148TrpfsTer?)
ClinVar dbSNP gnomAD v4
17g.50199316delCA8645709COL1A1c.386del (p.Pro129LeufsTer?)
n.607del
c.440del (p.Pro147LeufsTer?)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
17g.50199312G>ACA8645710COL1A1c.385C>T (p.Pro129Ser)
n.606C>T
c.439C>T (p.Pro147Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.50199312G>CCA400227504COL1A1c.385C>G (p.Pro129Ala)
n.606C>G
c.439C>G (p.Pro147Ala)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.50199312G=CA2263920639COL1A1c.385C= (p.Pro129=)
n.606C=
c.439C= (p.Pro147=)
17g.50199312G>TCA400227506COL1A1c.385C>A (p.Pro129Thr)
n.606C>A
c.439C>A (p.Pro147Thr)
gnomAD v4
17g.50199313G>ACA500852208COL1A1c.384C>T (p.Pro128=)
n.605C>T
c.438C>T (p.Pro146=)
gnomAD v4
17g.50199313G>CCA500852209COL1A1c.384C>G (p.Pro128=)
n.605C>G
c.438C>G (p.Pro146=)
dbSNP gnomAD v4
17g.50199313G=CA2263920640COL1A1c.384C= (p.Pro128=)
n.605C=
c.438C= (p.Pro146=)
17g.50199313G>TCA500852210COL1A1c.384C>A (p.Pro128=)
n.605C>A
c.438C>A (p.Pro146=)
ClinVar dbSNP gnomAD v4
17g.50199314G>ACA400227509COL1A1c.383C>T (p.Pro128Leu)
n.604C>T
c.437C>T (p.Pro146Leu)
dbSNP
17g.50199314G>CCA400227511COL1A1c.383C>G (p.Pro128Arg)
n.604C>G
c.437C>G (p.Pro146Arg)
17g.50199314G=CA2263920641COL1A1c.383C= (p.Pro128=)
n.604C=
c.437C= (p.Pro146=)
17g.50199314G>TCA400227515COL1A1c.383C>A (p.Pro128His)
n.604C>A
c.437C>A (p.Pro146His)
gnomAD v4
17g.50199317_50199324delCA2739268230COL1A1c.376_383del (p.Ala126ProfsTer?)
n.597_604del
c.430_437del (p.Ala144ProfsTer?)
ClinVar
17g.50199315G>ACA400227517COL1A1c.382C>T (p.Pro128Ser)
n.603C>T
c.436C>T (p.Pro146Ser)
dbSNP gnomAD v2 gnomAD v4
17g.50199315G>CCA400227520COL1A1c.382C>G (p.Pro128Ala)
n.603C>G
c.436C>G (p.Pro146Ala)
17g.50199315G=CA2263920642COL1A1c.382C= (p.Pro128=)
n.603C=
c.436C= (p.Pro146=)
17g.50199315G>TCA400227518COL1A1c.382C>A (p.Pro128Thr)
n.603C>A
c.436C>A (p.Pro146Thr)
gnomAD v4
17g.50199316G>ACA500852211COL1A1c.381C>T (p.Gly127=)
n.602C>T
c.435C>T (p.Gly145=)
ClinVar dbSNP gnomAD v2 gnomAD v4
17g.50199316G>CCA500852212COL1A1c.381C>G (p.Gly127=)
n.602C>G
c.435C>G (p.Gly145=)
ClinVar gnomAD v4
17g.50199316G=CA2263920643COL1A1c.381C= (p.Gly127=)
n.602C=
c.435C= (p.Gly145=)
17g.50199316G>TCA8645711COL1A1c.381C>A (p.Gly127=)
n.602C>A
c.435C>A (p.Gly145=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
17g.50199317C>ACA400227524COL1A1c.380G>T (p.Gly127Val)
n.601G>T
c.434G>T (p.Gly145Val)
17g.50199317C>GCA400227526COL1A1c.380G>C (p.Gly127Ala)
n.601G>C
c.434G>C (p.Gly145Ala)
gnomAD v4
17g.50199317C>TCA400227527COL1A1c.380G>A (p.Gly127Asp)
n.601G>A
c.434G>A (p.Gly145Asp)
gnomAD v4
17g.50199318delCA2573154239COL1A1c.380del (p.Gly127AlafsTer?)
n.601del
c.434del (p.Gly145AlafsTer?)
ClinVar dbSNP
17g.50199318C>ACA400227530COL1A1c.379G>T (p.Gly127Cys)
n.600G>T
c.433G>T (p.Gly145Cys)
gnomAD v4
17g.50199318C>GCA400227532COL1A1c.379G>C (p.Gly127Arg)
n.600G>C
c.433G>C (p.Gly145Arg)
17g.50199318C>TCA400227533COL1A1c.379G>A (p.Gly127Ser)
n.600G>A
c.433G>A (p.Gly145Ser)
gnomAD v4
17g.50199319T>ACA500852213COL1A1c.378A>T (p.Ala126=)
n.599A>T
c.432A>T (p.Ala144=)
17g.50199319T>CCA500852214COL1A1c.378A>G (p.Ala126=)
n.599A>G
c.432A>G (p.Ala144=)
gnomAD v4
17g.50199319T>GCA500852215COL1A1c.378A>C (p.Ala126=)
n.599A>C
c.432A>C (p.Ala144=)
gnomAD v4
17g.50199320G>ACA400227536COL1A1c.377C>T (p.Ala126Val)
n.598C>T
c.431C>T (p.Ala144Val)
gnomAD v4
17g.50199320G>CCA400227538COL1A1c.377C>G (p.Ala126Gly)
n.598C>G
c.431C>G (p.Ala144Gly)
17g.50199320G>TCA400227539COL1A1c.377C>A (p.Ala126Glu)
n.598C>A
c.431C>A (p.Ala144Glu)
gnomAD v4
17g.50199321C>ACA400227543COL1A1c.376G>T (p.Ala126Ser)
n.597G>T
c.430G>T (p.Ala144Ser)
ClinVar dbSNP gnomAD v2 gnomAD v4
17g.50199321C=CA2263920644COL1A1c.376G= (p.Ala126=)
n.597G=
c.430G= (p.Ala144=)
17g.50199321C>GCA400227545COL1A1c.376G>C (p.Ala126Pro)
n.597G>C
c.430G>C (p.Ala144Pro)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.50199321C>TCA400227541COL1A1c.376G>A (p.Ala126Thr)
n.597G>A
c.430G>A (p.Ala144Thr)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.50199322G>ACA500852216COL1A1c.375C>T (p.Pro125=)
n.596C>T
c.429C>T (p.Pro143=)
ClinVar dbSNP gnomAD v2 gnomAD v4
17g.50199322G>CCA500852217COL1A1c.375C>G (p.Pro125=)
n.596C>G
c.429C>G (p.Pro143=)
gnomAD v4
17g.50199322G=CA2263920645COL1A1c.375C= (p.Pro125=)
n.596C=
c.429C= (p.Pro143=)
17g.50199322G>TCA500852218COL1A1c.375C>A (p.Pro125=)
n.596C>A
c.429C>A (p.Pro143=)
gnomAD v4
17g.50199324dupCA2695226559COL1A1c.375dup (p.Ala126ArgfsTer?)
n.596dup
c.429dup (p.Ala144ArgfsTer?)
17g.50199323G>ACA400227548COL1A1c.374C>T (p.Pro125Leu)
n.595C>T
c.428C>T (p.Pro143Leu)
gnomAD v4
17g.50199323G>CCA400227549COL1A1c.374C>G (p.Pro125Arg)
n.595C>G
c.428C>G (p.Pro143Arg)
dbSNP
17g.50199323G=CA2263920646COL1A1c.374C= (p.Pro125=)
n.595C=
c.428C= (p.Pro143=)
17g.50199323G>TCA400227550COL1A1c.374C>A (p.Pro125His)
n.595C>A
c.428C>A (p.Pro143His)
gnomAD v4
17g.50199324G>ACA400227551COL1A1c.373C>T (p.Pro125Ser)
n.594C>T
c.427C>T (p.Pro143Ser)
dbSNP gnomAD v2 gnomAD v4
17g.50199324G>CCA400227552COL1A1c.373C>G (p.Pro125Ala)
n.594C>G
c.427C>G (p.Pro143Ala)
17g.50199324G=CA2263920647COL1A1c.373C= (p.Pro125=)
n.594C=
c.427C= (p.Pro143=)
17g.50199324G>TCA400227553COL1A1c.373C>A (p.Pro125Thr)
n.594C>A
c.427C>A (p.Pro143Thr)
gnomAD v4
17g.50199325T>ACA500852220COL1A1c.372A>T (p.Gly124=)
n.593A>T
c.426A>T (p.Gly142=)
ClinVar
17g.50199325T>CCA500852221COL1A1c.372A>G (p.Gly124=)
n.593A>G
c.426A>G (p.Gly142=)
dbSNP gnomAD v4
17g.50199325T>GCA500852219COL1A1c.372A>C (p.Gly124=)
n.593A>C
c.426A>C (p.Gly142=)
17g.50199325T=CA2263920648COL1A1c.372A= (p.Gly124=)
n.593A=
c.426A= (p.Gly142=)
17g.50199326C>ACA400227555COL1A1c.371G>T (p.Gly124Val)
n.592G>T
c.425G>T (p.Gly142Val)
gnomAD v4
17g.50199326C>GCA400227557COL1A1c.371G>C (p.Gly124Ala)
n.592G>C
c.425G>C (p.Gly142Ala)
17g.50199326C>TCA400227559COL1A1c.371G>A (p.Gly124Glu)
n.592G>A
c.425G>A (p.Gly142Glu)
gnomAD v4
17g.50199327C>ACA400227562COL1A1c.370G>T (p.Gly124Ter)
n.591G>T
c.424G>T (p.Gly142Ter)
17g.50199327C>GCA400227564COL1A1c.370G>C (p.Gly124Arg)
n.591G>C
c.424G>C (p.Gly142Arg)
17g.50199327C>TCA400227565COL1A1c.370G>A (p.Gly124Arg)
n.591G>A
c.424G>A (p.Gly142Arg)
17g.50199329_50199418delCA500852222COL1A1c.369+2_370del
n.590+2_591del
c.423+2_424del
17g.50199328C>ACA400227570COL1A1c.370-1G>T (n.370-1G>T)
n.591-1G>T
c.424-1G>T (n.424-1G>T)
ClinVar dbSNP gnomAD v4
17g.50199328C>GCA400227567COL1A1c.370-1G>C (n.370-1G>C)
n.591-1G>C
c.424-1G>C (n.424-1G>C)
17g.50199328C>TCA400227568COL1A1c.370-1G>A (n.370-1G>A)
n.591-1G>A
c.424-1G>A (n.424-1G>A)
ClinVar dbSNP
17g.50199328_50199330delinsGACA2695226560COL1A1c.370-3_370-1delinsTC (n.370-3_370-1delinsTC)
n.591-3_591-1delinsTC
c.424-3_424-1delinsTC (n.424-3_424-1delinsTC)
17g.50199329T>ACA400227572COL1A1c.370-2A>T (n.370-2A>T)
n.591-2A>T
c.424-2A>T (n.424-2A>T)
ClinVar
17g.50199329T>CCA260312COL1A1c.370-2A>G (n.370-2A>G)
n.591-2A>G
c.424-2A>G (n.424-2A>G)
ClinVar dbSNP gnomAD v4
17g.50199329T>GCA400227574COL1A1c.370-2A>C (n.370-2A>C)
n.591-2A>C
c.424-2A>C (n.424-2A>C)
17g.50199329T=CA2263920649COL1A1c.370-2A= (n.370-2A=)
n.591-2A=
c.424-2A= (n.424-2A=)
17g.50199331C>ACA2638682957COL1A1c.370-4G>T (n.370-4G>T)
n.591-4G>T
c.424-4G>T (n.424-4G>T)
gnomAD v4
17g.50199331C>TCA2638682959COL1A1c.370-4G>A (n.370-4G>A)
n.591-4G>A
c.424-4G>A (n.424-4G>A)
gnomAD v4
17g.50199332A>CCA2638682964COL1A1c.370-5T>G (n.370-5T>G)
n.591-5T>G
c.424-5T>G (n.424-5T>G)
gnomAD v4
17g.50199332_50199333delinsAGCA2263920650COL1A1c.370-6_370-5delinsCT (n.370-6_370-5delinsCT)
n.591-6_591-5delinsCT
c.424-6_424-5delinsCT (n.424-6_424-5delinsCT)
17g.50199333G>ACA2638682977COL1A1c.370-6C>T (n.370-6C>T)
n.591-6C>T
c.424-6C>T (n.424-6C>T)
gnomAD v4
17g.50199333G>CCA2740093785COL1A1c.370-6C>G (n.370-6C>G)
n.591-6C>G
c.424-6C>G (n.424-6C>G)
ClinVar
17g.50199337delCA291550439COL1A1c.370-6del (n.370-6del)
n.591-6del
c.424-6del (n.424-6del)
ClinVar dbSNP gnomAD v4
17g.50199334G>ACA626486285COL1A1c.370-7C>T (n.370-7C>T)
n.591-7C>T
c.424-7C>T (n.424-7C>T)
dbSNP gnomAD v2 gnomAD v4
17g.50199334G=CA2263920651COL1A1c.370-7C= (n.370-7C=)
n.591-7C=
c.424-7C= (n.424-7C=)
17g.50199334G>TCA2638682992COL1A1c.370-7C>A (n.370-7C>A)
n.591-7C>A
c.424-7C>A (n.424-7C>A)
gnomAD v4
17g.50199335G>ACA2638682995COL1A1c.370-8C>T (n.370-8C>T)
n.591-8C>T
c.424-8C>T (n.424-8C>T)
gnomAD v4
17g.50199335G>TCA2638682998COL1A1c.370-8C>A (n.370-8C>A)
n.591-8C>A
c.424-8C>A (n.424-8C>A)
gnomAD v4
17g.50199336G>ACA8645712COL1A1c.370-9C>T (n.370-9C>T)
n.591-9C>T
c.424-9C>T (n.424-9C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.50199336G=CA2263920652COL1A1c.370-9C= (n.370-9C=)
n.591-9C=
c.424-9C= (n.424-9C=)
17g.50199337G>CCA626486287COL1A1c.370-10C>G (n.370-10C>G)
n.591-10C>G
c.424-10C>G (n.424-10C>G)
dbSNP gnomAD v2
17g.50199337G=CA2263920653COL1A1c.370-10C= (n.370-10C=)
n.591-10C=
c.424-10C= (n.424-10C=)
17g.50199337G>TCA2638683014COL1A1c.370-10C>A (n.370-10C>A)
n.591-10C>A
c.424-10C>A (n.424-10C>A)
gnomAD v4
17g.50199338A>GCA2638683020COL1A1c.370-11T>C (n.370-11T>C)
n.591-11T>C
c.424-11T>C (n.424-11T>C)
gnomAD v4
17g.50199338A>TCA2638683025COL1A1c.370-11T>A (n.370-11T>A)
n.591-11T>A
c.424-11T>A (n.424-11T>A)
gnomAD v4
17g.50199339G>ACA626486288COL1A1c.370-12C>T (n.370-12C>T)
n.591-12C>T
c.424-12C>T (n.424-12C>T)
dbSNP gnomAD v2 gnomAD v4
17g.50199339G>CCA2638683034COL1A1c.370-12C>G (n.370-12C>G)
n.591-12C>G
c.424-12C>G (n.424-12C>G)
gnomAD v4
17g.50199339G=CA2263920654COL1A1c.370-12C= (n.370-12C=)
n.591-12C=
c.424-12C= (n.424-12C=)
17g.50199339G>TCA2638683039COL1A1c.370-12C>A (n.370-12C>A)
n.591-12C>A
c.424-12C>A (n.424-12C>A)
gnomAD v4

Number of alleles fetched