Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.43084851_43094146delCA645369660BRCA1c.1384_4186-2277del
c.1243_4045-2277del
c.787+597_877-2277del
n.1520_4322-2277del
n.1561_4363-2277del
c.670+1699_760-2277del
c.*1167_*3969-2277del
c.784+597_874-2277del
n.409+597_499-2277del
n.412+597_502-2277del
c.646+597_736-2277del
c.5-30196_5-20901del (p.=)
c.-43-19626_-43-10331del (p.=)
c.-99+31124_-98-34662del (p.=)
ClinVar
17g.43091681_43091691delCA10589719BRCA1c.3836_3846del (p.Gln1281ProfsTer2)
c.3695_3705del (p.Gln1234ProfsTer2)
c.788-663_788-653del (p.=)
n.3972_3982del
n.4013_4023del
c.671-663_671-653del (p.=)
c.*3619_*3629del (p.=)
n.130_140del
c.785-663_785-653del (p.=)
n.410-663_410-653del (p.=)
n.413-663_413-653del (p.=)
c.647-663_647-653del (p.=)
c.5-27744_5-27734del (p.=)
c.-43-17174_-43-17164del (p.=)
c.-99+33576_-99+33586del (p.=)
ClinVar dbSNP
17g.43091683T>ACA10594268BRCA1c.3848A>T (p.His1283Leu)
c.3707A>T (p.His1236Leu)
c.788-651A>T (p.=)
n.3984A>T
n.4025A>T
c.671-651A>T (p.=)
c.*3631A>T (p.=)
n.142A>T
c.785-651A>T (p.=)
n.410-651A>T (p.=)
n.413-651A>T (p.=)
c.647-651A>T (p.=)
c.5-27732A>T (p.=)
c.-43-17162A>T (p.=)
c.-99+33588A>T (p.=)
17g.43091683T>CCA002479BRCA1c.3848A>G (p.His1283Arg)
c.3707A>G (p.His1236Arg)
c.788-651A>G (p.=)
n.3984A>G
n.4025A>G
c.671-651A>G (p.=)
c.*3631A>G (p.=)
n.142A>G
c.785-651A>G (p.=)
n.410-651A>G (p.=)
n.413-651A>G (p.=)
c.647-651A>G (p.=)
c.5-27732A>G (p.=)
c.-43-17162A>G (p.=)
c.-99+33588A>G (p.=)
ClinVar dbSNP ExAC gnomAD
17g.43091683T>GCA10594269BRCA1c.3848A>C (p.His1283Pro)
c.3707A>C (p.His1236Pro)
c.788-651A>C (p.=)
n.3984A>C
n.4025A>C
c.671-651A>C (p.=)
c.*3631A>C (p.=)
n.142A>C
c.785-651A>C (p.=)
n.410-651A>C (p.=)
n.413-651A>C (p.=)
c.647-651A>C (p.=)
c.5-27732A>C (p.=)
c.-43-17162A>C (p.=)
c.-99+33588A>C (p.=)
17g.43091684G>ACA10594270BRCA1c.3847C>T (p.His1283Tyr)
c.3706C>T (p.His1236Tyr)
c.788-652C>T (p.=)
n.3983C>T
n.4024C>T
c.671-652C>T (p.=)
c.*3630C>T (p.=)
n.141C>T
c.785-652C>T (p.=)
n.410-652C>T (p.=)
n.413-652C>T (p.=)
c.647-652C>T (p.=)
c.5-27733C>T (p.=)
c.-43-17163C>T (p.=)
c.-99+33587C>T (p.=)
ClinVar
17g.43091684G>CCA10594271BRCA1c.3847C>G (p.His1283Asp)
c.3706C>G (p.His1236Asp)
c.788-652C>G (p.=)
n.3983C>G
n.4024C>G
c.671-652C>G (p.=)
c.*3630C>G (p.=)
n.141C>G
c.785-652C>G (p.=)
n.410-652C>G (p.=)
n.413-652C>G (p.=)
c.647-652C>G (p.=)
c.5-27733C>G (p.=)
c.-43-17163C>G (p.=)
c.-99+33587C>G (p.=)
17g.43091684G>TCA10594272BRCA1c.3847C>A (p.His1283Asn)
c.3706C>A (p.His1236Asn)
c.788-652C>A (p.=)
n.3983C>A
n.4024C>A
c.671-652C>A (p.=)
c.*3630C>A (p.=)
n.141C>A
c.785-652C>A (p.=)
n.410-652C>A (p.=)
n.413-652C>A (p.=)
c.647-652C>A (p.=)
c.5-27733C>A (p.=)
c.-43-17163C>A (p.=)
c.-99+33587C>A (p.=)
17g.43091685T>ACA10594273BRCA1c.3846A>T (p.Glu1282Asp)
c.3705A>T (p.Glu1235Asp)
c.788-653A>T (p.=)
n.3982A>T
n.4023A>T
c.671-653A>T (p.=)
c.*3629A>T (p.=)
n.140A>T
c.785-653A>T (p.=)
n.410-653A>T (p.=)
n.413-653A>T (p.=)
c.647-653A>T (p.=)
c.5-27734A>T (p.=)
c.-43-17164A>T (p.=)
c.-99+33586A>T (p.=)
17g.43091685T>CCA500232159BRCA1c.3846A>G (p.Glu1282=)
c.3705A>G (p.Glu1235=)
c.788-653A>G (p.=)
n.3982A>G
n.4023A>G
c.671-653A>G (p.=)
c.*3629A>G (p.=)
n.140A>G
c.785-653A>G (p.=)
n.410-653A>G (p.=)
n.413-653A>G (p.=)
c.647-653A>G (p.=)
c.5-27734A>G (p.=)
c.-43-17164A>G (p.=)
c.-99+33586A>G (p.=)
ClinVar
17g.43091685T>GCA10594274BRCA1c.3846A>C (p.Glu1282Asp)
c.3705A>C (p.Glu1235Asp)
c.788-653A>C (p.=)
n.3982A>C
n.4023A>C
c.671-653A>C (p.=)
c.*3629A>C (p.=)
n.140A>C
c.785-653A>C (p.=)
n.410-653A>C (p.=)
n.413-653A>C (p.=)
c.647-653A>C (p.=)
c.5-27734A>C (p.=)
c.-43-17164A>C (p.=)
c.-99+33586A>C (p.=)
17g.43091686T>ACA002478BRCA1c.3845A>T (p.Glu1282Val)
c.3704A>T (p.Glu1235Val)
c.788-654A>T (p.=)
n.3981A>T
n.4022A>T
c.671-654A>T (p.=)
c.*3628A>T (p.=)
n.139A>T
c.785-654A>T (p.=)
n.410-654A>T (p.=)
n.413-654A>T (p.=)
c.647-654A>T (p.=)
c.5-27735A>T (p.=)
c.-43-17165A>T (p.=)
c.-99+33585A>T (p.=)
ClinVar dbSNP gnomAD
17g.43091686T>CCA10594275BRCA1c.3845A>G (p.Glu1282Gly)
c.3704A>G (p.Glu1235Gly)
c.788-654A>G (p.=)
n.3981A>G
n.4022A>G
c.671-654A>G (p.=)
c.*3628A>G (p.=)
n.139A>G
c.785-654A>G (p.=)
n.410-654A>G (p.=)
n.413-654A>G (p.=)
c.647-654A>G (p.=)
c.5-27735A>G (p.=)
c.-43-17165A>G (p.=)
c.-99+33585A>G (p.=)
17g.43091686T>GCA10594276BRCA1c.3845A>C (p.Glu1282Ala)
c.3704A>C (p.Glu1235Ala)
c.788-654A>C (p.=)
n.3981A>C
n.4022A>C
c.671-654A>C (p.=)
c.*3628A>C (p.=)
n.139A>C
c.785-654A>C (p.=)
n.410-654A>C (p.=)
n.413-654A>C (p.=)
c.647-654A>C (p.=)
c.5-27735A>C (p.=)
c.-43-17165A>C (p.=)
c.-99+33585A>C (p.=)
17g.43091687C>ACA10594277BRCA1c.3844G>T (p.Glu1282Ter)
c.3703G>T (p.Glu1235Ter)
c.788-655G>T (p.=)
n.3980G>T
n.4021G>T
c.671-655G>T (p.=)
c.*3627G>T (p.=)
n.138G>T
c.785-655G>T (p.=)
n.410-655G>T (p.=)
n.413-655G>T (p.=)
c.647-655G>T (p.=)
c.5-27736G>T (p.=)
c.-43-17166G>T (p.=)
c.-99+33584G>T (p.=)
17g.43091687C>GCA10594278BRCA1c.3844G>C (p.Glu1282Gln)
c.3703G>C (p.Glu1235Gln)
c.788-655G>C (p.=)
n.3980G>C
n.4021G>C
c.671-655G>C (p.=)
c.*3627G>C (p.=)
n.138G>C
c.785-655G>C (p.=)
n.410-655G>C (p.=)
n.413-655G>C (p.=)
c.647-655G>C (p.=)
c.5-27736G>C (p.=)
c.-43-17166G>C (p.=)
c.-99+33584G>C (p.=)
17g.43091687C>TCA10594279BRCA1c.3844G>A (p.Glu1282Lys)
c.3703G>A (p.Glu1235Lys)
c.788-655G>A (p.=)
n.3980G>A
n.4021G>A
c.671-655G>A (p.=)
c.*3627G>A (p.=)
n.138G>A
c.785-655G>A (p.=)
n.410-655G>A (p.=)
n.413-655G>A (p.=)
c.647-655G>A (p.=)
c.5-27736G>A (p.=)
c.-43-17166G>A (p.=)
c.-99+33584G>A (p.=)
17g.43091687delCA002477BRCA1c.3843del (p.Glu1282AsnfsTer25)
c.3702del (p.Glu1235AsnfsTer25)
c.788-656del (p.=)
n.3979del
n.4020del
c.671-656del (p.=)
c.*3626del (p.=)
n.137del
c.785-656del (p.=)
n.410-656del (p.=)
n.413-656del (p.=)
c.647-656del (p.=)
c.5-27737del (p.=)
c.-43-17167del (p.=)
c.-99+33583del (p.=)
ClinVar dbSNP
17g.43091688C>ACA10594280BRCA1c.3843G>T (p.Gln1281His)
c.3702G>T (p.Gln1234His)
c.788-656G>T (p.=)
n.3979G>T
n.4020G>T
c.671-656G>T (p.=)
c.*3626G>T (p.=)
n.137G>T
c.785-656G>T (p.=)
n.410-656G>T (p.=)
n.413-656G>T (p.=)
c.647-656G>T (p.=)
c.5-27737G>T (p.=)
c.-43-17167G>T (p.=)
c.-99+33583G>T (p.=)
ClinVar
17g.43091688C>GCA10594281BRCA1c.3843G>C (p.Gln1281His)
c.3702G>C (p.Gln1234His)
c.788-656G>C (p.=)
n.3979G>C
n.4020G>C
c.671-656G>C (p.=)
c.*3626G>C (p.=)
n.137G>C
c.785-656G>C (p.=)
n.410-656G>C (p.=)
n.413-656G>C (p.=)
c.647-656G>C (p.=)
c.5-27737G>C (p.=)
c.-43-17167G>C (p.=)
c.-99+33583G>C (p.=)
17g.43091688C>TCA500232160BRCA1c.3843G>A (p.Gln1281=)
c.3702G>A (p.Gln1234=)
c.788-656G>A (p.=)
n.3979G>A
n.4020G>A
c.671-656G>A (p.=)
c.*3626G>A (p.=)
n.137G>A
c.785-656G>A (p.=)
n.410-656G>A (p.=)
n.413-656G>A (p.=)
c.647-656G>A (p.=)
c.5-27737G>A (p.=)
c.-43-17167G>A (p.=)
c.-99+33583G>A (p.=)
17g.43091688_43091690delCA002474BRCA1c.3841_3843del (p.Gln1281del)
c.3700_3702del (p.Gln1234del)
c.788-658_788-656del (p.=)
n.3977_3979del
n.4018_4020del
c.671-658_671-656del (p.=)
c.*3624_*3626del (p.=)
n.135_137del
c.785-658_785-656del (p.=)
n.410-658_410-656del (p.=)
n.413-658_413-656del (p.=)
c.647-658_647-656del (p.=)
c.5-27739_5-27737del (p.=)
c.-43-17169_-43-17167del (p.=)
c.-99+33581_-99+33583del (p.=)
ClinVar dbSNP
17g.43091688_43091692delCA10589720BRCA1c.3839_3843del (p.Ser1280Ter)
c.3698_3702del (p.Ser1233Ter)
c.788-660_788-656del (p.=)
n.3975_3979del
n.4016_4020del
c.671-660_671-656del (p.=)
c.*3622_*3626del (p.=)
n.133_137del
c.785-660_785-656del (p.=)
n.410-660_410-656del (p.=)
n.413-660_413-656del (p.=)
c.647-660_647-656del (p.=)
c.5-27741_5-27737del (p.=)
c.-43-17171_-43-17167del (p.=)
c.-99+33579_-99+33583del (p.=)
ClinVar dbSNP
17g.43091688_43091692delinsGCCTCA002470BRCA1c.3839_3843delinsAGGC (p.Ser1280Ter)
c.3698_3702delinsAGGC (p.Ser1233Ter)
c.788-660_788-656delinsAGGC (p.=)
n.3975_3979delinsAGGC
n.4016_4020delinsAGGC
c.671-660_671-656delinsAGGC (p.=)
c.*3622_*3626delinsAGGC (p.=)
n.133_137delinsAGGC
c.785-660_785-656delinsAGGC (p.=)
n.410-660_410-656delinsAGGC (p.=)
n.413-660_413-656delinsAGGC (p.=)
c.647-660_647-656delinsAGGC (p.=)
c.5-27741_5-27737delinsAGGC (p.=)
c.-43-17171_-43-17167delinsAGGC (p.=)
c.-99+33579_-99+33583delinsAGGC (p.=)
ClinVar dbSNP
17g.43091689T>ACA10594282BRCA1c.3842A>T (p.Gln1281Leu)
c.3701A>T (p.Gln1234Leu)
c.788-657A>T (p.=)
n.3978A>T
n.4019A>T
c.671-657A>T (p.=)
c.*3625A>T (p.=)
n.136A>T
c.785-657A>T (p.=)
n.410-657A>T (p.=)
n.413-657A>T (p.=)
c.647-657A>T (p.=)
c.5-27738A>T (p.=)
c.-43-17168A>T (p.=)
c.-99+33582A>T (p.=)
17g.43091689T>CCA10594283BRCA1c.3842A>G (p.Gln1281Arg)
c.3701A>G (p.Gln1234Arg)
c.788-657A>G (p.=)
n.3978A>G
n.4019A>G
c.671-657A>G (p.=)
c.*3625A>G (p.=)
n.136A>G
c.785-657A>G (p.=)
n.410-657A>G (p.=)
n.413-657A>G (p.=)
c.647-657A>G (p.=)
c.5-27738A>G (p.=)
c.-43-17168A>G (p.=)
c.-99+33582A>G (p.=)
17g.43091689T>GCA002476BRCA1c.3842A>C (p.Gln1281Pro)
c.3701A>C (p.Gln1234Pro)
c.788-657A>C (p.=)
n.3978A>C
n.4019A>C
c.671-657A>C (p.=)
c.*3625A>C (p.=)
n.136A>C
c.785-657A>C (p.=)
n.410-657A>C (p.=)
n.413-657A>C (p.=)
c.647-657A>C (p.=)
c.5-27738A>C (p.=)
c.-43-17168A>C (p.=)
c.-99+33582A>C (p.=)
ClinVar dbSNP ExAC gnomAD
17g.43091689_43091690delCA002472BRCA1c.3841_3842del (p.Gln1281GlyfsTer5)
c.3700_3701del (p.Gln1234GlyfsTer5)
c.788-658_788-657del (p.=)
n.3977_3978del
n.4018_4019del
c.671-658_671-657del (p.=)
c.*3624_*3625del (p.=)
n.135_136del
c.785-658_785-657del (p.=)
n.410-658_410-657del (p.=)
n.413-658_413-657del (p.=)
c.647-658_647-657del (p.=)
c.5-27739_5-27738del (p.=)
c.-43-17169_-43-17168del (p.=)
c.-99+33581_-99+33582del (p.=)
ClinVar dbSNP
17g.43091690G>ACA002475BRCA1c.3841C>T (p.Gln1281Ter)
c.3700C>T (p.Gln1234Ter)
c.788-658C>T (p.=)
n.3977C>T
n.4018C>T
c.671-658C>T (p.=)
c.*3624C>T (p.=)
n.135C>T
c.785-658C>T (p.=)
n.410-658C>T (p.=)
n.413-658C>T (p.=)
c.647-658C>T (p.=)
c.5-27739C>T (p.=)
c.-43-17169C>T (p.=)
c.-99+33581C>T (p.=)
ClinVar dbSNP COSMIC
17g.43091690G>CCA10594284BRCA1c.3841C>G (p.Gln1281Glu)
c.3700C>G (p.Gln1234Glu)
c.788-658C>G (p.=)
n.3977C>G
n.4018C>G
c.671-658C>G (p.=)
c.*3624C>G (p.=)
n.135C>G
c.785-658C>G (p.=)
n.410-658C>G (p.=)
n.413-658C>G (p.=)
c.647-658C>G (p.=)
c.5-27739C>G (p.=)
c.-43-17169C>G (p.=)
c.-99+33581C>G (p.=)
ClinVar
17g.43091690G>TCA10594285BRCA1c.3841C>A (p.Gln1281Lys)
c.3700C>A (p.Gln1234Lys)
c.788-658C>A (p.=)
n.3977C>A
n.4018C>A
c.671-658C>A (p.=)
c.*3624C>A (p.=)
n.135C>A
c.785-658C>A (p.=)
n.410-658C>A (p.=)
n.413-658C>A (p.=)
c.647-658C>A (p.=)
c.5-27739C>A (p.=)
c.-43-17169C>A (p.=)
c.-99+33581C>A (p.=)
17g.43091691A>CCA500232161BRCA1c.3840T>G (p.Ser1280=)
c.3699T>G (p.Ser1233=)
c.788-659T>G (p.=)
n.3976T>G
n.4017T>G
c.671-659T>G (p.=)
c.*3623T>G (p.=)
n.134T>G
c.785-659T>G (p.=)
n.410-659T>G (p.=)
n.413-659T>G (p.=)
c.647-659T>G (p.=)
c.5-27740T>G (p.=)
c.-43-17170T>G (p.=)
c.-99+33580T>G (p.=)
17g.43091691A>GCA500232162BRCA1c.3840T>C (p.Ser1280=)
c.3699T>C (p.Ser1233=)
c.788-659T>C (p.=)
n.3976T>C
n.4017T>C
c.671-659T>C (p.=)
c.*3623T>C (p.=)
n.134T>C
c.785-659T>C (p.=)
n.410-659T>C (p.=)
n.413-659T>C (p.=)
c.647-659T>C (p.=)
c.5-27740T>C (p.=)
c.-43-17170T>C (p.=)
c.-99+33580T>C (p.=)
17g.43091691A>TCA500232163BRCA1c.3840T>A (p.Ser1280=)
c.3699T>A (p.Ser1233=)
c.788-659T>A (p.=)
n.3976T>A
n.4017T>A
c.671-659T>A (p.=)
c.*3623T>A (p.=)
n.134T>A
c.785-659T>A (p.=)
n.410-659T>A (p.=)
n.413-659T>A (p.=)
c.647-659T>A (p.=)
c.5-27740T>A (p.=)
c.-43-17170T>A (p.=)
c.-99+33580T>A (p.=)
17g.43091691_43091694delCA10589721BRCA1c.3837_3840del (p.Ser1280ArgfsTer26)
c.3696_3699del (p.Ser1233ArgfsTer26)
c.788-662_788-659del (p.=)
n.3973_3976del
n.4014_4017del
c.671-662_671-659del (p.=)
c.*3620_*3623del (p.=)
n.131_134del
c.785-662_785-659del (p.=)
n.410-662_410-659del (p.=)
n.413-662_413-659del (p.=)
c.647-662_647-659del (p.=)
c.5-27743_5-27740del (p.=)
c.-43-17173_-43-17170del (p.=)
c.-99+33577_-99+33580del (p.=)
ClinVar dbSNP
17g.43091692G>ACA10594286BRCA1c.3839C>T (p.Ser1280Phe)
c.3698C>T (p.Ser1233Phe)
c.788-660C>T (p.=)
n.3975C>T
n.4016C>T
c.671-660C>T (p.=)
c.*3622C>T (p.=)
n.133C>T
c.785-660C>T (p.=)
n.410-660C>T (p.=)
n.413-660C>T (p.=)
c.647-660C>T (p.=)
c.5-27741C>T (p.=)
c.-43-17171C>T (p.=)
c.-99+33579C>T (p.=)
17g.43091692G>CCA10594287BRCA1c.3839C>G (p.Ser1280Cys)
c.3698C>G (p.Ser1233Cys)
c.788-660C>G (p.=)
n.3975C>G
n.4016C>G
c.671-660C>G (p.=)
c.*3622C>G (p.=)
n.133C>G
c.785-660C>G (p.=)
n.410-660C>G (p.=)
n.413-660C>G (p.=)
c.647-660C>G (p.=)
c.5-27741C>G (p.=)
c.-43-17171C>G (p.=)
c.-99+33579C>G (p.=)
17g.43091692G>TCA10594288BRCA1c.3839C>A (p.Ser1280Tyr)
c.3698C>A (p.Ser1233Tyr)
c.788-660C>A (p.=)
n.3975C>A
n.4016C>A
c.671-660C>A (p.=)
c.*3622C>A (p.=)
n.133C>A
c.785-660C>A (p.=)
n.410-660C>A (p.=)
n.413-660C>A (p.=)
c.647-660C>A (p.=)
c.5-27741C>A (p.=)
c.-43-17171C>A (p.=)
c.-99+33579C>A (p.=)
ClinVar
17g.43091693A>CCA10594289BRCA1c.3838T>G (p.Ser1280Ala)
c.3697T>G (p.Ser1233Ala)
c.788-661T>G (p.=)
n.3974T>G
n.4015T>G
c.671-661T>G (p.=)
c.*3621T>G (p.=)
n.132T>G
c.785-661T>G (p.=)
n.410-661T>G (p.=)
n.413-661T>G (p.=)
c.647-661T>G (p.=)
c.5-27742T>G (p.=)
c.-43-17172T>G (p.=)
c.-99+33578T>G (p.=)
17g.43091693A>GCA10594290BRCA1c.3838T>C (p.Ser1280Pro)
c.3697T>C (p.Ser1233Pro)
c.788-661T>C (p.=)
n.3974T>C
n.4015T>C
c.671-661T>C (p.=)
c.*3621T>C (p.=)
n.132T>C
c.785-661T>C (p.=)
n.410-661T>C (p.=)
n.413-661T>C (p.=)
c.647-661T>C (p.=)
c.5-27742T>C (p.=)
c.-43-17172T>C (p.=)
c.-99+33578T>C (p.=)
ClinVar
17g.43091693A>TCA10594291BRCA1c.3838T>A (p.Ser1280Thr)
c.3697T>A (p.Ser1233Thr)
c.788-661T>A (p.=)
n.3974T>A
n.4015T>A
c.671-661T>A (p.=)
c.*3621T>A (p.=)
n.132T>A
c.785-661T>A (p.=)
n.410-661T>A (p.=)
n.413-661T>A (p.=)
c.647-661T>A (p.=)
c.5-27742T>A (p.=)
c.-43-17172T>A (p.=)
c.-99+33578T>A (p.=)
17g.43091694T>ACA500232164BRCA1c.3837A>T (p.Ala1279=)
c.3696A>T (p.Ala1232=)
c.788-662A>T (p.=)
n.3973A>T
n.4014A>T
c.671-662A>T (p.=)
c.*3620A>T (p.=)
n.131A>T
c.785-662A>T (p.=)
n.410-662A>T (p.=)
n.413-662A>T (p.=)
c.647-662A>T (p.=)
c.5-27743A>T (p.=)
c.-43-17173A>T (p.=)
c.-99+33577A>T (p.=)
17g.43091694T>CCA500232165BRCA1c.3837A>G (p.Ala1279=)
c.3696A>G (p.Ala1232=)
c.788-662A>G (p.=)
n.3973A>G
n.4014A>G
c.671-662A>G (p.=)
c.*3620A>G (p.=)
n.131A>G
c.785-662A>G (p.=)
n.410-662A>G (p.=)
n.413-662A>G (p.=)
c.647-662A>G (p.=)
c.5-27743A>G (p.=)
c.-43-17173A>G (p.=)
c.-99+33577A>G (p.=)
17g.43091694T>GCA500232166BRCA1c.3837A>C (p.Ala1279=)
c.3696A>C (p.Ala1232=)
c.788-662A>C (p.=)
n.3973A>C
n.4014A>C
c.671-662A>C (p.=)
c.*3620A>C (p.=)
n.131A>C
c.785-662A>C (p.=)
n.410-662A>C (p.=)
n.413-662A>C (p.=)
c.647-662A>C (p.=)
c.5-27743A>C (p.=)
c.-43-17173A>C (p.=)
c.-99+33577A>C (p.=)
17g.43091695G>ACA10594292BRCA1c.3836C>T (p.Ala1279Val)
c.3695C>T (p.Ala1232Val)
c.788-663C>T (p.=)
n.3972C>T
n.4013C>T
c.671-663C>T (p.=)
c.*3619C>T (p.=)
n.130C>T
c.785-663C>T (p.=)
n.410-663C>T (p.=)
n.413-663C>T (p.=)
c.647-663C>T (p.=)
c.5-27744C>T (p.=)
c.-43-17174C>T (p.=)
c.-99+33576C>T (p.=)
ClinVar
17g.43091695G>CCA10594293BRCA1c.3836C>G (p.Ala1279Gly)
c.3695C>G (p.Ala1232Gly)
c.788-663C>G (p.=)
n.3972C>G
n.4013C>G
c.671-663C>G (p.=)
c.*3619C>G (p.=)
n.130C>G
c.785-663C>G (p.=)
n.410-663C>G (p.=)
n.413-663C>G (p.=)
c.647-663C>G (p.=)
c.5-27744C>G (p.=)
c.-43-17174C>G (p.=)
c.-99+33576C>G (p.=)
17g.43091695G>TCA10594294BRCA1c.3836C>A (p.Ala1279Glu)
c.3695C>A (p.Ala1232Glu)
c.788-663C>A (p.=)
n.3972C>A
n.4013C>A
c.671-663C>A (p.=)
c.*3619C>A (p.=)
n.130C>A
c.785-663C>A (p.=)
n.410-663C>A (p.=)
n.413-663C>A (p.=)
c.647-663C>A (p.=)
c.5-27744C>A (p.=)
c.-43-17174C>A (p.=)
c.-99+33576C>A (p.=)
17g.43091696C>ACA10594295BRCA1c.3835G>T (p.Ala1279Ser)
c.3694G>T (p.Ala1232Ser)
c.788-664G>T (p.=)
n.3971G>T
n.4012G>T
c.671-664G>T (p.=)
c.*3618G>T (p.=)
n.129G>T
c.785-664G>T (p.=)
n.410-664G>T (p.=)
n.413-664G>T (p.=)
c.647-664G>T (p.=)
c.5-27745G>T (p.=)
c.-43-17175G>T (p.=)
c.-99+33575G>T (p.=)
ClinVar dbSNP
17g.43091696C>GCA10594296BRCA1c.3835G>C (p.Ala1279Pro)
c.3694G>C (p.Ala1232Pro)
c.788-664G>C (p.=)
n.3971G>C
n.4012G>C
c.671-664G>C (p.=)
c.*3618G>C (p.=)
n.129G>C
c.785-664G>C (p.=)
n.410-664G>C (p.=)
n.413-664G>C (p.=)
c.647-664G>C (p.=)
c.5-27745G>C (p.=)
c.-43-17175G>C (p.=)
c.-99+33575G>C (p.=)
ClinVar
17g.43091696C>TCA002469BRCA1c.3835G>A (p.Ala1279Thr)
c.3694G>A (p.Ala1232Thr)
c.788-664G>A (p.=)
n.3971G>A
n.4012G>A
c.671-664G>A (p.=)
c.*3618G>A (p.=)
n.129G>A
c.785-664G>A (p.=)
n.410-664G>A (p.=)
n.413-664G>A (p.=)
c.647-664G>A (p.=)
c.5-27745G>A (p.=)
c.-43-17175G>A (p.=)
c.-99+33575G>A (p.=)
ClinVar dbSNP ExAC gnomAD

Number of alleles fetched