Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.32357847_32357906dupCA2580614662BRCA2c.7723_7782dup (p.Lys2594_Ala2595insThrGlyLysGlyIleGlnLeuAlaAspGlyGlyTrpLeuIleProSerAsnAspGlyLys)
c.7354_7413dup (p.Lys2471_Ala2472insThrGlyLysGlyIleGlnLeuAlaAspGlyGlyTrpLeuIleProSerAsnAspGlyLys)
c.190_249dup (p.Lys83_Ala84insThrGlyLysGlyIleGlnLeuAlaAspGlyGlyTrpLeuIleProSerAsnAspGlyLys)
c.288_347dup
n.7723_7782dup
c.7627_7686dup (p.Lys2562_Ala2563insThrGlyLysGlyIleGlnLeuAlaAspGlyGlyTrpLeuIleProSerAsnAspGlyLys)
ClinVar
13g.32357885_32357888delinsCATACA2082818783BRCA2c.7761_7764delinsCATA (p.Leu2587=)
c.7392_7395delinsCATA (p.Leu2464=)
c.228_231delinsCATA (p.Leu76=)
c.326_329delinsCATA
n.7761_7764delinsCATA
c.7665_7668delinsCATA (p.Leu2555=)
13g.32357886_32357890dupCA10589449BRCA2c.7762_7766dup (p.Ser2590TyrfsTer?)
c.7393_7397dup (p.Ser2467TyrfsTer?)
c.229_233dup (p.Ser79TyrfsTer?)
c.7762_7766dup (p.Ser2590TyrfsTer21)
c.327_331dup
n.7762_7766dup
c.7666_7670dup (p.Ser2558TyrfsTer?)
ClinVar dbSNP
13g.32357886_32357888delinsCCCA2580087360BRCA2c.7762_7764delinsCC (p.Ile2588ProfsTer?)
c.7393_7395delinsCC (p.Ile2465ProfsTer?)
c.229_231delinsCC (p.Ile77ProfsTer?)
c.7762_7764delinsCC (p.Ile2588ProfsTer21)
c.327_329delinsCC
n.7762_7764delinsCC
c.7666_7668delinsCC (p.Ile2556ProfsTer?)
ClinVar
13g.32357886_32357888delinsTTCA090898BRCA2c.7762_7764delinsTT (p.Ile2588PhefsTer?)
c.7393_7395delinsTT (p.Ile2465PhefsTer?)
c.229_231delinsTT (p.Ile77PhefsTer?)
c.7762_7764delinsTT (p.Ile2588PhefsTer21)
c.327_329delinsTT
n.7762_7764delinsTT
c.7666_7668delinsTT (p.Ile2556PhefsTer?)
ClinVar dbSNP
13g.32357888delCA2695217929BRCA2c.7764del (p.Ser2590ProfsTer?)
c.7395del (p.Ser2467ProfsTer?)
c.231del (p.Ser79ProfsTer?)
c.7764del (p.Ser2590ProfsTer19)
c.329del
n.7764del
c.7668del (p.Ser2558ProfsTer?)
13g.32357888A=CA2082818835BRCA2c.7764A= (p.Ile2588=)
c.7395A= (p.Ile2465=)
c.231A= (p.Ile77=)
c.329A=
n.7764A=
c.7668A= (p.Ile2556=)
13g.32357888A>CCA483439260BRCA2c.7764A>C (p.Ile2588=)
c.7395A>C (p.Ile2465=)
c.231A>C (p.Ile77=)
c.329A>C
n.7764A>C
c.7668A>C (p.Ile2556=)
13g.32357888A>GCA387745876BRCA2c.7764A>G (p.Ile2588Met)
c.7395A>G (p.Ile2465Met)
c.231A>G (p.Ile77Met)
c.329A>G
n.7764A>G
c.7668A>G (p.Ile2556Met)
13g.32357888A>TCA025266BRCA2c.7764A>T (p.Ile2588=)
c.7395A>T (p.Ile2465=)
c.231A>T (p.Ile77=)
c.329A>T
n.7764A>T
c.7668A>T (p.Ile2556=)
ClinVar dbSNP gnomAD v4
13g.32357889C>ACA6941137BRCA2c.7765C>A (p.Pro2589Thr)
c.7396C>A (p.Pro2466Thr)
c.232C>A (p.Pro78Thr)
c.330C>A
n.7765C>A
c.7669C>A (p.Pro2557Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32357889C=CA2082818848BRCA2c.7765C= (p.Pro2589=)
c.7396C= (p.Pro2466=)
c.232C= (p.Pro78=)
c.330C=
n.7765C=
c.7669C= (p.Pro2557=)
13g.32357889C>GCA387745884BRCA2c.7765C>G (p.Pro2589Ala)
c.7396C>G (p.Pro2466Ala)
c.232C>G (p.Pro78Ala)
c.330C>G
n.7765C>G
c.7669C>G (p.Pro2557Ala)
dbSNP
13g.32357889C>TCA387745881BRCA2c.7765C>T (p.Pro2589Ser)
c.7396C>T (p.Pro2466Ser)
c.232C>T (p.Pro78Ser)
c.330C>T
n.7765C>T
c.7669C>T (p.Pro2557Ser)
ClinVar dbSNP
13g.32357891delCA2499222306BRCA2c.7767del (p.Ser2590ProfsTer?)
c.7398del (p.Ser2467ProfsTer?)
c.234del (p.Ser79ProfsTer?)
c.7767del (p.Ser2590ProfsTer19)
c.332del
n.7767del
c.7671del (p.Ser2558ProfsTer?)
ClinVar dbSNP
13g.32357890C>ACA025267BRCA2c.7766C>A (p.Pro2589His)
c.7397C>A (p.Pro2466His)
c.233C>A (p.Pro78His)
c.331C>A
n.7766C>A
c.7670C>A (p.Pro2557His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32357890C=CA2082818874BRCA2c.7766C= (p.Pro2589=)
c.7397C= (p.Pro2466=)
c.233C= (p.Pro78=)
c.331C=
n.7766C=
c.7670C= (p.Pro2557=)
13g.32357890C>GCA387745888BRCA2c.7766C>G (p.Pro2589Arg)
c.7397C>G (p.Pro2466Arg)
c.233C>G (p.Pro78Arg)
c.331C>G
n.7766C>G
c.7670C>G (p.Pro2557Arg)
dbSNP
13g.32357890C>TCA10579752BRCA2c.7766C>T (p.Pro2589Leu)
c.7397C>T (p.Pro2466Leu)
c.233C>T (p.Pro78Leu)
c.331C>T
n.7766C>T
c.7670C>T (p.Pro2557Leu)
ClinVar dbSNP
13g.32357891C>ACA483439266BRCA2c.7767C>A (p.Pro2589=)
c.7398C>A (p.Pro2466=)
c.234C>A (p.Pro78=)
c.332C>A
n.7767C>A
c.7671C>A (p.Pro2557=)
dbSNP
13g.32357891C=CA2082818885BRCA2c.7767C= (p.Pro2589=)
c.7398C= (p.Pro2466=)
c.234C= (p.Pro78=)
c.332C=
n.7767C=
c.7671C= (p.Pro2557=)
13g.32357891C>GCA483439267BRCA2c.7767C>G (p.Pro2589=)
c.7398C>G (p.Pro2466=)
c.234C>G (p.Pro78=)
c.332C>G
n.7767C>G
c.7671C>G (p.Pro2557=)
ClinVar dbSNP gnomAD v4
13g.32357891C>TCA483439268BRCA2c.7767C>T (p.Pro2589=)
c.7398C>T (p.Pro2466=)
c.234C>T (p.Pro78=)
c.332C>T
n.7767C>T
c.7671C>T (p.Pro2557=)
ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32357892_32357893dupCA2499222307BRCA2c.7768_7769dup (p.Asn2591ProfsTer?)
c.7399_7400dup (p.Asn2468ProfsTer?)
c.235_236dup (p.Asn80ProfsTer?)
c.7768_7769dup (p.Asn2591ProfsTer19)
c.333_334dup
n.7768_7769dup
c.7672_7673dup (p.Asn2559ProfsTer?)
ClinVar dbSNP
13g.32357892T>ACA025268BRCA2c.7768T>A (p.Ser2590Thr)
c.7399T>A (p.Ser2467Thr)
c.235T>A (p.Ser79Thr)
c.333T>A
n.7768T>A
c.7672T>A (p.Ser2558Thr)
ClinVar dbSNP
13g.32357892T>CCA10579753BRCA2c.7768T>C (p.Ser2590Pro)
c.7399T>C (p.Ser2467Pro)
c.235T>C (p.Ser79Pro)
c.333T>C
n.7768T>C
c.7672T>C (p.Ser2558Pro)
ClinVar dbSNP gnomAD v4
13g.32357892T>GCA387745893BRCA2c.7768T>G (p.Ser2590Ala)
c.7399T>G (p.Ser2467Ala)
c.235T>G (p.Ser79Ala)
c.333T>G
n.7768T>G
c.7672T>G (p.Ser2558Ala)
13g.32357892T=CA2082818892BRCA2c.7768T= (p.Ser2590=)
c.7399T= (p.Ser2467=)
c.235T= (p.Ser79=)
c.333T=
n.7768T=
c.7672T= (p.Ser2558=)
13g.32357893C>ACA387745895BRCA2c.7769C>A (p.Ser2590Tyr)
c.7400C>A (p.Ser2467Tyr)
c.236C>A (p.Ser79Tyr)
c.334C>A
n.7769C>A
c.7673C>A (p.Ser2558Tyr)
13g.32357893C=CA2082818900BRCA2c.7769C= (p.Ser2590=)
c.7400C= (p.Ser2467=)
c.236C= (p.Ser79=)
c.334C=
n.7769C=
c.7673C= (p.Ser2558=)
13g.32357893C>GCA025269BRCA2c.7769C>G (p.Ser2590Cys)
c.7400C>G (p.Ser2467Cys)
c.236C>G (p.Ser79Cys)
c.334C>G
n.7769C>G
c.7673C>G (p.Ser2558Cys)
ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32357893C>TCA387745900BRCA2c.7769C>T (p.Ser2590Phe)
c.7400C>T (p.Ser2467Phe)
c.236C>T (p.Ser79Phe)
c.334C>T
n.7769C>T
c.7673C>T (p.Ser2558Phe)
ClinVar
13g.32357894C>ACA483439272BRCA2c.7770C>A (p.Ser2590=)
c.7401C>A (p.Ser2467=)
c.237C>A (p.Ser79=)
c.335C>A
n.7770C>A
c.7674C>A (p.Ser2558=)
dbSNP
13g.32357894C>GCA483439274BRCA2c.7770C>G (p.Ser2590=)
c.7401C>G (p.Ser2467=)
c.237C>G (p.Ser79=)
c.335C>G
n.7770C>G
c.7674C>G (p.Ser2558=)
dbSNP
13g.32357894C>TCA483439275BRCA2c.7770C>T (p.Ser2590=)
c.7401C>T (p.Ser2467=)
c.237C>T (p.Ser79=)
c.335C>T
n.7770C>T
c.7674C>T (p.Ser2558=)
dbSNP
13g.32357895A=CA2082818905BRCA2c.7771A= (p.Asn2591=)
c.7402A= (p.Asn2468=)
c.238A= (p.Asn80=)
c.336A=
n.7771A=
c.7675A= (p.Asn2559=)
13g.32357895A>CCA6941138BRCA2c.7771A>C (p.Asn2591His)
c.7402A>C (p.Asn2468His)
c.238A>C (p.Asn80His)
c.336A>C
n.7771A>C
c.7675A>C (p.Asn2559His)
dbSNP ExAC gnomAD v2 gnomAD v4
13g.32357895A>GCA16619770BRCA2c.7771A>G (p.Asn2591Asp)
c.7402A>G (p.Asn2468Asp)
c.238A>G (p.Asn80Asp)
c.336A>G
n.7771A>G
c.7675A>G (p.Asn2559Asp)
ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32357895A>TCA387745907BRCA2c.7771A>T (p.Asn2591Tyr)
c.7402A>T (p.Asn2468Tyr)
c.238A>T (p.Asn80Tyr)
c.336A>T
n.7771A>T
c.7675A>T (p.Asn2559Tyr)
13g.32357896A=CA2082818912BRCA2c.7772A= (p.Asn2591=)
c.7403A= (p.Asn2468=)
c.239A= (p.Asn80=)
c.337A=
n.7772A=
c.7676A= (p.Asn2559=)
13g.32357896A>CCA387745922BRCA2c.7772A>C (p.Asn2591Thr)
c.7403A>C (p.Asn2468Thr)
c.239A>C (p.Asn80Thr)
c.337A>C
n.7772A>C
c.7676A>C (p.Asn2559Thr)
13g.32357896A>GCA025270BRCA2c.7772A>G (p.Asn2591Ser)
c.7403A>G (p.Asn2468Ser)
c.239A>G (p.Asn80Ser)
c.337A>G
n.7772A>G
c.7676A>G (p.Asn2559Ser)
ClinVar dbSNP gnomAD v4
13g.32357896A>TCA387745916BRCA2c.7772A>T (p.Asn2591Ile)
c.7403A>T (p.Asn2468Ile)
c.239A>T (p.Asn80Ile)
c.337A>T
n.7772A>T
c.7676A>T (p.Asn2559Ile)
dbSNP
13g.32357897T>ACA387745927BRCA2c.7773T>A (p.Asn2591Lys)
c.7404T>A (p.Asn2468Lys)
c.240T>A (p.Asn80Lys)
c.338T>A
n.7773T>A
c.7677T>A (p.Asn2559Lys)
dbSNP
13g.32357897T>CCA483439276BRCA2c.7773T>C (p.Asn2591=)
c.7404T>C (p.Asn2468=)
c.240T>C (p.Asn80=)
c.338T>C
n.7773T>C
c.7677T>C (p.Asn2559=)
ClinVar dbSNP gnomAD v4
13g.32357897T>GCA387745930BRCA2c.7773T>G (p.Asn2591Lys)
c.7404T>G (p.Asn2468Lys)
c.240T>G (p.Asn80Lys)
c.338T>G
n.7773T>G
c.7677T>G (p.Asn2559Lys)
13g.32357897T=CA2082818921BRCA2c.7773T= (p.Asn2591=)
c.7404T= (p.Asn2468=)
c.240T= (p.Asn80=)
c.338T=
n.7773T=
c.7677T= (p.Asn2559=)
13g.32357898G>ACA387745936BRCA2c.7774G>A (p.Asp2592Asn)
c.7405G>A (p.Asp2469Asn)
c.241G>A (p.Asp81Asn)
c.339G>A
n.7774G>A
c.7678G>A (p.Asp2560Asn)
ClinVar dbSNP
13g.32357898G>CCA387745939BRCA2c.7774G>C (p.Asp2592His)
c.7405G>C (p.Asp2469His)
c.241G>C (p.Asp81His)
c.339G>C
n.7774G>C
c.7678G>C (p.Asp2560His)
dbSNP
13g.32357898G>TCA387745942BRCA2c.7774G>T (p.Asp2592Tyr)
c.7405G>T (p.Asp2469Tyr)
c.241G>T (p.Asp81Tyr)
c.339G>T
n.7774G>T
c.7678G>T (p.Asp2560Tyr)
dbSNP

Number of alleles fetched