Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.32357847_32357906dup | CA2580614662 | BRCA2 | c.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 |
13 | g.32357886_32357890dup | CA10589449 | BRCA2 | c.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 |
13 | g.32357891del | CA2499222306 | BRCA2 | c.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 |
13 | g.32357890C>A | CA025267 | BRCA2 | c.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 |
13 | g.32357890C= | CA2082818874 | BRCA2 | c.7766C= (p.Pro2589=) c.7397C= (p.Pro2466=) c.233C= (p.Pro78=) c.331C= n.7766C= c.7670C= (p.Pro2557=) | |
13 | g.32357890C>G | CA387745888 | BRCA2 | c.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 |
13 | g.32357890C>T | CA10579752 | BRCA2 | c.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 |
13 | g.32357891C>A | CA483439266 | BRCA2 | c.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 |
13 | g.32357891C= | CA2082818885 | BRCA2 | c.7767C= (p.Pro2589=) c.7398C= (p.Pro2466=) c.234C= (p.Pro78=) c.332C= n.7767C= c.7671C= (p.Pro2557=) | |
13 | g.32357891C>G | CA483439267 | BRCA2 | c.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 |
13 | g.32357891C>T | CA483439268 | BRCA2 | c.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 |
13 | g.32357892_32357893dup | CA2499222307 | BRCA2 | c.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 |
13 | g.32357892T>A | CA025268 | BRCA2 | c.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 |
13 | g.32357892T>C | CA10579753 | BRCA2 | c.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 |
13 | g.32357892T>G | CA387745893 | BRCA2 | c.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) | |
13 | g.32357892T= | CA2082818892 | BRCA2 | c.7768T= (p.Ser2590=) c.7399T= (p.Ser2467=) c.235T= (p.Ser79=) c.333T= n.7768T= c.7672T= (p.Ser2558=) | |
13 | g.32357893C>A | CA387745895 | BRCA2 | c.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) | |
13 | g.32357893C= | CA2082818900 | BRCA2 | c.7769C= (p.Ser2590=) c.7400C= (p.Ser2467=) c.236C= (p.Ser79=) c.334C= n.7769C= c.7673C= (p.Ser2558=) | |
13 | g.32357893C>G | CA025269 | BRCA2 | c.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 |
13 | g.32357893C>T | CA387745900 | BRCA2 | c.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 |
13 | g.32357894C>A | CA483439272 | BRCA2 | c.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 |
13 | g.32357894C>G | CA483439274 | BRCA2 | c.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 |
13 | g.32357894C>T | CA483439275 | BRCA2 | c.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 |
13 | g.32357895A= | CA2082818905 | BRCA2 | c.7771A= (p.Asn2591=) c.7402A= (p.Asn2468=) c.238A= (p.Asn80=) c.336A= n.7771A= c.7675A= (p.Asn2559=) | |
13 | g.32357895A>C | CA6941138 | BRCA2 | c.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 |
13 | g.32357895A>G | CA16619770 | BRCA2 | c.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 |
13 | g.32357895A>T | CA387745907 | BRCA2 | c.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) | |
13 | g.32357896A= | CA2082818912 | BRCA2 | c.7772A= (p.Asn2591=) c.7403A= (p.Asn2468=) c.239A= (p.Asn80=) c.337A= n.7772A= c.7676A= (p.Asn2559=) | |
13 | g.32357896A>C | CA387745922 | BRCA2 | c.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) | |
13 | g.32357896A>G | CA025270 | BRCA2 | c.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 |
13 | g.32357896A>T | CA387745916 | BRCA2 | c.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 |
13 | g.32357897T>A | CA387745927 | BRCA2 | c.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 |
13 | g.32357897T>C | CA483439276 | BRCA2 | c.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 |
13 | g.32357897T>G | CA387745930 | BRCA2 | c.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) | |
13 | g.32357897T= | CA2082818921 | BRCA2 | c.7773T= (p.Asn2591=) c.7404T= (p.Asn2468=) c.240T= (p.Asn80=) c.338T= n.7773T= c.7677T= (p.Asn2559=) | |
13 | g.32357898G>A | CA387745936 | BRCA2 | c.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 |
13 | g.32357898G>C | CA387745939 | BRCA2 | c.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 |
13 | g.32357898G>T | CA387745942 | BRCA2 | c.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 |
13 | g.32357899A= | CA2082818931 | BRCA2 | c.7775A= (p.Asp2592=) c.7406A= (p.Asp2469=) c.242A= (p.Asp81=) c.340A= n.7775A= c.7679A= (p.Asp2560=) | |
13 | g.32357899A>C | CA387745944 | BRCA2 | c.7775A>C (p.Asp2592Ala) c.7406A>C (p.Asp2469Ala) c.242A>C (p.Asp81Ala) c.340A>C n.7775A>C c.7679A>C (p.Asp2560Ala) | |
13 | g.32357899A>G | CA387745947 | BRCA2 | c.7775A>G (p.Asp2592Gly) c.7406A>G (p.Asp2469Gly) c.242A>G (p.Asp81Gly) c.340A>G n.7775A>G c.7679A>G (p.Asp2560Gly) | ClinVar dbSNP gnomAD v4 |
13 | g.32357899A>T | CA387745950 | BRCA2 | c.7775A>T (p.Asp2592Val) c.7406A>T (p.Asp2469Val) c.242A>T (p.Asp81Val) c.340A>T n.7775A>T c.7679A>T (p.Asp2560Val) | |
13 | g.32357900T>A | CA387745954 | BRCA2 | c.7776T>A (p.Asp2592Glu) c.7407T>A (p.Asp2469Glu) c.243T>A (p.Asp81Glu) c.341T>A n.7776T>A c.7680T>A (p.Asp2560Glu) | dbSNP |
13 | g.32357900T>C | CA483439282 | BRCA2 | c.7776T>C (p.Asp2592=) c.7407T>C (p.Asp2469=) c.243T>C (p.Asp81=) c.341T>C n.7776T>C c.7680T>C (p.Asp2560=) | ClinVar dbSNP |
13 | g.32357900T>G | CA387745958 | BRCA2 | c.7776T>G (p.Asp2592Glu) c.7407T>G (p.Asp2469Glu) c.243T>G (p.Asp81Glu) c.341T>G n.7776T>G c.7680T>G (p.Asp2560Glu) | |
13 | g.32357901G>A | CA387745960 | BRCA2 | c.7777G>A (p.Gly2593Arg) c.7408G>A (p.Gly2470Arg) c.244G>A (p.Gly82Arg) c.342G>A n.7777G>A c.7681G>A (p.Gly2561Arg) | ClinVar gnomAD v4 |
13 | g.32357901G>C | CA387745961 | BRCA2 | c.7777G>C (p.Gly2593Arg) c.7408G>C (p.Gly2470Arg) c.244G>C (p.Gly82Arg) c.342G>C n.7777G>C c.7681G>C (p.Gly2561Arg) | |
13 | g.32357901G= | CA2082818940 | BRCA2 | c.7777G= (p.Gly2593=) c.7408G= (p.Gly2470=) c.244G= (p.Gly82=) c.342G= n.7777G= c.7681G= (p.Gly2561=) | |
13 | g.32357901G>T | CA025271 | BRCA2 | c.7777G>T (p.Gly2593Ter) c.7408G>T (p.Gly2470Ter) c.244G>T (p.Gly82Ter) c.342G>T n.7777G>T c.7681G>T (p.Gly2561Ter) | ClinVar dbSNP COSMIC COSMIC |
13 | g.32357902G>A | CA387745964 | BRCA2 | c.7778G>A (p.Gly2593Glu) c.7409G>A (p.Gly2470Glu) c.245G>A (p.Gly82Glu) c.343G>A n.7778G>A c.7682G>A (p.Gly2561Glu) | ClinVar dbSNP |
13 | g.32357902G>C | CA387745966 | BRCA2 | c.7778G>C (p.Gly2593Ala) c.7409G>C (p.Gly2470Ala) c.245G>C (p.Gly82Ala) c.343G>C n.7778G>C c.7682G>C (p.Gly2561Ala) | dbSNP |
13 | g.32357902G= | CA2082818945 | BRCA2 | c.7778G= (p.Gly2593=) c.7409G= (p.Gly2470=) c.245G= (p.Gly82=) c.343G= n.7778G= c.7682G= (p.Gly2561=) | |
13 | g.32357902G>T | CA387745963 | BRCA2 | c.7778G>T (p.Gly2593Val) c.7409G>T (p.Gly2470Val) c.245G>T (p.Gly82Val) c.343G>T n.7778G>T c.7682G>T (p.Gly2561Val) | |
13 | g.32357903A= | CA2082818953 | BRCA2 | c.7779A= (p.Gly2593=) c.7410A= (p.Gly2470=) c.246A= (p.Gly82=) c.344A= n.7779A= c.7683A= (p.Gly2561=) | |
13 | g.32357903A>C | CA483439283 | BRCA2 | c.7779A>C (p.Gly2593=) c.7410A>C (p.Gly2470=) c.246A>C (p.Gly82=) c.344A>C n.7779A>C c.7683A>C (p.Gly2561=) | |
13 | g.32357903A>G | CA483439284 | BRCA2 | c.7779A>G (p.Gly2593=) c.7410A>G (p.Gly2470=) c.246A>G (p.Gly82=) c.344A>G n.7779A>G c.7683A>G (p.Gly2561=) | dbSNP |
13 | g.32357903A>T | CA483439285 | BRCA2 | c.7779A>T (p.Gly2593=) c.7410A>T (p.Gly2470=) c.246A>T (p.Gly82=) c.344A>T n.7779A>T c.7683A>T (p.Gly2561=) | ClinVar dbSNP |
13 | g.32357905dup | CA10589450 | BRCA2 | c.7781dup (p.Ala2595GlyfsTer8) c.7412dup (p.Ala2472GlyfsTer8) c.248dup (p.Ala84GlyfsTer8) c.346dup n.7781dup c.7685dup (p.Ala2563GlyfsTer8) | ClinVar dbSNP |
13 | g.32357905del | CA2573149412 | BRCA2 | c.7781del (p.Lys2594ArgfsTer?) c.7412del (p.Lys2471ArgfsTer?) c.248del (p.Lys83ArgfsTer?) c.7781del (p.Lys2594ArgfsTer15) c.346del n.7781del c.7685del (p.Lys2562ArgfsTer?) | ClinVar dbSNP |
13 | g.32357904A>C | CA387745970 | BRCA2 | c.7780A>C (p.Lys2594Gln) c.7411A>C (p.Lys2471Gln) c.247A>C (p.Lys83Gln) c.345A>C n.7780A>C c.7684A>C (p.Lys2562Gln) | |
13 | g.32357904A>G | CA387745967 | BRCA2 | c.7780A>G (p.Lys2594Glu) c.7411A>G (p.Lys2471Glu) c.247A>G (p.Lys83Glu) c.345A>G n.7780A>G c.7684A>G (p.Lys2562Glu) | |
13 | g.32357904A>T | CA387745972 | BRCA2 | c.7780A>T (p.Lys2594Ter) c.7411A>T (p.Lys2471Ter) c.247A>T (p.Lys83Ter) c.345A>T n.7780A>T c.7684A>T (p.Lys2562Ter) | dbSNP |
13 | g.32357905A= | CA2082818957 | BRCA2 | c.7781A= (p.Lys2594=) c.7412A= (p.Lys2471=) c.248A= (p.Lys83=) c.346A= n.7781A= c.7685A= (p.Lys2562=) | |
13 | g.32357905A>C | CA387745974 | BRCA2 | c.7781A>C (p.Lys2594Thr) c.7412A>C (p.Lys2471Thr) c.248A>C (p.Lys83Thr) c.346A>C n.7781A>C c.7685A>C (p.Lys2562Thr) | |
13 | g.32357905A>G | CA10579754 | BRCA2 | c.7781A>G (p.Lys2594Arg) c.7412A>G (p.Lys2471Arg) c.248A>G (p.Lys83Arg) c.346A>G n.7781A>G c.7685A>G (p.Lys2562Arg) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
13 | g.32357905A>T | CA387745975 | BRCA2 | c.7781A>T (p.Lys2594Met) c.7412A>T (p.Lys2471Met) c.248A>T (p.Lys83Met) c.346A>T n.7781A>T c.7685A>T (p.Lys2562Met) | |
13 | g.32357906G>A | CA483439288 | BRCA2 | c.7782G>A (p.Lys2594=) c.7413G>A (p.Lys2471=) c.249G>A (p.Lys83=) c.347G>A n.7782G>A c.7686G>A (p.Lys2562=) | dbSNP |
13 | g.32357906G>C | CA387745983 | BRCA2 | c.7782G>C (p.Lys2594Asn) c.7413G>C (p.Lys2471Asn) c.249G>C (p.Lys83Asn) c.347G>C n.7782G>C c.7686G>C (p.Lys2562Asn) | dbSNP |
13 | g.32357906G>T | CA387745986 | BRCA2 | c.7782G>T (p.Lys2594Asn) c.7413G>T (p.Lys2471Asn) c.249G>T (p.Lys83Asn) c.347G>T n.7782G>T c.7686G>T (p.Lys2562Asn) | gnomAD v4 |
13 | g.32357907del | CA2695202250 | BRCA2 | c.7783del (p.Ala2595LeufsTer?) c.7414del (p.Ala2472LeufsTer?) c.250del (p.Ala84LeufsTer?) c.7783del (p.Ala2595LeufsTer14) c.348del n.7783del c.7687del (p.Ala2563LeufsTer?) | |
13 | g.32357907G>A | CA10579755 | BRCA2 | c.7783G>A (p.Ala2595Thr) c.7414G>A (p.Ala2472Thr) c.250G>A (p.Ala84Thr) c.348G>A n.7783G>A c.7687G>A (p.Ala2563Thr) | ClinVar dbSNP |
13 | g.32357907G>C | CA387745989 | BRCA2 | c.7783G>C (p.Ala2595Pro) c.7414G>C (p.Ala2472Pro) c.250G>C (p.Ala84Pro) c.348G>C n.7783G>C c.7687G>C (p.Ala2563Pro) | gnomAD v4 |
13 | g.32357907G= | CA2082818971 | BRCA2 | c.7783G= (p.Ala2595=) c.7414G= (p.Ala2472=) c.250G= (p.Ala84=) c.348G= n.7783G= c.7687G= (p.Ala2563=) | |
13 | g.32357907G>T | CA025273 | BRCA2 | c.7783G>T (p.Ala2595Ser) c.7414G>T (p.Ala2472Ser) c.250G>T (p.Ala84Ser) c.348G>T n.7783G>T c.7687G>T (p.Ala2563Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
13 | g.32357908C>A | CA387745994 | BRCA2 | c.7784C>A (p.Ala2595Asp) c.7415C>A (p.Ala2472Asp) c.251C>A (p.Ala84Asp) c.349C>A n.7784C>A c.7688C>A (p.Ala2563Asp) | dbSNP |
13 | g.32357908C= | CA2082818984 | BRCA2 | c.7784C= (p.Ala2595=) c.7415C= (p.Ala2472=) c.251C= (p.Ala84=) c.349C= n.7784C= c.7688C= (p.Ala2563=) | |
13 | g.32357908C>G | CA387745996 | BRCA2 | c.7784C>G (p.Ala2595Gly) c.7415C>G (p.Ala2472Gly) c.251C>G (p.Ala84Gly) c.349C>G n.7784C>G c.7688C>G (p.Ala2563Gly) | ClinVar dbSNP COSMIC COSMIC |
13 | g.32357908C>T | CA387745999 | BRCA2 | c.7784C>T (p.Ala2595Val) c.7415C>T (p.Ala2472Val) c.251C>T (p.Ala84Val) c.349C>T n.7784C>T c.7688C>T (p.Ala2563Val) | dbSNP |
13 | g.32357909T>A | CA16613938 | BRCA2 | c.7785T>A (p.Ala2595=) c.7416T>A (p.Ala2472=) c.252T>A (p.Ala84=) c.350T>A n.7785T>A c.7689T>A (p.Ala2563=) | ClinVar dbSNP |
13 | g.32357909T>C | CA483439294 | BRCA2 | c.7785T>C (p.Ala2595=) c.7416T>C (p.Ala2472=) c.252T>C (p.Ala84=) c.350T>C n.7785T>C c.7689T>C (p.Ala2563=) | ClinVar dbSNP |
13 | g.32357909T>G | CA483439293 | BRCA2 | c.7785T>G (p.Ala2595=) c.7416T>G (p.Ala2472=) c.252T>G (p.Ala84=) c.350T>G n.7785T>G c.7689T>G (p.Ala2563=) | |
13 | g.32357909T= | CA2082818993 | BRCA2 | c.7785T= (p.Ala2595=) c.7416T= (p.Ala2472=) c.252T= (p.Ala84=) c.350T= n.7785T= c.7689T= (p.Ala2563=) | |
13 | g.32357910G>A | CA025274 | BRCA2 | c.7786G>A (p.Gly2596Arg) c.7417G>A (p.Gly2473Arg) c.253G>A (p.Gly85Arg) c.351G>A n.7786G>A c.7690G>A (p.Gly2564Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
13 | g.32357910G>C | CA387746004 | BRCA2 | c.7786G>C (p.Gly2596Arg) c.7417G>C (p.Gly2473Arg) c.253G>C (p.Gly85Arg) c.351G>C n.7786G>C c.7690G>C (p.Gly2564Arg) | ClinVar dbSNP |
13 | g.32357910G= | CA2082819003 | BRCA2 | c.7786G= (p.Gly2596=) c.7417G= (p.Gly2473=) c.253G= (p.Gly85=) c.351G= n.7786G= c.7690G= (p.Gly2564=) | |
13 | g.32357910G>T | CA387746007 | BRCA2 | c.7786G>T (p.Gly2596Ter) c.7417G>T (p.Gly2473Ter) c.253G>T (p.Gly85Ter) c.351G>T n.7786G>T c.7690G>T (p.Gly2564Ter) | |
13 | g.32357911_32357912insGGG | CA2622572192 | BRCA2 | c.7787_7788insGGG (p.Gly2596_Lys2597insGly) c.7418_7419insGGG (p.Gly2473_Lys2474insGly) c.254_255insGGG (p.Gly85_Lys86insGly) c.352_353insGGG n.7787_7788insGGG c.7691_7692insGGG (p.Gly2564_Lys2565insGly) | gnomAD v4 |
13 | g.32357911G>A | CA16619771 | BRCA2 | c.7787G>A (p.Gly2596Glu) c.7418G>A (p.Gly2473Glu) c.254G>A (p.Gly85Glu) c.352G>A n.7787G>A c.7691G>A (p.Gly2564Glu) | ClinVar dbSNP |
13 | g.32357911G>C | CA387746017 | BRCA2 | c.7787G>C (p.Gly2596Ala) c.7418G>C (p.Gly2473Ala) c.254G>C (p.Gly85Ala) c.352G>C n.7787G>C c.7691G>C (p.Gly2564Ala) | ClinVar dbSNP |
13 | g.32357911G= | CA2082819012 | BRCA2 | c.7787G= (p.Gly2596=) c.7418G= (p.Gly2473=) c.254G= (p.Gly85=) c.352G= n.7787G= c.7691G= (p.Gly2564=) | |
13 | g.32357911G>T | CA387746014 | BRCA2 | c.7787G>T (p.Gly2596Val) c.7418G>T (p.Gly2473Val) c.254G>T (p.Gly85Val) c.352G>T n.7787G>T c.7691G>T (p.Gly2564Val) | ClinVar dbSNP |
13 | g.32357911_32357912delinsGA | CA2082819014 | BRCA2 | c.7787_7788delinsGA (p.Gly2596=) c.7418_7419delinsGA (p.Gly2473=) c.254_255delinsGA (p.Gly85=) c.352_353delinsGA n.7787_7788delinsGA c.7691_7692delinsGA (p.Gly2564=) | |
13 | g.32357912A= | CA2082819037 | BRCA2 | c.7788A= (p.Gly2596=) c.7419A= (p.Gly2473=) c.255A= (p.Gly85=) c.353A= n.7788A= c.7692A= (p.Gly2564=) | |
13 | g.32357912A>C | CA483439300 | BRCA2 | c.7788A>C (p.Gly2596=) c.7419A>C (p.Gly2473=) c.255A>C (p.Gly85=) c.353A>C n.7788A>C c.7692A>C (p.Gly2564=) | |
13 | g.32357912A>G | CA483439301 | BRCA2 | c.7788A>G (p.Gly2596=) c.7419A>G (p.Gly2473=) c.255A>G (p.Gly85=) c.353A>G n.7788A>G c.7692A>G (p.Gly2564=) | |
13 | g.32357912A>T | CA483439303 | BRCA2 | c.7788A>T (p.Gly2596=) c.7419A>T (p.Gly2473=) c.255A>T (p.Gly85=) c.353A>T n.7788A>T c.7692A>T (p.Gly2564=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
13 | g.32357912delinsGGGT | CA913188540 | BRCA2 | c.7788delinsGGGT (p.Gly2596_Lys2597insGly) c.7419delinsGGGT (p.Gly2473_Lys2474insGly) c.255delinsGGGT (p.Gly85_Lys86insGly) c.353delinsGGGT n.7788delinsGGGT c.7692delinsGGGT (p.Gly2564_Lys2565insGly) | ClinVar dbSNP |
13 | g.32357915dup | CA025276 | BRCA2 | c.7791dup (p.Glu2598ArgfsTer5) c.7422dup (p.Glu2475ArgfsTer5) c.258dup (p.Glu87ArgfsTer5) c.356dup n.7791dup c.7695dup (p.Glu2566ArgfsTer5) | ClinVar dbSNP |
13 | g.32357915del | CA658823756 | BRCA2 | c.7791del (p.Glu2598LysfsTer?) c.7422del (p.Glu2475LysfsTer?) c.258del (p.Glu87LysfsTer?) c.7791del (p.Glu2598LysfsTer11) c.356del n.7791del c.7695del (p.Glu2566LysfsTer?) | ClinVar dbSNP |
13 | g.32357913A>C | CA387746018 | BRCA2 | c.7789A>C (p.Lys2597Gln) c.7420A>C (p.Lys2474Gln) c.256A>C (p.Lys86Gln) c.354A>C n.7789A>C c.7693A>C (p.Lys2565Gln) | |
13 | g.32357913A>G | CA387746019 | BRCA2 | c.7789A>G (p.Lys2597Glu) c.7420A>G (p.Lys2474Glu) c.256A>G (p.Lys86Glu) c.354A>G n.7789A>G c.7693A>G (p.Lys2565Glu) | dbSNP |
13 | g.32357913A>T | CA387746020 | BRCA2 | c.7789A>T (p.Lys2597Ter) c.7420A>T (p.Lys2474Ter) c.256A>T (p.Lys86Ter) c.354A>T n.7789A>T c.7693A>T (p.Lys2565Ter) | dbSNP |
13 | g.32357913_32357916delinsAAAG | CA2082819048 | BRCA2 | c.7789_7792delinsAAAG (p.Lys2597=) c.7420_7423delinsAAAG (p.Lys2474=) c.256_259delinsAAAG (p.Lys86=) c.354_357delinsAAAG n.7789_7792delinsAAAG c.7693_7696delinsAAAG (p.Lys2565=) | |
13 | g.32357914A>C | CA387746023 | BRCA2 | c.7790A>C (p.Lys2597Thr) c.7421A>C (p.Lys2474Thr) c.257A>C (p.Lys86Thr) c.355A>C n.7790A>C c.7694A>C (p.Lys2565Thr) | |
13 | g.32357914A>G | CA387746025 | BRCA2 | c.7790A>G (p.Lys2597Arg) c.7421A>G (p.Lys2474Arg) c.257A>G (p.Lys86Arg) c.355A>G n.7790A>G c.7694A>G (p.Lys2565Arg) | dbSNP |
13 | g.32357914A>T | CA387746026 | BRCA2 | c.7790A>T (p.Lys2597Ile) c.7421A>T (p.Lys2474Ile) c.257A>T (p.Lys86Ile) c.355A>T n.7790A>T c.7694A>T (p.Lys2565Ile) | |
13 | g.32357919_32357921del | CA025277 | BRCA2 | c.7795_7797del (p.Glu2599del) c.7426_7428del (p.Glu2476del) c.262_264del (p.Glu88del) c.360_362del n.7795_7797del c.7699_7701del (p.Glu2567del) | ClinVar dbSNP gnomAD v4 |
13 | g.32357915A= | CA2082819059 | BRCA2 | c.7791A= (p.Lys2597=) c.7422A= (p.Lys2474=) c.258A= (p.Lys86=) c.356A= n.7791A= c.7695A= (p.Lys2565=) | |
13 | g.32357915A>C | CA387746031 | BRCA2 | c.7791A>C (p.Lys2597Asn) c.7422A>C (p.Lys2474Asn) c.258A>C (p.Lys86Asn) c.356A>C n.7791A>C c.7695A>C (p.Lys2565Asn) | ClinVar dbSNP |
13 | g.32357915A>G | CA483439307 | BRCA2 | c.7791A>G (p.Lys2597=) c.7422A>G (p.Lys2474=) c.258A>G (p.Lys86=) c.356A>G n.7791A>G c.7695A>G (p.Lys2565=) | dbSNP |
13 | g.32357915A>T | CA387746033 | BRCA2 | c.7791A>T (p.Lys2597Asn) c.7422A>T (p.Lys2474Asn) c.258A>T (p.Lys86Asn) c.356A>T n.7791A>T c.7695A>T (p.Lys2565Asn) | |
13 | g.32357916G>A | CA387746035 | BRCA2 | c.7792G>A (p.Glu2598Lys) c.7423G>A (p.Glu2475Lys) c.259G>A (p.Glu87Lys) c.357G>A n.7792G>A c.7696G>A (p.Glu2566Lys) | dbSNP |
13 | g.32357916G>C | CA387746037 | BRCA2 | c.7792G>C (p.Glu2598Gln) c.7423G>C (p.Glu2475Gln) c.259G>C (p.Glu87Gln) c.357G>C n.7792G>C c.7696G>C (p.Glu2566Gln) | dbSNP |
13 | g.32357916G= | CA2082819070 | BRCA2 | c.7792G= (p.Glu2598=) c.7423G= (p.Glu2475=) c.259G= (p.Glu87=) c.357G= n.7792G= c.7696G= (p.Glu2566=) | |
13 | g.32357916G>T | CA387746039 | BRCA2 | c.7792G>T (p.Glu2598Ter) c.7423G>T (p.Glu2475Ter) c.259G>T (p.Glu87Ter) c.357G>T n.7792G>T c.7696G>T (p.Glu2566Ter) | ClinVar dbSNP |
13 | g.32357917A= | CA2082819083 | BRCA2 | c.7793A= (p.Glu2598=) c.7424A= (p.Glu2475=) c.260A= (p.Glu87=) c.358A= n.7793A= c.7697A= (p.Glu2566=) | |
13 | g.32357917A>C | CA387746056 | BRCA2 | c.7793A>C (p.Glu2598Ala) c.7424A>C (p.Glu2475Ala) c.260A>C (p.Glu87Ala) c.358A>C n.7793A>C c.7697A>C (p.Glu2566Ala) | |
13 | g.32357917A>G | CA387746059 | BRCA2 | c.7793A>G (p.Glu2598Gly) c.7424A>G (p.Glu2475Gly) c.260A>G (p.Glu87Gly) c.358A>G n.7793A>G c.7697A>G (p.Glu2566Gly) | |
13 | g.32357917A>T | CA387746043 | BRCA2 | c.7793A>T (p.Glu2598Val) c.7424A>T (p.Glu2475Val) c.260A>T (p.Glu87Val) c.358A>T n.7793A>T c.7697A>T (p.Glu2566Val) | dbSNP |
13 | g.32357917_32357918insCTCTGCATTTTTGCTGTT | CA2082819092 | BRCA2 | c.7793_7794insCTCTGCATTTTTGCTGTT (p.Glu2598delinsAspSerAlaPheLeuLeuLeu) c.7424_7425insCTCTGCATTTTTGCTGTT (p.Glu2475delinsAspSerAlaPheLeuLeuLeu) c.260_261insCTCTGCATTTTTGCTGTT (p.Glu87delinsAspSerAlaPheLeuLeuLeu) c.358_359insCTCTGCATTTTTGCTGTT n.7793_7794insCTCTGCATTTTTGCTGTT c.7697_7698insCTCTGCATTTTTGCTGTT (p.Glu2566delinsAspSerAlaPheLeuLeuLeu) | dbSNP |
13 | g.32357918A= | CA2082819088 | BRCA2 | c.7794A= (p.Glu2598=) c.7425A= (p.Glu2475=) c.261A= (p.Glu87=) c.359A= n.7794A= c.7698A= (p.Glu2566=) | |
13 | g.32357918A>C | CA387746062 | BRCA2 | c.7794A>C (p.Glu2598Asp) c.7425A>C (p.Glu2475Asp) c.261A>C (p.Glu87Asp) c.359A>C n.7794A>C c.7698A>C (p.Glu2566Asp) | |
13 | g.32357918A>G | CA483439309 | BRCA2 | c.7794A>G (p.Glu2598=) c.7425A>G (p.Glu2475=) c.261A>G (p.Glu87=) c.359A>G n.7794A>G c.7698A>G (p.Glu2566=) | |
13 | g.32357918A>T | CA387746066 | BRCA2 | c.7794A>T (p.Glu2598Asp) c.7425A>T (p.Glu2475Asp) c.261A>T (p.Glu87Asp) c.359A>T n.7794A>T c.7698A>T (p.Glu2566Asp) | |
13 | g.32357919_32357920del | CA1139770845 | BRCA2 | c.7795_7796del (p.Glu2599IlefsTer3) c.7426_7427del (p.Glu2476IlefsTer3) c.262_263del (p.Glu88IlefsTer3) c.360_361del n.7795_7796del c.7699_7700del (p.Glu2567IlefsTer3) | |
13 | g.32357919G>A | CA10579756 | BRCA2 | c.7795G>A (p.Glu2599Lys) c.7426G>A (p.Glu2476Lys) c.262G>A (p.Glu88Lys) c.360G>A n.7795G>A c.7699G>A (p.Glu2567Lys) | ClinVar dbSNP |
13 | g.32357919G>C | CA387746073 | BRCA2 | c.7795G>C (p.Glu2599Gln) c.7426G>C (p.Glu2476Gln) c.262G>C (p.Glu88Gln) c.360G>C n.7795G>C c.7699G>C (p.Glu2567Gln) | dbSNP |
13 | g.32357919G= | CA2082819102 | BRCA2 | c.7795G= (p.Glu2599=) c.7426G= (p.Glu2476=) c.262G= (p.Glu88=) c.360G= n.7795G= c.7699G= (p.Glu2567=) | |
13 | g.32357919G>T | CA10589451 | BRCA2 | c.7795G>T (p.Glu2599Ter) c.7426G>T (p.Glu2476Ter) c.262G>T (p.Glu88Ter) c.360G>T n.7795G>T c.7699G>T (p.Glu2567Ter) | ClinVar dbSNP COSMIC COSMIC |
13 | g.32357919dup | CA247471267 | BRCA2 | c.7795dup (p.Glu2599GlyfsTer4) c.7426dup (p.Glu2476GlyfsTer4) c.262dup (p.Glu88GlyfsTer4) c.360dup n.7795dup c.7699dup (p.Glu2567GlyfsTer4) | dbSNP |
13 | g.32357919_32357920insT | CA247471293 | BRCA2 | c.7795_7796insT (p.Glu2599ValfsTer4) c.7426_7427insT (p.Glu2476ValfsTer4) c.262_263insT (p.Glu88ValfsTer4) c.360_361insT n.7795_7796insT c.7699_7700insT (p.Glu2567ValfsTer4) | dbSNP |
13 | g.32357920A= | CA2082819114 | BRCA2 | c.7796A= (p.Glu2599=) c.7427A= (p.Glu2476=) c.263A= (p.Glu88=) c.361A= n.7796A= c.7700A= (p.Glu2567=) | |
13 | g.32357920A>C | CA6941139 | BRCA2 | c.7796A>C (p.Glu2599Ala) c.7427A>C (p.Glu2476Ala) c.263A>C (p.Glu88Ala) c.361A>C n.7796A>C c.7700A>C (p.Glu2567Ala) | dbSNP ExAC gnomAD v2 gnomAD v4 |
13 | g.32357920A>G | CA387746086 | BRCA2 | c.7796A>G (p.Glu2599Gly) c.7427A>G (p.Glu2476Gly) c.263A>G (p.Glu88Gly) c.361A>G n.7796A>G c.7700A>G (p.Glu2567Gly) | ClinVar dbSNP |
13 | g.32357920A>T | CA387746106 | BRCA2 | c.7796A>T (p.Glu2599Val) c.7427A>T (p.Glu2476Val) c.263A>T (p.Glu88Val) c.361A>T n.7796A>T c.7700A>T (p.Glu2567Val) | ClinVar dbSNP |
13 | g.32357921A= | CA2082819122 | BRCA2 | c.7797A= (p.Glu2599=) c.7428A= (p.Glu2476=) c.264A= (p.Glu88=) c.362A= n.7797A= c.7701A= (p.Glu2567=) | |
13 | g.32357921A>C | CA387746113 | BRCA2 | c.7797A>C (p.Glu2599Asp) c.7428A>C (p.Glu2476Asp) c.264A>C (p.Glu88Asp) c.362A>C n.7797A>C c.7701A>C (p.Glu2567Asp) | ClinVar dbSNP |
13 | g.32357921A>G | CA483439314 | BRCA2 | c.7797A>G (p.Glu2599=) c.7428A>G (p.Glu2476=) c.264A>G (p.Glu88=) c.362A>G n.7797A>G c.7701A>G (p.Glu2567=) | |
13 | g.32357921A>T | CA387746114 | BRCA2 | c.7797A>T (p.Glu2599Asp) c.7428A>T (p.Glu2476Asp) c.264A>T (p.Glu88Asp) c.362A>T n.7797A>T c.7701A>T (p.Glu2567Asp) | |
13 | g.32357922T>A | CA387746120 | BRCA2 | c.7798T>A (p.Phe2600Ile) c.7429T>A (p.Phe2477Ile) c.265T>A (p.Phe89Ile) c.363T>A n.7798T>A c.7702T>A (p.Phe2568Ile) | dbSNP |
13 | g.32357922T>C | CA387746117 | BRCA2 | c.7798T>C (p.Phe2600Leu) c.7429T>C (p.Phe2477Leu) c.265T>C (p.Phe89Leu) c.363T>C n.7798T>C c.7702T>C (p.Phe2568Leu) | dbSNP |
13 | g.32357922T>G | CA387746119 | BRCA2 | c.7798T>G (p.Phe2600Val) c.7429T>G (p.Phe2477Val) c.265T>G (p.Phe89Val) c.363T>G n.7798T>G c.7702T>G (p.Phe2568Val) | |
13 | g.32357925del | CA2727914535 | BRCA2 | c.7801del (p.Tyr2601IlefsTer?) c.7432del (p.Tyr2478IlefsTer?) c.268del (p.Tyr90IlefsTer?) c.7801del (p.Tyr2601IlefsTer8) c.366del n.7801del c.7705del (p.Tyr2569IlefsTer?) | dbSNP |
13 | g.32357923T>A | CA387746124 | BRCA2 | c.7799T>A (p.Phe2600Tyr) c.7430T>A (p.Phe2477Tyr) c.266T>A (p.Phe89Tyr) c.364T>A n.7799T>A c.7703T>A (p.Phe2568Tyr) | |
13 | g.32357923T>C | CA387746126 | BRCA2 | c.7799T>C (p.Phe2600Ser) c.7430T>C (p.Phe2477Ser) c.266T>C (p.Phe89Ser) c.364T>C n.7799T>C c.7703T>C (p.Phe2568Ser) | |
13 | g.32357923T>G | CA387746128 | BRCA2 | c.7799T>G (p.Phe2600Cys) c.7430T>G (p.Phe2477Cys) c.266T>G (p.Phe89Cys) c.364T>G n.7799T>G c.7703T>G (p.Phe2568Cys) | ClinVar dbSNP |
13 | g.32357923T= | CA2082819129 | BRCA2 | c.7799T= (p.Phe2600=) c.7430T= (p.Phe2477=) c.266T= (p.Phe89=) c.364T= n.7799T= c.7703T= (p.Phe2568=) | |
13 | g.32357924T>A | CA387746132 | BRCA2 | c.7800T>A (p.Phe2600Leu) c.7431T>A (p.Phe2477Leu) c.267T>A (p.Phe89Leu) c.365T>A n.7800T>A c.7704T>A (p.Phe2568Leu) | |
13 | g.32357924T>C | CA483439318 | BRCA2 | c.7800T>C (p.Phe2600=) c.7431T>C (p.Phe2477=) c.267T>C (p.Phe89=) c.365T>C n.7800T>C c.7704T>C (p.Phe2568=) | |
13 | g.32357924T>G | CA16614214 | BRCA2 | c.7800T>G (p.Phe2600Leu) c.7431T>G (p.Phe2477Leu) c.267T>G (p.Phe89Leu) c.365T>G n.7800T>G c.7704T>G (p.Phe2568Leu) | ClinVar dbSNP |
13 | g.32357924T= | CA2082819138 | BRCA2 | c.7800T= (p.Phe2600=) c.7431T= (p.Phe2477=) c.267T= (p.Phe89=) c.365T= n.7800T= c.7704T= (p.Phe2568=) | |
13 | g.32357924_32357925insAAAGTAAACATG | CA609453902 | BRCA2 | c.7800_7801insAAAGTAAACATG (p.Phe2600_Tyr2601insLysValAsnMet) c.7431_7432insAAAGTAAACATG (p.Phe2477_Tyr2478insLysValAsnMet) c.267_268insAAAGTAAACATG (p.Phe89_Tyr90insLysValAsnMet) c.365_366insAAAGTAAACATG n.7800_7801insAAAGTAAACATG c.7704_7705insAAAGTAAACATG (p.Phe2568_Tyr2569insLysValAsnMet) | dbSNP gnomAD v2 |
13 | g.32357925T>A | CA387746137 | BRCA2 | c.7801T>A (p.Tyr2601Asn) c.7432T>A (p.Tyr2478Asn) c.268T>A (p.Tyr90Asn) c.366T>A n.7801T>A c.7705T>A (p.Tyr2569Asn) | |
13 | g.32357925T>C | CA387746146 | BRCA2 | c.7801T>C (p.Tyr2601His) c.7432T>C (p.Tyr2478His) c.268T>C (p.Tyr90His) c.366T>C n.7801T>C c.7705T>C (p.Tyr2569His) | |
13 | g.32357925T>G | CA387746148 | BRCA2 | c.7801T>G (p.Tyr2601Asp) c.7432T>G (p.Tyr2478Asp) c.268T>G (p.Tyr90Asp) c.366T>G n.7801T>G c.7705T>G (p.Tyr2569Asp) | |
13 | g.32357928_32357938del | CA2580087366 | BRCA2 | c.7804_7805+9del c.7435_7436+9del c.271_272+9del c.369_370+9del n.7804_7805+9del c.7708_7709+9del | ClinVar |
13 | g.32357926A= | CA2082819146 | BRCA2 | c.7802A= (p.Tyr2601=) c.7433A= (p.Tyr2478=) c.269A= (p.Tyr90=) c.367A= n.7802A= c.7706A= (p.Tyr2569=) | |
13 | g.32357926A>C | CA387746150 | BRCA2 | c.7802A>C (p.Tyr2601Ser) c.7433A>C (p.Tyr2478Ser) c.269A>C (p.Tyr90Ser) c.367A>C n.7802A>C c.7706A>C (p.Tyr2569Ser) | dbSNP |
13 | g.32357926A>G | CA025278 | BRCA2 | c.7802A>G (p.Tyr2601Cys) c.7433A>G (p.Tyr2478Cys) c.269A>G (p.Tyr90Cys) c.367A>G n.7802A>G c.7706A>G (p.Tyr2569Cys) | ClinVar dbSNP |
13 | g.32357926A>T | CA387746155 | BRCA2 | c.7802A>T (p.Tyr2601Phe) c.7433A>T (p.Tyr2478Phe) c.269A>T (p.Tyr90Phe) c.367A>T n.7802A>T c.7706A>T (p.Tyr2569Phe) | dbSNP |
13 | g.32357927del | CA2582341811 | BRCA2 | c.7803del (p.Tyr2601Ter) c.7434del (p.Tyr2478Ter) c.270del (p.Tyr90Ter) c.368del n.7803del c.7707del (p.Tyr2569Ter) | ClinVar |
13 | g.32357927T>A | CA387746158 | BRCA2 | c.7803T>A (p.Tyr2601Ter) c.7434T>A (p.Tyr2478Ter) c.270T>A (p.Tyr90Ter) c.368T>A n.7803T>A c.7707T>A (p.Tyr2569Ter) | dbSNP |
13 | g.32357927T>C | CA483439324 | BRCA2 | c.7803T>C (p.Tyr2601=) c.7434T>C (p.Tyr2478=) c.270T>C (p.Tyr90=) c.368T>C n.7803T>C c.7707T>C (p.Tyr2569=) | ClinVar dbSNP |
13 | g.32357927T>G | CA387746160 | BRCA2 | c.7803T>G (p.Tyr2601Ter) c.7434T>G (p.Tyr2478Ter) c.270T>G (p.Tyr90Ter) c.368T>G n.7803T>G c.7707T>G (p.Tyr2569Ter) | |
13 | g.32357927T= | CA2082819161 | BRCA2 | c.7803T= (p.Tyr2601=) c.7434T= (p.Tyr2478=) c.270T= (p.Tyr90=) c.368T= n.7803T= c.7707T= (p.Tyr2569=) | |
13 | g.32357928A= | CA2082819165 | BRCA2 | c.7804A= (p.Arg2602=) c.7435A= (p.Arg2479=) c.271A= (p.Arg91=) c.7804A= (p.Ser2602=) c.369A= n.7804A= c.7708A= (p.Arg2570=) | |
13 | g.32357928A>C | CA483439325 | BRCA2 | c.7804A>C (p.Arg2602=) c.7435A>C (p.Arg2479=) c.271A>C (p.Arg91=) c.7804A>C (p.Ser2602Arg) c.369A>C n.7804A>C c.7708A>C (p.Arg2570=) | |
13 | g.32357928A>G | CA387746163 | BRCA2 | c.7804A>G (p.Arg2602Gly) c.7435A>G (p.Arg2479Gly) c.271A>G (p.Arg91Gly) c.7804A>G (p.Ser2602Gly) c.369A>G n.7804A>G c.7708A>G (p.Arg2570Gly) | dbSNP gnomAD v4 |
13 | g.32357928A>T | CA387746166 | BRCA2 | c.7804A>T (p.Arg2602Trp) c.7435A>T (p.Arg2479Trp) c.271A>T (p.Arg91Trp) c.7804A>T (p.Ser2602Cys) c.369A>T n.7804A>T c.7708A>T (p.Arg2570Trp) | dbSNP |
13 | g.32357928_32357929insTTGTTCAG | CA919242800 | BRCA2 | c.7804_7805insTTGTTCAG (p.Arg2602IlefsTer?) c.7435_7436insTTGTTCAG (p.Arg2479IlefsTer?) c.271_272insTTGTTCAG (p.Arg91IlefsTer?) c.7804_7805insTTGTTCAG (p.Ser2602IlefsTer10) c.369_370insTTGTTCAG n.7804_7805insTTGTTCAG c.7708_7709insTTGTTCAG (p.Arg2570IlefsTer?) | dbSNP |
13 | g.32357929G>A | CA387746169 | BRCA2 | c.7805G>A (p.Arg2602Lys) c.7436G>A (p.Arg2479Lys) c.272G>A (p.Arg91Lys) c.7805G>A (p.Ser2602Asn) c.370G>A n.7805G>A c.7709G>A (p.Arg2570Lys) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
13 | g.32357929G>C | CA025285 | BRCA2 | c.7805G>C (p.Arg2602Thr) c.7436G>C (p.Arg2479Thr) c.272G>C (p.Arg91Thr) c.7805G>C (p.Ser2602Thr) c.370G>C n.7805G>C c.7709G>C (p.Arg2570Thr) | ClinVar dbSNP |
13 | g.32357929G= | CA2082819172 | BRCA2 | c.7805G= (p.Arg2602=) c.7436G= (p.Arg2479=) c.272G= (p.Arg91=) c.7805G= (p.Ser2602=) c.370G= n.7805G= c.7709G= (p.Arg2570=) | |
13 | g.32357929G>T | CA387746172 | BRCA2 | c.7805G>T (p.Arg2602Met) c.7436G>T (p.Arg2479Met) c.272G>T (p.Arg91Met) c.7805G>T (p.Ser2602Ile) c.370G>T n.7805G>T c.7709G>T (p.Arg2570Met) | dbSNP |
13 | g.32357930G>A | CA025280 | BRCA2 | c.7805+1G>A (n.7805+1G>A) c.7436+1G>A (n.7436+1G>A) c.272+1G>A (n.272+1G>A) c.370+1G>A n.7805+1G>A c.7709+1G>A (n.7709+1G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC |
13 | g.32357930G>C | CA387746183 | BRCA2 | c.7805+1G>C (n.7805+1G>C) c.7436+1G>C (n.7436+1G>C) c.272+1G>C (n.272+1G>C) c.370+1G>C n.7805+1G>C c.7709+1G>C (n.7709+1G>C) | dbSNP |
13 | g.32357930G= | CA2082819185 | BRCA2 | c.7805+1G= (n.7805+1G=) c.7436+1G= (n.7436+1G=) c.272+1G= (n.272+1G=) c.370+1G= n.7805+1G= c.7709+1G= (n.7709+1G=) | |
13 | g.32357930G>T | CA387746185 | BRCA2 | c.7805+1G>T (n.7805+1G>T) c.7436+1G>T (n.7436+1G>T) c.272+1G>T (n.272+1G>T) c.370+1G>T n.7805+1G>T c.7709+1G>T (n.7709+1G>T) | dbSNP |
13 | g.32357930_32357932delinsGTA | CA2082819188 | BRCA2 | c.7805+1_7805+3delinsGTA (n.7805+1_7805+3delinsGTA) c.7436+1_7436+3delinsGTA (n.7436+1_7436+3delinsGTA) c.272+1_272+3delinsGTA (n.272+1_272+3delinsGTA) c.370+1_370+3delinsGTA n.7805+1_7805+3delinsGTA c.7709+1_7709+3delinsGTA (n.7709+1_7709+3delinsGTA) | |
13 | g.32357931T>A | CA387746187 | BRCA2 | c.7805+2T>A (n.7805+2T>A) c.7436+2T>A (n.7436+2T>A) c.272+2T>A (n.272+2T>A) c.370+2T>A n.7805+2T>A c.7709+2T>A (n.7709+2T>A) | ClinVar dbSNP |
13 | g.32357931T>C | CA387746189 | BRCA2 | c.7805+2T>C (n.7805+2T>C) c.7436+2T>C (n.7436+2T>C) c.272+2T>C (n.272+2T>C) c.370+2T>C n.7805+2T>C c.7709+2T>C (n.7709+2T>C) | ClinVar dbSNP |
13 | g.32357931T>G | CA10602541 | BRCA2 | c.7805+2T>G (n.7805+2T>G) c.7436+2T>G (n.7436+2T>G) c.272+2T>G (n.272+2T>G) c.370+2T>G n.7805+2T>G c.7709+2T>G (n.7709+2T>G) | ClinVar dbSNP |
13 | g.32357931T= | CA2082819202 | BRCA2 | c.7805+2T= (n.7805+2T=) c.7436+2T= (n.7436+2T=) c.272+2T= (n.272+2T=) c.370+2T= n.7805+2T= c.7709+2T= (n.7709+2T=) | |
13 | g.32357931_32357932del | CA1139663207 | BRCA2 | c.7805+2_7805+3del (n.7805+2_7805+3del) c.7436+2_7436+3del (n.7436+2_7436+3del) c.272+2_272+3del (n.272+2_272+3del) c.370+2_370+3del n.7805+2_7805+3del c.7709+2_7709+3del (n.7709+2_7709+3del) | ClinVar dbSNP |
13 | g.32357932A= | CA2082819207 | BRCA2 | c.7805+3A= (n.7805+3A=) c.7436+3A= (n.7436+3A=) c.272+3A= (n.272+3A=) c.370+3A= n.7805+3A= c.7709+3A= (n.7709+3A=) | |
13 | g.32357932A>C | CA025281 | BRCA2 | c.7805+3A>C (n.7805+3A>C) c.7436+3A>C (n.7436+3A>C) c.272+3A>C (n.272+3A>C) c.370+3A>C n.7805+3A>C c.7709+3A>C (n.7709+3A>C) | ClinVar dbSNP gnomAD v4 |
13 | g.32357932A>G | CA2727833969 | BRCA2 | c.7805+3A>G (n.7805+3A>G) c.7436+3A>G (n.7436+3A>G) c.272+3A>G (n.272+3A>G) c.370+3A>G n.7805+3A>G c.7709+3A>G (n.7709+3A>G) | dbSNP |
13 | g.32357932A>T | CA2727833968 | BRCA2 | c.7805+3A>T (n.7805+3A>T) c.7436+3A>T (n.7436+3A>T) c.272+3A>T (n.272+3A>T) c.370+3A>T n.7805+3A>T c.7709+3A>T (n.7709+3A>T) | dbSNP |
13 | g.32357933C>A | CA915946878 | BRCA2 | c.7805+4C>A (n.7805+4C>A) c.7436+4C>A (n.7436+4C>A) c.272+4C>A (n.272+4C>A) c.370+4C>A n.7805+4C>A c.7709+4C>A (n.7709+4C>A) | ClinVar dbSNP |
13 | g.32357933C= | CA2082819216 | BRCA2 | c.7805+4C= (n.7805+4C=) c.7436+4C= (n.7436+4C=) c.272+4C= (n.272+4C=) c.370+4C= n.7805+4C= c.7709+4C= (n.7709+4C=) | |
13 | g.32357933C>G | CA2727840307 | BRCA2 | c.7805+4C>G (n.7805+4C>G) c.7436+4C>G (n.7436+4C>G) c.272+4C>G (n.272+4C>G) c.370+4C>G n.7805+4C>G c.7709+4C>G (n.7709+4C>G) | dbSNP |
13 | g.32357933C>T | CA6941140 | BRCA2 | c.7805+4C>T (n.7805+4C>T) c.7436+4C>T (n.7436+4C>T) c.272+4C>T (n.272+4C>T) c.370+4C>T n.7805+4C>T c.7709+4C>T (n.7709+4C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
13 | g.32357934T>A | CA2727914551 | BRCA2 | c.7805+5T>A (n.7805+5T>A) c.7436+5T>A (n.7436+5T>A) c.272+5T>A (n.272+5T>A) c.370+5T>A n.7805+5T>A c.7709+5T>A (n.7709+5T>A) | dbSNP |
13 | g.32357934T>G | CA2580087369 | BRCA2 | c.7805+5T>G (n.7805+5T>G) c.7436+5T>G (n.7436+5T>G) c.272+5T>G (n.272+5T>G) c.370+5T>G n.7805+5T>G c.7709+5T>G (n.7709+5T>G) | ClinVar |
13 | g.32357935C>A | CA2727833970 | BRCA2 | c.7805+6C>A (n.7805+6C>A) c.7436+6C>A (n.7436+6C>A) c.272+6C>A (n.272+6C>A) c.370+6C>A n.7805+6C>A c.7709+6C>A (n.7709+6C>A) | dbSNP |
13 | g.32357935C= | CA2082819227 | BRCA2 | c.7805+6C= (n.7805+6C=) c.7436+6C= (n.7436+6C=) c.272+6C= (n.272+6C=) c.370+6C= n.7805+6C= c.7709+6C= (n.7709+6C=) | |
13 | g.32357935C>G | CA025282 | BRCA2 | c.7805+6C>G (n.7805+6C>G) c.7436+6C>G (n.7436+6C>G) c.272+6C>G (n.272+6C>G) c.370+6C>G n.7805+6C>G c.7709+6C>G (n.7709+6C>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.32357935C>T | CA913188544 | BRCA2 | c.7805+6C>T (n.7805+6C>T) c.7436+6C>T (n.7436+6C>T) c.272+6C>T (n.272+6C>T) c.370+6C>T n.7805+6C>T c.7709+6C>T (n.7709+6C>T) | ClinVar dbSNP |
13 | g.32357935_32357937delinsCTA | CA2082819233 | BRCA2 | c.7805+6_7805+8delinsCTA (n.7805+6_7805+8delinsCTA) c.7436+6_7436+8delinsCTA (n.7436+6_7436+8delinsCTA) c.272+6_272+8delinsCTA (n.272+6_272+8delinsCTA) c.370+6_370+8delinsCTA n.7805+6_7805+8delinsCTA c.7709+6_7709+8delinsCTA (n.7709+6_7709+8delinsCTA) | |
13 | g.32357936T>A | CA025283 | BRCA2 | c.7805+7T>A (n.7805+7T>A) c.7436+7T>A (n.7436+7T>A) c.272+7T>A (n.272+7T>A) c.370+7T>A n.7805+7T>A c.7709+7T>A (n.7709+7T>A) | ClinVar dbSNP |
13 | g.32357936T= | CA2082819241 | BRCA2 | c.7805+7T= (n.7805+7T=) c.7436+7T= (n.7436+7T=) c.272+7T= (n.272+7T=) c.370+7T= n.7805+7T= c.7709+7T= (n.7709+7T=) | |
13 | g.32357937_32357938del | CA954697467 | BRCA2 | c.7805+8_7805+9del (n.7805+8_7805+9del) c.7436+8_7436+9del (n.7436+8_7436+9del) c.272+8_272+9del (n.272+8_272+9del) c.370+8_370+9del n.7805+8_7805+9del c.7709+8_7709+9del (n.7709+8_7709+9del) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
13 | g.32357937A= | CA2082819290 | BRCA2 | c.7805+8A= (n.7805+8A=) c.7436+8A= (n.7436+8A=) c.272+8A= (n.272+8A=) c.370+8A= n.7805+8A= c.7709+8A= (n.7709+8A=) | |
13 | g.32357937A>C | CA913188545 | BRCA2 | c.7805+8A>C (n.7805+8A>C) c.7436+8A>C (n.7436+8A>C) c.272+8A>C (n.272+8A>C) c.370+8A>C n.7805+8A>C c.7709+8A>C (n.7709+8A>C) | ClinVar dbSNP |
13 | g.32357937A>G | CA025284 | BRCA2 | c.7805+8A>G (n.7805+8A>G) c.7436+8A>G (n.7436+8A>G) c.272+8A>G (n.272+8A>G) c.370+8A>G n.7805+8A>G c.7709+8A>G (n.7709+8A>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.32357938T>A | CA350397 | BRCA2 | c.7805+9T>A (n.7805+9T>A) c.7436+9T>A (n.7436+9T>A) c.272+9T>A (n.272+9T>A) c.370+9T>A n.7805+9T>A c.7709+9T>A (n.7709+9T>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.32357938T>C | CA2499222308 | BRCA2 | c.7805+9T>C (n.7805+9T>C) c.7436+9T>C (n.7436+9T>C) c.272+9T>C (n.272+9T>C) c.370+9T>C n.7805+9T>C c.7709+9T>C (n.7709+9T>C) | ClinVar dbSNP |
13 | g.32357938T= | CA2082819304 | BRCA2 | c.7805+9T= (n.7805+9T=) c.7436+9T= (n.7436+9T=) c.272+9T= (n.272+9T=) c.370+9T= n.7805+9T= c.7709+9T= (n.7709+9T=) | |
13 | g.32357939G>A | CA658798124 | BRCA2 | c.7805+10G>A (n.7805+10G>A) c.7436+10G>A (n.7436+10G>A) c.272+10G>A (n.272+10G>A) c.370+10G>A n.7805+10G>A c.7709+10G>A (n.7709+10G>A) | ClinVar dbSNP gnomAD v4 |
13 | g.32357939G>C | CA2727853380 | BRCA2 | c.7805+10G>C (n.7805+10G>C) c.7436+10G>C (n.7436+10G>C) c.272+10G>C (n.272+10G>C) c.370+10G>C n.7805+10G>C c.7709+10G>C (n.7709+10G>C) | dbSNP |
13 | g.32357939G= | CA2082819313 | BRCA2 | c.7805+10G= (n.7805+10G=) c.7436+10G= (n.7436+10G=) c.272+10G= (n.272+10G=) c.370+10G= n.7805+10G= c.7709+10G= (n.7709+10G=) | |
13 | g.32357939G>T | CA16606817 | BRCA2 | c.7805+10G>T (n.7805+10G>T) c.7436+10G>T (n.7436+10G>T) c.272+10G>T (n.272+10G>T) c.370+10G>T n.7805+10G>T c.7709+10G>T (n.7709+10G>T) | ClinVar dbSNP gnomAD v4 |
13 | g.32357940C>A | CA16614357 | BRCA2 | c.7805+11C>A (n.7805+11C>A) c.7436+11C>A (n.7436+11C>A) c.272+11C>A (n.272+11C>A) c.370+11C>A n.7805+11C>A c.7709+11C>A (n.7709+11C>A) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
13 | g.32357940C= | CA2082819327 | BRCA2 | c.7805+11C= (n.7805+11C=) c.7436+11C= (n.7436+11C=) c.272+11C= (n.272+11C=) c.370+11C= n.7805+11C= c.7709+11C= (n.7709+11C=) | |
13 | g.32357942A= | CA2082819330 | BRCA2 | c.7805+13A= (n.7805+13A=) c.7436+13A= (n.7436+13A=) c.272+13A= (n.272+13A=) c.370+13A= n.7805+13A= c.7709+13A= (n.7709+13A=) | |
13 | g.32357942A>G | CA025279 | BRCA2 | c.7805+13A>G (n.7805+13A>G) c.7436+13A>G (n.7436+13A>G) c.272+13A>G (n.272+13A>G) c.370+13A>G n.7805+13A>G c.7709+13A>G (n.7709+13A>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.32357943A>G | CA2499222309 | BRCA2 | c.7805+14A>G (n.7805+14A>G) c.7436+14A>G (n.7436+14A>G) c.272+14A>G (n.272+14A>G) c.370+14A>G n.7805+14A>G c.7709+14A>G (n.7709+14A>G) | ClinVar dbSNP |
13 | g.32357943A>T | CA2727914555 | BRCA2 | c.7805+14A>T (n.7805+14A>T) c.7436+14A>T (n.7436+14A>T) c.272+14A>T (n.272+14A>T) c.370+14A>T n.7805+14A>T c.7709+14A>T (n.7709+14A>T) | dbSNP |
13 | g.32357944A>G | CA2727914556 | BRCA2 | c.7805+15A>G (n.7805+15A>G) c.7436+15A>G (n.7436+15A>G) c.272+15A>G (n.272+15A>G) c.370+15A>G n.7805+15A>G c.7709+15A>G (n.7709+15A>G) | dbSNP |
13 | g.32357946G>A | CA337126 | BRCA2 | c.7805+17G>A (n.7805+17G>A) c.7436+17G>A (n.7436+17G>A) c.272+17G>A (n.272+17G>A) c.370+17G>A n.7805+17G>A c.7709+17G>A (n.7709+17G>A) | ClinVar dbSNP gnomAD v4 |
13 | g.32357946G>C | CA2727836150 | BRCA2 | c.7805+17G>C (n.7805+17G>C) c.7436+17G>C (n.7436+17G>C) c.272+17G>C (n.272+17G>C) c.370+17G>C n.7805+17G>C c.7709+17G>C (n.7709+17G>C) | dbSNP |
13 | g.32357946G= | CA2082819342 | BRCA2 | c.7805+17G= (n.7805+17G=) c.7436+17G= (n.7436+17G=) c.272+17G= (n.272+17G=) c.370+17G= n.7805+17G= c.7709+17G= (n.7709+17G=) | |
13 | g.32357946G>T | CA697352007 | BRCA2 | c.7805+17G>T (n.7805+17G>T) c.7436+17G>T (n.7436+17G>T) c.272+17G>T (n.272+17G>T) c.370+17G>T n.7805+17G>T c.7709+17G>T (n.7709+17G>T) | dbSNP |
13 | g.32357947A>G | CA2697551789 | BRCA2 | c.7805+18A>G (n.7805+18A>G) c.7436+18A>G (n.7436+18A>G) c.272+18A>G (n.272+18A>G) c.370+18A>G n.7805+18A>G c.7709+18A>G (n.7709+18A>G) | ClinVar |
13 | g.32357947A>T | CA2727914558 | BRCA2 | c.7805+18A>T (n.7805+18A>T) c.7436+18A>T (n.7436+18A>T) c.272+18A>T (n.272+18A>T) c.370+18A>T n.7805+18A>T c.7709+18A>T (n.7709+18A>T) | dbSNP |
13 | g.32357948T>A | CA2727912939 | BRCA2 | c.7805+19T>A (n.7805+19T>A) c.7436+19T>A (n.7436+19T>A) c.272+19T>A (n.272+19T>A) c.370+19T>A n.7805+19T>A c.7709+19T>A (n.7709+19T>A) | dbSNP |
13 | g.32357948T>G | CA2082819363 | BRCA2 | c.7805+19T>G (n.7805+19T>G) c.7436+19T>G (n.7436+19T>G) c.272+19T>G (n.272+19T>G) c.370+19T>G n.7805+19T>G c.7709+19T>G (n.7709+19T>G) | ClinVar dbSNP |
13 | g.32357948T= | CA2082819346 | BRCA2 | c.7805+19T= (n.7805+19T=) c.7436+19T= (n.7436+19T=) c.272+19T= (n.272+19T=) c.370+19T= n.7805+19T= c.7709+19T= (n.7709+19T=) | |
13 | g.32357949T>A | CA6941141 | BRCA2 | c.7805+20T>A (n.7805+20T>A) c.7436+20T>A (n.7436+20T>A) c.272+20T>A (n.272+20T>A) c.370+20T>A n.7805+20T>A c.7709+20T>A (n.7709+20T>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
13 | g.32357949T>G | CA2573149413 | BRCA2 | c.7805+20T>G (n.7805+20T>G) c.7436+20T>G (n.7436+20T>G) c.272+20T>G (n.272+20T>G) c.370+20T>G n.7805+20T>G c.7709+20T>G (n.7709+20T>G) | ClinVar dbSNP |
13 | g.32357949T= | CA2082819365 | BRCA2 | c.7805+20T= (n.7805+20T=) c.7436+20T= (n.7436+20T=) c.272+20T= (n.272+20T=) c.370+20T= n.7805+20T= c.7709+20T= (n.7709+20T=) | |
13 | g.32357950G>C | CA2727914559 | BRCA2 | c.7805+21G>C (n.7805+21G>C) c.7436+21G>C (n.7436+21G>C) c.272+21G>C (n.272+21G>C) c.370+21G>C n.7805+21G>C c.7709+21G>C (n.7709+21G>C) | dbSNP |
13 | g.32357951T>A | CA2727914561 | BRCA2 | c.7805+22T>A (n.7805+22T>A) c.7436+22T>A (n.7436+22T>A) c.272+22T>A (n.272+22T>A) c.370+22T>A n.7805+22T>A c.7709+22T>A (n.7709+22T>A) | dbSNP |
13 | g.32357951T>C | CA2622572256 | BRCA2 | c.7805+22T>C (n.7805+22T>C) c.7436+22T>C (n.7436+22T>C) c.272+22T>C (n.272+22T>C) c.370+22T>C n.7805+22T>C c.7709+22T>C (n.7709+22T>C) | gnomAD v4 |
13 | g.32357951T>G | CA2727914563 | BRCA2 | c.7805+22T>G (n.7805+22T>G) c.7436+22T>G (n.7436+22T>G) c.272+22T>G (n.272+22T>G) c.370+22T>G n.7805+22T>G c.7709+22T>G (n.7709+22T>G) | dbSNP |
13 | g.32357952G>A | CA6941142 | BRCA2 | c.7805+23G>A (n.7805+23G>A) c.7436+23G>A (n.7436+23G>A) c.272+23G>A (n.272+23G>A) c.370+23G>A n.7805+23G>A c.7709+23G>A (n.7709+23G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.32357952G>C | CA2727833971 | BRCA2 | c.7805+23G>C (n.7805+23G>C) c.7436+23G>C (n.7436+23G>C) c.272+23G>C (n.272+23G>C) c.370+23G>C n.7805+23G>C c.7709+23G>C (n.7709+23G>C) | dbSNP |
13 | g.32357952G= | CA2082819370 | BRCA2 | c.7805+23G= (n.7805+23G=) c.7436+23G= (n.7436+23G=) c.272+23G= (n.272+23G=) c.370+23G= n.7805+23G= c.7709+23G= (n.7709+23G=) | |
13 | g.32357954G>A | CA2622572264 | BRCA2 | c.7805+25G>A (n.7805+25G>A) c.7436+25G>A (n.7436+25G>A) c.272+25G>A (n.272+25G>A) c.370+25G>A n.7805+25G>A c.7709+25G>A (n.7709+25G>A) | dbSNP gnomAD v4 |
13 | g.32357954G>C | CA2727841189 | BRCA2 | c.7805+25G>C (n.7805+25G>C) c.7436+25G>C (n.7436+25G>C) c.272+25G>C (n.272+25G>C) c.370+25G>C n.7805+25G>C c.7709+25G>C (n.7709+25G>C) | dbSNP |
13 | g.32357954G= | CA2082819376 | BRCA2 | c.7805+25G= (n.7805+25G=) c.7436+25G= (n.7436+25G=) c.272+25G= (n.272+25G=) c.370+25G= n.7805+25G= c.7709+25G= (n.7709+25G=) | |
13 | g.32357954G>T | CA6941143 | BRCA2 | c.7805+25G>T (n.7805+25G>T) c.7436+25G>T (n.7436+25G>T) c.272+25G>T (n.272+25G>T) c.370+25G>T n.7805+25G>T c.7709+25G>T (n.7709+25G>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.32357955T>A | CA2727914565 | BRCA2 | c.7805+26T>A (n.7805+26T>A) c.7436+26T>A (n.7436+26T>A) c.272+26T>A (n.272+26T>A) c.370+26T>A n.7805+26T>A c.7709+26T>A (n.7709+26T>A) | dbSNP |
13 | g.32357955T>C | CA2622572273 | BRCA2 | c.7805+26T>C (n.7805+26T>C) c.7436+26T>C (n.7436+26T>C) c.272+26T>C (n.272+26T>C) c.370+26T>C n.7805+26T>C c.7709+26T>C (n.7709+26T>C) | gnomAD v4 |
13 | g.32357956T>A | CA2727914567 | BRCA2 | c.7805+27T>A (n.7805+27T>A) c.7436+27T>A (n.7436+27T>A) c.272+27T>A (n.272+27T>A) c.370+27T>A n.7805+27T>A c.7709+27T>A (n.7709+27T>A) | dbSNP |
13 | g.32357956T>C | CA2622572277 | BRCA2 | c.7805+27T>C (n.7805+27T>C) c.7436+27T>C (n.7436+27T>C) c.272+27T>C (n.272+27T>C) c.370+27T>C n.7805+27T>C c.7709+27T>C (n.7709+27T>C) | gnomAD v4 |
13 | g.32357958A= | CA2082819380 | BRCA2 | c.7805+29A= (n.7805+29A=) c.7436+29A= (n.7436+29A=) c.272+29A= (n.272+29A=) c.370+29A= n.7805+29A= c.7709+29A= (n.7709+29A=) | |
13 | g.32357958A>C | CA954697490 | BRCA2 | c.7805+29A>C (n.7805+29A>C) c.7436+29A>C (n.7436+29A>C) c.272+29A>C (n.272+29A>C) c.370+29A>C n.7805+29A>C c.7709+29A>C (n.7709+29A>C) | dbSNP gnomAD v3 gnomAD v4 |
13 | g.32357958A>T | CA2727912941 | BRCA2 | c.7805+29A>T (n.7805+29A>T) c.7436+29A>T (n.7436+29A>T) c.272+29A>T (n.272+29A>T) c.370+29A>T n.7805+29A>T c.7709+29A>T (n.7709+29A>T) | dbSNP |
13 | g.32357959C= | CA2082819386 | BRCA2 | c.7805+30C= (n.7805+30C=) c.7436+30C= (n.7436+30C=) c.272+30C= (n.272+30C=) c.370+30C= n.7805+30C= c.7709+30C= (n.7709+30C=) | |
13 | g.32357959C>T | CA2082819392 | BRCA2 | c.7805+30C>T (n.7805+30C>T) c.7436+30C>T (n.7436+30C>T) c.272+30C>T (n.272+30C>T) c.370+30C>T n.7805+30C>T c.7709+30C>T (n.7709+30C>T) | dbSNP |
13 | g.32357960_32357963del | CA2622572278 | BRCA2 | c.7805+31_7805+34del (n.7805+31_7805+34del) c.7436+31_7436+34del (n.7436+31_7436+34del) c.272+31_272+34del (n.272+31_272+34del) c.370+31_370+34del n.7805+31_7805+34del c.7709+31_7709+34del (n.7709+31_7709+34del) | gnomAD v4 |
13 | g.32357961T>A | CA2082819398 | BRCA2 | c.7805+32T>A (n.7805+32T>A) c.7436+32T>A (n.7436+32T>A) c.272+32T>A (n.272+32T>A) c.370+32T>A n.7805+32T>A c.7709+32T>A (n.7709+32T>A) | dbSNP |
13 | g.32357961T>G | CA2082819399 | BRCA2 | c.7805+32T>G (n.7805+32T>G) c.7436+32T>G (n.7436+32T>G) c.272+32T>G (n.272+32T>G) c.370+32T>G n.7805+32T>G c.7709+32T>G (n.7709+32T>G) | dbSNP |
13 | g.32357961T= | CA2082819397 | BRCA2 | c.7805+32T= (n.7805+32T=) c.7436+32T= (n.7436+32T=) c.272+32T= (n.272+32T=) c.370+32T= n.7805+32T= c.7709+32T= (n.7709+32T=) | |
13 | g.32357962T>C | CA6941144 | BRCA2 | c.7805+33T>C (n.7805+33T>C) c.7436+33T>C (n.7436+33T>C) c.272+33T>C (n.272+33T>C) c.370+33T>C n.7805+33T>C c.7709+33T>C (n.7709+33T>C) | dbSNP ExAC gnomAD v2 |
13 | g.32357962T= | CA2082819401 | BRCA2 | c.7805+33T= (n.7805+33T=) c.7436+33T= (n.7436+33T=) c.272+33T= (n.272+33T=) c.370+33T= n.7805+33T= c.7709+33T= (n.7709+33T=) | |
13 | g.32357963T>G | CA6941145 | BRCA2 | c.7805+34T>G (n.7805+34T>G) c.7436+34T>G (n.7436+34T>G) c.272+34T>G (n.272+34T>G) c.370+34T>G n.7805+34T>G c.7709+34T>G (n.7709+34T>G) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.32357963T= | CA2082819404 | BRCA2 | c.7805+34T= (n.7805+34T=) c.7436+34T= (n.7436+34T=) c.272+34T= (n.272+34T=) c.370+34T= n.7805+34T= c.7709+34T= (n.7709+34T=) | |
13 | g.32357964A= | CA2082819410 | BRCA2 | c.7805+35A= (n.7805+35A=) c.7436+35A= (n.7436+35A=) c.272+35A= (n.272+35A=) c.370+35A= n.7805+35A= c.7709+35A= (n.7709+35A=) | |
13 | g.32357964A>G | CA2622572280 | BRCA2 | c.7805+35A>G (n.7805+35A>G) c.7436+35A>G (n.7436+35A>G) c.272+35A>G (n.272+35A>G) c.370+35A>G n.7805+35A>G c.7709+35A>G (n.7709+35A>G) | gnomAD v4 |
13 | g.32357964A>T | CA2082819412 | BRCA2 | c.7805+35A>T (n.7805+35A>T) c.7436+35A>T (n.7436+35A>T) c.272+35A>T (n.272+35A>T) c.370+35A>T n.7805+35A>T c.7709+35A>T (n.7709+35A>T) | dbSNP |
13 | g.32357965T>G | CA2575388219 | BRCA2 | c.7805+36T>G (n.7805+36T>G) c.7436+36T>G (n.7436+36T>G) c.272+36T>G (n.272+36T>G) c.370+36T>G n.7805+36T>G c.7709+36T>G (n.7709+36T>G) | |
13 | g.32357966G>A | CA483260664 | BRCA2 | c.7805+37G>A (n.7805+37G>A) c.7436+37G>A (n.7436+37G>A) c.272+37G>A (n.272+37G>A) c.370+37G>A n.7805+37G>A c.7709+37G>A (n.7709+37G>A) | gnomAD v4 |
13 | g.32357966G>C | CA2727914570 | BRCA2 | c.7805+37G>C (n.7805+37G>C) c.7436+37G>C (n.7436+37G>C) c.272+37G>C (n.272+37G>C) c.370+37G>C n.7805+37G>C c.7709+37G>C (n.7709+37G>C) | dbSNP |
13 | g.32357966G>T | CA2622572283 | BRCA2 | c.7805+37G>T (n.7805+37G>T) c.7436+37G>T (n.7436+37G>T) c.272+37G>T (n.272+37G>T) c.370+37G>T n.7805+37G>T c.7709+37G>T (n.7709+37G>T) | gnomAD v4 |
13 | g.32357967T>C | CA609091404 | BRCA2 | c.7805+38T>C (n.7805+38T>C) c.7436+38T>C (n.7436+38T>C) c.272+38T>C (n.272+38T>C) c.370+38T>C n.7805+38T>C c.7709+38T>C (n.7709+38T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.32357967T= | CA2082819422 | BRCA2 | c.7805+38T= (n.7805+38T=) c.7436+38T= (n.7436+38T=) c.272+38T= (n.272+38T=) c.370+38T= n.7805+38T= c.7709+38T= (n.7709+38T=) | |
13 | g.32357968A= | CA2082819428 | BRCA2 | c.7805+39A= (n.7805+39A=) c.7436+39A= (n.7436+39A=) c.272+39A= (n.272+39A=) c.370+39A= n.7805+39A= c.7709+39A= (n.7709+39A=) | |
13 | g.32357968A>C | CA2727852922 | BRCA2 | c.7805+39A>C (n.7805+39A>C) c.7436+39A>C (n.7436+39A>C) c.272+39A>C (n.272+39A>C) c.370+39A>C n.7805+39A>C c.7709+39A>C (n.7709+39A>C) | dbSNP |
13 | g.32357968A>G | CA247471362 | BRCA2 | c.7805+39A>G (n.7805+39A>G) c.7436+39A>G (n.7436+39A>G) c.272+39A>G (n.272+39A>G) c.370+39A>G n.7805+39A>G c.7709+39A>G (n.7709+39A>G) | dbSNP gnomAD v2 gnomAD v4 |
13 | g.32357968A>T | CA2727852923 | BRCA2 | c.7805+39A>T (n.7805+39A>T) c.7436+39A>T (n.7436+39A>T) c.272+39A>T (n.272+39A>T) c.370+39A>T n.7805+39A>T c.7709+39A>T (n.7709+39A>T) | dbSNP |
13 | g.32357968_32357969insATG | CA2082819435 | BRCA2 | c.7805+39_7805+40insATG (n.7805+39_7805+40insATG) c.7436+39_7436+40insATG (n.7436+39_7436+40insATG) c.272+39_272+40insATG (n.272+39_272+40insATG) c.370+39_370+40insATG n.7805+39_7805+40insATG c.7709+39_7709+40insATG (n.7709+39_7709+40insATG) | dbSNP |
13 | g.32357968_32357969insATGT | CA6941146 | BRCA2 | c.7805+39_7805+40insATGT (n.7805+39_7805+40insATGT) c.7436+39_7436+40insATGT (n.7436+39_7436+40insATGT) c.272+39_272+40insATGT (n.272+39_272+40insATGT) c.370+39_370+40insATGT n.7805+39_7805+40insATGT c.7709+39_7709+40insATGT (n.7709+39_7709+40insATGT) | dbSNP ExAC |
13 | g.32357969T>C | CA654758724 | BRCA2 | c.7805+40T>C (n.7805+40T>C) c.7436+40T>C (n.7436+40T>C) c.272+40T>C (n.272+40T>C) c.370+40T>C n.7805+40T>C c.7709+40T>C (n.7709+40T>C) | COSMIC |
13 | g.32357970T>A | CA2798719423 | BRCA2 | c.7805+41T>A (n.7805+41T>A) c.7436+41T>A (n.7436+41T>A) c.272+41T>A (n.272+41T>A) c.370+41T>A n.7805+41T>A c.7709+41T>A (n.7709+41T>A) | |
13 | g.32357970T= | CA2082819440 | BRCA2 | c.7805+41T= (n.7805+41T=) c.7436+41T= (n.7436+41T=) c.272+41T= (n.272+41T=) c.370+41T= n.7805+41T= c.7709+41T= (n.7709+41T=) | |
13 | g.32357970_32357971insTAGAAA | CA2082819442 | BRCA2 | c.7805+41_7805+42insTAGAAA (n.7805+41_7805+42insTAGAAA) c.7436+41_7436+42insTAGAAA (n.7436+41_7436+42insTAGAAA) c.272+41_272+42insTAGAAA (n.272+41_272+42insTAGAAA) c.370+41_370+42insTAGAAA n.7805+41_7805+42insTAGAAA c.7709+41_7709+42insTAGAAA (n.7709+41_7709+42insTAGAAA) | dbSNP |
13 | g.32357971C>A | CA2622572287 | BRCA2 | c.7805+42C>A (n.7805+42C>A) c.7436+42C>A (n.7436+42C>A) c.272+42C>A (n.272+42C>A) c.370+42C>A n.7805+42C>A c.7709+42C>A (n.7709+42C>A) | dbSNP gnomAD v4 |
13 | g.32357971C>G | CA2727914573 | BRCA2 | c.7805+42C>G (n.7805+42C>G) c.7436+42C>G (n.7436+42C>G) c.272+42C>G (n.272+42C>G) c.370+42C>G n.7805+42C>G c.7709+42C>G (n.7709+42C>G) | dbSNP |
13 | g.32357971C>T | CA2727914572 | BRCA2 | c.7805+42C>T (n.7805+42C>T) c.7436+42C>T (n.7436+42C>T) c.272+42C>T (n.272+42C>T) c.370+42C>T n.7805+42C>T c.7709+42C>T (n.7709+42C>T) | dbSNP |
13 | g.32357972C= | CA2082819446 | BRCA2 | c.7805+43C= (n.7805+43C=) c.7436+43C= (n.7436+43C=) c.272+43C= (n.272+43C=) c.370+43C= n.7805+43C= c.7709+43C= (n.7709+43C=) | |
13 | g.32357972C>G | CA609091405 | BRCA2 | c.7805+43C>G (n.7805+43C>G) c.7436+43C>G (n.7436+43C>G) c.272+43C>G (n.272+43C>G) c.370+43C>G n.7805+43C>G c.7709+43C>G (n.7709+43C>G) | dbSNP gnomAD v2 gnomAD v4 |
13 | g.32357972C>T | CA2575388220 | BRCA2 | c.7805+43C>T (n.7805+43C>T) c.7436+43C>T (n.7436+43C>T) c.272+43C>T (n.272+43C>T) c.370+43C>T n.7805+43C>T c.7709+43C>T (n.7709+43C>T) | |
13 | g.32357972_32357973insTTTTCCAGTCCATAAA | CA609091406 | BRCA2 | c.7805+43_7805+44insTTTTCCAGTCCATAAA (n.7805+43_7805+44insTTTTCCAGTCCATAAA) c.7436+43_7436+44insTTTTCCAGTCCATAAA (n.7436+43_7436+44insTTTTCCAGTCCATAAA) c.272+43_272+44insTTTTCCAGTCCATAAA (n.272+43_272+44insTTTTCCAGTCCATAAA) c.370+43_370+44insTTTTCCAGTCCATAAA n.7805+43_7805+44insTTTTCCAGTCCATAAA c.7709+43_7709+44insTTTTCCAGTCCATAAA (n.7709+43_7709+44insTTTTCCAGTCCATAAA) | gnomAD v2 |
13 | g.32357973C= | CA2082819454 | BRCA2 | c.7805+44C= (n.7805+44C=) c.7436+44C= (n.7436+44C=) c.272+44C= (n.272+44C=) c.370+44C= n.7805+44C= c.7709+44C= (n.7709+44C=) | |
13 | g.32357973C>G | CA697352027 | BRCA2 | c.7805+44C>G (n.7805+44C>G) c.7436+44C>G (n.7436+44C>G) c.272+44C>G (n.272+44C>G) c.370+44C>G n.7805+44C>G c.7709+44C>G (n.7709+44C>G) | dbSNP gnomAD v4 |
13 | g.32357973C>T | CA6941147 | BRCA2 | c.7805+44C>T (n.7805+44C>T) c.7436+44C>T (n.7436+44C>T) c.272+44C>T (n.272+44C>T) c.370+44C>T n.7805+44C>T c.7709+44C>T (n.7709+44C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.32357974_32357975insAAAATTCCATCTTCATTTGGAATGCAACACCCCATTCTG | CA2798719429 | BRCA2 | c.7805+45_7805+46insAAAATTCCATCTTCATTTGGAATGCAACACCCCATTCTG (n.7805+45_7805+46insAAAATTCCATCTTCATTTGGAATGCAACACCCCATTCTG) c.7436+45_7436+46insAAAATTCCATCTTCATTTGGAATGCAACACCCCATTCTG (n.7436+45_7436+46insAAAATTCCATCTTCATTTGGAATGCAACACCCCATTCTG) c.272+45_272+46insAAAATTCCATCTTCATTTGGAATGCAACACCCCATTCTG (n.272+45_272+46insAAAATTCCATCTTCATTTGGAATGCAACACCCCATTCTG) c.370+45_370+46insAAAATTCCATCTTCATTTGGAATGCAACACCCCATTCTG n.7805+45_7805+46insAAAATTCCATCTTCATTTGGAATGCAACACCCCATTCTG c.7709+45_7709+46insAAAATTCCATCTTCATTTGGAATGCAACACCCCATTCTG (n.7709+45_7709+46insAAAATTCCATCTTCATTTGGAATGCAACACCCCATTCTG) | |
13 | g.32357975C>A | CA2622572296 | BRCA2 | c.7805+46C>A (n.7805+46C>A) c.7436+46C>A (n.7436+46C>A) c.272+46C>A (n.272+46C>A) c.370+46C>A n.7805+46C>A c.7709+46C>A (n.7709+46C>A) | dbSNP gnomAD v4 |
13 | g.32357975C>G | CA2727914574 | BRCA2 | c.7805+46C>G (n.7805+46C>G) c.7436+46C>G (n.7436+46C>G) c.272+46C>G (n.272+46C>G) c.370+46C>G n.7805+46C>G c.7709+46C>G (n.7709+46C>G) | dbSNP |
13 | g.32357976A= | CA2082819461 | BRCA2 | c.7805+47A= (n.7805+47A=) c.7436+47A= (n.7436+47A=) c.272+47A= (n.272+47A=) c.370+47A= n.7805+47A= c.7709+47A= (n.7709+47A=) | |
13 | g.32357976A>C | CA2727836938 | BRCA2 | c.7805+47A>C (n.7805+47A>C) c.7436+47A>C (n.7436+47A>C) c.272+47A>C (n.272+47A>C) c.370+47A>C n.7805+47A>C c.7709+47A>C (n.7709+47A>C) | dbSNP |
13 | g.32357976A>G | CA6941148 | BRCA2 | c.7805+47A>G (n.7805+47A>G) c.7436+47A>G (n.7436+47A>G) c.272+47A>G (n.272+47A>G) c.370+47A>G n.7805+47A>G c.7709+47A>G (n.7709+47A>G) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.32357976A>T | CA2727836937 | BRCA2 | c.7805+47A>T (n.7805+47A>T) c.7436+47A>T (n.7436+47A>T) c.272+47A>T (n.272+47A>T) c.370+47A>T n.7805+47A>T c.7709+47A>T (n.7709+47A>T) | dbSNP |
13 | g.32357978C>A | CA2622572301 | BRCA2 | c.7805+49C>A (n.7805+49C>A) c.7436+49C>A (n.7436+49C>A) c.272+49C>A (n.272+49C>A) c.370+49C>A n.7805+49C>A c.7709+49C>A (n.7709+49C>A) | dbSNP gnomAD v4 |
13 | g.32357978C= | CA2082819462 | BRCA2 | c.7805+49C= (n.7805+49C=) c.7436+49C= (n.7436+49C=) c.272+49C= (n.272+49C=) c.370+49C= n.7805+49C= c.7709+49C= (n.7709+49C=) | |
13 | g.32357978C>G | CA2727912942 | BRCA2 | c.7805+49C>G (n.7805+49C>G) c.7436+49C>G (n.7436+49C>G) c.272+49C>G (n.272+49C>G) c.370+49C>G n.7805+49C>G c.7709+49C>G (n.7709+49C>G) | dbSNP |
13 | g.32357978C>T | CA2082819465 | BRCA2 | c.7805+49C>T (n.7805+49C>T) c.7436+49C>T (n.7436+49C>T) c.272+49C>T (n.272+49C>T) c.370+49C>T n.7805+49C>T c.7709+49C>T (n.7709+49C>T) | dbSNP |
13 | g.32357979_32357981delinsCCT | CA2082819469 | BRCA2 | c.7805+50_7805+52delinsCCT (n.7805+50_7805+52delinsCCT) c.7436+50_7436+52delinsCCT (n.7436+50_7436+52delinsCCT) c.272+50_272+52delinsCCT (n.272+50_272+52delinsCCT) c.370+50_370+52delinsCCT n.7805+50_7805+52delinsCCT c.7709+50_7709+52delinsCCT (n.7709+50_7709+52delinsCCT) | |
13 | g.32357980C>A | CA2727914575 | BRCA2 | c.7805+51C>A (n.7805+51C>A) c.7436+51C>A (n.7436+51C>A) c.272+51C>A (n.272+51C>A) c.370+51C>A n.7805+51C>A c.7709+51C>A (n.7709+51C>A) | dbSNP |
13 | g.32357980C>T | CA2622572304 | BRCA2 | c.7805+51C>T (n.7805+51C>T) c.7436+51C>T (n.7436+51C>T) c.272+51C>T (n.272+51C>T) c.370+51C>T n.7805+51C>T c.7709+51C>T (n.7709+51C>T) | dbSNP gnomAD v4 |
13 | g.32357982_32357983del | CA6941149 | BRCA2 | c.7805+53_7805+54del (n.7805+53_7805+54del) c.7436+53_7436+54del (n.7436+53_7436+54del) c.272+53_272+54del (n.272+53_272+54del) c.370+53_370+54del n.7805+53_7805+54del c.7709+53_7709+54del (n.7709+53_7709+54del) | dbSNP ExAC gnomAD v2 |
13 | g.32357981T>C | CA2575388221 | BRCA2 | c.7805+52T>C (n.7805+52T>C) c.7436+52T>C (n.7436+52T>C) c.272+52T>C (n.272+52T>C) c.370+52T>C n.7805+52T>C c.7709+52T>C (n.7709+52T>C) | gnomAD v4 |
13 | g.32357982C>A | CA2727914576 | BRCA2 | c.7805+53C>A (n.7805+53C>A) c.7436+53C>A (n.7436+53C>A) c.272+53C>A (n.272+53C>A) c.370+53C>A n.7805+53C>A c.7709+53C>A (n.7709+53C>A) | dbSNP |
13 | g.32357982C>G | CA2727914577 | BRCA2 | c.7805+53C>G (n.7805+53C>G) c.7436+53C>G (n.7436+53C>G) c.272+53C>G (n.272+53C>G) c.370+53C>G n.7805+53C>G c.7709+53C>G (n.7709+53C>G) | dbSNP |
13 | g.32357982C>T | CA2622572310 | BRCA2 | c.7805+53C>T (n.7805+53C>T) c.7436+53C>T (n.7436+53C>T) c.272+53C>T (n.272+53C>T) c.370+53C>T n.7805+53C>T c.7709+53C>T (n.7709+53C>T) | dbSNP gnomAD v4 |
13 | g.32357983T>A | CA2727914578 | BRCA2 | c.7805+54T>A (n.7805+54T>A) c.7436+54T>A (n.7436+54T>A) c.272+54T>A (n.272+54T>A) c.370+54T>A n.7805+54T>A c.7709+54T>A (n.7709+54T>A) | dbSNP |
13 | g.32357983T>C | CA2622572314 | BRCA2 | c.7805+54T>C (n.7805+54T>C) c.7436+54T>C (n.7436+54T>C) c.272+54T>C (n.272+54T>C) c.370+54T>C n.7805+54T>C c.7709+54T>C (n.7709+54T>C) | gnomAD v4 |
13 | g.32357984_32357989delinsTTCTTC | CA2082819476 | BRCA2 | c.7805+55_7805+60delinsTTCTTC (n.7805+55_7805+60delinsTTCTTC) c.7436+55_7436+60delinsTTCTTC (n.7436+55_7436+60delinsTTCTTC) c.272+55_272+60delinsTTCTTC (n.272+55_272+60delinsTTCTTC) c.370+55_370+60delinsTTCTTC n.7805+55_7805+60delinsTTCTTC c.7709+55_7709+60delinsTTCTTC (n.7709+55_7709+60delinsTTCTTC) | |
13 | g.32357989_32357993del | CA2082819480 | BRCA2 | c.7805+60_7805+64del (n.7805+60_7805+64del) c.7436+60_7436+64del (n.7436+60_7436+64del) c.272+60_272+64del (n.272+60_272+64del) c.370+60_370+64del n.7805+60_7805+64del c.7709+60_7709+64del (n.7709+60_7709+64del) | dbSNP gnomAD v4 |
13 | g.32357986C>A | CA247471383 | BRCA2 | c.7805+57C>A (n.7805+57C>A) c.7436+57C>A (n.7436+57C>A) c.272+57C>A (n.272+57C>A) c.370+57C>A n.7805+57C>A c.7709+57C>A (n.7709+57C>A) | dbSNP gnomAD v4 |
13 | g.32357986C= | CA2082819484 | BRCA2 | c.7805+57C= (n.7805+57C=) c.7436+57C= (n.7436+57C=) c.272+57C= (n.272+57C=) c.370+57C= n.7805+57C= c.7709+57C= (n.7709+57C=) | |
13 | g.32357986C>G | CA2727843402 | BRCA2 | c.7805+57C>G (n.7805+57C>G) c.7436+57C>G (n.7436+57C>G) c.272+57C>G (n.272+57C>G) c.370+57C>G n.7805+57C>G c.7709+57C>G (n.7709+57C>G) | dbSNP |
13 | g.32357986C>T | CA2082819494 | BRCA2 | c.7805+57C>T (n.7805+57C>T) c.7436+57C>T (n.7436+57C>T) c.272+57C>T (n.272+57C>T) c.370+57C>T n.7805+57C>T c.7709+57C>T (n.7709+57C>T) | dbSNP |
13 | g.32357987T>C | CA2622572317 | BRCA2 | c.7805+58T>C (n.7805+58T>C) c.7436+58T>C (n.7436+58T>C) c.272+58T>C (n.272+58T>C) c.370+58T>C n.7805+58T>C c.7709+58T>C (n.7709+58T>C) | gnomAD v4 |
13 | g.32357988T>C | CA2727914579 | BRCA2 | c.7805+59T>C (n.7805+59T>C) c.7436+59T>C (n.7436+59T>C) c.272+59T>C (n.272+59T>C) c.370+59T>C n.7805+59T>C c.7709+59T>C (n.7709+59T>C) | dbSNP |
13 | g.32357989C>A | CA2622572320 | BRCA2 | c.7805+60C>A (n.7805+60C>A) c.7436+60C>A (n.7436+60C>A) c.272+60C>A (n.272+60C>A) c.370+60C>A n.7805+60C>A c.7709+60C>A (n.7709+60C>A) | dbSNP gnomAD v4 |
13 | g.32357989C>G | CA2622572321 | BRCA2 | c.7805+60C>G (n.7805+60C>G) c.7436+60C>G (n.7436+60C>G) c.272+60C>G (n.272+60C>G) c.370+60C>G n.7805+60C>G c.7709+60C>G (n.7709+60C>G) | dbSNP gnomAD v4 |
13 | g.32357989C>T | CA2727914581 | BRCA2 | c.7805+60C>T (n.7805+60C>T) c.7436+60C>T (n.7436+60C>T) c.272+60C>T (n.272+60C>T) c.370+60C>T n.7805+60C>T c.7709+60C>T (n.7709+60C>T) | dbSNP |
13 | g.32357989_32357991del | CA2622572319 | BRCA2 | c.7805+60_7805+62del (n.7805+60_7805+62del) c.7436+60_7436+62del (n.7436+60_7436+62del) c.272+60_272+62del (n.272+60_272+62del) c.370+60_370+62del n.7805+60_7805+62del c.7709+60_7709+62del (n.7709+60_7709+62del) | gnomAD v4 |
13 | g.32357990T>A | CA2727862874 | BRCA2 | c.7805+61T>A (n.7805+61T>A) c.7436+61T>A (n.7436+61T>A) c.272+61T>A (n.272+61T>A) c.370+61T>A n.7805+61T>A c.7709+61T>A (n.7709+61T>A) | dbSNP |
13 | g.32357990T>C | CA697352042 | BRCA2 | c.7805+61T>C (n.7805+61T>C) c.7436+61T>C (n.7436+61T>C) c.272+61T>C (n.272+61T>C) c.370+61T>C n.7805+61T>C c.7709+61T>C (n.7709+61T>C) | dbSNP gnomAD v3 gnomAD v4 |
13 | g.32357990T= | CA2082819501 | BRCA2 | c.7805+61T= (n.7805+61T=) c.7436+61T= (n.7436+61T=) c.272+61T= (n.272+61T=) c.370+61T= n.7805+61T= c.7709+61T= (n.7709+61T=) |