| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32359467_32364093del | CA2580087377 | BRCA2 | c.7805+1538_8331+560del c.7436+1538_7962+560del c.272+1538_798+560del c.7805+1538_8339+560del c.370+1538_896+560del c.7709+1538_8235+560del | ClinVar |
| 13 | g.32362795_32362807del | CA609091826 | BRCA2 | c.7976+102_7976+114del (n.7976+102_7976+114del) c.7607+102_7607+114del (n.7607+102_7607+114del) c.443+102_443+114del (n.443+102_443+114del) c.7984+102_7984+114del (n.7984+102_7984+114del) c.541+102_541+114del c.7880+102_7880+114del (n.7880+102_7880+114del) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32362806T>C | CA2082832765 | BRCA2 | c.7976+113T>C (n.7976+113T>C) c.7607+113T>C (n.7607+113T>C) c.443+113T>C (n.443+113T>C) c.7984+113T>C (n.7984+113T>C) c.541+113T>C c.7880+113T>C (n.7880+113T>C) | dbSNP |
| 13 | g.32362806T= | CA2082832761 | BRCA2 | c.7976+113T= (n.7976+113T=) c.7607+113T= (n.7607+113T=) c.443+113T= (n.443+113T=) c.7984+113T= (n.7984+113T=) c.541+113T= c.7880+113T= (n.7880+113T=) | |
| 13 | g.32362807G>A | CA2622572949 | BRCA2 | c.7976+114G>A (n.7976+114G>A) c.7607+114G>A (n.7607+114G>A) c.443+114G>A (n.443+114G>A) c.7984+114G>A (n.7984+114G>A) c.541+114G>A c.7880+114G>A (n.7880+114G>A) | gnomAD v4 |
| 13 | g.32362807G>T | CA2622572950 | BRCA2 | c.7976+114G>T (n.7976+114G>T) c.7607+114G>T (n.7607+114G>T) c.443+114G>T (n.443+114G>T) c.7984+114G>T (n.7984+114G>T) c.541+114G>T c.7880+114G>T (n.7880+114G>T) | gnomAD v4 |
| 13 | g.32362808C>A | CA2622572951 | BRCA2 | c.7976+115C>A (n.7976+115C>A) c.7607+115C>A (n.7607+115C>A) c.443+115C>A (n.443+115C>A) c.7984+115C>A (n.7984+115C>A) c.541+115C>A c.7880+115C>A (n.7880+115C>A) | gnomAD v4 |
| 13 | g.32362808C= | CA2082832771 | BRCA2 | c.7976+115C= (n.7976+115C=) c.7607+115C= (n.7607+115C=) c.443+115C= (n.443+115C=) c.7984+115C= (n.7984+115C=) c.541+115C= c.7880+115C= (n.7880+115C=) | |
| 13 | g.32362808C>T | CA2082832773 | BRCA2 | c.7976+115C>T (n.7976+115C>T) c.7607+115C>T (n.7607+115C>T) c.443+115C>T (n.443+115C>T) c.7984+115C>T (n.7984+115C>T) c.541+115C>T c.7880+115C>T (n.7880+115C>T) | dbSNP gnomAD v4 |
| 13 | g.32362809C>A | CA2622572952 | BRCA2 | c.7976+116C>A (n.7976+116C>A) c.7607+116C>A (n.7607+116C>A) c.443+116C>A (n.443+116C>A) c.7984+116C>A (n.7984+116C>A) c.541+116C>A c.7880+116C>A (n.7880+116C>A) | gnomAD v4 |
| 13 | g.32362809C>G | CA2622572953 | BRCA2 | c.7976+116C>G (n.7976+116C>G) c.7607+116C>G (n.7607+116C>G) c.443+116C>G (n.443+116C>G) c.7984+116C>G (n.7984+116C>G) c.541+116C>G c.7880+116C>G (n.7880+116C>G) | gnomAD v4 |
| 13 | g.32362809C>T | CA2622572954 | BRCA2 | c.7976+116C>T (n.7976+116C>T) c.7607+116C>T (n.7607+116C>T) c.443+116C>T (n.443+116C>T) c.7984+116C>T (n.7984+116C>T) c.541+116C>T c.7880+116C>T (n.7880+116C>T) | gnomAD v4 |
| 13 | g.32362811T>A | CA247475438 | BRCA2 | c.7976+118T>A (n.7976+118T>A) c.7607+118T>A (n.7607+118T>A) c.443+118T>A (n.443+118T>A) c.7984+118T>A (n.7984+118T>A) c.541+118T>A c.7880+118T>A (n.7880+118T>A) | dbSNP |
| 13 | g.32362811T= | CA2082832777 | BRCA2 | c.7976+118T= (n.7976+118T=) c.7607+118T= (n.7607+118T=) c.443+118T= (n.443+118T=) c.7984+118T= (n.7984+118T=) c.541+118T= c.7880+118T= (n.7880+118T=) | |
| 13 | g.32362812C>A | CA2622572956 | BRCA2 | c.7976+119C>A (n.7976+119C>A) c.7607+119C>A (n.7607+119C>A) c.443+119C>A (n.443+119C>A) c.7984+119C>A (n.7984+119C>A) c.541+119C>A c.7880+119C>A (n.7880+119C>A) | gnomAD v4 |
| 13 | g.32362814del | CA2622572955 | BRCA2 | c.7976+121del (n.7976+121del) c.7607+121del (n.7607+121del) c.443+121del (n.443+121del) c.7984+121del (n.7984+121del) c.541+121del c.7880+121del (n.7880+121del) | gnomAD v4 |
| 13 | g.32362813C>A | CA2622572957 | BRCA2 | c.7976+120C>A (n.7976+120C>A) c.7607+120C>A (n.7607+120C>A) c.443+120C>A (n.443+120C>A) c.7984+120C>A (n.7984+120C>A) c.541+120C>A c.7880+120C>A (n.7880+120C>A) | gnomAD v4 |
| 13 | g.32362813C>T | CA2622572958 | BRCA2 | c.7976+120C>T (n.7976+120C>T) c.7607+120C>T (n.7607+120C>T) c.443+120C>T (n.443+120C>T) c.7984+120C>T (n.7984+120C>T) c.541+120C>T c.7880+120C>T (n.7880+120C>T) | gnomAD v4 |
| 13 | g.32362814C>A | CA2622572959 | BRCA2 | c.7976+121C>A (n.7976+121C>A) c.7607+121C>A (n.7607+121C>A) c.443+121C>A (n.443+121C>A) c.7984+121C>A (n.7984+121C>A) c.541+121C>A c.7880+121C>A (n.7880+121C>A) | gnomAD v4 |
| 13 | g.32362815A>T | CA2535445232 | BRCA2 | c.7976+122A>T (n.7976+122A>T) c.7607+122A>T (n.7607+122A>T) c.443+122A>T (n.443+122A>T) c.7984+122A>T (n.7984+122A>T) c.541+122A>T c.7880+122A>T (n.7880+122A>T) | |
| 13 | g.32362816C>A | CA2622572960 | BRCA2 | c.7976+123C>A (n.7976+123C>A) c.7607+123C>A (n.7607+123C>A) c.443+123C>A (n.443+123C>A) c.7984+123C>A (n.7984+123C>A) c.541+123C>A c.7880+123C>A (n.7880+123C>A) | gnomAD v4 |
| 13 | g.32362816C= | CA2082832785 | BRCA2 | c.7976+123C= (n.7976+123C=) c.7607+123C= (n.7607+123C=) c.443+123C= (n.443+123C=) c.7984+123C= (n.7984+123C=) c.541+123C= c.7880+123C= (n.7880+123C=) | |
| 13 | g.32362816C>T | CA954700400 | BRCA2 | c.7976+123C>T (n.7976+123C>T) c.7607+123C>T (n.7607+123C>T) c.443+123C>T (n.443+123C>T) c.7984+123C>T (n.7984+123C>T) c.541+123C>T c.7880+123C>T (n.7880+123C>T) | dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32362817A= | CA2082832806 | BRCA2 | c.7976+124A= (n.7976+124A=) c.7607+124A= (n.7607+124A=) c.443+124A= (n.443+124A=) c.7984+124A= (n.7984+124A=) c.541+124A= c.7880+124A= (n.7880+124A=) | |
| 13 | g.32362817A>G | CA697355413 | BRCA2 | c.7976+124A>G (n.7976+124A>G) c.7607+124A>G (n.7607+124A>G) c.443+124A>G (n.443+124A>G) c.7984+124A>G (n.7984+124A>G) c.541+124A>G c.7880+124A>G (n.7880+124A>G) | dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32362817_32362820delinsACTG | CA2082832793 | BRCA2 | c.7976+124_7976+127delinsACTG (n.7976+124_7976+127delinsACTG) c.7607+124_7607+127delinsACTG (n.7607+124_7607+127delinsACTG) c.443+124_443+127delinsACTG (n.443+124_443+127delinsACTG) c.7984+124_7984+127delinsACTG (n.7984+124_7984+127delinsACTG) c.541+124_541+127delinsACTG c.7880+124_7880+127delinsACTG (n.7880+124_7880+127delinsACTG) | |
| 13 | g.32362818C>A | CA2622572962 | BRCA2 | c.7976+125C>A (n.7976+125C>A) c.7607+125C>A (n.7607+125C>A) c.443+125C>A (n.443+125C>A) c.7984+125C>A (n.7984+125C>A) c.541+125C>A c.7880+125C>A (n.7880+125C>A) | gnomAD v4 |
| 13 | g.32362818C>T | CA2622572961 | BRCA2 | c.7976+125C>T (n.7976+125C>T) c.7607+125C>T (n.7607+125C>T) c.443+125C>T (n.443+125C>T) c.7984+125C>T (n.7984+125C>T) c.541+125C>T c.7880+125C>T (n.7880+125C>T) | gnomAD v4 |
| 13 | g.32362821_32362823del | CA2082832813 | BRCA2 | c.7976+128_7976+130del (n.7976+128_7976+130del) c.7607+128_7607+130del (n.7607+128_7607+130del) c.443+128_443+130del (n.443+128_443+130del) c.7984+128_7984+130del (n.7984+128_7984+130del) c.541+128_541+130del c.7880+128_7880+130del (n.7880+128_7880+130del) | dbSNP |
| 13 | g.32362819T>G | CA609091829 | BRCA2 | c.7976+126T>G (n.7976+126T>G) c.7607+126T>G (n.7607+126T>G) c.443+126T>G (n.443+126T>G) c.7984+126T>G (n.7984+126T>G) c.541+126T>G c.7880+126T>G (n.7880+126T>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32362819T= | CA2082832816 | BRCA2 | c.7976+126T= (n.7976+126T=) c.7607+126T= (n.7607+126T=) c.443+126T= (n.443+126T=) c.7984+126T= (n.7984+126T=) c.541+126T= c.7880+126T= (n.7880+126T=) | |
| 13 | g.32362820G>A | CA247475442 | BRCA2 | c.7976+127G>A (n.7976+127G>A) c.7607+127G>A (n.7607+127G>A) c.443+127G>A (n.443+127G>A) c.7984+127G>A (n.7984+127G>A) c.541+127G>A c.7880+127G>A (n.7880+127G>A) | dbSNP gnomAD v4 |
| 13 | g.32362820G= | CA2082832821 | BRCA2 | c.7976+127G= (n.7976+127G=) c.7607+127G= (n.7607+127G=) c.443+127G= (n.443+127G=) c.7984+127G= (n.7984+127G=) c.541+127G= c.7880+127G= (n.7880+127G=) | |
| 13 | g.32362820G>T | CA2622572966 | BRCA2 | c.7976+127G>T (n.7976+127G>T) c.7607+127G>T (n.7607+127G>T) c.443+127G>T (n.443+127G>T) c.7984+127G>T (n.7984+127G>T) c.541+127G>T c.7880+127G>T (n.7880+127G>T) | gnomAD v4 |
| 13 | g.32362820_32362821insTC | CA2502264740 | BRCA2 | c.7976+127_7976+128insTC (n.7976+127_7976+128insTC) c.7607+127_7607+128insTC (n.7607+127_7607+128insTC) c.443+127_443+128insTC (n.443+127_443+128insTC) c.7984+127_7984+128insTC (n.7984+127_7984+128insTC) c.541+127_541+128insTC c.7880+127_7880+128insTC (n.7880+127_7880+128insTC) | |
| 13 | g.32362821C>A | CA2622572967 | BRCA2 | c.7976+128C>A (n.7976+128C>A) c.7607+128C>A (n.7607+128C>A) c.443+128C>A (n.443+128C>A) c.7984+128C>A (n.7984+128C>A) c.541+128C>A c.7880+128C>A (n.7880+128C>A) | gnomAD v4 |
| 13 | g.32362821C>T | CA2622572968 | BRCA2 | c.7976+128C>T (n.7976+128C>T) c.7607+128C>T (n.7607+128C>T) c.443+128C>T (n.443+128C>T) c.7984+128C>T (n.7984+128C>T) c.541+128C>T c.7880+128C>T (n.7880+128C>T) | gnomAD v4 |
| 13 | g.32362822_32362823insCACATCCCTGACTGGTACACAGTA | CA2555270366 | BRCA2 | c.7976+129_7976+130insCACATCCCTGACTGGTACACAGTA (n.7976+129_7976+130insCACATCCCTGACTGGTACACAGTA) c.7607+129_7607+130insCACATCCCTGACTGGTACACAGTA (n.7607+129_7607+130insCACATCCCTGACTGGTACACAGTA) c.443+129_443+130insCACATCCCTGACTGGTACACAGTA (n.443+129_443+130insCACATCCCTGACTGGTACACAGTA) c.7984+129_7984+130insCACATCCCTGACTGGTACACAGTA (n.7984+129_7984+130insCACATCCCTGACTGGTACACAGTA) c.541+129_541+130insCACATCCCTGACTGGTACACAGTA c.7880+129_7880+130insCACATCCCTGACTGGTACACAGTA (n.7880+129_7880+130insCACATCCCTGACTGGTACACAGTA) | |
| 13 | g.32362823G>A | CA2622572971 | BRCA2 | c.7976+130G>A (n.7976+130G>A) c.7607+130G>A (n.7607+130G>A) c.443+130G>A (n.443+130G>A) c.7984+130G>A (n.7984+130G>A) c.541+130G>A c.7880+130G>A (n.7880+130G>A) | gnomAD v4 |
| 13 | g.32362823G= | CA2082832826 | BRCA2 | c.7976+130G= (n.7976+130G=) c.7607+130G= (n.7607+130G=) c.443+130G= (n.443+130G=) c.7984+130G= (n.7984+130G=) c.541+130G= c.7880+130G= (n.7880+130G=) | |
| 13 | g.32362823G>T | CA954700402 | BRCA2 | c.7976+130G>T (n.7976+130G>T) c.7607+130G>T (n.7607+130G>T) c.443+130G>T (n.443+130G>T) c.7984+130G>T (n.7984+130G>T) c.541+130G>T c.7880+130G>T (n.7880+130G>T) | dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32362824T>A | CA2082832833 | BRCA2 | c.7976+131T>A (n.7976+131T>A) c.7607+131T>A (n.7607+131T>A) c.443+131T>A (n.443+131T>A) c.7984+131T>A (n.7984+131T>A) c.541+131T>A c.7880+131T>A (n.7880+131T>A) | dbSNP gnomAD v4 |
| 13 | g.32362824T= | CA2082832830 | BRCA2 | c.7976+131T= (n.7976+131T=) c.7607+131T= (n.7607+131T=) c.443+131T= (n.443+131T=) c.7984+131T= (n.7984+131T=) c.541+131T= c.7880+131T= (n.7880+131T=) | |
| 13 | g.32362825_32362828delinsTCTC | CA2082832852 | BRCA2 | c.7976+132_7976+135delinsTCTC (n.7976+132_7976+135delinsTCTC) c.7607+132_7607+135delinsTCTC (n.7607+132_7607+135delinsTCTC) c.443+132_443+135delinsTCTC (n.443+132_443+135delinsTCTC) c.7984+132_7984+135delinsTCTC (n.7984+132_7984+135delinsTCTC) c.541+132_541+135delinsTCTC c.7880+132_7880+135delinsTCTC (n.7880+132_7880+135delinsTCTC) | |
| 13 | g.32362826C>A | CA2622572975 | BRCA2 | c.7976+133C>A (n.7976+133C>A) c.7607+133C>A (n.7607+133C>A) c.443+133C>A (n.443+133C>A) c.7984+133C>A (n.7984+133C>A) c.541+133C>A c.7880+133C>A (n.7880+133C>A) | gnomAD v4 |
| 13 | g.32362826C= | CA2082832858 | BRCA2 | c.7976+133C= (n.7976+133C=) c.7607+133C= (n.7607+133C=) c.443+133C= (n.443+133C=) c.7984+133C= (n.7984+133C=) c.541+133C= c.7880+133C= (n.7880+133C=) | |
| 13 | g.32362826C>G | CA2082832855 | BRCA2 | c.7976+133C>G (n.7976+133C>G) c.7607+133C>G (n.7607+133C>G) c.443+133C>G (n.443+133C>G) c.7984+133C>G (n.7984+133C>G) c.541+133C>G c.7880+133C>G (n.7880+133C>G) | dbSNP |
| 13 | g.32362828_32362830del | CA697355414 | BRCA2 | c.7976+135_7976+137del (n.7976+135_7976+137del) c.7607+135_7607+137del (n.7607+135_7607+137del) c.443+135_443+137del (n.443+135_443+137del) c.7984+135_7984+137del (n.7984+135_7984+137del) c.541+135_541+137del c.7880+135_7880+137del (n.7880+135_7880+137del) | dbSNP gnomAD v4 |
| 13 | g.32362827T>A | CA2622572976 | BRCA2 | c.7976+134T>A (n.7976+134T>A) c.7607+134T>A (n.7607+134T>A) c.443+134T>A (n.443+134T>A) c.7984+134T>A (n.7984+134T>A) c.541+134T>A c.7880+134T>A (n.7880+134T>A) | gnomAD v4 |
| 13 | g.32362827T>C | CA2622572977 | BRCA2 | c.7976+134T>C (n.7976+134T>C) c.7607+134T>C (n.7607+134T>C) c.443+134T>C (n.443+134T>C) c.7984+134T>C (n.7984+134T>C) c.541+134T>C c.7880+134T>C (n.7880+134T>C) | gnomAD v4 |
| 13 | g.32362828C>A | CA2082832898 | BRCA2 | c.7976+135C>A (n.7976+135C>A) c.7607+135C>A (n.7607+135C>A) c.443+135C>A (n.443+135C>A) c.7984+135C>A (n.7984+135C>A) c.541+135C>A c.7880+135C>A (n.7880+135C>A) | dbSNP gnomAD v4 |
| 13 | g.32362828C= | CA2082832867 | BRCA2 | c.7976+135C= (n.7976+135C=) c.7607+135C= (n.7607+135C=) c.443+135C= (n.443+135C=) c.7984+135C= (n.7984+135C=) c.541+135C= c.7880+135C= (n.7880+135C=) | |
| 13 | g.32362828C>T | CA2082832900 | BRCA2 | c.7976+135C>T (n.7976+135C>T) c.7607+135C>T (n.7607+135C>T) c.443+135C>T (n.443+135C>T) c.7984+135C>T (n.7984+135C>T) c.541+135C>T c.7880+135C>T (n.7880+135C>T) | dbSNP gnomAD v4 |
| 13 | g.32362829C>A | CA2622572980 | BRCA2 | c.7976+136C>A (n.7976+136C>A) c.7607+136C>A (n.7607+136C>A) c.443+136C>A (n.443+136C>A) c.7984+136C>A (n.7984+136C>A) c.541+136C>A c.7880+136C>A (n.7880+136C>A) | gnomAD v4 |
| 13 | g.32362829C>T | CA2556409064 | BRCA2 | c.7976+136C>T (n.7976+136C>T) c.7607+136C>T (n.7607+136C>T) c.443+136C>T (n.443+136C>T) c.7984+136C>T (n.7984+136C>T) c.541+136C>T c.7880+136C>T (n.7880+136C>T) | |
| 13 | g.32362830T>C | CA2622572982 | BRCA2 | c.7976+137T>C (n.7976+137T>C) c.7607+137T>C (n.7607+137T>C) c.443+137T>C (n.443+137T>C) c.7984+137T>C (n.7984+137T>C) c.541+137T>C c.7880+137T>C (n.7880+137T>C) | gnomAD v4 |
| 13 | g.32362831G>A | CA2622572983 | BRCA2 | c.7976+138G>A (n.7976+138G>A) c.7607+138G>A (n.7607+138G>A) c.443+138G>A (n.443+138G>A) c.7984+138G>A (n.7984+138G>A) c.541+138G>A c.7880+138G>A (n.7880+138G>A) | gnomAD v4 |
| 13 | g.32362833C>A | CA2622572985 | BRCA2 | c.7976+140C>A (n.7976+140C>A) c.7607+140C>A (n.7607+140C>A) c.443+140C>A (n.443+140C>A) c.7984+140C>A (n.7984+140C>A) c.541+140C>A c.7880+140C>A (n.7880+140C>A) | gnomAD v4 |
| 13 | g.32362835T>C | CA2622572986 | BRCA2 | c.7976+142T>C (n.7976+142T>C) c.7607+142T>C (n.7607+142T>C) c.443+142T>C (n.443+142T>C) c.7984+142T>C (n.7984+142T>C) c.541+142T>C c.7880+142T>C (n.7880+142T>C) | gnomAD v4 |
| 13 | g.32362836C>A | CA2622572987 | BRCA2 | c.7976+143C>A (n.7976+143C>A) c.7607+143C>A (n.7607+143C>A) c.443+143C>A (n.443+143C>A) c.7984+143C>A (n.7984+143C>A) c.541+143C>A c.7880+143C>A (n.7880+143C>A) | gnomAD v4 |
| 13 | g.32362837C>A | CA2622572988 | BRCA2 | c.7976+144C>A (n.7976+144C>A) c.7607+144C>A (n.7607+144C>A) c.443+144C>A (n.443+144C>A) c.7984+144C>A (n.7984+144C>A) c.541+144C>A c.7880+144C>A (n.7880+144C>A) | gnomAD v4 |
| 13 | g.32362837C>T | CA2622572989 | BRCA2 | c.7976+144C>T (n.7976+144C>T) c.7607+144C>T (n.7607+144C>T) c.443+144C>T (n.443+144C>T) c.7984+144C>T (n.7984+144C>T) c.541+144C>T c.7880+144C>T (n.7880+144C>T) | gnomAD v4 |
| 13 | g.32362837_32362838insT | CA2502510589 | BRCA2 | c.7976+144_7976+145insT (n.7976+144_7976+145insT) c.7607+144_7607+145insT (n.7607+144_7607+145insT) c.443+144_443+145insT (n.443+144_443+145insT) c.7984+144_7984+145insT (n.7984+144_7984+145insT) c.541+144_541+145insT c.7880+144_7880+145insT (n.7880+144_7880+145insT) | |
| 13 | g.32362838C>A | CA2622572990 | BRCA2 | c.7976+145C>A (n.7976+145C>A) c.7607+145C>A (n.7607+145C>A) c.443+145C>A (n.443+145C>A) c.7984+145C>A (n.7984+145C>A) c.541+145C>A c.7880+145C>A (n.7880+145C>A) | gnomAD v4 |
| 13 | g.32362838C>G | CA2622572992 | BRCA2 | c.7976+145C>G (n.7976+145C>G) c.7607+145C>G (n.7607+145C>G) c.443+145C>G (n.443+145C>G) c.7984+145C>G (n.7984+145C>G) c.541+145C>G c.7880+145C>G (n.7880+145C>G) | gnomAD v4 |
| 13 | g.32362838C>T | CA2798720289 | BRCA2 | c.7976+145C>T (n.7976+145C>T) c.7607+145C>T (n.7607+145C>T) c.443+145C>T (n.443+145C>T) c.7984+145C>T (n.7984+145C>T) c.541+145C>T c.7880+145C>T (n.7880+145C>T) | |
| 13 | g.32362839T>C | CA2538143515 | BRCA2 | c.7976+146T>C (n.7976+146T>C) c.7607+146T>C (n.7607+146T>C) c.443+146T>C (n.443+146T>C) c.7984+146T>C (n.7984+146T>C) c.541+146T>C c.7880+146T>C (n.7880+146T>C) | |
| 13 | g.32362839T>G | CA2622572993 | BRCA2 | c.7976+146T>G (n.7976+146T>G) c.7607+146T>G (n.7607+146T>G) c.443+146T>G (n.443+146T>G) c.7984+146T>G (n.7984+146T>G) c.541+146T>G c.7880+146T>G (n.7880+146T>G) | gnomAD v4 |
| 13 | g.32362839_32362840insTTCCATTATCTTTTTTAT | CA2798720290 | BRCA2 | c.7976+146_7976+147insTTCCATTATCTTTTTTAT (n.7976+146_7976+147insTTCCATTATCTTTTTTAT) c.7607+146_7607+147insTTCCATTATCTTTTTTAT (n.7607+146_7607+147insTTCCATTATCTTTTTTAT) c.443+146_443+147insTTCCATTATCTTTTTTAT (n.443+146_443+147insTTCCATTATCTTTTTTAT) c.7984+146_7984+147insTTCCATTATCTTTTTTAT (n.7984+146_7984+147insTTCCATTATCTTTTTTAT) c.541+146_541+147insTTCCATTATCTTTTTTAT c.7880+146_7880+147insTTCCATTATCTTTTTTAT (n.7880+146_7880+147insTTCCATTATCTTTTTTAT) | |
| 13 | g.32362840A= | CA2082832902 | BRCA2 | c.7976+147A= (n.7976+147A=) c.7607+147A= (n.7607+147A=) c.443+147A= (n.443+147A=) c.7984+147A= (n.7984+147A=) c.541+147A= c.7880+147A= (n.7880+147A=) | |
| 13 | g.32362840A>C | CA609091830 | BRCA2 | c.7976+147A>C (n.7976+147A>C) c.7607+147A>C (n.7607+147A>C) c.443+147A>C (n.443+147A>C) c.7984+147A>C (n.7984+147A>C) c.541+147A>C c.7880+147A>C (n.7880+147A>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32362840A>G | CA2622572996 | BRCA2 | c.7976+147A>G (n.7976+147A>G) c.7607+147A>G (n.7607+147A>G) c.443+147A>G (n.443+147A>G) c.7984+147A>G (n.7984+147A>G) c.541+147A>G c.7880+147A>G (n.7880+147A>G) | gnomAD v4 |
| 13 | g.32362841G>A | CA2622572997 | BRCA2 | c.7976+148G>A (n.7976+148G>A) c.7607+148G>A (n.7607+148G>A) c.443+148G>A (n.443+148G>A) c.7984+148G>A (n.7984+148G>A) c.541+148G>A c.7880+148G>A (n.7880+148G>A) | gnomAD v4 |
| 13 | g.32362841G>T | CA2622572998 | BRCA2 | c.7976+148G>T (n.7976+148G>T) c.7607+148G>T (n.7607+148G>T) c.443+148G>T (n.443+148G>T) c.7984+148G>T (n.7984+148G>T) c.541+148G>T c.7880+148G>T (n.7880+148G>T) | gnomAD v4 |
| 13 | g.32362842C>A | CA2622572999 | BRCA2 | c.7976+149C>A (n.7976+149C>A) c.7607+149C>A (n.7607+149C>A) c.443+149C>A (n.443+149C>A) c.7984+149C>A (n.7984+149C>A) c.541+149C>A c.7880+149C>A (n.7880+149C>A) | gnomAD v4 |
| 13 | g.32362842C>T | CA2622573000 | BRCA2 | c.7976+149C>T (n.7976+149C>T) c.7607+149C>T (n.7607+149C>T) c.443+149C>T (n.443+149C>T) c.7984+149C>T (n.7984+149C>T) c.541+149C>T c.7880+149C>T (n.7880+149C>T) | gnomAD v4 |
| 13 | g.32362844C>T | CA2507397738 | BRCA2 | c.7976+151C>T (n.7976+151C>T) c.7607+151C>T (n.7607+151C>T) c.443+151C>T (n.443+151C>T) c.7984+151C>T (n.7984+151C>T) c.541+151C>T c.7880+151C>T (n.7880+151C>T) | |
| 13 | g.32362845C>A | CA2622573003 | BRCA2 | c.7976+152C>A (n.7976+152C>A) c.7607+152C>A (n.7607+152C>A) c.443+152C>A (n.443+152C>A) c.7984+152C>A (n.7984+152C>A) c.541+152C>A c.7880+152C>A (n.7880+152C>A) | gnomAD v4 |
| 13 | g.32362845C= | CA2082832937 | BRCA2 | c.7976+152C= (n.7976+152C=) c.7607+152C= (n.7607+152C=) c.443+152C= (n.443+152C=) c.7984+152C= (n.7984+152C=) c.541+152C= c.7880+152C= (n.7880+152C=) | |
| 13 | g.32362845C>G | CA2622573004 | BRCA2 | c.7976+152C>G (n.7976+152C>G) c.7607+152C>G (n.7607+152C>G) c.443+152C>G (n.443+152C>G) c.7984+152C>G (n.7984+152C>G) c.541+152C>G c.7880+152C>G (n.7880+152C>G) | gnomAD v4 |
| 13 | g.32362845C>T | CA247475443 | BRCA2 | c.7976+152C>T (n.7976+152C>T) c.7607+152C>T (n.7607+152C>T) c.443+152C>T (n.443+152C>T) c.7984+152C>T (n.7984+152C>T) c.541+152C>T c.7880+152C>T (n.7880+152C>T) | dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32362846_32362847del | CA2525978338 | BRCA2 | c.7976+153_7976+154del (n.7976+153_7976+154del) c.7607+153_7607+154del (n.7607+153_7607+154del) c.443+153_443+154del (n.443+153_443+154del) c.7984+153_7984+154del (n.7984+153_7984+154del) c.541+153_541+154del c.7880+153_7880+154del (n.7880+153_7880+154del) | |
| 13 | g.32362848T>C | CA2727918270 | BRCA2 | c.7976+155T>C (n.7976+155T>C) c.7607+155T>C (n.7607+155T>C) c.443+155T>C (n.443+155T>C) c.7984+155T>C (n.7984+155T>C) c.541+155T>C c.7880+155T>C (n.7880+155T>C) | dbSNP |
| 13 | g.32362851A>G | CA2536408235 | BRCA2 | c.7976+158A>G (n.7976+158A>G) c.7607+158A>G (n.7607+158A>G) c.443+158A>G (n.443+158A>G) c.7984+158A>G (n.7984+158A>G) c.541+158A>G c.7880+158A>G (n.7880+158A>G) | |
| 13 | g.32362855G>C | CA2082832941 | BRCA2 | c.7976+162G>C (n.7976+162G>C) c.7607+162G>C (n.7607+162G>C) c.443+162G>C (n.443+162G>C) c.7984+162G>C (n.7984+162G>C) c.541+162G>C c.7880+162G>C (n.7880+162G>C) | dbSNP |
| 13 | g.32362855G= | CA2082832940 | BRCA2 | c.7976+162G= (n.7976+162G=) c.7607+162G= (n.7607+162G=) c.443+162G= (n.443+162G=) c.7984+162G= (n.7984+162G=) c.541+162G= c.7880+162G= (n.7880+162G=) | |
| 13 | g.32362856A= | CA2082832943 | BRCA2 | c.7976+163A= (n.7976+163A=) c.7607+163A= (n.7607+163A=) c.443+163A= (n.443+163A=) c.7984+163A= (n.7984+163A=) c.541+163A= c.7880+163A= (n.7880+163A=) | |
| 13 | g.32362856A>G | CA697355428 | BRCA2 | c.7976+163A>G (n.7976+163A>G) c.7607+163A>G (n.7607+163A>G) c.443+163A>G (n.443+163A>G) c.7984+163A>G (n.7984+163A>G) c.541+163A>G c.7880+163A>G (n.7880+163A>G) | dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32362857G>A | CA2506648019 | BRCA2 | c.7976+164G>A (n.7976+164G>A) c.7607+164G>A (n.7607+164G>A) c.443+164G>A (n.443+164G>A) c.7984+164G>A (n.7984+164G>A) c.541+164G>A c.7880+164G>A (n.7880+164G>A) | |
| 13 | g.32362858A= | CA2082832944 | BRCA2 | c.7976+165A= (n.7976+165A=) c.7607+165A= (n.7607+165A=) c.443+165A= (n.443+165A=) c.7984+165A= (n.7984+165A=) c.541+165A= c.7880+165A= (n.7880+165A=) | |
| 13 | g.32362858A>G | CA247475444 | BRCA2 | c.7976+165A>G (n.7976+165A>G) c.7607+165A>G (n.7607+165A>G) c.443+165A>G (n.443+165A>G) c.7984+165A>G (n.7984+165A>G) c.541+165A>G c.7880+165A>G (n.7880+165A>G) | dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32362858A>T | CA2552841655 | BRCA2 | c.7976+165A>T (n.7976+165A>T) c.7607+165A>T (n.7607+165A>T) c.443+165A>T (n.443+165A>T) c.7984+165A>T (n.7984+165A>T) c.541+165A>T c.7880+165A>T (n.7880+165A>T) | |
| 13 | g.32362864C= | CA2082832948 | BRCA2 | c.7976+171C= (n.7976+171C=) c.7607+171C= (n.7607+171C=) c.443+171C= (n.443+171C=) c.7984+171C= (n.7984+171C=) c.541+171C= c.7880+171C= (n.7880+171C=) | |
| 13 | g.32362864C>T | CA609091831 | BRCA2 | c.7976+171C>T (n.7976+171C>T) c.7607+171C>T (n.7607+171C>T) c.443+171C>T (n.443+171C>T) c.7984+171C>T (n.7984+171C>T) c.541+171C>T c.7880+171C>T (n.7880+171C>T) | dbSNP gnomAD v2 |
| 13 | g.32362865A= | CA2082832953 | BRCA2 | c.7976+172A= (n.7976+172A=) c.7607+172A= (n.7607+172A=) c.443+172A= (n.443+172A=) c.7984+172A= (n.7984+172A=) c.541+172A= c.7880+172A= (n.7880+172A=) | |
| 13 | g.32362865A>G | CA954700409 | BRCA2 | c.7976+172A>G (n.7976+172A>G) c.7607+172A>G (n.7607+172A>G) c.443+172A>G (n.443+172A>G) c.7984+172A>G (n.7984+172A>G) c.541+172A>G c.7880+172A>G (n.7880+172A>G) | dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32362865A>T | CA247475447 | BRCA2 | c.7976+172A>T (n.7976+172A>T) c.7607+172A>T (n.7607+172A>T) c.443+172A>T (n.443+172A>T) c.7984+172A>T (n.7984+172A>T) c.541+172A>T c.7880+172A>T (n.7880+172A>T) | dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32362866T>G | CA247475459 | BRCA2 | c.7976+173T>G (n.7976+173T>G) c.7607+173T>G (n.7607+173T>G) c.443+173T>G (n.443+173T>G) c.7984+173T>G (n.7984+173T>G) c.541+173T>G c.7880+173T>G (n.7880+173T>G) | dbSNP |
| 13 | g.32362866T= | CA2082832958 | BRCA2 | c.7976+173T= (n.7976+173T=) c.7607+173T= (n.7607+173T=) c.443+173T= (n.443+173T=) c.7984+173T= (n.7984+173T=) c.541+173T= c.7880+173T= (n.7880+173T=) | |
| 13 | g.32362868C>T | CA2741308458 | BRCA2 | c.7976+175C>T (n.7976+175C>T) c.7607+175C>T (n.7607+175C>T) c.443+175C>T (n.443+175C>T) c.7984+175C>T (n.7984+175C>T) c.541+175C>T c.7880+175C>T (n.7880+175C>T) | |
| 13 | g.32362869A= | CA2082832967 | BRCA2 | c.7976+176A= (n.7976+176A=) c.7607+176A= (n.7607+176A=) c.443+176A= (n.443+176A=) c.7984+176A= (n.7984+176A=) c.541+176A= c.7880+176A= (n.7880+176A=) | |
| 13 | g.32362869A>G | CA247475470 | BRCA2 | c.7976+176A>G (n.7976+176A>G) c.7607+176A>G (n.7607+176A>G) c.443+176A>G (n.443+176A>G) c.7984+176A>G (n.7984+176A>G) c.541+176A>G c.7880+176A>G (n.7880+176A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32362872C= | CA2082832972 | BRCA2 | c.7976+179C= (n.7976+179C=) c.7607+179C= (n.7607+179C=) c.443+179C= (n.443+179C=) c.7984+179C= (n.7984+179C=) c.541+179C= c.7880+179C= (n.7880+179C=) | |
| 13 | g.32362872C>T | CA954700412 | BRCA2 | c.7976+179C>T (n.7976+179C>T) c.7607+179C>T (n.7607+179C>T) c.443+179C>T (n.443+179C>T) c.7984+179C>T (n.7984+179C>T) c.541+179C>T c.7880+179C>T (n.7880+179C>T) | dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32362873A= | CA2082832977 | BRCA2 | c.7976+180A= (n.7976+180A=) c.7607+180A= (n.7607+180A=) c.443+180A= (n.443+180A=) c.7984+180A= (n.7984+180A=) c.541+180A= c.7880+180A= (n.7880+180A=) | |
| 13 | g.32362874T>C | CA697355432 | BRCA2 | c.7976+181T>C (n.7976+181T>C) c.7607+181T>C (n.7607+181T>C) c.443+181T>C (n.443+181T>C) c.7984+181T>C (n.7984+181T>C) c.541+181T>C c.7880+181T>C (n.7880+181T>C) | dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32362874T= | CA2082832979 | BRCA2 | c.7976+181T= (n.7976+181T=) c.7607+181T= (n.7607+181T=) c.443+181T= (n.443+181T=) c.7984+181T= (n.7984+181T=) c.541+181T= c.7880+181T= (n.7880+181T=) | |
| 13 | g.32362906_32362907insTGCTTGCTTGCTTCCCTCTTTCCCCACCCCCTCCTT | CA954700415 | BRCA2 | c.7976+213_7976+214insTGCTTGCTTGCTTCCCTCTTTCCCCACCCCCTCCTT (n.7976+213_7976+214insTGCTTGCTTGCTTCCCTCTTTCCCCACCCCCTCCTT) c.7607+213_7607+214insTGCTTGCTTGCTTCCCTCTTTCCCCACCCCCTCCTT (n.7607+213_7607+214insTGCTTGCTTGCTTCCCTCTTTCCCCACCCCCTCCTT) c.443+213_443+214insTGCTTGCTTGCTTCCCTCTTTCCCCACCCCCTCCTT (n.443+213_443+214insTGCTTGCTTGCTTCCCTCTTTCCCCACCCCCTCCTT) c.7984+213_7984+214insTGCTTGCTTGCTTCCCTCTTTCCCCACCCCCTCCTT (n.7984+213_7984+214insTGCTTGCTTGCTTCCCTCTTTCCCCACCCCCTCCTT) c.541+213_541+214insTGCTTGCTTGCTTCCCTCTTTCCCCACCCCCTCCTT c.7880+213_7880+214insTGCTTGCTTGCTTCCCTCTTTCCCCACCCCCTCCTT (n.7880+213_7880+214insTGCTTGCTTGCTTCCCTCTTTCCCCACCCCCTCCTT) | dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32362876G>C | CA2082832981 | BRCA2 | c.7976+183G>C (n.7976+183G>C) c.7607+183G>C (n.7607+183G>C) c.443+183G>C (n.443+183G>C) c.7984+183G>C (n.7984+183G>C) c.541+183G>C c.7880+183G>C (n.7880+183G>C) | dbSNP |
| 13 | g.32362876G= | CA2082832980 | BRCA2 | c.7976+183G= (n.7976+183G=) c.7607+183G= (n.7607+183G=) c.443+183G= (n.443+183G=) c.7984+183G= (n.7984+183G=) c.541+183G= c.7880+183G= (n.7880+183G=) | |
| 13 | g.32362876G>T | CA697355433 | BRCA2 | c.7976+183G>T (n.7976+183G>T) c.7607+183G>T (n.7607+183G>T) c.443+183G>T (n.443+183G>T) c.7984+183G>T (n.7984+183G>T) c.541+183G>T c.7880+183G>T (n.7880+183G>T) | dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32362877C= | CA2082832984 | BRCA2 | c.7976+184C= (n.7976+184C=) c.7607+184C= (n.7607+184C=) c.443+184C= (n.443+184C=) c.7984+184C= (n.7984+184C=) c.541+184C= c.7880+184C= (n.7880+184C=) | |
| 13 | g.32362877C>T | CA697355435 | BRCA2 | c.7976+184C>T (n.7976+184C>T) c.7607+184C>T (n.7607+184C>T) c.443+184C>T (n.443+184C>T) c.7984+184C>T (n.7984+184C>T) c.541+184C>T c.7880+184C>T (n.7880+184C>T) | dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32362886C>T | CA2727918273 | BRCA2 | c.7976+193C>T (n.7976+193C>T) c.7607+193C>T (n.7607+193C>T) c.443+193C>T (n.443+193C>T) c.7984+193C>T (n.7984+193C>T) c.541+193C>T c.7880+193C>T (n.7880+193C>T) | dbSNP |
| 13 | g.32362887T>A | CA2082832988 | BRCA2 | c.7976+194T>A (n.7976+194T>A) c.7607+194T>A (n.7607+194T>A) c.443+194T>A (n.443+194T>A) c.7984+194T>A (n.7984+194T>A) c.541+194T>A c.7880+194T>A (n.7880+194T>A) | dbSNP |
| 13 | g.32362887T= | CA2082832989 | BRCA2 | c.7976+194T= (n.7976+194T=) c.7607+194T= (n.7607+194T=) c.443+194T= (n.443+194T=) c.7984+194T= (n.7984+194T=) c.541+194T= c.7880+194T= (n.7880+194T=) | |
| 13 | g.32362888C= | CA2082832993 | BRCA2 | c.7976+195C= (n.7976+195C=) c.7607+195C= (n.7607+195C=) c.443+195C= (n.443+195C=) c.7984+195C= (n.7984+195C=) c.541+195C= c.7880+195C= (n.7880+195C=) | |
| 13 | g.32362888C>G | CA247475473 | BRCA2 | c.7976+195C>G (n.7976+195C>G) c.7607+195C>G (n.7607+195C>G) c.443+195C>G (n.443+195C>G) c.7984+195C>G (n.7984+195C>G) c.541+195C>G c.7880+195C>G (n.7880+195C>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32362892C= | CA2082832997 | BRCA2 | c.7976+199C= (n.7976+199C=) c.7607+199C= (n.7607+199C=) c.443+199C= (n.443+199C=) c.7984+199C= (n.7984+199C=) c.541+199C= c.7880+199C= (n.7880+199C=) | |
| 13 | g.32362892C>T | CA2082832998 | BRCA2 | c.7976+199C>T (n.7976+199C>T) c.7607+199C>T (n.7607+199C>T) c.443+199C>T (n.443+199C>T) c.7984+199C>T (n.7984+199C>T) c.541+199C>T c.7880+199C>T (n.7880+199C>T) | dbSNP |
| 13 | g.32362893C>A | CA247475478 | BRCA2 | c.7976+200C>A (n.7976+200C>A) c.7607+200C>A (n.7607+200C>A) c.443+200C>A (n.443+200C>A) c.7984+200C>A (n.7984+200C>A) c.541+200C>A c.7880+200C>A (n.7880+200C>A) | dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32362893C= | CA2082833002 | BRCA2 | c.7976+200C= (n.7976+200C=) c.7607+200C= (n.7607+200C=) c.443+200C= (n.443+200C=) c.7984+200C= (n.7984+200C=) c.541+200C= c.7880+200C= (n.7880+200C=) | |
| 13 | g.32362893C>T | CA247475482 | BRCA2 | c.7976+200C>T (n.7976+200C>T) c.7607+200C>T (n.7607+200C>T) c.443+200C>T (n.443+200C>T) c.7984+200C>T (n.7984+200C>T) c.541+200C>T c.7880+200C>T (n.7880+200C>T) | dbSNP |
| 13 | g.32362896A= | CA2082833005 | BRCA2 | c.7976+203A= (n.7976+203A=) c.7607+203A= (n.7607+203A=) c.443+203A= (n.443+203A=) c.7984+203A= (n.7984+203A=) c.541+203A= c.7880+203A= (n.7880+203A=) | |
| 13 | g.32362896A>C | CA609091832 | BRCA2 | c.7976+203A>C (n.7976+203A>C) c.7607+203A>C (n.7607+203A>C) c.443+203A>C (n.443+203A>C) c.7984+203A>C (n.7984+203A>C) c.541+203A>C c.7880+203A>C (n.7880+203A>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32362896A>T | CA247475485 | BRCA2 | c.7976+203A>T (n.7976+203A>T) c.7607+203A>T (n.7607+203A>T) c.443+203A>T (n.443+203A>T) c.7984+203A>T (n.7984+203A>T) c.541+203A>T c.7880+203A>T (n.7880+203A>T) | dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32362897C>A | CA697355454 | BRCA2 | c.7976+204C>A (n.7976+204C>A) c.7607+204C>A (n.7607+204C>A) c.443+204C>A (n.443+204C>A) c.7984+204C>A (n.7984+204C>A) c.541+204C>A c.7880+204C>A (n.7880+204C>A) | dbSNP |
| 13 | g.32362897C= | CA2082833022 | BRCA2 | c.7976+204C= (n.7976+204C=) c.7607+204C= (n.7607+204C=) c.443+204C= (n.443+204C=) c.7984+204C= (n.7984+204C=) c.541+204C= c.7880+204C= (n.7880+204C=) | |
| 13 | g.32362898C>A | CA2082833030 | BRCA2 | c.7976+205C>A (n.7976+205C>A) c.7607+205C>A (n.7607+205C>A) c.443+205C>A (n.443+205C>A) c.7984+205C>A (n.7984+205C>A) c.541+205C>A c.7880+205C>A (n.7880+205C>A) | dbSNP |
| 13 | g.32362898C= | CA2082833026 | BRCA2 | c.7976+205C= (n.7976+205C=) c.7607+205C= (n.7607+205C=) c.443+205C= (n.443+205C=) c.7984+205C= (n.7984+205C=) c.541+205C= c.7880+205C= (n.7880+205C=) | |
| 13 | g.32362899C>A | CA247475489 | BRCA2 | c.7976+206C>A (n.7976+206C>A) c.7607+206C>A (n.7607+206C>A) c.443+206C>A (n.443+206C>A) c.7984+206C>A (n.7984+206C>A) c.541+206C>A c.7880+206C>A (n.7880+206C>A) | dbSNP |
| 13 | g.32362899C= | CA2082833035 | BRCA2 | c.7976+206C= (n.7976+206C=) c.7607+206C= (n.7607+206C=) c.443+206C= (n.443+206C=) c.7984+206C= (n.7984+206C=) c.541+206C= c.7880+206C= (n.7880+206C=) | |
| 13 | g.32362900C>A | CA697355455 | BRCA2 | c.7976+207C>A (n.7976+207C>A) c.7607+207C>A (n.7607+207C>A) c.443+207C>A (n.443+207C>A) c.7984+207C>A (n.7984+207C>A) c.541+207C>A c.7880+207C>A (n.7880+207C>A) | dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32362900C= | CA2082833044 | BRCA2 | c.7976+207C= (n.7976+207C=) c.7607+207C= (n.7607+207C=) c.443+207C= (n.443+207C=) c.7984+207C= (n.7984+207C=) c.541+207C= c.7880+207C= (n.7880+207C=) | |
| 13 | g.32362900C>G | CA2082833054 | BRCA2 | c.7976+207C>G (n.7976+207C>G) c.7607+207C>G (n.7607+207C>G) c.443+207C>G (n.443+207C>G) c.7984+207C>G (n.7984+207C>G) c.541+207C>G c.7880+207C>G (n.7880+207C>G) | dbSNP |
| 13 | g.32362900C>T | CA954700426 | BRCA2 | c.7976+207C>T (n.7976+207C>T) c.7607+207C>T (n.7607+207C>T) c.443+207C>T (n.443+207C>T) c.7984+207C>T (n.7984+207C>T) c.541+207C>T c.7880+207C>T (n.7880+207C>T) | dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32362901C= | CA2082833059 | BRCA2 | c.7976+208C= (n.7976+208C=) c.7607+208C= (n.7607+208C=) c.443+208C= (n.443+208C=) c.7984+208C= (n.7984+208C=) c.541+208C= c.7880+208C= (n.7880+208C=) | |
| 13 | g.32362901C>T | CA609091833 | BRCA2 | c.7976+208C>T (n.7976+208C>T) c.7607+208C>T (n.7607+208C>T) c.443+208C>T (n.443+208C>T) c.7984+208C>T (n.7984+208C>T) c.541+208C>T c.7880+208C>T (n.7880+208C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32362902T>C | CA954700429 | BRCA2 | c.7976+209T>C (n.7976+209T>C) c.7607+209T>C (n.7607+209T>C) c.443+209T>C (n.443+209T>C) c.7984+209T>C (n.7984+209T>C) c.541+209T>C c.7880+209T>C (n.7880+209T>C) | dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.32362902T= | CA2082833068 | BRCA2 | c.7976+209T= (n.7976+209T=) c.7607+209T= (n.7607+209T=) c.443+209T= (n.443+209T=) c.7984+209T= (n.7984+209T=) c.541+209T= c.7880+209T= (n.7880+209T=) | |
| 13 | g.32362903C= | CA2082833073 | BRCA2 | c.7976+210C= (n.7976+210C=) c.7607+210C= (n.7607+210C=) c.443+210C= (n.443+210C=) c.7984+210C= (n.7984+210C=) c.541+210C= c.7880+210C= (n.7880+210C=) | |
| 13 | g.32362903C>T | CA697355457 | BRCA2 | c.7976+210C>T (n.7976+210C>T) c.7607+210C>T (n.7607+210C>T) c.443+210C>T (n.443+210C>T) c.7984+210C>T (n.7984+210C>T) c.541+210C>T c.7880+210C>T (n.7880+210C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32362904C= | CA2082833076 | BRCA2 | c.7976+211C= (n.7976+211C=) c.7607+211C= (n.7607+211C=) c.443+211C= (n.443+211C=) c.7984+211C= (n.7984+211C=) c.541+211C= c.7880+211C= (n.7880+211C=) | |
| 13 | g.32362904C>G | CA2082833082 | BRCA2 | c.7976+211C>G (n.7976+211C>G) c.7607+211C>G (n.7607+211C>G) c.443+211C>G (n.443+211C>G) c.7984+211C>G (n.7984+211C>G) c.541+211C>G c.7880+211C>G (n.7880+211C>G) | dbSNP |