Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.32338516_32338520delCA2499222155BRCA2c.4161_4165del (p.Leu1387PhefsTer14)
c.3792_3796del (p.Leu1264PhefsTer14)
n.4161_4165del
13g.32338516A=CA2082809010BRCA2c.4161A= (p.Leu1387=)
c.3792A= (p.Leu1264=)
n.4161A=
13g.32338516A>CCA387780042BRCA2c.4161A>C (p.Leu1387Phe)
c.3792A>C (p.Leu1264Phe)
n.4161A>C
13g.32338516A>GCA483437841BRCA2c.4161A>G (p.Leu1387=)
c.3792A>G (p.Leu1264=)
n.4161A>G
 dbSNP
13g.32338516A>TCA387780040BRCA2c.4161A>T (p.Leu1387Phe)
c.3792A>T (p.Leu1264Phe)
n.4161A>T
 dbSNP
13g.32338516_32338521delinsAACTTTCA2082809007BRCA2c.4161_4166delinsAACTTT (p.Leu1387=)
c.3792_3797delinsAACTTT (p.Leu1264=)
n.4161_4166delinsAACTTT
13g.32338517A=CA2082809025BRCA2c.4162A= (p.Thr1388=)
c.3793A= (p.Thr1265=)
n.4162A=
13g.32338517A>CCA387780044BRCA2c.4162A>C (p.Thr1388Pro)
c.3793A>C (p.Thr1265Pro)
n.4162A>C
 ClinVar dbSNP
13g.32338517A>GCA387780047BRCA2c.4162A>G (p.Thr1388Ala)
c.3793A>G (p.Thr1265Ala)
n.4162A>G
13g.32338517A>TCA387780048BRCA2c.4162A>T (p.Thr1388Ser)
c.3793A>T (p.Thr1265Ser)
n.4162A>T
13g.32338517_32338519delinsACTCA2082809022BRCA2c.4162_4164delinsACT (p.Thr1388=)
c.3793_3795delinsACT (p.Thr1265=)
n.4162_4164delinsACT
13g.32338517_32338521delCA6940757BRCA2c.4162_4166del (p.Thr1388PhefsTer13)
c.3793_3797del (p.Thr1265PhefsTer13)
n.4162_4166del
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32338518delCA1139768323BRCA2c.4163del (p.Thr1388IlefsTer22)
c.3794del (p.Thr1265IlefsTer22)
n.4163del
 ClinVar gnomAD v4
13g.32338518C>ACA019646BRCA2c.4163C>A (p.Thr1388Asn)
c.3794C>A (p.Thr1265Asn)
n.4163C>A
 ClinVar dbSNP ExAC gnomAD v3 gnomAD v4
13g.32338518C=CA2082809040BRCA2c.4163C= (p.Thr1388=)
c.3794C= (p.Thr1265=)
n.4163C=
13g.32338518C>GCA387780049BRCA2c.4163C>G (p.Thr1388Ser)
c.3794C>G (p.Thr1265Ser)
n.4163C>G
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32338518C>TCA387780051BRCA2c.4163C>T (p.Thr1388Ile)
c.3794C>T (p.Thr1265Ile)
n.4163C>T
13g.32338518_32338519delinsACA019640BRCA2c.4163_4164delinsA (p.Thr1388AsnfsTer22)
c.3794_3795delinsA (p.Thr1265AsnfsTer22)
n.4163_4164delinsA
 ClinVar dbSNP
13g.32338518_32338520delinsCTTCA2082809048BRCA2c.4163_4165delinsCTT (p.Thr1388=)
c.3794_3796delinsCTT (p.Thr1265=)
n.4163_4165delinsCTT
13g.32338519T>ACA247507333BRCA2c.4164T>A (p.Thr1388=)
c.3795T>A (p.Thr1265=)
n.4164T>A
 ClinVar dbSNP gnomAD v4
13g.32338519T>CCA483437850BRCA2c.4164T>C (p.Thr1388=)
c.3795T>C (p.Thr1265=)
n.4164T>C
 ClinVar dbSNP
13g.32338519T>GCA483437851BRCA2c.4164T>G (p.Thr1388=)
c.3795T>G (p.Thr1265=)
n.4164T>G
 ClinVar
13g.32338519T=CA2082809073BRCA2c.4164T= (p.Thr1388=)
c.3795T= (p.Thr1265=)
n.4164T=
13g.32338524dupCA10589244BRCA2c.4169dup (p.Leu1390PhefsTer13)
c.3800dup (p.Leu1267PhefsTer13)
n.4169dup
 ClinVar dbSNP
13g.32338524delCA019655BRCA2c.4169del (p.Leu1390TrpfsTer20)
c.3800del (p.Leu1267TrpfsTer20)
n.4169del
 ClinVar dbSNP gnomAD v4
13g.32338523_32338524delCA019652BRCA2c.4168_4169del (p.Leu1390GlyfsTer12)
c.3799_3800del (p.Leu1267GlyfsTer12)
n.4168_4169del
 ClinVar dbSNP
13g.32338521_32338524delCA2499222156BRCA2c.4166_4169del (p.Phe1389TrpfsTer20)
c.3797_3800del (p.Phe1266TrpfsTer20)
n.4166_4169del
13g.32338520T>ACA387780057BRCA2c.4165T>A (p.Phe1389Ile)
c.3796T>A (p.Phe1266Ile)
n.4165T>A
 ClinVar dbSNP
13g.32338520T>CCA387780059BRCA2c.4165T>C (p.Phe1389Leu)
c.3796T>C (p.Phe1266Leu)
n.4165T>C
 ClinVar dbSNP
13g.32338520T>GCA16020672BRCA2c.4165T>G (p.Phe1389Val)
c.3796T>G (p.Phe1266Val)
n.4165T>G
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
13g.32338520T=CA2082809086BRCA2c.4165T= (p.Phe1389=)
c.3796T= (p.Phe1266=)
n.4165T=
13g.32338521T>ACA387780061BRCA2c.4166T>A (p.Phe1389Tyr)
c.3797T>A (p.Phe1266Tyr)
n.4166T>A
13g.32338521T>CCA387780063BRCA2c.4166T>C (p.Phe1389Ser)
c.3797T>C (p.Phe1266Ser)
n.4166T>C
 ClinVar dbSNP
13g.32338521T>GCA387780064BRCA2c.4166T>G (p.Phe1389Cys)
c.3797T>G (p.Phe1266Cys)
n.4166T>G
13g.32338521T=CA2082809094BRCA2c.4166T= (p.Phe1389=)
c.3797T= (p.Phe1266=)
n.4166T=
13g.32338522T>ACA387780069BRCA2c.4167T>A (p.Phe1389Leu)
c.3798T>A (p.Phe1266Leu)
n.4167T>A
13g.32338522T>CCA483437857BRCA2c.4167T>C (p.Phe1389=)
c.3798T>C (p.Phe1266=)
n.4167T>C
 ClinVar
13g.32338522T>GCA387780066BRCA2c.4167T>G (p.Phe1389Leu)
c.3798T>G (p.Phe1266Leu)
n.4167T>G
13g.32338523T>ACA387780071BRCA2c.4168T>A (p.Leu1390Met)
c.3799T>A (p.Leu1267Met)
n.4168T>A
 dbSNP
13g.32338523T>CCA483437861BRCA2c.4168T>C (p.Leu1390=)
c.3799T>C (p.Leu1267=)
n.4168T>C
 ClinVar dbSNP gnomAD v4
13g.32338523T>GCA387780070BRCA2c.4168T>G (p.Leu1390Val)
c.3799T>G (p.Leu1267Val)
n.4168T>G
13g.32338523T=CA2082809107BRCA2c.4168T= (p.Leu1390=)
c.3799T= (p.Leu1267=)
n.4168T=
13g.32338524T>ACA387780074BRCA2c.4169T>A (p.Leu1390Ter)
c.3800T>A (p.Leu1267Ter)
n.4169T>A
13g.32338524T>CCA387780075BRCA2c.4169T>C (p.Leu1390Ser)
c.3800T>C (p.Leu1267Ser)
n.4169T>C
13g.32338524T>GCA387780076BRCA2c.4169T>G (p.Leu1390Trp)
c.3800T>G (p.Leu1267Trp)
n.4169T>G
 ClinVar dbSNP
13g.32338524T=CA2082809126BRCA2c.4169T= (p.Leu1390=)
c.3800T= (p.Leu1267=)
n.4169T=
13g.32338524_32338525delinsTGCA2082809123BRCA2c.4169_4170delinsTG (p.Leu1390=)
c.3800_3801delinsTG (p.Leu1267=)
n.4169_4170delinsTG
13g.32338524_32338526delinsTGGCA2082809124BRCA2c.4169_4171delinsTGG (p.Leu1390=)
c.3800_3802delinsTGG (p.Leu1267=)
n.4169_4171delinsTGG
13g.32338525G>ACA483437865BRCA2c.4170G>A (p.Leu1390=)
c.3801G>A (p.Leu1267=)
n.4170G>A
 ClinVar dbSNP COSMIC COSMIC
13g.32338525G>CCA387780079BRCA2c.4170G>C (p.Leu1390Phe)
c.3801G>C (p.Leu1267Phe)
n.4170G>C
 dbSNP
13g.32338525G=CA2082809148BRCA2c.4170G= (p.Leu1390=)
c.3801G= (p.Leu1267=)
n.4170G=
13g.32338525G>TCA387780081BRCA2c.4170G>T (p.Leu1390Phe)
c.3801G>T (p.Leu1267Phe)
n.4170G>T
 dbSNP
13g.32338525_32338526delCA10583100BRCA2c.4170_4171del (p.Glu1391SerfsTer11)
c.3801_3802del (p.Glu1268SerfsTer11)
n.4170_4171del
 ClinVar dbSNP
13g.32338526dupCA2580087256BRCA2c.4171dup (p.Glu1391GlyfsTer12)
c.3802dup (p.Glu1268GlyfsTer12)
n.4171dup
 ClinVar
13g.32338526delCA019663BRCA2c.4171del (p.Glu1391LysfsTer19)
c.3802del (p.Glu1268LysfsTer19)
n.4171del
 ClinVar dbSNP
13g.32338526G>ACA387780084BRCA2c.4171G>A (p.Glu1391Lys)
c.3802G>A (p.Glu1268Lys)
n.4171G>A
 ClinVar dbSNP
13g.32338526G>CCA387780086BRCA2c.4171G>C (p.Glu1391Gln)
c.3802G>C (p.Glu1268Gln)
n.4171G>C
 dbSNP
13g.32338526G=CA2082809157BRCA2c.4171G= (p.Glu1391=)
c.3802G= (p.Glu1268=)
n.4171G=
13g.32338526G>TCA387780083BRCA2c.4171G>T (p.Glu1391Ter)
c.3802G>T (p.Glu1268Ter)
n.4171G>T
 ClinVar dbSNP
13g.32338527A>CCA387780088BRCA2c.4172A>C (p.Glu1391Ala)
c.3803A>C (p.Glu1268Ala)
n.4172A>C
13g.32338527A>GCA387780089BRCA2c.4172A>G (p.Glu1391Gly)
c.3803A>G (p.Glu1268Gly)
n.4172A>G
 ClinVar dbSNP
13g.32338527A>TCA387780091BRCA2c.4172A>T (p.Glu1391Val)
c.3803A>T (p.Glu1268Val)
n.4172A>T
 dbSNP
13g.32338527_32338530delCA2695218198BRCA2c.4172_4175del (p.Glu1391ValfsTer18)
c.3803_3806del (p.Glu1268ValfsTer18)
n.4172_4175del
13g.32338528A>CCA387780093BRCA2c.4173A>C (p.Glu1391Asp)
c.3804A>C (p.Glu1268Asp)
n.4173A>C
13g.32338528A>GCA483437868BRCA2c.4173A>G (p.Glu1391=)
c.3804A>G (p.Glu1268=)
n.4173A>G
 dbSNP gnomAD v4
13g.32338528A>TCA387780095BRCA2c.4173A>T (p.Glu1391Asp)
c.3804A>T (p.Glu1268Asp)
n.4173A>T
 dbSNP
13g.32338529G>ACA019667BRCA2c.4174G>A (p.Val1392Ile)
c.3805G>A (p.Val1269Ile)
n.4174G>A
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32338529G>CCA387780098BRCA2c.4174G>C (p.Val1392Leu)
c.3805G>C (p.Val1269Leu)
n.4174G>C
 dbSNP
13g.32338529G=CA2082809162BRCA2c.4174G= (p.Val1392=)
c.3805G= (p.Val1269=)
n.4174G=
13g.32338529G>TCA387780100BRCA2c.4174G>T (p.Val1392Phe)
c.3805G>T (p.Val1269Phe)
n.4174G>T
 dbSNP
13g.32338529_32338530delinsGTCA2082809167BRCA2c.4174_4175delinsGT (p.Val1392=)
c.3805_3806delinsGT (p.Val1269=)
n.4174_4175delinsGT
13g.32338530T>ACA387780102BRCA2c.4175T>A (p.Val1392Asp)
c.3806T>A (p.Val1269Asp)
n.4175T>A
 dbSNP
13g.32338530T>CCA387780104BRCA2c.4175T>C (p.Val1392Ala)
c.3806T>C (p.Val1269Ala)
n.4175T>C
 dbSNP
13g.32338530T>GCA387780106BRCA2c.4175T>G (p.Val1392Gly)
c.3806T>G (p.Val1269Gly)
n.4175T>G
 dbSNP
13g.32338531delCA335700BRCA2c.4176del (p.Ala1393ArgfsTer17)
c.3807del (p.Ala1270ArgfsTer17)
n.4176del
 ClinVar dbSNP gnomAD v4
13g.32338531T>ACA483437876BRCA2c.4176T>A (p.Val1392=)
c.3807T>A (p.Val1269=)
n.4176T>A
 dbSNP
13g.32338531T>CCA483437877BRCA2c.4176T>C (p.Val1392=)
c.3807T>C (p.Val1269=)
n.4176T>C
13g.32338531T>GCA483437878BRCA2c.4176T>G (p.Val1392=)
c.3807T>G (p.Val1269=)
n.4176T>G
13g.32338531T=CA2082809178BRCA2c.4176T= (p.Val1392=)
c.3807T= (p.Val1269=)
n.4176T=
13g.32338532G>ACA387780112BRCA2c.4177G>A (p.Ala1393Thr)
c.3808G>A (p.Ala1270Thr)
n.4177G>A
 dbSNP
13g.32338532G>CCA387780109BRCA2c.4177G>C (p.Ala1393Pro)
c.3808G>C (p.Ala1270Pro)
n.4177G>C
 dbSNP
13g.32338532G>TCA387780111BRCA2c.4177G>T (p.Ala1393Ser)
c.3808G>T (p.Ala1270Ser)
n.4177G>T
 dbSNP
13g.32338532dupCA10579602BRCA2c.4177dup (p.Ala1393GlyfsTer10)
c.3808dup (p.Ala1270GlyfsTer10)
n.4177dup
 ClinVar dbSNP gnomAD v4
13g.32338533C>ACA387780113BRCA2c.4178C>A (p.Ala1393Glu)
c.3809C>A (p.Ala1270Glu)
n.4178C>A
 dbSNP
13g.32338533C=CA2082809188BRCA2c.4178C= (p.Ala1393=)
c.3809C= (p.Ala1270=)
n.4178C=
13g.32338533C>GCA019671BRCA2c.4178C>G (p.Ala1393Gly)
c.3809C>G (p.Ala1270Gly)
n.4178C>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32338533C>TCA019676BRCA2c.4178C>T (p.Ala1393Val)
c.3809C>T (p.Ala1270Val)
n.4178C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
13g.32338534G>ACA019680BRCA2c.4179G>A (p.Ala1393=)
c.3810G>A (p.Ala1270=)
n.4179G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
13g.32338534G>CCA483437882BRCA2c.4179G>C (p.Ala1393=)
c.3810G>C (p.Ala1270=)
n.4179G>C
 ClinVar dbSNP
13g.32338534G=CA2082809208BRCA2c.4179G= (p.Ala1393=)
c.3810G= (p.Ala1270=)
n.4179G=
13g.32338534G>TCA483437883BRCA2c.4179G>T (p.Ala1393=)
c.3810G>T (p.Ala1270=)
n.4179G>T
 dbSNP
13g.32338535A>CCA387780117BRCA2c.4180A>C (p.Lys1394Gln)
c.3811A>C (p.Lys1271Gln)
n.4180A>C
13g.32338535A>GCA387780118BRCA2c.4180A>G (p.Lys1394Glu)
c.3811A>G (p.Lys1271Glu)
n.4180A>G
13g.32338535A>TCA387780120BRCA2c.4180A>T (p.Lys1394Ter)
c.3811A>T (p.Lys1271Ter)
n.4180A>T
 dbSNP
13g.32338536A>CCA387780122BRCA2c.4181A>C (p.Lys1394Thr)
c.3812A>C (p.Lys1271Thr)
n.4181A>C
13g.32338536A>GCA387780124BRCA2c.4181A>G (p.Lys1394Arg)
c.3812A>G (p.Lys1271Arg)
n.4181A>G
 dbSNP
13g.32338536A>TCA387780126BRCA2c.4181A>T (p.Lys1394Ile)
c.3812A>T (p.Lys1271Ile)
n.4181A>T
 dbSNP
13g.32338537A>CCA387780128BRCA2c.4182A>C (p.Lys1394Asn)
c.3813A>C (p.Lys1271Asn)
n.4182A>C
13g.32338537A>GCA483437886BRCA2c.4182A>G (p.Lys1394=)
c.3813A>G (p.Lys1271=)
n.4182A>G
 ClinVar dbSNP
13g.32338537A>TCA387780130BRCA2c.4182A>T (p.Lys1394Asn)
c.3813A>T (p.Lys1271Asn)
n.4182A>T
 dbSNP
13g.32338537_32338538delinsAGCA2082809211BRCA2c.4182_4183delinsAG (p.Lys1394=)
c.3813_3814delinsAG (p.Lys1271=)
n.4182_4183delinsAG
13g.32338538delCA1139663190BRCA2c.4183del (p.Ala1395LeufsTer15)
c.3814del (p.Ala1272LeufsTer15)
n.4183del
 ClinVar dbSNP
13g.32338538G>ACA387780133BRCA2c.4183G>A (p.Ala1395Thr)
c.3814G>A (p.Ala1272Thr)
n.4183G>A
 dbSNP
13g.32338538G>CCA387780135BRCA2c.4183G>C (p.Ala1395Pro)
c.3814G>C (p.Ala1272Pro)
n.4183G>C
 dbSNP
13g.32338538G=CA2082809217BRCA2c.4183G= (p.Ala1395=)
c.3814G= (p.Ala1272=)
n.4183G=
13g.32338538G>TCA019684BRCA2c.4183G>T (p.Ala1395Ser)
c.3814G>T (p.Ala1272Ser)
n.4183G>T
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32338539C>ACA387780141BRCA2c.4184C>A (p.Ala1395Asp)
c.3815C>A (p.Ala1272Asp)
n.4184C>A
 dbSNP
13g.32338539C=CA2082809231BRCA2c.4184C= (p.Ala1395=)
c.3815C= (p.Ala1272=)
n.4184C=
13g.32338539C>GCA387780137BRCA2c.4184C>G (p.Ala1395Gly)
c.3815C>G (p.Ala1272Gly)
n.4184C>G
 dbSNP
13g.32338539C>TCA387780139BRCA2c.4184C>T (p.Ala1395Val)
c.3815C>T (p.Ala1272Val)
n.4184C>T
 ClinVar dbSNP
13g.32338539dupCA2573053809BRCA2c.4184dup (p.Gln1396SerfsTer7)
c.3815dup (p.Gln1273SerfsTer7)
n.4184dup
 ClinVar dbSNP gnomAD v4
13g.32338540T>ACA483437891BRCA2c.4185T>A (p.Ala1395=)
c.3816T>A (p.Ala1272=)
n.4185T>A
 dbSNP
13g.32338540T>CCA483437892BRCA2c.4185T>C (p.Ala1395=)
c.3816T>C (p.Ala1272=)
n.4185T>C
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32338540T>GCA483437894BRCA2c.4185T>G (p.Ala1395=)
c.3816T>G (p.Ala1272=)
n.4185T>G
 ClinVar dbSNP
13g.32338540T=CA2082809236BRCA2c.4185T= (p.Ala1395=)
c.3816T= (p.Ala1272=)
n.4185T=
13g.32338540_32338576delCA2580087257BRCA2c.4185_4221del (p.Gln1396SerfsTer2)
c.3816_3852del (p.Gln1273SerfsTer2)
n.4185_4221del
 ClinVar
13g.32338541C>ACA387780143BRCA2c.4186C>A (p.Gln1396Lys)
c.3817C>A (p.Gln1273Lys)
n.4186C>A
 ClinVar dbSNP
13g.32338541C=CA2082809241BRCA2c.4186C= (p.Gln1396=)
c.3817C= (p.Gln1273=)
n.4186C=
13g.32338541C>GCA6940758BRCA2c.4186C>G (p.Gln1396Glu)
c.3817C>G (p.Gln1273Glu)
n.4186C>G
 dbSNP ExAC
13g.32338541C>TCA387780145BRCA2c.4186C>T (p.Gln1396Ter)
c.3817C>T (p.Gln1273Ter)
n.4186C>T
 ClinVar dbSNP
13g.32338541_32338542delinsCACA2082809240BRCA2c.4186_4187delinsCA (p.Gln1396=)
c.3817_3818delinsCA (p.Gln1273=)
n.4186_4187delinsCA
13g.32338542A=CA2082809249BRCA2c.4187A= (p.Gln1396=)
c.3818A= (p.Gln1273=)
n.4187A=
13g.32338542A>CCA387780151BRCA2c.4187A>C (p.Gln1396Pro)
c.3818A>C (p.Gln1273Pro)
n.4187A>C
13g.32338542A>GCA019687BRCA2c.4187A>G (p.Gln1396Arg)
c.3818A>G (p.Gln1273Arg)
n.4187A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32338542A>TCA387780149BRCA2c.4187A>T (p.Gln1396Leu)
c.3818A>T (p.Gln1273Leu)
n.4187A>T
 dbSNP gnomAD v4
13g.32338543delCA019693BRCA2c.4188del (p.Glu1397LysfsTer13)
c.3819del (p.Glu1274LysfsTer13)
n.4188del
 ClinVar dbSNP
13g.32338543A=CA2082809256BRCA2c.4188A= (p.Gln1396=)
c.3819A= (p.Gln1273=)
n.4188A=
13g.32338543A>CCA387780153BRCA2c.4188A>C (p.Gln1396His)
c.3819A>C (p.Gln1273His)
n.4188A>C
13g.32338543A>GCA483437899BRCA2c.4188A>G (p.Gln1396=)
c.3819A>G (p.Gln1273=)
n.4188A>G
 ClinVar dbSNP gnomAD v4
13g.32338543A>TCA387780156BRCA2c.4188A>T (p.Gln1396His)
c.3819A>T (p.Gln1273His)
n.4188A>T
13g.32338544G>ACA019698BRCA2c.4189G>A (p.Glu1397Lys)
c.3820G>A (p.Glu1274Lys)
n.4189G>A
 ClinVar dbSNP gnomAD v4
13g.32338544G>CCA387780160BRCA2c.4189G>C (p.Glu1397Gln)
c.3820G>C (p.Glu1274Gln)
n.4189G>C
 ClinVar dbSNP
13g.32338544G=CA2082809262BRCA2c.4189G= (p.Glu1397=)
c.3820G= (p.Glu1274=)
n.4189G=
13g.32338544G>TCA387780162BRCA2c.4189G>T (p.Glu1397Ter)
c.3820G>T (p.Glu1274Ter)
n.4189G>T
 dbSNP
13g.32338545A=CA2082809269BRCA2c.4190A= (p.Glu1397=)
c.3821A= (p.Glu1274=)
n.4190A=
13g.32338545A>CCA387780164BRCA2c.4190A>C (p.Glu1397Ala)
c.3821A>C (p.Glu1274Ala)
n.4190A>C
 ClinVar dbSNP
13g.32338545A>GCA387780168BRCA2c.4190A>G (p.Glu1397Gly)
c.3821A>G (p.Glu1274Gly)
n.4190A>G
13g.32338545A>TCA387780166BRCA2c.4190A>T (p.Glu1397Val)
c.3821A>T (p.Glu1274Val)
n.4190A>T
 dbSNP
13g.32338546A>CCA387780169BRCA2c.4191A>C (p.Glu1397Asp)
c.3822A>C (p.Glu1274Asp)
n.4191A>C
13g.32338546A>GCA483437902BRCA2c.4191A>G (p.Glu1397=)
c.3822A>G (p.Glu1274=)
n.4191A>G
13g.32338546A>TCA387780171BRCA2c.4191A>T (p.Glu1397Asp)
c.3822A>T (p.Glu1274Asp)
n.4191A>T
 dbSNP
13g.32338547G>ACA10579603BRCA2c.4192G>A (p.Ala1398Thr)
c.3823G>A (p.Ala1275Thr)
n.4192G>A
 ClinVar dbSNP gnomAD v4
13g.32338547G>CCA387780173BRCA2c.4192G>C (p.Ala1398Pro)
c.3823G>C (p.Ala1275Pro)
n.4192G>C
 ClinVar dbSNP gnomAD v4
13g.32338547G=CA2082809276BRCA2c.4192G= (p.Ala1398=)
c.3823G= (p.Ala1275=)
n.4192G=
13g.32338547G>TCA387780175BRCA2c.4192G>T (p.Ala1398Ser)
c.3823G>T (p.Ala1275Ser)
n.4192G>T
13g.32338548C>ACA387780177BRCA2c.4193C>A (p.Ala1398Glu)
c.3824C>A (p.Ala1275Glu)
n.4193C>A
 dbSNP gnomAD v4
13g.32338548C=CA2082809284BRCA2c.4193C= (p.Ala1398=)
c.3824C= (p.Ala1275=)
n.4193C=
13g.32338548C>GCA387780179BRCA2c.4193C>G (p.Ala1398Gly)
c.3824C>G (p.Ala1275Gly)
n.4193C>G
 dbSNP
13g.32338548C>TCA387780180BRCA2c.4193C>T (p.Ala1398Val)
c.3824C>T (p.Ala1275Val)
n.4193C>T
 ClinVar dbSNP
13g.32338549A=CA2082809289BRCA2c.4194A= (p.Ala1398=)
c.3825A= (p.Ala1275=)
n.4194A=
13g.32338549A>CCA483437905BRCA2c.4194A>C (p.Ala1398=)
c.3825A>C (p.Ala1275=)
n.4194A>C
13g.32338549A>GCA483437907BRCA2c.4194A>G (p.Ala1398=)
c.3825A>G (p.Ala1275=)
n.4194A>G
 ClinVar dbSNP gnomAD v4
13g.32338549A>TCA483437906BRCA2c.4194A>T (p.Ala1398=)
c.3825A>T (p.Ala1275=)
n.4194A>T
 dbSNP
13g.32338550T>ACA387780181BRCA2c.4195T>A (p.Cys1399Ser)
c.3826T>A (p.Cys1276Ser)
n.4195T>A
 dbSNP
13g.32338550T>CCA019706BRCA2c.4195T>C (p.Cys1399Arg)
c.3826T>C (p.Cys1276Arg)
n.4195T>C
 ClinVar dbSNP
13g.32338550T>GCA387780185BRCA2c.4195T>G (p.Cys1399Gly)
c.3826T>G (p.Cys1276Gly)
n.4195T>G
13g.32338550T=CA2082809295BRCA2c.4195T= (p.Cys1399=)
c.3826T= (p.Cys1276=)
n.4195T=
13g.32338551G>ACA387780190BRCA2c.4196G>A (p.Cys1399Tyr)
c.3827G>A (p.Cys1276Tyr)
n.4196G>A
 dbSNP
13g.32338551G>CCA387780187BRCA2c.4196G>C (p.Cys1399Ser)
c.3827G>C (p.Cys1276Ser)
n.4196G>C
 dbSNP
13g.32338551G=CA2082809302BRCA2c.4196G= (p.Cys1399=)
c.3827G= (p.Cys1276=)
n.4196G=
13g.32338551G>TCA6940759BRCA2c.4196G>T (p.Cys1399Phe)
c.3827G>T (p.Cys1276Phe)
n.4196G>T
 ClinVar dbSNP ExAC gnomAD v2
13g.32338552T>ACA387780191BRCA2c.4197T>A (p.Cys1399Ter)
c.3828T>A (p.Cys1276Ter)
n.4197T>A
 ClinVar dbSNP
13g.32338552T>CCA483437909BRCA2c.4197T>C (p.Cys1399=)
c.3828T>C (p.Cys1276=)
n.4197T>C
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32338552T>GCA387780193BRCA2c.4197T>G (p.Cys1399Trp)
c.3828T>G (p.Cys1276Trp)
n.4197T>G
 dbSNP
13g.32338552T=CA2082809309BRCA2c.4197T= (p.Cys1399=)
c.3828T= (p.Cys1276=)
n.4197T=
13g.32338553C>ACA387780195BRCA2c.4198C>A (p.His1400Asn)
c.3829C>A (p.His1277Asn)
n.4198C>A
 dbSNP
13g.32338553C=CA2082809314BRCA2c.4198C= (p.His1400=)
c.3829C= (p.His1277=)
n.4198C=
13g.32338553C>GCA387780197BRCA2c.4198C>G (p.His1400Asp)
c.3829C>G (p.His1277Asp)
n.4198C>G
 dbSNP
13g.32338553C>TCA387780199BRCA2c.4198C>T (p.His1400Tyr)
c.3829C>T (p.His1277Tyr)
n.4198C>T
 ClinVar dbSNP
13g.32338554A=CA2082809318BRCA2c.4199A= (p.His1400=)
c.3830A= (p.His1277=)
n.4199A=
13g.32338554A>CCA387780201BRCA2c.4199A>C (p.His1400Pro)
c.3830A>C (p.His1277Pro)
n.4199A>C
13g.32338554A>GCA387780202BRCA2c.4199A>G (p.His1400Arg)
c.3830A>G (p.His1277Arg)
n.4199A>G
 ClinVar dbSNP gnomAD v4
13g.32338554A>TCA387780207BRCA2c.4199A>T (p.His1400Leu)
c.3830A>T (p.His1277Leu)
n.4199A>T
 dbSNP gnomAD v2 gnomAD v4
13g.32338555T>ACA387780209BRCA2c.4200T>A (p.His1400Gln)
c.3831T>A (p.His1277Gln)
n.4200T>A
 dbSNP
13g.32338555T>CCA483437913BRCA2c.4200T>C (p.His1400=)
c.3831T>C (p.His1277=)
n.4200T>C
 ClinVar dbSNP gnomAD v4
13g.32338555T>GCA387780211BRCA2c.4200T>G (p.His1400Gln)
c.3831T>G (p.His1277Gln)
n.4200T>G
 dbSNP
13g.32338555T=CA2082809324BRCA2c.4200T= (p.His1400=)
c.3831T= (p.His1277=)
n.4200T=
13g.32338556G>ACA387780213BRCA2c.4201G>A (p.Gly1401Ser)
c.3832G>A (p.Gly1278Ser)
n.4201G>A
 ClinVar dbSNP
13g.32338556G>CCA387780215BRCA2c.4201G>C (p.Gly1401Arg)
c.3832G>C (p.Gly1278Arg)
n.4201G>C
 dbSNP
13g.32338556G=CA2082809353BRCA2c.4201G= (p.Gly1401=)
c.3832G= (p.Gly1278=)
n.4201G=
13g.32338556G>TCA387780216BRCA2c.4201G>T (p.Gly1401Cys)
c.3832G>T (p.Gly1278Cys)
n.4201G>T
 dbSNP gnomAD v4
13g.32338557G>ACA387780220BRCA2c.4202G>A (p.Gly1401Asp)
c.3833G>A (p.Gly1278Asp)
n.4202G>A
 dbSNP
13g.32338557G>CCA019711BRCA2c.4202G>C (p.Gly1401Ala)
c.3833G>C (p.Gly1278Ala)
n.4202G>C
 ClinVar dbSNP
13g.32338557G=CA2082809359BRCA2c.4202G= (p.Gly1401=)
c.3833G= (p.Gly1278=)
n.4202G=
13g.32338557G>TCA387780218BRCA2c.4202G>T (p.Gly1401Val)
c.3833G>T (p.Gly1278Val)
n.4202G>T
 dbSNP
13g.32338558T>ACA483437915BRCA2c.4203T>A (p.Gly1401=)
c.3834T>A (p.Gly1278=)
n.4203T>A
13g.32338558T>CCA483437916BRCA2c.4203T>C (p.Gly1401=)
c.3834T>C (p.Gly1278=)
n.4203T>C
 ClinVar dbSNP
13g.32338558T>GCA483437917BRCA2c.4203T>G (p.Gly1401=)
c.3834T>G (p.Gly1278=)
n.4203T>G
 ClinVar
13g.32338560_32338562dupCA2622601020BRCA2c.4205_4207dup (p.Asn1402_Thr1403insAsn)
c.3836_3838dup (p.Asn1279_Thr1280insAsn)
n.4205_4207dup
 gnomAD v4
13g.32338559A=CA2082809368BRCA2c.4204A= (p.Asn1402=)
c.3835A= (p.Asn1279=)
n.4204A=
13g.32338559A>CCA019715BRCA2c.4204A>C (p.Asn1402His)
c.3835A>C (p.Asn1279His)
n.4204A>C
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32338559A>GCA387780223BRCA2c.4204A>G (p.Asn1402Asp)
c.3835A>G (p.Asn1279Asp)
n.4204A>G
 dbSNP
13g.32338559A>TCA387780225BRCA2c.4204A>T (p.Asn1402Tyr)
c.3835A>T (p.Asn1279Tyr)
n.4204A>T
 dbSNP
13g.32338560A>CCA387780227BRCA2c.4205A>C (p.Asn1402Thr)
c.3836A>C (p.Asn1279Thr)
n.4205A>C
13g.32338560A>GCA387780230BRCA2c.4205A>G (p.Asn1402Ser)
c.3836A>G (p.Asn1279Ser)
n.4205A>G
 ClinVar dbSNP
13g.32338560A>TCA387780233BRCA2c.4205A>T (p.Asn1402Ile)
c.3836A>T (p.Asn1279Ile)
n.4205A>T
 dbSNP
13g.32338561T>ACA387780235BRCA2c.4206T>A (p.Asn1402Lys)
c.3837T>A (p.Asn1279Lys)
n.4206T>A
 dbSNP
13g.32338561T>CCA10583101BRCA2c.4206T>C (p.Asn1402=)
c.3837T>C (p.Asn1279=)
n.4206T>C
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32338561T>GCA387780238BRCA2c.4206T>G (p.Asn1402Lys)
c.3837T>G (p.Asn1279Lys)
n.4206T>G
 dbSNP
13g.32338561T=CA2082809375BRCA2c.4206T= (p.Asn1402=)
c.3837T= (p.Asn1279=)
n.4206T=
13g.32338562_32338564delCA2499222157BRCA2c.4207_4209del (p.Thr1403del)
c.3838_3840del (p.Thr1280del)
n.4207_4209del
 ClinVar dbSNP
13g.32338562A=CA2082809382BRCA2c.4207A= (p.Thr1403=)
c.3838A= (p.Thr1280=)
n.4207A=
13g.32338562A>CCA387780240BRCA2c.4207A>C (p.Thr1403Pro)
c.3838A>C (p.Thr1280Pro)
n.4207A>C
 dbSNP
13g.32338562A>GCA387780242BRCA2c.4207A>G (p.Thr1403Ala)
c.3838A>G (p.Thr1280Ala)
n.4207A>G
 ClinVar dbSNP
13g.32338562A>TCA387780244BRCA2c.4207A>T (p.Thr1403Ser)
c.3838A>T (p.Thr1280Ser)
n.4207A>T
 dbSNP
13g.32338562dupCA2499222158BRCA2c.4207dup (p.Thr1403AsnfsTer4)
c.3838dup (p.Thr1280AsnfsTer4)
n.4207dup
13g.32338562_32338565delinsACTTCA2082809385BRCA2c.4207_4210delinsACTT (p.Thr1403=)
c.3838_3841delinsACTT (p.Thr1280=)
n.4207_4210delinsACTT
13g.32338563_32338567delCA2499222159BRCA2c.4208_4212del (p.Thr1403LysfsTer2)
c.3839_3843del (p.Thr1280LysfsTer2)
n.4208_4212del
 ClinVar dbSNP
13g.32338563C>ACA387780246BRCA2c.4208C>A (p.Thr1403Asn)
c.3839C>A (p.Thr1280Asn)
n.4208C>A
 dbSNP
13g.32338563C=CA2082809403BRCA2c.4208C= (p.Thr1403=)
c.3839C= (p.Thr1280=)
n.4208C=
13g.32338563C>GCA387780250BRCA2c.4208C>G (p.Thr1403Ser)
c.3839C>G (p.Thr1280Ser)
n.4208C>G
 ClinVar dbSNP COSMIC COSMIC
13g.32338563C>TCA387780248BRCA2c.4208C>T (p.Thr1403Ile)
c.3839C>T (p.Thr1280Ile)
n.4208C>T
 ClinVar dbSNP gnomAD v4
13g.32338564_32338566delCA2082809396BRCA2c.4209_4211del (p.Ser1404del)
c.3840_3842del (p.Ser1281del)
n.4209_4211del
 ClinVar dbSNP
13g.32338564T>ACA483437930BRCA2c.4209T>A (p.Thr1403=)
c.3840T>A (p.Thr1280=)
n.4209T>A
 ClinVar dbSNP
13g.32338564T>CCA483437926BRCA2c.4209T>C (p.Thr1403=)
c.3840T>C (p.Thr1280=)
n.4209T>C
 ClinVar dbSNP gnomAD v4
13g.32338564T>GCA483437929BRCA2c.4209T>G (p.Thr1403=)
c.3840T>G (p.Thr1280=)
n.4209T>G
13g.32338564T=CA2082809412BRCA2c.4209T= (p.Thr1403=)
c.3840T= (p.Thr1280=)
n.4209T=
13g.32338564_32338569delinsTTCAAACA2082809415BRCA2c.4209_4214delinsTTCAAA (p.Thr1403=)
c.3840_3845delinsTTCAAA (p.Thr1280=)
n.4209_4214delinsTTCAAA
13g.32338565T>ACA387780252BRCA2c.4210T>A (p.Ser1404Thr)
c.3841T>A (p.Ser1281Thr)
n.4210T>A
 dbSNP
13g.32338565T>CCA387780257BRCA2c.4210T>C (p.Ser1404Pro)
c.3841T>C (p.Ser1281Pro)
n.4210T>C
13g.32338565T>GCA387780255BRCA2c.4210T>G (p.Ser1404Ala)
c.3841T>G (p.Ser1281Ala)
n.4210T>G
13g.32338565_32338566delinsTCCA2082809420BRCA2c.4210_4211delinsTC (p.Ser1404=)
c.3841_3842delinsTC (p.Ser1281=)
n.4210_4211delinsTC
13g.32338566_32338570delCA019721BRCA2c.4211_4215del (p.Ser1404Ter)
c.3842_3846del (p.Ser1281Ter)
n.4211_4215del
 ClinVar dbSNP
13g.32338566delCA019731BRCA2c.4211del (p.Ser1404Ter)
c.3842del (p.Ser1281Ter)
n.4211del
 ClinVar dbSNP gnomAD v4
13g.32338566C>ACA387780259BRCA2c.4211C>A (p.Ser1404Ter)
c.3842C>A (p.Ser1281Ter)
n.4211C>A
 ClinVar dbSNP
13g.32338566C=CA2082809467BRCA2c.4211C= (p.Ser1404=)
c.3842C= (p.Ser1281=)
n.4211C=
13g.32338566C>GCA10589245BRCA2c.4211C>G (p.Ser1404Ter)
c.3842C>G (p.Ser1281Ter)
n.4211C>G
 ClinVar dbSNP gnomAD v4
13g.32338566C>TCA019726BRCA2c.4211C>T (p.Ser1404Leu)
c.3842C>T (p.Ser1281Leu)
n.4211C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32338567A>CCA483437934BRCA2c.4212A>C (p.Ser1404=)
c.3843A>C (p.Ser1281=)
n.4212A>C
 ClinVar
13g.32338567A>GCA483437935BRCA2c.4212A>G (p.Ser1404=)
c.3843A>G (p.Ser1281=)
n.4212A>G
13g.32338567A>TCA483437936BRCA2c.4212A>T (p.Ser1404=)
c.3843A>T (p.Ser1281=)
n.4212A>T
 dbSNP
13g.32338569_32338573delCA2695199717BRCA2c.4214_4218del (p.Asn1405ArgfsTer7)
c.3845_3849del (p.Asn1282ArgfsTer7)
n.4214_4218del
 ClinVar
13g.32338568A=CA2082809486BRCA2c.4213A= (p.Asn1405=)
c.3844A= (p.Asn1282=)
n.4213A=
13g.32338568A>CCA387780266BRCA2c.4213A>C (p.Asn1405His)
c.3844A>C (p.Asn1282His)
n.4213A>C
 ClinVar dbSNP
13g.32338568A>GCA387780264BRCA2c.4213A>G (p.Asn1405Asp)
c.3844A>G (p.Asn1282Asp)
n.4213A>G
 ClinVar dbSNP gnomAD v4
13g.32338568A>TCA387780268BRCA2c.4213A>T (p.Asn1405Tyr)
c.3844A>T (p.Asn1282Tyr)
n.4213A>T
 dbSNP
13g.32338569A>CCA387780270BRCA2c.4214A>C (p.Asn1405Thr)
c.3845A>C (p.Asn1282Thr)
n.4214A>C
13g.32338569A>GCA387780274BRCA2c.4214A>G (p.Asn1405Ser)
c.3845A>G (p.Asn1282Ser)
n.4214A>G
 ClinVar dbSNP
13g.32338569A>TCA387780272BRCA2c.4214A>T (p.Asn1405Ile)
c.3845A>T (p.Asn1282Ile)
n.4214A>T
 dbSNP
13g.32338570T>ACA387780275BRCA2c.4215T>A (p.Asn1405Lys)
c.3846T>A (p.Asn1282Lys)
n.4215T>A
 ClinVar
13g.32338570T>CCA483437938BRCA2c.4215T>C (p.Asn1405=)
c.3846T>C (p.Asn1282=)
n.4215T>C
13g.32338570T>GCA387780277BRCA2c.4215T>G (p.Asn1405Lys)
c.3846T>G (p.Asn1282Lys)
n.4215T>G
13g.32338570_32338573delinsTAAACA2082809497BRCA2c.4215_4218delinsTAAA (p.Asn1405=)
c.3846_3849delinsTAAA (p.Asn1282=)
n.4215_4218delinsTAAA
13g.32338570_32338574delinsTAAAGCA2082809500BRCA2c.4215_4219delinsTAAAG (p.Asn1405=)
c.3846_3850delinsTAAAG (p.Asn1282=)
n.4215_4219delinsTAAAG
13g.32338571A=CA2082809528BRCA2c.4216A= (p.Lys1406=)
c.3847A= (p.Lys1283=)
n.4216A=
13g.32338571A>CCA387780278BRCA2c.4216A>C (p.Lys1406Gln)
c.3847A>C (p.Lys1283Gln)
n.4216A>C
13g.32338571A>GCA10579604BRCA2c.4216A>G (p.Lys1406Glu)
c.3847A>G (p.Lys1283Glu)
n.4216A>G
 ClinVar dbSNP gnomAD v4
13g.32338571A>TCA387780281BRCA2c.4216A>T (p.Lys1406Ter)
c.3847A>T (p.Lys1283Ter)
n.4216A>T
 dbSNP
13g.32338571_32338573delCA019735BRCA2c.4216_4218del (p.Lys1406del)
c.3847_3849del (p.Lys1283del)
n.4216_4218del
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32338573_32338576delCA019739BRCA2c.4218_4221del (p.Lys1406AsnfsTer3)
c.3849_3852del (p.Lys1283AsnfsTer3)
n.4218_4221del
 ClinVar dbSNP gnomAD v4 COSMIC
13g.32338572A>CCA387780285BRCA2c.4217A>C (p.Lys1406Thr)
c.3848A>C (p.Lys1283Thr)
n.4217A>C
13g.32338572A>GCA387780287BRCA2c.4217A>G (p.Lys1406Arg)
c.3848A>G (p.Lys1283Arg)
n.4217A>G
13g.32338572A>TCA387780288BRCA2c.4217A>T (p.Lys1406Ile)
c.3848A>T (p.Lys1283Ile)
n.4217A>T
 dbSNP
13g.32338573A=CA2082809535BRCA2c.4218A= (p.Lys1406=)
c.3849A= (p.Lys1283=)
n.4218A=
13g.32338573A>CCA387780291BRCA2c.4218A>C (p.Lys1406Asn)
c.3849A>C (p.Lys1283Asn)
n.4218A>C
 ClinVar dbSNP
13g.32338573A>GCA483437942BRCA2c.4218A>G (p.Lys1406=)
c.3849A>G (p.Lys1283=)
n.4218A>G
 ClinVar dbSNP
13g.32338573A>TCA387780292BRCA2c.4218A>T (p.Lys1406Asn)
c.3849A>T (p.Lys1283Asn)
n.4218A>T
 dbSNP
13g.32338574G>ACA387780294BRCA2c.4219G>A (p.Glu1407Lys)
c.3850G>A (p.Glu1284Lys)
n.4219G>A
 dbSNP
13g.32338574G>CCA387780298BRCA2c.4219G>C (p.Glu1407Gln)
c.3850G>C (p.Glu1284Gln)
n.4219G>C
 dbSNP COSMIC COSMIC
13g.32338574G>TCA387780296BRCA2c.4219G>T (p.Glu1407Ter)
c.3850G>T (p.Glu1284Ter)
n.4219G>T
 ClinVar dbSNP
13g.32338574_32338575delinsGACA2082809546BRCA2c.4219_4220delinsGA (p.Glu1407=)
c.3850_3851delinsGA (p.Glu1284=)
n.4219_4220delinsGA
13g.32338575A=CA2082809563BRCA2c.4220A= (p.Glu1407=)
c.3851A= (p.Glu1284=)
n.4220A=
13g.32338575A>CCA387780300BRCA2c.4220A>C (p.Glu1407Ala)
c.3851A>C (p.Glu1284Ala)
n.4220A>C
13g.32338575A>GCA387780302BRCA2c.4220A>G (p.Glu1407Gly)
c.3851A>G (p.Glu1284Gly)
n.4220A>G
 ClinVar dbSNP gnomAD v4
13g.32338575A>TCA387780304BRCA2c.4220A>T (p.Glu1407Val)
c.3851A>T (p.Glu1284Val)
n.4220A>T
 ClinVar dbSNP
13g.32338576delCA10589246BRCA2c.4221del (p.Glu1407AspfsTer3)
c.3852del (p.Glu1284AspfsTer3)
n.4221del
 ClinVar dbSNP
13g.32338576A>CCA387780307BRCA2c.4221A>C (p.Glu1407Asp)
c.3852A>C (p.Glu1284Asp)
n.4221A>C
 dbSNP
13g.32338576A>GCA483437948BRCA2c.4221A>G (p.Glu1407=)
c.3852A>G (p.Glu1284=)
n.4221A>G
 dbSNP
13g.32338576A>TCA387780309BRCA2c.4221A>T (p.Glu1407Asp)
c.3852A>T (p.Glu1284Asp)
n.4221A>T
 dbSNP
13g.32338577_32338578delCA2580087261BRCA2c.4222_4223del (p.Gln1408ValfsTer5)
c.3853_3854del (p.Gln1285ValfsTer5)
n.4222_4223del
 ClinVar
13g.32338577C>ACA387780311BRCA2c.4222C>A (p.Gln1408Lys)
c.3853C>A (p.Gln1285Lys)
n.4222C>A
 ClinVar dbSNP gnomAD v4
13g.32338577C=CA2082809588BRCA2c.4222C= (p.Gln1408=)
c.3853C= (p.Gln1285=)
n.4222C=
13g.32338577C>GCA387780313BRCA2c.4222C>G (p.Gln1408Glu)
c.3853C>G (p.Gln1285Glu)
n.4222C>G
 dbSNP gnomAD v4
13g.32338577C>TCA019744BRCA2c.4222C>T (p.Gln1408Ter)
c.3853C>T (p.Gln1285Ter)
n.4222C>T
 ClinVar dbSNP gnomAD v4
13g.32338577dupCA2573149372BRCA2c.4222dup (p.Gln1408ProfsTer6)
c.3853dup (p.Gln1285ProfsTer6)
n.4222dup
 ClinVar dbSNP
13g.32338577_32338578delinsCACA2082809581BRCA2c.4222_4223delinsCA (p.Gln1408=)
c.3853_3854delinsCA (p.Gln1285=)
n.4222_4223delinsCA
13g.32338577_32338581delinsCAGTTCA2082809578BRCA2c.4222_4226delinsCAGTT (p.Gln1408=)
c.3853_3857delinsCAGTT (p.Gln1285=)
n.4222_4226delinsCAGTT
13g.32338578delCA019749BRCA2c.4223del (p.Gln1408ArgfsTer2)
c.3854del (p.Gln1285ArgfsTer2)
n.4223del
 ClinVar dbSNP
13g.32338578A=CA2082809603BRCA2c.4223A= (p.Gln1408=)
c.3854A= (p.Gln1285=)
n.4223A=
13g.32338578A>CCA387780320BRCA2c.4223A>C (p.Gln1408Pro)
c.3854A>C (p.Gln1285Pro)
n.4223A>C
13g.32338578A>GCA6940760BRCA2c.4223A>G (p.Gln1408Arg)
c.3854A>G (p.Gln1285Arg)
n.4223A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32338578A>TCA387780318BRCA2c.4223A>T (p.Gln1408Leu)
c.3854A>T (p.Gln1285Leu)
n.4223A>T
 dbSNP
13g.32338579_32338582delCA954694064BRCA2c.4224_4227del (p.Thr1410LeufsTer8)
c.3855_3858del (p.Thr1287LeufsTer8)
n.4224_4227del
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32338579G>ACA337867BRCA2c.4224G>A (p.Gln1408=)
c.3855G>A (p.Gln1285=)
n.4224G>A
 ClinVar dbSNP gnomAD v4
13g.32338579G>CCA387780322BRCA2c.4224G>C (p.Gln1408His)
c.3855G>C (p.Gln1285His)
n.4224G>C
13g.32338579G=CA2082809612BRCA2c.4224G= (p.Gln1408=)
c.3855G= (p.Gln1285=)
n.4224G=
13g.32338579G>TCA387780324BRCA2c.4224G>T (p.Gln1408His)
c.3855G>T (p.Gln1285His)
n.4224G>T
13g.32338580T>ACA387780326BRCA2c.4225T>A (p.Leu1409Ile)
c.3856T>A (p.Leu1286Ile)
n.4225T>A
 dbSNP
13g.32338580T>CCA483437957BRCA2c.4225T>C (p.Leu1409=)
c.3856T>C (p.Leu1286=)
n.4225T>C
 dbSNP
13g.32338580T>GCA387780328BRCA2c.4225T>G (p.Leu1409Val)
c.3856T>G (p.Leu1286Val)
n.4225T>G
 ClinVar dbSNP
13g.32338580T=CA2082809628BRCA2c.4225T= (p.Leu1409=)
c.3856T= (p.Leu1286=)
n.4225T=
13g.32338581T>ACA16606423BRCA2c.4226T>A (p.Leu1409Ter)
c.3857T>A (p.Leu1286Ter)
n.4226T>A
 ClinVar dbSNP
13g.32338581T>CCA387780330BRCA2c.4226T>C (p.Leu1409Ser)
c.3857T>C (p.Leu1286Ser)
n.4226T>C
 gnomAD v4
13g.32338581T>GCA387780332BRCA2c.4226T>G (p.Leu1409Ter)
c.3857T>G (p.Leu1286Ter)
n.4226T>G
13g.32338581T=CA2082809640BRCA2c.4226T= (p.Leu1409=)
c.3857T= (p.Leu1286=)
n.4226T=
13g.32338582A>CCA387780335BRCA2c.4227A>C (p.Leu1409Phe)
c.3858A>C (p.Leu1286Phe)
n.4227A>C
13g.32338582A>GCA483437958BRCA2c.4227A>G (p.Leu1409=)
c.3858A>G (p.Leu1286=)
n.4227A>G
13g.32338582A>TCA387780336BRCA2c.4227A>T (p.Leu1409Phe)
c.3858A>T (p.Leu1286Phe)
n.4227A>T
 dbSNP
13g.32338583dupCA10586066BRCA2c.4228dup (p.Thr1410AsnfsTer4)
c.3859dup (p.Thr1287AsnfsTer4)
n.4228dup
 ClinVar dbSNP
13g.32338582_32338583dupCA2697551729BRCA2c.4227_4228dup (p.Thr1410LysfsTer10)
c.3858_3859dup (p.Thr1287LysfsTer10)
n.4227_4228dup
 ClinVar
13g.32338583A>CCA387780342BRCA2c.4228A>C (p.Thr1410Pro)
c.3859A>C (p.Thr1287Pro)
n.4228A>C
 dbSNP
13g.32338583A>GCA387780341BRCA2c.4228A>G (p.Thr1410Ala)
c.3859A>G (p.Thr1287Ala)
n.4228A>G
 dbSNP
13g.32338583A>TCA387780339BRCA2c.4228A>T (p.Thr1410Ser)
c.3859A>T (p.Thr1287Ser)
n.4228A>T
 ClinVar dbSNP
13g.32338584C>ACA387780344BRCA2c.4229C>A (p.Thr1410Asn)
c.3860C>A (p.Thr1287Asn)
n.4229C>A
 ClinVar dbSNP
13g.32338584C=CA2082809658BRCA2c.4229C= (p.Thr1410=)
c.3860C= (p.Thr1287=)
n.4229C=
13g.32338584C>GCA387780346BRCA2c.4229C>G (p.Thr1410Ser)
c.3860C>G (p.Thr1287Ser)
n.4229C>G
 dbSNP
13g.32338584C>TCA387780348BRCA2c.4229C>T (p.Thr1410Ile)
c.3860C>T (p.Thr1287Ile)
n.4229C>T
 dbSNP
13g.32338584dupCA2739291771BRCA2c.4229dup (p.Ala1411CysfsTer3)
c.3860dup (p.Ala1288CysfsTer3)
n.4229dup
13g.32338584_32338585insACA10589247BRCA2c.4229_4230insA (p.Ala1411CysfsTer3)
c.3860_3861insA (p.Ala1288CysfsTer3)
n.4229_4230insA
 ClinVar dbSNP
13g.32338585T>ACA483437960BRCA2c.4230T>A (p.Thr1410=)
c.3861T>A (p.Thr1287=)
n.4230T>A
 dbSNP
13g.32338585T>CCA483437961BRCA2c.4230T>C (p.Thr1410=)
c.3861T>C (p.Thr1287=)
n.4230T>C
 dbSNP
13g.32338585T>GCA483437962BRCA2c.4230T>G (p.Thr1410=)
c.3861T>G (p.Thr1287=)
n.4230T>G
 ClinVar
13g.32338586G>ACA387780352BRCA2c.4231G>A (p.Ala1411Thr)
c.3862G>A (p.Ala1288Thr)
n.4231G>A
 dbSNP
13g.32338586G>CCA387780353BRCA2c.4231G>C (p.Ala1411Pro)
c.3862G>C (p.Ala1288Pro)
n.4231G>C
 dbSNP
13g.32338586G=CA2082809667BRCA2c.4231G= (p.Ala1411=)
c.3862G= (p.Ala1288=)
n.4231G=
13g.32338586G>TCA387780355BRCA2c.4231G>T (p.Ala1411Ser)
c.3862G>T (p.Ala1288Ser)
n.4231G>T
 ClinVar dbSNP gnomAD v2
13g.32338587C>ACA387780356BRCA2c.4232C>A (p.Ala1411Asp)
c.3863C>A (p.Ala1288Asp)
n.4232C>A
 dbSNP
13g.32338587C=CA2082809692BRCA2c.4232C= (p.Ala1411=)
c.3863C= (p.Ala1288=)
n.4232C=
13g.32338587C>GCA019754BRCA2c.4232C>G (p.Ala1411Gly)
c.3863C>G (p.Ala1288Gly)
n.4232C>G
 ClinVar dbSNP
13g.32338587C>TCA387780359BRCA2c.4232C>T (p.Ala1411Val)
c.3863C>T (p.Ala1288Val)
n.4232C>T
 dbSNP
13g.32338588T>ACA483437965BRCA2c.4233T>A (p.Ala1411=)
c.3864T>A (p.Ala1288=)
n.4233T>A
 dbSNP
13g.32338588T>CCA483437966BRCA2c.4233T>C (p.Ala1411=)
c.3864T>C (p.Ala1288=)
n.4233T>C
 ClinVar dbSNP
13g.32338588T>GCA483437969BRCA2c.4233T>G (p.Ala1411=)
c.3864T>G (p.Ala1288=)
n.4233T>G
13g.32338588T=CA2082809703BRCA2c.4233T= (p.Ala1411=)
c.3864T= (p.Ala1288=)
n.4233T=
13g.32338589A=CA2082809716BRCA2c.4234A= (p.Thr1412=)
c.3865A= (p.Thr1289=)
n.4234A=
13g.32338589A>CCA387780361BRCA2c.4234A>C (p.Thr1412Pro)
c.3865A>C (p.Thr1289Pro)
n.4234A>C
 ClinVar dbSNP
13g.32338589A>GCA387780363BRCA2c.4234A>G (p.Thr1412Ala)
c.3865A>G (p.Thr1289Ala)
n.4234A>G
 dbSNP
13g.32338589A>TCA387780365BRCA2c.4234A>T (p.Thr1412Ser)
c.3865A>T (p.Thr1289Ser)
n.4234A>T
 dbSNP
13g.32338589_32338591delinsCCA2831039687BRCA2c.4234_4236delinsC (p.Thr1412GlnfsTer10)
c.3865_3867delinsC (p.Thr1289GlnfsTer10)
n.4234_4236delinsC
13g.32338590C>ACA387780369BRCA2c.4235C>A (p.Thr1412Asn)
c.3866C>A (p.Thr1289Asn)
n.4235C>A
 dbSNP
13g.32338590C>GCA387780371BRCA2c.4235C>G (p.Thr1412Ser)
c.3866C>G (p.Thr1289Ser)
n.4235C>G
 dbSNP
13g.32338590C>TCA387780367BRCA2c.4235C>T (p.Thr1412Ile)
c.3866C>T (p.Thr1289Ile)
n.4235C>T
 dbSNP
13g.32338591T>ACA483437970BRCA2c.4236T>A (p.Thr1412=)
c.3867T>A (p.Thr1289=)
n.4236T>A
13g.32338591T>CCA483437971BRCA2c.4236T>C (p.Thr1412=)
c.3867T>C (p.Thr1289=)
n.4236T>C
13g.32338591T>GCA483437972BRCA2c.4236T>G (p.Thr1412=)
c.3867T>G (p.Thr1289=)
n.4236T>G
13g.32338591_32338592delinsTACA2082809717BRCA2c.4236_4237delinsTA (p.Thr1412=)
c.3867_3868delinsTA (p.Thr1289=)
n.4236_4237delinsTA
13g.32338592A=CA2082809724BRCA2c.4237A= (p.Lys1413=)
c.3868A= (p.Lys1290=)
n.4237A=
13g.32338592A>CCA387780375BRCA2c.4237A>C (p.Lys1413Gln)
c.3868A>C (p.Lys1290Gln)
n.4237A>C
13g.32338592A>GCA10577470BRCA2c.4237A>G (p.Lys1413Glu)
c.3868A>G (p.Lys1290Glu)
n.4237A>G
 ClinVar dbSNP gnomAD v4
13g.32338592A>TCA387780374BRCA2c.4237A>T (p.Lys1413Ter)
c.3868A>T (p.Lys1290Ter)
n.4237A>T
13g.32338595delCA919242550BRCA2c.4240del (p.Thr1414ArgfsTer5)
c.3871del (p.Thr1291ArgfsTer5)
n.4240del
 dbSNP
13g.32338593A>CCA387780378BRCA2c.4238A>C (p.Lys1413Thr)
c.3869A>C (p.Lys1290Thr)
n.4238A>C
13g.32338593A>GCA387780380BRCA2c.4238A>G (p.Lys1413Arg)
c.3869A>G (p.Lys1290Arg)
n.4238A>G
13g.32338593A>TCA387780381BRCA2c.4238A>T (p.Lys1413Ile)
c.3869A>T (p.Lys1290Ile)
n.4238A>T
 dbSNP
13g.32338594A>CCA387780385BRCA2c.4239A>C (p.Lys1413Asn)
c.3870A>C (p.Lys1290Asn)
n.4239A>C
 dbSNP
13g.32338594A>GCA483437975BRCA2c.4239A>G (p.Lys1413=)
c.3870A>G (p.Lys1290=)
n.4239A>G
 dbSNP
13g.32338594A>TCA387780386BRCA2c.4239A>T (p.Lys1413Asn)
c.3870A>T (p.Lys1290Asn)
n.4239A>T
 dbSNP
13g.32338595A=CA2082809733BRCA2c.4240A= (p.Thr1414=)
c.3871A= (p.Thr1291=)
n.4240A=
13g.32338595A>CCA387780388BRCA2c.4240A>C (p.Thr1414Pro)
c.3871A>C (p.Thr1291Pro)
n.4240A>C
 dbSNP
13g.32338595A>GCA10583102BRCA2c.4240A>G (p.Thr1414Ala)
c.3871A>G (p.Thr1291Ala)
n.4240A>G
 ClinVar dbSNP gnomAD v4
13g.32338595A>TCA387780390BRCA2c.4240A>T (p.Thr1414Ser)
c.3871A>T (p.Thr1291Ser)
n.4240A>T
 dbSNP
13g.32338596C>ACA387780394BRCA2c.4241C>A (p.Thr1414Lys)
c.3872C>A (p.Thr1291Lys)
n.4241C>A
 dbSNP
13g.32338596C=CA2082809753BRCA2c.4241C= (p.Thr1414=)
c.3872C= (p.Thr1291=)
n.4241C=
13g.32338596C>GCA387780392BRCA2c.4241C>G (p.Thr1414Arg)
c.3872C>G (p.Thr1291Arg)
n.4241C>G
13g.32338596C>TCA019759BRCA2c.4241C>T (p.Thr1414Met)
c.3872C>T (p.Thr1291Met)
n.4241C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32338597G>ACA10579605BRCA2c.4242G>A (p.Thr1414=)
c.3873G>A (p.Thr1291=)
n.4242G>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32338597G>CCA483437979BRCA2c.4242G>C (p.Thr1414=)
c.3873G>C (p.Thr1291=)
n.4242G>C
 dbSNP
13g.32338597G=CA2082809764BRCA2c.4242G= (p.Thr1414=)
c.3873G= (p.Thr1291=)
n.4242G=
13g.32338597G>TCA019766BRCA2c.4242G>T (p.Thr1414=)
c.3873G>T (p.Thr1291=)
n.4242G>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32338598G>ACA6940761BRCA2c.4243G>A (p.Glu1415Lys)
c.3874G>A (p.Glu1292Lys)
n.4243G>A
 dbSNP ExAC gnomAD v2 gnomAD v4
13g.32338598G>CCA387780398BRCA2c.4243G>C (p.Glu1415Gln)
c.3874G>C (p.Glu1292Gln)
n.4243G>C
 ClinVar dbSNP
13g.32338598G=CA2082809776BRCA2c.4243G= (p.Glu1415=)
c.3874G= (p.Glu1292=)
n.4243G=
13g.32338598G>TCA019770BRCA2c.4243G>T (p.Glu1415Ter)
c.3874G>T (p.Glu1292Ter)
n.4243G>T
 ClinVar dbSNP gnomAD v4
13g.32338599A=CA2082809788BRCA2c.4244A= (p.Glu1415=)
c.3875A= (p.Glu1292=)
n.4244A=
13g.32338599A>CCA387780401BRCA2c.4244A>C (p.Glu1415Ala)
c.3875A>C (p.Glu1292Ala)
n.4244A>C
13g.32338599A>GCA16613961BRCA2c.4244A>G (p.Glu1415Gly)
c.3875A>G (p.Glu1292Gly)
n.4244A>G
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32338599A>TCA387780403BRCA2c.4244A>T (p.Glu1415Val)
c.3875A>T (p.Glu1292Val)
n.4244A>T
13g.32338599_32338600delinsAGCA2082809782BRCA2c.4244_4245delinsAG (p.Glu1415=)
c.3875_3876delinsAG (p.Glu1292=)
n.4244_4245delinsAG
13g.32338600delCA6940762BRCA2c.4245del (p.Glu1415AspfsTer4)
c.3876del (p.Glu1292AspfsTer4)
n.4245del
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32338600G>ACA019776BRCA2c.4245G>A (p.Glu1415=)
c.3876G>A (p.Glu1292=)
n.4245G>A
 ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC
13g.32338600G>CCA387780407BRCA2c.4245G>C (p.Glu1415Asp)
c.3876G>C (p.Glu1292Asp)
n.4245G>C
 dbSNP gnomAD v4
13g.32338600G=CA2082809799BRCA2c.4245G= (p.Glu1415=)
c.3876G= (p.Glu1292=)
n.4245G=
13g.32338600G>TCA387780409BRCA2c.4245G>T (p.Glu1415Asp)
c.3876G>T (p.Glu1292Asp)
n.4245G>T
 dbSNP
13g.32338601C>ACA387780413BRCA2c.4246C>A (p.Gln1416Lys)
c.3877C>A (p.Gln1293Lys)
n.4246C>A
 dbSNP gnomAD v4
13g.32338601C=CA2082809826BRCA2c.4246C= (p.Gln1416=)
c.3877C= (p.Gln1293=)
n.4246C=
13g.32338601C>GCA387780415BRCA2c.4246C>G (p.Gln1416Glu)
c.3877C>G (p.Gln1293Glu)
n.4246C>G
 dbSNP
13g.32338601C>TCA019781BRCA2c.4246C>T (p.Gln1416Ter)
c.3877C>T (p.Gln1293Ter)
n.4246C>T
 ClinVar dbSNP
13g.32338601_32338602delinsCACA2082809822BRCA2c.4246_4247delinsCA (p.Gln1416=)
c.3877_3878delinsCA (p.Gln1293=)
n.4246_4247delinsCA
13g.32338602A=CA2082809839BRCA2c.4247A= (p.Gln1416=)
c.3878A= (p.Gln1293=)
n.4247A=
13g.32338602A>CCA387780416BRCA2c.4247A>C (p.Gln1416Pro)
c.3878A>C (p.Gln1293Pro)
n.4247A>C
13g.32338602A>GCA387780419BRCA2c.4247A>G (p.Gln1416Arg)
c.3878A>G (p.Gln1293Arg)
n.4247A>G
 ClinVar dbSNP
13g.32338602A>TCA387780420BRCA2c.4247A>T (p.Gln1416Leu)
c.3878A>T (p.Gln1293Leu)
n.4247A>T
 ClinVar
13g.32338605dupCA1139663192BRCA2c.4250dup (p.Asn1417LysfsTer6)
c.3881dup (p.Asn1294LysfsTer6)
n.4250dup
 ClinVar dbSNP
13g.32338605delCA247507399BRCA2c.4250del (p.Asn1417IlefsTer2)
c.3881del (p.Asn1294IlefsTer2)
n.4250del
 dbSNP
13g.32338603A=CA2082809846BRCA2c.4248A= (p.Gln1416=)
c.3879A= (p.Gln1293=)
n.4248A=
13g.32338603A>CCA387780424BRCA2c.4248A>C (p.Gln1416His)
c.3879A>C (p.Gln1293His)
n.4248A>C
13g.32338603A>GCA019784BRCA2c.4248A>G (p.Gln1416=)
c.3879A>G (p.Gln1293=)
n.4248A>G
 ClinVar dbSNP gnomAD v4
13g.32338603A>TCA387780426BRCA2c.4248A>T (p.Gln1416His)
c.3879A>T (p.Gln1293His)
n.4248A>T
 dbSNP
13g.32338604A>CCA387780428BRCA2c.4249A>C (p.Asn1417His)
c.3880A>C (p.Asn1294His)
n.4249A>C
13g.32338604A>GCA387780430BRCA2c.4249A>G (p.Asn1417Asp)
c.3880A>G (p.Asn1294Asp)
n.4249A>G
13g.32338604A>TCA387780432BRCA2c.4249A>T (p.Asn1417Tyr)
c.3880A>T (p.Asn1294Tyr)
n.4249A>T
13g.32338605A>CCA387780435BRCA2c.4250A>C (p.Asn1417Thr)
c.3881A>C (p.Asn1294Thr)
n.4250A>C
13g.32338605A>GCA387780436BRCA2c.4250A>G (p.Asn1417Ser)
c.3881A>G (p.Asn1294Ser)
n.4250A>G
13g.32338605A>TCA387780438BRCA2c.4250A>T (p.Asn1417Ile)
c.3881A>T (p.Asn1294Ile)
n.4250A>T
 dbSNP
13g.32338606T>ACA387780442BRCA2c.4251T>A (p.Asn1417Lys)
c.3882T>A (p.Asn1294Lys)
n.4251T>A
 dbSNP
13g.32338606T>CCA16606682BRCA2c.4251T>C (p.Asn1417=)
c.3882T>C (p.Asn1294=)
n.4251T>C
 ClinVar dbSNP gnomAD v3 gnomAD v4
13g.32338606T>GCA387780440BRCA2c.4251T>G (p.Asn1417Lys)
c.3882T>G (p.Asn1294Lys)
n.4251T>G
13g.32338606T=CA2082809853BRCA2c.4251T= (p.Asn1417=)
c.3882T= (p.Asn1294=)
n.4251T=
13g.32338606_32338610delinsTATAACA2082809852BRCA2c.4251_4255delinsTATAA (p.Asn1417=)
c.3882_3886delinsTATAA (p.Asn1294=)
n.4251_4255delinsTATAA
13g.32338607A=CA2082809864BRCA2c.4252A= (p.Ile1418=)
c.3883A= (p.Ile1295=)
n.4252A=
13g.32338607A>CCA6940763BRCA2c.4252A>C (p.Ile1418Leu)
c.3883A>C (p.Ile1295Leu)
n.4252A>C
 dbSNP ExAC gnomAD v2
13g.32338607A>GCA019793BRCA2c.4252A>G (p.Ile1418Val)
c.3883A>G (p.Ile1295Val)
n.4252A>G
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.32338607A>TCA387780446BRCA2c.4252A>T (p.Ile1418Leu)
c.3883A>T (p.Ile1295Leu)
n.4252A>T
 dbSNP
13g.32338607_32338610delinsTCA10586521BRCA2c.4252_4255delinsT (p.Ile1418Ter)
c.3883_3886delinsT (p.Ile1295Ter)
n.4252_4255delinsT
 ClinVar dbSNP
13g.32338608delCA2580087267BRCA2c.4253del (p.Ile1418LysfsTer30)
c.3884del (p.Ile1295LysfsTer30)
n.4253del
 ClinVar
13g.32338608T>ACA387780449BRCA2c.4253T>A (p.Ile1418Lys)
c.3884T>A (p.Ile1295Lys)
n.4253T>A
13g.32338608T>CCA6940764BRCA2c.4253T>C (p.Ile1418Thr)
c.3884T>C (p.Ile1295Thr)
n.4253T>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32338608T>GCA387780451BRCA2c.4253T>G (p.Ile1418Arg)
c.3884T>G (p.Ile1295Arg)
n.4253T>G
13g.32338608T=CA2082809892BRCA2c.4253T= (p.Ile1418=)
c.3884T= (p.Ile1295=)
n.4253T=
13g.32338608_32338610delinsTAACA2082809883BRCA2c.4253_4255delinsTAA (p.Ile1418=)
c.3884_3886delinsTAA (p.Ile1295=)
n.4253_4255delinsTAA
13g.32338609A=CA2082809899BRCA2c.4254A= (p.Ile1418=)
c.3885A= (p.Ile1295=)
n.4254A=
13g.32338609A>CCA483437995BRCA2c.4254A>C (p.Ile1418=)
c.3885A>C (p.Ile1295=)
n.4254A>C
13g.32338609A>GCA16619702BRCA2c.4254A>G (p.Ile1418Met)
c.3885A>G (p.Ile1295Met)
n.4254A>G
 ClinVar dbSNP gnomAD v4
13g.32338609A>TCA483437996BRCA2c.4254A>T (p.Ile1418=)
c.3885A>T (p.Ile1295=)
n.4254A>T
 dbSNP
13g.32338612delCA2573053810BRCA2c.4257del (p.Asp1420IlefsTer28)
c.3888del (p.Asp1297IlefsTer28)
n.4257del
 ClinVar dbSNP
13g.32338611_32338612delCA609453787BRCA2c.4256_4257del (p.Lys1419ArgfsTer3)
c.3887_3888del (p.Lys1296ArgfsTer3)
n.4256_4257del
 ClinVar dbSNP gnomAD v2 gnomAD v4
13g.32338610A=CA2082809906BRCA2c.4255A= (p.Lys1419=)
c.3886A= (p.Lys1296=)
n.4255A=
13g.32338610A>CCA387780454BRCA2c.4255A>C (p.Lys1419Gln)
c.3886A>C (p.Lys1296Gln)
n.4255A>C
 ClinVar dbSNP
13g.32338610A>GCA387780456BRCA2c.4255A>G (p.Lys1419Glu)
c.3886A>G (p.Lys1296Glu)
n.4255A>G
 dbSNP
13g.32338610A>TCA387780457BRCA2c.4255A>T (p.Lys1419Ter)
c.3886A>T (p.Lys1296Ter)
n.4255A>T
 dbSNP
13g.32338611A=CA2082809914BRCA2c.4256A= (p.Lys1419=)
c.3887A= (p.Lys1296=)
n.4256A=
13g.32338611A>CCA387780460BRCA2c.4256A>C (p.Lys1419Thr)
c.3887A>C (p.Lys1296Thr)
n.4256A>C
 ClinVar
13g.32338611A>GCA387780461BRCA2c.4256A>G (p.Lys1419Arg)
c.3887A>G (p.Lys1296Arg)
n.4256A>G
 gnomAD v4
13g.32338611A>TCA387780462BRCA2c.4256A>T (p.Lys1419Ile)
c.3887A>T (p.Lys1296Ile)
n.4256A>T
 ClinVar dbSNP
13g.32338612A>CCA387780466BRCA2c.4257A>C (p.Lys1419Asn)
c.3888A>C (p.Lys1296Asn)
n.4257A>C
13g.32338612A>GCA483437998BRCA2c.4257A>G (p.Lys1419=)
c.3888A>G (p.Lys1296=)
n.4257A>G
 dbSNP
13g.32338612A>TCA387780464BRCA2c.4257A>T (p.Lys1419Asn)
c.3888A>T (p.Lys1296Asn)
n.4257A>T
 dbSNP
13g.32338612_32338613delinsAGCA2082809917BRCA2c.4257_4258delinsAG (p.Lys1419=)
c.3888_3889delinsAG (p.Lys1296=)
n.4257_4258delinsAG
13g.32338613delCA019805BRCA2c.4258del (p.Asp1420IlefsTer28)
c.3889del (p.Asp1297IlefsTer28)
n.4258del
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
13g.32338613G>ACA387780469BRCA2c.4258G>A (p.Asp1420Asn)
c.3889G>A (p.Asp1297Asn)
n.4258G>A
 dbSNP COSMIC COSMIC
13g.32338613G>CCA387780470BRCA2c.4258G>C (p.Asp1420His)
c.3889G>C (p.Asp1297His)
n.4258G>C
 dbSNP
13g.32338613G=CA2082809925BRCA2c.4258G= (p.Asp1420=)
c.3889G= (p.Asp1297=)
n.4258G=
13g.32338613G>TCA019810BRCA2c.4258G>T (p.Asp1420Tyr)
c.3889G>T (p.Asp1297Tyr)
n.4258G>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.32338614A=CA2082809933BRCA2c.4259A= (p.Asp1420=)
c.3890A= (p.Asp1297=)
n.4259A=
13g.32338614A>CCA387780473BRCA2c.4259A>C (p.Asp1420Ala)
c.3890A>C (p.Asp1297Ala)
n.4259A>C
13g.32338614A>GCA387780475BRCA2c.4259A>G (p.Asp1420Gly)
c.3890A>G (p.Asp1297Gly)
n.4259A>G
13g.32338614A>TCA387780477BRCA2c.4259A>T (p.Asp1420Val)
c.3890A>T (p.Asp1297Val)
n.4259A>T
 ClinVar dbSNP
13g.32338614dupCA2575387649BRCA2c.4259dup (p.Asp1420GlufsTer3)
c.3890dup (p.Asp1297GlufsTer3)
n.4259dup
13g.32338615T>ACA387780481BRCA2c.4260T>A (p.Asp1420Glu)
c.3891T>A (p.Asp1297Glu)
n.4260T>A
 dbSNP
13g.32338615T>CCA483438002BRCA2c.4260T>C (p.Asp1420=)
c.3891T>C (p.Asp1297=)
n.4260T>C
13g.32338615T>GCA387780479BRCA2c.4260T>G (p.Asp1420Glu)
c.3891T>G (p.Asp1297Glu)
n.4260T>G
 dbSNP
13g.32338615delinsAACA2499222161BRCA2c.4260delinsAA (p.Asp1420GlufsTer3)
c.3891delinsAA (p.Asp1297GlufsTer3)
n.4260delinsAA
 ClinVar dbSNP
13g.32338618dupCA16619703BRCA2c.4263dup (p.Glu1422Ter)
c.3894dup (p.Glu1299Ter)
n.4263dup
 ClinVar dbSNP gnomAD v4
13g.32338619_32338638delCA2499222160BRCA2c.4264_4283del (p.Glu1422SerfsTer9)
c.3895_3914del (p.Glu1299SerfsTer9)
n.4264_4283del
13g.32338616T>ACA387780484BRCA2c.4261T>A (p.Phe1421Ile)
c.3892T>A (p.Phe1298Ile)
n.4261T>A
 dbSNP
13g.32338616T>CCA10583103BRCA2c.4261T>C (p.Phe1421Leu)
c.3892T>C (p.Phe1298Leu)
n.4261T>C
 ClinVar dbSNP gnomAD v4
13g.32338616T>GCA387780495BRCA2c.4261T>G (p.Phe1421Val)
c.3892T>G (p.Phe1298Val)
n.4261T>G
13g.32338616T=CA2082809951BRCA2c.4261T= (p.Phe1421=)
c.3892T= (p.Phe1298=)
n.4261T=
13g.32338616_32338623delinsTTTGAGACCA2082809955BRCA2c.4261_4268delinsTTTGAGAC (p.Phe1421=)
c.3892_3899delinsTTTGAGAC (p.Phe1298=)
n.4261_4268delinsTTTGAGAC

Number of alleles fetched