Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.16825001C>ACA5422272CUBNc.10846G>T (p.Ala3616Ser)
c.6832G>T (p.Ala2278Ser)
c.6808G>T (p.Ala2270Ser)
c.6688G>T (p.Ala2230Ser)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.16825001C=CA1893309963CUBNc.10846G= (p.Ala3616=)
c.6832G= (p.Ala2278=)
c.6808G= (p.Ala2270=)
c.6688G= (p.Ala2230=)
10g.16825001C>GCA376118607CUBNc.10846G>C (p.Ala3616Pro)
c.6832G>C (p.Ala2278Pro)
c.6808G>C (p.Ala2270Pro)
c.6688G>C (p.Ala2230Pro)
10g.16825001C>TCA5422271CUBNc.10846G>A (p.Ala3616Thr)
c.6832G>A (p.Ala2278Thr)
c.6808G>A (p.Ala2270Thr)
c.6688G>A (p.Ala2230Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.16825002G>ACA5422273CUBNc.10845C>T (p.Ser3615=)
c.6831C>T (p.Ser2277=)
c.6807C>T (p.Ser2269=)
c.6687C>T (p.Ser2229=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.16825002G>CCA468298478CUBNc.10845C>G (p.Ser3615=)
c.6831C>G (p.Ser2277=)
c.6807C>G (p.Ser2269=)
c.6687C>G (p.Ser2229=)
10g.16825002G=CA1893309964CUBNc.10845C= (p.Ser3615=)
c.6831C= (p.Ser2277=)
c.6807C= (p.Ser2269=)
c.6687C= (p.Ser2229=)
10g.16825002G>TCA468298479CUBNc.10845C>A (p.Ser3615=)
c.6831C>A (p.Ser2277=)
c.6807C>A (p.Ser2269=)
c.6687C>A (p.Ser2229=)
10g.16825003G>ACA203531531CUBNc.10844C>T (p.Ser3615Phe)
c.6830C>T (p.Ser2277Phe)
c.6806C>T (p.Ser2269Phe)
c.6686C>T (p.Ser2229Phe)
dbSNP
10g.16825003G>CCA376118612CUBNc.10844C>G (p.Ser3615Cys)
c.6830C>G (p.Ser2277Cys)
c.6806C>G (p.Ser2269Cys)
c.6686C>G (p.Ser2229Cys)
10g.16825003G=CA1893309966CUBNc.10844C= (p.Ser3615=)
c.6830C= (p.Ser2277=)
c.6806C= (p.Ser2269=)
c.6686C= (p.Ser2229=)
10g.16825003G>TCA376118613CUBNc.10844C>A (p.Ser3615Tyr)
c.6830C>A (p.Ser2277Tyr)
c.6806C>A (p.Ser2269Tyr)
c.6686C>A (p.Ser2229Tyr)
10g.16825004A=CA1893309970CUBNc.10843T= (p.Ser3615=)
c.6829T= (p.Ser2277=)
c.6805T= (p.Ser2269=)
c.6685T= (p.Ser2229=)
10g.16825004A>CCA376118615CUBNc.10843T>G (p.Ser3615Ala)
c.6829T>G (p.Ser2277Ala)
c.6805T>G (p.Ser2269Ala)
c.6685T>G (p.Ser2229Ala)
10g.16825004A>GCA376118616CUBNc.10843T>C (p.Ser3615Pro)
c.6829T>C (p.Ser2277Pro)
c.6805T>C (p.Ser2269Pro)
c.6685T>C (p.Ser2229Pro)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.16825004A>TCA376118619CUBNc.10843T>A (p.Ser3615Thr)
c.6829T>A (p.Ser2277Thr)
c.6805T>A (p.Ser2269Thr)
c.6685T>A (p.Ser2229Thr)
10g.16825005T>ACA468298480CUBNc.10842A>T (p.Pro3614=)
c.6828A>T (p.Pro2276=)
c.6804A>T (p.Pro2268=)
c.6684A>T (p.Pro2228=)
10g.16825005T>CCA468298481CUBNc.10842A>G (p.Pro3614=)
c.6828A>G (p.Pro2276=)
c.6804A>G (p.Pro2268=)
c.6684A>G (p.Pro2228=)
10g.16825005T>GCA468298482CUBNc.10842A>C (p.Pro3614=)
c.6828A>C (p.Pro2276=)
c.6804A>C (p.Pro2268=)
c.6684A>C (p.Pro2228=)
10g.16825006G>ACA376118626CUBNc.10841C>T (p.Pro3614Leu)
c.6827C>T (p.Pro2276Leu)
c.6803C>T (p.Pro2268Leu)
c.6683C>T (p.Pro2228Leu)
10g.16825006G>CCA376118622CUBNc.10841C>G (p.Pro3614Arg)
c.6827C>G (p.Pro2276Arg)
c.6803C>G (p.Pro2268Arg)
c.6683C>G (p.Pro2228Arg)
gnomAD v4
10g.16825006G>TCA376118624CUBNc.10841C>A (p.Pro3614Gln)
c.6827C>A (p.Pro2276Gln)
c.6803C>A (p.Pro2268Gln)
c.6683C>A (p.Pro2228Gln)
10g.16825006_16825013delCA2608396282CUBNc.10834_10841del (p.Arg3612IlefsTer13)
c.6820_6827del (p.Arg2274IlefsTer13)
c.6796_6803del (p.Arg2266IlefsTer13)
c.6676_6683del (p.Arg2226IlefsTer13)
gnomAD v4
10g.16825007G>ACA376118628CUBNc.10840C>T (p.Pro3614Ser)
c.6826C>T (p.Pro2276Ser)
c.6802C>T (p.Pro2268Ser)
c.6682C>T (p.Pro2228Ser)
10g.16825007G>CCA376118630CUBNc.10840C>G (p.Pro3614Ala)
c.6826C>G (p.Pro2276Ala)
c.6802C>G (p.Pro2268Ala)
c.6682C>G (p.Pro2228Ala)
10g.16825007G>TCA376118631CUBNc.10840C>A (p.Pro3614Thr)
c.6826C>A (p.Pro2276Thr)
c.6802C>A (p.Pro2268Thr)
c.6682C>A (p.Pro2228Thr)
gnomAD v4
10g.16825008A>CCA468298483CUBNc.10839T>G (p.Arg3613=)
c.6825T>G (p.Arg2275=)
c.6801T>G (p.Arg2267=)
c.6681T>G (p.Arg2227=)
10g.16825008A>GCA468298484CUBNc.10839T>C (p.Arg3613=)
c.6825T>C (p.Arg2275=)
c.6801T>C (p.Arg2267=)
c.6681T>C (p.Arg2227=)
gnomAD v4
10g.16825008A>TCA468298485CUBNc.10839T>A (p.Arg3613=)
c.6825T>A (p.Arg2275=)
c.6801T>A (p.Arg2267=)
c.6681T>A (p.Arg2227=)
10g.16825009C>ACA376118634CUBNc.10838G>T (p.Arg3613Leu)
c.6824G>T (p.Arg2275Leu)
c.6800G>T (p.Arg2267Leu)
c.6680G>T (p.Arg2227Leu)
10g.16825009C=CA1893309972CUBNc.10838G= (p.Arg3613=)
c.6824G= (p.Arg2275=)
c.6800G= (p.Arg2267=)
c.6680G= (p.Arg2227=)
10g.16825009C>GCA376118635CUBNc.10838G>C (p.Arg3613Pro)
c.6824G>C (p.Arg2275Pro)
c.6800G>C (p.Arg2267Pro)
c.6680G>C (p.Arg2227Pro)
10g.16825009C>TCA5422274CUBNc.10838G>A (p.Arg3613His)
c.6824G>A (p.Arg2275His)
c.6800G>A (p.Arg2267His)
c.6680G>A (p.Arg2227His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.16825010G>ACA5422275CUBNc.10837C>T (p.Arg3613Cys)
c.6823C>T (p.Arg2275Cys)
c.6799C>T (p.Arg2267Cys)
c.6679C>T (p.Arg2227Cys)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.16825010G>CCA376118637CUBNc.10837C>G (p.Arg3613Gly)
c.6823C>G (p.Arg2275Gly)
c.6799C>G (p.Arg2267Gly)
c.6679C>G (p.Arg2227Gly)
10g.16825010G=CA1893309974CUBNc.10837C= (p.Arg3613=)
c.6823C= (p.Arg2275=)
c.6799C= (p.Arg2267=)
c.6679C= (p.Arg2227=)
10g.16825010G>TCA376118638CUBNc.10837C>A (p.Arg3613Ser)
c.6823C>A (p.Arg2275Ser)
c.6799C>A (p.Arg2267Ser)
c.6679C>A (p.Arg2227Ser)
COSMIC
10g.16825010_16825011delinsGCCA1893309977CUBNc.10836_10837delinsGC (p.Arg3612=)
c.6822_6823delinsGC (p.Arg2274=)
c.6798_6799delinsGC (p.Arg2266=)
c.6678_6679delinsGC (p.Arg2226=)
10g.16825011C>ACA468298486CUBNc.10836G>T (p.Arg3612=)
c.6822G>T (p.Arg2274=)
c.6798G>T (p.Arg2266=)
c.6678G>T (p.Arg2226=)
10g.16825011C>GCA468298487CUBNc.10836G>C (p.Arg3612=)
c.6822G>C (p.Arg2274=)
c.6798G>C (p.Arg2266=)
c.6678G>C (p.Arg2226=)
10g.16825011C>TCA468298488CUBNc.10836G>A (p.Arg3612=)
c.6822G>A (p.Arg2274=)
c.6798G>A (p.Arg2266=)
c.6678G>A (p.Arg2226=)
10g.16825012delCA1893309981CUBNc.10836del (p.Arg3613ValfsTer7)
c.6822del (p.Arg2275ValfsTer7)
c.6798del (p.Arg2267ValfsTer7)
c.6678del (p.Arg2227ValfsTer7)
dbSNP
10g.16825012C>ACA376118640CUBNc.10835G>T (p.Arg3612Leu)
c.6821G>T (p.Arg2274Leu)
c.6797G>T (p.Arg2266Leu)
c.6677G>T (p.Arg2226Leu)
10g.16825012C=CA1893309985CUBNc.10835G= (p.Arg3612=)
c.6821G= (p.Arg2274=)
c.6797G= (p.Arg2266=)
c.6677G= (p.Arg2226=)
10g.16825012C>GCA376118642CUBNc.10835G>C (p.Arg3612Pro)
c.6821G>C (p.Arg2274Pro)
c.6797G>C (p.Arg2266Pro)
c.6677G>C (p.Arg2226Pro)
10g.16825012C>TCA5422276CUBNc.10835G>A (p.Arg3612Gln)
c.6821G>A (p.Arg2274Gln)
c.6797G>A (p.Arg2266Gln)
c.6677G>A (p.Arg2226Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.16825013G>ACA5422277CUBNc.10834C>T (p.Arg3612Trp)
c.6820C>T (p.Arg2274Trp)
c.6796C>T (p.Arg2266Trp)
c.6676C>T (p.Arg2226Trp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.16825013G>CCA376118645CUBNc.10834C>G (p.Arg3612Gly)
c.6820C>G (p.Arg2274Gly)
c.6796C>G (p.Arg2266Gly)
c.6676C>G (p.Arg2226Gly)
10g.16825013G=CA1893309989CUBNc.10834C= (p.Arg3612=)
c.6820C= (p.Arg2274=)
c.6796C= (p.Arg2266=)
c.6676C= (p.Arg2226=)
10g.16825013G>TCA468298489CUBNc.10834C>A (p.Arg3612=)
c.6820C>A (p.Arg2274=)
c.6796C>A (p.Arg2266=)
c.6676C>A (p.Arg2226=)

Number of alleles fetched