Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.16828817T>ACA10635349CUBNc.10752A>T (p.Pro3584=)
c.6738A>T (p.Pro2246=)
c.6714A>T (p.Pro2238=)
c.6594A>T (p.Pro2198=)
ClinVar dbSNP gnomAD v4
10g.16828817T>CCA468407417CUBNc.10752A>G (p.Pro3584=)
c.6738A>G (p.Pro2246=)
c.6714A>G (p.Pro2238=)
c.6594A>G (p.Pro2198=)
dbSNP gnomAD v4
10g.16828817T>GCA468407416CUBNc.10752A>C (p.Pro3584=)
c.6738A>C (p.Pro2246=)
c.6714A>C (p.Pro2238=)
c.6594A>C (p.Pro2198=)
10g.16828817T=CA1893313736CUBNc.10752A= (p.Pro3584=)
c.6738A= (p.Pro2246=)
c.6714A= (p.Pro2238=)
c.6594A= (p.Pro2198=)
10g.16828818G>ACA376119762CUBNc.10751C>T (p.Pro3584Leu)
c.6737C>T (p.Pro2246Leu)
c.6713C>T (p.Pro2238Leu)
c.6593C>T (p.Pro2198Leu)
10g.16828818G>CCA376119764CUBNc.10751C>G (p.Pro3584Arg)
c.6737C>G (p.Pro2246Arg)
c.6713C>G (p.Pro2238Arg)
c.6593C>G (p.Pro2198Arg)
10g.16828818G>TCA376119766CUBNc.10751C>A (p.Pro3584Gln)
c.6737C>A (p.Pro2246Gln)
c.6713C>A (p.Pro2238Gln)
c.6593C>A (p.Pro2198Gln)
10g.16828819G>ACA376119768CUBNc.10750C>T (p.Pro3584Ser)
c.6736C>T (p.Pro2246Ser)
c.6712C>T (p.Pro2238Ser)
c.6592C>T (p.Pro2198Ser)
10g.16828819G>CCA376119770CUBNc.10750C>G (p.Pro3584Ala)
c.6736C>G (p.Pro2246Ala)
c.6712C>G (p.Pro2238Ala)
c.6592C>G (p.Pro2198Ala)
10g.16828819G>TCA376119772CUBNc.10750C>A (p.Pro3584Thr)
c.6736C>A (p.Pro2246Thr)
c.6712C>A (p.Pro2238Thr)
c.6592C>A (p.Pro2198Thr)
10g.16828820T>ACA468407423CUBNc.10749A>T (p.Gly3583=)
c.6735A>T (p.Gly2245=)
c.6711A>T (p.Gly2237=)
c.6591A>T (p.Gly2197=)
10g.16828820T>CCA468407424CUBNc.10749A>G (p.Gly3583=)
c.6735A>G (p.Gly2245=)
c.6711A>G (p.Gly2237=)
c.6591A>G (p.Gly2197=)
dbSNP gnomAD v3 gnomAD v4
10g.16828820T>GCA468407426CUBNc.10749A>C (p.Gly3583=)
c.6735A>C (p.Gly2245=)
c.6711A>C (p.Gly2237=)
c.6591A>C (p.Gly2197=)
10g.16828820T=CA1893313738CUBNc.10749A= (p.Gly3583=)
c.6735A= (p.Gly2245=)
c.6711A= (p.Gly2237=)
c.6591A= (p.Gly2197=)
10g.16828821C>ACA376119773CUBNc.10748G>T (p.Gly3583Val)
c.6734G>T (p.Gly2245Val)
c.6710G>T (p.Gly2237Val)
c.6590G>T (p.Gly2197Val)
10g.16828821C>GCA376119774CUBNc.10748G>C (p.Gly3583Ala)
c.6734G>C (p.Gly2245Ala)
c.6710G>C (p.Gly2237Ala)
c.6590G>C (p.Gly2197Ala)
10g.16828821C>TCA376119775CUBNc.10748G>A (p.Gly3583Glu)
c.6734G>A (p.Gly2245Glu)
c.6710G>A (p.Gly2237Glu)
c.6590G>A (p.Gly2197Glu)
10g.16828822C>ACA376119778CUBNc.10747G>T (p.Gly3583Ter)
c.6733G>T (p.Gly2245Ter)
c.6709G>T (p.Gly2237Ter)
c.6589G>T (p.Gly2197Ter)
10g.16828822C>GCA376119780CUBNc.10747G>C (p.Gly3583Arg)
c.6733G>C (p.Gly2245Arg)
c.6709G>C (p.Gly2237Arg)
c.6589G>C (p.Gly2197Arg)
10g.16828822C>TCA376119782CUBNc.10747G>A (p.Gly3583Arg)
c.6733G>A (p.Gly2245Arg)
c.6709G>A (p.Gly2237Arg)
c.6589G>A (p.Gly2197Arg)
10g.16828822_16828824delinsCAGCA1893313739CUBNc.10745_10747delinsCTG (p.Ser3582=)
c.6731_6733delinsCTG (p.Ser2244=)
c.6707_6709delinsCTG (p.Ser2236=)
c.6587_6589delinsCTG (p.Ser2196=)
10g.16828823A=CA1893313742CUBNc.10746T= (p.Ser3582=)
c.6732T= (p.Ser2244=)
c.6708T= (p.Ser2236=)
c.6588T= (p.Ser2196=)
10g.16828823A>CCA468407445CUBNc.10746T>G (p.Ser3582=)
c.6732T>G (p.Ser2244=)
c.6708T>G (p.Ser2236=)
c.6588T>G (p.Ser2196=)
10g.16828823A>GCA203533530CUBNc.10746T>C (p.Ser3582=)
c.6732T>C (p.Ser2244=)
c.6708T>C (p.Ser2236=)
c.6588T>C (p.Ser2196=)
dbSNP
10g.16828823A>TCA468407447CUBNc.10746T>A (p.Ser3582=)
c.6732T>A (p.Ser2244=)
c.6708T>A (p.Ser2236=)
c.6588T>A (p.Ser2196=)
10g.16828825_16828826dupCA2608396465CUBNc.10745_10746dup (p.Gly3583LeufsTer11)
c.6731_6732dup (p.Gly2245LeufsTer11)
c.6707_6708dup (p.Gly2237LeufsTer11)
c.6587_6588dup (p.Gly2197LeufsTer11)
gnomAD v4
10g.16828825_16828826delCA925381904CUBNc.10745_10746del (p.Ser3582TrpfsTer27)
c.6731_6732del (p.Ser2244TrpfsTer27)
c.6707_6708del (p.Ser2236TrpfsTer27)
c.6587_6588del (p.Ser2196TrpfsTer27)
dbSNP gnomAD v3 gnomAD v4
10g.16828824G>ACA376119788CUBNc.10745C>T (p.Ser3582Phe)
c.6731C>T (p.Ser2244Phe)
c.6707C>T (p.Ser2236Phe)
c.6587C>T (p.Ser2196Phe)
COSMIC
10g.16828824G>CCA376119789CUBNc.10745C>G (p.Ser3582Cys)
c.6731C>G (p.Ser2244Cys)
c.6707C>G (p.Ser2236Cys)
c.6587C>G (p.Ser2196Cys)
10g.16828824G>TCA376119792CUBNc.10745C>A (p.Ser3582Tyr)
c.6731C>A (p.Ser2244Tyr)
c.6707C>A (p.Ser2236Tyr)
c.6587C>A (p.Ser2196Tyr)
10g.16828825A>CCA376119794CUBNc.10744T>G (p.Ser3582Ala)
c.6730T>G (p.Ser2244Ala)
c.6706T>G (p.Ser2236Ala)
c.6586T>G (p.Ser2196Ala)
10g.16828825A>GCA376119795CUBNc.10744T>C (p.Ser3582Pro)
c.6730T>C (p.Ser2244Pro)
c.6706T>C (p.Ser2236Pro)
c.6586T>C (p.Ser2196Pro)
10g.16828825A>TCA376119796CUBNc.10744T>A (p.Ser3582Thr)
c.6730T>A (p.Ser2244Thr)
c.6706T>A (p.Ser2236Thr)
c.6586T>A (p.Ser2196Thr)
10g.16828826G>ACA468407452CUBNc.10743C>T (p.Ser3581=)
c.6729C>T (p.Ser2243=)
c.6705C>T (p.Ser2235=)
c.6585C>T (p.Ser2195=)
10g.16828826G>CCA468407450CUBNc.10743C>G (p.Ser3581=)
c.6729C>G (p.Ser2243=)
c.6705C>G (p.Ser2235=)
c.6585C>G (p.Ser2195=)
gnomAD v4
10g.16828826G>TCA468407451CUBNc.10743C>A (p.Ser3581=)
c.6729C>A (p.Ser2243=)
c.6705C>A (p.Ser2235=)
c.6585C>A (p.Ser2195=)
COSMIC
10g.16828826_16828848delCA2574500155CUBNc.10721_10743del (p.Gly3574ValfsTer28)
c.6707_6729del (p.Gly2236ValfsTer28)
c.6683_6705del (p.Gly2228ValfsTer28)
c.6563_6585del (p.Gly2188ValfsTer28)
10g.16828827G>ACA376119799CUBNc.10742C>T (p.Ser3581Phe)
c.6728C>T (p.Ser2243Phe)
c.6704C>T (p.Ser2235Phe)
c.6584C>T (p.Ser2195Phe)
ClinVar dbSNP
10g.16828827G>CCA376119800CUBNc.10742C>G (p.Ser3581Cys)
c.6728C>G (p.Ser2243Cys)
c.6704C>G (p.Ser2235Cys)
c.6584C>G (p.Ser2195Cys)
COSMIC
10g.16828827G>TCA376119802CUBNc.10742C>A (p.Ser3581Tyr)
c.6728C>A (p.Ser2243Tyr)
c.6704C>A (p.Ser2235Tyr)
c.6584C>A (p.Ser2195Tyr)
10g.16828828A>CCA376119804CUBNc.10741T>G (p.Ser3581Ala)
c.6727T>G (p.Ser2243Ala)
c.6703T>G (p.Ser2235Ala)
c.6583T>G (p.Ser2195Ala)
10g.16828828A>GCA376119806CUBNc.10741T>C (p.Ser3581Pro)
c.6727T>C (p.Ser2243Pro)
c.6703T>C (p.Ser2235Pro)
c.6583T>C (p.Ser2195Pro)
10g.16828828A>TCA376119808CUBNc.10741T>A (p.Ser3581Thr)
c.6727T>A (p.Ser2243Thr)
c.6703T>A (p.Ser2235Thr)
c.6583T>A (p.Ser2195Thr)
10g.16828829T>ACA468407456CUBNc.10740A>T (p.Pro3580=)
c.6726A>T (p.Pro2242=)
c.6702A>T (p.Pro2234=)
c.6582A>T (p.Pro2194=)
10g.16828829T>CCA468407457CUBNc.10740A>G (p.Pro3580=)
c.6726A>G (p.Pro2242=)
c.6702A>G (p.Pro2234=)
c.6582A>G (p.Pro2194=)
10g.16828829T>GCA468407458CUBNc.10740A>C (p.Pro3580=)
c.6726A>C (p.Pro2242=)
c.6702A>C (p.Pro2234=)
c.6582A>C (p.Pro2194=)
10g.16828830G>ACA376119810CUBNc.10739C>T (p.Pro3580Leu)
c.6725C>T (p.Pro2242Leu)
c.6701C>T (p.Pro2234Leu)
c.6581C>T (p.Pro2194Leu)
gnomAD v4
10g.16828830G>CCA376119812CUBNc.10739C>G (p.Pro3580Arg)
c.6725C>G (p.Pro2242Arg)
c.6701C>G (p.Pro2234Arg)
c.6581C>G (p.Pro2194Arg)
10g.16828830G>TCA376119809CUBNc.10739C>A (p.Pro3580Gln)
c.6725C>A (p.Pro2242Gln)
c.6701C>A (p.Pro2234Gln)
c.6581C>A (p.Pro2194Gln)
10g.16828831G>ACA376119814CUBNc.10738C>T (p.Pro3580Ser)
c.6724C>T (p.Pro2242Ser)
c.6700C>T (p.Pro2234Ser)
c.6580C>T (p.Pro2194Ser)

Number of alleles fetched