Chr Mutation (hg38) CAid Gene Transcript Linkouts
20g.61928150C>ACA2653589312CDH4c.1772-40C>A (n.1772-40C>A)
c.1550-40C>A (n.1550-40C>A)
c.1490-40C>A (n.1490-40C>A)
c.1661-40C>A (n.1661-40C>A)
gnomAD v4
20g.61928150C=CA2373989163CDH4c.1772-40C= (n.1772-40C=)
c.1550-40C= (n.1550-40C=)
c.1490-40C= (n.1490-40C=)
c.1661-40C= (n.1661-40C=)
20g.61928150C>TCA636608668CDH4c.1772-40C>T (n.1772-40C>T)
c.1550-40C>T (n.1550-40C>T)
c.1490-40C>T (n.1490-40C>T)
c.1661-40C>T (n.1661-40C>T)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
20g.61928151delCA1019134440CDH4c.1772-39del (n.1772-39del)
c.1550-39del (n.1550-39del)
c.1490-39del (n.1490-39del)
c.1661-39del (n.1661-39del)
20g.61928151C>ACA636608669CDH4c.1772-39C>A (n.1772-39C>A)
c.1550-39C>A (n.1550-39C>A)
c.1490-39C>A (n.1490-39C>A)
c.1661-39C>A (n.1661-39C>A)
dbSNP gnomAD v2 gnomAD v4
20g.61928151C=CA2373989164CDH4c.1772-39C= (n.1772-39C=)
c.1550-39C= (n.1550-39C=)
c.1490-39C= (n.1490-39C=)
c.1661-39C= (n.1661-39C=)
20g.61928153G>ACA1019134445CDH4c.1772-37G>A (n.1772-37G>A)
c.1550-37G>A (n.1550-37G>A)
c.1490-37G>A (n.1490-37G>A)
c.1661-37G>A (n.1661-37G>A)
gnomAD v4
20g.61928153G>CCA2595659491CDH4c.1772-37G>C (n.1772-37G>C)
c.1550-37G>C (n.1550-37G>C)
c.1490-37G>C (n.1490-37G>C)
c.1661-37G>C (n.1661-37G>C)
dbSNP gnomAD v3 gnomAD v4
20g.61928153G=CA2373989165CDH4c.1772-37G= (n.1772-37G=)
c.1550-37G= (n.1550-37G=)
c.1490-37G= (n.1490-37G=)
c.1661-37G= (n.1661-37G=)
20g.61928153G>TCA636608670CDH4c.1772-37G>T (n.1772-37G>T)
c.1550-37G>T (n.1550-37G>T)
c.1490-37G>T (n.1490-37G>T)
c.1661-37G>T (n.1661-37G>T)
dbSNP gnomAD v2 gnomAD v4
20g.61928154G>ACA636608671CDH4c.1772-36G>A (n.1772-36G>A)
c.1550-36G>A (n.1550-36G>A)
c.1490-36G>A (n.1490-36G>A)
c.1661-36G>A (n.1661-36G>A)
dbSNP gnomAD v2
20g.61928154G=CA2373989166CDH4c.1772-36G= (n.1772-36G=)
c.1550-36G= (n.1550-36G=)
c.1490-36G= (n.1490-36G=)
c.1661-36G= (n.1661-36G=)
20g.61928156G>ACA9934866CDH4c.1772-34G>A (n.1772-34G>A)
c.1550-34G>A (n.1550-34G>A)
c.1490-34G>A (n.1490-34G>A)
c.1661-34G>A (n.1661-34G>A)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.61928156G=CA2373989167CDH4c.1772-34G= (n.1772-34G=)
c.1550-34G= (n.1550-34G=)
c.1490-34G= (n.1490-34G=)
c.1661-34G= (n.1661-34G=)
20g.61928157T>CCA636608672CDH4c.1772-33T>C (n.1772-33T>C)
c.1550-33T>C (n.1550-33T>C)
c.1490-33T>C (n.1490-33T>C)
c.1661-33T>C (n.1661-33T>C)
dbSNP gnomAD v2 gnomAD v4
20g.61928157T=CA2373989168CDH4c.1772-33T= (n.1772-33T=)
c.1550-33T= (n.1550-33T=)
c.1490-33T= (n.1490-33T=)
c.1661-33T= (n.1661-33T=)
20g.61928158G>ACA2653589313CDH4c.1772-32G>A (n.1772-32G>A)
c.1550-32G>A (n.1550-32G>A)
c.1490-32G>A (n.1490-32G>A)
c.1661-32G>A (n.1661-32G>A)
gnomAD v4
20g.61928159G>CCA2653589314CDH4c.1772-31G>C (n.1772-31G>C)
c.1550-31G>C (n.1550-31G>C)
c.1490-31G>C (n.1490-31G>C)
c.1661-31G>C (n.1661-31G>C)
gnomAD v4
20g.61928159_61928160delinsGCCA2373989169CDH4c.1772-31_1772-30delinsGC (n.1772-31_1772-30delinsGC)
c.1550-31_1550-30delinsGC (n.1550-31_1550-30delinsGC)
c.1490-31_1490-30delinsGC (n.1490-31_1490-30delinsGC)
c.1661-31_1661-30delinsGC (n.1661-31_1661-30delinsGC)
20g.61928160C>ACA2653589315CDH4c.1772-30C>A (n.1772-30C>A)
c.1550-30C>A (n.1550-30C>A)
c.1490-30C>A (n.1490-30C>A)
c.1661-30C>A (n.1661-30C>A)
gnomAD v4
20g.61928160C>TCA2653589316CDH4c.1772-30C>T (n.1772-30C>T)
c.1550-30C>T (n.1550-30C>T)
c.1490-30C>T (n.1490-30C>T)
c.1661-30C>T (n.1661-30C>T)
gnomAD v4
20g.61928162delCA636608674CDH4c.1772-28del (n.1772-28del)
c.1550-28del (n.1550-28del)
c.1490-28del (n.1490-28del)
c.1661-28del (n.1661-28del)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
20g.61928162C>ACA9934867CDH4c.1772-28C>A (n.1772-28C>A)
c.1550-28C>A (n.1550-28C>A)
c.1490-28C>A (n.1490-28C>A)
c.1661-28C>A (n.1661-28C>A)
dbSNP ExAC gnomAD v2 gnomAD v4
20g.61928162C=CA2373989170CDH4c.1772-28C= (n.1772-28C=)
c.1550-28C= (n.1550-28C=)
c.1490-28C= (n.1490-28C=)
c.1661-28C= (n.1661-28C=)
20g.61928162C>GCA636608675CDH4c.1772-28C>G (n.1772-28C>G)
c.1550-28C>G (n.1550-28C>G)
c.1490-28C>G (n.1490-28C>G)
c.1661-28C>G (n.1661-28C>G)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
20g.61928162C>TCA636608676CDH4c.1772-28C>T (n.1772-28C>T)
c.1550-28C>T (n.1550-28C>T)
c.1490-28C>T (n.1490-28C>T)
c.1661-28C>T (n.1661-28C>T)
dbSNP gnomAD v2 gnomAD v4
20g.61928163G>ACA9934868CDH4c.1772-27G>A (n.1772-27G>A)
c.1550-27G>A (n.1550-27G>A)
c.1490-27G>A (n.1490-27G>A)
c.1661-27G>A (n.1661-27G>A)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.61928163G=CA2373989171CDH4c.1772-27G= (n.1772-27G=)
c.1550-27G= (n.1550-27G=)
c.1490-27G= (n.1490-27G=)
c.1661-27G= (n.1661-27G=)
20g.61928163G>TCA2653589317CDH4c.1772-27G>T (n.1772-27G>T)
c.1550-27G>T (n.1550-27G>T)
c.1490-27G>T (n.1490-27G>T)
c.1661-27G>T (n.1661-27G>T)
gnomAD v4
20g.61928164T>CCA2577441270CDH4c.1772-26T>C (n.1772-26T>C)
c.1550-26T>C (n.1550-26T>C)
c.1490-26T>C (n.1490-26T>C)
c.1661-26T>C (n.1661-26T>C)
20g.61928164T>GCA9934869CDH4c.1772-26T>G (n.1772-26T>G)
c.1550-26T>G (n.1550-26T>G)
c.1490-26T>G (n.1490-26T>G)
c.1661-26T>G (n.1661-26T>G)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.61928164T=CA2373989172CDH4c.1772-26T= (n.1772-26T=)
c.1550-26T= (n.1550-26T=)
c.1490-26T= (n.1490-26T=)
c.1661-26T= (n.1661-26T=)
20g.61928164_61928167delinsTGTGCA2373989173CDH4c.1772-26_1772-23delinsTGTG (n.1772-26_1772-23delinsTGTG)
c.1550-26_1550-23delinsTGTG (n.1550-26_1550-23delinsTGTG)
c.1490-26_1490-23delinsTGTG (n.1490-26_1490-23delinsTGTG)
c.1661-26_1661-23delinsTGTG (n.1661-26_1661-23delinsTGTG)
20g.61928165G>ACA2373989175CDH4c.1772-25G>A (n.1772-25G>A)
c.1550-25G>A (n.1550-25G>A)
c.1490-25G>A (n.1490-25G>A)
c.1661-25G>A (n.1661-25G>A)
dbSNP
20g.61928165G=CA2373989176CDH4c.1772-25G= (n.1772-25G=)
c.1550-25G= (n.1550-25G=)
c.1490-25G= (n.1490-25G=)
c.1661-25G= (n.1661-25G=)
20g.61928165G>TCA2653589318CDH4c.1772-25G>T (n.1772-25G>T)
c.1550-25G>T (n.1550-25G>T)
c.1490-25G>T (n.1490-25G>T)
c.1661-25G>T (n.1661-25G>T)
gnomAD v4
20g.61928168_61928170delCA2373989174CDH4c.1772-22_1772-20del (n.1772-22_1772-20del)
c.1550-22_1550-20del (n.1550-22_1550-20del)
c.1490-22_1490-20del (n.1490-22_1490-20del)
c.1661-22_1661-20del (n.1661-22_1661-20del)
dbSNP
20g.61928166T>CCA2373989178CDH4c.1772-24T>C (n.1772-24T>C)
c.1550-24T>C (n.1550-24T>C)
c.1490-24T>C (n.1490-24T>C)
c.1661-24T>C (n.1661-24T>C)
dbSNP
20g.61928166T=CA2373989177CDH4c.1772-24T= (n.1772-24T=)
c.1550-24T= (n.1550-24T=)
c.1490-24T= (n.1490-24T=)
c.1661-24T= (n.1661-24T=)
20g.61928167G>CCA2653589319CDH4c.1772-23G>C (n.1772-23G>C)
c.1550-23G>C (n.1550-23G>C)
c.1490-23G>C (n.1490-23G>C)
c.1661-23G>C (n.1661-23G>C)
gnomAD v4
20g.61928167G>TCA2653589320CDH4c.1772-23G>T (n.1772-23G>T)
c.1550-23G>T (n.1550-23G>T)
c.1490-23G>T (n.1490-23G>T)
c.1661-23G>T (n.1661-23G>T)
gnomAD v4
20g.61928168G>ACA1019134455CDH4c.1772-22G>A (n.1772-22G>A)
c.1550-22G>A (n.1550-22G>A)
c.1490-22G>A (n.1490-22G>A)
c.1661-22G>A (n.1661-22G>A)
dbSNP gnomAD v3 gnomAD v4
20g.61928168G=CA2373989179CDH4c.1772-22G= (n.1772-22G=)
c.1550-22G= (n.1550-22G=)
c.1490-22G= (n.1490-22G=)
c.1661-22G= (n.1661-22G=)
20g.61928168G>TCA2653589321CDH4c.1772-22G>T (n.1772-22G>T)
c.1550-22G>T (n.1550-22G>T)
c.1490-22G>T (n.1490-22G>T)
c.1661-22G>T (n.1661-22G>T)
gnomAD v4
20g.61928170G>ACA636608677CDH4c.1772-20G>A (n.1772-20G>A)
c.1550-20G>A (n.1550-20G>A)
c.1490-20G>A (n.1490-20G>A)
c.1661-20G>A (n.1661-20G>A)
dbSNP gnomAD v2 gnomAD v4
20g.61928170G=CA2373989180CDH4c.1772-20G= (n.1772-20G=)
c.1550-20G= (n.1550-20G=)
c.1490-20G= (n.1490-20G=)
c.1661-20G= (n.1661-20G=)
20g.61928170G>TCA2653589322CDH4c.1772-20G>T (n.1772-20G>T)
c.1550-20G>T (n.1550-20G>T)
c.1490-20G>T (n.1490-20G>T)
c.1661-20G>T (n.1661-20G>T)
gnomAD v4
20g.61928172C>ACA2653589323CDH4c.1772-18C>A (n.1772-18C>A)
c.1550-18C>A (n.1550-18C>A)
c.1490-18C>A (n.1490-18C>A)
c.1661-18C>A (n.1661-18C>A)
gnomAD v4
20g.61928172C=CA2373989181CDH4c.1772-18C= (n.1772-18C=)
c.1550-18C= (n.1550-18C=)
c.1490-18C= (n.1490-18C=)
c.1661-18C= (n.1661-18C=)
20g.61928172C>TCA9934870CDH4c.1772-18C>T (n.1772-18C>T)
c.1550-18C>T (n.1550-18C>T)
c.1490-18C>T (n.1490-18C>T)
c.1661-18C>T (n.1661-18C>T)
dbSNP ExAC gnomAD v2
20g.61928173C>ACA2653589324CDH4c.1772-17C>A (n.1772-17C>A)
c.1550-17C>A (n.1550-17C>A)
c.1490-17C>A (n.1490-17C>A)
c.1661-17C>A (n.1661-17C>A)
gnomAD v4
20g.61928173C>TCA2653589325CDH4c.1772-17C>T (n.1772-17C>T)
c.1550-17C>T (n.1550-17C>T)
c.1490-17C>T (n.1490-17C>T)
c.1661-17C>T (n.1661-17C>T)
gnomAD v4
20g.61928174T>CCA2577441271CDH4c.1772-16T>C (n.1772-16T>C)
c.1550-16T>C (n.1550-16T>C)
c.1490-16T>C (n.1490-16T>C)
c.1661-16T>C (n.1661-16T>C)
20g.61928177_61928178delCA2653589326CDH4c.1772-13_1772-12del (n.1772-13_1772-12del)
c.1550-13_1550-12del (n.1550-13_1550-12del)
c.1490-13_1490-12del (n.1490-13_1490-12del)
c.1661-13_1661-12del (n.1661-13_1661-12del)
gnomAD v4
20g.61928175G=CA2373989182CDH4c.1772-15G= (n.1772-15G=)
c.1550-15G= (n.1550-15G=)
c.1490-15G= (n.1490-15G=)
c.1661-15G= (n.1661-15G=)
20g.61928175G>TCA2653589327CDH4c.1772-15G>T (n.1772-15G>T)
c.1550-15G>T (n.1550-15G>T)
c.1490-15G>T (n.1490-15G>T)
c.1661-15G>T (n.1661-15G>T)
gnomAD v4
20g.61928175_61928179delinsGTGTCCA2373989183CDH4c.1772-15_1772-11delinsGTGTC (n.1772-15_1772-11delinsGTGTC)
c.1550-15_1550-11delinsGTGTC (n.1550-15_1550-11delinsGTGTC)
c.1490-15_1490-11delinsGTGTC (n.1490-15_1490-11delinsGTGTC)
c.1661-15_1661-11delinsGTGTC (n.1661-15_1661-11delinsGTGTC)
20g.61928176T>CCA746323720CDH4c.1772-14T>C (n.1772-14T>C)
c.1550-14T>C (n.1550-14T>C)
c.1490-14T>C (n.1490-14T>C)
c.1661-14T>C (n.1661-14T>C)
dbSNP gnomAD v3 gnomAD v4
20g.61928176T=CA2373989184CDH4c.1772-14T= (n.1772-14T=)
c.1550-14T= (n.1550-14T=)
c.1490-14T= (n.1490-14T=)
c.1661-14T= (n.1661-14T=)
20g.61928176dupCA746323718CDH4c.1772-14dup (n.1772-14dup)
c.1550-14dup (n.1550-14dup)
c.1490-14dup (n.1490-14dup)
c.1661-14dup (n.1661-14dup)
dbSNP gnomAD v3 gnomAD v4
20g.61928179_61928182delCA2373989185CDH4c.1772-11_1772-8del (n.1772-11_1772-8del)
c.1550-11_1550-8del (n.1550-11_1550-8del)
c.1490-11_1490-8del (n.1490-11_1490-8del)
c.1661-11_1661-8del (n.1661-11_1661-8del)
dbSNP gnomAD v4
20g.61928177G>TCA2653589328CDH4c.1772-13G>T (n.1772-13G>T)
c.1550-13G>T (n.1550-13G>T)
c.1490-13G>T (n.1490-13G>T)
c.1661-13G>T (n.1661-13G>T)
gnomAD v4
20g.61928178T>ACA2373989187CDH4c.1772-12T>A (n.1772-12T>A)
c.1550-12T>A (n.1550-12T>A)
c.1490-12T>A (n.1490-12T>A)
c.1661-12T>A (n.1661-12T>A)
dbSNP gnomAD v4
20g.61928178T=CA2373989186CDH4c.1772-12T= (n.1772-12T=)
c.1550-12T= (n.1550-12T=)
c.1490-12T= (n.1490-12T=)
c.1661-12T= (n.1661-12T=)
20g.61928179C>ACA2653589329CDH4c.1772-11C>A (n.1772-11C>A)
c.1550-11C>A (n.1550-11C>A)
c.1490-11C>A (n.1490-11C>A)
c.1661-11C>A (n.1661-11C>A)
gnomAD v4
20g.61928179C>GCA2653589330CDH4c.1772-11C>G (n.1772-11C>G)
c.1550-11C>G (n.1550-11C>G)
c.1490-11C>G (n.1490-11C>G)
c.1661-11C>G (n.1661-11C>G)
gnomAD v4
20g.61928180T>GCA2736964107CDH4c.1772-10T>G (n.1772-10T>G)
c.1550-10T>G (n.1550-10T>G)
c.1490-10T>G (n.1490-10T>G)
c.1661-10T>G (n.1661-10T>G)
dbSNP
20g.61928181G>ACA9934871CDH4c.1772-9G>A (n.1772-9G>A)
c.1550-9G>A (n.1550-9G>A)
c.1490-9G>A (n.1490-9G>A)
c.1661-9G>A (n.1661-9G>A)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.61928181G>CCA2653589331CDH4c.1772-9G>C (n.1772-9G>C)
c.1550-9G>C (n.1550-9G>C)
c.1490-9G>C (n.1490-9G>C)
c.1661-9G>C (n.1661-9G>C)
gnomAD v4
20g.61928181G=CA2373989188CDH4c.1772-9G= (n.1772-9G=)
c.1550-9G= (n.1550-9G=)
c.1490-9G= (n.1490-9G=)
c.1661-9G= (n.1661-9G=)
20g.61928181G>TCA2653589332CDH4c.1772-9G>T (n.1772-9G>T)
c.1550-9G>T (n.1550-9G>T)
c.1490-9G>T (n.1490-9G>T)
c.1661-9G>T (n.1661-9G>T)
gnomAD v4
20g.61928182T>CCA2577441272CDH4c.1772-8T>C (n.1772-8T>C)
c.1550-8T>C (n.1550-8T>C)
c.1490-8T>C (n.1490-8T>C)
c.1661-8T>C (n.1661-8T>C)
gnomAD v4
20g.61928184C>TCA2653589334CDH4c.1772-6C>T (n.1772-6C>T)
c.1550-6C>T (n.1550-6C>T)
c.1490-6C>T (n.1490-6C>T)
c.1661-6C>T (n.1661-6C>T)
gnomAD v4
20g.61928185delCA2653589333CDH4c.1772-5del (n.1772-5del)
c.1550-5del (n.1550-5del)
c.1490-5del (n.1490-5del)
c.1661-5del (n.1661-5del)
gnomAD v4
20g.61928185C>TCA2653589335CDH4c.1772-5C>T (n.1772-5C>T)
c.1550-5C>T (n.1550-5C>T)
c.1490-5C>T (n.1490-5C>T)
c.1661-5C>T (n.1661-5C>T)
gnomAD v4
20g.61928186A=CA2373989189CDH4c.1772-4A= (n.1772-4A=)
c.1550-4A= (n.1550-4A=)
c.1490-4A= (n.1490-4A=)
c.1661-4A= (n.1661-4A=)
20g.61928186A>CCA746323722CDH4c.1772-4A>C (n.1772-4A>C)
c.1550-4A>C (n.1550-4A>C)
c.1490-4A>C (n.1490-4A>C)
c.1661-4A>C (n.1661-4A>C)
dbSNP
20g.61928187C>ACA2653589336CDH4c.1772-3C>A (n.1772-3C>A)
c.1550-3C>A (n.1550-3C>A)
c.1490-3C>A (n.1490-3C>A)
c.1661-3C>A (n.1661-3C>A)
gnomAD v4
20g.61928187C>TCA2653589337CDH4c.1772-3C>T (n.1772-3C>T)
c.1550-3C>T (n.1550-3C>T)
c.1490-3C>T (n.1490-3C>T)
c.1661-3C>T (n.1661-3C>T)
gnomAD v4
20g.61928188A>CCA409508549CDH4c.1772-2A>C (n.1772-2A>C)
c.1550-2A>C (n.1550-2A>C)
c.1490-2A>C (n.1490-2A>C)
c.1661-2A>C (n.1661-2A>C)
20g.61928188A>GCA409508550CDH4c.1772-2A>G (n.1772-2A>G)
c.1550-2A>G (n.1550-2A>G)
c.1490-2A>G (n.1490-2A>G)
c.1661-2A>G (n.1661-2A>G)
20g.61928188A>TCA409508551CDH4c.1772-2A>T (n.1772-2A>T)
c.1550-2A>T (n.1550-2A>T)
c.1490-2A>T (n.1490-2A>T)
c.1661-2A>T (n.1661-2A>T)
20g.61928189G>ACA409508552CDH4c.1772-1G>A (n.1772-1G>A)
c.1550-1G>A (n.1550-1G>A)
c.1490-1G>A (n.1490-1G>A)
c.1661-1G>A (n.1661-1G>A)
20g.61928189G>CCA409508553CDH4c.1772-1G>C (n.1772-1G>C)
c.1550-1G>C (n.1550-1G>C)
c.1490-1G>C (n.1490-1G>C)
c.1661-1G>C (n.1661-1G>C)
20g.61928189G>TCA409508554CDH4c.1772-1G>T (n.1772-1G>T)
c.1550-1G>T (n.1550-1G>T)
c.1490-1G>T (n.1490-1G>T)
c.1661-1G>T (n.1661-1G>T)
gnomAD v4
20g.61928190G>ACA409508555CDH4c.1772G>A (p.Gly591Glu)
c.1550G>A (p.Gly517Glu)
c.1490G>A (p.Gly497Glu)
c.1661G>A (p.Gly554Glu)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
20g.61928190G>CCA409508557CDH4c.1772G>C (p.Gly591Ala)
c.1550G>C (p.Gly517Ala)
c.1490G>C (p.Gly497Ala)
c.1661G>C (p.Gly554Ala)
20g.61928190G=CA2373989190CDH4c.1772G= (p.Gly591=)
c.1550G= (p.Gly517=)
c.1490G= (p.Gly497=)
c.1661G= (p.Gly554=)
20g.61928190G>TCA409508556CDH4c.1772G>T (p.Gly591Val)
c.1550G>T (p.Gly517Val)
c.1490G>T (p.Gly497Val)
c.1661G>T (p.Gly554Val)
gnomAD v4
20g.61928191G>ACA511321928CDH4c.1773G>A (p.Gly591=)
c.1551G>A (p.Gly517=)
c.1491G>A (p.Gly497=)
c.1662G>A (p.Gly554=)
20g.61928191G>CCA511321929CDH4c.1773G>C (p.Gly591=)
c.1551G>C (p.Gly517=)
c.1491G>C (p.Gly497=)
c.1662G>C (p.Gly554=)
20g.61928191G=CA2373989191CDH4c.1773G= (p.Gly591=)
c.1551G= (p.Gly517=)
c.1491G= (p.Gly497=)
c.1662G= (p.Gly554=)
20g.61928191G>TCA511321930CDH4c.1773G>T (p.Gly591=)
c.1551G>T (p.Gly517=)
c.1491G>T (p.Gly497=)
c.1662G>T (p.Gly554=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
20g.61928192A=CA2373989192CDH4c.1774A= (p.Ile592=)
c.1552A= (p.Ile518=)
c.1492A= (p.Ile498=)
c.1663A= (p.Ile555=)
20g.61928192A>CCA409508558CDH4c.1774A>C (p.Ile592Leu)
c.1552A>C (p.Ile518Leu)
c.1492A>C (p.Ile498Leu)
c.1663A>C (p.Ile555Leu)
20g.61928192A>GCA409508559CDH4c.1774A>G (p.Ile592Val)
c.1552A>G (p.Ile518Val)
c.1492A>G (p.Ile498Val)
c.1663A>G (p.Ile555Val)
dbSNP gnomAD v2 gnomAD v4
20g.61928192A>TCA409508560CDH4c.1774A>T (p.Ile592Leu)
c.1552A>T (p.Ile518Leu)
c.1492A>T (p.Ile498Leu)
c.1663A>T (p.Ile555Leu)
20g.61928193T>ACA409508561CDH4c.1775T>A (p.Ile592Lys)
c.1553T>A (p.Ile518Lys)
c.1493T>A (p.Ile498Lys)
c.1664T>A (p.Ile555Lys)
20g.61928193T>CCA409508562CDH4c.1775T>C (p.Ile592Thr)
c.1553T>C (p.Ile518Thr)
c.1493T>C (p.Ile498Thr)
c.1664T>C (p.Ile555Thr)
dbSNP
20g.61928193T>GCA409508563CDH4c.1775T>G (p.Ile592Arg)
c.1553T>G (p.Ile518Arg)
c.1493T>G (p.Ile498Arg)
c.1664T>G (p.Ile555Arg)
20g.61928193T=CA2373989193CDH4c.1775T= (p.Ile592=)
c.1553T= (p.Ile518=)
c.1493T= (p.Ile498=)
c.1664T= (p.Ile555=)
20g.61928194A=CA2373989195CDH4c.1776A= (p.Ile592=)
c.1554A= (p.Ile518=)
c.1494A= (p.Ile498=)
c.1665A= (p.Ile555=)
20g.61928194A>CCA511321934CDH4c.1776A>C (p.Ile592=)
c.1554A>C (p.Ile518=)
c.1494A>C (p.Ile498=)
c.1665A>C (p.Ile555=)
dbSNP
20g.61928194A>GCA409508564CDH4c.1776A>G (p.Ile592Met)
c.1554A>G (p.Ile518Met)
c.1494A>G (p.Ile498Met)
c.1665A>G (p.Ile555Met)
gnomAD v4
20g.61928194A>TCA511321932CDH4c.1776A>T (p.Ile592=)
c.1554A>T (p.Ile518=)
c.1494A>T (p.Ile498=)
c.1665A>T (p.Ile555=)
20g.61928194_61928195delinsACCA2373989194CDH4c.1776_1777delinsAC (p.Ile592=)
c.1554_1555delinsAC (p.Ile518=)
c.1494_1495delinsAC (p.Ile498=)
c.1665_1666delinsAC (p.Ile555=)
20g.61928194_61928200delCA2653589338CDH4c.1776_1782del (p.Ile592MetfsTer?)
c.1554_1560del (p.Ile518MetfsTer?)
c.1494_1500del (p.Ile498MetfsTer?)
c.1665_1671del (p.Ile555MetfsTer?)
gnomAD v4
20g.61928195C>ACA409508565CDH4c.1777C>A (p.Pro593Thr)
c.1555C>A (p.Pro519Thr)
c.1495C>A (p.Pro499Thr)
c.1666C>A (p.Pro556Thr)
20g.61928195C>GCA409508566CDH4c.1777C>G (p.Pro593Ala)
c.1555C>G (p.Pro519Ala)
c.1495C>G (p.Pro499Ala)
c.1666C>G (p.Pro556Ala)
20g.61928195C>TCA409508567CDH4c.1777C>T (p.Pro593Ser)
c.1555C>T (p.Pro519Ser)
c.1495C>T (p.Pro499Ser)
c.1666C>T (p.Pro556Ser)
20g.61928199delCA636608678CDH4c.1781del (p.Pro594ArgfsTer?)
c.1559del (p.Pro520ArgfsTer?)
c.1499del (p.Pro500ArgfsTer?)
c.1670del (p.Pro557ArgfsTer?)
dbSNP gnomAD v2 gnomAD v4 COSMIC
20g.61928196C>ACA409508570CDH4c.1778C>A (p.Pro593His)
c.1556C>A (p.Pro519His)
c.1496C>A (p.Pro499His)
c.1667C>A (p.Pro556His)
20g.61928196C>GCA409508569CDH4c.1778C>G (p.Pro593Arg)
c.1556C>G (p.Pro519Arg)
c.1496C>G (p.Pro499Arg)
c.1667C>G (p.Pro556Arg)
20g.61928196C>TCA409508568CDH4c.1778C>T (p.Pro593Leu)
c.1556C>T (p.Pro519Leu)
c.1496C>T (p.Pro499Leu)
c.1667C>T (p.Pro556Leu)
gnomAD v4
20g.61928197C>ACA317137335CDH4c.1779C>A (p.Pro593=)
c.1557C>A (p.Pro519=)
c.1497C>A (p.Pro499=)
c.1668C>A (p.Pro556=)
dbSNP gnomAD v3 gnomAD v4
20g.61928197C=CA2373989196CDH4c.1779C= (p.Pro593=)
c.1557C= (p.Pro519=)
c.1497C= (p.Pro499=)
c.1668C= (p.Pro556=)
20g.61928197C>GCA511321935CDH4c.1779C>G (p.Pro593=)
c.1557C>G (p.Pro519=)
c.1497C>G (p.Pro499=)
c.1668C>G (p.Pro556=)
20g.61928197C>TCA511321936CDH4c.1779C>T (p.Pro593=)
c.1557C>T (p.Pro519=)
c.1497C>T (p.Pro499=)
c.1668C>T (p.Pro556=)
20g.61928198C>ACA409508571CDH4c.1780C>A (p.Pro594Thr)
c.1558C>A (p.Pro520Thr)
c.1498C>A (p.Pro500Thr)
c.1669C>A (p.Pro557Thr)
gnomAD v4
20g.61928198C>GCA409508573CDH4c.1780C>G (p.Pro594Ala)
c.1558C>G (p.Pro520Ala)
c.1498C>G (p.Pro500Ala)
c.1669C>G (p.Pro557Ala)
20g.61928198C>TCA409508575CDH4c.1780C>T (p.Pro594Ser)
c.1558C>T (p.Pro520Ser)
c.1498C>T (p.Pro500Ser)
c.1669C>T (p.Pro557Ser)
gnomAD v4
20g.61928199C>ACA409508577CDH4c.1781C>A (p.Pro594Gln)
c.1559C>A (p.Pro520Gln)
c.1499C>A (p.Pro500Gln)
c.1670C>A (p.Pro557Gln)
dbSNP
20g.61928199C=CA2373989197CDH4c.1781C= (p.Pro594=)
c.1559C= (p.Pro520=)
c.1499C= (p.Pro500=)
c.1670C= (p.Pro557=)
20g.61928199C>GCA409508579CDH4c.1781C>G (p.Pro594Arg)
c.1559C>G (p.Pro520Arg)
c.1499C>G (p.Pro500Arg)
c.1670C>G (p.Pro557Arg)
20g.61928199C>TCA9934872CDH4c.1781C>T (p.Pro594Leu)
c.1559C>T (p.Pro520Leu)
c.1499C>T (p.Pro500Leu)
c.1670C>T (p.Pro557Leu)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
20g.61928200G>ACA9934873CDH4c.1782G>A (p.Pro594=)
c.1560G>A (p.Pro520=)
c.1500G>A (p.Pro500=)
c.1671G>A (p.Pro557=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
20g.61928200G>CCA511321939CDH4c.1782G>C (p.Pro594=)
c.1560G>C (p.Pro520=)
c.1500G>C (p.Pro500=)
c.1671G>C (p.Pro557=)
dbSNP gnomAD v4
20g.61928200G=CA2373989198CDH4c.1782G= (p.Pro594=)
c.1560G= (p.Pro520=)
c.1500G= (p.Pro500=)
c.1671G= (p.Pro557=)
20g.61928200G>TCA511321937CDH4c.1782G>T (p.Pro594=)
c.1560G>T (p.Pro520=)
c.1500G>T (p.Pro500=)
c.1671G>T (p.Pro557=)
gnomAD v4
20g.61928201G>ACA409508583CDH4c.1783G>A (p.Ala595Thr)
c.1561G>A (p.Ala521Thr)
c.1501G>A (p.Ala501Thr)
c.1672G>A (p.Ala558Thr)
20g.61928201G>CCA409508585CDH4c.1783G>C (p.Ala595Pro)
c.1561G>C (p.Ala521Pro)
c.1501G>C (p.Ala501Pro)
c.1672G>C (p.Ala558Pro)
20g.61928201G>TCA409508587CDH4c.1783G>T (p.Ala595Ser)
c.1561G>T (p.Ala521Ser)
c.1501G>T (p.Ala501Ser)
c.1672G>T (p.Ala558Ser)
gnomAD v4
20g.61928202C>ACA409508588CDH4c.1784C>A (p.Ala595Asp)
c.1562C>A (p.Ala521Asp)
c.1502C>A (p.Ala501Asp)
c.1673C>A (p.Ala558Asp)
20g.61928202C=CA2373989199CDH4c.1784C= (p.Ala595=)
c.1562C= (p.Ala521=)
c.1502C= (p.Ala501=)
c.1673C= (p.Ala558=)
20g.61928202C>GCA409508590CDH4c.1784C>G (p.Ala595Gly)
c.1562C>G (p.Ala521Gly)
c.1502C>G (p.Ala501Gly)
c.1673C>G (p.Ala558Gly)
dbSNP
20g.61928202C>TCA409508592CDH4c.1784C>T (p.Ala595Val)
c.1562C>T (p.Ala521Val)
c.1502C>T (p.Ala501Val)
c.1673C>T (p.Ala558Val)
gnomAD v4
20g.61928203C>ACA511321943CDH4c.1785C>A (p.Ala595=)
c.1563C>A (p.Ala521=)
c.1503C>A (p.Ala501=)
c.1674C>A (p.Ala558=)
20g.61928203C>GCA511321940CDH4c.1785C>G (p.Ala595=)
c.1563C>G (p.Ala521=)
c.1503C>G (p.Ala501=)
c.1674C>G (p.Ala558=)
20g.61928203C>TCA511321941CDH4c.1785C>T (p.Ala595=)
c.1563C>T (p.Ala521=)
c.1503C>T (p.Ala501=)
c.1674C>T (p.Ala558=)
20g.61928204A>CCA409508595CDH4c.1786A>C (p.Ser596Arg)
c.1564A>C (p.Ser522Arg)
c.1504A>C (p.Ser502Arg)
c.1675A>C (p.Ser559Arg)
20g.61928204A>GCA409508599CDH4c.1786A>G (p.Ser596Gly)
c.1564A>G (p.Ser522Gly)
c.1504A>G (p.Ser502Gly)
c.1675A>G (p.Ser559Gly)
dbSNP
20g.61928204A>TCA409508597CDH4c.1786A>T (p.Ser596Cys)
c.1564A>T (p.Ser522Cys)
c.1504A>T (p.Ser502Cys)
c.1675A>T (p.Ser559Cys)
20g.61928205G>ACA409508600CDH4c.1787G>A (p.Ser596Asn)
c.1565G>A (p.Ser522Asn)
c.1505G>A (p.Ser502Asn)
c.1676G>A (p.Ser559Asn)
dbSNP gnomAD v3 gnomAD v4
20g.61928205G>CCA409508602CDH4c.1787G>C (p.Ser596Thr)
c.1565G>C (p.Ser522Thr)
c.1505G>C (p.Ser502Thr)
c.1676G>C (p.Ser559Thr)
ClinVar dbSNP gnomAD v3 gnomAD v4
20g.61928205G=CA2373989200CDH4c.1787G= (p.Ser596=)
c.1565G= (p.Ser522=)
c.1505G= (p.Ser502=)
c.1676G= (p.Ser559=)
20g.61928205G>TCA409508604CDH4c.1787G>T (p.Ser596Ile)
c.1565G>T (p.Ser522Ile)
c.1505G>T (p.Ser502Ile)
c.1676G>T (p.Ser559Ile)
gnomAD v4
20g.61928206C>ACA409508606CDH4c.1788C>A (p.Ser596Arg)
c.1566C>A (p.Ser522Arg)
c.1506C>A (p.Ser502Arg)
c.1677C>A (p.Ser559Arg)
gnomAD v4
20g.61928206C=CA2373989201CDH4c.1788C= (p.Ser596=)
c.1566C= (p.Ser522=)
c.1506C= (p.Ser502=)
c.1677C= (p.Ser559=)
20g.61928206C>GCA409508609CDH4c.1788C>G (p.Ser596Arg)
c.1566C>G (p.Ser522Arg)
c.1506C>G (p.Ser502Arg)
c.1677C>G (p.Ser559Arg)
20g.61928206C>TCA511321946CDH4c.1788C>T (p.Ser596=)
c.1566C>T (p.Ser522=)
c.1506C>T (p.Ser502=)
c.1677C>T (p.Ser559=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
20g.61928207G>ACA9934874CDH4c.1789G>A (p.Gly597Ser)
c.1567G>A (p.Gly523Ser)
c.1507G>A (p.Gly503Ser)
c.1678G>A (p.Gly560Ser)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
20g.61928207G>CCA409508611CDH4c.1789G>C (p.Gly597Arg)
c.1567G>C (p.Gly523Arg)
c.1507G>C (p.Gly503Arg)
c.1678G>C (p.Gly560Arg)
20g.61928207G=CA2373989202CDH4c.1789G= (p.Gly597=)
c.1567G= (p.Gly523=)
c.1507G= (p.Gly503=)
c.1678G= (p.Gly560=)
20g.61928207G>TCA409508613CDH4c.1789G>T (p.Gly597Cys)
c.1567G>T (p.Gly523Cys)
c.1507G>T (p.Gly503Cys)
c.1678G>T (p.Gly560Cys)
gnomAD v4
20g.61928208G>ACA409508614CDH4c.1790G>A (p.Gly597Asp)
c.1568G>A (p.Gly523Asp)
c.1508G>A (p.Gly503Asp)
c.1679G>A (p.Gly560Asp)
dbSNP gnomAD v4
20g.61928208G>CCA409508616CDH4c.1790G>C (p.Gly597Ala)
c.1568G>C (p.Gly523Ala)
c.1508G>C (p.Gly503Ala)
c.1679G>C (p.Gly560Ala)
20g.61928208G=CA2373989203CDH4c.1790G= (p.Gly597=)
c.1568G= (p.Gly523=)
c.1508G= (p.Gly503=)
c.1679G= (p.Gly560=)
20g.61928208G>TCA409508617CDH4c.1790G>T (p.Gly597Val)
c.1568G>T (p.Gly523Val)
c.1508G>T (p.Gly503Val)
c.1679G>T (p.Gly560Val)
gnomAD v4
20g.61928209C>ACA511321949CDH4c.1791C>A (p.Gly597=)
c.1569C>A (p.Gly523=)
c.1509C>A (p.Gly503=)
c.1680C>A (p.Gly560=)
20g.61928209C>GCA511321950CDH4c.1791C>G (p.Gly597=)
c.1569C>G (p.Gly523=)
c.1509C>G (p.Gly503=)
c.1680C>G (p.Gly560=)
20g.61928209C>TCA511321951CDH4c.1791C>T (p.Gly597=)
c.1569C>T (p.Gly523=)
c.1509C>T (p.Gly503=)
c.1680C>T (p.Gly560=)
20g.61928210A>CCA409508622CDH4c.1792A>C (p.Thr598Pro)
c.1570A>C (p.Thr524Pro)
c.1510A>C (p.Thr504Pro)
c.1681A>C (p.Thr561Pro)
20g.61928210A>GCA409508623CDH4c.1792A>G (p.Thr598Ala)
c.1570A>G (p.Thr524Ala)
c.1510A>G (p.Thr504Ala)
c.1681A>G (p.Thr561Ala)
20g.61928210A>TCA409508620CDH4c.1792A>T (p.Thr598Ser)
c.1570A>T (p.Thr524Ser)
c.1510A>T (p.Thr504Ser)
c.1681A>T (p.Thr561Ser)
20g.61928211C>ACA409508627CDH4c.1793C>A (p.Thr598Asn)
c.1571C>A (p.Thr524Asn)
c.1511C>A (p.Thr504Asn)
c.1682C>A (p.Thr561Asn)
20g.61928211C>GCA409508626CDH4c.1793C>G (p.Thr598Ser)
c.1571C>G (p.Thr524Ser)
c.1511C>G (p.Thr504Ser)
c.1682C>G (p.Thr561Ser)
20g.61928211C>TCA409508630CDH4c.1793C>T (p.Thr598Ile)
c.1571C>T (p.Thr524Ile)
c.1511C>T (p.Thr504Ile)
c.1682C>T (p.Thr561Ile)
gnomAD v4
20g.61928212C>ACA511321953CDH4c.1794C>A (p.Thr598=)
c.1572C>A (p.Thr524=)
c.1512C>A (p.Thr504=)
c.1683C>A (p.Thr561=)
20g.61928212C=CA2373989204CDH4c.1794C= (p.Thr598=)
c.1572C= (p.Thr524=)
c.1512C= (p.Thr504=)
c.1683C= (p.Thr561=)
20g.61928212C>GCA511321954CDH4c.1794C>G (p.Thr598=)
c.1572C>G (p.Thr524=)
c.1512C>G (p.Thr504=)
c.1683C>G (p.Thr561=)
20g.61928212C>TCA9934875CDH4c.1794C>T (p.Thr598=)
c.1572C>T (p.Thr524=)
c.1512C>T (p.Thr504=)
c.1683C>T (p.Thr561=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
20g.61928213G>ACA9934876CDH4c.1795G>A (p.Gly599Arg)
c.1573G>A (p.Gly525Arg)
c.1513G>A (p.Gly505Arg)
c.1684G>A (p.Gly562Arg)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.61928213G>CCA409508634CDH4c.1795G>C (p.Gly599Arg)
c.1573G>C (p.Gly525Arg)
c.1513G>C (p.Gly505Arg)
c.1684G>C (p.Gly562Arg)
20g.61928213G=CA2373989205CDH4c.1795G= (p.Gly599=)
c.1573G= (p.Gly525=)
c.1513G= (p.Gly505=)
c.1684G= (p.Gly562=)
20g.61928213G>TCA409508636CDH4c.1795G>T (p.Gly599Trp)
c.1573G>T (p.Gly525Trp)
c.1513G>T (p.Gly505Trp)
c.1684G>T (p.Gly562Trp)
gnomAD v4
20g.61928214G>ACA409508638CDH4c.1796G>A (p.Gly599Glu)
c.1574G>A (p.Gly525Glu)
c.1514G>A (p.Gly505Glu)
c.1685G>A (p.Gly562Glu)
gnomAD v4
20g.61928214G>CCA409508640CDH4c.1796G>C (p.Gly599Ala)
c.1574G>C (p.Gly525Ala)
c.1514G>C (p.Gly505Ala)
c.1685G>C (p.Gly562Ala)
20g.61928214G>TCA409508642CDH4c.1796G>T (p.Gly599Val)
c.1574G>T (p.Gly525Val)
c.1514G>T (p.Gly505Val)
c.1685G>T (p.Gly562Val)
gnomAD v4
20g.61928215G>ACA511321956CDH4c.1797G>A (p.Gly599=)
c.1575G>A (p.Gly525=)
c.1515G>A (p.Gly505=)
c.1686G>A (p.Gly562=)
gnomAD v4
20g.61928215G>CCA9934877CDH4c.1797G>C (p.Gly599=)
c.1575G>C (p.Gly525=)
c.1515G>C (p.Gly505=)
c.1686G>C (p.Gly562=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.61928215G=CA2373989206CDH4c.1797G= (p.Gly599=)
c.1575G= (p.Gly525=)
c.1515G= (p.Gly505=)
c.1686G= (p.Gly562=)
20g.61928215G>TCA9934878CDH4c.1797G>T (p.Gly599=)
c.1575G>T (p.Gly525=)
c.1515G>T (p.Gly505=)
c.1686G>T (p.Gly562=)
dbSNP ExAC gnomAD v2 gnomAD v4
20g.61928216A=CA2373989207CDH4c.1798A= (p.Thr600=)
c.1576A= (p.Thr526=)
c.1516A= (p.Thr506=)
c.1687A= (p.Thr563=)
20g.61928216A>CCA409508647CDH4c.1798A>C (p.Thr600Pro)
c.1576A>C (p.Thr526Pro)
c.1516A>C (p.Thr506Pro)
c.1687A>C (p.Thr563Pro)
20g.61928216A>GCA9934879CDH4c.1798A>G (p.Thr600Ala)
c.1576A>G (p.Thr526Ala)
c.1516A>G (p.Thr506Ala)
c.1687A>G (p.Thr563Ala)
dbSNP ExAC gnomAD v2
20g.61928216A>TCA409508649CDH4c.1798A>T (p.Thr600Ser)
c.1576A>T (p.Thr526Ser)
c.1516A>T (p.Thr506Ser)
c.1687A>T (p.Thr563Ser)
20g.61928217C>ACA409508651CDH4c.1799C>A (p.Thr600Asn)
c.1577C>A (p.Thr526Asn)
c.1517C>A (p.Thr506Asn)
c.1688C>A (p.Thr563Asn)
20g.61928217C=CA2373989208CDH4c.1799C= (p.Thr600=)
c.1577C= (p.Thr526=)
c.1517C= (p.Thr506=)
c.1688C= (p.Thr563=)
20g.61928217C>GCA409508653CDH4c.1799C>G (p.Thr600Ser)
c.1577C>G (p.Thr526Ser)
c.1517C>G (p.Thr506Ser)
c.1688C>G (p.Thr563Ser)
20g.61928217C>TCA317137439CDH4c.1799C>T (p.Thr600Ile)
c.1577C>T (p.Thr526Ile)
c.1517C>T (p.Thr506Ile)
c.1688C>T (p.Thr563Ile)
dbSNP gnomAD v2 gnomAD v4
20g.61928218C>ACA511321960CDH4c.1800C>A (p.Thr600=)
c.1578C>A (p.Thr526=)
c.1518C>A (p.Thr506=)
c.1689C>A (p.Thr563=)
20g.61928218C>GCA511321961CDH4c.1800C>G (p.Thr600=)
c.1578C>G (p.Thr526=)
c.1518C>G (p.Thr506=)
c.1689C>G (p.Thr563=)
20g.61928218C>TCA511321962CDH4c.1800C>T (p.Thr600=)
c.1578C>T (p.Thr526=)
c.1518C>T (p.Thr506=)
c.1689C>T (p.Thr563=)
gnomAD v4
20g.61928219C>ACA409508657CDH4c.1801C>A (p.Leu601Ile)
c.1579C>A (p.Leu527Ile)
c.1519C>A (p.Leu507Ile)
c.1690C>A (p.Leu564Ile)
20g.61928219C=CA2373989209CDH4c.1801C= (p.Leu601=)
c.1579C= (p.Leu527=)
c.1519C= (p.Leu507=)
c.1690C= (p.Leu564=)
20g.61928219C>GCA409508660CDH4c.1801C>G (p.Leu601Val)
c.1579C>G (p.Leu527Val)
c.1519C>G (p.Leu507Val)
c.1690C>G (p.Leu564Val)
20g.61928219C>TCA317137442CDH4c.1801C>T (p.Leu601Phe)
c.1579C>T (p.Leu527Phe)
c.1519C>T (p.Leu507Phe)
c.1690C>T (p.Leu564Phe)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
20g.61928220T>ACA409508662CDH4c.1802T>A (p.Leu601His)
c.1580T>A (p.Leu527His)
c.1520T>A (p.Leu507His)
c.1691T>A (p.Leu564His)
20g.61928220T>CCA409508664CDH4c.1802T>C (p.Leu601Pro)
c.1580T>C (p.Leu527Pro)
c.1520T>C (p.Leu507Pro)
c.1691T>C (p.Leu564Pro)
gnomAD v4
20g.61928220T>GCA409508666CDH4c.1802T>G (p.Leu601Arg)
c.1580T>G (p.Leu527Arg)
c.1520T>G (p.Leu507Arg)
c.1691T>G (p.Leu564Arg)
20g.61928221C>ACA511321966CDH4c.1803C>A (p.Leu601=)
c.1581C>A (p.Leu527=)
c.1521C>A (p.Leu507=)
c.1692C>A (p.Leu564=)
20g.61928221C=CA2373989210CDH4c.1803C= (p.Leu601=)
c.1581C= (p.Leu527=)
c.1521C= (p.Leu507=)
c.1692C= (p.Leu564=)
20g.61928221C>GCA511321967CDH4c.1803C>G (p.Leu601=)
c.1581C>G (p.Leu527=)
c.1521C>G (p.Leu507=)
c.1692C>G (p.Leu564=)
COSMIC
20g.61928221C>TCA317137448CDH4c.1803C>T (p.Leu601=)
c.1581C>T (p.Leu527=)
c.1521C>T (p.Leu507=)
c.1692C>T (p.Leu564=)
dbSNP
20g.61928222C>ACA409508668CDH4c.1804C>A (p.Gln602Lys)
c.1582C>A (p.Gln528Lys)
c.1522C>A (p.Gln508Lys)
c.1693C>A (p.Gln565Lys)
20g.61928222C>GCA409508670CDH4c.1804C>G (p.Gln602Glu)
c.1582C>G (p.Gln528Glu)
c.1522C>G (p.Gln508Glu)
c.1693C>G (p.Gln565Glu)
20g.61928222C>TCA409508672CDH4c.1804C>T (p.Gln602Ter)
c.1582C>T (p.Gln528Ter)
c.1522C>T (p.Gln508Ter)
c.1693C>T (p.Gln565Ter)
20g.61928223A=CA2373989211CDH4c.1805A= (p.Gln602=)
c.1583A= (p.Gln528=)
c.1523A= (p.Gln508=)
c.1694A= (p.Gln565=)
20g.61928223A>CCA409508675CDH4c.1805A>C (p.Gln602Pro)
c.1583A>C (p.Gln528Pro)
c.1523A>C (p.Gln508Pro)
c.1694A>C (p.Gln565Pro)
20g.61928223A>GCA409508677CDH4c.1805A>G (p.Gln602Arg)
c.1583A>G (p.Gln528Arg)
c.1523A>G (p.Gln508Arg)
c.1694A>G (p.Gln565Arg)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
20g.61928223A>TCA409508678CDH4c.1805A>T (p.Gln602Leu)
c.1583A>T (p.Gln528Leu)
c.1523A>T (p.Gln508Leu)
c.1694A>T (p.Gln565Leu)
20g.61928224G>ACA511321969CDH4c.1806G>A (p.Gln602=)
c.1584G>A (p.Gln528=)
c.1524G>A (p.Gln508=)
c.1695G>A (p.Gln565=)
gnomAD v4
20g.61928224G>CCA409508681CDH4c.1806G>C (p.Gln602His)
c.1584G>C (p.Gln528His)
c.1524G>C (p.Gln508His)
c.1695G>C (p.Gln565His)
dbSNP
20g.61928224G=CA2373989212CDH4c.1806G= (p.Gln602=)
c.1584G= (p.Gln528=)
c.1524G= (p.Gln508=)
c.1695G= (p.Gln565=)
20g.61928224G>TCA9934880CDH4c.1806G>T (p.Gln602His)
c.1584G>T (p.Gln528His)
c.1524G>T (p.Gln508His)
c.1695G>T (p.Gln565His)
dbSNP ExAC gnomAD v2 gnomAD v4
20g.61928225A>CCA409508684CDH4c.1807A>C (p.Ile603Leu)
c.1585A>C (p.Ile529Leu)
c.1525A>C (p.Ile509Leu)
c.1696A>C (p.Ile566Leu)
20g.61928225A>GCA409508687CDH4c.1807A>G (p.Ile603Val)
c.1585A>G (p.Ile529Val)
c.1525A>G (p.Ile509Val)
c.1696A>G (p.Ile566Val)
20g.61928225A>TCA409508686CDH4c.1807A>T (p.Ile603Phe)
c.1585A>T (p.Ile529Phe)
c.1525A>T (p.Ile509Phe)
c.1696A>T (p.Ile566Phe)
20g.61928229_61928232dupCA2653589339CDH4c.1811_1814dup (p.Ile606SerfsTer3)
c.1589_1592dup (p.Ile532SerfsTer3)
c.1529_1532dup (p.Ile512SerfsTer3)
c.1700_1703dup (p.Ile569SerfsTer3)
gnomAD v4
20g.61928226T>ACA409508689CDH4c.1808T>A (p.Ile603Asn)
c.1586T>A (p.Ile529Asn)
c.1526T>A (p.Ile509Asn)
c.1697T>A (p.Ile566Asn)
20g.61928226T>CCA409508691CDH4c.1808T>C (p.Ile603Thr)
c.1586T>C (p.Ile529Thr)
c.1526T>C (p.Ile509Thr)
c.1697T>C (p.Ile566Thr)
20g.61928226T>GCA409508692CDH4c.1808T>G (p.Ile603Ser)
c.1586T>G (p.Ile529Ser)
c.1526T>G (p.Ile509Ser)
c.1697T>G (p.Ile566Ser)
20g.61928227C>ACA511322095CDH4c.1809C>A (p.Ile603=)
c.1587C>A (p.Ile529=)
c.1527C>A (p.Ile509=)
c.1698C>A (p.Ile566=)
20g.61928227C>GCA409508694CDH4c.1809C>G (p.Ile603Met)
c.1587C>G (p.Ile529Met)
c.1527C>G (p.Ile509Met)
c.1698C>G (p.Ile566Met)
20g.61928227C>TCA511322098CDH4c.1809C>T (p.Ile603=)
c.1587C>T (p.Ile529=)
c.1527C>T (p.Ile509=)
c.1698C>T (p.Ile566=)
COSMIC
20g.61928228T>ACA409508696CDH4c.1810T>A (p.Tyr604Asn)
c.1588T>A (p.Tyr530Asn)
c.1528T>A (p.Tyr510Asn)
c.1699T>A (p.Tyr567Asn)
20g.61928228T>CCA409508699CDH4c.1810T>C (p.Tyr604His)
c.1588T>C (p.Tyr530His)
c.1528T>C (p.Tyr510His)
c.1699T>C (p.Tyr567His)
gnomAD v4
20g.61928228T>GCA409508701CDH4c.1810T>G (p.Tyr604Asp)
c.1588T>G (p.Tyr530Asp)
c.1528T>G (p.Tyr510Asp)
c.1699T>G (p.Tyr567Asp)
20g.61928229A=CA2373989213CDH4c.1811A= (p.Tyr604=)
c.1589A= (p.Tyr530=)
c.1529A= (p.Tyr510=)
c.1700A= (p.Tyr567=)
20g.61928229A>CCA409508704CDH4c.1811A>C (p.Tyr604Ser)
c.1589A>C (p.Tyr530Ser)
c.1529A>C (p.Tyr510Ser)
c.1700A>C (p.Tyr567Ser)
dbSNP
20g.61928229A>GCA409508705CDH4c.1811A>G (p.Tyr604Cys)
c.1589A>G (p.Tyr530Cys)
c.1529A>G (p.Tyr510Cys)
c.1700A>G (p.Tyr567Cys)
20g.61928229A>TCA409508707CDH4c.1811A>T (p.Tyr604Phe)
c.1589A>T (p.Tyr530Phe)
c.1529A>T (p.Tyr510Phe)
c.1700A>T (p.Tyr567Phe)
gnomAD v4
20g.61928230T>ACA409508710CDH4c.1812T>A (p.Tyr604Ter)
c.1590T>A (p.Tyr530Ter)
c.1530T>A (p.Tyr510Ter)
c.1701T>A (p.Tyr567Ter)
20g.61928230T>CCA511322100CDH4c.1812T>C (p.Tyr604=)
c.1590T>C (p.Tyr530=)
c.1530T>C (p.Tyr510=)
c.1701T>C (p.Tyr567=)
gnomAD v4
20g.61928230T>GCA409508711CDH4c.1812T>G (p.Tyr604Ter)
c.1590T>G (p.Tyr530Ter)
c.1530T>G (p.Tyr510Ter)
c.1701T>G (p.Tyr567Ter)
20g.61928231C>ACA409508717CDH4c.1813C>A (p.Leu605Ile)
c.1591C>A (p.Leu531Ile)
c.1531C>A (p.Leu511Ile)
c.1702C>A (p.Leu568Ile)
20g.61928231C>GCA409508714CDH4c.1813C>G (p.Leu605Val)
c.1591C>G (p.Leu531Val)
c.1531C>G (p.Leu511Val)
c.1702C>G (p.Leu568Val)
COSMIC
20g.61928231C>TCA409508716CDH4c.1813C>T (p.Leu605Phe)
c.1591C>T (p.Leu531Phe)
c.1531C>T (p.Leu511Phe)
c.1702C>T (p.Leu568Phe)
20g.61928232T>ACA409508720CDH4c.1814T>A (p.Leu605His)
c.1592T>A (p.Leu531His)
c.1532T>A (p.Leu511His)
c.1703T>A (p.Leu568His)
20g.61928232T>CCA409508722CDH4c.1814T>C (p.Leu605Pro)
c.1592T>C (p.Leu531Pro)
c.1532T>C (p.Leu511Pro)
c.1703T>C (p.Leu568Pro)
20g.61928232T>GCA409508723CDH4c.1814T>G (p.Leu605Arg)
c.1592T>G (p.Leu531Arg)
c.1532T>G (p.Leu511Arg)
c.1703T>G (p.Leu568Arg)
20g.61928233C>ACA511322106CDH4c.1815C>A (p.Leu605=)
c.1593C>A (p.Leu531=)
c.1533C>A (p.Leu511=)
c.1704C>A (p.Leu568=)
20g.61928233C=CA2373989214CDH4c.1815C= (p.Leu605=)
c.1593C= (p.Leu531=)
c.1533C= (p.Leu511=)
c.1704C= (p.Leu568=)
20g.61928233C>GCA9934881CDH4c.1815C>G (p.Leu605=)
c.1593C>G (p.Leu531=)
c.1533C>G (p.Leu511=)
c.1704C>G (p.Leu568=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.61928233C>TCA511322107CDH4c.1815C>T (p.Leu605=)
c.1593C>T (p.Leu531=)
c.1533C>T (p.Leu511=)
c.1704C>T (p.Leu568=)
COSMIC
20g.61928234A=CA2373989215CDH4c.1816A= (p.Ile606=)
c.1594A= (p.Ile532=)
c.1534A= (p.Ile512=)
c.1705A= (p.Ile569=)
20g.61928234A>CCA409508727CDH4c.1816A>C (p.Ile606Leu)
c.1594A>C (p.Ile532Leu)
c.1534A>C (p.Ile512Leu)
c.1705A>C (p.Ile569Leu)
dbSNP gnomAD v4
20g.61928234A>GCA409508729CDH4c.1816A>G (p.Ile606Val)
c.1594A>G (p.Ile532Val)
c.1534A>G (p.Ile512Val)
c.1705A>G (p.Ile569Val)
dbSNP gnomAD v3 gnomAD v4
20g.61928234A>TCA409508731CDH4c.1816A>T (p.Ile606Phe)
c.1594A>T (p.Ile532Phe)
c.1534A>T (p.Ile512Phe)
c.1705A>T (p.Ile569Phe)
20g.61928235T>ACA409508733CDH4c.1817T>A (p.Ile606Asn)
c.1595T>A (p.Ile532Asn)
c.1535T>A (p.Ile512Asn)
c.1706T>A (p.Ile569Asn)
20g.61928235T>CCA317137454CDH4c.1817T>C (p.Ile606Thr)
c.1595T>C (p.Ile532Thr)
c.1535T>C (p.Ile512Thr)
c.1706T>C (p.Ile569Thr)
dbSNP gnomAD v3 gnomAD v4
20g.61928235T>GCA409508735CDH4c.1817T>G (p.Ile606Ser)
c.1595T>G (p.Ile532Ser)
c.1535T>G (p.Ile512Ser)
c.1706T>G (p.Ile569Ser)
20g.61928235T=CA2373989216CDH4c.1817T= (p.Ile606=)
c.1595T= (p.Ile532=)
c.1535T= (p.Ile512=)
c.1706T= (p.Ile569=)
20g.61928236T>ACA511322111CDH4c.1818T>A (p.Ile606=)
c.1596T>A (p.Ile532=)
c.1536T>A (p.Ile512=)
c.1707T>A (p.Ile569=)
20g.61928236T>CCA511322112CDH4c.1818T>C (p.Ile606=)
c.1596T>C (p.Ile532=)
c.1536T>C (p.Ile512=)
c.1707T>C (p.Ile569=)
20g.61928236T>GCA409508737CDH4c.1818T>G (p.Ile606Met)
c.1596T>G (p.Ile532Met)
c.1536T>G (p.Ile512Met)
c.1707T>G (p.Ile569Met)
20g.61928237G>ACA409508743CDH4c.1819G>A (p.Asp607Asn)
c.1597G>A (p.Asp533Asn)
c.1537G>A (p.Asp513Asn)
c.1708G>A (p.Asp570Asn)
20g.61928237G>CCA409508741CDH4c.1819G>C (p.Asp607His)
c.1597G>C (p.Asp533His)
c.1537G>C (p.Asp513His)
c.1708G>C (p.Asp570His)
20g.61928237G>TCA409508739CDH4c.1819G>T (p.Asp607Tyr)
c.1597G>T (p.Asp533Tyr)
c.1537G>T (p.Asp513Tyr)
c.1708G>T (p.Asp570Tyr)
gnomAD v4
20g.61928238A>CCA409508745CDH4c.1820A>C (p.Asp607Ala)
c.1598A>C (p.Asp533Ala)
c.1538A>C (p.Asp513Ala)
c.1709A>C (p.Asp570Ala)
20g.61928238A>GCA409508749CDH4c.1820A>G (p.Asp607Gly)
c.1598A>G (p.Asp533Gly)
c.1538A>G (p.Asp513Gly)
c.1709A>G (p.Asp570Gly)
20g.61928238A>TCA409508747CDH4c.1820A>T (p.Asp607Val)
c.1598A>T (p.Asp533Val)
c.1538A>T (p.Asp513Val)
c.1709A>T (p.Asp570Val)
20g.61928239C>ACA409508751CDH4c.1821C>A (p.Asp607Glu)
c.1599C>A (p.Asp533Glu)
c.1539C>A (p.Asp513Glu)
c.1710C>A (p.Asp570Glu)
20g.61928239C=CA2373989217CDH4c.1821C= (p.Asp607=)
c.1599C= (p.Asp533=)
c.1539C= (p.Asp513=)
c.1710C= (p.Asp570=)
20g.61928239C>GCA409508753CDH4c.1821C>G (p.Asp607Glu)
c.1599C>G (p.Asp533Glu)
c.1539C>G (p.Asp513Glu)
c.1710C>G (p.Asp570Glu)
dbSNP gnomAD v2 gnomAD v4
20g.61928239C>TCA511322119CDH4c.1821C>T (p.Asp607=)
c.1599C>T (p.Asp533=)
c.1539C>T (p.Asp513=)
c.1710C>T (p.Asp570=)
20g.61928240A>CCA409508756CDH4c.1822A>C (p.Ile608Leu)
c.1600A>C (p.Ile534Leu)
c.1540A>C (p.Ile514Leu)
c.1711A>C (p.Ile571Leu)
20g.61928240A>GCA409508757CDH4c.1822A>G (p.Ile608Val)
c.1600A>G (p.Ile534Val)
c.1540A>G (p.Ile514Val)
c.1711A>G (p.Ile571Val)
20g.61928240A>TCA409508758CDH4c.1822A>T (p.Ile608Phe)
c.1600A>T (p.Ile534Phe)
c.1540A>T (p.Ile514Phe)
c.1711A>T (p.Ile571Phe)
gnomAD v4
20g.61928241T>ACA409508760CDH4c.1823T>A (p.Ile608Asn)
c.1601T>A (p.Ile534Asn)
c.1541T>A (p.Ile514Asn)
c.1712T>A (p.Ile571Asn)
20g.61928241T>CCA409508762CDH4c.1823T>C (p.Ile608Thr)
c.1601T>C (p.Ile534Thr)
c.1541T>C (p.Ile514Thr)
c.1712T>C (p.Ile571Thr)
20g.61928241T>GCA409508764CDH4c.1823T>G (p.Ile608Ser)
c.1601T>G (p.Ile534Ser)
c.1541T>G (p.Ile514Ser)
c.1712T>G (p.Ile571Ser)
20g.61928242C>ACA511322124CDH4c.1824C>A (p.Ile608=)
c.1602C>A (p.Ile534=)
c.1542C>A (p.Ile514=)
c.1713C>A (p.Ile571=)
20g.61928242C>GCA409508766CDH4c.1824C>G (p.Ile608Met)
c.1602C>G (p.Ile534Met)
c.1542C>G (p.Ile514Met)
c.1713C>G (p.Ile571Met)
gnomAD v4 COSMIC
20g.61928242C>TCA511322125CDH4c.1824C>T (p.Ile608=)
c.1602C>T (p.Ile534=)
c.1542C>T (p.Ile514=)
c.1713C>T (p.Ile571=)
gnomAD v4
20g.61928243A>CCA409508768CDH4c.1825A>C (p.Asn609His)
c.1603A>C (p.Asn535His)
c.1543A>C (p.Asn515His)
c.1714A>C (p.Asn572His)
20g.61928243A>GCA409508770CDH4c.1825A>G (p.Asn609Asp)
c.1603A>G (p.Asn535Asp)
c.1543A>G (p.Asn515Asp)
c.1714A>G (p.Asn572Asp)
gnomAD v4
20g.61928243A>TCA409508772CDH4c.1825A>T (p.Asn609Tyr)
c.1603A>T (p.Asn535Tyr)
c.1543A>T (p.Asn515Tyr)
c.1714A>T (p.Asn572Tyr)
20g.61928244A>CCA409508779CDH4c.1826A>C (p.Asn609Thr)
c.1604A>C (p.Asn535Thr)
c.1544A>C (p.Asn515Thr)
c.1715A>C (p.Asn572Thr)
20g.61928244A>GCA409508775CDH4c.1826A>G (p.Asn609Ser)
c.1604A>G (p.Asn535Ser)
c.1544A>G (p.Asn515Ser)
c.1715A>G (p.Asn572Ser)
20g.61928244A>TCA409508777CDH4c.1826A>T (p.Asn609Ile)
c.1604A>T (p.Asn535Ile)
c.1544A>T (p.Asn515Ile)
c.1715A>T (p.Asn572Ile)
20g.61928246_61928248delCA2653589340CDH4c.1828_1830del (p.Asp610del)
c.1606_1608del (p.Asp536del)
c.1546_1548del (p.Asp516del)
c.1717_1719del (p.Asp573del)
gnomAD v4
20g.61928245C>ACA409508781CDH4c.1827C>A (p.Asn609Lys)
c.1605C>A (p.Asn535Lys)
c.1545C>A (p.Asn515Lys)
c.1716C>A (p.Asn572Lys)
20g.61928245C=CA2373989218CDH4c.1827C= (p.Asn609=)
c.1605C= (p.Asn535=)
c.1545C= (p.Asn515=)
c.1716C= (p.Asn572=)
20g.61928245C>GCA409508783CDH4c.1827C>G (p.Asn609Lys)
c.1605C>G (p.Asn535Lys)
c.1545C>G (p.Asn515Lys)
c.1716C>G (p.Asn572Lys)
20g.61928245C>TCA9934882CDH4c.1827C>T (p.Asn609=)
c.1605C>T (p.Asn535=)
c.1545C>T (p.Asn515=)
c.1716C>T (p.Asn572=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
20g.61928246G>ACA409508785CDH4c.1828G>A (p.Asp610Asn)
c.1606G>A (p.Asp536Asn)
c.1546G>A (p.Asp516Asn)
c.1717G>A (p.Asp573Asn)
dbSNP gnomAD v2 gnomAD v4 COSMIC
20g.61928246G>CCA409508787CDH4c.1828G>C (p.Asp610His)
c.1606G>C (p.Asp536His)
c.1546G>C (p.Asp516His)
c.1717G>C (p.Asp573His)
20g.61928246G=CA2373989219CDH4c.1828G= (p.Asp610=)
c.1606G= (p.Asp536=)
c.1546G= (p.Asp516=)
c.1717G= (p.Asp573=)
20g.61928246G>TCA409508788CDH4c.1828G>T (p.Asp610Tyr)
c.1606G>T (p.Asp536Tyr)
c.1546G>T (p.Asp516Tyr)
c.1717G>T (p.Asp573Tyr)
gnomAD v4
20g.61928247A>CCA409508790CDH4c.1829A>C (p.Asp610Ala)
c.1607A>C (p.Asp536Ala)
c.1547A>C (p.Asp516Ala)
c.1718A>C (p.Asp573Ala)
20g.61928247A>GCA409508792CDH4c.1829A>G (p.Asp610Gly)
c.1607A>G (p.Asp536Gly)
c.1547A>G (p.Asp516Gly)
c.1718A>G (p.Asp573Gly)
COSMIC
20g.61928247A>TCA409508794CDH4c.1829A>T (p.Asp610Val)
c.1607A>T (p.Asp536Val)
c.1547A>T (p.Asp516Val)
c.1718A>T (p.Asp573Val)
20g.61928248C>ACA409508796CDH4c.1830C>A (p.Asp610Glu)
c.1608C>A (p.Asp536Glu)
c.1548C>A (p.Asp516Glu)
c.1719C>A (p.Asp573Glu)
20g.61928248C>GCA409508798CDH4c.1830C>G (p.Asp610Glu)
c.1608C>G (p.Asp536Glu)
c.1548C>G (p.Asp516Glu)
c.1719C>G (p.Asp573Glu)
20g.61928248C>TCA511322134CDH4c.1830C>T (p.Asp610=)
c.1608C>T (p.Asp536=)
c.1548C>T (p.Asp516=)
c.1719C>T (p.Asp573=)
gnomAD v4
20g.61928249A>CCA409508805CDH4c.1831A>C (p.Asn611His)
c.1609A>C (p.Asn537His)
c.1549A>C (p.Asn517His)
c.1720A>C (p.Asn574His)
gnomAD v4
20g.61928249A>GCA409508802CDH4c.1831A>G (p.Asn611Asp)
c.1609A>G (p.Asn537Asp)
c.1549A>G (p.Asn517Asp)
c.1720A>G (p.Asn574Asp)
20g.61928249A>TCA409508800CDH4c.1831A>T (p.Asn611Tyr)
c.1609A>T (p.Asn537Tyr)
c.1549A>T (p.Asn517Tyr)
c.1720A>T (p.Asn574Tyr)
gnomAD v4

Number of alleles fetched