Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.156760135_156760147dup | CA1083312701 | SGCD | c.*745_*757dup (n.*745_*757dup) | dbSNP gnomAD v3 gnomAD v4 |
5 | g.156760143C>A | CA130642341 | SGCD | c.*753C>A (n.*753C>A) | dbSNP gnomAD v3 gnomAD v4 |
5 | g.156760143C= | CA1593857077 | SGCD | c.*753C= (n.*753C=) | |
5 | g.156760143C>T | CA10619781 | SGCD | c.*753C>T (n.*753C>T) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.156760144A= | CA1593857078 | SGCD | c.*754A= (n.*754A=) | |
5 | g.156760145A>G | CA2550743986 | SGCD | c.*755A>G (n.*755A>G) | |
5 | g.156760147_156760150dup | CA130642342 | SGCD | c.*757_*760dup (n.*757_*760dup) | dbSNP |
5 | g.156760148T>G | CA1083312716 | SGCD | c.*758T>G (n.*758T>G) | dbSNP gnomAD v3 gnomAD v4 |
5 | g.156760148T= | CA1593857079 | SGCD | c.*758T= (n.*758T=) | |
5 | g.156760150A= | CA1593857080 | SGCD | c.*760A= (n.*760A=) | |
5 | g.156760150A>G | CA1593857081 | SGCD | c.*760A>G (n.*760A>G) | dbSNP |
5 | g.156760150A>T | CA2676179817 | SGCD | c.*760A>T (n.*760A>T) | gnomAD v4 |
5 | g.156760152A= | CA1593857082 | SGCD | c.*762A= (n.*762A=) | |
5 | g.156760152A>G | CA130642343 | SGCD | c.*762A>G (n.*762A>G) | dbSNP gnomAD v3 gnomAD v4 |
5 | g.156760153T>C | CA1593857084 | SGCD | c.*763T>C (n.*763T>C) | dbSNP |
5 | g.156760153T= | CA1593857083 | SGCD | c.*763T= (n.*763T=) | |
5 | g.156760155A= | CA1593857085 | SGCD | c.*765A= (n.*765A=) | |
5 | g.156760155A>G | CA130642344 | SGCD | c.*765A>G (n.*765A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.156760156C= | CA1593857086 | SGCD | c.*766C= (n.*766C=) | |
5 | g.156760156C>T | CA1593857087 | SGCD | c.*766C>T (n.*766C>T) | dbSNP |
5 | g.156760157A= | CA1593857088 | SGCD | c.*767A= (n.*767A=) | |
5 | g.156760157A>T | CA10623848 | SGCD | c.*767A>T (n.*767A>T) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
5 | g.156760158G>T | CA2676179818 | SGCD | c.*768G>T (n.*768G>T) | gnomAD v4 |
5 | g.156760161G>A | CA2676179819 | SGCD | c.*771G>A (n.*771G>A) | gnomAD v4 |
5 | g.156760161G>T | CA2676179820 | SGCD | c.*771G>T (n.*771G>T) | gnomAD v4 |
5 | g.156760162T>C | CA2676179821 | SGCD | c.*772T>C (n.*772T>C) | gnomAD v4 |
5 | g.156760165C>A | CA2676179822 | SGCD | c.*775C>A (n.*775C>A) | gnomAD v4 |
5 | g.156760166T>C | CA1083312724 | SGCD | c.*776T>C (n.*776T>C) | dbSNP gnomAD v3 gnomAD v4 |
5 | g.156760166T= | CA1593857089 | SGCD | c.*776T= (n.*776T=) | |
5 | g.156760167C= | CA1593857090 | SGCD | c.*777C= (n.*777C=) | |
5 | g.156760167C>T | CA806148285 | SGCD | c.*777C>T (n.*777C>T) | dbSNP gnomAD v3 gnomAD v4 |
5 | g.156760168A= | CA1593857091 | SGCD | c.*778A= (n.*778A=) | |
5 | g.156760168A>C | CA806148287 | SGCD | c.*778A>C (n.*778A>C) | dbSNP gnomAD v3 gnomAD v4 |
5 | g.156760168A>T | CA130642345 | SGCD | c.*778A>T (n.*778A>T) | dbSNP |
5 | g.156760169G>A | CA806148302 | SGCD | c.*779G>A (n.*779G>A) | dbSNP gnomAD v3 gnomAD v4 |
5 | g.156760169G= | CA1593857092 | SGCD | c.*779G= (n.*779G=) | |
5 | g.156760170T>C | CA2769042282 | SGCD | c.*780T>C (n.*780T>C) | |
5 | g.156760171G>A | CA806148314 | SGCD | c.*781G>A (n.*781G>A) | dbSNP gnomAD v3 gnomAD v4 |
5 | g.156760171G>C | CA10621024 | SGCD | c.*781G>C (n.*781G>C) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.156760171G= | CA1593857093 | SGCD | c.*781G= (n.*781G=) | |
5 | g.156760171G>T | CA2581526289 | SGCD | c.*781G>T (n.*781G>T) | |
5 | g.156760172A= | CA1593857094 | SGCD | c.*782A= (n.*782A=) | |
5 | g.156760172A>G | CA1593857095 | SGCD | c.*782A>G (n.*782A>G) | dbSNP |
5 | g.156760173G>A | CA806148316 | SGCD | c.*783G>A (n.*783G>A) | dbSNP |
5 | g.156760173G= | CA1593857096 | SGCD | c.*783G= (n.*783G=) | |
5 | g.156760173G>T | CA2676179823 | SGCD | c.*783G>T (n.*783G>T) | gnomAD v4 |
5 | g.156760176G>A | CA2676179824 | SGCD | c.*786G>A (n.*786G>A) | gnomAD v4 |
5 | g.156760178A>G | CA2676179825 | SGCD | c.*788A>G (n.*788A>G) | gnomAD v4 |
5 | g.156760179A>G | CA2676179826 | SGCD | c.*789A>G (n.*789A>G) | gnomAD v4 |
5 | g.156760180G>C | CA1593857098 | SGCD | c.*790G>C (n.*790G>C) | dbSNP |