Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.128852754T>A | CA369210835 | FLNC,FLNC-AS1 | c.6004+2T>A (n.6004+2T>A) c.5905+2T>A (n.5905+2T>A) n.215+531A>T | |
7 | g.128852754T>C | CA16622133 | FLNC,FLNC-AS1 | c.6004+2T>C (n.6004+2T>C) c.5905+2T>C (n.5905+2T>C) n.215+531A>G | ClinVar dbSNP |
7 | g.128852754T>G | CA369210838 | FLNC,FLNC-AS1 | c.6004+2T>G (n.6004+2T>G) c.5905+2T>G (n.5905+2T>G) n.215+531A>C | |
7 | g.128852754T= | CA1742575152 | FLNC,FLNC-AS1 | c.6004+2T= (n.6004+2T=) c.5905+2T= (n.5905+2T=) n.215+531A= | |
7 | g.128852755G>A | CA833141398 | FLNC,FLNC-AS1 | c.6004+3G>A (n.6004+3G>A) c.5905+3G>A (n.5905+3G>A) n.215+530C>T | ClinVar dbSNP |
7 | g.128852755G= | CA1742575155 | FLNC,FLNC-AS1 | c.6004+3G= (n.6004+3G=) c.5905+3G= (n.5905+3G=) n.215+530C= | |
7 | g.128852757G>A | CA1742575158 | FLNC,FLNC-AS1 | c.6004+5G>A (n.6004+5G>A) c.5905+5G>A (n.5905+5G>A) n.215+528C>T | dbSNP gnomAD v4 |
7 | g.128852757G= | CA1742575156 | FLNC,FLNC-AS1 | c.6004+5G= (n.6004+5G=) c.5905+5G= (n.5905+5G=) n.215+528C= | |
7 | g.128852757G>T | CA2684813209 | FLNC,FLNC-AS1 | c.6004+5G>T (n.6004+5G>T) c.5905+5G>T (n.5905+5G>T) n.215+528C>A | gnomAD v4 |
7 | g.128852758C= | CA1742575179 | FLNC,FLNC-AS1 | c.6004+6C= (n.6004+6C=) c.5905+6C= (n.5905+6C=) n.215+527G= | |
7 | g.128852758C>T | CA4475850 | FLNC,FLNC-AS1 | c.6004+6C>T (n.6004+6C>T) c.5905+6C>T (n.5905+6C>T) n.215+527G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128852759G>A | CA4475851 | FLNC,FLNC-AS1 | c.6004+7G>A (n.6004+7G>A) c.5905+7G>A (n.5905+7G>A) n.215+526C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128852759G>C | CA578150593 | FLNC,FLNC-AS1 | c.6004+7G>C (n.6004+7G>C) c.5905+7G>C (n.5905+7G>C) n.215+526C>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
7 | g.128852759G= | CA1742575196 | FLNC,FLNC-AS1 | c.6004+7G= (n.6004+7G=) c.5905+7G= (n.5905+7G=) n.215+526C= | |
7 | g.128852760T>C | CA2684813227 | FLNC,FLNC-AS1 | c.6004+8T>C (n.6004+8T>C) c.5905+8T>C (n.5905+8T>C) n.215+525A>G | gnomAD v4 |
7 | g.128852760T= | CA1742575205 | FLNC,FLNC-AS1 | c.6004+8T= (n.6004+8T=) c.5905+8T= (n.5905+8T=) n.215+525A= | |
7 | g.128852764dup | CA4475852 | FLNC,FLNC-AS1 | c.6004+12dup (n.6004+12dup) c.5905+12dup (n.5905+12dup) n.215+524dup | ClinVar dbSNP ExAC gnomAD v2 |
7 | g.128852762G>A | CA2573141601 | FLNC,FLNC-AS1 | c.6004+10G>A (n.6004+10G>A) c.5905+10G>A (n.5905+10G>A) n.215+523C>T | ClinVar dbSNP |
7 | g.128852763G>A | CA4475853 | FLNC,FLNC-AS1 | c.6004+11G>A (n.6004+11G>A) c.5905+11G>A (n.5905+11G>A) n.215+522C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128852763G= | CA1742575209 | FLNC,FLNC-AS1 | c.6004+11G= (n.6004+11G=) c.5905+11G= (n.5905+11G=) n.215+522C= | |
7 | g.128852763G>T | CA1742575216 | FLNC,FLNC-AS1 | c.6004+11G>T (n.6004+11G>T) c.5905+11G>T (n.5905+11G>T) n.215+522C>A | dbSNP gnomAD v4 |
7 | g.128852764G>A | CA2684813231 | FLNC,FLNC-AS1 | c.6004+12G>A (n.6004+12G>A) c.5905+12G>A (n.5905+12G>A) n.215+521C>T | gnomAD v4 |
7 | g.128852764G>C | CA4475854 | FLNC,FLNC-AS1 | c.6004+12G>C (n.6004+12G>C) c.5905+12G>C (n.5905+12G>C) n.215+521C>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.128852764G= | CA1742575222 | FLNC,FLNC-AS1 | c.6004+12G= (n.6004+12G=) c.5905+12G= (n.5905+12G=) n.215+521C= | |
7 | g.128852770_128852780del | CA2684813234 | FLNC,FLNC-AS1 | c.6004+18_6004+28del (n.6004+18_6004+28del) c.5905+18_5905+28del (n.5905+18_5905+28del) n.215+510_215+520del | gnomAD v4 |
7 | g.128852766C= | CA1742575225 | FLNC,FLNC-AS1 | c.6004+14C= (n.6004+14C=) c.5905+14C= (n.5905+14C=) n.215+519G= | |
7 | g.128852766C>T | CA1742575226 | FLNC,FLNC-AS1 | c.6004+14C>T (n.6004+14C>T) c.5905+14C>T (n.5905+14C>T) n.215+519G>A | dbSNP gnomAD v4 |
7 | g.128852770C= | CA1742575228 | FLNC,FLNC-AS1 | c.6004+18C= (n.6004+18C=) c.5905+18C= (n.5905+18C=) n.215+515G= | |
7 | g.128852770C>T | CA578150595 | FLNC,FLNC-AS1 | c.6004+18C>T (n.6004+18C>T) c.5905+18C>T (n.5905+18C>T) n.215+515G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
7 | g.128852771G>A | CA4475855 | FLNC,FLNC-AS1 | c.6004+19G>A (n.6004+19G>A) c.5905+19G>A (n.5905+19G>A) n.215+514C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128852771G= | CA1742575234 | FLNC,FLNC-AS1 | c.6004+19G= (n.6004+19G=) c.5905+19G= (n.5905+19G=) n.215+514C= | |
7 | g.128852771G>T | CA2684813244 | FLNC,FLNC-AS1 | c.6004+19G>T (n.6004+19G>T) c.5905+19G>T (n.5905+19G>T) n.215+514C>A | gnomAD v4 |
7 | g.128852774dup | CA2843264450 | FLNC,FLNC-AS1 | c.6004+22dup (n.6004+22dup) c.5905+22dup (n.5905+22dup) n.215+514dup | |
7 | g.128852775_128852784del | CA2511669735 | FLNC,FLNC-AS1 | c.6004+23_6004+32del (n.6004+23_6004+32del) c.5905+23_5905+32del (n.5905+23_5905+32del) n.215+505_215+514del | |
7 | g.128852772G>A | CA4475856 | FLNC,FLNC-AS1 | c.6004+20G>A (n.6004+20G>A) c.5905+20G>A (n.5905+20G>A) n.215+513C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.128852772G= | CA1742575265 | FLNC,FLNC-AS1 | c.6004+20G= (n.6004+20G=) c.5905+20G= (n.5905+20G=) n.215+513C= | |
7 | g.128852774G>A | CA578150596 | FLNC,FLNC-AS1 | c.6004+22G>A (n.6004+22G>A) c.5905+22G>A (n.5905+22G>A) n.215+511C>T | dbSNP gnomAD v2 gnomAD v4 |
7 | g.128852774G= | CA1742575273 | FLNC,FLNC-AS1 | c.6004+22G= (n.6004+22G=) c.5905+22G= (n.5905+22G=) n.215+511C= | |
7 | g.128852775A>G | CA2579014562 | FLNC,FLNC-AS1 | c.6004+23A>G (n.6004+23A>G) c.5905+23A>G (n.5905+23A>G) n.215+510T>C | gnomAD v4 |
7 | g.128852777C>A | CA2715890733 | FLNC,FLNC-AS1 | c.6004+25C>A (n.6004+25C>A) c.5905+25C>A (n.5905+25C>A) n.215+508G>T | dbSNP |
7 | g.128852777C>T | CA2684813253 | FLNC,FLNC-AS1 | c.6004+25C>T (n.6004+25C>T) c.5905+25C>T (n.5905+25C>T) n.215+508G>A | gnomAD v4 |
7 | g.128852779C>T | CA2684813255 | FLNC,FLNC-AS1 | c.6004+27C>T (n.6004+27C>T) c.5905+27C>T (n.5905+27C>T) n.215+506G>A | gnomAD v4 |
7 | g.128852779_128852780delinsCA | CA1742575288 | FLNC,FLNC-AS1 | c.6004+27_6004+28delinsCA (n.6004+27_6004+28delinsCA) c.5905+27_5905+28delinsCA (n.5905+27_5905+28delinsCA) n.215+505_215+506delinsTG | |
7 | g.128852779_128852781delinsCAG | CA1742575277 | FLNC,FLNC-AS1 | c.6004+27_6004+29delinsCAG (n.6004+27_6004+29delinsCAG) c.5905+27_5905+29delinsCAG (n.5905+27_5905+29delinsCAG) n.215+504_215+506delinsCTG | |
7 | g.128852780del | CA166190043 | FLNC,FLNC-AS1 | c.6004+28del (n.6004+28del) c.5905+28del (n.5905+28del) n.215+505del | dbSNP gnomAD v4 |
7 | g.128852780_128852781del | CA4475857 | FLNC,FLNC-AS1 | c.6004+28_6004+29del (n.6004+28_6004+29del) c.5905+28_5905+29del (n.5905+28_5905+29del) n.215+504_215+505del | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128852781G>A | CA4475858 | FLNC,FLNC-AS1 | c.6004+29G>A (n.6004+29G>A) c.5905+29G>A (n.5905+29G>A) n.215+504C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.128852781G>C | CA2684813262 | FLNC,FLNC-AS1 | c.6004+29G>C (n.6004+29G>C) c.5905+29G>C (n.5905+29G>C) n.215+504C>G | gnomAD v4 |
7 | g.128852781G= | CA1742575297 | FLNC,FLNC-AS1 | c.6004+29G= (n.6004+29G=) c.5905+29G= (n.5905+29G=) n.215+504C= | |
7 | g.128852782G>C | CA2604393589 | FLNC,FLNC-AS1 | c.6004+30G>C (n.6004+30G>C) c.5905+30G>C (n.5905+30G>C) n.215+503C>G | dbSNP gnomAD v3 gnomAD v4 |
7 | g.128852783G>A | CA4475859 | FLNC,FLNC-AS1 | c.6004+31G>A (n.6004+31G>A) c.5905+31G>A (n.5905+31G>A) n.215+502C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.128852783G= | CA1742575321 | FLNC,FLNC-AS1 | c.6004+31G= (n.6004+31G=) c.5905+31G= (n.5905+31G=) n.215+502C= | |
7 | g.128852784G>A | CA2835019123 | FLNC,FLNC-AS1 | c.6004+32G>A (n.6004+32G>A) c.5905+32G>A (n.5905+32G>A) n.215+501C>T | |
7 | g.128852785_128852786delinsTG | CA1742575325 | FLNC,FLNC-AS1 | c.6004+33_6004+34delinsTG (n.6004+33_6004+34delinsTG) c.5905+33_5905+34delinsTG (n.5905+33_5905+34delinsTG) n.215+499_215+500delinsCA | |
7 | g.128852786G>A | CA2684813270 | FLNC,FLNC-AS1 | c.6004+34G>A (n.6004+34G>A) c.5905+34G>A (n.5905+34G>A) n.215+499C>T | gnomAD v4 |
7 | g.128852786G>C | CA2715890736 | FLNC,FLNC-AS1 | c.6004+34G>C (n.6004+34G>C) c.5905+34G>C (n.5905+34G>C) n.215+499C>G | dbSNP |
7 | g.128852789_128852790dup | CA4475860 | FLNC,FLNC-AS1 | c.6004+37_6005-38dup (n.6004+37_6005-38dup) c.5905+37_5906-38dup (n.5905+37_5906-38dup) n.215+498_215+499dup | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128852790del | CA578150597 | FLNC,FLNC-AS1 | c.6005-38del (n.6005-38del) c.5906-38del (n.5906-38del) n.215+499del | dbSNP gnomAD v2 gnomAD v4 |
7 | g.128852788G>A | CA1742575344 | FLNC,FLNC-AS1 | c.6004+36G>A (n.6004+36G>A) c.5905+36G>A (n.5905+36G>A) n.215+497C>T | dbSNP |
7 | g.128852788G= | CA1742575343 | FLNC,FLNC-AS1 | c.6004+36G= (n.6004+36G=) c.5905+36G= (n.5905+36G=) n.215+497C= | |
7 | g.128852788G>T | CA578150598 | FLNC,FLNC-AS1 | c.6004+36G>T (n.6004+36G>T) c.5905+36G>T (n.5905+36G>T) n.215+497C>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128852789G>C | CA2684813274 | FLNC,FLNC-AS1 | c.6004+37G>C (n.6004+37G>C) c.5905+37G>C (n.5905+37G>C) n.215+496C>G | gnomAD v4 |
7 | g.128852790G>A | CA833141414 | FLNC,FLNC-AS1 | c.6005-38G>A (n.6005-38G>A) c.5906-38G>A (n.5906-38G>A) n.215+495C>T | dbSNP gnomAD v3 gnomAD v4 |
7 | g.128852790G= | CA1742575345 | FLNC,FLNC-AS1 | c.6005-38G= (n.6005-38G=) c.5906-38G= (n.5906-38G=) n.215+495C= | |
7 | g.128852790G>T | CA4475861 | FLNC,FLNC-AS1 | c.6005-38G>T (n.6005-38G>T) c.5906-38G>T (n.5906-38G>T) n.215+495C>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.128852793_128852808del | CA2684813277 | FLNC,FLNC-AS1 | c.6005-35_6005-20del (n.6005-35_6005-20del) c.5906-35_5906-20del (n.5906-35_5906-20del) n.215+480_215+495del | gnomAD v4 |
7 | g.128852793C= | CA1742575349 | FLNC,FLNC-AS1 | c.6005-35C= (n.6005-35C=) c.5906-35C= (n.5906-35C=) n.215+492G= | |
7 | g.128852793C>T | CA1742575350 | FLNC,FLNC-AS1 | c.6005-35C>T (n.6005-35C>T) c.5906-35C>T (n.5906-35C>T) n.215+492G>A | dbSNP |
7 | g.128852794A= | CA1742575352 | FLNC,FLNC-AS1 | c.6005-34A= (n.6005-34A=) c.5906-34A= (n.5906-34A=) n.215+491T= | |
7 | g.128852794A>G | CA1742575353 | FLNC,FLNC-AS1 | c.6005-34A>G (n.6005-34A>G) c.5906-34A>G (n.5906-34A>G) n.215+491T>C | dbSNP gnomAD v4 |
7 | g.128852795C>A | CA2684813284 | FLNC,FLNC-AS1 | c.6005-33C>A (n.6005-33C>A) c.5906-33C>A (n.5906-33C>A) n.215+490G>T | gnomAD v4 |
7 | g.128852795C= | CA1742575355 | FLNC,FLNC-AS1 | c.6005-33C= (n.6005-33C=) c.5906-33C= (n.5906-33C=) n.215+490G= | |
7 | g.128852795C>G | CA4475862 | FLNC,FLNC-AS1 | c.6005-33C>G (n.6005-33C>G) c.5906-33C>G (n.5906-33C>G) n.215+490G>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128852795C>T | CA2684813287 | FLNC,FLNC-AS1 | c.6005-33C>T (n.6005-33C>T) c.5906-33C>T (n.5906-33C>T) n.215+490G>A | gnomAD v4 |
7 | g.128852798G>A | CA2684813288 | FLNC,FLNC-AS1 | c.6005-30G>A (n.6005-30G>A) c.5906-30G>A (n.5906-30G>A) n.215+487C>T | gnomAD v4 |
7 | g.128852798G= | CA1742575356 | FLNC,FLNC-AS1 | c.6005-30G= (n.6005-30G=) c.5906-30G= (n.5906-30G=) n.215+487C= | |
7 | g.128852798G>T | CA1742575357 | FLNC,FLNC-AS1 | c.6005-30G>T (n.6005-30G>T) c.5906-30G>T (n.5906-30G>T) n.215+487C>A | dbSNP gnomAD v4 |
7 | g.128852799A>T | CA2684813289 | FLNC,FLNC-AS1 | c.6005-29A>T (n.6005-29A>T) c.5906-29A>T (n.5906-29A>T) n.215+486T>A | gnomAD v4 |
7 | g.128852800T>G | CA4475863 | FLNC,FLNC-AS1 | c.6005-28T>G (n.6005-28T>G) c.5906-28T>G (n.5906-28T>G) n.215+485A>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.128852800T= | CA1742575361 | FLNC,FLNC-AS1 | c.6005-28T= (n.6005-28T=) c.5906-28T= (n.5906-28T=) n.215+485A= | |
7 | g.128852802C>T | CA2579014563 | FLNC,FLNC-AS1 | c.6005-26C>T (n.6005-26C>T) c.5906-26C>T (n.5906-26C>T) n.215+483G>A | gnomAD v4 |
7 | g.128852803T>C | CA4475864 | FLNC,FLNC-AS1 | c.6005-25T>C (n.6005-25T>C) c.5906-25T>C (n.5906-25T>C) n.215+482A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.128852803T>G | CA578150599 | FLNC,FLNC-AS1 | c.6005-25T>G (n.6005-25T>G) c.5906-25T>G (n.5906-25T>G) n.215+482A>C | dbSNP gnomAD v2 gnomAD v4 |
7 | g.128852803T= | CA1742575399 | FLNC,FLNC-AS1 | c.6005-25T= (n.6005-25T=) c.5906-25T= (n.5906-25T=) n.215+482A= | |
7 | g.128852804C= | CA1742575406 | FLNC,FLNC-AS1 | c.6005-24C= (n.6005-24C=) c.5906-24C= (n.5906-24C=) n.215+481G= | |
7 | g.128852804C>T | CA4475865 | FLNC,FLNC-AS1 | c.6005-24C>T (n.6005-24C>T) c.5906-24C>T (n.5906-24C>T) n.215+481G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128852806G>A | CA4475866 | FLNC,FLNC-AS1 | c.6005-22G>A (n.6005-22G>A) c.5906-22G>A (n.5906-22G>A) n.215+479C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.128852806G>C | CA2684813299 | FLNC,FLNC-AS1 | c.6005-22G>C (n.6005-22G>C) c.5906-22G>C (n.5906-22G>C) n.215+479C>G | dbSNP gnomAD v4 |
7 | g.128852806G= | CA1742575411 | FLNC,FLNC-AS1 | c.6005-22G= (n.6005-22G=) c.5906-22G= (n.5906-22G=) n.215+479C= | |
7 | g.128852808C= | CA1742575417 | FLNC,FLNC-AS1 | c.6005-20C= (n.6005-20C=) c.5906-20C= (n.5906-20C=) n.215+477G= | |
7 | g.128852808C>T | CA578150600 | FLNC,FLNC-AS1 | c.6005-20C>T (n.6005-20C>T) c.5906-20C>T (n.5906-20C>T) n.215+477G>A | dbSNP gnomAD v2 gnomAD v4 |
7 | g.128852810A= | CA1742575423 | FLNC,FLNC-AS1 | c.6005-18A= (n.6005-18A=) c.5906-18A= (n.5906-18A=) n.215+475T= | |
7 | g.128852810A>G | CA833141418 | FLNC,FLNC-AS1 | c.6005-18A>G (n.6005-18A>G) c.5906-18A>G (n.5906-18A>G) n.215+475T>C | dbSNP gnomAD v3 gnomAD v4 |
7 | g.128852812C= | CA1742575426 | FLNC,FLNC-AS1 | c.6005-16C= (n.6005-16C=) c.5906-16C= (n.5906-16C=) n.215+473G= | |
7 | g.128852812C>T | CA4475867 | FLNC,FLNC-AS1 | c.6005-16C>T (n.6005-16C>T) c.5906-16C>T (n.5906-16C>T) n.215+473G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128852814C>A | CA2777853348 | FLNC,FLNC-AS1 | c.6005-14C>A (n.6005-14C>A) c.5906-14C>A (n.5906-14C>A) n.215+471G>T | |
7 | g.128852814C= | CA1742575430 | FLNC,FLNC-AS1 | c.6005-14C= (n.6005-14C=) c.5906-14C= (n.5906-14C=) n.215+471G= | |
7 | g.128852814C>G | CA2573141602 | FLNC,FLNC-AS1 | c.6005-14C>G (n.6005-14C>G) c.5906-14C>G (n.5906-14C>G) n.215+471G>C | ClinVar dbSNP |
7 | g.128852814C>T | CA166190094 | FLNC,FLNC-AS1 | c.6005-14C>T (n.6005-14C>T) c.5906-14C>T (n.5906-14C>T) n.215+471G>A | ClinVar dbSNP gnomAD v4 |
7 | g.128852816del | CA2740094865 | FLNC,FLNC-AS1 | c.6005-12del (n.6005-12del) c.5906-12del (n.5906-12del) n.215+471del | ClinVar |
7 | g.128852815C>T | CA2684813305 | FLNC,FLNC-AS1 | c.6005-13C>T (n.6005-13C>T) c.5906-13C>T (n.5906-13C>T) n.215+470G>A | gnomAD v4 |
7 | g.128852816C>G | CA2579014564 | FLNC,FLNC-AS1 | c.6005-12C>G (n.6005-12C>G) c.5906-12C>G (n.5906-12C>G) n.215+469G>C | |
7 | g.128852816C>T | CA2684813306 | FLNC,FLNC-AS1 | c.6005-12C>T (n.6005-12C>T) c.5906-12C>T (n.5906-12C>T) n.215+469G>A | gnomAD v4 |
7 | g.128852817A= | CA1742575433 | FLNC,FLNC-AS1 | c.6005-11A= (n.6005-11A=) c.5906-11A= (n.5906-11A=) n.215+468T= | |
7 | g.128852817A>G | CA578150601 | FLNC,FLNC-AS1 | c.6005-11A>G (n.6005-11A>G) c.5906-11A>G (n.5906-11A>G) n.215+468T>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128852817A>T | CA4475868 | FLNC,FLNC-AS1 | c.6005-11A>T (n.6005-11A>T) c.5906-11A>T (n.5906-11A>T) n.215+468T>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128852818C= | CA1742575447 | FLNC,FLNC-AS1 | c.6005-10C= (n.6005-10C=) c.5906-10C= (n.5906-10C=) n.215+467G= | |
7 | g.128852818C>T | CA578150602 | FLNC,FLNC-AS1 | c.6005-10C>T (n.6005-10C>T) c.5906-10C>T (n.5906-10C>T) n.215+467G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
7 | g.128852819T>C | CA202655 | FLNC,FLNC-AS1 | c.6005-9T>C (n.6005-9T>C) c.5906-9T>C (n.5906-9T>C) n.215+466A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128852819T= | CA1742575450 | FLNC,FLNC-AS1 | c.6005-9T= (n.6005-9T=) c.5906-9T= (n.5906-9T=) n.215+466A= | |
7 | g.128852821T>C | CA915945514 | FLNC,FLNC-AS1 | c.6005-7T>C (n.6005-7T>C) c.5906-7T>C (n.5906-7T>C) n.215+464A>G | ClinVar dbSNP gnomAD v4 |
7 | g.128852821T= | CA1742575460 | FLNC,FLNC-AS1 | c.6005-7T= (n.6005-7T=) c.5906-7T= (n.5906-7T=) n.215+464A= | |
7 | g.128852822C= | CA1742575468 | FLNC,FLNC-AS1 | c.6005-6C= (n.6005-6C=) c.5906-6C= (n.5906-6C=) n.215+463G= | |
7 | g.128852822C>T | CA166190100 | FLNC,FLNC-AS1 | c.6005-6C>T (n.6005-6C>T) c.5906-6C>T (n.5906-6C>T) n.215+463G>A | dbSNP |
7 | g.128852823C>T | CA2579014565 | FLNC,FLNC-AS1 | c.6005-5C>T (n.6005-5C>T) c.5906-5C>T (n.5906-5C>T) n.215+462G>A | ClinVar gnomAD v4 |
7 | g.128852825C= | CA1742575471 | FLNC,FLNC-AS1 | c.6005-3C= (n.6005-3C=) c.5906-3C= (n.5906-3C=) n.215+460G= | |
7 | g.128852825C>T | CA166190102 | FLNC,FLNC-AS1 | c.6005-3C>T (n.6005-3C>T) c.5906-3C>T (n.5906-3C>T) n.215+460G>A | dbSNP |
7 | g.128852826A= | CA1742575473 | FLNC,FLNC-AS1 | c.6005-2A= (n.6005-2A=) c.5906-2A= (n.5906-2A=) n.215+459T= | |
7 | g.128852826A>C | CA369210854 | FLNC,FLNC-AS1 | c.6005-2A>C (n.6005-2A>C) c.5906-2A>C (n.5906-2A>C) n.215+459T>G | |
7 | g.128852826A>G | CA369210856 | FLNC,FLNC-AS1 | c.6005-2A>G (n.6005-2A>G) c.5906-2A>G (n.5906-2A>G) n.215+459T>C | |
7 | g.128852826A>T | CA166190104 | FLNC,FLNC-AS1 | c.6005-2A>T (n.6005-2A>T) c.5906-2A>T (n.5906-2A>T) n.215+459T>A | dbSNP |
7 | g.128852827G>A | CA369210861 | FLNC,FLNC-AS1 | c.6005-1G>A (n.6005-1G>A) c.5906-1G>A (n.5906-1G>A) n.215+458C>T | |
7 | g.128852827G>C | CA369210858 | FLNC,FLNC-AS1 | c.6005-1G>C (n.6005-1G>C) c.5906-1G>C (n.5906-1G>C) n.215+458C>G | |
7 | g.128852827G>T | CA369210860 | FLNC,FLNC-AS1 | c.6005-1G>T (n.6005-1G>T) c.5906-1G>T (n.5906-1G>T) n.215+458C>A | |
7 | g.128852828G>A | CA369210864 | FLNC,FLNC-AS1 | c.6005G>A (p.Gly2002Glu) c.5906G>A (p.Gly1969Glu) n.215+457C>T | |
7 | g.128852828G>C | CA369210866 | FLNC,FLNC-AS1 | c.6005G>C (p.Gly2002Ala) c.5906G>C (p.Gly1969Ala) n.215+457C>G | gnomAD v4 |
7 | g.128852828G= | CA1742575482 | FLNC,FLNC-AS1 | c.6005G= (p.Gly2002=) c.5906G= (p.Gly1969=) n.215+457C= | |
7 | g.128852828G>T | CA4475869 | FLNC,FLNC-AS1 | c.6005G>T (p.Gly2002Val) c.5906G>T (p.Gly1969Val) n.215+457C>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128852829G>A | CA166190122 | FLNC,FLNC-AS1 | c.6006G>A (p.Gly2002=) c.5907G>A (p.Gly1969=) n.215+456C>T | dbSNP gnomAD v3 gnomAD v4 |
7 | g.128852829G>C | CA457849430 | FLNC,FLNC-AS1 | c.6006G>C (p.Gly2002=) c.5907G>C (p.Gly1969=) n.215+456C>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
7 | g.128852829G= | CA1742575488 | FLNC,FLNC-AS1 | c.6006G= (p.Gly2002=) c.5907G= (p.Gly1969=) n.215+456C= | |
7 | g.128852829G>T | CA457849431 | FLNC,FLNC-AS1 | c.6006G>T (p.Gly2002=) c.5907G>T (p.Gly1969=) n.215+456C>A | |
7 | g.128852830A>C | CA369210869 | FLNC,FLNC-AS1 | c.6007A>C (p.Ile2003Leu) c.5908A>C (p.Ile1970Leu) n.215+455T>G | |
7 | g.128852830A>G | CA369210871 | FLNC,FLNC-AS1 | c.6007A>G (p.Ile2003Val) c.5908A>G (p.Ile1970Val) n.215+455T>C | |
7 | g.128852830A>T | CA369210873 | FLNC,FLNC-AS1 | c.6007A>T (p.Ile2003Phe) c.5908A>T (p.Ile1970Phe) n.215+455T>A | |
7 | g.128852831T>A | CA369210875 | FLNC,FLNC-AS1 | c.6008T>A (p.Ile2003Asn) c.5909T>A (p.Ile1970Asn) n.215+454A>T | ClinVar |
7 | g.128852831T>C | CA369210877 | FLNC,FLNC-AS1 | c.6008T>C (p.Ile2003Thr) c.5909T>C (p.Ile1970Thr) n.215+454A>G | dbSNP |
7 | g.128852831T>G | CA369210879 | FLNC,FLNC-AS1 | c.6008T>G (p.Ile2003Ser) c.5909T>G (p.Ile1970Ser) n.215+454A>C | |
7 | g.128852831T= | CA1742575494 | FLNC,FLNC-AS1 | c.6008T= (p.Ile2003=) c.5909T= (p.Ile1970=) n.215+454A= | |
7 | g.128852832del | CA2580611033 | FLNC,FLNC-AS1 | c.6009del (p.Ser2004ProfsTer12) c.5910del (p.Ser1971ProfsTer12) n.215+453del | ClinVar |
7 | g.128852832C>A | CA457849433 | FLNC,FLNC-AS1 | c.6009C>A (p.Ile2003=) c.5910C>A (p.Ile1970=) n.215+453G>T | ClinVar dbSNP gnomAD v4 |
7 | g.128852832C>G | CA369210881 | FLNC,FLNC-AS1 | c.6009C>G (p.Ile2003Met) c.5910C>G (p.Ile1970Met) n.215+453G>C | |
7 | g.128852832C>T | CA457849434 | FLNC,FLNC-AS1 | c.6009C>T (p.Ile2003=) c.5910C>T (p.Ile1970=) n.215+453G>A | ClinVar gnomAD v4 |
7 | g.128852834_128852836del | CA2695203152 | FLNC,FLNC-AS1 | c.6011_6013del (p.Ser2004del) c.5912_5914del (p.Ser1971del) n.215+451_215+453del | |
7 | g.128852833T>A | CA369210883 | FLNC,FLNC-AS1 | c.6010T>A (p.Ser2004Thr) c.5911T>A (p.Ser1971Thr) n.215+452A>T | |
7 | g.128852833T>C | CA369210885 | FLNC,FLNC-AS1 | c.6010T>C (p.Ser2004Pro) c.5911T>C (p.Ser1971Pro) n.215+452A>G | |
7 | g.128852833T>G | CA369210887 | FLNC,FLNC-AS1 | c.6010T>G (p.Ser2004Ala) c.5911T>G (p.Ser1971Ala) n.215+452A>C | |
7 | g.128852834C>A | CA369210890 | FLNC,FLNC-AS1 | c.6011C>A (p.Ser2004Tyr) c.5912C>A (p.Ser1971Tyr) n.215+451G>T | |
7 | g.128852834C>G | CA369210893 | FLNC,FLNC-AS1 | c.6011C>G (p.Ser2004Cys) c.5912C>G (p.Ser1971Cys) n.215+451G>C | |
7 | g.128852834C>T | CA369210891 | FLNC,FLNC-AS1 | c.6011C>T (p.Ser2004Phe) c.5912C>T (p.Ser1971Phe) n.215+451G>A | ClinVar |
7 | g.128852835C>A | CA457849436 | FLNC,FLNC-AS1 | c.6012C>A (p.Ser2004=) c.5913C>A (p.Ser1971=) n.215+450G>T | gnomAD v4 |
7 | g.128852835C>G | CA457849437 | FLNC,FLNC-AS1 | c.6012C>G (p.Ser2004=) c.5913C>G (p.Ser1971=) n.215+450G>C | ClinVar |
7 | g.128852835C>T | CA457849438 | FLNC,FLNC-AS1 | c.6012C>T (p.Ser2004=) c.5913C>T (p.Ser1971=) n.215+450G>A | |
7 | g.128852836T>A | CA369210896 | FLNC,FLNC-AS1 | c.6013T>A (p.Phe2005Ile) c.5914T>A (p.Phe1972Ile) n.215+449A>T | |
7 | g.128852836T>C | CA369210898 | FLNC,FLNC-AS1 | c.6013T>C (p.Phe2005Leu) c.5914T>C (p.Phe1972Leu) n.215+449A>G | |
7 | g.128852836T>G | CA369210900 | FLNC,FLNC-AS1 | c.6013T>G (p.Phe2005Val) c.5914T>G (p.Phe1972Val) n.215+449A>C | |
7 | g.128852837T>A | CA369210901 | FLNC,FLNC-AS1 | c.6014T>A (p.Phe2005Tyr) c.5915T>A (p.Phe1972Tyr) n.215+448A>T | |
7 | g.128852837T>C | CA369210903 | FLNC,FLNC-AS1 | c.6014T>C (p.Phe2005Ser) c.5915T>C (p.Phe1972Ser) n.215+448A>G | dbSNP gnomAD v2 gnomAD v4 |
7 | g.128852837T>G | CA369210905 | FLNC,FLNC-AS1 | c.6014T>G (p.Phe2005Cys) c.5915T>G (p.Phe1972Cys) n.215+448A>C | |
7 | g.128852837T= | CA1742575511 | FLNC,FLNC-AS1 | c.6014T= (p.Phe2005=) c.5915T= (p.Phe1972=) n.215+448A= | |
7 | g.128852838C>A | CA369210907 | FLNC,FLNC-AS1 | c.6015C>A (p.Phe2005Leu) c.5916C>A (p.Phe1972Leu) n.215+447G>T | |
7 | g.128852838C= | CA1742575524 | FLNC,FLNC-AS1 | c.6015C= (p.Phe2005=) c.5916C= (p.Phe1972=) n.215+447G= | |
7 | g.128852838C>G | CA369210909 | FLNC,FLNC-AS1 | c.6015C>G (p.Phe2005Leu) c.5916C>G (p.Phe1972Leu) n.215+447G>C | |
7 | g.128852838C>T | CA4475870 | FLNC,FLNC-AS1 | c.6015C>T (p.Phe2005=) c.5916C>T (p.Phe1972=) n.215+447G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
7 | g.128852839A= | CA1742575527 | FLNC,FLNC-AS1 | c.6016A= (p.Thr2006=) c.5917A= (p.Thr1973=) n.215+446T= | |
7 | g.128852839A>C | CA369210911 | FLNC,FLNC-AS1 | c.6016A>C (p.Thr2006Pro) c.5917A>C (p.Thr1973Pro) n.215+446T>G | |
7 | g.128852839A>G | CA369210913 | FLNC,FLNC-AS1 | c.6016A>G (p.Thr2006Ala) c.5917A>G (p.Thr1973Ala) n.215+446T>C | dbSNP |
7 | g.128852839A>T | CA369210914 | FLNC,FLNC-AS1 | c.6016A>T (p.Thr2006Ser) c.5917A>T (p.Thr1973Ser) n.215+446T>A | gnomAD v4 |
7 | g.128852840C>A | CA369210920 | FLNC,FLNC-AS1 | c.6017C>A (p.Thr2006Asn) c.5918C>A (p.Thr1973Asn) n.215+445G>T | |
7 | g.128852840C>G | CA369210916 | FLNC,FLNC-AS1 | c.6017C>G (p.Thr2006Ser) c.5918C>G (p.Thr1973Ser) n.215+445G>C | |
7 | g.128852840C>T | CA369210918 | FLNC,FLNC-AS1 | c.6017C>T (p.Thr2006Ile) c.5918C>T (p.Thr1973Ile) n.215+445G>A | ClinVar |
7 | g.128852841C>A | CA457849444 | FLNC,FLNC-AS1 | c.6018C>A (p.Thr2006=) c.5919C>A (p.Thr1973=) n.215+444G>T | gnomAD v4 |
7 | g.128852841C>G | CA457849445 | FLNC,FLNC-AS1 | c.6018C>G (p.Thr2006=) c.5919C>G (p.Thr1973=) n.215+444G>C | |
7 | g.128852841C>T | CA457849446 | FLNC,FLNC-AS1 | c.6018C>T (p.Thr2006=) c.5919C>T (p.Thr1973=) n.215+444G>A | |
7 | g.128852842C>A | CA369210922 | FLNC,FLNC-AS1 | c.6019C>A (p.Pro2007Thr) c.5920C>A (p.Pro1974Thr) n.215+443G>T | |
7 | g.128852842C>G | CA369210924 | FLNC,FLNC-AS1 | c.6019C>G (p.Pro2007Ala) c.5920C>G (p.Pro1974Ala) n.215+443G>C | |
7 | g.128852842C>T | CA369210926 | FLNC,FLNC-AS1 | c.6019C>T (p.Pro2007Ser) c.5920C>T (p.Pro1974Ser) n.215+443G>A | |
7 | g.128852843C>A | CA369210928 | FLNC,FLNC-AS1 | c.6020C>A (p.Pro2007His) c.5921C>A (p.Pro1974His) n.215+442G>T | |
7 | g.128852843C>G | CA369210930 | FLNC,FLNC-AS1 | c.6020C>G (p.Pro2007Arg) c.5921C>G (p.Pro1974Arg) n.215+442G>C | |
7 | g.128852843C>T | CA369210932 | FLNC,FLNC-AS1 | c.6020C>T (p.Pro2007Leu) c.5921C>T (p.Pro1974Leu) n.215+442G>A | ClinVar dbSNP |
7 | g.128852844C>A | CA457849447 | FLNC,FLNC-AS1 | c.6021C>A (p.Pro2007=) c.5922C>A (p.Pro1974=) n.215+441G>T | dbSNP gnomAD v3 gnomAD v4 |
7 | g.128852844C= | CA1742575531 | FLNC,FLNC-AS1 | c.6021C= (p.Pro2007=) c.5922C= (p.Pro1974=) n.215+441G= | |
7 | g.128852844C>G | CA457849448 | FLNC,FLNC-AS1 | c.6021C>G (p.Pro2007=) c.5922C>G (p.Pro1974=) n.215+441G>C | |
7 | g.128852844C>T | CA457849449 | FLNC,FLNC-AS1 | c.6021C>T (p.Pro2007=) c.5922C>T (p.Pro1974=) n.215+441G>A | |
7 | g.128852845A= | CA1742575540 | FLNC,FLNC-AS1 | c.6022A= (p.Lys2008=) c.5923A= (p.Lys1975=) n.215+440T= | |
7 | g.128852845A>C | CA369210934 | FLNC,FLNC-AS1 | c.6022A>C (p.Lys2008Gln) c.5923A>C (p.Lys1975Gln) n.215+440T>G | |
7 | g.128852845A>G | CA4475871 | FLNC,FLNC-AS1 | c.6022A>G (p.Lys2008Glu) c.5923A>G (p.Lys1975Glu) n.215+440T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128852845A>T | CA369210937 | FLNC,FLNC-AS1 | c.6022A>T (p.Lys2008Ter) c.5923A>T (p.Lys1975Ter) n.215+440T>A | |
7 | g.128852846dup | CA2580076671 | FLNC,FLNC-AS1 | c.6023dup (p.Glu2009GlyfsTer29) c.5924dup (p.Glu1976GlyfsTer29) n.215+440dup | ClinVar |
7 | g.128852846A>C | CA369210939 | FLNC,FLNC-AS1 | c.6023A>C (p.Lys2008Thr) c.5924A>C (p.Lys1975Thr) n.215+439T>G | |
7 | g.128852846A>G | CA369210941 | FLNC,FLNC-AS1 | c.6023A>G (p.Lys2008Arg) c.5924A>G (p.Lys1975Arg) n.215+439T>C | ClinVar |
7 | g.128852846A>T | CA369210943 | FLNC,FLNC-AS1 | c.6023A>T (p.Lys2008Met) c.5924A>T (p.Lys1975Met) n.215+439T>A | |
7 | g.128852847G>A | CA457849453 | FLNC,FLNC-AS1 | c.6024G>A (p.Lys2008=) c.5925G>A (p.Lys1975=) n.215+438C>T | gnomAD v4 COSMIC |
7 | g.128852847G>C | CA369210947 | FLNC,FLNC-AS1 | c.6024G>C (p.Lys2008Asn) c.5925G>C (p.Lys1975Asn) n.215+438C>G | |
7 | g.128852847G>T | CA369210945 | FLNC,FLNC-AS1 | c.6024G>T (p.Lys2008Asn) c.5925G>T (p.Lys1975Asn) n.215+438C>A | |
7 | g.128852848G>A | CA369210950 | FLNC,FLNC-AS1 | c.6025G>A (p.Glu2009Lys) c.5926G>A (p.Glu1976Lys) n.215+437C>T | |
7 | g.128852848G>C | CA369210953 | FLNC,FLNC-AS1 | c.6025G>C (p.Glu2009Gln) c.5926G>C (p.Glu1976Gln) n.215+437C>G | |
7 | g.128852848G>T | CA369210952 | FLNC,FLNC-AS1 | c.6025G>T (p.Glu2009Ter) c.5926G>T (p.Glu1976Ter) n.215+437C>A | |
7 | g.128852849A>C | CA369210956 | FLNC,FLNC-AS1 | c.6026A>C (p.Glu2009Ala) c.5927A>C (p.Glu1976Ala) n.215+436T>G | |
7 | g.128852849A>G | CA369210960 | FLNC,FLNC-AS1 | c.6026A>G (p.Glu2009Gly) c.5927A>G (p.Glu1976Gly) n.215+436T>C | |
7 | g.128852849A>T | CA369210958 | FLNC,FLNC-AS1 | c.6026A>T (p.Glu2009Val) c.5927A>T (p.Glu1976Val) n.215+436T>A | |
7 | g.128852850G>A | CA457849457 | FLNC,FLNC-AS1 | c.6027G>A (p.Glu2009=) c.5928G>A (p.Glu1976=) n.215+435C>T | gnomAD v4 |
7 | g.128852850G>C | CA369210962 | FLNC,FLNC-AS1 | c.6027G>C (p.Glu2009Asp) c.5928G>C (p.Glu1976Asp) n.215+435C>G | gnomAD v4 |
7 | g.128852850G>T | CA369210964 | FLNC,FLNC-AS1 | c.6027G>T (p.Glu2009Asp) c.5928G>T (p.Glu1976Asp) n.215+435C>A | |
7 | g.128852851G>A | CA369210966 | FLNC,FLNC-AS1 | c.6028G>A (p.Val2010Ile) c.5929G>A (p.Val1977Ile) n.215+434C>T | |
7 | g.128852851G>C | CA369210967 | FLNC,FLNC-AS1 | c.6028G>C (p.Val2010Leu) c.5929G>C (p.Val1977Leu) n.215+434C>G | |
7 | g.128852851G>T | CA369210969 | FLNC,FLNC-AS1 | c.6028G>T (p.Val2010Phe) c.5929G>T (p.Val1977Phe) n.215+434C>A | |
7 | g.128852852T>A | CA369210972 | FLNC,FLNC-AS1 | c.6029T>A (p.Val2010Asp) c.5930T>A (p.Val1977Asp) n.215+433A>T | |
7 | g.128852852T>C | CA369210974 | FLNC,FLNC-AS1 | c.6029T>C (p.Val2010Ala) c.5930T>C (p.Val1977Ala) n.215+433A>G | dbSNP gnomAD v2 |
7 | g.128852852T>G | CA369210975 | FLNC,FLNC-AS1 | c.6029T>G (p.Val2010Gly) c.5930T>G (p.Val1977Gly) n.215+433A>C | |
7 | g.128852852T= | CA1742575546 | FLNC,FLNC-AS1 | c.6029T= (p.Val2010=) c.5930T= (p.Val1977=) n.215+433A= | |
7 | g.128852853C>A | CA4475873 | FLNC,FLNC-AS1 | c.6030C>A (p.Val2010=) c.5931C>A (p.Val1977=) n.215+432G>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.128852853C= | CA1742575553 | FLNC,FLNC-AS1 | c.6030C= (p.Val2010=) c.5931C= (p.Val1977=) n.215+432G= | |
7 | g.128852853C>G | CA457849458 | FLNC,FLNC-AS1 | c.6030C>G (p.Val2010=) c.5931C>G (p.Val1977=) n.215+432G>C | gnomAD v4 |
7 | g.128852853C>T | CA4475872 | FLNC,FLNC-AS1 | c.6030C>T (p.Val2010=) c.5931C>T (p.Val1977=) n.215+432G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128852854G>A | CA369210984 | FLNC,FLNC-AS1 | c.6031G>A (p.Gly2011Arg) c.5932G>A (p.Gly1978Arg) n.215+431C>T | ClinVar dbSNP |
7 | g.128852854G>C | CA369210981 | FLNC,FLNC-AS1 | c.6031G>C (p.Gly2011Arg) c.5932G>C (p.Gly1978Arg) n.215+431C>G | |
7 | g.128852854G= | CA1742575562 | FLNC,FLNC-AS1 | c.6031G= (p.Gly2011=) c.5932G= (p.Gly1978=) n.215+431C= | |
7 | g.128852854G>T | CA369210979 | FLNC,FLNC-AS1 | c.6031G>T (p.Gly2011Trp) c.5932G>T (p.Gly1978Trp) n.215+431C>A | dbSNP |