Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.56968820_56968822delCA977671256CETPc.234-566_234-564del (p.=)
c.39-566_39-564del (p.=)
n.232-566_232-564del
16g.56968820T>ACA2224395669CETPc.234-566T>A (p.=)
c.39-566T>A (p.=)
n.232-566T>A
16g.56968820T>CCA2224395668CETPc.234-566T>C (p.=)
c.39-566T>C (p.=)
n.232-566T>C
16g.56968820T>GCA14266406CETPc.234-566T>G (p.=)
c.39-566T>G (p.=)
n.232-566T>G
dbSNP gnomAD
16g.56968820T=CA2224395667CETPc.234-566T= (p.=)
c.39-566T= (p.=)
n.232-566T=
16g.56968821T>CCA722013215CETPc.234-565T>C (p.=)
c.39-565T>C (p.=)
n.232-565T>C
16g.56968821T=CA2224395670CETPc.234-565T= (p.=)
c.39-565T= (p.=)
n.232-565T=
16g.56968821_56968822insGTCA977671264CETPc.234-565_234-564insGT (p.=)
c.39-565_39-564insGT (p.=)
n.232-565_232-564insGT
dbSNP
16g.56968821_56968822insCACCGATTGTTGTTGTCA977671263CETPc.234-565_234-564insCACCGATTGTTGTTGT (p.=)
c.39-565_39-564insCACCGATTGTTGTTGT (p.=)
n.232-565_232-564insCACCGATTGTTGTTGT
16g.56968823G>TCA977671267CETPc.234-563G>T (p.=)
c.39-563G>T (p.=)
n.232-563G>T
16g.56968826C>TCA977671269CETPc.234-560C>T (p.=)
c.39-560C>T (p.=)
n.232-560C>T
16g.56968828A>TCA977671275CETPc.234-558A>T (p.=)
c.39-558A>T (p.=)
n.232-558A>T
16g.56968829T>GCA722013217CETPc.234-557T>G (p.=)
c.39-557T>G (p.=)
n.232-557T>G
16g.56968829T=CA2224395671CETPc.234-557T= (p.=)
c.39-557T= (p.=)
n.232-557T=
16g.56968831A>TCA977671276CETPc.234-555A>T (p.=)
c.39-555A>T (p.=)
n.232-555A>T
16g.56968831_56968843delinsATTTCATTCATAGCA2224395672CETPc.234-555_234-543delinsATTTCATTCATAG (p.=)
c.39-555_39-543delinsATTTCATTCATAG (p.=)
n.232-555_232-543delinsATTTCATTCATAG
16g.56968832_56968843delCA2224395673CETPc.234-554_234-543del (p.=)
c.39-554_39-543del (p.=)
n.232-554_232-543del
dbSNP
16g.56968840A=CA2224395674CETPc.234-546A= (p.=)
c.39-546A= (p.=)
n.232-546A=
16g.56968840A>GCA281521291CETPc.234-546A>G (p.=)
c.39-546A>G (p.=)
n.232-546A>G
dbSNP gnomAD
16g.56968841T>CCA977671288CETPc.234-545T>C (p.=)
c.39-545T>C (p.=)
n.232-545T>C
16g.56968841T=CA2224395675CETPc.234-545T= (p.=)
c.39-545T= (p.=)
n.232-545T=
16g.56968845C=CA2224395676CETPc.234-541C= (p.=)
c.39-541C= (p.=)
n.232-541C=
16g.56968845C>TCA2224395677CETPc.234-541C>T (p.=)
c.39-541C>T (p.=)
n.232-541C>T
16g.56968846A=CA2224395678CETPc.234-540A= (p.=)
c.39-540A= (p.=)
n.232-540A=
16g.56968846A>GCA2224395679CETPc.234-540A>G (p.=)
c.39-540A>G (p.=)
n.232-540A>G
16g.56968851G>ACA281521294CETPc.234-535G>A (p.=)
c.39-535G>A (p.=)
n.232-535G>A
dbSNP
16g.56968851G=CA2224395680CETPc.234-535G= (p.=)
c.39-535G= (p.=)
n.232-535G=
16g.56968861_56968865delinsACTTCCA2224395681CETPc.234-525_234-521delinsACTTC (p.=)
c.39-525_39-521delinsACTTC (p.=)
n.232-525_232-521delinsACTTC
16g.56968862C=CA2224395682CETPc.234-524C= (p.=)
c.39-524C= (p.=)
n.232-524C=
16g.56968862C>GCA977671299CETPc.234-524C>G (p.=)
c.39-524C>G (p.=)
n.232-524C>G
16g.56968870_56968873delCA622341239CETPc.234-516_234-513del (p.=)
c.39-516_39-513del (p.=)
n.232-516_232-513del
dbSNP gnomAD
16g.56968865C>ACA977671306CETPc.234-521C>A (p.=)
c.39-521C>A (p.=)
n.232-521C>A
16g.56968865C=CA2224395683CETPc.234-521C= (p.=)
c.39-521C= (p.=)
n.232-521C=
16g.56968865C>GCA977671307CETPc.234-521C>G (p.=)
c.39-521C>G (p.=)
n.232-521C>G
16g.56968866C>ACA977671309CETPc.234-520C>A (p.=)
c.39-520C>A (p.=)
n.232-520C>A
16g.56968866C=CA2224395684CETPc.234-520C= (p.=)
c.39-520C= (p.=)
n.232-520C=
16g.56968866C>GCA977671319CETPc.234-520C>G (p.=)
c.39-520C>G (p.=)
n.232-520C>G
16g.56968866C>TCA977671310CETPc.234-520C>T (p.=)
c.39-520C>T (p.=)
n.232-520C>T
16g.56968867T>CCA722013330CETPc.234-519T>C (p.=)
c.39-519T>C (p.=)
n.232-519T>C
16g.56968867T=CA2224395685CETPc.234-519T= (p.=)
c.39-519T= (p.=)
n.232-519T=
16g.56968877T>CCA622341240CETPc.234-509T>C (p.=)
c.39-509T>C (p.=)
n.232-509T>C
gnomAD
16g.56968877T=CA2224395686CETPc.234-509T= (p.=)
c.39-509T= (p.=)
n.232-509T=
16g.56968882T>GCA2224395688CETPc.234-504T>G (p.=)
c.39-504T>G (p.=)
n.232-504T>G
16g.56968882T=CA2224395687CETPc.234-504T= (p.=)
c.39-504T= (p.=)
n.232-504T=
16g.56968886G=CA2224395689CETPc.234-500G= (p.=)
c.39-500G= (p.=)
n.232-500G=
16g.56968886G>TCA977671329CETPc.234-500G>T (p.=)
c.39-500G>T (p.=)
n.232-500G>T
16g.56968887_56968888delinsCTCA2224395690CETPc.234-499_234-498delinsCT (p.=)
c.39-499_39-498delinsCT (p.=)
n.232-499_232-498delinsCT
16g.56968889delCA2224395691CETPc.234-497del (p.=)
c.39-497del (p.=)
n.232-497del
dbSNP
16g.56968889T>CCA622341243CETPc.234-497T>C (p.=)
c.39-497T>C (p.=)
n.232-497T>C
gnomAD
16g.56968889T=CA2224395692CETPc.234-497T= (p.=)
c.39-497T= (p.=)
n.232-497T=

Number of alleles fetched