Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.2166893G>ACA472414305THc.835C>T (p.Leu279=)
c.*524C>T (n.*524C>T)
c.696-344C>T (n.696-344C>T)
c.*555C>T (n.*555C>T)
c.916C>T (p.Leu306=)
c.928C>T (p.Leu310=)
c.136-344C>T
c.136-125C>T
n.384C>T
c.847C>T (p.Leu283=)
11g.2166893G>CCA379126503THc.835C>G (p.Leu279Val)
c.*524C>G (n.*524C>G)
c.696-344C>G (n.696-344C>G)
c.*555C>G (n.*555C>G)
c.916C>G (p.Leu306Val)
c.928C>G (p.Leu310Val)
c.136-344C>G
c.136-125C>G
n.384C>G
c.847C>G (p.Leu283Val)
11g.2166893G>TCA379126506THc.835C>A (p.Leu279Met)
c.*524C>A (n.*524C>A)
c.696-344C>A (n.696-344C>A)
c.*555C>A (n.*555C>A)
c.916C>A (p.Leu306Met)
c.928C>A (p.Leu310Met)
c.136-344C>A
c.136-125C>A
n.384C>A
c.847C>A (p.Leu283Met)
11g.2166894dupCA2580082666THc.835dup (p.Leu279ProfsTer?)
c.*524dup (n.*524dup)
c.696-344dup (n.696-344dup)
c.*555dup (n.*555dup)
c.916dup (p.Leu306ProfsTer?)
c.928dup (p.Leu310ProfsTer?)
c.136-344dup
c.136-125dup
n.384dup
c.847dup (p.Leu283ProfsTer?)
ClinVar
11g.2166894G>ACA472414306THc.834C>T (p.Phe278=)
c.*523C>T (n.*523C>T)
c.696-345C>T (n.696-345C>T)
c.*554C>T (n.*554C>T)
c.915C>T (p.Phe305=)
c.927C>T (p.Phe309=)
c.136-345C>T
c.136-126C>T
n.963C>T
n.383C>T
c.846C>T (p.Phe282=)
11g.2166894G>CCA379126510THc.834C>G (p.Phe278Leu)
c.*523C>G (n.*523C>G)
c.696-345C>G (n.696-345C>G)
c.*554C>G (n.*554C>G)
c.915C>G (p.Phe305Leu)
c.927C>G (p.Phe309Leu)
c.136-345C>G
c.136-126C>G
n.963C>G
n.383C>G
c.846C>G (p.Phe282Leu)
11g.2166894G>TCA379126508THc.834C>A (p.Phe278Leu)
c.*523C>A (n.*523C>A)
c.696-345C>A (n.696-345C>A)
c.*554C>A (n.*554C>A)
c.915C>A (p.Phe305Leu)
c.927C>A (p.Phe309Leu)
c.136-345C>A
c.136-126C>A
n.963C>A
n.383C>A
c.846C>A (p.Phe282Leu)
11g.2166895_2166899dupCA2611964147THc.830_834dup (p.Leu279AlafsTer3)
c.*519_*523dup (n.*519_*523dup)
c.696-349_696-345dup (n.696-349_696-345dup)
c.*550_*554dup (n.*550_*554dup)
c.911_915dup (p.Leu306AlafsTer3)
c.923_927dup (p.Leu310AlafsTer3)
c.136-349_136-345dup
c.136-130_136-126dup
n.379_383dup
c.842_846dup (p.Leu283AlafsTer3)
gnomAD v4
11g.2166895A>CCA379126513THc.833T>G (p.Phe278Cys)
c.*522T>G (n.*522T>G)
c.696-346T>G (n.696-346T>G)
c.*553T>G (n.*553T>G)
c.914T>G (p.Phe305Cys)
c.926T>G (p.Phe309Cys)
c.136-346T>G
c.136-127T>G
n.962T>G
n.382T>G
c.845T>G (p.Phe282Cys)
11g.2166895A>GCA379126515THc.833T>C (p.Phe278Ser)
c.*522T>C (n.*522T>C)
c.696-346T>C (n.696-346T>C)
c.*553T>C (n.*553T>C)
c.914T>C (p.Phe305Ser)
c.926T>C (p.Phe309Ser)
c.136-346T>C
c.136-127T>C
n.962T>C
n.382T>C
c.845T>C (p.Phe282Ser)
11g.2166895A>TCA379126514THc.833T>A (p.Phe278Tyr)
c.*522T>A (n.*522T>A)
c.696-346T>A (n.696-346T>A)
c.*553T>A (n.*553T>A)
c.914T>A (p.Phe305Tyr)
c.926T>A (p.Phe309Tyr)
c.136-346T>A
c.136-127T>A
n.962T>A
n.382T>A
c.845T>A (p.Phe282Tyr)
gnomAD v4
11g.2166896A>CCA379126516THc.832T>G (p.Phe278Val)
c.*521T>G (n.*521T>G)
c.696-347T>G (n.696-347T>G)
c.*552T>G (n.*552T>G)
c.913T>G (p.Phe305Val)
c.925T>G (p.Phe309Val)
c.136-347T>G
c.136-128T>G
n.961T>G
n.381T>G
c.844T>G (p.Phe282Val)
11g.2166896A>GCA379126519THc.832T>C (p.Phe278Leu)
c.*521T>C (n.*521T>C)
c.696-347T>C (n.696-347T>C)
c.*552T>C (n.*552T>C)
c.913T>C (p.Phe305Leu)
c.925T>C (p.Phe309Leu)
c.136-347T>C
c.136-128T>C
n.961T>C
n.381T>C
c.844T>C (p.Phe282Leu)
11g.2166896A>TCA379126517THc.832T>A (p.Phe278Ile)
c.*521T>A (n.*521T>A)
c.696-347T>A (n.696-347T>A)
c.*552T>A (n.*552T>A)
c.913T>A (p.Phe305Ile)
c.925T>A (p.Phe309Ile)
c.136-347T>A
c.136-128T>A
n.961T>A
n.381T>A
c.844T>A (p.Phe282Ile)
11g.2166897G>ACA472414307THc.831C>T (p.Arg277=)
c.*520C>T (n.*520C>T)
c.696-348C>T (n.696-348C>T)
c.*551C>T (n.*551C>T)
c.912C>T (p.Arg304=)
c.924C>T (p.Arg308=)
c.136-348C>T
c.136-129C>T
n.960C>T
n.380C>T
c.843C>T (p.Arg281=)
11g.2166897G>CCA472414308THc.831C>G (p.Arg277=)
c.*520C>G (n.*520C>G)
c.696-348C>G (n.696-348C>G)
c.*551C>G (n.*551C>G)
c.912C>G (p.Arg304=)
c.924C>G (p.Arg308=)
c.136-348C>G
c.136-129C>G
n.960C>G
n.380C>G
c.843C>G (p.Arg281=)
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.2166897G=CA1948005763THc.831C= (p.Arg277=)
c.*520C= (n.*520C=)
c.696-348C= (n.696-348C=)
c.*551C= (n.*551C=)
c.912C= (p.Arg304=)
c.924C= (p.Arg308=)
c.136-348C=
c.136-129C=
n.960C=
n.380C=
c.843C= (p.Arg281=)
11g.2166897G>TCA472414309THc.831C>A (p.Arg277=)
c.*520C>A (n.*520C>A)
c.696-348C>A (n.696-348C>A)
c.*551C>A (n.*551C>A)
c.912C>A (p.Arg304=)
c.924C>A (p.Arg308=)
c.136-348C>A
c.136-129C>A
n.960C>A
n.380C>A
c.843C>A (p.Arg281=)
11g.2166898C>ACA379126521THc.830G>T (p.Arg277Leu)
c.*519G>T (n.*519G>T)
c.696-349G>T (n.696-349G>T)
c.*550G>T (n.*550G>T)
c.911G>T (p.Arg304Leu)
c.923G>T (p.Arg308Leu)
c.136-349G>T
c.136-130G>T
n.959G>T
n.379G>T
c.842G>T (p.Arg281Leu)
gnomAD v4
11g.2166898C=CA1948005766THc.830G= (p.Arg277=)
c.*519G= (n.*519G=)
c.696-349G= (n.696-349G=)
c.*550G= (n.*550G=)
c.911G= (p.Arg304=)
c.923G= (p.Arg308=)
c.136-349G=
c.136-130G=
n.959G=
n.379G=
c.842G= (p.Arg281=)
11g.2166898C>GCA379126522THc.830G>C (p.Arg277Pro)
c.*519G>C (n.*519G>C)
c.696-349G>C (n.696-349G>C)
c.*550G>C (n.*550G>C)
c.911G>C (p.Arg304Pro)
c.923G>C (p.Arg308Pro)
c.136-349G>C
c.136-130G>C
n.959G>C
n.379G>C
c.842G>C (p.Arg281Pro)
11g.2166898C>TCA379126524THc.830G>A (p.Arg277His)
c.*519G>A (n.*519G>A)
c.696-349G>A (n.696-349G>A)
c.*550G>A (n.*550G>A)
c.911G>A (p.Arg304His)
c.923G>A (p.Arg308His)
c.136-349G>A
c.136-130G>A
n.959G>A
n.379G>A
c.842G>A (p.Arg281His)
dbSNP gnomAD v2 gnomAD v4
11g.2166898_2166899delinsCGCA1948005768THc.829_830delinsCG (p.Arg277=)
c.*518_*519delinsCG (n.*518_*519delinsCG)
c.696-350_696-349delinsCG (n.696-350_696-349delinsCG)
c.*549_*550delinsCG (n.*549_*550delinsCG)
c.910_911delinsCG (p.Arg304=)
c.922_923delinsCG (p.Arg308=)
c.136-350_136-349delinsCG
c.136-131_136-130delinsCG
n.958_959delinsCG
n.378_379delinsCG
c.841_842delinsCG (p.Arg281=)
11g.2166899G>ACA379126526THc.829C>T (p.Arg277Cys)
c.*518C>T (n.*518C>T)
c.696-350C>T (n.696-350C>T)
c.*549C>T (n.*549C>T)
c.910C>T (p.Arg304Cys)
c.922C>T (p.Arg308Cys)
c.136-350C>T
c.136-131C>T
n.958C>T
n.378C>T
c.841C>T (p.Arg281Cys)
gnomAD v4
11g.2166899G>CCA379126528THc.829C>G (p.Arg277Gly)
c.*518C>G (n.*518C>G)
c.696-350C>G (n.696-350C>G)
c.*549C>G (n.*549C>G)
c.910C>G (p.Arg304Gly)
c.922C>G (p.Arg308Gly)
c.136-350C>G
c.136-131C>G
n.958C>G
n.378C>G
c.841C>G (p.Arg281Gly)
gnomAD v4
11g.2166899G>TCA379126529THc.829C>A (p.Arg277Ser)
c.*518C>A (n.*518C>A)
c.696-350C>A (n.696-350C>A)
c.*549C>A (n.*549C>A)
c.910C>A (p.Arg304Ser)
c.922C>A (p.Arg308Ser)
c.136-350C>A
c.136-131C>A
n.958C>A
n.378C>A
c.841C>A (p.Arg281Ser)
ClinVar dbSNP gnomAD v4
11g.2166901delCA934419392THc.829del (p.Arg277AlafsTer3)
c.*518del (n.*518del)
c.696-350del (n.696-350del)
c.*549del (n.*549del)
c.910del (p.Arg304AlafsTer3)
c.922del (p.Arg308AlafsTer3)
c.136-350del
c.136-131del
n.958del
n.378del
c.841del (p.Arg281AlafsTer3)
dbSNP gnomAD v3 gnomAD v4
11g.2166900G>ACA472414310THc.828C>T (p.Ser276=)
c.*517C>T (n.*517C>T)
c.696-351C>T (n.696-351C>T)
c.*548C>T (n.*548C>T)
c.909C>T (p.Ser303=)
c.921C>T (p.Ser307=)
c.136-351C>T
c.136-132C>T
n.957C>T
n.377C>T
c.840C>T (p.Ser280=)
gnomAD v4
11g.2166900G>CCA5818476THc.828C>G (p.Ser276=)
c.*517C>G (n.*517C>G)
c.696-351C>G (n.696-351C>G)
c.*548C>G (n.*548C>G)
c.909C>G (p.Ser303=)
c.921C>G (p.Ser307=)
c.136-351C>G
c.136-132C>G
n.957C>G
n.377C>G
c.840C>G (p.Ser280=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.2166900G=CA1948005773THc.828C= (p.Ser276=)
c.*517C= (n.*517C=)
c.696-351C= (n.696-351C=)
c.*548C= (n.*548C=)
c.909C= (p.Ser303=)
c.921C= (p.Ser307=)
c.136-351C=
c.136-132C=
n.957C=
n.377C=
c.840C= (p.Ser280=)
11g.2166900G>TCA472414311THc.828C>A (p.Ser276=)
c.*517C>A (n.*517C>A)
c.696-351C>A (n.696-351C>A)
c.*548C>A (n.*548C>A)
c.909C>A (p.Ser303=)
c.921C>A (p.Ser307=)
c.136-351C>A
c.136-132C>A
n.957C>A
n.377C>A
c.840C>A (p.Ser280=)
gnomAD v4
11g.2166901G>ACA379126533THc.827C>T (p.Ser276Phe)
c.*516C>T (n.*516C>T)
c.696-352C>T (n.696-352C>T)
c.*547C>T (n.*547C>T)
c.908C>T (p.Ser303Phe)
c.920C>T (p.Ser307Phe)
c.136-352C>T
c.136-133C>T
n.956C>T
n.376C>T
c.839C>T (p.Ser280Phe)
11g.2166901G>CCA379126538THc.827C>G (p.Ser276Cys)
c.*516C>G (n.*516C>G)
c.696-352C>G (n.696-352C>G)
c.*547C>G (n.*547C>G)
c.908C>G (p.Ser303Cys)
c.920C>G (p.Ser307Cys)
c.136-352C>G
c.136-133C>G
n.956C>G
n.376C>G
c.839C>G (p.Ser280Cys)
gnomAD v4
11g.2166901G>TCA379126540THc.827C>A (p.Ser276Tyr)
c.*516C>A (n.*516C>A)
c.696-352C>A (n.696-352C>A)
c.*547C>A (n.*547C>A)
c.908C>A (p.Ser303Tyr)
c.920C>A (p.Ser307Tyr)
c.136-352C>A
c.136-133C>A
n.956C>A
n.376C>A
c.839C>A (p.Ser280Tyr)
ClinVar
11g.2166902A=CA1948005777THc.826T= (p.Ser276=)
c.*515T= (n.*515T=)
c.696-353T= (n.696-353T=)
c.*546T= (n.*546T=)
c.907T= (p.Ser303=)
c.919T= (p.Ser307=)
c.136-353T=
c.136-134T=
n.955T=
n.375T=
c.838T= (p.Ser280=)
11g.2166902A>CCA379126542THc.826T>G (p.Ser276Ala)
c.*515T>G (n.*515T>G)
c.696-353T>G (n.696-353T>G)
c.*546T>G (n.*546T>G)
c.907T>G (p.Ser303Ala)
c.919T>G (p.Ser307Ala)
c.136-353T>G
c.136-134T>G
n.955T>G
n.375T>G
c.838T>G (p.Ser280Ala)
dbSNP gnomAD v2 gnomAD v4
11g.2166902A>GCA379126543THc.826T>C (p.Ser276Pro)
c.*515T>C (n.*515T>C)
c.696-353T>C (n.696-353T>C)
c.*546T>C (n.*546T>C)
c.907T>C (p.Ser303Pro)
c.919T>C (p.Ser307Pro)
c.136-353T>C
c.136-134T>C
n.955T>C
n.375T>C
c.838T>C (p.Ser280Pro)
11g.2166902A>TCA379126545THc.826T>A (p.Ser276Thr)
c.*515T>A (n.*515T>A)
c.696-353T>A (n.696-353T>A)
c.*546T>A (n.*546T>A)
c.907T>A (p.Ser303Thr)
c.919T>A (p.Ser307Thr)
c.136-353T>A
c.136-134T>A
n.955T>A
n.375T>A
c.838T>A (p.Ser280Thr)
11g.2166903G>ACA472414312THc.825C>T (p.Val275=)
c.*514C>T (n.*514C>T)
c.696-354C>T (n.696-354C>T)
c.*545C>T (n.*545C>T)
c.906C>T (p.Val302=)
c.918C>T (p.Val306=)
c.136-354C>T
c.136-135C>T
n.954C>T
n.374C>T
c.837C>T (p.Val279=)
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.2166903G>CCA472414314THc.825C>G (p.Val275=)
c.*514C>G (n.*514C>G)
c.696-354C>G (n.696-354C>G)
c.*545C>G (n.*545C>G)
c.906C>G (p.Val302=)
c.918C>G (p.Val306=)
c.136-354C>G
c.136-135C>G
n.954C>G
n.374C>G
c.837C>G (p.Val279=)
11g.2166903G=CA1948005784THc.825C= (p.Val275=)
c.*514C= (n.*514C=)
c.696-354C= (n.696-354C=)
c.*545C= (n.*545C=)
c.906C= (p.Val302=)
c.918C= (p.Val306=)
c.136-354C=
c.136-135C=
n.954C=
n.374C=
c.837C= (p.Val279=)
11g.2166903G>TCA472414313THc.825C>A (p.Val275=)
c.*514C>A (n.*514C>A)
c.696-354C>A (n.696-354C>A)
c.*545C>A (n.*545C>A)
c.906C>A (p.Val302=)
c.918C>A (p.Val306=)
c.136-354C>A
c.136-135C>A
n.954C>A
n.374C>A
c.837C>A (p.Val279=)
gnomAD v4
11g.2166904_2166906dupCA2574757483THc.823_825dup (p.Val275_Ser276insVal)
c.*512_*514dup (n.*512_*514dup)
c.696-356_696-354dup (n.696-356_696-354dup)
c.*543_*545dup (n.*543_*545dup)
c.904_906dup (p.Val302_Ser303insVal)
c.916_918dup (p.Val306_Ser307insVal)
c.136-356_136-354dup
c.136-137_136-135dup
n.952_954dup
n.372_374dup
c.835_837dup (p.Val279_Ser280insVal)
gnomAD v4
11g.2166905_2166922dupCA597431466THc.808_825dup (p.Val275_Ser276insProGlnLeuGluAspVal)
c.*497_*514dup (n.*497_*514dup)
c.696-371_696-354dup (n.696-371_696-354dup)
c.*528_*545dup (n.*528_*545dup)
c.889_906dup (p.Val302_Ser303insProGlnLeuGluAspVal)
c.901_918dup (p.Val306_Ser307insProGlnLeuGluAspVal)
c.136-371_136-354dup
c.136-152_136-135dup
n.937_954dup
n.357_374dup
c.820_837dup (p.Val279_Ser280insProGlnLeuGluAspVal)
dbSNP gnomAD v2 gnomAD v4
11g.2166904A>CCA379126547THc.824T>G (p.Val275Gly)
c.*513T>G (n.*513T>G)
c.696-355T>G (n.696-355T>G)
c.*544T>G (n.*544T>G)
c.905T>G (p.Val302Gly)
c.917T>G (p.Val306Gly)
c.136-355T>G
c.136-136T>G
n.953T>G
n.373T>G
c.836T>G (p.Val279Gly)
ClinVar dbSNP
11g.2166904A>GCA379126550THc.824T>C (p.Val275Ala)
c.*513T>C (n.*513T>C)
c.696-355T>C (n.696-355T>C)
c.*544T>C (n.*544T>C)
c.905T>C (p.Val302Ala)
c.917T>C (p.Val306Ala)
c.136-355T>C
c.136-136T>C
n.953T>C
n.373T>C
c.836T>C (p.Val279Ala)
11g.2166904A>TCA379126548THc.824T>A (p.Val275Asp)
c.*513T>A (n.*513T>A)
c.696-355T>A (n.696-355T>A)
c.*544T>A (n.*544T>A)
c.905T>A (p.Val302Asp)
c.917T>A (p.Val306Asp)
c.136-355T>A
c.136-136T>A
n.953T>A
n.373T>A
c.836T>A (p.Val279Asp)
11g.2166904_2166908delinsACGTCCA1948005786THc.820_824delinsGACGT (p.Asp274=)
c.*509_*513delinsGACGT (n.*509_*513delinsGACGT)
c.696-359_696-355delinsGACGT (n.696-359_696-355delinsGACGT)
c.*540_*544delinsGACGT (n.*540_*544delinsGACGT)
c.901_905delinsGACGT (p.Asp301=)
c.913_917delinsGACGT (p.Asp305=)
c.136-359_136-355delinsGACGT
c.136-140_136-136delinsGACGT
n.949_953delinsGACGT
n.369_373delinsGACGT
c.832_836delinsGACGT (p.Asp278=)
11g.2166905C>ACA379126552THc.823G>T (p.Val275Phe)
c.*512G>T (n.*512G>T)
c.696-356G>T (n.696-356G>T)
c.*543G>T (n.*543G>T)
c.904G>T (p.Val302Phe)
c.916G>T (p.Val306Phe)
c.136-356G>T
c.136-137G>T
n.952G>T
n.372G>T
c.835G>T (p.Val279Phe)
11g.2166905C=CA1948005790THc.823G= (p.Val275=)
c.*512G= (n.*512G=)
c.696-356G= (n.696-356G=)
c.*543G= (n.*543G=)
c.904G= (p.Val302=)
c.916G= (p.Val306=)
c.136-356G=
c.136-137G=
n.952G=
n.372G=
c.835G= (p.Val279=)
11g.2166905C>GCA379126553THc.823G>C (p.Val275Leu)
c.*512G>C (n.*512G>C)
c.696-356G>C (n.696-356G>C)
c.*543G>C (n.*543G>C)
c.904G>C (p.Val302Leu)
c.916G>C (p.Val306Leu)
c.136-356G>C
c.136-137G>C
n.952G>C
n.372G>C
c.835G>C (p.Val279Leu)
11g.2166905C>TCA5818478THc.823G>A (p.Val275Ile)
c.*512G>A (n.*512G>A)
c.696-356G>A (n.696-356G>A)
c.*543G>A (n.*543G>A)
c.904G>A (p.Val302Ile)
c.916G>A (p.Val306Ile)
c.136-356G>A
c.136-137G>A
n.952G>A
n.372G>A
c.835G>A (p.Val279Ile)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.2166905_2166906delinsCGCA1948005791THc.822_823delinsCG (p.Asp274=)
c.*511_*512delinsCG (n.*511_*512delinsCG)
c.696-357_696-356delinsCG (n.696-357_696-356delinsCG)
c.*542_*543delinsCG (n.*542_*543delinsCG)
c.903_904delinsCG (p.Asp301=)
c.915_916delinsCG (p.Asp305=)
c.136-357_136-356delinsCG
c.136-138_136-137delinsCG
n.951_952delinsCG
n.371_372delinsCG
c.834_835delinsCG (p.Asp278=)
11g.2166906_2166909delCA674607087THc.820_823del (p.Asp274SerfsTer5)
c.*509_*512del (n.*509_*512del)
c.696-359_696-356del (n.696-359_696-356del)
c.*540_*543del (n.*540_*543del)
c.901_904del (p.Asp301SerfsTer5)
c.913_916del (p.Asp305SerfsTer5)
c.136-359_136-356del
c.136-140_136-137del
n.949_952del
n.369_372del
c.832_835del (p.Asp278SerfsTer5)
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.2166906delCA5818477THc.822del (p.Asp274GlufsTer6)
c.*511del (n.*511del)
c.696-357del (n.696-357del)
c.*542del (n.*542del)
c.903del (p.Asp301GlufsTer6)
c.915del (p.Asp305GlufsTer6)
c.136-357del
c.136-138del
n.951del
n.371del
c.834del (p.Asp278GlufsTer6)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.2166906G>ACA5818479THc.822C>T (p.Asp274=)
c.*511C>T (n.*511C>T)
c.696-357C>T (n.696-357C>T)
c.*542C>T (n.*542C>T)
c.903C>T (p.Asp301=)
c.915C>T (p.Asp305=)
c.136-357C>T
c.136-138C>T
n.951C>T
n.371C>T
c.834C>T (p.Asp278=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.2166906G>CCA5818480THc.822C>G (p.Asp274Glu)
c.*511C>G (n.*511C>G)
c.696-357C>G (n.696-357C>G)
c.*542C>G (n.*542C>G)
c.903C>G (p.Asp301Glu)
c.915C>G (p.Asp305Glu)
c.136-357C>G
c.136-138C>G
n.951C>G
n.371C>G
c.834C>G (p.Asp278Glu)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.2166906G=CA1948005796THc.822C= (p.Asp274=)
c.*511C= (n.*511C=)
c.696-357C= (n.696-357C=)
c.*542C= (n.*542C=)
c.903C= (p.Asp301=)
c.915C= (p.Asp305=)
c.136-357C=
c.136-138C=
n.951C=
n.371C=
c.834C= (p.Asp278=)
11g.2166906G>TCA379126554THc.822C>A (p.Asp274Glu)
c.*511C>A (n.*511C>A)
c.696-357C>A (n.696-357C>A)
c.*542C>A (n.*542C>A)
c.903C>A (p.Asp301Glu)
c.915C>A (p.Asp305Glu)
c.136-357C>A
c.136-138C>A
n.951C>A
n.371C>A
c.834C>A (p.Asp278Glu)
gnomAD v4
11g.2166907T>ACA379126557THc.821A>T (p.Asp274Val)
c.*510A>T (n.*510A>T)
c.696-358A>T (n.696-358A>T)
c.*541A>T (n.*541A>T)
c.902A>T (p.Asp301Val)
c.914A>T (p.Asp305Val)
c.136-358A>T
c.136-139A>T
n.950A>T
n.370A>T
c.833A>T (p.Asp278Val)
11g.2166907T>CCA379126558THc.821A>G (p.Asp274Gly)
c.*510A>G (n.*510A>G)
c.696-358A>G (n.696-358A>G)
c.*541A>G (n.*541A>G)
c.902A>G (p.Asp301Gly)
c.914A>G (p.Asp305Gly)
c.136-358A>G
c.136-139A>G
n.950A>G
n.370A>G
c.833A>G (p.Asp278Gly)
ClinVar
11g.2166907T>GCA379126559THc.821A>C (p.Asp274Ala)
c.*510A>C (n.*510A>C)
c.696-358A>C (n.696-358A>C)
c.*541A>C (n.*541A>C)
c.902A>C (p.Asp301Ala)
c.914A>C (p.Asp305Ala)
c.136-358A>C
c.136-139A>C
n.950A>C
n.370A>C
c.833A>C (p.Asp278Ala)
11g.2166908C>ACA379126563THc.820G>T (p.Asp274Tyr)
c.*509G>T (n.*509G>T)
c.696-359G>T (n.696-359G>T)
c.*540G>T (n.*540G>T)
c.901G>T (p.Asp301Tyr)
c.913G>T (p.Asp305Tyr)
c.136-359G>T
c.136-140G>T
n.949G>T
n.369G>T
c.832G>T (p.Asp278Tyr)
gnomAD v4
11g.2166908C=CA1948005799THc.820G= (p.Asp274=)
c.*509G= (n.*509G=)
c.696-359G= (n.696-359G=)
c.*540G= (n.*540G=)
c.901G= (p.Asp301=)
c.913G= (p.Asp305=)
c.136-359G=
c.136-140G=
n.949G=
n.369G=
c.832G= (p.Asp278=)
11g.2166908C>GCA379126561THc.820G>C (p.Asp274His)
c.*509G>C (n.*509G>C)
c.696-359G>C (n.696-359G>C)
c.*540G>C (n.*540G>C)
c.901G>C (p.Asp301His)
c.913G>C (p.Asp305His)
c.136-359G>C
c.136-140G>C
n.949G>C
n.369G>C
c.832G>C (p.Asp278His)
11g.2166908C>TCA379126560THc.820G>A (p.Asp274Asn)
c.*509G>A (n.*509G>A)
c.696-359G>A (n.696-359G>A)
c.*540G>A (n.*540G>A)
c.901G>A (p.Asp301Asn)
c.913G>A (p.Asp305Asn)
c.136-359G>A
c.136-140G>A
n.949G>A
n.369G>A
c.832G>A (p.Asp278Asn)
dbSNP gnomAD v2 gnomAD v4
11g.2166909C>ACA379126565THc.819G>T (p.Glu273Asp)
c.*508G>T (n.*508G>T)
c.696-360G>T (n.696-360G>T)
c.*539G>T (n.*539G>T)
c.900G>T (p.Glu300Asp)
c.912G>T (p.Glu304Asp)
c.136-360G>T
c.136-141G>T
n.948G>T
n.368G>T
c.831G>T (p.Glu277Asp)
COSMIC
11g.2166909C=CA1948005803THc.819G= (p.Glu273=)
c.*508G= (n.*508G=)
c.696-360G= (n.696-360G=)
c.*539G= (n.*539G=)
c.900G= (p.Glu300=)
c.912G= (p.Glu304=)
c.136-360G=
c.136-141G=
n.948G=
n.368G=
c.831G= (p.Glu277=)
11g.2166909C>GCA379126566THc.819G>C (p.Glu273Asp)
c.*508G>C (n.*508G>C)
c.696-360G>C (n.696-360G>C)
c.*539G>C (n.*539G>C)
c.900G>C (p.Glu300Asp)
c.912G>C (p.Glu304Asp)
c.136-360G>C
c.136-141G>C
n.948G>C
n.368G>C
c.831G>C (p.Glu277Asp)
11g.2166909C>TCA472414315THc.819G>A (p.Glu273=)
c.*508G>A (n.*508G>A)
c.696-360G>A (n.696-360G>A)
c.*539G>A (n.*539G>A)
c.900G>A (p.Glu300=)
c.912G>A (p.Glu304=)
c.136-360G>A
c.136-141G>A
n.948G>A
n.368G>A
c.831G>A (p.Glu277=)
dbSNP gnomAD v2
11g.2166910T>ACA379126567THc.818A>T (p.Glu273Val)
c.*507A>T (n.*507A>T)
c.696-361A>T (n.696-361A>T)
c.*538A>T (n.*538A>T)
c.899A>T (p.Glu300Val)
c.911A>T (p.Glu304Val)
c.136-361A>T
c.136-142A>T
n.947A>T
n.367A>T
c.830A>T (p.Glu277Val)
11g.2166910T>CCA379126568THc.818A>G (p.Glu273Gly)
c.*507A>G (n.*507A>G)
c.696-361A>G (n.696-361A>G)
c.*538A>G (n.*538A>G)
c.899A>G (p.Glu300Gly)
c.911A>G (p.Glu304Gly)
c.136-361A>G
c.136-142A>G
n.947A>G
n.367A>G
c.830A>G (p.Glu277Gly)
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.2166910T>GCA379126569THc.818A>C (p.Glu273Ala)
c.*507A>C (n.*507A>C)
c.696-361A>C (n.696-361A>C)
c.*538A>C (n.*538A>C)
c.899A>C (p.Glu300Ala)
c.911A>C (p.Glu304Ala)
c.136-361A>C
c.136-142A>C
n.947A>C
n.367A>C
c.830A>C (p.Glu277Ala)
ClinVar dbSNP gnomAD v4
11g.2166910T=CA1948005808THc.818A= (p.Glu273=)
c.*507A= (n.*507A=)
c.696-361A= (n.696-361A=)
c.*538A= (n.*538A=)
c.899A= (p.Glu300=)
c.911A= (p.Glu304=)
c.136-361A=
c.136-142A=
n.947A=
n.367A=
c.830A= (p.Glu277=)
11g.2166911C>ACA379126571THc.817G>T (p.Glu273Ter)
c.*506G>T (n.*506G>T)
c.696-362G>T (n.696-362G>T)
c.*537G>T (n.*537G>T)
c.898G>T (p.Glu300Ter)
c.910G>T (p.Glu304Ter)
c.136-362G>T
c.136-143G>T
n.946G>T
n.366G>T
c.829G>T (p.Glu277Ter)
gnomAD v4 COSMIC
11g.2166911C>GCA379126573THc.817G>C (p.Glu273Gln)
c.*506G>C (n.*506G>C)
c.696-362G>C (n.696-362G>C)
c.*537G>C (n.*537G>C)
c.898G>C (p.Glu300Gln)
c.910G>C (p.Glu304Gln)
c.136-362G>C
c.136-143G>C
n.946G>C
n.366G>C
c.829G>C (p.Glu277Gln)
11g.2166911C>TCA379126575THc.817G>A (p.Glu273Lys)
c.*506G>A (n.*506G>A)
c.696-362G>A (n.696-362G>A)
c.*537G>A (n.*537G>A)
c.898G>A (p.Glu300Lys)
c.910G>A (p.Glu304Lys)
c.136-362G>A
c.136-143G>A
n.946G>A
n.366G>A
c.829G>A (p.Glu277Lys)
11g.2166912C>ACA472414317THc.816G>T (p.Leu272=)
c.*505G>T (n.*505G>T)
c.696-363G>T (n.696-363G>T)
c.*536G>T (n.*536G>T)
c.897G>T (p.Leu299=)
c.909G>T (p.Leu303=)
c.136-363G>T
c.136-144G>T
n.945G>T
n.365G>T
c.828G>T (p.Leu276=)
gnomAD v4
11g.2166912C=CA1948005811THc.816G= (p.Leu272=)
c.*505G= (n.*505G=)
c.696-363G= (n.696-363G=)
c.*536G= (n.*536G=)
c.897G= (p.Leu299=)
c.909G= (p.Leu303=)
c.136-363G=
c.136-144G=
n.945G=
n.365G=
c.828G= (p.Leu276=)
11g.2166912C>GCA472414316THc.816G>C (p.Leu272=)
c.*505G>C (n.*505G>C)
c.696-363G>C (n.696-363G>C)
c.*536G>C (n.*536G>C)
c.897G>C (p.Leu299=)
c.909G>C (p.Leu303=)
c.136-363G>C
c.136-144G>C
n.945G>C
n.365G>C
c.828G>C (p.Leu276=)
11g.2166912C>TCA5818481THc.816G>A (p.Leu272=)
c.*505G>A (n.*505G>A)
c.696-363G>A (n.696-363G>A)
c.*536G>A (n.*536G>A)
c.897G>A (p.Leu299=)
c.909G>A (p.Leu303=)
c.136-363G>A
c.136-144G>A
n.945G>A
n.365G>A
c.828G>A (p.Leu276=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.2166913A=CA1948005814THc.815T= (p.Leu272=)
c.*504T= (n.*504T=)
c.696-364T= (n.696-364T=)
c.*535T= (n.*535T=)
c.896T= (p.Leu299=)
c.908T= (p.Leu303=)
c.136-364T=
c.136-145T=
n.944T=
n.364T=
c.827T= (p.Leu276=)
11g.2166913A>CCA5818482THc.815T>G (p.Leu272Arg)
c.*504T>G (n.*504T>G)
c.696-364T>G (n.696-364T>G)
c.*535T>G (n.*535T>G)
c.896T>G (p.Leu299Arg)
c.908T>G (p.Leu303Arg)
c.136-364T>G
c.136-145T>G
n.944T>G
n.364T>G
c.827T>G (p.Leu276Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.2166913A>GCA379126595THc.815T>C (p.Leu272Pro)
c.*504T>C (n.*504T>C)
c.696-364T>C (n.696-364T>C)
c.*535T>C (n.*535T>C)
c.896T>C (p.Leu299Pro)
c.908T>C (p.Leu303Pro)
c.136-364T>C
c.136-145T>C
n.944T>C
n.364T>C
c.827T>C (p.Leu276Pro)
gnomAD v4
11g.2166913A>TCA379126596THc.815T>A (p.Leu272Gln)
c.*504T>A (n.*504T>A)
c.696-364T>A (n.696-364T>A)
c.*535T>A (n.*535T>A)
c.896T>A (p.Leu299Gln)
c.908T>A (p.Leu303Gln)
c.136-364T>A
c.136-145T>A
n.944T>A
n.364T>A
c.827T>A (p.Leu276Gln)
11g.2166914G>ACA472414318THc.814C>T (p.Leu272=)
c.*503C>T (n.*503C>T)
c.696-365C>T (n.696-365C>T)
c.*534C>T (n.*534C>T)
c.895C>T (p.Leu299=)
c.907C>T (p.Leu303=)
c.136-365C>T
c.136-146C>T
n.943C>T
n.363C>T
c.826C>T (p.Leu276=)
11g.2166914G>CCA379126598THc.814C>G (p.Leu272Val)
c.*503C>G (n.*503C>G)
c.696-365C>G (n.696-365C>G)
c.*534C>G (n.*534C>G)
c.895C>G (p.Leu299Val)
c.907C>G (p.Leu303Val)
c.136-365C>G
c.136-146C>G
n.943C>G
n.363C>G
c.826C>G (p.Leu276Val)
gnomAD v4
11g.2166914G>TCA379126600THc.814C>A (p.Leu272Met)
c.*503C>A (n.*503C>A)
c.696-365C>A (n.696-365C>A)
c.*534C>A (n.*534C>A)
c.895C>A (p.Leu299Met)
c.907C>A (p.Leu303Met)
c.136-365C>A
c.136-146C>A
n.943C>A
n.363C>A
c.826C>A (p.Leu276Met)
gnomAD v4
11g.2166915C>ACA379126602THc.813G>T (p.Gln271His)
c.*502G>T (n.*502G>T)
c.696-366G>T (n.696-366G>T)
c.*533G>T (n.*533G>T)
c.894G>T (p.Gln298His)
c.906G>T (p.Gln302His)
c.136-366G>T
c.136-147G>T
n.942G>T
n.362G>T
c.825G>T (p.Gln275His)
11g.2166915C>GCA379126604THc.813G>C (p.Gln271His)
c.*502G>C (n.*502G>C)
c.696-366G>C (n.696-366G>C)
c.*533G>C (n.*533G>C)
c.894G>C (p.Gln298His)
c.906G>C (p.Gln302His)
c.136-366G>C
c.136-147G>C
n.942G>C
n.362G>C
c.825G>C (p.Gln275His)
11g.2166915C>TCA472414319THc.813G>A (p.Gln271=)
c.*502G>A (n.*502G>A)
c.696-366G>A (n.696-366G>A)
c.*533G>A (n.*533G>A)
c.894G>A (p.Gln298=)
c.906G>A (p.Gln302=)
c.136-366G>A
c.136-147G>A
n.942G>A
n.362G>A
c.825G>A (p.Gln275=)
11g.2166916T>ACA379126607THc.812A>T (p.Gln271Leu)
c.*501A>T (n.*501A>T)
c.696-367A>T (n.696-367A>T)
c.*532A>T (n.*532A>T)
c.893A>T (p.Gln298Leu)
c.905A>T (p.Gln302Leu)
c.136-367A>T
c.136-148A>T
n.941A>T
n.361A>T
c.824A>T (p.Gln275Leu)
11g.2166916T>CCA379126609THc.812A>G (p.Gln271Arg)
c.*501A>G (n.*501A>G)
c.696-367A>G (n.696-367A>G)
c.*532A>G (n.*532A>G)
c.893A>G (p.Gln298Arg)
c.905A>G (p.Gln302Arg)
c.136-367A>G
c.136-148A>G
n.941A>G
n.361A>G
c.824A>G (p.Gln275Arg)
11g.2166916T>GCA379126610THc.812A>C (p.Gln271Pro)
c.*501A>C (n.*501A>C)
c.696-367A>C (n.696-367A>C)
c.*532A>C (n.*532A>C)
c.893A>C (p.Gln298Pro)
c.905A>C (p.Gln302Pro)
c.136-367A>C
c.136-148A>C
n.941A>C
n.361A>C
c.824A>C (p.Gln275Pro)
11g.2166917G>ACA379126612THc.811C>T (p.Gln271Ter)
c.*500C>T (n.*500C>T)
c.696-368C>T (n.696-368C>T)
c.*531C>T (n.*531C>T)
c.892C>T (p.Gln298Ter)
c.904C>T (p.Gln302Ter)
c.136-368C>T
c.136-149C>T
n.940C>T
n.360C>T
c.823C>T (p.Gln275Ter)
ClinVar gnomAD v4
11g.2166917G>CCA379126614THc.811C>G (p.Gln271Glu)
c.*500C>G (n.*500C>G)
c.696-368C>G (n.696-368C>G)
c.*531C>G (n.*531C>G)
c.892C>G (p.Gln298Glu)
c.904C>G (p.Gln302Glu)
c.136-368C>G
c.136-149C>G
n.940C>G
n.360C>G
c.823C>G (p.Gln275Glu)
11g.2166917G>TCA379126615THc.811C>A (p.Gln271Lys)
c.*500C>A (n.*500C>A)
c.696-368C>A (n.696-368C>A)
c.*531C>A (n.*531C>A)
c.892C>A (p.Gln298Lys)
c.904C>A (p.Gln302Lys)
c.136-368C>A
c.136-149C>A
n.940C>A
n.360C>A
c.823C>A (p.Gln275Lys)
11g.2166921delCA2611964347THc.811del (p.Gln271SerfsTer9)
c.*500del (n.*500del)
c.696-368del (n.696-368del)
c.*531del (n.*531del)
c.892del (p.Gln298SerfsTer9)
c.904del (p.Gln302SerfsTer9)
c.136-368del
c.136-149del
n.940del
n.360del
c.823del (p.Gln275SerfsTer9)
gnomAD v4
11g.2166918G>ACA472414320THc.810C>T (p.Pro270=)
c.*499C>T (n.*499C>T)
c.696-369C>T (n.696-369C>T)
c.*530C>T (n.*530C>T)
c.891C>T (p.Pro297=)
c.903C>T (p.Pro301=)
c.136-369C>T
c.136-150C>T
n.939C>T
n.359C>T
c.822C>T (p.Pro274=)
ClinVar dbSNP gnomAD v4 COSMIC
11g.2166918G>CCA472414321THc.810C>G (p.Pro270=)
c.*499C>G (n.*499C>G)
c.696-369C>G (n.696-369C>G)
c.*530C>G (n.*530C>G)
c.891C>G (p.Pro297=)
c.903C>G (p.Pro301=)
c.136-369C>G
c.136-150C>G
n.939C>G
n.359C>G
c.822C>G (p.Pro274=)
ClinVar dbSNP gnomAD v4
11g.2166918G=CA1948005817THc.810C= (p.Pro270=)
c.*499C= (n.*499C=)
c.696-369C= (n.696-369C=)
c.*530C= (n.*530C=)
c.891C= (p.Pro297=)
c.903C= (p.Pro301=)
c.136-369C=
c.136-150C=
n.939C=
n.359C=
c.822C= (p.Pro274=)
11g.2166918G>TCA472414322THc.810C>A (p.Pro270=)
c.*499C>A (n.*499C>A)
c.696-369C>A (n.696-369C>A)
c.*530C>A (n.*530C>A)
c.891C>A (p.Pro297=)
c.903C>A (p.Pro301=)
c.136-369C>A
c.136-150C>A
n.939C>A
n.359C>A
c.822C>A (p.Pro274=)
gnomAD v4
11g.2166919G>ACA379126616THc.809C>T (p.Pro270Leu)
c.*498C>T (n.*498C>T)
c.696-370C>T (n.696-370C>T)
c.*529C>T (n.*529C>T)
c.890C>T (p.Pro297Leu)
c.902C>T (p.Pro301Leu)
c.136-370C>T
c.136-151C>T
n.938C>T
n.358C>T
c.821C>T (p.Pro274Leu)
11g.2166919G>CCA5818483THc.809C>G (p.Pro270Arg)
c.*498C>G (n.*498C>G)
c.696-370C>G (n.696-370C>G)
c.*529C>G (n.*529C>G)
c.890C>G (p.Pro297Arg)
c.902C>G (p.Pro301Arg)
c.136-370C>G
c.136-151C>G
n.938C>G
n.358C>G
c.821C>G (p.Pro274Arg)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.2166919G=CA1948005819THc.809C= (p.Pro270=)
c.*498C= (n.*498C=)
c.696-370C= (n.696-370C=)
c.*529C= (n.*529C=)
c.890C= (p.Pro297=)
c.902C= (p.Pro301=)
c.136-370C=
c.136-151C=
n.938C=
n.358C=
c.821C= (p.Pro274=)
11g.2166919G>TCA379126618THc.809C>A (p.Pro270His)
c.*498C>A (n.*498C>A)
c.696-370C>A (n.696-370C>A)
c.*529C>A (n.*529C>A)
c.890C>A (p.Pro297His)
c.902C>A (p.Pro301His)
c.136-370C>A
c.136-151C>A
n.938C>A
n.358C>A
c.821C>A (p.Pro274His)
gnomAD v4
11g.2166920G>ACA379126620THc.808C>T (p.Pro270Ser)
c.*497C>T (n.*497C>T)
c.696-371C>T (n.696-371C>T)
c.*528C>T (n.*528C>T)
c.889C>T (p.Pro297Ser)
c.901C>T (p.Pro301Ser)
c.136-371C>T
c.136-152C>T
n.937C>T
n.357C>T
c.820C>T (p.Pro274Ser)
11g.2166920G>CCA379126622THc.808C>G (p.Pro270Ala)
c.*497C>G (n.*497C>G)
c.696-371C>G (n.696-371C>G)
c.*528C>G (n.*528C>G)
c.889C>G (p.Pro297Ala)
c.901C>G (p.Pro301Ala)
c.136-371C>G
c.136-152C>G
n.937C>G
n.357C>G
c.820C>G (p.Pro274Ala)
11g.2166920G>TCA379126624THc.808C>A (p.Pro270Thr)
c.*497C>A (n.*497C>A)
c.696-371C>A (n.696-371C>A)
c.*528C>A (n.*528C>A)
c.889C>A (p.Pro297Thr)
c.901C>A (p.Pro301Thr)
c.136-371C>A
c.136-152C>A
n.937C>A
n.357C>A
c.820C>A (p.Pro274Thr)
11g.2166921G>ACA472414323THc.807C>T (p.Ile269=)
c.*496C>T (n.*496C>T)
c.696-372C>T (n.696-372C>T)
c.*527C>T (n.*527C>T)
c.888C>T (p.Ile296=)
c.900C>T (p.Ile300=)
c.136-372C>T
c.136-153C>T
n.936C>T
n.356C>T
c.819C>T (p.Ile273=)
ClinVar dbSNP gnomAD v4
11g.2166921G>CCA5818484THc.807C>G (p.Ile269Met)
c.*496C>G (n.*496C>G)
c.696-372C>G (n.696-372C>G)
c.*527C>G (n.*527C>G)
c.888C>G (p.Ile296Met)
c.900C>G (p.Ile300Met)
c.136-372C>G
c.136-153C>G
n.936C>G
n.356C>G
c.819C>G (p.Ile273Met)
dbSNP ExAC gnomAD v2
11g.2166921G=CA1948005821THc.807C= (p.Ile269=)
c.*496C= (n.*496C=)
c.696-372C= (n.696-372C=)
c.*527C= (n.*527C=)
c.888C= (p.Ile296=)
c.900C= (p.Ile300=)
c.136-372C=
c.136-153C=
n.936C=
n.356C=
c.819C= (p.Ile273=)
11g.2166921G>TCA472414324THc.807C>A (p.Ile269=)
c.*496C>A (n.*496C>A)
c.696-372C>A (n.696-372C>A)
c.*527C>A (n.*527C>A)
c.888C>A (p.Ile296=)
c.900C>A (p.Ile300=)
c.136-372C>A
c.136-153C>A
n.936C>A
n.356C>A
c.819C>A (p.Ile273=)
ClinVar dbSNP gnomAD v4
11g.2166922A>CCA379126632THc.806T>G (p.Ile269Ser)
c.*495T>G (n.*495T>G)
c.696-373T>G (n.696-373T>G)
c.*526T>G (n.*526T>G)
c.887T>G (p.Ile296Ser)
c.899T>G (p.Ile300Ser)
c.136-373T>G
c.136-154T>G
n.935T>G
n.355T>G
c.818T>G (p.Ile273Ser)
11g.2166922A>GCA379126628THc.806T>C (p.Ile269Thr)
c.*495T>C (n.*495T>C)
c.696-373T>C (n.696-373T>C)
c.*526T>C (n.*526T>C)
c.887T>C (p.Ile296Thr)
c.899T>C (p.Ile300Thr)
c.136-373T>C
c.136-154T>C
n.935T>C
n.355T>C
c.818T>C (p.Ile273Thr)
11g.2166922A>TCA379126630THc.806T>A (p.Ile269Asn)
c.*495T>A (n.*495T>A)
c.696-373T>A (n.696-373T>A)
c.*526T>A (n.*526T>A)
c.887T>A (p.Ile296Asn)
c.899T>A (p.Ile300Asn)
c.136-373T>A
c.136-154T>A
n.935T>A
n.355T>A
c.818T>A (p.Ile273Asn)
gnomAD v4
11g.2166923T>ACA379126634THc.805A>T (p.Ile269Phe)
c.*494A>T (n.*494A>T)
c.696-374A>T (n.696-374A>T)
c.*525A>T (n.*525A>T)
c.886A>T (p.Ile296Phe)
c.898A>T (p.Ile300Phe)
c.136-374A>T
c.136-155A>T
n.934A>T
n.354A>T
c.817A>T (p.Ile273Phe)
11g.2166923T>CCA379126636THc.805A>G (p.Ile269Val)
c.*494A>G (n.*494A>G)
c.696-374A>G (n.696-374A>G)
c.*525A>G (n.*525A>G)
c.886A>G (p.Ile296Val)
c.898A>G (p.Ile300Val)
c.136-374A>G
c.136-155A>G
n.934A>G
n.354A>G
c.817A>G (p.Ile273Val)
11g.2166923T>GCA379126638THc.805A>C (p.Ile269Leu)
c.*494A>C (n.*494A>C)
c.696-374A>C (n.696-374A>C)
c.*525A>C (n.*525A>C)
c.886A>C (p.Ile296Leu)
c.898A>C (p.Ile300Leu)
c.136-374A>C
c.136-155A>C
n.934A>C
n.354A>C
c.817A>C (p.Ile273Leu)
11g.2166924A=CA1948005823THc.804T= (p.Asn268=)
c.*493T= (n.*493T=)
c.696-375T= (n.696-375T=)
c.*524T= (n.*524T=)
c.885T= (p.Asn295=)
c.897T= (p.Asn299=)
c.136-375T=
c.136-156T=
n.933T=
n.353T=
c.816T= (p.Asn272=)
11g.2166924A>CCA379126640THc.804T>G (p.Asn268Lys)
c.*493T>G (n.*493T>G)
c.696-375T>G (n.696-375T>G)
c.*524T>G (n.*524T>G)
c.885T>G (p.Asn295Lys)
c.897T>G (p.Asn299Lys)
c.136-375T>G
c.136-156T>G
n.933T>G
n.353T>G
c.816T>G (p.Asn272Lys)
11g.2166924A>GCA472414325THc.804T>C (p.Asn268=)
c.*493T>C (n.*493T>C)
c.696-375T>C (n.696-375T>C)
c.*524T>C (n.*524T>C)
c.885T>C (p.Asn295=)
c.897T>C (p.Asn299=)
c.136-375T>C
c.136-156T>C
n.933T>C
n.353T>C
c.816T>C (p.Asn272=)
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.2166924A>TCA379126641THc.804T>A (p.Asn268Lys)
c.*493T>A (n.*493T>A)
c.696-375T>A (n.696-375T>A)
c.*524T>A (n.*524T>A)
c.885T>A (p.Asn295Lys)
c.897T>A (p.Asn299Lys)
c.136-375T>A
c.136-156T>A
n.933T>A
n.353T>A
c.816T>A (p.Asn272Lys)
11g.2166925T>ACA379126647THc.803A>T (p.Asn268Ile)
c.*492A>T (n.*492A>T)
c.696-376A>T (n.696-376A>T)
c.*523A>T (n.*523A>T)
c.884A>T (p.Asn295Ile)
c.896A>T (p.Asn299Ile)
c.136-376A>T
c.136-157A>T
n.932A>T
n.352A>T
c.815A>T (p.Asn272Ile)
gnomAD v4
11g.2166925T>CCA379126643THc.803A>G (p.Asn268Ser)
c.*492A>G (n.*492A>G)
c.696-376A>G (n.696-376A>G)
c.*523A>G (n.*523A>G)
c.884A>G (p.Asn295Ser)
c.896A>G (p.Asn299Ser)
c.136-376A>G
c.136-157A>G
n.932A>G
n.352A>G
c.815A>G (p.Asn272Ser)
dbSNP gnomAD v3 gnomAD v4
11g.2166925T>GCA379126645THc.803A>C (p.Asn268Thr)
c.*492A>C (n.*492A>C)
c.696-376A>C (n.696-376A>C)
c.*523A>C (n.*523A>C)
c.884A>C (p.Asn295Thr)
c.896A>C (p.Asn299Thr)
c.136-376A>C
c.136-157A>C
n.932A>C
n.352A>C
c.815A>C (p.Asn272Thr)
11g.2166925T=CA1948005825THc.803A= (p.Asn268=)
c.*492A= (n.*492A=)
c.696-376A= (n.696-376A=)
c.*523A= (n.*523A=)
c.884A= (p.Asn295=)
c.896A= (p.Asn299=)
c.136-376A=
c.136-157A=
n.932A=
n.352A=
c.815A= (p.Asn272=)
11g.2166927_2166931dupCA2611964395THc.799_803dup (p.Asn268LysfsTer14)
c.*488_*492dup (n.*488_*492dup)
c.696-380_696-376dup (n.696-380_696-376dup)
c.*519_*523dup (n.*519_*523dup)
c.880_884dup (p.Asn295LysfsTer14)
c.892_896dup (p.Asn299LysfsTer14)
c.136-380_136-376dup
c.136-161_136-157dup
n.928_932dup
n.348_352dup
c.811_815dup (p.Asn272LysfsTer14)
gnomAD v4
11g.2166926T>ACA379126649THc.802A>T (p.Asn268Tyr)
c.*491A>T (n.*491A>T)
c.696-377A>T (n.696-377A>T)
c.*522A>T (n.*522A>T)
c.883A>T (p.Asn295Tyr)
c.895A>T (p.Asn299Tyr)
c.136-377A>T
c.136-158A>T
n.931A>T
n.351A>T
c.814A>T (p.Asn272Tyr)
11g.2166926T>CCA379126651THc.802A>G (p.Asn268Asp)
c.*491A>G (n.*491A>G)
c.696-377A>G (n.696-377A>G)
c.*522A>G (n.*522A>G)
c.883A>G (p.Asn295Asp)
c.895A>G (p.Asn299Asp)
c.136-377A>G
c.136-158A>G
n.931A>G
n.351A>G
c.814A>G (p.Asn272Asp)
dbSNP gnomAD v3 gnomAD v4
11g.2166926T>GCA379126653THc.802A>C (p.Asn268His)
c.*491A>C (n.*491A>C)
c.696-377A>C (n.696-377A>C)
c.*522A>C (n.*522A>C)
c.883A>C (p.Asn295His)
c.895A>C (p.Asn299His)
c.136-377A>C
c.136-158A>C
n.931A>C
n.351A>C
c.814A>C (p.Asn272His)
11g.2166926T=CA1948005828THc.802A= (p.Asn268=)
c.*491A= (n.*491A=)
c.696-377A= (n.696-377A=)
c.*522A= (n.*522A=)
c.883A= (p.Asn295=)
c.895A= (p.Asn299=)
c.136-377A=
c.136-158A=
n.931A=
n.351A=
c.814A= (p.Asn272=)
11g.2166927G>ACA472414326THc.801C>T (p.Asp267=)
c.*490C>T (n.*490C>T)
c.696-378C>T (n.696-378C>T)
c.*521C>T (n.*521C>T)
c.882C>T (p.Asp294=)
c.894C>T (p.Asp298=)
c.136-378C>T
c.136-159C>T
n.930C>T
n.350C>T
c.813C>T (p.Asp271=)
gnomAD v4
11g.2166927G>CCA379126655THc.801C>G (p.Asp267Glu)
c.*490C>G (n.*490C>G)
c.696-378C>G (n.696-378C>G)
c.*521C>G (n.*521C>G)
c.882C>G (p.Asp294Glu)
c.894C>G (p.Asp298Glu)
c.136-378C>G
c.136-159C>G
n.930C>G
n.350C>G
c.813C>G (p.Asp271Glu)
11g.2166927G>TCA379126657THc.801C>A (p.Asp267Glu)
c.*490C>A (n.*490C>A)
c.696-378C>A (n.696-378C>A)
c.*521C>A (n.*521C>A)
c.882C>A (p.Asp294Glu)
c.894C>A (p.Asp298Glu)
c.136-378C>A
c.136-159C>A
n.930C>A
n.350C>A
c.813C>A (p.Asp271Glu)
11g.2166928T>ACA379126660THc.800A>T (p.Asp267Val)
c.*489A>T (n.*489A>T)
c.696-379A>T (n.696-379A>T)
c.*520A>T (n.*520A>T)
c.881A>T (p.Asp294Val)
c.893A>T (p.Asp298Val)
c.136-379A>T
c.136-160A>T
n.929A>T
n.349A>T
c.812A>T (p.Asp271Val)
11g.2166928T>CCA379126664THc.800A>G (p.Asp267Gly)
c.*489A>G (n.*489A>G)
c.696-379A>G (n.696-379A>G)
c.*520A>G (n.*520A>G)
c.881A>G (p.Asp294Gly)
c.893A>G (p.Asp298Gly)
c.136-379A>G
c.136-160A>G
n.929A>G
n.349A>G
c.812A>G (p.Asp271Gly)
11g.2166928T>GCA379126662THc.800A>C (p.Asp267Ala)
c.*489A>C (n.*489A>C)
c.696-379A>C (n.696-379A>C)
c.*520A>C (n.*520A>C)
c.881A>C (p.Asp294Ala)
c.893A>C (p.Asp298Ala)
c.136-379A>C
c.136-160A>C
n.929A>C
n.349A>C
c.812A>C (p.Asp271Ala)
11g.2166929C>ACA379126666THc.799G>T (p.Asp267Tyr)
c.*488G>T (n.*488G>T)
c.696-380G>T (n.696-380G>T)
c.*519G>T (n.*519G>T)
c.880G>T (p.Asp294Tyr)
c.892G>T (p.Asp298Tyr)
c.136-380G>T
c.136-161G>T
n.928G>T
n.348G>T
c.811G>T (p.Asp271Tyr)
gnomAD v4
11g.2166929C=CA1948005833THc.799G= (p.Asp267=)
c.*488G= (n.*488G=)
c.696-380G= (n.696-380G=)
c.*519G= (n.*519G=)
c.880G= (p.Asp294=)
c.892G= (p.Asp298=)
c.136-380G=
c.136-161G=
n.928G=
n.348G=
c.811G= (p.Asp271=)
11g.2166929C>GCA16606213THc.799G>C (p.Asp267His)
c.*488G>C (n.*488G>C)
c.696-380G>C (n.696-380G>C)
c.*519G>C (n.*519G>C)
c.880G>C (p.Asp294His)
c.892G>C (p.Asp298His)
c.136-380G>C
c.136-161G>C
n.928G>C
n.348G>C
c.811G>C (p.Asp271His)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.2166929C>TCA379126669THc.799G>A (p.Asp267Asn)
c.*488G>A (n.*488G>A)
c.696-380G>A (n.696-380G>A)
c.*519G>A (n.*519G>A)
c.880G>A (p.Asp294Asn)
c.892G>A (p.Asp298Asn)
c.136-380G>A
c.136-161G>A
n.928G>A
n.348G>A
c.811G>A (p.Asp271Asn)
dbSNP gnomAD v3 gnomAD v4
11g.2166929_2166930delinsCTCA1948005836THc.798_799delinsAG (p.Glu266=)
c.*487_*488delinsAG (n.*487_*488delinsAG)
c.696-381_696-380delinsAG (n.696-381_696-380delinsAG)
c.*518_*519delinsAG (n.*518_*519delinsAG)
c.879_880delinsAG (p.Glu293=)
c.891_892delinsAG (p.Glu297=)
c.136-381_136-380delinsAG
c.136-162_136-161delinsAG
n.927_928delinsAG
n.347_348delinsAG
c.810_811delinsAG (p.Glu270=)
11g.2166930T>ACA379126671THc.798A>T (p.Glu266Asp)
c.*487A>T (n.*487A>T)
c.696-381A>T (n.696-381A>T)
c.*518A>T (n.*518A>T)
c.879A>T (p.Glu293Asp)
c.891A>T (p.Glu297Asp)
c.136-381A>T
c.136-162A>T
n.927A>T
n.347A>T
c.810A>T (p.Glu270Asp)
11g.2166930T>CCA472414327THc.798A>G (p.Glu266=)
c.*487A>G (n.*487A>G)
c.696-381A>G (n.696-381A>G)
c.*518A>G (n.*518A>G)
c.879A>G (p.Glu293=)
c.891A>G (p.Glu297=)
c.136-381A>G
c.136-162A>G
n.927A>G
n.347A>G
c.810A>G (p.Glu270=)
dbSNP gnomAD v2 gnomAD v4
11g.2166930T>GCA379126673THc.798A>C (p.Glu266Asp)
c.*487A>C (n.*487A>C)
c.696-381A>C (n.696-381A>C)
c.*518A>C (n.*518A>C)
c.879A>C (p.Glu293Asp)
c.891A>C (p.Glu297Asp)
c.136-381A>C
c.136-162A>C
n.927A>C
n.347A>C
c.810A>C (p.Glu270Asp)
COSMIC
11g.2166930T=CA1948005839THc.798A= (p.Glu266=)
c.*487A= (n.*487A=)
c.696-381A= (n.696-381A=)
c.*518A= (n.*518A=)
c.879A= (p.Glu293=)
c.891A= (p.Glu297=)
c.136-381A=
c.136-162A=
n.927A=
n.347A=
c.810A= (p.Glu270=)
11g.2166931delCA934419400THc.798del (p.Asp267ThrfsTer13)
c.*487del (n.*487del)
c.696-381del (n.696-381del)
c.*518del (n.*518del)
c.879del (p.Asp294ThrfsTer13)
c.891del (p.Asp298ThrfsTer13)
c.136-381del
c.136-162del
n.927del
n.347del
c.810del (p.Asp271ThrfsTer13)
dbSNP gnomAD v3 gnomAD v4
11g.2166931T>ACA379126675THc.797A>T (p.Glu266Val)
c.*486A>T (n.*486A>T)
c.696-382A>T (n.696-382A>T)
c.*517A>T (n.*517A>T)
c.878A>T (p.Glu293Val)
c.890A>T (p.Glu297Val)
c.136-382A>T
c.136-163A>T
n.926A>T
n.346A>T
c.809A>T (p.Glu270Val)
11g.2166931T>CCA379126678THc.797A>G (p.Glu266Gly)
c.*486A>G (n.*486A>G)
c.696-382A>G (n.696-382A>G)
c.*517A>G (n.*517A>G)
c.878A>G (p.Glu293Gly)
c.890A>G (p.Glu297Gly)
c.136-382A>G
c.136-163A>G
n.926A>G
n.346A>G
c.809A>G (p.Glu270Gly)
11g.2166931T>GCA379126680THc.797A>C (p.Glu266Ala)
c.*486A>C (n.*486A>C)
c.696-382A>C (n.696-382A>C)
c.*517A>C (n.*517A>C)
c.878A>C (p.Glu293Ala)
c.890A>C (p.Glu297Ala)
c.136-382A>C
c.136-163A>C
n.926A>C
n.346A>C
c.809A>C (p.Glu270Ala)
11g.2166932C>ACA379126684THc.796G>T (p.Glu266Ter)
c.*485G>T (n.*485G>T)
c.696-383G>T (n.696-383G>T)
c.*516G>T (n.*516G>T)
c.877G>T (p.Glu293Ter)
c.889G>T (p.Glu297Ter)
c.136-383G>T
c.136-164G>T
n.925G>T
n.345G>T
c.808G>T (p.Glu270Ter)
ClinVar dbSNP gnomAD v4
11g.2166932C=CA1948005845THc.796G= (p.Glu266=)
c.*485G= (n.*485G=)
c.696-383G= (n.696-383G=)
c.*516G= (n.*516G=)
c.877G= (p.Glu293=)
c.889G= (p.Glu297=)
c.136-383G=
c.136-164G=
n.925G=
n.345G=
c.808G= (p.Glu270=)
11g.2166932C>GCA379126685THc.796G>C (p.Glu266Gln)
c.*485G>C (n.*485G>C)
c.696-383G>C (n.696-383G>C)
c.*516G>C (n.*516G>C)
c.877G>C (p.Glu293Gln)
c.889G>C (p.Glu297Gln)
c.136-383G>C
c.136-164G>C
n.925G>C
n.345G>C
c.808G>C (p.Glu270Gln)
gnomAD v4
11g.2166932C>TCA379126687THc.796G>A (p.Glu266Lys)
c.*485G>A (n.*485G>A)
c.696-383G>A (n.696-383G>A)
c.*516G>A (n.*516G>A)
c.877G>A (p.Glu293Lys)
c.889G>A (p.Glu297Lys)
c.136-383G>A
c.136-164G>A
n.925G>A
n.345G>A
c.808G>A (p.Glu270Lys)
11g.2166933C>ACA472414328THc.795G>T (p.Arg265=)
c.*484G>T (n.*484G>T)
c.696-384G>T (n.696-384G>T)
c.*515G>T (n.*515G>T)
c.876G>T (p.Arg292=)
c.888G>T (p.Arg296=)
c.136-384G>T
c.136-165G>T
n.924G>T
n.344G>T
c.807G>T (p.Arg269=)
ClinVar dbSNP gnomAD v4
11g.2166933C=CA1948005847THc.795G= (p.Arg265=)
c.*484G= (n.*484G=)
c.696-384G= (n.696-384G=)
c.*515G= (n.*515G=)
c.876G= (p.Arg292=)
c.888G= (p.Arg296=)
c.136-384G=
c.136-165G=
n.924G=
n.344G=
c.807G= (p.Arg269=)
11g.2166933C>GCA472414329THc.795G>C (p.Arg265=)
c.*484G>C (n.*484G>C)
c.696-384G>C (n.696-384G>C)
c.*515G>C (n.*515G>C)
c.876G>C (p.Arg292=)
c.888G>C (p.Arg296=)
c.136-384G>C
c.136-165G>C
n.924G>C
n.344G>C
c.807G>C (p.Arg269=)
ClinVar
11g.2166933C>TCA5818485THc.795G>A (p.Arg265=)
c.*484G>A (n.*484G>A)
c.696-384G>A (n.696-384G>A)
c.*515G>A (n.*515G>A)
c.876G>A (p.Arg292=)
c.888G>A (p.Arg296=)
c.136-384G>A
c.136-165G>A
n.924G>A
n.344G>A
c.807G>A (p.Arg269=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.2166936_2166942dupCA2695201060THc.789_795dup (p.Glu266LeufsTer?)
c.*478_*484dup (n.*478_*484dup)
c.696-390_696-384dup (n.696-390_696-384dup)
c.*509_*515dup (n.*509_*515dup)
c.870_876dup (p.Glu293LeufsTer?)
c.882_888dup (p.Glu297LeufsTer?)
c.136-390_136-384dup
c.136-171_136-165dup
n.918_924dup
n.338_344dup
c.801_807dup (p.Glu270LeufsTer?)
ClinVar
11g.2166934C>ACA379126692THc.794G>T (p.Arg265Leu)
c.*483G>T (n.*483G>T)
c.696-385G>T (n.696-385G>T)
c.*514G>T (n.*514G>T)
c.875G>T (p.Arg292Leu)
c.887G>T (p.Arg296Leu)
c.136-385G>T
c.136-166G>T
n.923G>T
n.343G>T
c.806G>T (p.Arg269Leu)
gnomAD v4
11g.2166934C=CA1948005853THc.794G= (p.Arg265=)
c.*483G= (n.*483G=)
c.696-385G= (n.696-385G=)
c.*514G= (n.*514G=)
c.875G= (p.Arg292=)
c.887G= (p.Arg296=)
c.136-385G=
c.136-166G=
n.923G=
n.343G=
c.806G= (p.Arg269=)
11g.2166934C>GCA379126696THc.794G>C (p.Arg265Pro)
c.*483G>C (n.*483G>C)
c.696-385G>C (n.696-385G>C)
c.*514G>C (n.*514G>C)
c.875G>C (p.Arg292Pro)
c.887G>C (p.Arg296Pro)
c.136-385G>C
c.136-166G>C
n.923G>C
n.343G>C
c.806G>C (p.Arg269Pro)
gnomAD v4
11g.2166934C>TCA5818486THc.794G>A (p.Arg265Gln)
c.*483G>A (n.*483G>A)
c.696-385G>A (n.696-385G>A)
c.*514G>A (n.*514G>A)
c.875G>A (p.Arg292Gln)
c.887G>A (p.Arg296Gln)
c.136-385G>A
c.136-166G>A
n.923G>A
n.343G>A
c.806G>A (p.Arg269Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.2166935G>ACA379126700THc.793C>T (p.Arg265Trp)
c.*482C>T (n.*482C>T)
c.696-386C>T (n.696-386C>T)
c.*513C>T (n.*513C>T)
c.874C>T (p.Arg292Trp)
c.886C>T (p.Arg296Trp)
c.136-386C>T
c.136-167C>T
n.922C>T
n.342C>T
c.805C>T (p.Arg269Trp)
gnomAD v4
11g.2166935G>CCA379126702THc.793C>G (p.Arg265Gly)
c.*482C>G (n.*482C>G)
c.696-386C>G (n.696-386C>G)
c.*513C>G (n.*513C>G)
c.874C>G (p.Arg292Gly)
c.886C>G (p.Arg296Gly)
c.136-386C>G
c.136-167C>G
n.922C>G
n.342C>G
c.805C>G (p.Arg269Gly)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.2166935G=CA1948005858THc.793C= (p.Arg265=)
c.*482C= (n.*482C=)
c.696-386C= (n.696-386C=)
c.*513C= (n.*513C=)
c.874C= (p.Arg292=)
c.886C= (p.Arg296=)
c.136-386C=
c.136-167C=
n.922C=
n.342C=
c.805C= (p.Arg269=)
11g.2166935G>TCA472414330THc.793C>A (p.Arg265=)
c.*482C>A (n.*482C>A)
c.696-386C>A (n.696-386C>A)
c.*513C>A (n.*513C>A)
c.874C>A (p.Arg292=)
c.886C>A (p.Arg296=)
c.136-386C>A
c.136-167C>A
n.922C>A
n.342C>A
c.805C>A (p.Arg269=)
gnomAD v4
11g.2166936G>ACA5818488THc.792C>T (p.Tyr264=)
c.*481C>T (n.*481C>T)
c.696-387C>T (n.696-387C>T)
c.*512C>T (n.*512C>T)
c.873C>T (p.Tyr291=)
c.885C>T (p.Tyr295=)
c.136-387C>T
c.136-168C>T
n.921C>T
n.341C>T
c.804C>T (p.Tyr268=)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.2166936G>CCA379126704THc.792C>G (p.Tyr264Ter)
c.*481C>G (n.*481C>G)
c.696-387C>G (n.696-387C>G)
c.*512C>G (n.*512C>G)
c.873C>G (p.Tyr291Ter)
c.885C>G (p.Tyr295Ter)
c.136-387C>G
c.136-168C>G
n.921C>G
n.341C>G
c.804C>G (p.Tyr268Ter)
ClinVar
11g.2166936G=CA1948005861THc.792C= (p.Tyr264=)
c.*481C= (n.*481C=)
c.696-387C= (n.696-387C=)
c.*512C= (n.*512C=)
c.873C= (p.Tyr291=)
c.885C= (p.Tyr295=)
c.136-387C=
c.136-168C=
n.921C=
n.341C=
c.804C= (p.Tyr268=)
11g.2166936G>TCA5818487THc.792C>A (p.Tyr264Ter)
c.*481C>A (n.*481C>A)
c.696-387C>A (n.696-387C>A)
c.*512C>A (n.*512C>A)
c.873C>A (p.Tyr291Ter)
c.885C>A (p.Tyr295Ter)
c.136-387C>A
c.136-168C>A
n.921C>A
n.341C>A
c.804C>A (p.Tyr268Ter)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.2166937_2166942delCA2611964483THc.787_792del (p.Gly263_Tyr264del)
c.*476_*481del (n.*476_*481del)
c.696-392_696-387del (n.696-392_696-387del)
c.*507_*512del (n.*507_*512del)
c.868_873del (p.Gly290_Tyr291del)
c.880_885del (p.Gly294_Tyr295del)
c.136-392_136-387del
c.136-173_136-168del
n.916_921del
n.336_341del
c.799_804del (p.Gly267_Tyr268del)
gnomAD v4
11g.2166937_2166945delCA2611964486THc.784_792del (p.Ser262_Tyr264del)
c.*473_*481del (n.*473_*481del)
c.696-395_696-387del (n.696-395_696-387del)
c.*504_*512del (n.*504_*512del)
c.865_873del (p.Ser289_Tyr291del)
c.877_885del (p.Ser293_Tyr295del)
c.136-395_136-387del
c.136-176_136-168del
n.913_921del
n.333_341del
c.796_804del (p.Ser266_Tyr268del)
gnomAD v4
11g.2166937_2166956delCA2611964487THc.773_792del (p.Leu258ProfsTer?)
c.*462_*481del (n.*462_*481del)
c.696-406_696-387del (n.696-406_696-387del)
c.*493_*512del (n.*493_*512del)
c.854_873del (p.Leu285ProfsTer?)
c.866_885del (p.Leu289ProfsTer?)
c.136-406_136-387del
c.136-187_136-168del
n.902_921del
n.322_341del
c.785_804del (p.Leu262ProfsTer?)
gnomAD v4
11g.2166937T>ACA379126713THc.791A>T (p.Tyr264Phe)
c.*480A>T (n.*480A>T)
c.696-388A>T (n.696-388A>T)
c.*511A>T (n.*511A>T)
c.872A>T (p.Tyr291Phe)
c.884A>T (p.Tyr295Phe)
c.136-388A>T
c.136-169A>T
n.920A>T
n.340A>T
c.803A>T (p.Tyr268Phe)
11g.2166937T>CCA379126711THc.791A>G (p.Tyr264Cys)
c.*480A>G (n.*480A>G)
c.696-388A>G (n.696-388A>G)
c.*511A>G (n.*511A>G)
c.872A>G (p.Tyr291Cys)
c.884A>G (p.Tyr295Cys)
c.136-388A>G
c.136-169A>G
n.920A>G
n.340A>G
c.803A>G (p.Tyr268Cys)
11g.2166937T>GCA379126709THc.791A>C (p.Tyr264Ser)
c.*480A>C (n.*480A>C)
c.696-388A>C (n.696-388A>C)
c.*511A>C (n.*511A>C)
c.872A>C (p.Tyr291Ser)
c.884A>C (p.Tyr295Ser)
c.136-388A>C
c.136-169A>C
n.920A>C
n.340A>C
c.803A>C (p.Tyr268Ser)
11g.2166938A>CCA379126715THc.790T>G (p.Tyr264Asp)
c.*479T>G (n.*479T>G)
c.696-389T>G (n.696-389T>G)
c.*510T>G (n.*510T>G)
c.871T>G (p.Tyr291Asp)
c.883T>G (p.Tyr295Asp)
c.136-389T>G
c.136-170T>G
n.919T>G
n.339T>G
c.802T>G (p.Tyr268Asp)
11g.2166938A>GCA379126717THc.790T>C (p.Tyr264His)
c.*479T>C (n.*479T>C)
c.696-389T>C (n.696-389T>C)
c.*510T>C (n.*510T>C)
c.871T>C (p.Tyr291His)
c.883T>C (p.Tyr295His)
c.136-389T>C
c.136-170T>C
n.919T>C
n.339T>C
c.802T>C (p.Tyr268His)
11g.2166938A>TCA379126719THc.790T>A (p.Tyr264Asn)
c.*479T>A (n.*479T>A)
c.696-389T>A (n.696-389T>A)
c.*510T>A (n.*510T>A)
c.871T>A (p.Tyr291Asn)
c.883T>A (p.Tyr295Asn)
c.136-389T>A
c.136-170T>A
n.919T>A
n.339T>A
c.802T>A (p.Tyr268Asn)
11g.2166939G>ACA472414331THc.789C>T (p.Gly263=)
c.*478C>T (n.*478C>T)
c.696-390C>T (n.696-390C>T)
c.*509C>T (n.*509C>T)
c.870C>T (p.Gly290=)
c.882C>T (p.Gly294=)
c.136-390C>T
c.136-171C>T
n.918C>T
n.338C>T
c.801C>T (p.Gly267=)
dbSNP
11g.2166939G>CCA472414332THc.789C>G (p.Gly263=)
c.*478C>G (n.*478C>G)
c.696-390C>G (n.696-390C>G)
c.*509C>G (n.*509C>G)
c.870C>G (p.Gly290=)
c.882C>G (p.Gly294=)
c.136-390C>G
c.136-171C>G
n.918C>G
n.338C>G
c.801C>G (p.Gly267=)
11g.2166939G=CA1948005865THc.789C= (p.Gly263=)
c.*478C= (n.*478C=)
c.696-390C= (n.696-390C=)
c.*509C= (n.*509C=)
c.870C= (p.Gly290=)
c.882C= (p.Gly294=)
c.136-390C=
c.136-171C=
n.918C=
n.338C=
c.801C= (p.Gly267=)
11g.2166939G>TCA472414333THc.789C>A (p.Gly263=)
c.*478C>A (n.*478C>A)
c.696-390C>A (n.696-390C>A)
c.*509C>A (n.*509C>A)
c.870C>A (p.Gly290=)
c.882C>A (p.Gly294=)
c.136-390C>A
c.136-171C>A
n.918C>A
n.338C>A
c.801C>A (p.Gly267=)
11g.2166940C>ACA379126722THc.788G>T (p.Gly263Val)
c.*477G>T (n.*477G>T)
c.696-391G>T (n.696-391G>T)
c.*508G>T (n.*508G>T)
c.869G>T (p.Gly290Val)
c.881G>T (p.Gly294Val)
c.136-391G>T
c.136-172G>T
n.917G>T
n.337G>T
c.800G>T (p.Gly267Val)
gnomAD v4
11g.2166940C>GCA379126724THc.788G>C (p.Gly263Ala)
c.*477G>C (n.*477G>C)
c.696-391G>C (n.696-391G>C)
c.*508G>C (n.*508G>C)
c.869G>C (p.Gly290Ala)
c.881G>C (p.Gly294Ala)
c.136-391G>C
c.136-172G>C
n.917G>C
n.337G>C
c.800G>C (p.Gly267Ala)
11g.2166940C>TCA379126726THc.788G>A (p.Gly263Asp)
c.*477G>A (n.*477G>A)
c.696-391G>A (n.696-391G>A)
c.*508G>A (n.*508G>A)
c.869G>A (p.Gly290Asp)
c.881G>A (p.Gly294Asp)
c.136-391G>A
c.136-172G>A
n.917G>A
n.337G>A
c.800G>A (p.Gly267Asp)
gnomAD v4
11g.2166941delCA912971960THc.788del (p.Gly263AlafsTer17)
c.*477del (n.*477del)
c.696-391del (n.696-391del)
c.*508del (n.*508del)
c.869del (p.Gly290AlafsTer17)
c.881del (p.Gly294AlafsTer17)
c.136-391del
c.136-172del
n.917del
n.337del
c.800del (p.Gly267AlafsTer17)
ClinVar dbSNP gnomAD v4
11g.2166941C>ACA379126728THc.787G>T (p.Gly263Cys)
c.*476G>T (n.*476G>T)
c.696-392G>T (n.696-392G>T)
c.*507G>T (n.*507G>T)
c.868G>T (p.Gly290Cys)
c.880G>T (p.Gly294Cys)
c.136-392G>T
c.136-173G>T
n.916G>T
n.336G>T
c.799G>T (p.Gly267Cys)
dbSNP gnomAD v2
11g.2166941C=CA1948005870THc.787G= (p.Gly263=)
c.*476G= (n.*476G=)
c.696-392G= (n.696-392G=)
c.*507G= (n.*507G=)
c.868G= (p.Gly290=)
c.880G= (p.Gly294=)
c.136-392G=
c.136-173G=
n.916G=
n.336G=
c.799G= (p.Gly267=)
11g.2166941C>GCA5818489THc.787G>C (p.Gly263Arg)
c.*476G>C (n.*476G>C)
c.696-392G>C (n.696-392G>C)
c.*507G>C (n.*507G>C)
c.868G>C (p.Gly290Arg)
c.880G>C (p.Gly294Arg)
c.136-392G>C
c.136-173G>C
n.916G>C
n.336G>C
c.799G>C (p.Gly267Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.2166941C>TCA5818490THc.787G>A (p.Gly263Ser)
c.*476G>A (n.*476G>A)
c.696-392G>A (n.696-392G>A)
c.*507G>A (n.*507G>A)
c.868G>A (p.Gly290Ser)
c.880G>A (p.Gly294Ser)
c.136-392G>A
c.136-173G>A
n.916G>A
n.336G>A
c.799G>A (p.Gly267Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.2166942G>ACA5818491THc.786C>T (p.Ser262=)
c.*475C>T (n.*475C>T)
c.696-393C>T (n.696-393C>T)
c.*506C>T (n.*506C>T)
c.867C>T (p.Ser289=)
c.879C>T (p.Ser293=)
c.136-393C>T
c.136-174C>T
n.915C>T
n.335C>T
c.798C>T (p.Ser266=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.2166942G>CCA379126735THc.786C>G (p.Ser262Arg)
c.*475C>G (n.*475C>G)
c.696-393C>G (n.696-393C>G)
c.*506C>G (n.*506C>G)
c.867C>G (p.Ser289Arg)
c.879C>G (p.Ser293Arg)
c.136-393C>G
c.136-174C>G
n.915C>G
n.335C>G
c.798C>G (p.Ser266Arg)
gnomAD v4
11g.2166942G=CA1948005872THc.786C= (p.Ser262=)
c.*475C= (n.*475C=)
c.696-393C= (n.696-393C=)
c.*506C= (n.*506C=)
c.867C= (p.Ser289=)
c.879C= (p.Ser293=)
c.136-393C=
c.136-174C=
n.915C=
n.335C=
c.798C= (p.Ser266=)
11g.2166942G>TCA379126737THc.786C>A (p.Ser262Arg)
c.*475C>A (n.*475C>A)
c.696-393C>A (n.696-393C>A)
c.*506C>A (n.*506C>A)
c.867C>A (p.Ser289Arg)
c.879C>A (p.Ser293Arg)
c.136-393C>A
c.136-174C>A
n.915C>A
n.335C>A
c.798C>A (p.Ser266Arg)
gnomAD v4
11g.2166943C>ACA379126739THc.785G>T (p.Ser262Ile)
c.*474G>T (n.*474G>T)
c.696-394G>T (n.696-394G>T)
c.*505G>T (n.*505G>T)
c.866G>T (p.Ser289Ile)
c.878G>T (p.Ser293Ile)
c.136-394G>T
c.136-175G>T
n.914G>T
n.334G>T
c.797G>T (p.Ser266Ile)
11g.2166943C>GCA379126742THc.785G>C (p.Ser262Thr)
c.*474G>C (n.*474G>C)
c.696-394G>C (n.696-394G>C)
c.*505G>C (n.*505G>C)
c.866G>C (p.Ser289Thr)
c.878G>C (p.Ser293Thr)
c.136-394G>C
c.136-175G>C
n.914G>C
n.334G>C
c.797G>C (p.Ser266Thr)
11g.2166943C>TCA379126744THc.785G>A (p.Ser262Asn)
c.*474G>A (n.*474G>A)
c.696-394G>A (n.696-394G>A)
c.*505G>A (n.*505G>A)
c.866G>A (p.Ser289Asn)
c.878G>A (p.Ser293Asn)
c.136-394G>A
c.136-175G>A
n.914G>A
n.334G>A
c.797G>A (p.Ser266Asn)
11g.2166944T>ACA379126746THc.784A>T (p.Ser262Cys)
c.*473A>T (n.*473A>T)
c.696-395A>T (n.696-395A>T)
c.*504A>T (n.*504A>T)
c.865A>T (p.Ser289Cys)
c.877A>T (p.Ser293Cys)
c.136-395A>T
c.136-176A>T
n.913A>T
n.333A>T
c.796A>T (p.Ser266Cys)
11g.2166944T>CCA379126748THc.784A>G (p.Ser262Gly)
c.*473A>G (n.*473A>G)
c.696-395A>G (n.696-395A>G)
c.*504A>G (n.*504A>G)
c.865A>G (p.Ser289Gly)
c.877A>G (p.Ser293Gly)
c.136-395A>G
c.136-176A>G
n.913A>G
n.333A>G
c.796A>G (p.Ser266Gly)
11g.2166944T>GCA379126751THc.784A>C (p.Ser262Arg)
c.*473A>C (n.*473A>C)
c.696-395A>C (n.696-395A>C)
c.*504A>C (n.*504A>C)
c.865A>C (p.Ser289Arg)
c.877A>C (p.Ser293Arg)
c.136-395A>C
c.136-176A>C
n.913A>C
n.333A>C
c.796A>C (p.Ser266Arg)
gnomAD v4
11g.2166945G>ACA472414334THc.783C>T (p.Phe261=)
c.*472C>T (n.*472C>T)
c.696-396C>T (n.696-396C>T)
c.*503C>T (n.*503C>T)
c.864C>T (p.Phe288=)
c.876C>T (p.Phe292=)
c.136-396C>T
c.136-177C>T
n.912C>T
n.332C>T
c.795C>T (p.Phe265=)
11g.2166945G>CCA379126753THc.783C>G (p.Phe261Leu)
c.*472C>G (n.*472C>G)
c.696-396C>G (n.696-396C>G)
c.*503C>G (n.*503C>G)
c.864C>G (p.Phe288Leu)
c.876C>G (p.Phe292Leu)
c.136-396C>G
c.136-177C>G
n.912C>G
n.332C>G
c.795C>G (p.Phe265Leu)
11g.2166945G>TCA379126755THc.783C>A (p.Phe261Leu)
c.*472C>A (n.*472C>A)
c.696-396C>A (n.696-396C>A)
c.*503C>A (n.*503C>A)
c.864C>A (p.Phe288Leu)
c.876C>A (p.Phe292Leu)
c.136-396C>A
c.136-177C>A
n.912C>A
n.332C>A
c.795C>A (p.Phe265Leu)
gnomAD v4
11g.2166946A>CCA379126760THc.782T>G (p.Phe261Cys)
c.*471T>G (n.*471T>G)
c.696-397T>G (n.696-397T>G)
c.*502T>G (n.*502T>G)
c.863T>G (p.Phe288Cys)
c.875T>G (p.Phe292Cys)
c.136-397T>G
c.136-178T>G
n.911T>G
n.331T>G
c.794T>G (p.Phe265Cys)
11g.2166946A>GCA379126759THc.782T>C (p.Phe261Ser)
c.*471T>C (n.*471T>C)
c.696-397T>C (n.696-397T>C)
c.*502T>C (n.*502T>C)
c.863T>C (p.Phe288Ser)
c.875T>C (p.Phe292Ser)
c.136-397T>C
c.136-178T>C
n.911T>C
n.331T>C
c.794T>C (p.Phe265Ser)
11g.2166946A>TCA379126758THc.782T>A (p.Phe261Tyr)
c.*471T>A (n.*471T>A)
c.696-397T>A (n.696-397T>A)
c.*502T>A (n.*502T>A)
c.863T>A (p.Phe288Tyr)
c.875T>A (p.Phe292Tyr)
c.136-397T>A
c.136-178T>A
n.911T>A
n.331T>A
c.794T>A (p.Phe265Tyr)
11g.2166947A>CCA379126765THc.781T>G (p.Phe261Val)
c.*470T>G (n.*470T>G)
c.696-398T>G (n.696-398T>G)
c.*501T>G (n.*501T>G)
c.862T>G (p.Phe288Val)
c.874T>G (p.Phe292Val)
c.136-398T>G
c.136-179T>G
n.910T>G
n.330T>G
c.793T>G (p.Phe265Val)
11g.2166947A>GCA379126763THc.781T>C (p.Phe261Leu)
c.*470T>C (n.*470T>C)
c.696-398T>C (n.696-398T>C)
c.*501T>C (n.*501T>C)
c.862T>C (p.Phe288Leu)
c.874T>C (p.Phe292Leu)
c.136-398T>C
c.136-179T>C
n.910T>C
n.330T>C
c.793T>C (p.Phe265Leu)
gnomAD v4
11g.2166947A>TCA379126767THc.781T>A (p.Phe261Ile)
c.*470T>A (n.*470T>A)
c.696-398T>A (n.696-398T>A)
c.*501T>A (n.*501T>A)
c.862T>A (p.Phe288Ile)
c.874T>A (p.Phe292Ile)
c.136-398T>A
c.136-179T>A
n.910T>A
n.330T>A
c.793T>A (p.Phe265Ile)
11g.2166948delCA2573146038THc.780del (p.Phe261SerfsTer19)
c.*469del (n.*469del)
c.696-399del (n.696-399del)
c.*500del (n.*500del)
c.861del (p.Phe288SerfsTer19)
c.873del (p.Phe292SerfsTer19)
c.136-399del
c.136-180del
n.909del
n.329del
c.792del (p.Phe265SerfsTer19)
dbSNP
11g.2166948G>ACA472414337THc.780C>T (p.Arg260=)
c.*469C>T (n.*469C>T)
c.696-399C>T (n.696-399C>T)
c.*500C>T (n.*500C>T)
c.861C>T (p.Arg287=)
c.873C>T (p.Arg291=)
c.136-399C>T
c.136-180C>T
n.909C>T
n.329C>T
c.792C>T (p.Arg264=)
11g.2166948G>CCA472414335THc.780C>G (p.Arg260=)
c.*469C>G (n.*469C>G)
c.696-399C>G (n.696-399C>G)
c.*500C>G (n.*500C>G)
c.861C>G (p.Arg287=)
c.873C>G (p.Arg291=)
c.136-399C>G
c.136-180C>G
n.909C>G
n.329C>G
c.792C>G (p.Arg264=)
11g.2166948G>TCA472414336THc.780C>A (p.Arg260=)
c.*469C>A (n.*469C>A)
c.696-399C>A (n.696-399C>A)
c.*500C>A (n.*500C>A)
c.861C>A (p.Arg287=)
c.873C>A (p.Arg291=)
c.136-399C>A
c.136-180C>A
n.909C>A
n.329C>A
c.792C>A (p.Arg264=)
11g.2166949delCA2580082587THc.779del (p.Arg260ProfsTer20)
c.*468del (n.*468del)
c.696-400del (n.696-400del)
c.*499del (n.*499del)
c.860del (p.Arg287ProfsTer20)
c.872del (p.Arg291ProfsTer20)
c.136-400del
c.136-181del
n.908del
n.328del
c.791del (p.Arg264ProfsTer20)
ClinVar
11g.2166949C>ACA216285419THc.779G>T (p.Arg260Leu)
c.*468G>T (n.*468G>T)
c.696-400G>T (n.696-400G>T)
c.*499G>T (n.*499G>T)
c.860G>T (p.Arg287Leu)
c.872G>T (p.Arg291Leu)
c.136-400G>T
c.136-181G>T
n.908G>T
n.328G>T
c.791G>T (p.Arg264Leu)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.2166949C=CA1948005876THc.779G= (p.Arg260=)
c.*468G= (n.*468G=)
c.696-400G= (n.696-400G=)
c.*499G= (n.*499G=)
c.860G= (p.Arg287=)
c.872G= (p.Arg291=)
c.136-400G=
c.136-181G=
n.908G=
n.328G=
c.791G= (p.Arg264=)
11g.2166949C>GCA379126773THc.779G>C (p.Arg260Pro)
c.*468G>C (n.*468G>C)
c.696-400G>C (n.696-400G>C)
c.*499G>C (n.*499G>C)
c.860G>C (p.Arg287Pro)
c.872G>C (p.Arg291Pro)
c.136-400G>C
c.136-181G>C
n.908G>C
n.328G>C
c.791G>C (p.Arg264Pro)
gnomAD v4
11g.2166949C>TCA379126770THc.779G>A (p.Arg260His)
c.*468G>A (n.*468G>A)
c.696-400G>A (n.696-400G>A)
c.*499G>A (n.*499G>A)
c.860G>A (p.Arg287His)
c.872G>A (p.Arg291His)
c.136-400G>A
c.136-181G>A
n.908G>A
n.328G>A
c.791G>A (p.Arg264His)
dbSNP gnomAD v2 gnomAD v4
11g.2166950delCA2580082589THc.778del (p.Arg260AlafsTer20)
c.*467del (n.*467del)
c.696-401del (n.696-401del)
c.*498del (n.*498del)
c.859del (p.Arg287AlafsTer20)
c.871del (p.Arg291AlafsTer20)
c.136-401del
c.136-182del
n.907del
n.327del
c.790del (p.Arg264AlafsTer20)
ClinVar
11g.2166950G>ACA5818493THc.778C>T (p.Arg260Cys)
c.*467C>T (n.*467C>T)
c.696-401C>T (n.696-401C>T)
c.*498C>T (n.*498C>T)
c.859C>T (p.Arg287Cys)
c.871C>T (p.Arg291Cys)
c.136-401C>T
c.136-182C>T
n.907C>T
n.327C>T
c.790C>T (p.Arg264Cys)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.2166950G>CCA379126778THc.778C>G (p.Arg260Gly)
c.*467C>G (n.*467C>G)
c.696-401C>G (n.696-401C>G)
c.*498C>G (n.*498C>G)
c.859C>G (p.Arg287Gly)
c.871C>G (p.Arg291Gly)
c.136-401C>G
c.136-182C>G
n.907C>G
n.327C>G
c.790C>G (p.Arg264Gly)
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.2166950G=CA1948005878THc.778C= (p.Arg260=)
c.*467C= (n.*467C=)
c.696-401C= (n.696-401C=)
c.*498C= (n.*498C=)
c.859C= (p.Arg287=)
c.871C= (p.Arg291=)
c.136-401C=
c.136-182C=
n.907C=
n.327C=
c.790C= (p.Arg264=)
11g.2166950G>TCA5818492THc.778C>A (p.Arg260Ser)
c.*467C>A (n.*467C>A)
c.696-401C>A (n.696-401C>A)
c.*498C>A (n.*498C>A)
c.859C>A (p.Arg287Ser)
c.871C>A (p.Arg291Ser)
c.136-401C>A
c.136-182C>A
n.907C>A
n.327C>A
c.790C>A (p.Arg264Ser)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.2166951C>ACA379126779THc.777G>T (p.Glu259Asp)
c.*466G>T (n.*466G>T)
c.696-402G>T (n.696-402G>T)
c.*497G>T (n.*497G>T)
c.858G>T (p.Glu286Asp)
c.870G>T (p.Glu290Asp)
c.136-402G>T
c.136-183G>T
n.906G>T
n.326G>T
c.789G>T (p.Glu263Asp)
11g.2166951C=CA1948005882THc.777G= (p.Glu259=)
c.*466G= (n.*466G=)
c.696-402G= (n.696-402G=)
c.*497G= (n.*497G=)
c.858G= (p.Glu286=)
c.870G= (p.Glu290=)
c.136-402G=
c.136-183G=
n.906G=
n.326G=
c.789G= (p.Glu263=)
11g.2166951C>GCA379126780THc.777G>C (p.Glu259Asp)
c.*466G>C (n.*466G>C)
c.696-402G>C (n.696-402G>C)
c.*497G>C (n.*497G>C)
c.858G>C (p.Glu286Asp)
c.870G>C (p.Glu290Asp)
c.136-402G>C
c.136-183G>C
n.906G>C
n.326G>C
c.789G>C (p.Glu263Asp)
gnomAD v4
11g.2166951C>TCA216285439THc.777G>A (p.Glu259=)
c.*466G>A (n.*466G>A)
c.696-402G>A (n.696-402G>A)
c.*497G>A (n.*497G>A)
c.858G>A (p.Glu286=)
c.870G>A (p.Glu290=)
c.136-402G>A
c.136-183G>A
n.906G>A
n.326G>A
c.789G>A (p.Glu263=)
ClinVar dbSNP gnomAD v4
11g.2166952T>ACA379126783THc.776A>T (p.Glu259Val)
c.*465A>T (n.*465A>T)
c.696-403A>T (n.696-403A>T)
c.*496A>T (n.*496A>T)
c.857A>T (p.Glu286Val)
c.869A>T (p.Glu290Val)
c.136-403A>T
c.136-184A>T
n.905A>T
n.325A>T
c.788A>T (p.Glu263Val)
11g.2166952T>CCA379126787THc.776A>G (p.Glu259Gly)
c.*465A>G (n.*465A>G)
c.696-403A>G (n.696-403A>G)
c.*496A>G (n.*496A>G)
c.857A>G (p.Glu286Gly)
c.869A>G (p.Glu290Gly)
c.136-403A>G
c.136-184A>G
n.905A>G
n.325A>G
c.788A>G (p.Glu263Gly)
gnomAD v4
11g.2166952T>GCA379126785THc.776A>C (p.Glu259Ala)
c.*465A>C (n.*465A>C)
c.696-403A>C (n.696-403A>C)
c.*496A>C (n.*496A>C)
c.857A>C (p.Glu286Ala)
c.869A>C (p.Glu290Ala)
c.136-403A>C
c.136-184A>C
n.905A>C
n.325A>C
c.788A>C (p.Glu263Ala)
11g.2166953C>ACA379126791THc.775G>T (p.Glu259Ter)
c.*464G>T (n.*464G>T)
c.696-404G>T (n.696-404G>T)
c.*495G>T (n.*495G>T)
c.856G>T (p.Glu286Ter)
c.868G>T (p.Glu290Ter)
c.136-404G>T
c.136-185G>T
n.904G>T
n.324G>T
c.787G>T (p.Glu263Ter)
11g.2166953C>GCA379126793THc.775G>C (p.Glu259Gln)
c.*464G>C (n.*464G>C)
c.696-404G>C (n.696-404G>C)
c.*495G>C (n.*495G>C)
c.856G>C (p.Glu286Gln)
c.868G>C (p.Glu290Gln)
c.136-404G>C
c.136-185G>C
n.904G>C
n.324G>C
c.787G>C (p.Glu263Gln)
11g.2166953C>TCA379126795THc.775G>A (p.Glu259Lys)
c.*464G>A (n.*464G>A)
c.696-404G>A (n.696-404G>A)
c.*495G>A (n.*495G>A)
c.856G>A (p.Glu286Lys)
c.868G>A (p.Glu290Lys)
c.136-404G>A
c.136-185G>A
n.904G>A
n.324G>A
c.787G>A (p.Glu263Lys)
11g.2166954C>ACA472414338THc.774G>T (p.Leu258=)
c.*463G>T (n.*463G>T)
c.696-405G>T (n.696-405G>T)
c.*494G>T (n.*494G>T)
c.855G>T (p.Leu285=)
c.867G>T (p.Leu289=)
c.136-405G>T
c.136-186G>T
n.903G>T
n.323G>T
c.786G>T (p.Leu262=)
11g.2166954C>GCA472414339THc.774G>C (p.Leu258=)
c.*463G>C (n.*463G>C)
c.696-405G>C (n.696-405G>C)
c.*494G>C (n.*494G>C)
c.855G>C (p.Leu285=)
c.867G>C (p.Leu289=)
c.136-405G>C
c.136-186G>C
n.903G>C
n.323G>C
c.786G>C (p.Leu262=)
11g.2166954C>TCA472414340THc.774G>A (p.Leu258=)
c.*463G>A (n.*463G>A)
c.696-405G>A (n.696-405G>A)
c.*494G>A (n.*494G>A)
c.855G>A (p.Leu285=)
c.867G>A (p.Leu289=)
c.136-405G>A
c.136-186G>A
n.903G>A
n.323G>A
c.786G>A (p.Leu262=)
11g.2166955A=CA1948005887THc.773T= (p.Leu258=)
c.*462T= (n.*462T=)
c.696-406T= (n.696-406T=)
c.*493T= (n.*493T=)
c.854T= (p.Leu285=)
c.866T= (p.Leu289=)
c.136-406T=
c.136-187T=
n.902T=
n.322T=
c.785T= (p.Leu262=)
11g.2166955A>CCA379126798THc.773T>G (p.Leu258Arg)
c.*462T>G (n.*462T>G)
c.696-406T>G (n.696-406T>G)
c.*493T>G (n.*493T>G)
c.854T>G (p.Leu285Arg)
c.866T>G (p.Leu289Arg)
c.136-406T>G
c.136-187T>G
n.902T>G
n.322T>G
c.785T>G (p.Leu262Arg)
11g.2166955A>GCA379126799THc.773T>C (p.Leu258Pro)
c.*462T>C (n.*462T>C)
c.696-406T>C (n.696-406T>C)
c.*493T>C (n.*493T>C)
c.854T>C (p.Leu285Pro)
c.866T>C (p.Leu289Pro)
c.136-406T>C
c.136-187T>C
n.902T>C
n.322T>C
c.785T>C (p.Leu262Pro)
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.2166955A>TCA379126802THc.773T>A (p.Leu258Gln)
c.*462T>A (n.*462T>A)
c.696-406T>A (n.696-406T>A)
c.*493T>A (n.*493T>A)
c.854T>A (p.Leu285Gln)
c.866T>A (p.Leu289Gln)
c.136-406T>A
c.136-187T>A
n.902T>A
n.322T>A
c.785T>A (p.Leu262Gln)
11g.2166962_2166966delCA2611964590THc.769_773del (p.Leu257GlyfsTer?)
c.*458_*462del (n.*458_*462del)
c.696-410_696-406del (n.696-410_696-406del)
c.*489_*493del (n.*489_*493del)
c.850_854del (p.Leu284GlyfsTer?)
c.862_866del (p.Leu288GlyfsTer?)
c.136-410_136-406del
c.136-191_136-187del
n.898_902del
n.318_322del
c.781_785del (p.Leu261GlyfsTer?)
gnomAD v4
11g.2166956G>ACA472414341THc.772C>T (p.Leu258=)
c.*461C>T (n.*461C>T)
c.696-407C>T (n.696-407C>T)
c.*492C>T (n.*492C>T)
c.853C>T (p.Leu285=)
c.865C>T (p.Leu289=)
c.136-407C>T
c.136-188C>T
n.901C>T
n.321C>T
c.784C>T (p.Leu262=)
gnomAD v4
11g.2166956G>CCA379126804THc.772C>G (p.Leu258Val)
c.*461C>G (n.*461C>G)
c.696-407C>G (n.696-407C>G)
c.*492C>G (n.*492C>G)
c.853C>G (p.Leu285Val)
c.865C>G (p.Leu289Val)
c.136-407C>G
c.136-188C>G
n.901C>G
n.321C>G
c.784C>G (p.Leu262Val)
11g.2166956G>TCA379126806THc.772C>A (p.Leu258Met)
c.*461C>A (n.*461C>A)
c.696-407C>A (n.696-407C>A)
c.*492C>A (n.*492C>A)
c.853C>A (p.Leu285Met)
c.865C>A (p.Leu289Met)
c.136-407C>A
c.136-188C>A
n.901C>A
n.321C>A
c.784C>A (p.Leu262Met)
11g.2166957C>ACA379126808THc.771G>T (p.Leu257Phe)
c.*460G>T (n.*460G>T)
c.696-408G>T (n.696-408G>T)
c.*491G>T (n.*491G>T)
c.852G>T (p.Leu284Phe)
c.864G>T (p.Leu288Phe)
c.136-408G>T
c.136-189G>T
n.900G>T
n.320G>T
c.783G>T (p.Leu261Phe)
gnomAD v4
11g.2166957C=CA1948005892THc.771G= (p.Leu257=)
c.*460G= (n.*460G=)
c.696-408G= (n.696-408G=)
c.*491G= (n.*491G=)
c.852G= (p.Leu284=)
c.864G= (p.Leu288=)
c.136-408G=
c.136-189G=
n.900G=
n.320G=
c.783G= (p.Leu261=)
11g.2166957C>GCA379126809THc.771G>C (p.Leu257Phe)
c.*460G>C (n.*460G>C)
c.696-408G>C (n.696-408G>C)
c.*491G>C (n.*491G>C)
c.852G>C (p.Leu284Phe)
c.864G>C (p.Leu288Phe)
c.136-408G>C
c.136-189G>C
n.900G>C
n.320G>C
c.783G>C (p.Leu261Phe)
dbSNP
11g.2166957C>TCA472414342THc.771G>A (p.Leu257=)
c.*460G>A (n.*460G>A)
c.696-408G>A (n.696-408G>A)
c.*491G>A (n.*491G>A)
c.852G>A (p.Leu284=)
c.864G>A (p.Leu288=)
c.136-408G>A
c.136-189G>A
n.900G>A
n.320G>A
c.783G>A (p.Leu261=)
11g.2166958A>CCA379126812THc.770T>G (p.Leu257Trp)
c.*459T>G (n.*459T>G)
c.696-409T>G (n.696-409T>G)
c.*490T>G (n.*490T>G)
c.851T>G (p.Leu284Trp)
c.863T>G (p.Leu288Trp)
c.136-409T>G
c.136-190T>G
n.899T>G
n.319T>G
c.782T>G (p.Leu261Trp)
11g.2166958A>GCA379126814THc.770T>C (p.Leu257Ser)
c.*459T>C (n.*459T>C)
c.696-409T>C (n.696-409T>C)
c.*490T>C (n.*490T>C)
c.851T>C (p.Leu284Ser)
c.863T>C (p.Leu288Ser)
c.136-409T>C
c.136-190T>C
n.899T>C
n.319T>C
c.782T>C (p.Leu261Ser)
gnomAD v4
11g.2166958A>TCA379126815THc.770T>A (p.Leu257Ter)
c.*459T>A (n.*459T>A)
c.696-409T>A (n.696-409T>A)
c.*490T>A (n.*490T>A)
c.851T>A (p.Leu284Ter)
c.863T>A (p.Leu288Ter)
c.136-409T>A
c.136-190T>A
n.899T>A
n.319T>A
c.782T>A (p.Leu261Ter)
11g.2166959A=CA1948005898THc.769T= (p.Leu257=)
c.*458T= (n.*458T=)
c.696-410T= (n.696-410T=)
c.*489T= (n.*489T=)
c.850T= (p.Leu284=)
c.862T= (p.Leu288=)
c.136-410T=
c.136-191T=
n.898T=
n.318T=
c.781T= (p.Leu261=)
11g.2166959A>CCA379126818THc.769T>G (p.Leu257Val)
c.*458T>G (n.*458T>G)
c.696-410T>G (n.696-410T>G)
c.*489T>G (n.*489T>G)
c.850T>G (p.Leu284Val)
c.862T>G (p.Leu288Val)
c.136-410T>G
c.136-191T>G
n.898T>G
n.318T>G
c.781T>G (p.Leu261Val)
11g.2166959A>GCA5818494THc.769T>C (p.Leu257=)
c.*458T>C (n.*458T>C)
c.696-410T>C (n.696-410T>C)
c.*489T>C (n.*489T>C)
c.850T>C (p.Leu284=)
c.862T>C (p.Leu288=)
c.136-410T>C
c.136-191T>C
n.898T>C
n.318T>C
c.781T>C (p.Leu261=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.2166959A>TCA379126820THc.769T>A (p.Leu257Met)
c.*458T>A (n.*458T>A)
c.696-410T>A (n.696-410T>A)
c.*489T>A (n.*489T>A)
c.850T>A (p.Leu284Met)
c.862T>A (p.Leu288Met)
c.136-410T>A
c.136-191T>A
n.898T>A
n.318T>A
c.781T>A (p.Leu261Met)
11g.2166960A=CA1948005901THc.768T= (p.Ala256=)
c.*457T= (n.*457T=)
c.696-411T= (n.696-411T=)
c.*488T= (n.*488T=)
c.849T= (p.Ala283=)
c.861T= (p.Ala287=)
c.136-411T=
c.136-192T=
n.897T=
n.317T=
c.780T= (p.Ala260=)
11g.2166960A>CCA472414345THc.768T>G (p.Ala256=)
c.*457T>G (n.*457T>G)
c.696-411T>G (n.696-411T>G)
c.*488T>G (n.*488T>G)
c.849T>G (p.Ala283=)
c.861T>G (p.Ala287=)
c.136-411T>G
c.136-192T>G
n.897T>G
n.317T>G
c.780T>G (p.Ala260=)
11g.2166960A>GCA472414343THc.768T>C (p.Ala256=)
c.*457T>C (n.*457T>C)
c.696-411T>C (n.696-411T>C)
c.*488T>C (n.*488T>C)
c.849T>C (p.Ala283=)
c.861T>C (p.Ala287=)
c.136-411T>C
c.136-192T>C
n.897T>C
n.317T>C
c.780T>C (p.Ala260=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.2166960A>TCA472414344THc.768T>A (p.Ala256=)
c.*457T>A (n.*457T>A)
c.696-411T>A (n.696-411T>A)
c.*488T>A (n.*488T>A)
c.849T>A (p.Ala283=)
c.861T>A (p.Ala287=)
c.136-411T>A
c.136-192T>A
n.897T>A
n.317T>A
c.780T>A (p.Ala260=)
11g.2166961_2166963delCA2611964602THc.766_768del (p.Ala256del)
c.*455_*457del (n.*455_*457del)
c.696-413_696-411del (n.696-413_696-411del)
c.*486_*488del (n.*486_*488del)
c.847_849del (p.Ala283del)
c.859_861del (p.Ala287del)
c.136-413_136-411del
c.136-194_136-192del
n.895_897del
n.315_317del
c.778_780del (p.Ala260del)
gnomAD v4
11g.2166961G>ACA5818495THc.767C>T (p.Ala256Val)
c.*456C>T (n.*456C>T)
c.696-412C>T (n.696-412C>T)
c.*487C>T (n.*487C>T)
c.848C>T (p.Ala283Val)
c.860C>T (p.Ala287Val)
c.136-412C>T
c.136-193C>T
n.896C>T
n.316C>T
c.779C>T (p.Ala260Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.2166961G>CCA379126825THc.767C>G (p.Ala256Gly)
c.*456C>G (n.*456C>G)
c.696-412C>G (n.696-412C>G)
c.*487C>G (n.*487C>G)
c.848C>G (p.Ala283Gly)
c.860C>G (p.Ala287Gly)
c.136-412C>G
c.136-193C>G
n.896C>G
n.316C>G
c.779C>G (p.Ala260Gly)
dbSNP gnomAD v2 gnomAD v4
11g.2166961G=CA1948005903THc.767C= (p.Ala256=)
c.*456C= (n.*456C=)
c.696-412C= (n.696-412C=)
c.*487C= (n.*487C=)
c.848C= (p.Ala283=)
c.860C= (p.Ala287=)
c.136-412C=
c.136-193C=
n.896C=
n.316C=
c.779C= (p.Ala260=)
11g.2166961G>TCA379126827THc.767C>A (p.Ala256Asp)
c.*456C>A (n.*456C>A)
c.696-412C>A (n.696-412C>A)
c.*487C>A (n.*487C>A)
c.848C>A (p.Ala283Asp)
c.860C>A (p.Ala287Asp)
c.136-412C>A
c.136-193C>A
n.896C>A
n.316C>A
c.779C>A (p.Ala260Asp)
COSMIC
11g.2166962C>ACA5818496THc.766G>T (p.Ala256Ser)
c.*455G>T (n.*455G>T)
c.696-413G>T (n.696-413G>T)
c.*486G>T (n.*486G>T)
c.847G>T (p.Ala283Ser)
c.859G>T (p.Ala287Ser)
c.136-413G>T
c.136-194G>T
n.895G>T
n.315G>T
c.778G>T (p.Ala260Ser)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.2166962C=CA1948005908THc.766G= (p.Ala256=)
c.*455G= (n.*455G=)
c.696-413G= (n.696-413G=)
c.*486G= (n.*486G=)
c.847G= (p.Ala283=)
c.859G= (p.Ala287=)
c.136-413G=
c.136-194G=
n.895G=
n.315G=
c.778G= (p.Ala260=)
11g.2166962C>GCA379126832THc.766G>C (p.Ala256Pro)
c.*455G>C (n.*455G>C)
c.696-413G>C (n.696-413G>C)
c.*486G>C (n.*486G>C)
c.847G>C (p.Ala283Pro)
c.859G>C (p.Ala287Pro)
c.136-413G>C
c.136-194G>C
n.895G>C
n.315G>C
c.778G>C (p.Ala260Pro)
11g.2166962C>TCA379126834THc.766G>A (p.Ala256Thr)
c.*455G>A (n.*455G>A)
c.696-413G>A (n.696-413G>A)
c.*486G>A (n.*486G>A)
c.847G>A (p.Ala283Thr)
c.859G>A (p.Ala287Thr)
c.136-413G>A
c.136-194G>A
n.895G>A
n.315G>A
c.778G>A (p.Ala260Thr)
11g.2166963A=CA1948005917THc.765T= (p.Phe255=)
c.*454T= (n.*454T=)
c.696-414T= (n.696-414T=)
c.*485T= (n.*485T=)
c.846T= (p.Phe282=)
c.858T= (p.Phe286=)
c.136-414T=
c.136-195T=
n.894T=
n.314T=
c.777T= (p.Phe259=)
11g.2166963A>CCA379126837THc.765T>G (p.Phe255Leu)
c.*454T>G (n.*454T>G)
c.696-414T>G (n.696-414T>G)
c.*485T>G (n.*485T>G)
c.846T>G (p.Phe282Leu)
c.858T>G (p.Phe286Leu)
c.136-414T>G
c.136-195T>G
n.894T>G
n.314T>G
c.777T>G (p.Phe259Leu)
ClinVar gnomAD v4
11g.2166963A>GCA5818497THc.765T>C (p.Phe255=)
c.*454T>C (n.*454T>C)
c.696-414T>C (n.696-414T>C)
c.*485T>C (n.*485T>C)
c.846T>C (p.Phe282=)
c.858T>C (p.Phe286=)
c.136-414T>C
c.136-195T>C
n.894T>C
n.314T>C
c.777T>C (p.Phe259=)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.2166963A>TCA379126840THc.765T>A (p.Phe255Leu)
c.*454T>A (n.*454T>A)
c.696-414T>A (n.696-414T>A)
c.*485T>A (n.*485T>A)
c.846T>A (p.Phe282Leu)
c.858T>A (p.Phe286Leu)
c.136-414T>A
c.136-195T>A
n.894T>A
n.314T>A
c.777T>A (p.Phe259Leu)
11g.2166965dupCA597431467THc.765dup (p.Ala256CysfsTer?)
c.*454dup (n.*454dup)
c.696-414dup (n.696-414dup)
c.*485dup (n.*485dup)
c.846dup (p.Ala283CysfsTer?)
c.858dup (p.Ala287CysfsTer?)
c.136-414dup
c.136-195dup
n.894dup
n.314dup
c.777dup (p.Ala260CysfsTer?)
dbSNP gnomAD v2 gnomAD v4
11g.2166964A>CCA379126847THc.764T>G (p.Phe255Cys)
c.*453T>G (n.*453T>G)
c.696-415T>G (n.696-415T>G)
c.*484T>G (n.*484T>G)
c.845T>G (p.Phe282Cys)
c.857T>G (p.Phe286Cys)
c.136-415T>G
c.136-196T>G
n.893T>G
n.313T>G
c.776T>G (p.Phe259Cys)
11g.2166964A>GCA379126845THc.764T>C (p.Phe255Ser)
c.*453T>C (n.*453T>C)
c.696-415T>C (n.696-415T>C)
c.*484T>C (n.*484T>C)
c.845T>C (p.Phe282Ser)
c.857T>C (p.Phe286Ser)
c.136-415T>C
c.136-196T>C
n.893T>C
n.313T>C
c.776T>C (p.Phe259Ser)
11g.2166964A>TCA379126842THc.764T>A (p.Phe255Tyr)
c.*453T>A (n.*453T>A)
c.696-415T>A (n.696-415T>A)
c.*484T>A (n.*484T>A)
c.845T>A (p.Phe282Tyr)
c.857T>A (p.Phe286Tyr)
c.136-415T>A
c.136-196T>A
n.893T>A
n.313T>A
c.776T>A (p.Phe259Tyr)
11g.2166965A>CCA379126849THc.763T>G (p.Phe255Val)
c.*452T>G (n.*452T>G)
c.696-416T>G (n.696-416T>G)
c.*483T>G (n.*483T>G)
c.844T>G (p.Phe282Val)
c.856T>G (p.Phe286Val)
c.136-416T>G
c.136-197T>G
n.892T>G
n.312T>G
c.775T>G (p.Phe259Val)
11g.2166965A>GCA379126851THc.763T>C (p.Phe255Leu)
c.*452T>C (n.*452T>C)
c.696-416T>C (n.696-416T>C)
c.*483T>C (n.*483T>C)
c.844T>C (p.Phe282Leu)
c.856T>C (p.Phe286Leu)
c.136-416T>C
c.136-197T>C
n.892T>C
n.312T>C
c.775T>C (p.Phe259Leu)
11g.2166965A>TCA379126853THc.763T>A (p.Phe255Ile)
c.*452T>A (n.*452T>A)
c.696-416T>A (n.696-416T>A)
c.*483T>A (n.*483T>A)
c.844T>A (p.Phe282Ile)
c.856T>A (p.Phe286Ile)
c.136-416T>A
c.136-197T>A
n.892T>A
n.312T>A
c.775T>A (p.Phe259Ile)
11g.2166965_2166966delinsAGCA1948005920THc.762_763delinsCT (p.Ala254=)
c.*451_*452delinsCT (n.*451_*452delinsCT)
c.696-417_696-416delinsCT (n.696-417_696-416delinsCT)
c.*482_*483delinsCT (n.*482_*483delinsCT)
c.843_844delinsCT (p.Ala281=)
c.855_856delinsCT (p.Ala285=)
c.136-417_136-416delinsCT
c.136-198_136-197delinsCT
n.891_892delinsCT
n.311_312delinsCT
c.774_775delinsCT (p.Ala258=)
11g.2166966G>ACA472414346THc.762C>T (p.Ala254=)
c.*451C>T (n.*451C>T)
c.696-417C>T (n.696-417C>T)
c.*482C>T (n.*482C>T)
c.843C>T (p.Ala281=)
c.855C>T (p.Ala285=)
c.136-417C>T
c.136-198C>T
n.891C>T
n.311C>T
c.774C>T (p.Ala258=)
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.2166966G>CCA472414347THc.762C>G (p.Ala254=)
c.*451C>G (n.*451C>G)
c.696-417C>G (n.696-417C>G)
c.*482C>G (n.*482C>G)
c.843C>G (p.Ala281=)
c.855C>G (p.Ala285=)
c.136-417C>G
c.136-198C>G
n.891C>G
n.311C>G
c.774C>G (p.Ala258=)
11g.2166966G=CA1948005923THc.762C= (p.Ala254=)
c.*451C= (n.*451C=)
c.696-417C= (n.696-417C=)
c.*482C= (n.*482C=)
c.843C= (p.Ala281=)
c.855C= (p.Ala285=)
c.136-417C=
c.136-198C=
n.891C=
n.311C=
c.774C= (p.Ala258=)
11g.2166966G>TCA472414348THc.762C>A (p.Ala254=)
c.*451C>A (n.*451C>A)
c.696-417C>A (n.696-417C>A)
c.*482C>A (n.*482C>A)
c.843C>A (p.Ala281=)
c.855C>A (p.Ala285=)
c.136-417C>A
c.136-198C>A
n.891C>A
n.311C>A
c.774C>A (p.Ala258=)
gnomAD v4
11g.2166967delCA1948005922THc.762del (p.Phe255LeufsTer25)
c.*451del (n.*451del)
c.696-417del (n.696-417del)
c.*482del (n.*482del)
c.843del (p.Phe282LeufsTer25)
c.855del (p.Phe286LeufsTer25)
c.136-417del
c.136-198del
n.891del
n.311del
c.774del (p.Phe259LeufsTer25)
dbSNP
11g.2166967G>ACA379126856THc.761C>T (p.Ala254Val)
c.*450C>T (n.*450C>T)
c.696-418C>T (n.696-418C>T)
c.*481C>T (n.*481C>T)
c.842C>T (p.Ala281Val)
c.854C>T (p.Ala285Val)
c.136-418C>T
c.136-199C>T
n.890C>T
n.310C>T
c.773C>T (p.Ala258Val)
gnomAD v4
11g.2166967G>CCA379126858THc.761C>G (p.Ala254Gly)
c.*450C>G (n.*450C>G)
c.696-418C>G (n.696-418C>G)
c.*481C>G (n.*481C>G)
c.842C>G (p.Ala281Gly)
c.854C>G (p.Ala285Gly)
c.136-418C>G
c.136-199C>G
n.890C>G
n.310C>G
c.773C>G (p.Ala258Gly)
11g.2166967G>TCA379126860THc.761C>A (p.Ala254Asp)
c.*450C>A (n.*450C>A)
c.696-418C>A (n.696-418C>A)
c.*481C>A (n.*481C>A)
c.842C>A (p.Ala281Asp)
c.854C>A (p.Ala285Asp)
c.136-418C>A
c.136-199C>A
n.890C>A
n.310C>A
c.773C>A (p.Ala258Asp)
gnomAD v4
11g.2166968C>ACA379126863THc.760G>T (p.Ala254Ser)
c.*449G>T (n.*449G>T)
c.696-419G>T (n.696-419G>T)
c.*480G>T (n.*480G>T)
c.841G>T (p.Ala281Ser)
c.853G>T (p.Ala285Ser)
c.136-419G>T
c.136-200G>T
n.889G>T
n.309G>T
c.772G>T (p.Ala258Ser)
gnomAD v4
11g.2166968C>GCA379126865THc.760G>C (p.Ala254Pro)
c.*449G>C (n.*449G>C)
c.696-419G>C (n.696-419G>C)
c.*480G>C (n.*480G>C)
c.841G>C (p.Ala281Pro)
c.853G>C (p.Ala285Pro)
c.136-419G>C
c.136-200G>C
n.889G>C
n.309G>C
c.772G>C (p.Ala258Pro)
gnomAD v4
11g.2166968C>TCA379126867THc.760G>A (p.Ala254Thr)
c.*449G>A (n.*449G>A)
c.696-419G>A (n.696-419G>A)
c.*480G>A (n.*480G>A)
c.841G>A (p.Ala281Thr)
c.853G>A (p.Ala285Thr)
c.136-419G>A
c.136-200G>A
n.889G>A
n.309G>A
c.772G>A (p.Ala258Thr)
11g.2166969C>ACA379126870THc.759G>T (p.Glu253Asp)
c.*448G>T (n.*448G>T)
c.696-420G>T (n.696-420G>T)
c.*479G>T (n.*479G>T)
c.840G>T (p.Glu280Asp)
c.852G>T (p.Glu284Asp)
c.136-420G>T
c.136-201G>T
n.888G>T
n.308G>T
c.771G>T (p.Glu257Asp)
11g.2166969C=CA1948005927THc.759G= (p.Glu253=)
c.*448G= (n.*448G=)
c.696-420G= (n.696-420G=)
c.*479G= (n.*479G=)
c.840G= (p.Glu280=)
c.852G= (p.Glu284=)
c.136-420G=
c.136-201G=
n.888G=
n.308G=
c.771G= (p.Glu257=)
11g.2166969C>GCA5818498THc.759G>C (p.Glu253Asp)
c.*448G>C (n.*448G>C)
c.696-420G>C (n.696-420G>C)
c.*479G>C (n.*479G>C)
c.840G>C (p.Glu280Asp)
c.852G>C (p.Glu284Asp)
c.136-420G>C
c.136-201G>C
n.888G>C
n.308G>C
c.771G>C (p.Glu257Asp)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.2166969C>TCA472414349THc.759G>A (p.Glu253=)
c.*448G>A (n.*448G>A)
c.696-420G>A (n.696-420G>A)
c.*479G>A (n.*479G>A)
c.840G>A (p.Glu280=)
c.852G>A (p.Glu284=)
c.136-420G>A
c.136-201G>A
n.888G>A
n.308G>A
c.771G>A (p.Glu257=)
ClinVar dbSNP
11g.2166970T>ACA5818499THc.758A>T (p.Glu253Val)
c.*447A>T (n.*447A>T)
c.696-421A>T (n.696-421A>T)
c.*478A>T (n.*478A>T)
c.839A>T (p.Glu280Val)
c.851A>T (p.Glu284Val)
c.136-421A>T
c.136-202A>T
n.887A>T
n.307A>T
c.770A>T (p.Glu257Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.2166970T>CCA379126875THc.758A>G (p.Glu253Gly)
c.*447A>G (n.*447A>G)
c.696-421A>G (n.696-421A>G)
c.*478A>G (n.*478A>G)
c.839A>G (p.Glu280Gly)
c.851A>G (p.Glu284Gly)
c.136-421A>G
c.136-202A>G
n.887A>G
n.307A>G
c.770A>G (p.Glu257Gly)
gnomAD v4
11g.2166970T>GCA379126874THc.758A>C (p.Glu253Ala)
c.*447A>C (n.*447A>C)
c.696-421A>C (n.696-421A>C)
c.*478A>C (n.*478A>C)
c.839A>C (p.Glu280Ala)
c.851A>C (p.Glu284Ala)
c.136-421A>C
c.136-202A>C
n.887A>C
n.307A>C
c.770A>C (p.Glu257Ala)
11g.2166970T=CA1948005931THc.758A= (p.Glu253=)
c.*447A= (n.*447A=)
c.696-421A= (n.696-421A=)
c.*478A= (n.*478A=)
c.839A= (p.Glu280=)
c.851A= (p.Glu284=)
c.136-421A=
c.136-202A=
n.887A=
n.307A=
c.770A= (p.Glu257=)
11g.2166970_2166971insACA2790191070THc.757_758insT (p.Glu253ValfsTer?)
c.*446_*447insT (n.*446_*447insT)
c.696-422_696-421insT (n.696-422_696-421insT)
c.*477_*478insT (n.*477_*478insT)
c.838_839insT (p.Glu280ValfsTer?)
c.850_851insT (p.Glu284ValfsTer?)
c.136-422_136-421insT
c.136-203_136-202insT
n.886_887insT
n.306_307insT
c.769_770insT (p.Glu257ValfsTer?)
11g.2166971C>ACA379126878THc.757G>T (p.Glu253Ter)
c.*446G>T (n.*446G>T)
c.696-422G>T (n.696-422G>T)
c.*477G>T (n.*477G>T)
c.838G>T (p.Glu280Ter)
c.850G>T (p.Glu284Ter)
c.136-422G>T
c.136-203G>T
n.886G>T
n.306G>T
c.769G>T (p.Glu257Ter)
gnomAD v4
11g.2166971C=CA1948005936THc.757G= (p.Glu253=)
c.*446G= (n.*446G=)
c.696-422G= (n.696-422G=)
c.*477G= (n.*477G=)
c.838G= (p.Glu280=)
c.850G= (p.Glu284=)
c.136-422G=
c.136-203G=
n.886G=
n.306G=
c.769G= (p.Glu257=)
11g.2166971C>GCA379126881THc.757G>C (p.Glu253Gln)
c.*446G>C (n.*446G>C)
c.696-422G>C (n.696-422G>C)
c.*477G>C (n.*477G>C)
c.838G>C (p.Glu280Gln)
c.850G>C (p.Glu284Gln)
c.136-422G>C
c.136-203G>C
n.886G>C
n.306G>C
c.769G>C (p.Glu257Gln)
11g.2166971C>TCA379126883THc.757G>A (p.Glu253Lys)
c.*446G>A (n.*446G>A)
c.696-422G>A (n.696-422G>A)
c.*477G>A (n.*477G>A)
c.838G>A (p.Glu280Lys)
c.850G>A (p.Glu284Lys)
c.136-422G>A
c.136-203G>A
n.886G>A
n.306G>A
c.769G>A (p.Glu257Lys)
dbSNP gnomAD v4
11g.2166972C>ACA472414352THc.756G>T (p.Leu252=)
c.*445G>T (n.*445G>T)
c.696-423G>T (n.696-423G>T)
c.*476G>T (n.*476G>T)
c.837G>T (p.Leu279=)
c.849G>T (p.Leu283=)
c.136-423G>T
c.136-204G>T
n.885G>T
n.305G>T
c.768G>T (p.Leu256=)
gnomAD v4
11g.2166972C=CA1948005938THc.756G= (p.Leu252=)
c.*445G= (n.*445G=)
c.696-423G= (n.696-423G=)
c.*476G= (n.*476G=)
c.837G= (p.Leu279=)
c.849G= (p.Leu283=)
c.136-423G=
c.136-204G=
n.885G=
n.305G=
c.768G= (p.Leu256=)
11g.2166972C>GCA472414350THc.756G>C (p.Leu252=)
c.*445G>C (n.*445G>C)
c.696-423G>C (n.696-423G>C)
c.*476G>C (n.*476G>C)
c.837G>C (p.Leu279=)
c.849G>C (p.Leu283=)
c.136-423G>C
c.136-204G>C
n.885G>C
n.305G>C
c.768G>C (p.Leu256=)
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.2166972C>TCA472414351THc.756G>A (p.Leu252=)
c.*445G>A (n.*445G>A)
c.696-423G>A (n.696-423G>A)
c.*476G>A (n.*476G>A)
c.837G>A (p.Leu279=)
c.849G>A (p.Leu283=)
c.136-423G>A
c.136-204G>A
n.885G>A
n.305G>A
c.768G>A (p.Leu256=)
11g.2166973A=CA1948005942THc.755T= (p.Leu252=)
c.*444T= (n.*444T=)
c.696-424T= (n.696-424T=)
c.*475T= (n.*475T=)
c.836T= (p.Leu279=)
c.848T= (p.Leu283=)
c.136-424T=
c.136-205T=
n.884T=
n.304T=
c.767T= (p.Leu256=)
11g.2166973A>CCA216285510THc.755T>G (p.Leu252Arg)
c.*444T>G (n.*444T>G)
c.696-424T>G (n.696-424T>G)
c.*475T>G (n.*475T>G)
c.836T>G (p.Leu279Arg)
c.848T>G (p.Leu283Arg)
c.136-424T>G
c.136-205T>G
n.884T>G
n.304T>G
c.767T>G (p.Leu256Arg)
dbSNP gnomAD v3 gnomAD v4
11g.2166973A>GCA379126887THc.755T>C (p.Leu252Pro)
c.*444T>C (n.*444T>C)
c.696-424T>C (n.696-424T>C)
c.*475T>C (n.*475T>C)
c.836T>C (p.Leu279Pro)
c.848T>C (p.Leu283Pro)
c.136-424T>C
c.136-205T>C
n.884T>C
n.304T>C
c.767T>C (p.Leu256Pro)
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.2166973A>TCA379126888THc.755T>A (p.Leu252Gln)
c.*444T>A (n.*444T>A)
c.696-424T>A (n.696-424T>A)
c.*475T>A (n.*475T>A)
c.836T>A (p.Leu279Gln)
c.848T>A (p.Leu283Gln)
c.136-424T>A
c.136-205T>A
n.884T>A
n.304T>A
c.767T>A (p.Leu256Gln)
11g.2166974G>ACA472414353THc.754C>T (p.Leu252=)
c.*443C>T (n.*443C>T)
c.696-425C>T (n.696-425C>T)
c.*474C>T (n.*474C>T)
c.835C>T (p.Leu279=)
c.847C>T (p.Leu283=)
c.136-425C>T
c.136-206C>T
n.883C>T
n.303C>T
c.766C>T (p.Leu256=)
11g.2166974G>CCA379126892THc.754C>G (p.Leu252Val)
c.*443C>G (n.*443C>G)
c.696-425C>G (n.696-425C>G)
c.*474C>G (n.*474C>G)
c.835C>G (p.Leu279Val)
c.847C>G (p.Leu283Val)
c.136-425C>G
c.136-206C>G
n.883C>G
n.303C>G
c.766C>G (p.Leu256Val)
dbSNP gnomAD v2 gnomAD v4
11g.2166974G=CA1948005946THc.754C= (p.Leu252=)
c.*443C= (n.*443C=)
c.696-425C= (n.696-425C=)
c.*474C= (n.*474C=)
c.835C= (p.Leu279=)
c.847C= (p.Leu283=)
c.136-425C=
c.136-206C=
n.883C=
n.303C=
c.766C= (p.Leu256=)
11g.2166974G>TCA379126893THc.754C>A (p.Leu252Met)
c.*443C>A (n.*443C>A)
c.696-425C>A (n.696-425C>A)
c.*474C>A (n.*474C>A)
c.835C>A (p.Leu279Met)
c.847C>A (p.Leu283Met)
c.136-425C>A
c.136-206C>A
n.883C>A
n.303C>A
c.766C>A (p.Leu256Met)
11g.2166975G>ACA472414354THc.753C>T (p.His251=)
c.*442C>T (n.*442C>T)
c.696-426C>T (n.696-426C>T)
c.*473C>T (n.*473C>T)
c.834C>T (p.His278=)
c.846C>T (p.His282=)
c.136-426C>T
c.136-207C>T
n.882C>T
n.302C>T
c.765C>T (p.His255=)
gnomAD v4
11g.2166975G>CCA379126896THc.753C>G (p.His251Gln)
c.*442C>G (n.*442C>G)
c.696-426C>G (n.696-426C>G)
c.*473C>G (n.*473C>G)
c.834C>G (p.His278Gln)
c.846C>G (p.His282Gln)
c.136-426C>G
c.136-207C>G
n.882C>G
n.302C>G
c.765C>G (p.His255Gln)
dbSNP gnomAD v2 gnomAD v4
11g.2166975G=CA1948005948THc.753C= (p.His251=)
c.*442C= (n.*442C=)
c.696-426C= (n.696-426C=)
c.*473C= (n.*473C=)
c.834C= (p.His278=)
c.846C= (p.His282=)
c.136-426C=
c.136-207C=
n.882C=
n.302C=
c.765C= (p.His255=)
11g.2166975G>TCA379126898THc.753C>A (p.His251Gln)
c.*442C>A (n.*442C>A)
c.696-426C>A (n.696-426C>A)
c.*473C>A (n.*473C>A)
c.834C>A (p.His278Gln)
c.846C>A (p.His282Gln)
c.136-426C>A
c.136-207C>A
n.882C>A
n.302C>A
c.765C>A (p.His255Gln)
11g.2166976T>ACA379126900THc.752A>T (p.His251Leu)
c.*441A>T (n.*441A>T)
c.696-427A>T (n.696-427A>T)
c.*472A>T (n.*472A>T)
c.833A>T (p.His278Leu)
c.845A>T (p.His282Leu)
c.136-427A>T
c.136-208A>T
n.881A>T
n.301A>T
c.764A>T (p.His255Leu)
11g.2166976T>CCA379126903THc.752A>G (p.His251Arg)
c.*441A>G (n.*441A>G)
c.696-427A>G (n.696-427A>G)
c.*472A>G (n.*472A>G)
c.833A>G (p.His278Arg)
c.845A>G (p.His282Arg)
c.136-427A>G
c.136-208A>G
n.881A>G
n.301A>G
c.764A>G (p.His255Arg)
11g.2166976T>GCA379126905THc.752A>C (p.His251Pro)
c.*441A>C (n.*441A>C)
c.696-427A>C (n.696-427A>C)
c.*472A>C (n.*472A>C)
c.833A>C (p.His278Pro)
c.845A>C (p.His282Pro)
c.136-427A>C
c.136-208A>C
n.881A>C
n.301A>C
c.764A>C (p.His255Pro)
11g.2166977G>ACA379126912THc.751C>T (p.His251Tyr)
c.*440C>T (n.*440C>T)
c.696-428C>T (n.696-428C>T)
c.*471C>T (n.*471C>T)
c.832C>T (p.His278Tyr)
c.844C>T (p.His282Tyr)
c.136-428C>T
c.136-209C>T
n.880C>T
n.300C>T
c.763C>T (p.His255Tyr)
dbSNP gnomAD v3 gnomAD v4
11g.2166977G>CCA379126909THc.751C>G (p.His251Asp)
c.*440C>G (n.*440C>G)
c.696-428C>G (n.696-428C>G)
c.*471C>G (n.*471C>G)
c.832C>G (p.His278Asp)
c.844C>G (p.His282Asp)
c.136-428C>G
c.136-209C>G
n.880C>G
n.300C>G
c.763C>G (p.His255Asp)
11g.2166977G=CA1948005952THc.751C= (p.His251=)
c.*440C= (n.*440C=)
c.696-428C= (n.696-428C=)
c.*471C= (n.*471C=)
c.832C= (p.His278=)
c.844C= (p.His282=)
c.136-428C=
c.136-209C=
n.880C=
n.300C=
c.763C= (p.His255=)
11g.2166977G>TCA379126907THc.751C>A (p.His251Asn)
c.*440C>A (n.*440C>A)
c.696-428C>A (n.696-428C>A)
c.*471C>A (n.*471C>A)
c.832C>A (p.His278Asn)
c.844C>A (p.His282Asn)
c.136-428C>A
c.136-209C>A
n.880C>A
n.300C>A
c.763C>A (p.His255Asn)
gnomAD v4
11g.2166978C>ACA379126917THc.750G>T (p.Glu250Asp)
c.*439G>T (n.*439G>T)
c.696-429G>T (n.696-429G>T)
c.*470G>T (n.*470G>T)
c.831G>T (p.Glu277Asp)
c.843G>T (p.Glu281Asp)
c.136-429G>T
c.136-210G>T
n.879G>T
n.299G>T
c.762G>T (p.Glu254Asp)
gnomAD v4
11g.2166978C>GCA379126914THc.750G>C (p.Glu250Asp)
c.*439G>C (n.*439G>C)
c.696-429G>C (n.696-429G>C)
c.*470G>C (n.*470G>C)
c.831G>C (p.Glu277Asp)
c.843G>C (p.Glu281Asp)
c.136-429G>C
c.136-210G>C
n.879G>C
n.299G>C
c.762G>C (p.Glu254Asp)
11g.2166978C>TCA472414355THc.750G>A (p.Glu250=)
c.*439G>A (n.*439G>A)
c.696-429G>A (n.696-429G>A)
c.*470G>A (n.*470G>A)
c.831G>A (p.Glu277=)
c.843G>A (p.Glu281=)
c.136-429G>A
c.136-210G>A
n.879G>A
n.299G>A
c.762G>A (p.Glu254=)
11g.2166979T>ACA10582880THc.749A>T (p.Glu250Val)
c.*438A>T (n.*438A>T)
c.696-430A>T (n.696-430A>T)
c.*469A>T (n.*469A>T)
c.830A>T (p.Glu277Val)
c.842A>T (p.Glu281Val)
c.136-430A>T
c.136-211A>T
n.878A>T
n.298A>T
c.761A>T (p.Glu254Val)
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.2166979T>CCA379126919THc.749A>G (p.Glu250Gly)
c.*438A>G (n.*438A>G)
c.696-430A>G (n.696-430A>G)
c.*469A>G (n.*469A>G)
c.830A>G (p.Glu277Gly)
c.842A>G (p.Glu281Gly)
c.136-430A>G
c.136-211A>G
n.878A>G
n.298A>G
c.761A>G (p.Glu254Gly)
11g.2166979T>GCA379126921THc.749A>C (p.Glu250Ala)
c.*438A>C (n.*438A>C)
c.696-430A>C (n.696-430A>C)
c.*469A>C (n.*469A>C)
c.830A>C (p.Glu277Ala)
c.842A>C (p.Glu281Ala)
c.136-430A>C
c.136-211A>C
n.878A>C
n.298A>C
c.761A>C (p.Glu254Ala)
11g.2166979T=CA1948005955THc.749A= (p.Glu250=)
c.*438A= (n.*438A=)
c.696-430A= (n.696-430A=)
c.*469A= (n.*469A=)
c.830A= (p.Glu277=)
c.842A= (p.Glu281=)
c.136-430A=
c.136-211A=
n.878A=
n.298A=
c.761A= (p.Glu254=)
11g.2166980C>ACA379126925THc.748G>T (p.Glu250Ter)
c.*437G>T (n.*437G>T)
c.696-431G>T (n.696-431G>T)
c.*468G>T (n.*468G>T)
c.829G>T (p.Glu277Ter)
c.841G>T (p.Glu281Ter)
c.136-431G>T
c.136-212G>T
n.877G>T
n.297G>T
c.760G>T (p.Glu254Ter)
gnomAD v4 COSMIC
11g.2166980C=CA1948005962THc.748G= (p.Glu250=)
c.*437G= (n.*437G=)
c.696-431G= (n.696-431G=)
c.*468G= (n.*468G=)
c.829G= (p.Glu277=)
c.841G= (p.Glu281=)
c.136-431G=
c.136-212G=
n.877G=
n.297G=
c.760G= (p.Glu254=)
11g.2166980C>GCA247843THc.748G>C (p.Glu250Gln)
c.*437G>C (n.*437G>C)
c.696-431G>C (n.696-431G>C)
c.*468G>C (n.*468G>C)
c.829G>C (p.Glu277Gln)
c.841G>C (p.Glu281Gln)
c.136-431G>C
c.136-212G>C
n.877G>C
n.297G>C
c.760G>C (p.Glu254Gln)
ClinVar dbSNP
11g.2166980C>TCA379126929THc.748G>A (p.Glu250Lys)
c.*437G>A (n.*437G>A)
c.696-431G>A (n.696-431G>A)
c.*468G>A (n.*468G>A)
c.829G>A (p.Glu277Lys)
c.841G>A (p.Glu281Lys)
c.136-431G>A
c.136-212G>A
n.877G>A
n.297G>A
c.760G>A (p.Glu254Lys)
11g.2166983delCA2580082590THc.748del (p.Glu250SerfsTer30)
c.*437del (n.*437del)
c.696-431del (n.696-431del)
c.*468del (n.*468del)
c.829del (p.Glu277SerfsTer30)
c.841del (p.Glu281SerfsTer30)
c.136-431del
c.136-212del
n.877del
n.297del
c.760del (p.Glu254SerfsTer30)
ClinVar gnomAD v4
11g.2166981C>ACA472414356THc.747G>T (p.Gly249=)
c.*436G>T (n.*436G>T)
c.696-432G>T (n.696-432G>T)
c.*467G>T (n.*467G>T)
c.828G>T (p.Gly276=)
c.840G>T (p.Gly280=)
c.136-432G>T
c.136-213G>T
n.876G>T
n.296G>T
c.759G>T (p.Gly253=)
gnomAD v4
11g.2166981C>GCA472414358THc.747G>C (p.Gly249=)
c.*436G>C (n.*436G>C)
c.696-432G>C (n.696-432G>C)
c.*467G>C (n.*467G>C)
c.828G>C (p.Gly276=)
c.840G>C (p.Gly280=)
c.136-432G>C
c.136-213G>C
n.876G>C
n.296G>C
c.759G>C (p.Gly253=)
11g.2166981C>TCA472414357THc.747G>A (p.Gly249=)
c.*436G>A (n.*436G>A)
c.696-432G>A (n.696-432G>A)
c.*467G>A (n.*467G>A)
c.828G>A (p.Gly276=)
c.840G>A (p.Gly280=)
c.136-432G>A
c.136-213G>A
n.876G>A
n.296G>A
c.759G>A (p.Gly253=)
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.2166982C>ACA379126932THc.746G>T (p.Gly249Val)
c.*435G>T (n.*435G>T)
c.696-433G>T (n.696-433G>T)
c.*466G>T (n.*466G>T)
c.827G>T (p.Gly276Val)
c.839G>T (p.Gly280Val)
c.136-433G>T
c.136-214G>T
n.875G>T
n.295G>T
c.758G>T (p.Gly253Val)
gnomAD v4
11g.2166982C>GCA379126934THc.746G>C (p.Gly249Ala)
c.*435G>C (n.*435G>C)
c.696-433G>C (n.696-433G>C)
c.*466G>C (n.*466G>C)
c.827G>C (p.Gly276Ala)
c.839G>C (p.Gly280Ala)
c.136-433G>C
c.136-214G>C
n.875G>C
n.295G>C
c.758G>C (p.Gly253Ala)
11g.2166982C>TCA379126936THc.746G>A (p.Gly249Glu)
c.*435G>A (n.*435G>A)
c.696-433G>A (n.696-433G>A)
c.*466G>A (n.*466G>A)
c.827G>A (p.Gly276Glu)
c.839G>A (p.Gly280Glu)
c.136-433G>A
c.136-214G>A
n.875G>A
n.295G>A
c.758G>A (p.Gly253Glu)
gnomAD v4
11g.2166983C>ACA216285541THc.745G>T (p.Gly249Trp)
c.*434G>T (n.*434G>T)
c.696-434G>T (n.696-434G>T)
c.*465G>T (n.*465G>T)
c.826G>T (p.Gly276Trp)
c.838G>T (p.Gly280Trp)
c.136-434G>T
c.136-215G>T
n.874G>T
n.294G>T
c.757G>T (p.Gly253Trp)
dbSNP gnomAD v4
11g.2166983C=CA1948005967THc.745G= (p.Gly249=)
c.*434G= (n.*434G=)
c.696-434G= (n.696-434G=)
c.*465G= (n.*465G=)
c.826G= (p.Gly276=)
c.838G= (p.Gly280=)
c.136-434G=
c.136-215G=
n.874G=
n.294G=
c.757G= (p.Gly253=)
11g.2166983C>GCA379126940THc.745G>C (p.Gly249Arg)
c.*434G>C (n.*434G>C)
c.696-434G>C (n.696-434G>C)
c.*465G>C (n.*465G>C)
c.826G>C (p.Gly276Arg)
c.838G>C (p.Gly280Arg)
c.136-434G>C
c.136-215G>C
n.874G>C
n.294G>C
c.757G>C (p.Gly253Arg)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.2166983C>TCA5818500THc.745G>A (p.Gly249Arg)
c.*434G>A (n.*434G>A)
c.696-434G>A (n.696-434G>A)
c.*465G>A (n.*465G>A)
c.826G>A (p.Gly276Arg)
c.838G>A (p.Gly280Arg)
c.136-434G>A
c.136-215G>A
n.874G>A
n.294G>A
c.757G>A (p.Gly253Arg)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.2166984G>ACA472414359THc.744C>T (p.Cys248=)
c.*433C>T (n.*433C>T)
c.696-435C>T (n.696-435C>T)
c.*464C>T (n.*464C>T)
c.825C>T (p.Cys275=)
c.837C>T (p.Cys279=)
c.136-435C>T
c.136-216C>T
n.873C>T
n.293C>T
c.756C>T (p.Cys252=)
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.2166984G>CCA379126943THc.744C>G (p.Cys248Trp)
c.*433C>G (n.*433C>G)
c.696-435C>G (n.696-435C>G)
c.*464C>G (n.*464C>G)
c.825C>G (p.Cys275Trp)
c.837C>G (p.Cys279Trp)
c.136-435C>G
c.136-216C>G
n.873C>G
n.293C>G
c.756C>G (p.Cys252Trp)
11g.2166984G=CA1948005971THc.744C= (p.Cys248=)
c.*433C= (n.*433C=)
c.696-435C= (n.696-435C=)
c.*464C= (n.*464C=)
c.825C= (p.Cys275=)
c.837C= (p.Cys279=)
c.136-435C=
c.136-216C=
n.873C=
n.293C=
c.756C= (p.Cys252=)
11g.2166984G>TCA379126945THc.744C>A (p.Cys248Ter)
c.*433C>A (n.*433C>A)
c.696-435C>A (n.696-435C>A)
c.*464C>A (n.*464C>A)
c.825C>A (p.Cys275Ter)
c.837C>A (p.Cys279Ter)
c.136-435C>A
c.136-216C>A
n.873C>A
n.293C>A
c.756C>A (p.Cys252Ter)
gnomAD v4
11g.2166985C>ACA379126952THc.743G>T (p.Cys248Phe)
c.*432G>T (n.*432G>T)
c.696-436G>T (n.696-436G>T)
c.*463G>T (n.*463G>T)
c.824G>T (p.Cys275Phe)
c.836G>T (p.Cys279Phe)
c.136-436G>T
c.136-217G>T
n.872G>T
n.292G>T
c.755G>T (p.Cys252Phe)
dbSNP gnomAD v2 gnomAD v4
11g.2166985C=CA1948005974THc.743G= (p.Cys248=)
c.*432G= (n.*432G=)
c.696-436G= (n.696-436G=)
c.*463G= (n.*463G=)
c.824G= (p.Cys275=)
c.836G= (p.Cys279=)
c.136-436G=
c.136-217G=
n.872G=
n.292G=
c.755G= (p.Cys252=)
11g.2166985C>GCA379126948THc.743G>C (p.Cys248Ser)
c.*432G>C (n.*432G>C)
c.696-436G>C (n.696-436G>C)
c.*463G>C (n.*463G>C)
c.824G>C (p.Cys275Ser)
c.836G>C (p.Cys279Ser)
c.136-436G>C
c.136-217G>C
n.872G>C
n.292G>C
c.755G>C (p.Cys252Ser)
11g.2166985C>TCA379126950THc.743G>A (p.Cys248Tyr)
c.*432G>A (n.*432G>A)
c.696-436G>A (n.696-436G>A)
c.*463G>A (n.*463G>A)
c.824G>A (p.Cys275Tyr)
c.836G>A (p.Cys279Tyr)
c.136-436G>A
c.136-217G>A
n.872G>A
n.292G>A
c.755G>A (p.Cys252Tyr)
gnomAD v4
11g.2166985_2166989dupCA2580082591THc.739_743dup (p.Cys248TrpfsTer?)
c.*428_*432dup (n.*428_*432dup)
c.696-440_696-436dup (n.696-440_696-436dup)
c.*459_*463dup (n.*459_*463dup)
c.820_824dup (p.Cys275TrpfsTer?)
c.832_836dup (p.Cys279TrpfsTer?)
c.136-440_136-436dup
c.136-221_136-217dup
n.868_872dup
n.288_292dup
c.751_755dup (p.Cys252TrpfsTer?)
ClinVar
11g.2166986A>CCA379126953THc.742T>G (p.Cys248Gly)
c.*431T>G (n.*431T>G)
c.696-437T>G (n.696-437T>G)
c.*462T>G (n.*462T>G)
c.823T>G (p.Cys275Gly)
c.835T>G (p.Cys279Gly)
c.136-437T>G
c.136-218T>G
n.871T>G
n.291T>G
c.754T>G (p.Cys252Gly)
11g.2166986A>GCA379126954THc.742T>C (p.Cys248Arg)
c.*431T>C (n.*431T>C)
c.696-437T>C (n.696-437T>C)
c.*462T>C (n.*462T>C)
c.823T>C (p.Cys275Arg)
c.835T>C (p.Cys279Arg)
c.136-437T>C
c.136-218T>C
n.871T>C
n.291T>C
c.754T>C (p.Cys252Arg)
11g.2166986A>TCA379126956THc.742T>A (p.Cys248Ser)
c.*431T>A (n.*431T>A)
c.696-437T>A (n.696-437T>A)
c.*462T>A (n.*462T>A)
c.823T>A (p.Cys275Ser)
c.835T>A (p.Cys279Ser)
c.136-437T>A
c.136-218T>A
n.871T>A
n.291T>A
c.754T>A (p.Cys252Ser)
gnomAD v4
11g.2166987G>ACA472414360THc.741C>T (p.Ala247=)
c.*430C>T (n.*430C>T)
c.696-438C>T (n.696-438C>T)
c.*461C>T (n.*461C>T)
c.822C>T (p.Ala274=)
c.834C>T (p.Ala278=)
c.136-438C>T
c.136-219C>T
n.870C>T
n.290C>T
c.753C>T (p.Ala251=)
11g.2166987G>CCA472414361THc.741C>G (p.Ala247=)
c.*430C>G (n.*430C>G)
c.696-438C>G (n.696-438C>G)
c.*461C>G (n.*461C>G)
c.822C>G (p.Ala274=)
c.834C>G (p.Ala278=)
c.136-438C>G
c.136-219C>G
n.870C>G
n.290C>G
c.753C>G (p.Ala251=)
11g.2166987G>TCA472414362THc.741C>A (p.Ala247=)
c.*430C>A (n.*430C>A)
c.696-438C>A (n.696-438C>A)
c.*461C>A (n.*461C>A)
c.822C>A (p.Ala274=)
c.834C>A (p.Ala278=)
c.136-438C>A
c.136-219C>A
n.870C>A
n.290C>A
c.753C>A (p.Ala251=)
11g.2166988G>ACA379126959THc.740C>T (p.Ala247Val)
c.*429C>T (n.*429C>T)
c.696-439C>T (n.696-439C>T)
c.*460C>T (n.*460C>T)
c.821C>T (p.Ala274Val)
c.833C>T (p.Ala278Val)
c.136-439C>T
c.136-220C>T
n.869C>T
n.289C>T
c.752C>T (p.Ala251Val)
dbSNP gnomAD v4
11g.2166988G>CCA379126961THc.740C>G (p.Ala247Gly)
c.*429C>G (n.*429C>G)
c.696-439C>G (n.696-439C>G)
c.*460C>G (n.*460C>G)
c.821C>G (p.Ala274Gly)
c.833C>G (p.Ala278Gly)
c.136-439C>G
c.136-220C>G
n.869C>G
n.289C>G
c.752C>G (p.Ala251Gly)
11g.2166988G=CA1948005976THc.740C= (p.Ala247=)
c.*429C= (n.*429C=)
c.696-439C= (n.696-439C=)
c.*460C= (n.*460C=)
c.821C= (p.Ala274=)
c.833C= (p.Ala278=)
c.136-439C=
c.136-220C=
n.869C=
n.289C=
c.752C= (p.Ala251=)
11g.2166988G>TCA5818501THc.740C>A (p.Ala247Asp)
c.*429C>A (n.*429C>A)
c.696-439C>A (n.696-439C>A)
c.*460C>A (n.*460C>A)
c.821C>A (p.Ala274Asp)
c.833C>A (p.Ala278Asp)
c.136-439C>A
c.136-220C>A
n.869C>A
n.289C>A
c.752C>A (p.Ala251Asp)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.2166989C>ACA379126965THc.739G>T (p.Ala247Ser)
c.*428G>T (n.*428G>T)
c.696-440G>T (n.696-440G>T)
c.*459G>T (n.*459G>T)
c.820G>T (p.Ala274Ser)
c.832G>T (p.Ala278Ser)
c.136-440G>T
c.136-221G>T
n.868G>T
n.288G>T
c.751G>T (p.Ala251Ser)
gnomAD v4
11g.2166989C=CA1948005980THc.739G= (p.Ala247=)
c.*428G= (n.*428G=)
c.696-440G= (n.696-440G=)
c.*459G= (n.*459G=)
c.820G= (p.Ala274=)
c.832G= (p.Ala278=)
c.136-440G=
c.136-221G=
n.868G=
n.288G=
c.751G= (p.Ala251=)
11g.2166989C>GCA5818502THc.739G>C (p.Ala247Pro)
c.*428G>C (n.*428G>C)
c.696-440G>C (n.696-440G>C)
c.*459G>C (n.*459G>C)
c.820G>C (p.Ala274Pro)
c.832G>C (p.Ala278Pro)
c.136-440G>C
c.136-221G>C
n.868G>C
n.288G>C
c.751G>C (p.Ala251Pro)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.2166989C>TCA379126968THc.739G>A (p.Ala247Thr)
c.*428G>A (n.*428G>A)
c.696-440G>A (n.696-440G>A)
c.*459G>A (n.*459G>A)
c.820G>A (p.Ala274Thr)
c.832G>A (p.Ala278Thr)
c.136-440G>A
c.136-221G>A
n.868G>A
n.288G>A
c.751G>A (p.Ala251Thr)
ClinVar dbSNP gnomAD v4
11g.2166990G>ACA472414363THc.738C>T (p.His246=)
c.*427C>T (n.*427C>T)
c.696-441C>T (n.696-441C>T)
c.*458C>T (n.*458C>T)
c.819C>T (p.His273=)
c.831C>T (p.His277=)
c.136-441C>T
c.136-222C>T
n.867C>T
n.287C>T
c.750C>T (p.His250=)
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.2166990G>CCA379126971THc.738C>G (p.His246Gln)
c.*427C>G (n.*427C>G)
c.696-441C>G (n.696-441C>G)
c.*458C>G (n.*458C>G)
c.819C>G (p.His273Gln)
c.831C>G (p.His277Gln)
c.136-441C>G
c.136-222C>G
n.867C>G
n.287C>G
c.750C>G (p.His250Gln)
dbSNP
11g.2166990G=CA1948005984THc.738C= (p.His246=)
c.*427C= (n.*427C=)
c.696-441C= (n.696-441C=)
c.*458C= (n.*458C=)
c.819C= (p.His273=)
c.831C= (p.His277=)
c.136-441C=
c.136-222C=
n.867C=
n.287C=
c.750C= (p.His250=)
11g.2166990G>TCA5818503THc.738C>A (p.His246Gln)
c.*427C>A (n.*427C>A)
c.696-441C>A (n.696-441C>A)
c.*458C>A (n.*458C>A)
c.819C>A (p.His273Gln)
c.831C>A (p.His277Gln)
c.136-441C>A
c.136-222C>A
n.867C>A
n.287C>A
c.750C>A (p.His250Gln)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.2166991T>ACA379126980THc.737A>T (p.His246Leu)
c.*426A>T (n.*426A>T)
c.696-442A>T (n.696-442A>T)
c.*457A>T (n.*457A>T)
c.818A>T (p.His273Leu)
c.830A>T (p.His277Leu)
c.136-442A>T
c.136-223A>T
n.866A>T
n.286A>T
c.749A>T (p.His250Leu)
11g.2166991T>CCA379126977THc.737A>G (p.His246Arg)
c.*426A>G (n.*426A>G)
c.696-442A>G (n.696-442A>G)
c.*457A>G (n.*457A>G)
c.818A>G (p.His273Arg)
c.830A>G (p.His277Arg)
c.136-442A>G
c.136-223A>G
n.866A>G
n.286A>G
c.749A>G (p.His250Arg)
gnomAD v4
11g.2166991T>GCA379126975THc.737A>C (p.His246Pro)
c.*426A>C (n.*426A>C)
c.696-442A>C (n.696-442A>C)
c.*457A>C (n.*457A>C)
c.818A>C (p.His273Pro)
c.830A>C (p.His277Pro)
c.136-442A>C
c.136-223A>C
n.866A>C
n.286A>C
c.749A>C (p.His250Pro)
11g.2166992G>ACA379126982THc.736C>T (p.His246Tyr)
c.*425C>T (n.*425C>T)
c.696-443C>T (n.696-443C>T)
c.*456C>T (n.*456C>T)
c.817C>T (p.His273Tyr)
c.829C>T (p.His277Tyr)
c.136-443C>T
c.136-224C>T
n.865C>T
n.285C>T
c.748C>T (p.His250Tyr)
gnomAD v4
11g.2166992G>CCA379126984THc.736C>G (p.His246Asp)
c.*425C>G (n.*425C>G)
c.696-443C>G (n.696-443C>G)
c.*456C>G (n.*456C>G)
c.817C>G (p.His273Asp)
c.829C>G (p.His277Asp)
c.136-443C>G
c.136-224C>G
n.865C>G
n.285C>G
c.748C>G (p.His250Asp)
11g.2166992G>TCA379126986THc.736C>A (p.His246Asn)
c.*425C>A (n.*425C>A)
c.696-443C>A (n.696-443C>A)
c.*456C>A (n.*456C>A)
c.817C>A (p.His273Asn)
c.829C>A (p.His277Asn)
c.136-443C>A
c.136-224C>A
n.865C>A
n.285C>A
c.748C>A (p.His250Asn)
gnomAD v4
11g.2166993C>ACA5818504THc.735G>T (p.Thr245=)
c.*424G>T (n.*424G>T)
c.695+442G>T (n.695+442G>T)
c.*455G>T (n.*455G>T)
c.816G>T (p.Thr272=)
c.828G>T (p.Thr276=)
c.135+442G>T
c.136-225G>T
n.864G>T
n.284G>T
c.747G>T (p.Thr249=)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.2166993C=CA1948005992THc.735G= (p.Thr245=)
c.*424G= (n.*424G=)
c.695+442G= (n.695+442G=)
c.*455G= (n.*455G=)
c.816G= (p.Thr272=)
c.828G= (p.Thr276=)
c.135+442G=
c.136-225G=
n.864G=
n.284G=
c.747G= (p.Thr249=)
11g.2166993C>GCA472414365THc.735G>C (p.Thr245=)
c.*424G>C (n.*424G>C)
c.695+442G>C (n.695+442G>C)
c.*455G>C (n.*455G>C)
c.816G>C (p.Thr272=)
c.828G>C (p.Thr276=)
c.135+442G>C
c.136-225G>C
n.864G>C
n.284G>C
c.747G>C (p.Thr249=)
gnomAD v4
11g.2166993C>TCA472414364THc.735G>A (p.Thr245=)
c.*424G>A (n.*424G>A)
c.695+442G>A (n.695+442G>A)
c.*455G>A (n.*455G>A)
c.816G>A (p.Thr272=)
c.828G>A (p.Thr276=)
c.135+442G>A
c.136-225G>A
n.864G>A
n.284G>A
c.747G>A (p.Thr249=)
dbSNP gnomAD v2 gnomAD v4
11g.2166993_2166998dupCA2611964843THc.730_735dup (p.Thr245_His246insAlaThr)
c.*419_*424dup (n.*419_*424dup)
c.695+437_695+442dup (n.695+437_695+442dup)
c.*450_*455dup (n.*450_*455dup)
c.811_816dup (p.Thr272_His273insAlaThr)
c.823_828dup (p.Thr276_His277insAlaThr)
c.135+437_135+442dup
c.136-230_136-225dup
n.859_864dup
n.279_284dup
c.742_747dup (p.Thr249_His250insAlaThr)
gnomAD v4

Number of alleles fetched