Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.24081457_24081476dupCA2624298556NRLc.476_495dup (p.Thr166GlyfsTer2)
c.59_78dup (p.Thr27GlyfsTer2)
c.575_594dup (p.Thr199GlyfsTer2)
c.260_279dup (p.Thr94GlyfsTer2)
c.161_180dup (p.Thr61GlyfsTer2)
c.782_801dup (p.Thr268GlyfsTer2)
c.467_486dup (p.Thr163GlyfsTer2)
gnomAD v4
14g.24081457_24081477delinsGGCGCCTCTGCTTCAGCCGCACA2123777720NRLc.473_493delinsTGCGGCTGAAGCAGAGGCGCC (p.Leu158=)
c.56_76delinsTGCGGCTGAAGCAGAGGCGCC (p.Leu19=)
c.572_592delinsTGCGGCTGAAGCAGAGGCGCC (p.Leu191=)
c.257_277delinsTGCGGCTGAAGCAGAGGCGCC (p.Leu86=)
c.158_178delinsTGCGGCTGAAGCAGAGGCGCC (p.Leu53=)
c.779_799delinsTGCGGCTGAAGCAGAGGCGCC (p.Leu260=)
c.464_484delinsTGCGGCTGAAGCAGAGGCGCC (p.Leu155=)
14g.24081465_24081484dupCA2624298569NRLc.473_492dup (p.Arg165CysfsTer3)
c.56_75dup (p.Arg26CysfsTer3)
c.572_591dup (p.Arg198CysfsTer3)
c.257_276dup (p.Arg93CysfsTer3)
c.158_177dup (p.Arg60CysfsTer3)
c.779_798dup (p.Arg267CysfsTer3)
c.464_483dup (p.Arg162CysfsTer3)
gnomAD v4
14g.24081465_24081484delCA613319080NRLc.473_492del (p.Leu158ProfsTer?)
c.56_75del (p.Leu19ProfsTer?)
c.572_591del (p.Leu191ProfsTer?)
c.257_276del (p.Leu86ProfsTer?)
c.158_177del (p.Leu53ProfsTer?)
c.779_798del (p.Leu260ProfsTer?)
c.464_483del (p.Leu155ProfsTer?)
dbSNP gnomAD v2
14g.24081471A=CA2123777754NRLc.479T= (p.Leu160=)
c.62T= (p.Leu21=)
c.578T= (p.Leu193=)
c.263T= (p.Leu88=)
c.164T= (p.Leu55=)
c.785T= (p.Leu262=)
c.470T= (p.Leu157=)
14g.24081471A>CCA389278293NRLc.479T>G (p.Leu160Arg)
c.62T>G (p.Leu21Arg)
c.578T>G (p.Leu193Arg)
c.263T>G (p.Leu88Arg)
c.164T>G (p.Leu55Arg)
c.785T>G (p.Leu262Arg)
c.470T>G (p.Leu157Arg)
14g.24081471A>GCA123731NRLc.479T>C (p.Leu160Pro)
c.62T>C (p.Leu21Pro)
c.578T>C (p.Leu193Pro)
c.263T>C (p.Leu88Pro)
c.164T>C (p.Leu55Pro)
c.785T>C (p.Leu262Pro)
c.470T>C (p.Leu157Pro)
ClinVar dbSNP gnomAD v4
14g.24081471A>TCA389278300NRLc.479T>A (p.Leu160Gln)
c.62T>A (p.Leu21Gln)
c.578T>A (p.Leu193Gln)
c.263T>A (p.Leu88Gln)
c.164T>A (p.Leu55Gln)
c.785T>A (p.Leu262Gln)
c.470T>A (p.Leu157Gln)
14g.24081472G>ACA485775957NRLc.478C>T (p.Leu160=)
c.61C>T (p.Leu21=)
c.577C>T (p.Leu193=)
c.262C>T (p.Leu88=)
c.163C>T (p.Leu55=)
c.784C>T (p.Leu262=)
c.469C>T (p.Leu157=)
dbSNP gnomAD v3 gnomAD v4
14g.24081472G>CCA389278312NRLc.478C>G (p.Leu160Val)
c.61C>G (p.Leu21Val)
c.577C>G (p.Leu193Val)
c.262C>G (p.Leu88Val)
c.163C>G (p.Leu55Val)
c.784C>G (p.Leu262Val)
c.469C>G (p.Leu157Val)
14g.24081472G=CA2123777755NRLc.478C= (p.Leu160=)
c.61C= (p.Leu21=)
c.577C= (p.Leu193=)
c.262C= (p.Leu88=)
c.163C= (p.Leu55=)
c.784C= (p.Leu262=)
c.469C= (p.Leu157=)
14g.24081472G>TCA389278315NRLc.478C>A (p.Leu160Met)
c.61C>A (p.Leu21Met)
c.577C>A (p.Leu193Met)
c.262C>A (p.Leu88Met)
c.163C>A (p.Leu55Met)
c.784C>A (p.Leu262Met)
c.469C>A (p.Leu157Met)
gnomAD v4
14g.24081473C>ACA485775964NRLc.477G>T (p.Arg159=)
c.60G>T (p.Arg20=)
c.576G>T (p.Arg192=)
c.261G>T (p.Arg87=)
c.162G>T (p.Arg54=)
c.783G>T (p.Arg261=)
c.468G>T (p.Arg156=)
gnomAD v4
14g.24081473C=CA2123777760NRLc.477G= (p.Arg159=)
c.60G= (p.Arg20=)
c.576G= (p.Arg192=)
c.261G= (p.Arg87=)
c.162G= (p.Arg54=)
c.783G= (p.Arg261=)
c.468G= (p.Arg156=)
14g.24081473C>GCA485775965NRLc.477G>C (p.Arg159=)
c.60G>C (p.Arg20=)
c.576G>C (p.Arg192=)
c.261G>C (p.Arg87=)
c.162G>C (p.Arg54=)
c.783G>C (p.Arg261=)
c.468G>C (p.Arg156=)
14g.24081473C>TCA485775966NRLc.477G>A (p.Arg159=)
c.60G>A (p.Arg20=)
c.576G>A (p.Arg192=)
c.261G>A (p.Arg87=)
c.162G>A (p.Arg54=)
c.783G>A (p.Arg261=)
c.468G>A (p.Arg156=)
dbSNP gnomAD v2 gnomAD v4
14g.24081480_24081498dupCA7122825NRLc.459_477dup (p.Leu160AlafsTer?)
c.42_60dup (p.Leu21AlafsTer?)
c.558_576dup (p.Leu193AlafsTer?)
c.243_261dup (p.Leu88AlafsTer?)
c.144_162dup (p.Leu55AlafsTer?)
c.765_783dup (p.Leu262AlafsTer?)
c.450_468dup (p.Leu157AlafsTer?)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.24081473_24081474insGTGCA2624298620NRLc.476_477insCAC (p.Arg159_Leu160insThr)
c.59_60insCAC (p.Arg20_Leu21insThr)
c.575_576insCAC (p.Arg192_Leu193insThr)
c.260_261insCAC (p.Arg87_Leu88insThr)
c.161_162insCAC (p.Arg54_Leu55insThr)
c.782_783insCAC (p.Arg261_Leu262insThr)
c.467_468insCAC (p.Arg156_Leu157insThr)
gnomAD v4
14g.24081474C>ACA389278320NRLc.476G>T (p.Arg159Leu)
c.59G>T (p.Arg20Leu)
c.575G>T (p.Arg192Leu)
c.260G>T (p.Arg87Leu)
c.161G>T (p.Arg54Leu)
c.782G>T (p.Arg261Leu)
c.467G>T (p.Arg156Leu)
14g.24081474C=CA2123777767NRLc.476G= (p.Arg159=)
c.59G= (p.Arg20=)
c.575G= (p.Arg192=)
c.260G= (p.Arg87=)
c.161G= (p.Arg54=)
c.782G= (p.Arg261=)
c.467G= (p.Arg156=)
14g.24081474C>GCA389278324NRLc.476G>C (p.Arg159Pro)
c.59G>C (p.Arg20Pro)
c.575G>C (p.Arg192Pro)
c.260G>C (p.Arg87Pro)
c.161G>C (p.Arg54Pro)
c.782G>C (p.Arg261Pro)
c.467G>C (p.Arg156Pro)
14g.24081474C>TCA389278343NRLc.476G>A (p.Arg159Gln)
c.59G>A (p.Arg20Gln)
c.575G>A (p.Arg192Gln)
c.260G>A (p.Arg87Gln)
c.161G>A (p.Arg54Gln)
c.782G>A (p.Arg261Gln)
c.467G>A (p.Arg156Gln)
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.24081475G>ACA389278349NRLc.475C>T (p.Arg159Trp)
c.58C>T (p.Arg20Trp)
c.574C>T (p.Arg192Trp)
c.259C>T (p.Arg87Trp)
c.160C>T (p.Arg54Trp)
c.781C>T (p.Arg261Trp)
c.466C>T (p.Arg156Trp)
dbSNP gnomAD v4
14g.24081475G>CCA389278352NRLc.475C>G (p.Arg159Gly)
c.58C>G (p.Arg20Gly)
c.574C>G (p.Arg192Gly)
c.259C>G (p.Arg87Gly)
c.160C>G (p.Arg54Gly)
c.781C>G (p.Arg261Gly)
c.466C>G (p.Arg156Gly)
14g.24081475G=CA2123777775NRLc.475C= (p.Arg159=)
c.58C= (p.Arg20=)
c.574C= (p.Arg192=)
c.259C= (p.Arg87=)
c.160C= (p.Arg54=)
c.781C= (p.Arg261=)
c.466C= (p.Arg156=)
14g.24081475G>TCA485775974NRLc.475C>A (p.Arg159=)
c.58C>A (p.Arg20=)
c.574C>A (p.Arg192=)
c.259C>A (p.Arg87=)
c.160C>A (p.Arg54=)
c.781C>A (p.Arg261=)
c.466C>A (p.Arg156=)
gnomAD v4
14g.24081475_24081476insTCA7122826NRLc.474_475insA (p.Arg159ThrfsTer?)
c.57_58insA (p.Arg20ThrfsTer?)
c.573_574insA (p.Arg192ThrfsTer?)
c.258_259insA (p.Arg87ThrfsTer?)
c.159_160insA (p.Arg54ThrfsTer?)
c.780_781insA (p.Arg261ThrfsTer?)
c.465_466insA (p.Arg156ThrfsTer?)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.24081475_24081476insGCGCCTCTGCTTCAGCCTCA2624298635NRLc.474_475insAGGCTGAAGCAGAGGCGC (p.Leu158_Arg159insArgLeuLysGlnArgArg)
c.57_58insAGGCTGAAGCAGAGGCGC (p.Leu19_Arg20insArgLeuLysGlnArgArg)
c.573_574insAGGCTGAAGCAGAGGCGC (p.Leu191_Arg192insArgLeuLysGlnArgArg)
c.258_259insAGGCTGAAGCAGAGGCGC (p.Leu86_Arg87insArgLeuLysGlnArgArg)
c.159_160insAGGCTGAAGCAGAGGCGC (p.Leu53_Arg54insArgLeuLysGlnArgArg)
c.780_781insAGGCTGAAGCAGAGGCGC (p.Leu260_Arg261insArgLeuLysGlnArgArg)
c.465_466insAGGCTGAAGCAGAGGCGC (p.Leu155_Arg156insArgLeuLysGlnArgArg)
gnomAD v4
14g.24081476C>ACA485775975NRLc.474G>T (p.Leu158=)
c.57G>T (p.Leu19=)
c.573G>T (p.Leu191=)
c.258G>T (p.Leu86=)
c.159G>T (p.Leu53=)
c.780G>T (p.Leu260=)
c.465G>T (p.Leu155=)
gnomAD v4
14g.24081476C=CA2123777781NRLc.474G= (p.Leu158=)
c.57G= (p.Leu19=)
c.573G= (p.Leu191=)
c.258G= (p.Leu86=)
c.159G= (p.Leu53=)
c.780G= (p.Leu260=)
c.465G= (p.Leu155=)
14g.24081476C>GCA485775976NRLc.474G>C (p.Leu158=)
c.57G>C (p.Leu19=)
c.573G>C (p.Leu191=)
c.258G>C (p.Leu86=)
c.159G>C (p.Leu53=)
c.780G>C (p.Leu260=)
c.465G>C (p.Leu155=)
14g.24081476C>TCA7122827NRLc.474G>A (p.Leu158=)
c.57G>A (p.Leu19=)
c.573G>A (p.Leu191=)
c.258G>A (p.Leu86=)
c.159G>A (p.Leu53=)
c.780G>A (p.Leu260=)
c.465G>A (p.Leu155=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.24081477A=CA2123777787NRLc.473T= (p.Leu158=)
c.56T= (p.Leu19=)
c.572T= (p.Leu191=)
c.257T= (p.Leu86=)
c.158T= (p.Leu53=)
c.779T= (p.Leu260=)
c.464T= (p.Leu155=)
14g.24081477A>CCA389278382NRLc.473T>G (p.Leu158Arg)
c.56T>G (p.Leu19Arg)
c.572T>G (p.Leu191Arg)
c.257T>G (p.Leu86Arg)
c.158T>G (p.Leu53Arg)
c.779T>G (p.Leu260Arg)
c.464T>G (p.Leu155Arg)
14g.24081477A>GCA389278383NRLc.473T>C (p.Leu158Pro)
c.56T>C (p.Leu19Pro)
c.572T>C (p.Leu191Pro)
c.257T>C (p.Leu86Pro)
c.158T>C (p.Leu53Pro)
c.779T>C (p.Leu260Pro)
c.464T>C (p.Leu155Pro)
dbSNP gnomAD v4
14g.24081477A>TCA389278385NRLc.473T>A (p.Leu158Gln)
c.56T>A (p.Leu19Gln)
c.572T>A (p.Leu191Gln)
c.257T>A (p.Leu86Gln)
c.158T>A (p.Leu53Gln)
c.779T>A (p.Leu260Gln)
c.464T>A (p.Leu155Gln)
14g.24081478G>ACA485775977NRLc.472C>T (p.Leu158=)
c.55C>T (p.Leu19=)
c.571C>T (p.Leu191=)
c.256C>T (p.Leu86=)
c.157C>T (p.Leu53=)
c.778C>T (p.Leu260=)
c.463C>T (p.Leu155=)
gnomAD v4
14g.24081478G>CCA389278388NRLc.472C>G (p.Leu158Val)
c.55C>G (p.Leu19Val)
c.571C>G (p.Leu191Val)
c.256C>G (p.Leu86Val)
c.157C>G (p.Leu53Val)
c.778C>G (p.Leu260Val)
c.463C>G (p.Leu155Val)
14g.24081478G>TCA389278396NRLc.472C>A (p.Leu158Met)
c.55C>A (p.Leu19Met)
c.571C>A (p.Leu191Met)
c.256C>A (p.Leu86Met)
c.157C>A (p.Leu53Met)
c.778C>A (p.Leu260Met)
c.463C>A (p.Leu155Met)
gnomAD v4
14g.24081479C>ACA485775980NRLc.471G>T (p.Ala157=)
c.54G>T (p.Ala18=)
c.570G>T (p.Ala190=)
c.255G>T (p.Ala85=)
c.156G>T (p.Ala52=)
c.777G>T (p.Ala259=)
c.462G>T (p.Ala154=)
gnomAD v4
14g.24081479C>GCA485775981NRLc.471G>C (p.Ala157=)
c.54G>C (p.Ala18=)
c.570G>C (p.Ala190=)
c.255G>C (p.Ala85=)
c.156G>C (p.Ala52=)
c.777G>C (p.Ala259=)
c.462G>C (p.Ala154=)
14g.24081479C>TCA485775979NRLc.471G>A (p.Ala157=)
c.54G>A (p.Ala18=)
c.570G>A (p.Ala190=)
c.255G>A (p.Ala85=)
c.156G>A (p.Ala52=)
c.777G>A (p.Ala259=)
c.462G>A (p.Ala154=)
gnomAD v4
14g.24081480G>ACA389278409NRLc.470C>T (p.Ala157Val)
c.53C>T (p.Ala18Val)
c.569C>T (p.Ala190Val)
c.254C>T (p.Ala85Val)
c.155C>T (p.Ala52Val)
c.776C>T (p.Ala259Val)
c.461C>T (p.Ala154Val)
dbSNP gnomAD v2 gnomAD v4
14g.24081480G>CCA257868097NRLc.470C>G (p.Ala157Gly)
c.53C>G (p.Ala18Gly)
c.569C>G (p.Ala190Gly)
c.254C>G (p.Ala85Gly)
c.155C>G (p.Ala52Gly)
c.776C>G (p.Ala259Gly)
c.461C>G (p.Ala154Gly)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.24081480G=CA2123777795NRLc.470C= (p.Ala157=)
c.53C= (p.Ala18=)
c.569C= (p.Ala190=)
c.254C= (p.Ala85=)
c.155C= (p.Ala52=)
c.776C= (p.Ala259=)
c.461C= (p.Ala154=)
14g.24081480G>TCA389278400NRLc.470C>A (p.Ala157Glu)
c.53C>A (p.Ala18Glu)
c.569C>A (p.Ala190Glu)
c.254C>A (p.Ala85Glu)
c.155C>A (p.Ala52Glu)
c.776C>A (p.Ala259Glu)
c.461C>A (p.Ala154Glu)
gnomAD v4
14g.24081481C>ACA389278412NRLc.469G>T (p.Ala157Ser)
c.52G>T (p.Ala18Ser)
c.568G>T (p.Ala190Ser)
c.253G>T (p.Ala85Ser)
c.154G>T (p.Ala52Ser)
c.775G>T (p.Ala259Ser)
c.460G>T (p.Ala154Ser)
ClinVar dbSNP gnomAD v4
14g.24081481C=CA2123777799NRLc.469G= (p.Ala157=)
c.52G= (p.Ala18=)
c.568G= (p.Ala190=)
c.253G= (p.Ala85=)
c.154G= (p.Ala52=)
c.775G= (p.Ala259=)
c.460G= (p.Ala154=)
14g.24081481C>GCA389278415NRLc.469G>C (p.Ala157Pro)
c.52G>C (p.Ala18Pro)
c.568G>C (p.Ala190Pro)
c.253G>C (p.Ala85Pro)
c.154G>C (p.Ala52Pro)
c.775G>C (p.Ala259Pro)
c.460G>C (p.Ala154Pro)
14g.24081481C>TCA389278413NRLc.469G>A (p.Ala157Thr)
c.52G>A (p.Ala18Thr)
c.568G>A (p.Ala190Thr)
c.253G>A (p.Ala85Thr)
c.154G>A (p.Ala52Thr)
c.775G>A (p.Ala259Thr)
c.460G>A (p.Ala154Thr)
ClinVar dbSNP gnomAD v4

Number of alleles fetched