Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.16144994A>CCA362797771MYLIPc.925A>C (p.Lys309Gln)
c.382A>C (p.Lys128Gln)
c.760A>C (p.Lys254Gln)
6g.16144994A>GCA362797773MYLIPc.925A>G (p.Lys309Glu)
c.382A>G (p.Lys128Glu)
c.760A>G (p.Lys254Glu)
6g.16144994A>TCA362797769MYLIPc.925A>T (p.Lys309Ter)
c.382A>T (p.Lys128Ter)
c.760A>T (p.Lys254Ter)
6g.16144995A>CCA362797781MYLIPc.926A>C (p.Lys309Thr)
c.383A>C (p.Lys128Thr)
c.761A>C (p.Lys254Thr)
6g.16144995A>GCA362797777MYLIPc.926A>G (p.Lys309Arg)
c.383A>G (p.Lys128Arg)
c.761A>G (p.Lys254Arg)
 gnomAD v4
6g.16144995A>TCA362797779MYLIPc.926A>T (p.Lys309Met)
c.383A>T (p.Lys128Met)
c.761A>T (p.Lys254Met)
6g.16144996G>ACA448954031MYLIPc.927G>A (p.Lys309=)
c.384G>A (p.Lys128=)
c.762G>A (p.Lys254=)
 dbSNP gnomAD v2 gnomAD v4
6g.16144996G>CCA362797784MYLIPc.927G>C (p.Lys309Asn)
c.384G>C (p.Lys128Asn)
c.762G>C (p.Lys254Asn)
6g.16144996G=CA1612565303MYLIPc.927G= (p.Lys309=)
c.384G= (p.Lys128=)
c.762G= (p.Lys254=)
6g.16144996G>TCA362797786MYLIPc.927G>T (p.Lys309Asn)
c.384G>T (p.Lys128Asn)
c.762G>T (p.Lys254Asn)
6g.16144997A=CA1612565308MYLIPc.928A= (p.Lys310=)
c.385A= (p.Lys129=)
c.763A= (p.Lys255=)
6g.16144997A>CCA362797790MYLIPc.928A>C (p.Lys310Gln)
c.385A>C (p.Lys129Gln)
c.763A>C (p.Lys255Gln)
6g.16144997A>GCA362797792MYLIPc.928A>G (p.Lys310Glu)
c.385A>G (p.Lys129Glu)
c.763A>G (p.Lys255Glu)
6g.16144997A>TCA362797795MYLIPc.928A>T (p.Lys310Ter)
c.385A>T (p.Lys129Ter)
c.763A>T (p.Lys255Ter)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.16144998A>CCA362797799MYLIPc.929A>C (p.Lys310Thr)
c.386A>C (p.Lys129Thr)
c.764A>C (p.Lys255Thr)
6g.16144998A>GCA362797801MYLIPc.929A>G (p.Lys310Arg)
c.386A>G (p.Lys129Arg)
c.764A>G (p.Lys255Arg)
6g.16144998A>TCA362797804MYLIPc.929A>T (p.Lys310Ile)
c.386A>T (p.Lys129Ile)
c.764A>T (p.Lys255Ile)
6g.16144999A>CCA362797807MYLIPc.930A>C (p.Lys310Asn)
c.387A>C (p.Lys129Asn)
c.765A>C (p.Lys255Asn)
6g.16144999A>GCA448954036MYLIPc.930A>G (p.Lys310=)
c.387A>G (p.Lys129=)
c.765A>G (p.Lys255=)
6g.16144999A>TCA362797809MYLIPc.930A>T (p.Lys310Asn)
c.387A>T (p.Lys129Asn)
c.765A>T (p.Lys255Asn)
6g.16145000T>ACA362797816MYLIPc.931T>A (p.Tyr311Asn)
c.388T>A (p.Tyr130Asn)
c.766T>A (p.Tyr256Asn)
6g.16145000T>CCA362797812MYLIPc.931T>C (p.Tyr311His)
c.388T>C (p.Tyr130His)
c.766T>C (p.Tyr256His)
 gnomAD v4
6g.16145000T>GCA362797814MYLIPc.931T>G (p.Tyr311Asp)
c.388T>G (p.Tyr130Asp)
c.766T>G (p.Tyr256Asp)
6g.16145001A>CCA362797818MYLIPc.932A>C (p.Tyr311Ser)
c.389A>C (p.Tyr130Ser)
c.767A>C (p.Tyr256Ser)
6g.16145001A>GCA362797821MYLIPc.932A>G (p.Tyr311Cys)
c.389A>G (p.Tyr130Cys)
c.767A>G (p.Tyr256Cys)
 gnomAD v4
6g.16145001A>TCA362797822MYLIPc.932A>T (p.Tyr311Phe)
c.389A>T (p.Tyr130Phe)
c.767A>T (p.Tyr256Phe)
6g.16145002T>ACA362797826MYLIPc.933T>A (p.Tyr311Ter)
c.390T>A (p.Tyr130Ter)
c.768T>A (p.Tyr256Ter)
6g.16145002T>CCA448954041MYLIPc.933T>C (p.Tyr311=)
c.390T>C (p.Tyr130=)
c.768T>C (p.Tyr256=)
 gnomAD v4
6g.16145002T>GCA362797828MYLIPc.933T>G (p.Tyr311Ter)
c.390T>G (p.Tyr130Ter)
c.768T>G (p.Tyr256Ter)
6g.16145003G>ACA134851650MYLIPc.934G>A (p.Val312Ile)
c.391G>A (p.Val131Ile)
c.769G>A (p.Val257Ile)
 dbSNP
6g.16145003G>CCA362797832MYLIPc.934G>C (p.Val312Leu)
c.391G>C (p.Val131Leu)
c.769G>C (p.Val257Leu)
6g.16145003G=CA1612565310MYLIPc.934G= (p.Val312=)
c.391G= (p.Val131=)
c.769G= (p.Val257=)
6g.16145003G>TCA362797834MYLIPc.934G>T (p.Val312Phe)
c.391G>T (p.Val131Phe)
c.769G>T (p.Val257Phe)
6g.16145004T>ACA362797837MYLIPc.935T>A (p.Val312Asp)
c.392T>A (p.Val131Asp)
c.770T>A (p.Val257Asp)
6g.16145004T>CCA362797839MYLIPc.935T>C (p.Val312Ala)
c.392T>C (p.Val131Ala)
c.770T>C (p.Val257Ala)
6g.16145004T>GCA362797842MYLIPc.935T>G (p.Val312Gly)
c.392T>G (p.Val131Gly)
c.770T>G (p.Val257Gly)
6g.16145005C>ACA448954045MYLIPc.936C>A (p.Val312=)
c.393C>A (p.Val131=)
c.771C>A (p.Val257=)
6g.16145005C>GCA448954047MYLIPc.936C>G (p.Val312=)
c.393C>G (p.Val131=)
c.771C>G (p.Val257=)
6g.16145005C>TCA448954049MYLIPc.936C>T (p.Val312=)
c.393C>T (p.Val131=)
c.771C>T (p.Val257=)
6g.16145006T>ACA362797847MYLIPc.937T>A (p.Phe313Ile)
c.394T>A (p.Phe132Ile)
c.772T>A (p.Phe258Ile)
6g.16145006T>CCA362797849MYLIPc.937T>C (p.Phe313Leu)
c.394T>C (p.Phe132Leu)
c.772T>C (p.Phe258Leu)
6g.16145006T>GCA362797845MYLIPc.937T>G (p.Phe313Val)
c.394T>G (p.Phe132Val)
c.772T>G (p.Phe258Val)
6g.16145007T>ACA362797853MYLIPc.938T>A (p.Phe313Tyr)
c.395T>A (p.Phe132Tyr)
c.773T>A (p.Phe258Tyr)
6g.16145007T>CCA362797855MYLIPc.938T>C (p.Phe313Ser)
c.395T>C (p.Phe132Ser)
c.773T>C (p.Phe258Ser)
 gnomAD v4
6g.16145007T>GCA362797857MYLIPc.938T>G (p.Phe313Cys)
c.395T>G (p.Phe132Cys)
c.773T>G (p.Phe258Cys)
6g.16145008T>ACA362797861MYLIPc.939T>A (p.Phe313Leu)
c.396T>A (p.Phe132Leu)
c.774T>A (p.Phe258Leu)
6g.16145008T>CCA448954055MYLIPc.939T>C (p.Phe313=)
c.396T>C (p.Phe132=)
c.774T>C (p.Phe258=)
6g.16145008T>GCA362797863MYLIPc.939T>G (p.Phe313Leu)
c.396T>G (p.Phe132Leu)
c.774T>G (p.Phe258Leu)
6g.16145009G>ACA362797866MYLIPc.940G>A (p.Asp314Asn)
c.397G>A (p.Asp133Asn)
c.775G>A (p.Asp259Asn)
6g.16145009G>CCA362797867MYLIPc.940G>C (p.Asp314His)
c.397G>C (p.Asp133His)
c.775G>C (p.Asp259His)
6g.16145009G>TCA362797870MYLIPc.940G>T (p.Asp314Tyr)
c.397G>T (p.Asp133Tyr)
c.775G>T (p.Asp259Tyr)
6g.16145010A>CCA362797874MYLIPc.941A>C (p.Asp314Ala)
c.398A>C (p.Asp133Ala)
c.776A>C (p.Asp259Ala)
6g.16145010A>GCA362797875MYLIPc.941A>G (p.Asp314Gly)
c.398A>G (p.Asp133Gly)
c.776A>G (p.Asp259Gly)
6g.16145010A>TCA362797878MYLIPc.941A>T (p.Asp314Val)
c.398A>T (p.Asp133Val)
c.776A>T (p.Asp259Val)
6g.16145011T>ACA362797882MYLIPc.942T>A (p.Asp314Glu)
c.399T>A (p.Asp133Glu)
c.777T>A (p.Asp259Glu)
6g.16145011T>CCA448954057MYLIPc.942T>C (p.Asp314=)
c.399T>C (p.Asp133=)
c.777T>C (p.Asp259=)
6g.16145011T>GCA362797884MYLIPc.942T>G (p.Asp314Glu)
c.399T>G (p.Asp133Glu)
c.777T>G (p.Asp259Glu)
6g.16145012A>CCA362797892MYLIPc.943A>C (p.Ile315Leu)
c.400A>C (p.Ile134Leu)
c.778A>C (p.Ile260Leu)
6g.16145012A>GCA362797890MYLIPc.943A>G (p.Ile315Val)
c.400A>G (p.Ile134Val)
c.778A>G (p.Ile260Val)
6g.16145012A>TCA362797888MYLIPc.943A>T (p.Ile315Phe)
c.400A>T (p.Ile134Phe)
c.778A>T (p.Ile260Phe)
6g.16145013T>ACA362797895MYLIPc.944T>A (p.Ile315Asn)
c.401T>A (p.Ile134Asn)
c.779T>A (p.Ile260Asn)
6g.16145013T>CCA362797897MYLIPc.944T>C (p.Ile315Thr)
c.401T>C (p.Ile134Thr)
c.779T>C (p.Ile260Thr)
6g.16145013T>GCA362797899MYLIPc.944T>G (p.Ile315Ser)
c.401T>G (p.Ile134Ser)
c.779T>G (p.Ile260Ser)
6g.16145014T>ACA448954061MYLIPc.945T>A (p.Ile315=)
c.402T>A (p.Ile134=)
c.780T>A (p.Ile260=)
6g.16145014T>CCA448954064MYLIPc.945T>C (p.Ile315=)
c.402T>C (p.Ile134=)
c.780T>C (p.Ile260=)
6g.16145014T>GCA362797902MYLIPc.945T>G (p.Ile315Met)
c.402T>G (p.Ile134Met)
c.780T>G (p.Ile260Met)
6g.16145015A>CCA362797906MYLIPc.946A>C (p.Lys316Gln)
c.403A>C (p.Lys135Gln)
c.781A>C (p.Lys261Gln)
6g.16145015A>GCA362797908MYLIPc.946A>G (p.Lys316Glu)
c.403A>G (p.Lys135Glu)
c.781A>G (p.Lys261Glu)
6g.16145015A>TCA362797910MYLIPc.946A>T (p.Lys316Ter)
c.403A>T (p.Lys135Ter)
c.781A>T (p.Lys261Ter)
6g.16145016A>CCA362797913MYLIPc.947A>C (p.Lys316Thr)
c.404A>C (p.Lys135Thr)
c.782A>C (p.Lys261Thr)
6g.16145016A>GCA362797916MYLIPc.947A>G (p.Lys316Arg)
c.404A>G (p.Lys135Arg)
c.782A>G (p.Lys261Arg)
6g.16145016A>TCA362797917MYLIPc.947A>T (p.Lys316Ile)
c.404A>T (p.Lys135Ile)
c.782A>T (p.Lys261Ile)
6g.16145017A>CCA362797920MYLIPc.948A>C (p.Lys316Asn)
c.405A>C (p.Lys135Asn)
c.783A>C (p.Lys261Asn)
6g.16145017A>GCA448954068MYLIPc.948A>G (p.Lys316=)
c.405A>G (p.Lys135=)
c.783A>G (p.Lys261=)
 COSMIC
6g.16145017A>TCA362797922MYLIPc.948A>T (p.Lys316Asn)
c.405A>T (p.Lys135Asn)
c.783A>T (p.Lys261Asn)
6g.16145018A>CCA448954069MYLIPc.949A>C (p.Arg317=)
c.406A>C (p.Arg136=)
c.784A>C (p.Arg262=)
6g.16145018A>GCA362797926MYLIPc.949A>G (p.Arg317Gly)
c.406A>G (p.Arg136Gly)
c.784A>G (p.Arg262Gly)
6g.16145018A>TCA362797929MYLIPc.949A>T (p.Arg317Ter)
c.406A>T (p.Arg136Ter)
c.784A>T (p.Arg262Ter)
6g.16145019G>ACA362797935MYLIPc.950G>A (p.Arg317Lys)
c.407G>A (p.Arg136Lys)
c.785G>A (p.Arg262Lys)
6g.16145019G>CCA362797937MYLIPc.950G>C (p.Arg317Thr)
c.407G>C (p.Arg136Thr)
c.785G>C (p.Arg262Thr)
6g.16145019G>TCA362797933MYLIPc.950G>T (p.Arg317Ile)
c.407G>T (p.Arg136Ile)
c.785G>T (p.Arg262Ile)
6g.16145020A>CCA362797943MYLIPc.951A>C (p.Arg317Ser)
c.408A>C (p.Arg136Ser)
c.786A>C (p.Arg262Ser)
6g.16145020A>GCA448954071MYLIPc.951A>G (p.Arg317=)
c.408A>G (p.Arg136=)
c.786A>G (p.Arg262=)
6g.16145020A>TCA362797940MYLIPc.951A>T (p.Arg317Ser)
c.408A>T (p.Arg136Ser)
c.786A>T (p.Arg262Ser)
6g.16145021A>CCA362797946MYLIPc.952A>C (p.Thr318Pro)
c.409A>C (p.Thr137Pro)
c.787A>C (p.Thr263Pro)
6g.16145021A>GCA362797948MYLIPc.952A>G (p.Thr318Ala)
c.409A>G (p.Thr137Ala)
c.787A>G (p.Thr263Ala)
 gnomAD v4
6g.16145021A>TCA362797950MYLIPc.952A>T (p.Thr318Ser)
c.409A>T (p.Thr137Ser)
c.787A>T (p.Thr263Ser)
6g.16145022C>ACA362797954MYLIPc.953C>A (p.Thr318Lys)
c.410C>A (p.Thr137Lys)
c.788C>A (p.Thr263Lys)
6g.16145022C=CA1612565312MYLIPc.953C= (p.Thr318=)
c.410C= (p.Thr137=)
c.788C= (p.Thr263=)
6g.16145022C>GCA362797956MYLIPc.953C>G (p.Thr318Arg)
c.410C>G (p.Thr137Arg)
c.788C>G (p.Thr263Arg)
6g.16145022C>TCA134851659MYLIPc.953C>T (p.Thr318Ile)
c.410C>T (p.Thr137Ile)
c.788C>T (p.Thr263Ile)
 dbSNP
6g.16145023A=CA1612565314MYLIPc.954A= (p.Thr318=)
c.411A= (p.Thr137=)
c.789A= (p.Thr263=)
6g.16145023A>CCA448954075MYLIPc.954A>C (p.Thr318=)
c.411A>C (p.Thr137=)
c.789A>C (p.Thr263=)
6g.16145023A>GCA448954072MYLIPc.954A>G (p.Thr318=)
c.411A>G (p.Thr137=)
c.789A>G (p.Thr263=)
 dbSNP gnomAD v3 gnomAD v4
6g.16145023A>TCA448954074MYLIPc.954A>T (p.Thr318=)
c.411A>T (p.Thr137=)
c.789A>T (p.Thr263=)
 dbSNP gnomAD v4
6g.16145024T>ACA362797960MYLIPc.955T>A (p.Ser319Thr)
c.412T>A (p.Ser138Thr)
c.790T>A (p.Ser264Thr)
6g.16145024T>CCA362797961MYLIPc.955T>C (p.Ser319Pro)
c.412T>C (p.Ser138Pro)
c.790T>C (p.Ser264Pro)
6g.16145024T>GCA362797964MYLIPc.955T>G (p.Ser319Ala)
c.412T>G (p.Ser138Ala)
c.790T>G (p.Ser264Ala)
6g.16145025C>ACA362797967MYLIPc.956C>A (p.Ser319Ter)
c.413C>A (p.Ser138Ter)
c.791C>A (p.Ser264Ter)
6g.16145025C>GCA362797969MYLIPc.956C>G (p.Ser319Ter)
c.413C>G (p.Ser138Ter)
c.791C>G (p.Ser264Ter)
6g.16145025C>TCA362797971MYLIPc.956C>T (p.Ser319Leu)
c.413C>T (p.Ser138Leu)
c.791C>T (p.Ser264Leu)
6g.16145026A>CCA448954076MYLIPc.957A>C (p.Ser319=)
c.414A>C (p.Ser138=)
c.792A>C (p.Ser264=)
 gnomAD v4
6g.16145026A>GCA448954077MYLIPc.957A>G (p.Ser319=)
c.414A>G (p.Ser138=)
c.792A>G (p.Ser264=)
6g.16145026A>TCA448954078MYLIPc.957A>T (p.Ser319=)
c.414A>T (p.Ser138=)
c.792A>T (p.Ser264=)
6g.16145027A>CCA362797978MYLIPc.958A>C (p.Lys320Gln)
c.415A>C (p.Lys139Gln)
c.793A>C (p.Lys265Gln)
6g.16145027A>GCA362797976MYLIPc.958A>G (p.Lys320Glu)
c.415A>G (p.Lys139Glu)
c.793A>G (p.Lys265Glu)
 gnomAD v4
6g.16145027A>TCA362797974MYLIPc.958A>T (p.Lys320Ter)
c.415A>T (p.Lys139Ter)
c.793A>T (p.Lys265Ter)
6g.16145028A>CCA362797981MYLIPc.959A>C (p.Lys320Thr)
c.416A>C (p.Lys139Thr)
c.794A>C (p.Lys265Thr)
6g.16145028A>GCA362797984MYLIPc.959A>G (p.Lys320Arg)
c.416A>G (p.Lys139Arg)
c.794A>G (p.Lys265Arg)
6g.16145028A>TCA362797986MYLIPc.959A>T (p.Lys320Met)
c.416A>T (p.Lys139Met)
c.794A>T (p.Lys265Met)
6g.16145029G>ACA448954080MYLIPc.960G>A (p.Lys320=)
c.417G>A (p.Lys139=)
c.795G>A (p.Lys265=)
6g.16145029G>CCA362797990MYLIPc.960G>C (p.Lys320Asn)
c.417G>C (p.Lys139Asn)
c.795G>C (p.Lys265Asn)
6g.16145029G>TCA362797992MYLIPc.960G>T (p.Lys320Asn)
c.417G>T (p.Lys139Asn)
c.795G>T (p.Lys265Asn)
6g.16145030G>ACA362797995MYLIPc.961G>A (p.Glu321Lys)
c.418G>A (p.Glu140Lys)
c.796G>A (p.Glu266Lys)
6g.16145030G>CCA362797998MYLIPc.961G>C (p.Glu321Gln)
c.418G>C (p.Glu140Gln)
c.796G>C (p.Glu266Gln)
6g.16145030G>TCA362798000MYLIPc.961G>T (p.Glu321Ter)
c.418G>T (p.Glu140Ter)
c.796G>T (p.Glu266Ter)
6g.16145031A>CCA362798003MYLIPc.962A>C (p.Glu321Ala)
c.419A>C (p.Glu140Ala)
c.797A>C (p.Glu266Ala)
6g.16145031A>GCA362798006MYLIPc.962A>G (p.Glu321Gly)
c.419A>G (p.Glu140Gly)
c.797A>G (p.Glu266Gly)
 COSMIC
6g.16145031A>TCA362798008MYLIPc.962A>T (p.Glu321Val)
c.419A>T (p.Glu140Val)
c.797A>T (p.Glu266Val)
6g.16145032G>ACA448954082MYLIPc.963G>A (p.Glu321=)
c.420G>A (p.Glu140=)
c.798G>A (p.Glu266=)
6g.16145032G>CCA3644617MYLIPc.963G>C (p.Glu321Asp)
c.420G>C (p.Glu140Asp)
c.798G>C (p.Glu266Asp)
 dbSNP ExAC gnomAD v2
6g.16145032G=CA1612565316MYLIPc.963G= (p.Glu321=)
c.420G= (p.Glu140=)
c.798G= (p.Glu266=)
6g.16145032G>TCA362798012MYLIPc.963G>T (p.Glu321Asp)
c.420G>T (p.Glu140Asp)
c.798G>T (p.Glu266Asp)
 gnomAD v4
6g.16145033G>ACA362798018MYLIPc.964G>A (p.Val322Met)
c.421G>A (p.Val141Met)
c.799G>A (p.Val267Met)
6g.16145033G>CCA362798020MYLIPc.964G>C (p.Val322Leu)
c.421G>C (p.Val141Leu)
c.799G>C (p.Val267Leu)
6g.16145033G=CA1612565319MYLIPc.964G= (p.Val322=)
c.421G= (p.Val141=)
c.799G= (p.Val267=)
6g.16145033G>TCA362798015MYLIPc.964G>T (p.Val322Leu)
c.421G>T (p.Val141Leu)
c.799G>T (p.Val267Leu)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.16145034T>ACA362798023MYLIPc.965T>A (p.Val322Glu)
c.422T>A (p.Val141Glu)
c.800T>A (p.Val267Glu)
6g.16145034T>CCA362798025MYLIPc.965T>C (p.Val322Ala)
c.422T>C (p.Val141Ala)
c.800T>C (p.Val267Ala)
6g.16145034T>GCA362798027MYLIPc.965T>G (p.Val322Gly)
c.422T>G (p.Val141Gly)
c.800T>G (p.Val267Gly)
6g.16145035G>ACA448954083MYLIPc.966G>A (p.Val322=)
c.423G>A (p.Val141=)
c.801G>A (p.Val267=)
 dbSNP gnomAD v4
6g.16145035G>CCA448954084MYLIPc.966G>C (p.Val322=)
c.423G>C (p.Val141=)
c.801G>C (p.Val267=)
6g.16145035G=CA1612565321MYLIPc.966G= (p.Val322=)
c.423G= (p.Val141=)
c.801G= (p.Val267=)
6g.16145035G>TCA448954085MYLIPc.966G>T (p.Val322=)
c.423G>T (p.Val141=)
c.801G>T (p.Val267=)
6g.16145036T>ACA362798030MYLIPc.967T>A (p.Tyr323Asn)
c.424T>A (p.Tyr142Asn)
c.802T>A (p.Tyr268Asn)
6g.16145036T>CCA362798032MYLIPc.967T>C (p.Tyr323His)
c.424T>C (p.Tyr142His)
c.802T>C (p.Tyr268His)
 COSMIC
6g.16145036T>GCA362798035MYLIPc.967T>G (p.Tyr323Asp)
c.424T>G (p.Tyr142Asp)
c.802T>G (p.Tyr268Asp)
6g.16145037A>CCA362798038MYLIPc.968A>C (p.Tyr323Ser)
c.425A>C (p.Tyr142Ser)
c.803A>C (p.Tyr268Ser)
6g.16145037A>GCA362798040MYLIPc.968A>G (p.Tyr323Cys)
c.425A>G (p.Tyr142Cys)
c.803A>G (p.Tyr268Cys)
6g.16145037A>TCA362798043MYLIPc.968A>T (p.Tyr323Phe)
c.425A>T (p.Tyr142Phe)
c.803A>T (p.Tyr268Phe)
6g.16145038T>ACA362798046MYLIPc.969T>A (p.Tyr323Ter)
c.426T>A (p.Tyr142Ter)
c.804T>A (p.Tyr268Ter)
6g.16145038T>CCA448954087MYLIPc.969T>C (p.Tyr323=)
c.426T>C (p.Tyr142=)
c.804T>C (p.Tyr268=)
6g.16145038T>GCA362798048MYLIPc.969T>G (p.Tyr323Ter)
c.426T>G (p.Tyr142Ter)
c.804T>G (p.Tyr268Ter)
6g.16145039G>ACA362798057MYLIPc.970G>A (p.Asp324Asn)
c.427G>A (p.Asp143Asn)
c.805G>A (p.Asp269Asn)
6g.16145039G>CCA362798055MYLIPc.970G>C (p.Asp324His)
c.427G>C (p.Asp143His)
c.805G>C (p.Asp269His)
6g.16145039G>TCA362798053MYLIPc.970G>T (p.Asp324Tyr)
c.427G>T (p.Asp143Tyr)
c.805G>T (p.Asp269Tyr)
 gnomAD v4
6g.16145040A>CCA362798061MYLIPc.971A>C (p.Asp324Ala)
c.428A>C (p.Asp143Ala)
c.806A>C (p.Asp269Ala)
6g.16145040A>GCA362798064MYLIPc.971A>G (p.Asp324Gly)
c.428A>G (p.Asp143Gly)
c.806A>G (p.Asp269Gly)
6g.16145040A>TCA362798067MYLIPc.971A>T (p.Asp324Val)
c.428A>T (p.Asp143Val)
c.806A>T (p.Asp269Val)
6g.16145040_16145041delinsACCA1612565324MYLIPc.971_972delinsAC (p.Asp324=)
c.428_429delinsAC (p.Asp143=)
c.806_807delinsAC (p.Asp269=)
6g.16145041C>ACA362798070MYLIPc.972C>A (p.Asp324Glu)
c.429C>A (p.Asp143Glu)
c.807C>A (p.Asp269Glu)
6g.16145041C=CA1612565327MYLIPc.972C= (p.Asp324=)
c.429C= (p.Asp143=)
c.807C= (p.Asp269=)
6g.16145041C>GCA3644618MYLIPc.972C>G (p.Asp324Glu)
c.429C>G (p.Asp143Glu)
c.807C>G (p.Asp269Glu)
 dbSNP ExAC gnomAD v2 gnomAD v4
6g.16145041C>TCA448954090MYLIPc.972C>T (p.Asp324=)
c.429C>T (p.Asp143=)
c.807C>T (p.Asp269=)
6g.16145042delCA1612565325MYLIPc.973del (p.His325MetfsTer27)
c.430del (p.His144MetfsTer27)
c.808del (p.His270MetfsTer27)
 ClinVar dbSNP
6g.16145042C>ACA362798077MYLIPc.973C>A (p.His325Asn)
c.430C>A (p.His144Asn)
c.808C>A (p.His270Asn)
6g.16145042C>GCA362798079MYLIPc.973C>G (p.His325Asp)
c.430C>G (p.His144Asp)
c.808C>G (p.His270Asp)
6g.16145042C>TCA362798082MYLIPc.973C>T (p.His325Tyr)
c.430C>T (p.His144Tyr)
c.808C>T (p.His270Tyr)
6g.16145043A=CA1612565329MYLIPc.974A= (p.His325=)
c.431A= (p.His144=)
c.809A= (p.His270=)
6g.16145043A>CCA362798087MYLIPc.974A>C (p.His325Pro)
c.431A>C (p.His144Pro)
c.809A>C (p.His270Pro)
6g.16145043A>GCA134851695MYLIPc.974A>G (p.His325Arg)
c.431A>G (p.His144Arg)
c.809A>G (p.His270Arg)
 dbSNP gnomAD v3 gnomAD v4
6g.16145043A>TCA362798091MYLIPc.974A>T (p.His325Leu)
c.431A>T (p.His144Leu)
c.809A>T (p.His270Leu)
6g.16145044T>ACA362798094MYLIPc.975T>A (p.His325Gln)
c.432T>A (p.His144Gln)
c.810T>A (p.His270Gln)
 gnomAD v4
6g.16145044T>CCA448954094MYLIPc.975T>C (p.His325=)
c.432T>C (p.His144=)
c.810T>C (p.His270=)
6g.16145044T>GCA362798097MYLIPc.975T>G (p.His325Gln)
c.432T>G (p.His144Gln)
c.810T>G (p.His270Gln)
6g.16145045G>ACA362798105MYLIPc.976G>A (p.Ala326Thr)
c.433G>A (p.Ala145Thr)
c.811G>A (p.Ala271Thr)
 gnomAD v4
6g.16145045G>CCA362798108MYLIPc.976G>C (p.Ala326Pro)
c.433G>C (p.Ala145Pro)
c.811G>C (p.Ala271Pro)
6g.16145045G>TCA362798103MYLIPc.976G>T (p.Ala326Ser)
c.433G>T (p.Ala145Ser)
c.811G>T (p.Ala271Ser)
 COSMIC
6g.16145046C>ACA362798119MYLIPc.977C>A (p.Ala326Asp)
c.434C>A (p.Ala145Asp)
c.812C>A (p.Ala271Asp)
6g.16145046C>GCA362798112MYLIPc.977C>G (p.Ala326Gly)
c.434C>G (p.Ala145Gly)
c.812C>G (p.Ala271Gly)
6g.16145046C>TCA362798115MYLIPc.977C>T (p.Ala326Val)
c.434C>T (p.Ala145Val)
c.812C>T (p.Ala271Val)
6g.16145047C>ACA448954097MYLIPc.978C>A (p.Ala326=)
c.435C>A (p.Ala145=)
c.813C>A (p.Ala271=)
6g.16145047C>GCA448954098MYLIPc.978C>G (p.Ala326=)
c.435C>G (p.Ala145=)
c.813C>G (p.Ala271=)
6g.16145047C>TCA448954099MYLIPc.978C>T (p.Ala326=)
c.435C>T (p.Ala145=)
c.813C>T (p.Ala271=)
6g.16145048A>CCA448954100MYLIPc.979A>C (p.Arg327=)
c.436A>C (p.Arg146=)
c.814A>C (p.Arg272=)
6g.16145048A>GCA362798124MYLIPc.979A>G (p.Arg327Gly)
c.436A>G (p.Arg146Gly)
c.814A>G (p.Arg272Gly)
6g.16145048A>TCA362798127MYLIPc.979A>T (p.Arg327Trp)
c.436A>T (p.Arg146Trp)
c.814A>T (p.Arg272Trp)
 gnomAD v4
6g.16145049G>ACA362798131MYLIPc.980G>A (p.Arg327Lys)
c.437G>A (p.Arg146Lys)
c.815G>A (p.Arg272Lys)
6g.16145049G>CCA362798134MYLIPc.980G>C (p.Arg327Thr)
c.437G>C (p.Arg146Thr)
c.815G>C (p.Arg272Thr)
6g.16145049G>TCA362798137MYLIPc.980G>T (p.Arg327Met)
c.437G>T (p.Arg146Met)
c.815G>T (p.Arg272Met)
6g.16145050G>ACA448954103MYLIPc.981G>A (p.Arg327=)
c.438G>A (p.Arg146=)
c.816G>A (p.Arg272=)
 dbSNP gnomAD v3 gnomAD v4
6g.16145050G>CCA362798142MYLIPc.981G>C (p.Arg327Ser)
c.438G>C (p.Arg146Ser)
c.816G>C (p.Arg272Ser)
6g.16145050G=CA1612565331MYLIPc.981G= (p.Arg327=)
c.438G= (p.Arg146=)
c.816G= (p.Arg272=)
6g.16145050G>TCA362798144MYLIPc.981G>T (p.Arg327Ser)
c.438G>T (p.Arg146Ser)
c.816G>T (p.Arg272Ser)
6g.16145051A>CCA448954104MYLIPc.982A>C (p.Arg328=)
c.439A>C (p.Arg147=)
c.817A>C (p.Arg273=)
6g.16145051A>GCA362798154MYLIPc.982A>G (p.Arg328Gly)
c.439A>G (p.Arg147Gly)
c.817A>G (p.Arg273Gly)
6g.16145051A>TCA362798158MYLIPc.982A>T (p.Arg328Trp)
c.439A>T (p.Arg147Trp)
c.817A>T (p.Arg273Trp)
6g.16145052G>ACA362798168MYLIPc.983G>A (p.Arg328Lys)
c.440G>A (p.Arg147Lys)
c.818G>A (p.Arg273Lys)
6g.16145052G>CCA362798165MYLIPc.983G>C (p.Arg328Thr)
c.440G>C (p.Arg147Thr)
c.818G>C (p.Arg273Thr)
6g.16145052G>TCA362798162MYLIPc.983G>T (p.Arg328Met)
c.440G>T (p.Arg147Met)
c.818G>T (p.Arg273Met)
6g.16145053G>ACA448954107MYLIPc.984G>A (p.Arg328=)
c.441G>A (p.Arg147=)
c.819G>A (p.Arg273=)
 gnomAD v4
6g.16145053G>CCA362798171MYLIPc.984G>C (p.Arg328Ser)
c.441G>C (p.Arg147Ser)
c.819G>C (p.Arg273Ser)
6g.16145053G>TCA362798175MYLIPc.984G>T (p.Arg328Ser)
c.441G>T (p.Arg147Ser)
c.819G>T (p.Arg273Ser)
 ClinVar
6g.16145054G>ACA3644619MYLIPc.985G>A (p.Ala329Thr)
c.442G>A (p.Ala148Thr)
c.820G>A (p.Ala274Thr)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.16145054G>CCA362798181MYLIPc.985G>C (p.Ala329Pro)
c.442G>C (p.Ala148Pro)
c.820G>C (p.Ala274Pro)
6g.16145054G=CA1612565333MYLIPc.985G= (p.Ala329=)
c.442G= (p.Ala148=)
c.820G= (p.Ala274=)
6g.16145054G>TCA362798184MYLIPc.985G>T (p.Ala329Ser)
c.442G>T (p.Ala148Ser)
c.820G>T (p.Ala274Ser)
 gnomAD v4 COSMIC
6g.16145055C>ACA362798189MYLIPc.986C>A (p.Ala329Asp)
c.443C>A (p.Ala148Asp)
c.821C>A (p.Ala274Asp)
6g.16145055C>GCA362798191MYLIPc.986C>G (p.Ala329Gly)
c.443C>G (p.Ala148Gly)
c.821C>G (p.Ala274Gly)
6g.16145055C>TCA362798193MYLIPc.986C>T (p.Ala329Val)
c.443C>T (p.Ala148Val)
c.821C>T (p.Ala274Val)
6g.16145056T>ACA448954113MYLIPc.987T>A (p.Ala329=)
c.444T>A (p.Ala148=)
c.822T>A (p.Ala274=)
6g.16145056T>CCA448954115MYLIPc.987T>C (p.Ala329=)
c.444T>C (p.Ala148=)
c.822T>C (p.Ala274=)
6g.16145056T>GCA448954116MYLIPc.987T>G (p.Ala329=)
c.444T>G (p.Ala148=)
c.822T>G (p.Ala274=)
6g.16145057C>ACA362798200MYLIPc.988C>A (p.Leu330Met)
c.445C>A (p.Leu149Met)
c.823C>A (p.Leu275Met)
6g.16145057C>GCA362798206MYLIPc.988C>G (p.Leu330Val)
c.445C>G (p.Leu149Val)
c.823C>G (p.Leu275Val)
 COSMIC
6g.16145057C>TCA448954118MYLIPc.988C>T (p.Leu330=)
c.445C>T (p.Leu149=)
c.823C>T (p.Leu275=)
6g.16145058T>ACA362798209MYLIPc.989T>A (p.Leu330Gln)
c.446T>A (p.Leu149Gln)
c.824T>A (p.Leu275Gln)
6g.16145058T>CCA362798212MYLIPc.989T>C (p.Leu330Pro)
c.446T>C (p.Leu149Pro)
c.824T>C (p.Leu275Pro)
 gnomAD v4
6g.16145058T>GCA362798214MYLIPc.989T>G (p.Leu330Arg)
c.446T>G (p.Leu149Arg)
c.824T>G (p.Leu275Arg)
6g.16145059G>ACA448954122MYLIPc.990G>A (p.Leu330=)
c.447G>A (p.Leu149=)
c.825G>A (p.Leu275=)
6g.16145059G>CCA448954123MYLIPc.990G>C (p.Leu330=)
c.447G>C (p.Leu149=)
c.825G>C (p.Leu275=)
6g.16145059G>TCA448954124MYLIPc.990G>T (p.Leu330=)
c.447G>T (p.Leu149=)
c.825G>T (p.Leu275=)
6g.16145060T>ACA362798221MYLIPc.991T>A (p.Tyr331Asn)
c.448T>A (p.Tyr150Asn)
c.826T>A (p.Tyr276Asn)
6g.16145060T>CCA362798224MYLIPc.991T>C (p.Tyr331His)
c.448T>C (p.Tyr150His)
c.826T>C (p.Tyr276His)
6g.16145060T>GCA362798218MYLIPc.991T>G (p.Tyr331Asp)
c.448T>G (p.Tyr150Asp)
c.826T>G (p.Tyr276Asp)
6g.16145061A>CCA362798228MYLIPc.992A>C (p.Tyr331Ser)
c.449A>C (p.Tyr150Ser)
c.827A>C (p.Tyr276Ser)
6g.16145061A>GCA362798231MYLIPc.992A>G (p.Tyr331Cys)
c.449A>G (p.Tyr150Cys)
c.827A>G (p.Tyr276Cys)
 gnomAD v4
6g.16145061A>TCA362798234MYLIPc.992A>T (p.Tyr331Phe)
c.449A>T (p.Tyr150Phe)
c.827A>T (p.Tyr276Phe)
6g.16145062C>ACA362798236MYLIPc.993C>A (p.Tyr331Ter)
c.450C>A (p.Tyr150Ter)
c.828C>A (p.Tyr276Ter)
 dbSNP gnomAD v4
6g.16145062C=CA1612565336MYLIPc.993C= (p.Tyr331=)
c.450C= (p.Tyr150=)
c.828C= (p.Tyr276=)
6g.16145062C>GCA362798239MYLIPc.993C>G (p.Tyr331Ter)
c.450C>G (p.Tyr150Ter)
c.828C>G (p.Tyr276Ter)
6g.16145062C>TCA448954127MYLIPc.993C>T (p.Tyr331=)
c.450C>T (p.Tyr150=)
c.828C>T (p.Tyr276=)
6g.16145063A=CA1612565339MYLIPc.994A= (p.Asn332=)
c.451A= (p.Asn151=)
c.829A= (p.Asn277=)
6g.16145063A>CCA362798241MYLIPc.994A>C (p.Asn332His)
c.451A>C (p.Asn151His)
c.829A>C (p.Asn277His)
6g.16145063A>GCA362798243MYLIPc.994A>G (p.Asn332Asp)
c.451A>G (p.Asn151Asp)
c.829A>G (p.Asn277Asp)
 ClinVar dbSNP gnomAD v3 gnomAD v4
6g.16145063A>TCA362798245MYLIPc.994A>T (p.Asn332Tyr)
c.451A>T (p.Asn151Tyr)
c.829A>T (p.Asn277Tyr)
6g.16145064A=CA1612565341MYLIPc.995A= (p.Asn332=)
c.452A= (p.Asn151=)
c.830A= (p.Asn277=)
6g.16145064A>CCA3644620MYLIPc.995A>C (p.Asn332Thr)
c.452A>C (p.Asn151Thr)
c.830A>C (p.Asn277Thr)
 dbSNP ExAC gnomAD v2 gnomAD v4
6g.16145064A>GCA362798249MYLIPc.995A>G (p.Asn332Ser)
c.452A>G (p.Asn151Ser)
c.830A>G (p.Asn277Ser)
 gnomAD v4
6g.16145064A>TCA362798251MYLIPc.995A>T (p.Asn332Ile)
c.452A>T (p.Asn151Ile)
c.830A>T (p.Asn277Ile)
6g.16145065T>ACA362798254MYLIPc.996T>A (p.Asn332Lys)
c.453T>A (p.Asn151Lys)
c.831T>A (p.Asn277Lys)
6g.16145065T>CCA3644621MYLIPc.996T>C (p.Asn332=)
c.453T>C (p.Asn151=)
c.831T>C (p.Asn277=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.16145065T>GCA362798259MYLIPc.996T>G (p.Asn332Lys)
c.453T>G (p.Asn151Lys)
c.831T>G (p.Asn277Lys)
6g.16145065T=CA1612565343MYLIPc.996T= (p.Asn332=)
c.453T= (p.Asn151=)
c.831T= (p.Asn277=)
6g.16145066G>ACA362798267MYLIPc.997G>A (p.Ala333Thr)
c.454G>A (p.Ala152Thr)
c.832G>A (p.Ala278Thr)
6g.16145066G>CCA362798264MYLIPc.997G>C (p.Ala333Pro)
c.454G>C (p.Ala152Pro)
c.832G>C (p.Ala278Pro)
6g.16145066G>TCA362798262MYLIPc.997G>T (p.Ala333Ser)
c.454G>T (p.Ala152Ser)
c.832G>T (p.Ala278Ser)
6g.16145067C>ACA362798270MYLIPc.998C>A (p.Ala333Asp)
c.455C>A (p.Ala152Asp)
c.833C>A (p.Ala278Asp)
6g.16145067C=CA1612565348MYLIPc.998C= (p.Ala333=)
c.455C= (p.Ala152=)
c.833C= (p.Ala278=)
6g.16145067C>GCA362798276MYLIPc.998C>G (p.Ala333Gly)
c.455C>G (p.Ala152Gly)
c.833C>G (p.Ala278Gly)
6g.16145067C>TCA134851712MYLIPc.998C>T (p.Ala333Val)
c.455C>T (p.Ala152Val)
c.833C>T (p.Ala278Val)
 dbSNP
6g.16145068T>ACA448954134MYLIPc.999T>A (p.Ala333=)
c.456T>A (p.Ala152=)
c.834T>A (p.Ala278=)
6g.16145068T>CCA448954135MYLIPc.999T>C (p.Ala333=)
c.456T>C (p.Ala152=)
c.834T>C (p.Ala278=)
 gnomAD v4
6g.16145068T>GCA448954136MYLIPc.999T>G (p.Ala333=)
c.456T>G (p.Ala152=)
c.834T>G (p.Ala278=)
 dbSNP
6g.16145068T=CA1612565350MYLIPc.999T= (p.Ala333=)
c.456T= (p.Ala152=)
c.834T= (p.Ala278=)
6g.16145069G>ACA362798282MYLIPc.1000G>A (p.Gly334Ser)
c.457G>A (p.Gly153Ser)
c.835G>A (p.Gly279Ser)
6g.16145069G>CCA362798284MYLIPc.1000G>C (p.Gly334Arg)
c.457G>C (p.Gly153Arg)
c.835G>C (p.Gly279Arg)
6g.16145069G>TCA362798287MYLIPc.1000G>T (p.Gly334Cys)
c.457G>T (p.Gly153Cys)
c.835G>T (p.Gly279Cys)
6g.16145070G>ACA362798290MYLIPc.1001G>A (p.Gly334Asp)
c.458G>A (p.Gly153Asp)
c.836G>A (p.Gly279Asp)
6g.16145070G>CCA362798292MYLIPc.1001G>C (p.Gly334Ala)
c.458G>C (p.Gly153Ala)
c.836G>C (p.Gly279Ala)
6g.16145070G=CA1612565352MYLIPc.1001G= (p.Gly334=)
c.458G= (p.Gly153=)
c.836G= (p.Gly279=)
6g.16145070G>TCA362798293MYLIPc.1001G>T (p.Gly334Val)
c.458G>T (p.Gly153Val)
c.836G>T (p.Gly279Val)
 dbSNP
6g.16145071C>ACA3644622MYLIPc.1002C>A (p.Gly334=)
c.459C>A (p.Gly153=)
c.837C>A (p.Gly279=)
 dbSNP ExAC
6g.16145071C=CA1612565359MYLIPc.1002C= (p.Gly334=)
c.459C= (p.Gly153=)
c.837C= (p.Gly279=)
6g.16145071C>GCA448954142MYLIPc.1002C>G (p.Gly334=)
c.459C>G (p.Gly153=)
c.837C>G (p.Gly279=)
6g.16145071C>TCA3644623MYLIPc.1002C>T (p.Gly334=)
c.459C>T (p.Gly153=)
c.837C>T (p.Gly279=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.16145072G>ACA3644624MYLIPc.1003G>A (p.Val335Ile)
c.460G>A (p.Val154Ile)
c.838G>A (p.Val280Ile)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
6g.16145072G>CCA362798299MYLIPc.1003G>C (p.Val335Leu)
c.460G>C (p.Val154Leu)
c.838G>C (p.Val280Leu)
6g.16145072G=CA1612565362MYLIPc.1003G= (p.Val335=)
c.460G= (p.Val154=)
c.838G= (p.Val280=)
6g.16145072G>TCA362798301MYLIPc.1003G>T (p.Val335Phe)
c.460G>T (p.Val154Phe)
c.838G>T (p.Val280Phe)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.16145073T>ACA362798315MYLIPc.1004T>A (p.Val335Asp)
c.461T>A (p.Val154Asp)
c.839T>A (p.Val280Asp)
6g.16145073T>CCA362798312MYLIPc.1004T>C (p.Val335Ala)
c.461T>C (p.Val154Ala)
c.839T>C (p.Val280Ala)
 dbSNP
6g.16145073T>GCA362798305MYLIPc.1004T>G (p.Val335Gly)
c.461T>G (p.Val154Gly)
c.839T>G (p.Val280Gly)
6g.16145074delCA2677410808MYLIPc.1005del (p.Val336TrpfsTer16)
c.462del (p.Val155TrpfsTer16)
c.840del (p.Val281TrpfsTer16)
 gnomAD v4
6g.16145074T>ACA448954146MYLIPc.1005T>A (p.Val335=)
c.462T>A (p.Val154=)
c.840T>A (p.Val280=)
 COSMIC
6g.16145074T>CCA448954145MYLIPc.1005T>C (p.Val335=)
c.462T>C (p.Val154=)
c.840T>C (p.Val280=)
6g.16145074T>GCA448954144MYLIPc.1005T>G (p.Val335=)
c.462T>G (p.Val154=)
c.840T>G (p.Val280=)
6g.16145075G>ACA362798333MYLIPc.1006G>A (p.Val336Met)
c.463G>A (p.Val155Met)
c.841G>A (p.Val281Met)
 gnomAD v4
6g.16145075G>CCA362798325MYLIPc.1006G>C (p.Val336Leu)
c.463G>C (p.Val155Leu)
c.841G>C (p.Val281Leu)
6g.16145075G>TCA362798343MYLIPc.1006G>T (p.Val336Leu)
c.463G>T (p.Val155Leu)
c.841G>T (p.Val281Leu)
6g.16145076T>ACA362798347MYLIPc.1007T>A (p.Val336Glu)
c.464T>A (p.Val155Glu)
c.842T>A (p.Val281Glu)
6g.16145076T>CCA362798351MYLIPc.1007T>C (p.Val336Ala)
c.464T>C (p.Val155Ala)
c.842T>C (p.Val281Ala)
 gnomAD v4
6g.16145076T>GCA362798349MYLIPc.1007T>G (p.Val336Gly)
c.464T>G (p.Val155Gly)
c.842T>G (p.Val281Gly)
6g.16145077G>ACA134851730MYLIPc.1008G>A (p.Val336=)
c.465G>A (p.Val155=)
c.843G>A (p.Val281=)
 dbSNP gnomAD v2 gnomAD v4
6g.16145077G>CCA448954152MYLIPc.1008G>C (p.Val336=)
c.465G>C (p.Val155=)
c.843G>C (p.Val281=)
6g.16145077G=CA1612565365MYLIPc.1008G= (p.Val336=)
c.465G= (p.Val155=)
c.843G= (p.Val281=)
6g.16145077G>TCA448954151MYLIPc.1008G>T (p.Val336=)
c.465G>T (p.Val155=)
c.843G>T (p.Val281=)
6g.16145078G>ACA362798356MYLIPc.1009G>A (p.Asp337Asn)
c.466G>A (p.Asp156Asn)
c.844G>A (p.Asp282Asn)
 gnomAD v4
6g.16145078G>CCA362798360MYLIPc.1009G>C (p.Asp337His)
c.466G>C (p.Asp156His)
c.844G>C (p.Asp282His)
6g.16145078G>TCA362798358MYLIPc.1009G>T (p.Asp337Tyr)
c.466G>T (p.Asp156Tyr)
c.844G>T (p.Asp282Tyr)
 dbSNP
6g.16145079A>CCA362798363MYLIPc.1010A>C (p.Asp337Ala)
c.467A>C (p.Asp156Ala)
c.845A>C (p.Asp282Ala)
6g.16145079A>GCA362798374MYLIPc.1010A>G (p.Asp337Gly)
c.467A>G (p.Asp156Gly)
c.845A>G (p.Asp282Gly)
6g.16145079A>TCA362798366MYLIPc.1010A>T (p.Asp337Val)
c.467A>T (p.Asp156Val)
c.845A>T (p.Asp282Val)
6g.16145080C>ACA362798377MYLIPc.1011C>A (p.Asp337Glu)
c.468C>A (p.Asp156Glu)
c.846C>A (p.Asp282Glu)
 gnomAD v4
6g.16145080C>GCA362798380MYLIPc.1011C>G (p.Asp337Glu)
c.468C>G (p.Asp156Glu)
c.846C>G (p.Asp282Glu)
6g.16145080C>TCA448954156MYLIPc.1011C>T (p.Asp337=)
c.468C>T (p.Asp156=)
c.846C>T (p.Asp282=)
6g.16145081C>ACA362798385MYLIPc.1012C>A (p.Leu338Ile)
c.469C>A (p.Leu157Ile)
c.847C>A (p.Leu283Ile)
6g.16145081C>GCA362798387MYLIPc.1012C>G (p.Leu338Val)
c.469C>G (p.Leu157Val)
c.847C>G (p.Leu283Val)
6g.16145081C>TCA362798392MYLIPc.1012C>T (p.Leu338Phe)
c.469C>T (p.Leu157Phe)
c.847C>T (p.Leu283Phe)
6g.16145082T>ACA362798396MYLIPc.1013T>A (p.Leu338His)
c.470T>A (p.Leu157His)
c.848T>A (p.Leu283His)
6g.16145082T>CCA362798398MYLIPc.1013T>C (p.Leu338Pro)
c.470T>C (p.Leu157Pro)
c.848T>C (p.Leu283Pro)
6g.16145082T>GCA362798399MYLIPc.1013T>G (p.Leu338Arg)
c.470T>G (p.Leu157Arg)
c.848T>G (p.Leu283Arg)
6g.16145082T=CA1612565367MYLIPc.1013T= (p.Leu338=)
c.470T= (p.Leu157=)
c.848T= (p.Leu283=)
6g.16145083C>ACA448954158MYLIPc.1014C>A (p.Leu338=)
c.471C>A (p.Leu157=)
c.849C>A (p.Leu283=)
6g.16145083C=CA1612565371MYLIPc.1014C= (p.Leu338=)
c.471C= (p.Leu157=)
c.849C= (p.Leu283=)
6g.16145083C>GCA448954159MYLIPc.1014C>G (p.Leu338=)
c.471C>G (p.Leu157=)
c.849C>G (p.Leu283=)
6g.16145083C>TCA3644625MYLIPc.1014C>T (p.Leu338=)
c.471C>T (p.Leu157=)
c.849C>T (p.Leu283=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.16145083dupCA565828453MYLIPc.1014dup (p.Val339ArgfsTer?)
c.471dup (p.Val158ArgfsTer?)
c.849dup (p.Val284ArgfsTer?)
 dbSNP gnomAD v2 gnomAD v4
6g.16145084G>ACA3644626MYLIPc.1015G>A (p.Val339Ile)
c.472G>A (p.Val158Ile)
c.850G>A (p.Val284Ile)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.16145084G>CCA362798401MYLIPc.1015G>C (p.Val339Leu)
c.472G>C (p.Val158Leu)
c.850G>C (p.Val284Leu)
6g.16145084G=CA1612565375MYLIPc.1015G= (p.Val339=)
c.472G= (p.Val158=)
c.850G= (p.Val284=)
6g.16145084G>TCA362798400MYLIPc.1015G>T (p.Val339Phe)
c.472G>T (p.Val158Phe)
c.850G>T (p.Val284Phe)
6g.16145085T>ACA362798404MYLIPc.1016T>A (p.Val339Asp)
c.473T>A (p.Val158Asp)
c.851T>A (p.Val284Asp)
6g.16145085T>CCA362798409MYLIPc.1016T>C (p.Val339Ala)
c.473T>C (p.Val158Ala)
c.851T>C (p.Val284Ala)
6g.16145085T>GCA362798412MYLIPc.1016T>G (p.Val339Gly)
c.473T>G (p.Val158Gly)
c.851T>G (p.Val284Gly)
6g.16145086T>ACA448954161MYLIPc.1017T>A (p.Val339=)
c.474T>A (p.Val158=)
c.852T>A (p.Val284=)
 gnomAD v4
6g.16145086T>CCA448954163MYLIPc.1017T>C (p.Val339=)
c.474T>C (p.Val158=)
c.852T>C (p.Val284=)
6g.16145086T>GCA448954165MYLIPc.1017T>G (p.Val339=)
c.474T>G (p.Val158=)
c.852T>G (p.Val284=)
6g.16145087T>ACA362798415MYLIPc.1018T>A (p.Ser340Thr)
c.475T>A (p.Ser159Thr)
c.853T>A (p.Ser285Thr)
6g.16145087T>CCA362798417MYLIPc.1018T>C (p.Ser340Pro)
c.475T>C (p.Ser159Pro)
c.853T>C (p.Ser285Pro)
6g.16145087T>GCA362798418MYLIPc.1018T>G (p.Ser340Ala)
c.475T>G (p.Ser159Ala)
c.853T>G (p.Ser285Ala)
6g.16145088C>ACA362798419MYLIPc.1019C>A (p.Ser340Ter)
c.476C>A (p.Ser159Ter)
c.854C>A (p.Ser285Ter)
 dbSNP
6g.16145088C=CA1612565377MYLIPc.1019C= (p.Ser340=)
c.476C= (p.Ser159=)
c.854C= (p.Ser285=)
6g.16145088C>GCA362798420MYLIPc.1019C>G (p.Ser340Ter)
c.476C>G (p.Ser159Ter)
c.854C>G (p.Ser285Ter)
6g.16145088C>TCA362798421MYLIPc.1019C>T (p.Ser340Leu)
c.476C>T (p.Ser159Leu)
c.854C>T (p.Ser285Leu)
6g.16145089A=CA1612565379MYLIPc.1020A= (p.Ser340=)
c.477A= (p.Ser159=)
c.855A= (p.Ser285=)
6g.16145089A>CCA448954167MYLIPc.1020A>C (p.Ser340=)
c.477A>C (p.Ser159=)
c.855A>C (p.Ser285=)
6g.16145089A>GCA448954168MYLIPc.1020A>G (p.Ser340=)
c.477A>G (p.Ser159=)
c.855A>G (p.Ser285=)
 dbSNP gnomAD v2 gnomAD v4
6g.16145089A>TCA448954169MYLIPc.1020A>T (p.Ser340=)
c.477A>T (p.Ser159=)
c.855A>T (p.Ser285=)
6g.16145090A=CA1612565383MYLIPc.1021A= (p.Arg341=)
c.478A= (p.Arg160=)
c.856A= (p.Arg286=)
6g.16145090A>CCA448954170MYLIPc.1021A>C (p.Arg341=)
c.478A>C (p.Arg160=)
c.856A>C (p.Arg286=)
6g.16145090A>GCA134851784MYLIPc.1021A>G (p.Arg341Gly)
c.478A>G (p.Arg160Gly)
c.856A>G (p.Arg286Gly)
 dbSNP
6g.16145090A>TCA362798429MYLIPc.1021A>T (p.Arg341Ter)
c.478A>T (p.Arg160Ter)
c.856A>T (p.Arg286Ter)
6g.16145091G>ACA362798438MYLIPc.1022G>A (p.Arg341Lys)
c.479G>A (p.Arg160Lys)
c.857G>A (p.Arg286Lys)
6g.16145091G>CCA362798439MYLIPc.1022G>C (p.Arg341Thr)
c.479G>C (p.Arg160Thr)
c.857G>C (p.Arg286Thr)
6g.16145091G>TCA362798435MYLIPc.1022G>T (p.Arg341Ile)
c.479G>T (p.Arg160Ile)
c.857G>T (p.Arg286Ile)
6g.16145092A>CCA362798441MYLIPc.1023A>C (p.Arg341Ser)
c.480A>C (p.Arg160Ser)
c.858A>C (p.Arg286Ser)
6g.16145092A>GCA448954171MYLIPc.1023A>G (p.Arg341=)
c.480A>G (p.Arg160=)
c.858A>G (p.Arg286=)
6g.16145092A>TCA362798444MYLIPc.1023A>T (p.Arg341Ser)
c.480A>T (p.Arg160Ser)
c.858A>T (p.Arg286Ser)
6g.16145093A>CCA362798447MYLIPc.1024A>C (p.Asn342His)
c.481A>C (p.Asn161His)
c.859A>C (p.Asn287His)
6g.16145093A>GCA362798449MYLIPc.1024A>G (p.Asn342Asp)
c.481A>G (p.Asn161Asp)
c.859A>G (p.Asn287Asp)
6g.16145093A>TCA362798451MYLIPc.1024A>T (p.Asn342Tyr)
c.481A>T (p.Asn161Tyr)
c.859A>T (p.Asn287Tyr)
6g.16145094A=CA1612565386MYLIPc.1025A= (p.Asn342=)
c.482A= (p.Asn161=)
c.860A= (p.Asn287=)
6g.16145094A>CCA362798455MYLIPc.1025A>C (p.Asn342Thr)
c.482A>C (p.Asn161Thr)
c.860A>C (p.Asn287Thr)
 dbSNP
6g.16145094A>GCA3644627MYLIPc.1025A>G (p.Asn342Ser)
c.482A>G (p.Asn161Ser)
c.860A>G (p.Asn287Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.16145094A>TCA362798454MYLIPc.1025A>T (p.Asn342Ile)
c.482A>T (p.Asn161Ile)
c.860A>T (p.Asn287Ile)
 dbSNP

Number of alleles fetched