Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.44006572G>ACA399726117NAGS,PYYc.959G>A (p.Cys320Tyr)
c.866G>A (p.Cys289Tyr)
n.234G>A
c.461G>A (p.Cys154Tyr)
c.-463+17000C>T (n.-463+17000C>T)
 gnomAD v4
17g.44006572G>CCA290853106NAGS,PYYc.959G>C (p.Cys320Ser)
c.866G>C (p.Cys289Ser)
n.234G>C
c.461G>C (p.Cys154Ser)
c.-463+17000C>G (n.-463+17000C>G)
 dbSNP gnomAD v4
17g.44006572G=CA2261182192NAGS,PYYc.959G= (p.Cys320=)
c.866G= (p.Cys289=)
n.234G=
c.461G= (p.Cys154=)
c.-463+17000C= (n.-463+17000C=)
17g.44006572G>TCA399726120NAGS,PYYc.959G>T (p.Cys320Phe)
c.866G>T (p.Cys289Phe)
n.234G>T
c.461G>T (p.Cys154Phe)
c.-463+17000C>A (n.-463+17000C>A)
17g.44006573C>ACA399726122NAGS,PYYc.960C>A (p.Cys320Ter)
c.867C>A (p.Cys289Ter)
n.235C>A
c.462C>A (p.Cys154Ter)
c.-463+16999G>T (n.-463+16999G>T)
 gnomAD v4
17g.44006573C>GCA399726124NAGS,PYYc.960C>G (p.Cys320Trp)
c.867C>G (p.Cys289Trp)
n.235C>G
c.462C>G (p.Cys154Trp)
c.-463+16999G>C (n.-463+16999G>C)
17g.44006573C>TCA500241088NAGS,PYYc.960C>T (p.Cys320=)
c.867C>T (p.Cys289=)
n.235C>T
c.462C>T (p.Cys154=)
c.-463+16999G>A (n.-463+16999G>A)
 gnomAD v4
17g.44006574A=CA2261182193NAGS,PYYc.961A= (p.Asn321=)
c.868A= (p.Asn290=)
n.236A=
c.463A= (p.Asn155=)
c.-463+16998T= (n.-463+16998T=)
17g.44006574A>CCA399726126NAGS,PYYc.961A>C (p.Asn321His)
c.868A>C (p.Asn290His)
n.236A>C
c.463A>C (p.Asn155His)
c.-463+16998T>G (n.-463+16998T>G)
 dbSNP gnomAD v2 gnomAD v4
17g.44006574A>GCA399726129NAGS,PYYc.961A>G (p.Asn321Asp)
c.868A>G (p.Asn290Asp)
n.236A>G
c.463A>G (p.Asn155Asp)
c.-463+16998T>C (n.-463+16998T>C)
 gnomAD v4
17g.44006574A>TCA399726128NAGS,PYYc.961A>T (p.Asn321Tyr)
c.868A>T (p.Asn290Tyr)
n.236A>T
c.463A>T (p.Asn155Tyr)
c.-463+16998T>A (n.-463+16998T>A)
17g.44006575A=CA2261182194NAGS,PYYc.962A= (p.Asn321=)
c.869A= (p.Asn290=)
n.237A=
c.464A= (p.Asn155=)
c.-463+16997T= (n.-463+16997T=)
17g.44006575A>CCA399726131NAGS,PYYc.962A>C (p.Asn321Thr)
c.869A>C (p.Asn290Thr)
n.237A>C
c.464A>C (p.Asn155Thr)
c.-463+16997T>G (n.-463+16997T>G)
17g.44006575A>GCA399726133NAGS,PYYc.962A>G (p.Asn321Ser)
c.869A>G (p.Asn290Ser)
n.237A>G
c.464A>G (p.Asn155Ser)
c.-463+16997T>C (n.-463+16997T>C)
 dbSNP
17g.44006575A>TCA8595281NAGS,PYYc.962A>T (p.Asn321Ile)
c.869A>T (p.Asn290Ile)
n.237A>T
c.464A>T (p.Asn155Ile)
c.-463+16997T>A (n.-463+16997T>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.44006576C>ACA399726136NAGS,PYYc.963C>A (p.Asn321Lys)
c.870C>A (p.Asn290Lys)
n.238C>A
c.465C>A (p.Asn155Lys)
c.-463+16996G>T (n.-463+16996G>T)
 gnomAD v4
17g.44006576C=CA2261182195NAGS,PYYc.963C= (p.Asn321=)
c.870C= (p.Asn290=)
n.238C=
c.465C= (p.Asn155=)
c.-463+16996G= (n.-463+16996G=)
17g.44006576C>GCA399726137NAGS,PYYc.963C>G (p.Asn321Lys)
c.870C>G (p.Asn290Lys)
n.238C>G
c.465C>G (p.Asn155Lys)
c.-463+16996G>C (n.-463+16996G>C)
17g.44006576C>TCA8595282NAGS,PYYc.963C>T (p.Asn321=)
c.870C>T (p.Asn290=)
n.238C>T
c.465C>T (p.Asn155=)
c.-463+16996G>A (n.-463+16996G>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.44006577G>ACA399726140NAGS,PYYc.964G>A (p.Ala322Thr)
c.871G>A (p.Ala291Thr)
n.239G>A
c.466G>A (p.Ala156Thr)
c.-463+16995C>T (n.-463+16995C>T)
 gnomAD v4
17g.44006577G>CCA399726141NAGS,PYYc.964G>C (p.Ala322Pro)
c.871G>C (p.Ala291Pro)
n.239G>C
c.466G>C (p.Ala156Pro)
c.-463+16995C>G (n.-463+16995C>G)
17g.44006577G>TCA399726142NAGS,PYYc.964G>T (p.Ala322Ser)
c.871G>T (p.Ala291Ser)
n.239G>T
c.466G>T (p.Ala156Ser)
c.-463+16995C>A (n.-463+16995C>A)
 gnomAD v4
17g.44006577dupCA2638146936NAGS,PYYc.964dup (p.Ala322GlyfsTer?)
c.871dup (p.Ala291GlyfsTer?)
n.239dup
c.466dup (p.Ala156GlyfsTer?)
c.-463+16995dup (n.-463+16995dup)
 gnomAD v4
17g.44006578C>ACA399726143NAGS,PYYc.965C>A (p.Ala322Asp)
c.872C>A (p.Ala291Asp)
n.240C>A
c.467C>A (p.Ala156Asp)
c.-463+16994G>T (n.-463+16994G>T)
 gnomAD v4
17g.44006578C=CA2261182196NAGS,PYYc.965C= (p.Ala322=)
c.872C= (p.Ala291=)
n.240C=
c.467C= (p.Ala156=)
c.-463+16994G= (n.-463+16994G=)
17g.44006578C>GCA399726145NAGS,PYYc.965C>G (p.Ala322Gly)
c.872C>G (p.Ala291Gly)
n.240C>G
c.467C>G (p.Ala156Gly)
c.-463+16994G>C (n.-463+16994G>C)
17g.44006578C>TCA8595283NAGS,PYYc.965C>T (p.Ala322Val)
c.872C>T (p.Ala291Val)
n.240C>T
c.467C>T (p.Ala156Val)
c.-463+16994G>A (n.-463+16994G>A)
 dbSNP ExAC gnomAD v2 gnomAD v4
17g.44006579C>ACA500241089NAGS,PYYc.966C>A (p.Ala322=)
c.873C>A (p.Ala291=)
n.241C>A
c.468C>A (p.Ala156=)
c.-463+16993G>T (n.-463+16993G>T)
17g.44006579C>GCA500241090NAGS,PYYc.966C>G (p.Ala322=)
c.873C>G (p.Ala291=)
n.241C>G
c.468C>G (p.Ala156=)
c.-463+16993G>C (n.-463+16993G>C)
17g.44006579C>TCA500241091NAGS,PYYc.966C>T (p.Ala322=)
c.873C>T (p.Ala291=)
n.241C>T
c.468C>T (p.Ala156=)
c.-463+16993G>A (n.-463+16993G>A)
 ClinVar dbSNP gnomAD v4
17g.44006580G>ACA8595284NAGS,PYYc.967G>A (p.Glu323Lys)
c.874G>A (p.Glu292Lys)
n.242G>A
c.469G>A (p.Glu157Lys)
c.-463+16992C>T (n.-463+16992C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.44006580G>CCA399726149NAGS,PYYc.967G>C (p.Glu323Gln)
c.874G>C (p.Glu292Gln)
n.242G>C
c.469G>C (p.Glu157Gln)
c.-463+16992C>G (n.-463+16992C>G)
 gnomAD v4
17g.44006580G=CA2261182197NAGS,PYYc.967G= (p.Glu323=)
c.874G= (p.Glu292=)
n.242G=
c.469G= (p.Glu157=)
c.-463+16992C= (n.-463+16992C=)
17g.44006580G>TCA399726148NAGS,PYYc.967G>T (p.Glu323Ter)
c.874G>T (p.Glu292Ter)
n.242G>T
c.469G>T (p.Glu157Ter)
c.-463+16992C>A (n.-463+16992C>A)
 gnomAD v4
17g.44006581A>CCA399726152NAGS,PYYc.968A>C (p.Glu323Ala)
c.875A>C (p.Glu292Ala)
n.243A>C
c.470A>C (p.Glu157Ala)
c.-463+16991T>G (n.-463+16991T>G)
17g.44006581A>GCA399726155NAGS,PYYc.968A>G (p.Glu323Gly)
c.875A>G (p.Glu292Gly)
n.243A>G
c.470A>G (p.Glu157Gly)
c.-463+16991T>C (n.-463+16991T>C)
17g.44006581A>TCA399726154NAGS,PYYc.968A>T (p.Glu323Val)
c.875A>T (p.Glu292Val)
n.243A>T
c.470A>T (p.Glu157Val)
c.-463+16991T>A (n.-463+16991T>A)
17g.44006581_44006585delinsAGTGGCA2261182198NAGS,PYYc.968_972delinsAGTGG (p.Glu323=)
c.875_879delinsAGTGG (p.Glu292=)
n.243_247delinsAGTGG
c.470_474delinsAGTGG (p.Glu157=)
c.-463+16987_-463+16991delinsCCACT (n.-463+16987_-463+16991delinsCCACT)
17g.44006582G>ACA500241092NAGS,PYYc.969G>A (p.Glu323=)
c.876G>A (p.Glu292=)
n.244G>A
c.471G>A (p.Glu157=)
c.-463+16990C>T (n.-463+16990C>T)
 dbSNP gnomAD v2
17g.44006582G>CCA399726158NAGS,PYYc.969G>C (p.Glu323Asp)
c.876G>C (p.Glu292Asp)
n.244G>C
c.471G>C (p.Glu157Asp)
c.-463+16990C>G (n.-463+16990C>G)
 gnomAD v4
17g.44006582G=CA2261182199NAGS,PYYc.969G= (p.Glu323=)
c.876G= (p.Glu292=)
n.244G=
c.471G= (p.Glu157=)
c.-463+16990C= (n.-463+16990C=)
17g.44006582G>TCA399726160NAGS,PYYc.969G>T (p.Glu323Asp)
c.876G>T (p.Glu292Asp)
n.244G>T
c.471G>T (p.Glu157Asp)
c.-463+16990C>A (n.-463+16990C>A)
 gnomAD v4
17g.44006585_44006588dupCA8595285NAGS,PYYc.972_975dup (p.Ser326GlyfsTer31)
c.879_882dup (p.Ser295GlyfsTer31)
n.247_250dup
c.474_477dup (p.Ser160GlyfsTer31)
c.-463+16987_-463+16990dup (n.-463+16987_-463+16990dup)
 dbSNP ExAC gnomAD v2 gnomAD v4
17g.44006585_44006588delCA8595286NAGS,PYYc.972_975del (p.Trp324Ter)
c.879_882del (p.Trp293Ter)
n.247_250del
c.474_477del (p.Trp158Ter)
c.-463+16987_-463+16990del (n.-463+16987_-463+16990del)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.44006583T>ACA399726162NAGS,PYYc.970T>A (p.Trp324Arg)
c.877T>A (p.Trp293Arg)
n.245T>A
c.472T>A (p.Trp158Arg)
c.-463+16989A>T (n.-463+16989A>T)
17g.44006583T>CCA399726164NAGS,PYYc.970T>C (p.Trp324Arg)
c.877T>C (p.Trp293Arg)
n.245T>C
c.472T>C (p.Trp158Arg)
c.-463+16989A>G (n.-463+16989A>G)
 gnomAD v4
17g.44006583T>GCA399726165NAGS,PYYc.970T>G (p.Trp324Gly)
c.877T>G (p.Trp293Gly)
n.245T>G
c.472T>G (p.Trp158Gly)
c.-463+16989A>C (n.-463+16989A>C)
 gnomAD v4
17g.44006584G>ACA115543NAGS,PYYc.971G>A (p.Trp324Ter)
c.878G>A (p.Trp293Ter)
n.246G>A
c.473G>A (p.Trp158Ter)
c.-463+16988C>T (n.-463+16988C>T)
 ClinVar dbSNP gnomAD v4
17g.44006584G>CCA399726168NAGS,PYYc.971G>C (p.Trp324Ser)
c.878G>C (p.Trp293Ser)
n.246G>C
c.473G>C (p.Trp158Ser)
c.-463+16988C>G (n.-463+16988C>G)
17g.44006584G=CA2261182200NAGS,PYYc.971G= (p.Trp324=)
c.878G= (p.Trp293=)
n.246G=
c.473G= (p.Trp158=)
c.-463+16988C= (n.-463+16988C=)
17g.44006584G>TCA399726170NAGS,PYYc.971G>T (p.Trp324Leu)
c.878G>T (p.Trp293Leu)
n.246G>T
c.473G>T (p.Trp158Leu)
c.-463+16988C>A (n.-463+16988C>A)
 gnomAD v4
17g.44006585G>ACA399726172NAGS,PYYc.972G>A (p.Trp324Ter)
c.879G>A (p.Trp293Ter)
n.247G>A
c.474G>A (p.Trp158Ter)
c.-463+16987C>T (n.-463+16987C>T)
 gnomAD v4
17g.44006585G>CCA399726173NAGS,PYYc.972G>C (p.Trp324Cys)
c.879G>C (p.Trp293Cys)
n.247G>C
c.474G>C (p.Trp158Cys)
c.-463+16987C>G (n.-463+16987C>G)
 gnomAD v4
17g.44006585G=CA2261182201NAGS,PYYc.972G= (p.Trp324=)
c.879G= (p.Trp293=)
n.247G=
c.474G= (p.Trp158=)
c.-463+16987C= (n.-463+16987C=)
17g.44006585G>TCA290853133NAGS,PYYc.972G>T (p.Trp324Cys)
c.879G>T (p.Trp293Cys)
n.247G>T
c.474G>T (p.Trp158Cys)
c.-463+16987C>A (n.-463+16987C>A)
 dbSNP gnomAD v4
17g.44006586G>ACA399726175NAGS,PYYc.973G>A (p.Val325Met)
c.880G>A (p.Val294Met)
n.248G>A
c.475G>A (p.Val159Met)
c.-463+16986C>T (n.-463+16986C>T)
17g.44006586G>CCA399726176NAGS,PYYc.973G>C (p.Val325Leu)
c.880G>C (p.Val294Leu)
n.248G>C
c.475G>C (p.Val159Leu)
c.-463+16986C>G (n.-463+16986C>G)
17g.44006586G=CA2261182202NAGS,PYYc.973G= (p.Val325=)
c.880G= (p.Val294=)
n.248G=
c.475G= (p.Val159=)
c.-463+16986C= (n.-463+16986C=)
17g.44006586G>TCA399726178NAGS,PYYc.973G>T (p.Val325Leu)
c.880G>T (p.Val294Leu)
n.248G>T
c.475G>T (p.Val159Leu)
c.-463+16986C>A (n.-463+16986C>A)
 dbSNP gnomAD v2 gnomAD v4
17g.44006587T>ACA399726180NAGS,PYYc.974T>A (p.Val325Glu)
c.881T>A (p.Val294Glu)
n.249T>A
c.476T>A (p.Val159Glu)
c.-463+16985A>T (n.-463+16985A>T)
 gnomAD v4
17g.44006587T>CCA399726183NAGS,PYYc.974T>C (p.Val325Ala)
c.881T>C (p.Val294Ala)
n.249T>C
c.476T>C (p.Val159Ala)
c.-463+16985A>G (n.-463+16985A>G)
 dbSNP gnomAD v3 gnomAD v4
17g.44006587T>GCA399726181NAGS,PYYc.974T>G (p.Val325Gly)
c.881T>G (p.Val294Gly)
n.249T>G
c.476T>G (p.Val159Gly)
c.-463+16985A>C (n.-463+16985A>C)
 gnomAD v4
17g.44006587T=CA2261182203NAGS,PYYc.974T= (p.Val325=)
c.881T= (p.Val294=)
n.249T=
c.476T= (p.Val159=)
c.-463+16985A= (n.-463+16985A=)
17g.44006588G>ACA8595287NAGS,PYYc.975G>A (p.Val325=)
c.882G>A (p.Val294=)
n.250G>A
c.477G>A (p.Val159=)
c.-463+16984C>T (n.-463+16984C>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
17g.44006588G>CCA500241093NAGS,PYYc.975G>C (p.Val325=)
c.882G>C (p.Val294=)
n.250G>C
c.477G>C (p.Val159=)
c.-463+16984C>G (n.-463+16984C>G)
17g.44006588G=CA2261182204NAGS,PYYc.975G= (p.Val325=)
c.882G= (p.Val294=)
n.250G=
c.477G= (p.Val159=)
c.-463+16984C= (n.-463+16984C=)
17g.44006588G>TCA500241094NAGS,PYYc.975G>T (p.Val325=)
c.882G>T (p.Val294=)
n.250G>T
c.477G>T (p.Val159=)
c.-463+16984C>A (n.-463+16984C>A)
17g.44006589A>CCA399726186NAGS,PYYc.976A>C (p.Ser326Arg)
c.883A>C (p.Ser295Arg)
n.251A>C
c.478A>C (p.Ser160Arg)
c.-463+16983T>G (n.-463+16983T>G)
17g.44006589A>GCA399726188NAGS,PYYc.976A>G (p.Ser326Gly)
c.883A>G (p.Ser295Gly)
n.251A>G
c.478A>G (p.Ser160Gly)
c.-463+16983T>C (n.-463+16983T>C)
17g.44006589A>TCA399726190NAGS,PYYc.976A>T (p.Ser326Cys)
c.883A>T (p.Ser295Cys)
n.251A>T
c.478A>T (p.Ser160Cys)
c.-463+16983T>A (n.-463+16983T>A)
 gnomAD v4
17g.44006590G>ACA399726192NAGS,PYYc.977G>A (p.Ser326Asn)
c.884G>A (p.Ser295Asn)
n.252G>A
c.479G>A (p.Ser160Asn)
c.-463+16982C>T (n.-463+16982C>T)
 dbSNP gnomAD v4
17g.44006590G>CCA399726193NAGS,PYYc.977G>C (p.Ser326Thr)
c.884G>C (p.Ser295Thr)
n.252G>C
c.479G>C (p.Ser160Thr)
c.-463+16982C>G (n.-463+16982C>G)
17g.44006590G=CA2261182205NAGS,PYYc.977G= (p.Ser326=)
c.884G= (p.Ser295=)
n.252G=
c.479G= (p.Ser160=)
c.-463+16982C= (n.-463+16982C=)
17g.44006590G>TCA399726194NAGS,PYYc.977G>T (p.Ser326Ile)
c.884G>T (p.Ser295Ile)
n.252G>T
c.479G>T (p.Ser160Ile)
c.-463+16982C>A (n.-463+16982C>A)
17g.44006591C>ACA399726197NAGS,PYYc.978C>A (p.Ser326Arg)
c.885C>A (p.Ser295Arg)
n.253C>A
c.480C>A (p.Ser160Arg)
c.-463+16981G>T (n.-463+16981G>T)
 gnomAD v4
17g.44006591C>GCA399726198NAGS,PYYc.978C>G (p.Ser326Arg)
c.885C>G (p.Ser295Arg)
n.253C>G
c.480C>G (p.Ser160Arg)
c.-463+16981G>C (n.-463+16981G>C)
17g.44006591C>TCA500241095NAGS,PYYc.978C>T (p.Ser326=)
c.885C>T (p.Ser295=)
n.253C>T
c.480C>T (p.Ser160=)
c.-463+16981G>A (n.-463+16981G>A)
 gnomAD v4 COSMIC
17g.44006592A=CA2261182206NAGS,PYYc.979A= (p.Thr327=)
c.886A= (p.Thr296=)
n.254A=
c.481A= (p.Thr161=)
c.-463+16980T= (n.-463+16980T=)
17g.44006592A>CCA399726203NAGS,PYYc.979A>C (p.Thr327Pro)
c.886A>C (p.Thr296Pro)
n.254A>C
c.481A>C (p.Thr161Pro)
c.-463+16980T>G (n.-463+16980T>G)
 dbSNP gnomAD v3 gnomAD v4
17g.44006592A>GCA399726202NAGS,PYYc.979A>G (p.Thr327Ala)
c.886A>G (p.Thr296Ala)
n.254A>G
c.481A>G (p.Thr161Ala)
c.-463+16980T>C (n.-463+16980T>C)
17g.44006592A>TCA399726200NAGS,PYYc.979A>T (p.Thr327Ser)
c.886A>T (p.Thr296Ser)
n.254A>T
c.481A>T (p.Thr161Ser)
c.-463+16980T>A (n.-463+16980T>A)
17g.44006593C>ACA399726205NAGS,PYYc.980C>A (p.Thr327Lys)
c.887C>A (p.Thr296Lys)
n.255C>A
c.482C>A (p.Thr161Lys)
c.-463+16979G>T (n.-463+16979G>T)
17g.44006593C>GCA399726207NAGS,PYYc.980C>G (p.Thr327Arg)
c.887C>G (p.Thr296Arg)
n.255C>G
c.482C>G (p.Thr161Arg)
c.-463+16979G>C (n.-463+16979G>C)
17g.44006593C>TCA399726208NAGS,PYYc.980C>T (p.Thr327Ile)
c.887C>T (p.Thr296Ile)
n.255C>T
c.482C>T (p.Thr161Ile)
c.-463+16979G>A (n.-463+16979G>A)
 gnomAD v4
17g.44006594A=CA2261182207NAGS,PYYc.981A= (p.Thr327=)
c.888A= (p.Thr296=)
n.256A=
c.483A= (p.Thr161=)
c.-463+16978T= (n.-463+16978T=)
17g.44006594A>CCA500241096NAGS,PYYc.981A>C (p.Thr327=)
c.888A>C (p.Thr296=)
n.256A>C
c.483A>C (p.Thr161=)
c.-463+16978T>G (n.-463+16978T>G)
17g.44006594A>GCA500241097NAGS,PYYc.981A>G (p.Thr327=)
c.888A>G (p.Thr296=)
n.256A>G
c.483A>G (p.Thr161=)
c.-463+16978T>C (n.-463+16978T>C)
17g.44006594A>TCA500241098NAGS,PYYc.981A>T (p.Thr327=)
c.888A>T (p.Thr296=)
n.256A>T
c.483A>T (p.Thr161=)
c.-463+16978T>A (n.-463+16978T>A)
 dbSNP gnomAD v2 gnomAD v4
17g.44006595A=CA2261182208NAGS,PYYc.982A= (p.Lys328=)
c.889A= (p.Lys297=)
n.257A=
c.484A= (p.Lys162=)
c.-463+16977T= (n.-463+16977T=)
17g.44006595A>CCA399726210NAGS,PYYc.982A>C (p.Lys328Gln)
c.889A>C (p.Lys297Gln)
n.257A>C
c.484A>C (p.Lys162Gln)
c.-463+16977T>G (n.-463+16977T>G)
17g.44006595A>GCA399726211NAGS,PYYc.982A>G (p.Lys328Glu)
c.889A>G (p.Lys297Glu)
n.257A>G
c.484A>G (p.Lys162Glu)
c.-463+16977T>C (n.-463+16977T>C)
 dbSNP gnomAD v4
17g.44006595A>TCA399726212NAGS,PYYc.982A>T (p.Lys328Ter)
c.889A>T (p.Lys297Ter)
n.257A>T
c.484A>T (p.Lys162Ter)
c.-463+16977T>A (n.-463+16977T>A)
17g.44006596A>CCA399726215NAGS,PYYc.983A>C (p.Lys328Thr)
c.890A>C (p.Lys297Thr)
n.258A>C
c.485A>C (p.Lys162Thr)
c.-463+16976T>G (n.-463+16976T>G)
17g.44006596A>GCA399726216NAGS,PYYc.983A>G (p.Lys328Arg)
c.890A>G (p.Lys297Arg)
n.258A>G
c.485A>G (p.Lys162Arg)
c.-463+16976T>C (n.-463+16976T>C)
17g.44006596A>TCA399726218NAGS,PYYc.983A>T (p.Lys328Ile)
c.890A>T (p.Lys297Ile)
n.258A>T
c.485A>T (p.Lys162Ile)
c.-463+16976T>A (n.-463+16976T>A)
17g.44006597A>CCA399726219NAGS,PYYc.984A>C (p.Lys328Asn)
c.891A>C (p.Lys297Asn)
n.259A>C
c.486A>C (p.Lys162Asn)
c.-463+16975T>G (n.-463+16975T>G)
 ClinVar
17g.44006597A>GCA500241099NAGS,PYYc.984A>G (p.Lys328=)
c.891A>G (p.Lys297=)
n.259A>G
c.486A>G (p.Lys162=)
c.-463+16975T>C (n.-463+16975T>C)
17g.44006597A>TCA399726221NAGS,PYYc.984A>T (p.Lys328Asn)
c.891A>T (p.Lys297Asn)
n.259A>T
c.486A>T (p.Lys162Asn)
c.-463+16975T>A (n.-463+16975T>A)
 gnomAD v4
17g.44006598G>ACA399726225NAGS,PYYc.985G>A (p.Glu329Lys)
c.892G>A (p.Glu298Lys)
n.260G>A
c.487G>A (p.Glu163Lys)
c.-463+16974C>T (n.-463+16974C>T)
17g.44006598G>CCA399726223NAGS,PYYc.985G>C (p.Glu329Gln)
c.892G>C (p.Glu298Gln)
n.260G>C
c.487G>C (p.Glu163Gln)
c.-463+16974C>G (n.-463+16974C>G)
17g.44006598G>TCA399726222NAGS,PYYc.985G>T (p.Glu329Ter)
c.892G>T (p.Glu298Ter)
n.260G>T
c.487G>T (p.Glu163Ter)
c.-463+16974C>A (n.-463+16974C>A)
 gnomAD v4
17g.44006599A>CCA399726226NAGS,PYYc.986A>C (p.Glu329Ala)
c.893A>C (p.Glu298Ala)
n.261A>C
c.488A>C (p.Glu163Ala)
c.-463+16973T>G (n.-463+16973T>G)
17g.44006599A>GCA399726228NAGS,PYYc.986A>G (p.Glu329Gly)
c.893A>G (p.Glu298Gly)
n.261A>G
c.488A>G (p.Glu163Gly)
c.-463+16973T>C (n.-463+16973T>C)
17g.44006599A>TCA399726230NAGS,PYYc.986A>T (p.Glu329Val)
c.893A>T (p.Glu298Val)
n.261A>T
c.488A>T (p.Glu163Val)
c.-463+16973T>A (n.-463+16973T>A)
17g.44006600A>CCA399726232NAGS,PYYc.987A>C (p.Glu329Asp)
c.894A>C (p.Glu298Asp)
n.262A>C
c.489A>C (p.Glu163Asp)
c.-463+16972T>G (n.-463+16972T>G)
17g.44006600A>GCA500241100NAGS,PYYc.987A>G (p.Glu329=)
c.894A>G (p.Glu298=)
n.262A>G
c.489A>G (p.Glu163=)
c.-463+16972T>C (n.-463+16972T>C)
17g.44006600A>TCA399726233NAGS,PYYc.987A>T (p.Glu329Asp)
c.894A>T (p.Glu298Asp)
n.262A>T
c.489A>T (p.Glu163Asp)
c.-463+16972T>A (n.-463+16972T>A)
17g.44006601C>ACA500241101NAGS,PYYc.988C>A (p.Arg330=)
c.895C>A (p.Arg299=)
n.263C>A
c.490C>A (p.Arg164=)
c.-463+16971G>T (n.-463+16971G>T)
17g.44006601C=CA2261182209NAGS,PYYc.988C= (p.Arg330=)
c.895C= (p.Arg299=)
n.263C=
c.490C= (p.Arg164=)
c.-463+16971G= (n.-463+16971G=)
17g.44006601C>GCA399726235NAGS,PYYc.988C>G (p.Arg330Gly)
c.895C>G (p.Arg299Gly)
n.263C>G
c.490C>G (p.Arg164Gly)
c.-463+16971G>C (n.-463+16971G>C)
17g.44006601C>TCA8595288NAGS,PYYc.988C>T (p.Arg330Trp)
c.895C>T (p.Arg299Trp)
n.263C>T
c.490C>T (p.Arg164Trp)
c.-463+16971G>A (n.-463+16971G>A)
 dbSNP ExAC gnomAD v2 gnomAD v4
17g.44006602G>ACA399726238NAGS,PYYc.989G>A (p.Arg330Gln)
c.896G>A (p.Arg299Gln)
n.264G>A
c.491G>A (p.Arg164Gln)
c.-463+16970C>T (n.-463+16970C>T)
 dbSNP gnomAD v3 gnomAD v4
17g.44006602G>CCA399726240NAGS,PYYc.989G>C (p.Arg330Pro)
c.896G>C (p.Arg299Pro)
n.264G>C
c.491G>C (p.Arg164Pro)
c.-463+16970C>G (n.-463+16970C>G)
 dbSNP gnomAD v2 gnomAD v4
17g.44006602G=CA2261182210NAGS,PYYc.989G= (p.Arg330=)
c.896G= (p.Arg299=)
n.264G=
c.491G= (p.Arg164=)
c.-463+16970C= (n.-463+16970C=)
17g.44006602G>TCA399726242NAGS,PYYc.989G>T (p.Arg330Leu)
c.896G>T (p.Arg299Leu)
n.264G>T
c.491G>T (p.Arg164Leu)
c.-463+16970C>A (n.-463+16970C>A)
 gnomAD v4
17g.44006603G>ACA500241102NAGS,PYYc.990G>A (p.Arg330=)
c.897G>A (p.Arg299=)
n.265G>A
c.492G>A (p.Arg164=)
c.-463+16969C>T (n.-463+16969C>T)
17g.44006603G>CCA500241103NAGS,PYYc.990G>C (p.Arg330=)
c.897G>C (p.Arg299=)
n.265G>C
c.492G>C (p.Arg164=)
c.-463+16969C>G (n.-463+16969C>G)
17g.44006603G>TCA500241104NAGS,PYYc.990G>T (p.Arg330=)
c.897G>T (p.Arg299=)
n.265G>T
c.492G>T (p.Arg164=)
c.-463+16969C>A (n.-463+16969C>A)
 gnomAD v4
17g.44006604C>ACA399726244NAGS,PYYc.991C>A (p.Gln331Lys)
c.898C>A (p.Gln300Lys)
n.266C>A
c.493C>A (p.Gln165Lys)
c.-463+16968G>T (n.-463+16968G>T)
17g.44006604C=CA2261182211NAGS,PYYc.991C= (p.Gln331=)
c.898C= (p.Gln300=)
n.266C=
c.493C= (p.Gln165=)
c.-463+16968G= (n.-463+16968G=)
17g.44006604C>GCA399726245NAGS,PYYc.991C>G (p.Gln331Glu)
c.898C>G (p.Gln300Glu)
n.266C>G
c.493C>G (p.Gln165Glu)
c.-463+16968G>C (n.-463+16968G>C)
17g.44006604C>TCA399726246NAGS,PYYc.991C>T (p.Gln331Ter)
c.898C>T (p.Gln300Ter)
n.266C>T
c.493C>T (p.Gln165Ter)
c.-463+16968G>A (n.-463+16968G>A)
 dbSNP gnomAD v2 gnomAD v4
17g.44006605A>CCA399726252NAGS,PYYc.992A>C (p.Gln331Pro)
c.899A>C (p.Gln300Pro)
n.267A>C
c.494A>C (p.Gln165Pro)
c.-463+16967T>G (n.-463+16967T>G)
17g.44006605A>GCA399726250NAGS,PYYc.992A>G (p.Gln331Arg)
c.899A>G (p.Gln300Arg)
n.267A>G
c.494A>G (p.Gln165Arg)
c.-463+16967T>C (n.-463+16967T>C)
 gnomAD v4
17g.44006605A>TCA399726249NAGS,PYYc.992A>T (p.Gln331Leu)
c.899A>T (p.Gln300Leu)
n.267A>T
c.494A>T (p.Gln165Leu)
c.-463+16967T>A (n.-463+16967T>A)
17g.44006606G>ACA500241105NAGS,PYYc.993G>A (p.Gln331=)
c.900G>A (p.Gln300=)
n.268G>A
c.495G>A (p.Gln165=)
c.-463+16966C>T (n.-463+16966C>T)
 dbSNP gnomAD v4
17g.44006606G>CCA399726255NAGS,PYYc.993G>C (p.Gln331His)
c.900G>C (p.Gln300His)
n.268G>C
c.495G>C (p.Gln165His)
c.-463+16966C>G (n.-463+16966C>G)
17g.44006606G=CA2261182212NAGS,PYYc.993G= (p.Gln331=)
c.900G= (p.Gln300=)
n.268G=
c.495G= (p.Gln165=)
c.-463+16966C= (n.-463+16966C=)
17g.44006606G>TCA399726253NAGS,PYYc.993G>T (p.Gln331His)
c.900G>T (p.Gln300His)
n.268G>T
c.495G>T (p.Gln165His)
c.-463+16966C>A (n.-463+16966C>A)
17g.44006607C>ACA399726257NAGS,PYYc.994C>A (p.Gln332Lys)
c.901C>A (p.Gln301Lys)
n.269C>A
c.496C>A (p.Gln166Lys)
c.-463+16965G>T (n.-463+16965G>T)
 gnomAD v4
17g.44006607C=CA2261182213NAGS,PYYc.994C= (p.Gln332=)
c.901C= (p.Gln301=)
n.269C=
c.496C= (p.Gln166=)
c.-463+16965G= (n.-463+16965G=)
17g.44006607C>GCA8595289NAGS,PYYc.994C>G (p.Gln332Glu)
c.901C>G (p.Gln301Glu)
n.269C>G
c.496C>G (p.Gln166Glu)
c.-463+16965G>C (n.-463+16965G>C)
 dbSNP ExAC gnomAD v2 gnomAD v4
17g.44006607C>TCA399726259NAGS,PYYc.994C>T (p.Gln332Ter)
c.901C>T (p.Gln301Ter)
n.269C>T
c.496C>T (p.Gln166Ter)
c.-463+16965G>A (n.-463+16965G>A)
17g.44006608A>CCA399726261NAGS,PYYc.995A>C (p.Gln332Pro)
c.902A>C (p.Gln301Pro)
n.270A>C
c.497A>C (p.Gln166Pro)
c.-463+16964T>G (n.-463+16964T>G)
 gnomAD v4
17g.44006608A>GCA399726263NAGS,PYYc.995A>G (p.Gln332Arg)
c.902A>G (p.Gln301Arg)
n.270A>G
c.497A>G (p.Gln166Arg)
c.-463+16964T>C (n.-463+16964T>C)
 dbSNP
17g.44006608A>TCA399726264NAGS,PYYc.995A>T (p.Gln332Leu)
c.902A>T (p.Gln301Leu)
n.270A>T
c.497A>T (p.Gln166Leu)
c.-463+16964T>A (n.-463+16964T>A)
17g.44006609G>ACA500241106NAGS,PYYc.996G>A (p.Gln332=)
c.903G>A (p.Gln301=)
n.271G>A
c.498G>A (p.Gln166=)
c.-463+16963C>T (n.-463+16963C>T)
17g.44006609G>CCA399726266NAGS,PYYc.996G>C (p.Gln332His)
c.903G>C (p.Gln301His)
n.271G>C
c.498G>C (p.Gln166His)
c.-463+16963C>G (n.-463+16963C>G)
17g.44006609G>TCA399726265NAGS,PYYc.996G>T (p.Gln332His)
c.903G>T (p.Gln301His)
n.271G>T
c.498G>T (p.Gln166His)
c.-463+16963C>A (n.-463+16963C>A)
17g.44006610A=CA2261182214NAGS,PYYc.997A= (p.Met333=)
c.904A= (p.Met302=)
n.272A=
c.499A= (p.Met167=)
c.-463+16962T= (n.-463+16962T=)
17g.44006610A>CCA399726267NAGS,PYYc.997A>C (p.Met333Leu)
c.904A>C (p.Met302Leu)
n.272A>C
c.499A>C (p.Met167Leu)
c.-463+16962T>G (n.-463+16962T>G)
17g.44006610A>GCA399726268NAGS,PYYc.997A>G (p.Met333Val)
c.904A>G (p.Met302Val)
n.272A>G
c.499A>G (p.Met167Val)
c.-463+16962T>C (n.-463+16962T>C)
17g.44006610A>TCA399726269NAGS,PYYc.997A>T (p.Met333Leu)
c.904A>T (p.Met302Leu)
n.272A>T
c.499A>T (p.Met167Leu)
c.-463+16962T>A (n.-463+16962T>A)
 dbSNP
17g.44006611T>ACA399726270NAGS,PYYc.998T>A (p.Met333Lys)
c.905T>A (p.Met302Lys)
n.273T>A
c.500T>A (p.Met167Lys)
c.-463+16961A>T (n.-463+16961A>T)
17g.44006611T>CCA399726271NAGS,PYYc.998T>C (p.Met333Thr)
c.905T>C (p.Met302Thr)
n.273T>C
c.500T>C (p.Met167Thr)
c.-463+16961A>G (n.-463+16961A>G)
17g.44006611T>GCA399726272NAGS,PYYc.998T>G (p.Met333Arg)
c.905T>G (p.Met302Arg)
n.273T>G
c.500T>G (p.Met167Arg)
c.-463+16961A>C (n.-463+16961A>C)
17g.44006611_44006629delCA2739267562NAGS,PYYc.998_1016del (p.Met333SerfsTer?)
c.905_923del (p.Met302SerfsTer?)
n.273_291del
c.500_518del (p.Met167SerfsTer?)
c.-463+16943_-463+16961del (n.-463+16943_-463+16961del)
 ClinVar
17g.44006612G>ACA399726273NAGS,PYYc.999G>A (p.Met333Ile)
c.906G>A (p.Met302Ile)
n.274G>A
c.501G>A (p.Met167Ile)
c.-463+16960C>T (n.-463+16960C>T)
17g.44006612G>CCA399726275NAGS,PYYc.999G>C (p.Met333Ile)
c.906G>C (p.Met302Ile)
n.274G>C
c.501G>C (p.Met167Ile)
c.-463+16960C>G (n.-463+16960C>G)
17g.44006612G>TCA399726274NAGS,PYYc.999G>T (p.Met333Ile)
c.906G>T (p.Met302Ile)
n.274G>T
c.501G>T (p.Met167Ile)
c.-463+16960C>A (n.-463+16960C>A)
17g.44006613C>ACA8595290NAGS,PYYc.1000C>A (p.Arg334=)
c.907C>A (p.Arg303=)
n.275C>A
c.502C>A (p.Arg168=)
c.-463+16959G>T (n.-463+16959G>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.44006613C=CA2261182215NAGS,PYYc.1000C= (p.Arg334=)
c.907C= (p.Arg303=)
n.275C=
c.502C= (p.Arg168=)
c.-463+16959G= (n.-463+16959G=)
17g.44006613C>GCA399726276NAGS,PYYc.1000C>G (p.Arg334Gly)
c.907C>G (p.Arg303Gly)
n.275C>G
c.502C>G (p.Arg168Gly)
c.-463+16959G>C (n.-463+16959G>C)
 dbSNP gnomAD v4
17g.44006613C>TCA399726277NAGS,PYYc.1000C>T (p.Arg334Trp)
c.907C>T (p.Arg303Trp)
n.275C>T
c.502C>T (p.Arg168Trp)
c.-463+16959G>A (n.-463+16959G>A)
 gnomAD v4
17g.44006614G>ACA8595291NAGS,PYYc.1001G>A (p.Arg334Gln)
c.908G>A (p.Arg303Gln)
n.276G>A
c.503G>A (p.Arg168Gln)
c.-463+16958C>T (n.-463+16958C>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
17g.44006614G>CCA399726278NAGS,PYYc.1001G>C (p.Arg334Pro)
c.908G>C (p.Arg303Pro)
n.276G>C
c.503G>C (p.Arg168Pro)
c.-463+16958C>G (n.-463+16958C>G)
17g.44006614G=CA2261182216NAGS,PYYc.1001G= (p.Arg334=)
c.908G= (p.Arg303=)
n.276G=
c.503G= (p.Arg168=)
c.-463+16958C= (n.-463+16958C=)
17g.44006614G>TCA399726279NAGS,PYYc.1001G>T (p.Arg334Leu)
c.908G>T (p.Arg303Leu)
n.276G>T
c.503G>T (p.Arg168Leu)
c.-463+16958C>A (n.-463+16958C>A)
17g.44006615G>ACA500241108NAGS,PYYc.1002G>A (p.Arg334=)
c.909G>A (p.Arg303=)
n.277G>A
c.504G>A (p.Arg168=)
c.-463+16957C>T (n.-463+16957C>T)
 gnomAD v4
17g.44006615G>CCA500241109NAGS,PYYc.1002G>C (p.Arg334=)
c.909G>C (p.Arg303=)
n.277G>C
c.504G>C (p.Arg168=)
c.-463+16957C>G (n.-463+16957C>G)
17g.44006615G>TCA500241110NAGS,PYYc.1002G>T (p.Arg334=)
c.909G>T (p.Arg303=)
n.277G>T
c.504G>T (p.Arg168=)
c.-463+16957C>A (n.-463+16957C>A)
 gnomAD v4
17g.44006616C>ACA399726282NAGS,PYYc.1003C>A (p.Leu335Ile)
c.910C>A (p.Leu304Ile)
n.278C>A
c.505C>A (p.Leu169Ile)
c.-463+16956G>T (n.-463+16956G>T)
17g.44006616C=CA2261182217NAGS,PYYc.1003C= (p.Leu335=)
c.910C= (p.Leu304=)
n.278C=
c.505C= (p.Leu169=)
c.-463+16956G= (n.-463+16956G=)
17g.44006616C>GCA399726283NAGS,PYYc.1003C>G (p.Leu335Val)
c.910C>G (p.Leu304Val)
n.278C>G
c.505C>G (p.Leu169Val)
c.-463+16956G>C (n.-463+16956G>C)
17g.44006616C>TCA8595292NAGS,PYYc.1003C>T (p.Leu335Phe)
c.910C>T (p.Leu304Phe)
n.278C>T
c.505C>T (p.Leu169Phe)
c.-463+16956G>A (n.-463+16956G>A)
 dbSNP ExAC gnomAD v2 gnomAD v4
17g.44006617T>ACA399726285NAGS,PYYc.1004T>A (p.Leu335His)
c.911T>A (p.Leu304His)
n.279T>A
c.506T>A (p.Leu169His)
c.-463+16955A>T (n.-463+16955A>T)
17g.44006617T>CCA399726286NAGS,PYYc.1004T>C (p.Leu335Pro)
c.911T>C (p.Leu304Pro)
n.279T>C
c.506T>C (p.Leu169Pro)
c.-463+16955A>G (n.-463+16955A>G)
17g.44006617T>GCA399726288NAGS,PYYc.1004T>G (p.Leu335Arg)
c.911T>G (p.Leu304Arg)
n.279T>G
c.506T>G (p.Leu169Arg)
c.-463+16955A>C (n.-463+16955A>C)
17g.44006618C>ACA500241111NAGS,PYYc.1005C>A (p.Leu335=)
c.912C>A (p.Leu304=)
n.280C>A
c.507C>A (p.Leu169=)
c.-463+16954G>T (n.-463+16954G>T)
17g.44006618C=CA2261182218NAGS,PYYc.1005C= (p.Leu335=)
c.912C= (p.Leu304=)
n.280C=
c.507C= (p.Leu169=)
c.-463+16954G= (n.-463+16954G=)
17g.44006618C>GCA500241113NAGS,PYYc.1005C>G (p.Leu335=)
c.912C>G (p.Leu304=)
n.280C>G
c.507C>G (p.Leu169=)
c.-463+16954G>C (n.-463+16954G>C)
17g.44006618C>TCA500241112NAGS,PYYc.1005C>T (p.Leu335=)
c.912C>T (p.Leu304=)
n.280C>T
c.507C>T (p.Leu169=)
c.-463+16954G>A (n.-463+16954G>A)
 dbSNP gnomAD v3 gnomAD v4
17g.44006619A>CCA399726290NAGS,PYYc.1006A>C (p.Ile336Leu)
c.913A>C (p.Ile305Leu)
n.281A>C
c.508A>C (p.Ile170Leu)
c.-463+16953T>G (n.-463+16953T>G)
17g.44006619A>GCA399726293NAGS,PYYc.1006A>G (p.Ile336Val)
c.913A>G (p.Ile305Val)
n.281A>G
c.508A>G (p.Ile170Val)
c.-463+16953T>C (n.-463+16953T>C)
17g.44006619A>TCA399726292NAGS,PYYc.1006A>T (p.Ile336Phe)
c.913A>T (p.Ile305Phe)
n.281A>T
c.508A>T (p.Ile170Phe)
c.-463+16953T>A (n.-463+16953T>A)
 gnomAD v4
17g.44006620T>ACA399726295NAGS,PYYc.1007T>A (p.Ile336Asn)
c.914T>A (p.Ile305Asn)
n.282T>A
c.509T>A (p.Ile170Asn)
c.-463+16952A>T (n.-463+16952A>T)
17g.44006620T>CCA399726296NAGS,PYYc.1007T>C (p.Ile336Thr)
c.914T>C (p.Ile305Thr)
n.282T>C
c.509T>C (p.Ile170Thr)
c.-463+16952A>G (n.-463+16952A>G)
17g.44006620T>GCA399726298NAGS,PYYc.1007T>G (p.Ile336Ser)
c.914T>G (p.Ile305Ser)
n.282T>G
c.509T>G (p.Ile170Ser)
c.-463+16952A>C (n.-463+16952A>C)
17g.44006621C>ACA500241116NAGS,PYYc.1008C>A (p.Ile336=)
c.915C>A (p.Ile305=)
n.283C>A
c.510C>A (p.Ile170=)
c.-463+16951G>T (n.-463+16951G>T)
17g.44006621C=CA2261182219NAGS,PYYc.1008C= (p.Ile336=)
c.915C= (p.Ile305=)
n.283C=
c.510C= (p.Ile170=)
c.-463+16951G= (n.-463+16951G=)
17g.44006621C>GCA399726300NAGS,PYYc.1008C>G (p.Ile336Met)
c.915C>G (p.Ile305Met)
n.283C>G
c.510C>G (p.Ile170Met)
c.-463+16951G>C (n.-463+16951G>C)
 dbSNP
17g.44006621C>TCA500241115NAGS,PYYc.1008C>T (p.Ile336=)
c.915C>T (p.Ile305=)
n.283C>T
c.510C>T (p.Ile170=)
c.-463+16951G>A (n.-463+16951G>A)
 ClinVar dbSNP gnomAD v3 gnomAD v4
17g.44006622G>ACA399726302NAGS,PYYc.1009G>A (p.Val337Met)
c.916G>A (p.Val306Met)
n.284G>A
c.511G>A (p.Val171Met)
c.-463+16950C>T (n.-463+16950C>T)
 dbSNP gnomAD v2 gnomAD v4
17g.44006622G>CCA399726303NAGS,PYYc.1009G>C (p.Val337Leu)
c.916G>C (p.Val306Leu)
n.284G>C
c.511G>C (p.Val171Leu)
c.-463+16950C>G (n.-463+16950C>G)
17g.44006622G=CA2261182220NAGS,PYYc.1009G= (p.Val337=)
c.916G= (p.Val306=)
n.284G=
c.511G= (p.Val171=)
c.-463+16950C= (n.-463+16950C=)
17g.44006622G>TCA399726305NAGS,PYYc.1009G>T (p.Val337Leu)
c.916G>T (p.Val306Leu)
n.284G>T
c.511G>T (p.Val171Leu)
c.-463+16950C>A (n.-463+16950C>A)
 gnomAD v4 COSMIC
17g.44006623T>ACA399726307NAGS,PYYc.1010T>A (p.Val337Glu)
c.917T>A (p.Val306Glu)
n.285T>A
c.512T>A (p.Val171Glu)
c.-463+16949A>T (n.-463+16949A>T)
17g.44006623T>CCA399726308NAGS,PYYc.1010T>C (p.Val337Ala)
c.917T>C (p.Val306Ala)
n.285T>C
c.512T>C (p.Val171Ala)
c.-463+16949A>G (n.-463+16949A>G)
 dbSNP gnomAD v2 gnomAD v4
17g.44006623T>GCA399726310NAGS,PYYc.1010T>G (p.Val337Gly)
c.917T>G (p.Val306Gly)
n.285T>G
c.512T>G (p.Val171Gly)
c.-463+16949A>C (n.-463+16949A>C)
17g.44006623T=CA2261182221NAGS,PYYc.1010T= (p.Val337=)
c.917T= (p.Val306=)
n.285T=
c.512T= (p.Val171=)
c.-463+16949A= (n.-463+16949A=)
17g.44006624G>ACA500241117NAGS,PYYc.1011G>A (p.Val337=)
c.918G>A (p.Val306=)
n.286G>A
c.513G>A (p.Val171=)
c.-463+16948C>T (n.-463+16948C>T)
17g.44006624G>CCA500241119NAGS,PYYc.1011G>C (p.Val337=)
c.918G>C (p.Val306=)
n.286G>C
c.513G>C (p.Val171=)
c.-463+16948C>G (n.-463+16948C>G)
 dbSNP
17g.44006624G=CA2261182222NAGS,PYYc.1011G= (p.Val337=)
c.918G= (p.Val306=)
n.286G=
c.513G= (p.Val171=)
c.-463+16948C= (n.-463+16948C=)
17g.44006624G>TCA500241118NAGS,PYYc.1011G>T (p.Val337=)
c.918G>T (p.Val306=)
n.286G>T
c.513G>T (p.Val171=)
c.-463+16948C>A (n.-463+16948C>A)
17g.44006625G>ACA399726312NAGS,PYYc.1012G>A (p.Asp338Asn)
c.919G>A (p.Asp307Asn)
n.287G>A
c.514G>A (p.Asp172Asn)
c.-463+16947C>T (n.-463+16947C>T)
17g.44006625G>CCA399726314NAGS,PYYc.1012G>C (p.Asp338His)
c.919G>C (p.Asp307His)
n.287G>C
c.514G>C (p.Asp172His)
c.-463+16947C>G (n.-463+16947C>G)
 gnomAD v4
17g.44006625G>TCA399726315NAGS,PYYc.1012G>T (p.Asp338Tyr)
c.919G>T (p.Asp307Tyr)
n.287G>T
c.514G>T (p.Asp172Tyr)
c.-463+16947C>A (n.-463+16947C>A)
17g.44006626A>CCA399726316NAGS,PYYc.1013A>C (p.Asp338Ala)
c.920A>C (p.Asp307Ala)
n.288A>C
c.515A>C (p.Asp172Ala)
c.-463+16946T>G (n.-463+16946T>G)
17g.44006626A>GCA399726320NAGS,PYYc.1013A>G (p.Asp338Gly)
c.920A>G (p.Asp307Gly)
n.288A>G
c.515A>G (p.Asp172Gly)
c.-463+16946T>C (n.-463+16946T>C)
17g.44006626A>TCA399726318NAGS,PYYc.1013A>T (p.Asp338Val)
c.920A>T (p.Asp307Val)
n.288A>T
c.515A>T (p.Asp172Val)
c.-463+16946T>A (n.-463+16946T>A)
17g.44006627C>ACA399726322NAGS,PYYc.1014C>A (p.Asp338Glu)
c.921C>A (p.Asp307Glu)
n.289C>A
c.516C>A (p.Asp172Glu)
c.-463+16945G>T (n.-463+16945G>T)
 dbSNP gnomAD v3 gnomAD v4
17g.44006627C>GCA399726323NAGS,PYYc.1014C>G (p.Asp338Glu)
c.921C>G (p.Asp307Glu)
n.289C>G
c.516C>G (p.Asp172Glu)
c.-463+16945G>C (n.-463+16945G>C)
17g.44006627C>TCA500241120NAGS,PYYc.1014C>T (p.Asp338=)
c.921C>T (p.Asp307=)
n.289C>T
c.516C>T (p.Asp172=)
c.-463+16945G>A (n.-463+16945G>A)
17g.44006628G>ACA399726324NAGS,PYYc.1015G>A (p.Val339Met)
c.922G>A (p.Val308Met)
n.290G>A
c.517G>A (p.Val173Met)
c.-463+16944C>T (n.-463+16944C>T)
 dbSNP gnomAD v4
17g.44006628G>CCA399726326NAGS,PYYc.1015G>C (p.Val339Leu)
c.922G>C (p.Val308Leu)
n.290G>C
c.517G>C (p.Val173Leu)
c.-463+16944C>G (n.-463+16944C>G)
17g.44006628G=CA2261182223NAGS,PYYc.1015G= (p.Val339=)
c.922G= (p.Val308=)
n.290G=
c.517G= (p.Val173=)
c.-463+16944C= (n.-463+16944C=)
17g.44006628G>TCA8595293NAGS,PYYc.1015G>T (p.Val339Leu)
c.922G>T (p.Val308Leu)
n.290G>T
c.517G>T (p.Val173Leu)
c.-463+16944C>A (n.-463+16944C>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.44006629T>ACA399726329NAGS,PYYc.1016T>A (p.Val339Glu)
c.923T>A (p.Val308Glu)
n.291T>A
c.518T>A (p.Val173Glu)
c.-463+16943A>T (n.-463+16943A>T)
17g.44006629T>CCA399726330NAGS,PYYc.1016T>C (p.Val339Ala)
c.923T>C (p.Val308Ala)
n.291T>C
c.518T>C (p.Val173Ala)
c.-463+16943A>G (n.-463+16943A>G)
17g.44006629T>GCA399726331NAGS,PYYc.1016T>G (p.Val339Gly)
c.923T>G (p.Val308Gly)
n.291T>G
c.518T>G (p.Val173Gly)
c.-463+16943A>C (n.-463+16943A>C)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.44006629T=CA2261182224NAGS,PYYc.1016T= (p.Val339=)
c.923T= (p.Val308=)
n.291T=
c.518T= (p.Val173=)
c.-463+16943A= (n.-463+16943A=)
17g.44006630G>ACA500241121NAGS,PYYc.1017G>A (p.Val339=)
c.924G>A (p.Val308=)
n.292G>A
c.519G>A (p.Val173=)
c.-463+16942C>T (n.-463+16942C>T)
 gnomAD v4
17g.44006630G>CCA500241122NAGS,PYYc.1017G>C (p.Val339=)
c.924G>C (p.Val308=)
n.292G>C
c.519G>C (p.Val173=)
c.-463+16942C>G (n.-463+16942C>G)
 gnomAD v4
17g.44006630G=CA2261182225NAGS,PYYc.1017G= (p.Val339=)
c.924G= (p.Val308=)
n.292G=
c.519G= (p.Val173=)
c.-463+16942C= (n.-463+16942C=)
17g.44006630G>TCA500241123NAGS,PYYc.1017G>T (p.Val339=)
c.924G>T (p.Val308=)
n.292G>T
c.519G>T (p.Val173=)
c.-463+16942C>A (n.-463+16942C>A)
 dbSNP
17g.44006631C>ACA399726332NAGS,PYYc.1018C>A (p.Leu340Ile)
c.925C>A (p.Leu309Ile)
n.293C>A
c.520C>A (p.Leu174Ile)
c.-463+16941G>T (n.-463+16941G>T)
17g.44006631C>GCA399726333NAGS,PYYc.1018C>G (p.Leu340Val)
c.925C>G (p.Leu309Val)
n.293C>G
c.520C>G (p.Leu174Val)
c.-463+16941G>C (n.-463+16941G>C)
17g.44006631C>TCA399726335NAGS,PYYc.1018C>T (p.Leu340Phe)
c.925C>T (p.Leu309Phe)
n.293C>T
c.520C>T (p.Leu174Phe)
c.-463+16941G>A (n.-463+16941G>A)
 ClinVar dbSNP
17g.44006632T>ACA399726337NAGS,PYYc.1019T>A (p.Leu340His)
c.926T>A (p.Leu309His)
n.294T>A
c.521T>A (p.Leu174His)
c.-463+16940A>T (n.-463+16940A>T)
17g.44006632T>CCA399726338NAGS,PYYc.1019T>C (p.Leu340Pro)
c.926T>C (p.Leu309Pro)
n.294T>C
c.521T>C (p.Leu174Pro)
c.-463+16940A>G (n.-463+16940A>G)
17g.44006632T>GCA399726336NAGS,PYYc.1019T>G (p.Leu340Arg)
c.926T>G (p.Leu309Arg)
n.294T>G
c.521T>G (p.Leu174Arg)
c.-463+16940A>C (n.-463+16940A>C)
17g.44006633C>ACA500241124NAGS,PYYc.1020C>A (p.Leu340=)
c.927C>A (p.Leu309=)
n.295C>A
c.522C>A (p.Leu174=)
c.-463+16939G>T (n.-463+16939G>T)
17g.44006633C>GCA500241125NAGS,PYYc.1020C>G (p.Leu340=)
c.927C>G (p.Leu309=)
n.295C>G
c.522C>G (p.Leu174=)
c.-463+16939G>C (n.-463+16939G>C)
17g.44006633C>TCA500241126NAGS,PYYc.1020C>T (p.Leu340=)
c.927C>T (p.Leu309=)
n.295C>T
c.522C>T (p.Leu174=)
c.-463+16939G>A (n.-463+16939G>A)
 gnomAD v4
17g.44006634A=CA2261182226NAGS,PYYc.1021A= (p.Ser341=)
c.928A= (p.Ser310=)
n.296A=
c.523A= (p.Ser175=)
c.-463+16938T= (n.-463+16938T=)
17g.44006634A>CCA399726340NAGS,PYYc.1021A>C (p.Ser341Arg)
c.928A>C (p.Ser310Arg)
n.296A>C
c.523A>C (p.Ser175Arg)
c.-463+16938T>G (n.-463+16938T>G)
17g.44006634A>GCA399726343NAGS,PYYc.1021A>G (p.Ser341Gly)
c.928A>G (p.Ser310Gly)
n.296A>G
c.523A>G (p.Ser175Gly)
c.-463+16938T>C (n.-463+16938T>C)
17g.44006634A>TCA8595294NAGS,PYYc.1021A>T (p.Ser341Cys)
c.928A>T (p.Ser310Cys)
n.296A>T
c.523A>T (p.Ser175Cys)
c.-463+16938T>A (n.-463+16938T>A)
 dbSNP ExAC gnomAD v2 gnomAD v4
17g.44006635G>ACA399726345NAGS,PYYc.1022G>A (p.Ser341Asn)
c.929G>A (p.Ser310Asn)
n.297G>A
c.524G>A (p.Ser175Asn)
c.-463+16937C>T (n.-463+16937C>T)
17g.44006635G>CCA399726347NAGS,PYYc.1022G>C (p.Ser341Thr)
c.929G>C (p.Ser310Thr)
n.297G>C
c.524G>C (p.Ser175Thr)
c.-463+16937C>G (n.-463+16937C>G)
 dbSNP
17g.44006635G=CA2261182227NAGS,PYYc.1022G= (p.Ser341=)
c.929G= (p.Ser310=)
n.297G=
c.524G= (p.Ser175=)
c.-463+16937C= (n.-463+16937C=)
17g.44006635G>TCA8595295NAGS,PYYc.1022G>T (p.Ser341Ile)
c.929G>T (p.Ser310Ile)
n.297G>T
c.524G>T (p.Ser175Ile)
c.-463+16937C>A (n.-463+16937C>A)
 dbSNP ExAC gnomAD v2 gnomAD v4
17g.44006636C>ACA399726349NAGS,PYYc.1023C>A (p.Ser341Arg)
c.930C>A (p.Ser310Arg)
n.298C>A
c.525C>A (p.Ser175Arg)
c.-463+16936G>T (n.-463+16936G>T)
17g.44006636C>GCA399726351NAGS,PYYc.1023C>G (p.Ser341Arg)
c.930C>G (p.Ser310Arg)
n.298C>G
c.525C>G (p.Ser175Arg)
c.-463+16936G>C (n.-463+16936G>C)
17g.44006636C>TCA500241127NAGS,PYYc.1023C>T (p.Ser341=)
c.930C>T (p.Ser310=)
n.298C>T
c.525C>T (p.Ser175=)
c.-463+16936G>A (n.-463+16936G>A)
17g.44006637C>ACA399726353NAGS,PYYc.1024C>A (p.Arg342Ser)
c.931C>A (p.Arg311Ser)
n.299C>A
c.526C>A (p.Arg176Ser)
c.-463+16935G>T (n.-463+16935G>T)
17g.44006637C=CA2261182229NAGS,PYYc.1024C= (p.Arg342=)
c.931C= (p.Arg311=)
n.299C=
c.526C= (p.Arg176=)
c.-463+16935G= (n.-463+16935G=)
17g.44006637C>GCA399726354NAGS,PYYc.1024C>G (p.Arg342Gly)
c.931C>G (p.Arg311Gly)
n.299C>G
c.526C>G (p.Arg176Gly)
c.-463+16935G>C (n.-463+16935G>C)
17g.44006637C>TCA399726355NAGS,PYYc.1024C>T (p.Arg342Cys)
c.931C>T (p.Arg311Cys)
n.299C>T
c.526C>T (p.Arg176Cys)
c.-463+16935G>A (n.-463+16935G>A)
 dbSNP gnomAD v4
17g.44006637_44006638delinsCGCA2261182228NAGS,PYYc.1024_1025delinsCG (p.Arg342=)
c.931_932delinsCG (p.Arg311=)
n.299_300delinsCG
c.526_527delinsCG (p.Arg176=)
c.-463+16934_-463+16935delinsCG (n.-463+16934_-463+16935delinsCG)
17g.44006638delCA115542NAGS,PYYc.1025del (p.Arg342ProfsTer?)
c.932del (p.Arg311ProfsTer?)
n.300del
c.527del (p.Arg176ProfsTer?)
c.-463+16934del (n.-463+16934del)
 ClinVar dbSNP gnomAD v3 gnomAD v4
17g.44006638G>ACA399726357NAGS,PYYc.1025G>A (p.Arg342His)
c.932G>A (p.Arg311His)
n.300G>A
c.527G>A (p.Arg176His)
c.-463+16934C>T (n.-463+16934C>T)
 dbSNP gnomAD v3 gnomAD v4
17g.44006638G>CCA399726359NAGS,PYYc.1025G>C (p.Arg342Pro)
c.932G>C (p.Arg311Pro)
n.300G>C
c.527G>C (p.Arg176Pro)
c.-463+16934C>G (n.-463+16934C>G)
17g.44006638G=CA2261182230NAGS,PYYc.1025G= (p.Arg342=)
c.932G= (p.Arg311=)
n.300G=
c.527G= (p.Arg176=)
c.-463+16934C= (n.-463+16934C=)
17g.44006638G>TCA399726360NAGS,PYYc.1025G>T (p.Arg342Leu)
c.932G>T (p.Arg311Leu)
n.300G>T
c.527G>T (p.Arg176Leu)
c.-463+16934C>A (n.-463+16934C>A)
17g.44006639C>ACA500241129NAGS,PYYc.1026C>A (p.Arg342=)
c.933C>A (p.Arg311=)
n.301C>A
c.528C>A (p.Arg176=)
c.-463+16933G>T (n.-463+16933G>T)
 ClinVar dbSNP
17g.44006639C>GCA500241130NAGS,PYYc.1026C>G (p.Arg342=)
c.933C>G (p.Arg311=)
n.301C>G
c.528C>G (p.Arg176=)
c.-463+16933G>C (n.-463+16933G>C)
17g.44006639C>TCA500241128NAGS,PYYc.1026C>T (p.Arg342=)
c.933C>T (p.Arg311=)
n.301C>T
c.528C>T (p.Arg176=)
c.-463+16933G>A (n.-463+16933G>A)
17g.44006640C>ACA399726363NAGS,PYYc.1027C>A (p.Leu343Met)
c.934C>A (p.Leu312Met)
n.302C>A
c.529C>A (p.Leu177Met)
c.-463+16932G>T (n.-463+16932G>T)
17g.44006640C>GCA399726364NAGS,PYYc.1027C>G (p.Leu343Val)
c.934C>G (p.Leu312Val)
n.302C>G
c.529C>G (p.Leu177Val)
c.-463+16932G>C (n.-463+16932G>C)
17g.44006640C>TCA500241131NAGS,PYYc.1027C>T (p.Leu343=)
c.934C>T (p.Leu312=)
n.302C>T
c.529C>T (p.Leu177=)
c.-463+16932G>A (n.-463+16932G>A)
 gnomAD v4
17g.44006641T>ACA399726366NAGS,PYYc.1028T>A (p.Leu343Gln)
c.935T>A (p.Leu312Gln)
n.303T>A
c.530T>A (p.Leu177Gln)
c.-463+16931A>T (n.-463+16931A>T)
17g.44006641T>CCA399726368NAGS,PYYc.1028T>C (p.Leu343Pro)
c.935T>C (p.Leu312Pro)
n.303T>C
c.530T>C (p.Leu177Pro)
c.-463+16931A>G (n.-463+16931A>G)
17g.44006641T>GCA399726369NAGS,PYYc.1028T>G (p.Leu343Arg)
c.935T>G (p.Leu312Arg)
n.303T>G
c.530T>G (p.Leu177Arg)
c.-463+16931A>C (n.-463+16931A>C)
17g.44006642G>ACA500241132NAGS,PYYc.1029G>A (p.Leu343=)
c.936G>A (p.Leu312=)
n.304G>A
c.531G>A (p.Leu177=)
c.-463+16930C>T (n.-463+16930C>T)
 ClinVar dbSNP gnomAD v2 gnomAD v4
17g.44006642G>CCA500241135NAGS,PYYc.1029G>C (p.Leu343=)
c.936G>C (p.Leu312=)
n.304G>C
c.531G>C (p.Leu177=)
c.-463+16930C>G (n.-463+16930C>G)
17g.44006642G=CA2261182231NAGS,PYYc.1029G= (p.Leu343=)
c.936G= (p.Leu312=)
n.304G=
c.531G= (p.Leu177=)
c.-463+16930C= (n.-463+16930C=)
17g.44006642G>TCA500241137NAGS,PYYc.1029G>T (p.Leu343=)
c.936G>T (p.Leu312=)
n.304G>T
c.531G>T (p.Leu177=)
c.-463+16930C>A (n.-463+16930C>A)
 dbSNP gnomAD v3 gnomAD v4
17g.44006643C>ACA399726371NAGS,PYYc.1030C>A (p.Pro344Thr)
c.937C>A (p.Pro313Thr)
n.305C>A
c.532C>A (p.Pro178Thr)
c.-463+16929G>T (n.-463+16929G>T)
17g.44006643C>GCA399726374NAGS,PYYc.1030C>G (p.Pro344Ala)
c.937C>G (p.Pro313Ala)
n.305C>G
c.532C>G (p.Pro178Ala)
c.-463+16929G>C (n.-463+16929G>C)
17g.44006643C>TCA399726373NAGS,PYYc.1030C>T (p.Pro344Ser)
c.937C>T (p.Pro313Ser)
n.305C>T
c.532C>T (p.Pro178Ser)
c.-463+16929G>A (n.-463+16929G>A)
17g.44006644C>ACA399726375NAGS,PYYc.1031C>A (p.Pro344His)
c.938C>A (p.Pro313His)
n.306C>A
c.533C>A (p.Pro178His)
c.-463+16928G>T (n.-463+16928G>T)
17g.44006644C>GCA399726376NAGS,PYYc.1031C>G (p.Pro344Arg)
c.938C>G (p.Pro313Arg)
n.306C>G
c.533C>G (p.Pro178Arg)
c.-463+16928G>C (n.-463+16928G>C)
17g.44006644C>TCA399726378NAGS,PYYc.1031C>T (p.Pro344Leu)
c.938C>T (p.Pro313Leu)
n.306C>T
c.533C>T (p.Pro178Leu)
c.-463+16928G>A (n.-463+16928G>A)
17g.44006644_44006647delinsCCCACA2261182232NAGS,PYYc.1031_1034delinsCCCA (p.Pro344=)
c.938_941delinsCCCA (p.Pro313=)
n.306_309delinsCCCA
c.533_536delinsCCCA (p.Pro178=)
c.-463+16925_-463+16928delinsTGGG (n.-463+16925_-463+16928delinsTGGG)
17g.44006645C>ACA8595296NAGS,PYYc.1032C>A (p.Pro344=)
c.939C>A (p.Pro313=)
n.307C>A
c.534C>A (p.Pro178=)
c.-463+16927G>T (n.-463+16927G>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.44006645C=CA2261182233NAGS,PYYc.1032C= (p.Pro344=)
c.939C= (p.Pro313=)
n.307C=
c.534C= (p.Pro178=)
c.-463+16927G= (n.-463+16927G=)
17g.44006645C>GCA500241153NAGS,PYYc.1032C>G (p.Pro344=)
c.939C>G (p.Pro313=)
n.307C>G
c.534C>G (p.Pro178=)
c.-463+16927G>C (n.-463+16927G>C)
17g.44006645C>TCA500241151NAGS,PYYc.1032C>T (p.Pro344=)
c.939C>T (p.Pro313=)
n.307C>T
c.534C>T (p.Pro178=)
c.-463+16927G>A (n.-463+16927G>A)
 ClinVar dbSNP
17g.44006649_44006651delCA2261182234NAGS,PYYc.1036_1038del (p.His346del)
c.943_945del (p.His315del)
n.311_313del
c.538_540del (p.His180del)
c.-463+16925_-463+16927del (n.-463+16925_-463+16927del)
 dbSNP
17g.44006646C>ACA399726381NAGS,PYYc.1033C>A (p.His345Asn)
c.940C>A (p.His314Asn)
n.308C>A
c.535C>A (p.His179Asn)
c.-463+16926G>T (n.-463+16926G>T)
17g.44006646C=CA2261182235NAGS,PYYc.1033C= (p.His345=)
c.940C= (p.His314=)
n.308C=
c.535C= (p.His179=)
c.-463+16926G= (n.-463+16926G=)
17g.44006646C>GCA399726382NAGS,PYYc.1033C>G (p.His345Asp)
c.940C>G (p.His314Asp)
n.308C>G
c.535C>G (p.His179Asp)
c.-463+16926G>C (n.-463+16926G>C)
17g.44006646C>TCA290853184NAGS,PYYc.1033C>T (p.His345Tyr)
c.940C>T (p.His314Tyr)
n.308C>T
c.535C>T (p.His179Tyr)
c.-463+16926G>A (n.-463+16926G>A)
 dbSNP gnomAD v4
17g.44006647A>CCA399726385NAGS,PYYc.1034A>C (p.His345Pro)
c.941A>C (p.His314Pro)
n.309A>C
c.536A>C (p.His179Pro)
c.-463+16925T>G (n.-463+16925T>G)
17g.44006647A>GCA399726386NAGS,PYYc.1034A>G (p.His345Arg)
c.941A>G (p.His314Arg)
n.309A>G
c.536A>G (p.His179Arg)
c.-463+16925T>C (n.-463+16925T>C)
 gnomAD v4
17g.44006647A>TCA399726387NAGS,PYYc.1034A>T (p.His345Leu)
c.941A>T (p.His314Leu)
n.309A>T
c.536A>T (p.His179Leu)
c.-463+16925T>A (n.-463+16925T>A)
17g.44006648C>ACA399726390NAGS,PYYc.1035C>A (p.His345Gln)
c.942C>A (p.His314Gln)
n.310C>A
c.537C>A (p.His179Gln)
c.-463+16924G>T (n.-463+16924G>T)
17g.44006648C>GCA399726388NAGS,PYYc.1035C>G (p.His345Gln)
c.942C>G (p.His314Gln)
n.310C>G
c.537C>G (p.His179Gln)
c.-463+16924G>C (n.-463+16924G>C)
17g.44006648C>TCA500241168NAGS,PYYc.1035C>T (p.His345=)
c.942C>T (p.His314=)
n.310C>T
c.537C>T (p.His179=)
c.-463+16924G>A (n.-463+16924G>A)
 ClinVar gnomAD v4
17g.44006649dupCA913203446NAGS,PYYc.1036dup (p.His346ProfsTer10)
c.943dup (p.His315ProfsTer10)
n.311dup
c.538dup (p.His180ProfsTer10)
c.-463+16924dup (n.-463+16924dup)
17g.44006649C>ACA399726392NAGS,PYYc.1036C>A (p.His346Asn)
c.943C>A (p.His315Asn)
n.311C>A
c.538C>A (p.His180Asn)
c.-463+16923G>T (n.-463+16923G>T)
17g.44006649C=CA2261182236NAGS,PYYc.1036C= (p.His346=)
c.943C= (p.His315=)
n.311C=
c.538C= (p.His180=)
c.-463+16923G= (n.-463+16923G=)
17g.44006649C>GCA399726393NAGS,PYYc.1036C>G (p.His346Asp)
c.943C>G (p.His315Asp)
n.311C>G
c.538C>G (p.His180Asp)
c.-463+16923G>C (n.-463+16923G>C)
17g.44006649C>TCA399726395NAGS,PYYc.1036C>T (p.His346Tyr)
c.943C>T (p.His315Tyr)
n.311C>T
c.538C>T (p.His180Tyr)
c.-463+16923G>A (n.-463+16923G>A)
 dbSNP
17g.44006650A>CCA399726397NAGS,PYYc.1037A>C (p.His346Pro)
c.944A>C (p.His315Pro)
n.312A>C
c.539A>C (p.His180Pro)
c.-463+16922T>G (n.-463+16922T>G)
17g.44006650A>GCA399726399NAGS,PYYc.1037A>G (p.His346Arg)
c.944A>G (p.His315Arg)
n.312A>G
c.539A>G (p.His180Arg)
c.-463+16922T>C (n.-463+16922T>C)
17g.44006650A>TCA399726400NAGS,PYYc.1037A>T (p.His346Leu)
c.944A>T (p.His315Leu)
n.312A>T
c.539A>T (p.His180Leu)
c.-463+16922T>A (n.-463+16922T>A)
17g.44006650_44006683delCA2580093934NAGS,PYYc.1037_1070del (p.His346ArgfsTer?)
c.944_977del (p.His315ArgfsTer?)
n.312_345del
c.539_572del (p.His180ArgfsTer?)
c.-463+16889_-463+16922del (n.-463+16889_-463+16922del)
 ClinVar
17g.44006651C>ACA399726402NAGS,PYYc.1038C>A (p.His346Gln)
c.945C>A (p.His315Gln)
n.313C>A
c.540C>A (p.His180Gln)
c.-463+16921G>T (n.-463+16921G>T)
 gnomAD v4
17g.44006651C=CA2261182237NAGS,PYYc.1038C= (p.His346=)
c.945C= (p.His315=)
n.313C=
c.540C= (p.His180=)
c.-463+16921G= (n.-463+16921G=)
17g.44006651C>GCA399726404NAGS,PYYc.1038C>G (p.His346Gln)
c.945C>G (p.His315Gln)
n.313C>G
c.540C>G (p.His180Gln)
c.-463+16921G>C (n.-463+16921G>C)
17g.44006651C>TCA8595297NAGS,PYYc.1038C>T (p.His346=)
c.945C>T (p.His315=)
n.313C>T
c.540C>T (p.His180=)
c.-463+16921G>A (n.-463+16921G>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.44006652T>ACA399726407NAGS,PYYc.1039T>A (p.Ser347Thr)
c.946T>A (p.Ser316Thr)
n.314T>A
c.541T>A (p.Ser181Thr)
c.-463+16920A>T (n.-463+16920A>T)
17g.44006652T>CCA399726408NAGS,PYYc.1039T>C (p.Ser347Pro)
c.946T>C (p.Ser316Pro)
n.314T>C
c.541T>C (p.Ser181Pro)
c.-463+16920A>G (n.-463+16920A>G)
 gnomAD v4
17g.44006652T>GCA399726410NAGS,PYYc.1039T>G (p.Ser347Ala)
c.946T>G (p.Ser316Ala)
n.314T>G
c.541T>G (p.Ser181Ala)
c.-463+16920A>C (n.-463+16920A>C)
 dbSNP gnomAD v2 gnomAD v4
17g.44006652T=CA2261182238NAGS,PYYc.1039T= (p.Ser347=)
c.946T= (p.Ser316=)
n.314T=
c.541T= (p.Ser181=)
c.-463+16920A= (n.-463+16920A=)
17g.44006653C>ACA399726413NAGS,PYYc.1040C>A (p.Ser347Tyr)
c.947C>A (p.Ser316Tyr)
n.315C>A
c.542C>A (p.Ser181Tyr)
c.-463+16919G>T (n.-463+16919G>T)
17g.44006653C>GCA399726412NAGS,PYYc.1040C>G (p.Ser347Cys)
c.947C>G (p.Ser316Cys)
n.315C>G
c.542C>G (p.Ser181Cys)
c.-463+16919G>C (n.-463+16919G>C)
17g.44006653C>TCA399726411NAGS,PYYc.1040C>T (p.Ser347Phe)
c.947C>T (p.Ser316Phe)
n.315C>T
c.542C>T (p.Ser181Phe)
c.-463+16919G>A (n.-463+16919G>A)
 gnomAD v4
17g.44006654C>ACA500241201NAGS,PYYc.1041C>A (p.Ser347=)
c.948C>A (p.Ser316=)
n.316C>A
c.543C>A (p.Ser181=)
c.-463+16918G>T (n.-463+16918G>T)
17g.44006654C>GCA500241197NAGS,PYYc.1041C>G (p.Ser347=)
c.948C>G (p.Ser316=)
n.316C>G
c.543C>G (p.Ser181=)
c.-463+16918G>C (n.-463+16918G>C)
17g.44006654C>TCA500241198NAGS,PYYc.1041C>T (p.Ser347=)
c.948C>T (p.Ser316=)
n.316C>T
c.543C>T (p.Ser181=)
c.-463+16918G>A (n.-463+16918G>A)
 ClinVar dbSNP gnomAD v4
17g.44006655T>ACA399726415NAGS,PYYc.1042T>A (p.Ser348Thr)
c.949T>A (p.Ser317Thr)
n.317T>A
c.544T>A (p.Ser182Thr)
c.-463+16917A>T (n.-463+16917A>T)
17g.44006655T>CCA399726417NAGS,PYYc.1042T>C (p.Ser348Pro)
c.949T>C (p.Ser317Pro)
n.317T>C
c.544T>C (p.Ser182Pro)
c.-463+16917A>G (n.-463+16917A>G)
17g.44006655T>GCA399726419NAGS,PYYc.1042T>G (p.Ser348Ala)
c.949T>G (p.Ser317Ala)
n.317T>G
c.544T>G (p.Ser182Ala)
c.-463+16917A>C (n.-463+16917A>C)
17g.44006656C>ACA399726420NAGS,PYYc.1043C>A (p.Ser348Ter)
c.950C>A (p.Ser317Ter)
n.318C>A
c.545C>A (p.Ser182Ter)
c.-463+16916G>T (n.-463+16916G>T)
17g.44006656C=CA2261182239NAGS,PYYc.1043C= (p.Ser348=)
c.950C= (p.Ser317=)
n.318C=
c.545C= (p.Ser182=)
c.-463+16916G= (n.-463+16916G=)
17g.44006656C>GCA399726421NAGS,PYYc.1043C>G (p.Ser348Trp)
c.950C>G (p.Ser317Trp)
n.318C>G
c.545C>G (p.Ser182Trp)
c.-463+16916G>C (n.-463+16916G>C)
17g.44006656C>TCA399726423NAGS,PYYc.1043C>T (p.Ser348Leu)
c.950C>T (p.Ser317Leu)
n.318C>T
c.545C>T (p.Ser182Leu)
c.-463+16916G>A (n.-463+16916G>A)
 dbSNP gnomAD v2
17g.44006657G>ACA500241212NAGS,PYYc.1044G>A (p.Ser348=)
c.951G>A (p.Ser317=)
n.319G>A
c.546G>A (p.Ser182=)
c.-463+16915C>T (n.-463+16915C>T)
 ClinVar gnomAD v4
17g.44006657G>CCA500241214NAGS,PYYc.1044G>C (p.Ser348=)
c.951G>C (p.Ser317=)
n.319G>C
c.546G>C (p.Ser182=)
c.-463+16915C>G (n.-463+16915C>G)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.44006657G=CA2261182240NAGS,PYYc.1044G= (p.Ser348=)
c.951G= (p.Ser317=)
n.319G=
c.546G= (p.Ser182=)
c.-463+16915C= (n.-463+16915C=)
17g.44006657G>TCA500241216NAGS,PYYc.1044G>T (p.Ser348=)
c.951G>T (p.Ser317=)
n.319G>T
c.546G>T (p.Ser182=)
c.-463+16915C>A (n.-463+16915C>A)
17g.44006657_44006660delinsGGCCCA2261182241NAGS,PYYc.1044_1047delinsGGCC (p.Ser348=)
c.951_954delinsGGCC (p.Ser317=)
n.319_322delinsGGCC
c.546_549delinsGGCC (p.Ser182=)
c.-463+16912_-463+16915delinsGGCC (n.-463+16912_-463+16915delinsGGCC)
17g.44006658G>ACA399726424NAGS,PYYc.1045G>A (p.Ala349Thr)
c.952G>A (p.Ala318Thr)
n.320G>A
c.547G>A (p.Ala183Thr)
c.-463+16914C>T (n.-463+16914C>T)
17g.44006658G>CCA399726426NAGS,PYYc.1045G>C (p.Ala349Pro)
c.952G>C (p.Ala318Pro)
n.320G>C
c.547G>C (p.Ala183Pro)
c.-463+16914C>G (n.-463+16914C>G)
17g.44006658G>TCA399726427NAGS,PYYc.1045G>T (p.Ala349Ser)
c.952G>T (p.Ala318Ser)
n.320G>T
c.547G>T (p.Ala183Ser)
c.-463+16914C>A (n.-463+16914C>A)
17g.44006659_44006661delCA772278245NAGS,PYYc.1046_1048del (p.Ala349del)
c.953_955del (p.Ala318del)
n.321_323del
c.548_550del (p.Ala183del)
c.-463+16912_-463+16914del (n.-463+16912_-463+16914del)
 dbSNP gnomAD v3 gnomAD v4
17g.44006659C>ACA399726428NAGS,PYYc.1046C>A (p.Ala349Asp)
c.953C>A (p.Ala318Asp)
n.321C>A
c.548C>A (p.Ala183Asp)
c.-463+16913G>T (n.-463+16913G>T)
17g.44006659C>GCA399726430NAGS,PYYc.1046C>G (p.Ala349Gly)
c.953C>G (p.Ala318Gly)
n.321C>G
c.548C>G (p.Ala183Gly)
c.-463+16913G>C (n.-463+16913G>C)
17g.44006659C>TCA399726432NAGS,PYYc.1046C>T (p.Ala349Val)
c.953C>T (p.Ala318Val)
n.321C>T
c.548C>T (p.Ala183Val)
c.-463+16913G>A (n.-463+16913G>A)
17g.44006660C>ACA500241226NAGS,PYYc.1047C>A (p.Ala349=)
c.954C>A (p.Ala318=)
n.322C>A
c.549C>A (p.Ala183=)
c.-463+16912G>T (n.-463+16912G>T)
 gnomAD v4
17g.44006660C=CA2261182243NAGS,PYYc.1047C= (p.Ala349=)
c.954C= (p.Ala318=)
n.322C=
c.549C= (p.Ala183=)
c.-463+16912G= (n.-463+16912G=)
17g.44006660C>GCA500241231NAGS,PYYc.1047C>G (p.Ala349=)
c.954C>G (p.Ala318=)
n.322C>G
c.549C>G (p.Ala183=)
c.-463+16912G>C (n.-463+16912G>C)
 dbSNP
17g.44006660C>TCA500241228NAGS,PYYc.1047C>T (p.Ala349=)
c.954C>T (p.Ala318=)
n.322C>T
c.549C>T (p.Ala183=)
c.-463+16912G>A (n.-463+16912G>A)
 ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC
17g.44006660_44006667delinsCGTCATCACA2261182242NAGS,PYYc.1047_1054delinsCGTCATCA (p.Ala349=)
c.954_961delinsCGTCATCA (p.Ala318=)
n.322_329delinsCGTCATCA
c.549_556delinsCGTCATCA (p.Ala183=)
c.-463+16905_-463+16912delinsTGATGACG (n.-463+16905_-463+16912delinsTGATGACG)
17g.44006661G>ACA399726435NAGS,PYYc.1048G>A (p.Val350Ile)
c.955G>A (p.Val319Ile)
n.323G>A
c.550G>A (p.Val184Ile)
c.-463+16911C>T (n.-463+16911C>T)
 gnomAD v4 COSMIC
17g.44006661G>CCA399726436NAGS,PYYc.1048G>C (p.Val350Leu)
c.955G>C (p.Val319Leu)
n.323G>C
c.550G>C (p.Val184Leu)
c.-463+16911C>G (n.-463+16911C>G)
17g.44006661G>TCA399726434NAGS,PYYc.1048G>T (p.Val350Phe)
c.955G>T (p.Val319Phe)
n.323G>T
c.550G>T (p.Val184Phe)
c.-463+16911C>A (n.-463+16911C>A)
 gnomAD v4
17g.44006661_44006667delCA290853191NAGS,PYYc.1048_1054del (p.Val350ProfsTer?)
c.955_961del (p.Val319ProfsTer?)
n.323_329del
c.550_556del (p.Val184ProfsTer?)
c.-463+16905_-463+16911del (n.-463+16905_-463+16911del)
 dbSNP
17g.44006661_44006667dupCA2261182244NAGS,PYYc.1048_1054dup (p.Thr352SerfsTer6)
c.955_961dup (p.Thr321SerfsTer6)
n.323_329dup
c.550_556dup (p.Thr186SerfsTer6)
c.-463+16905_-463+16911dup (n.-463+16905_-463+16911dup)
 dbSNP
17g.44006662T>ACA399726440NAGS,PYYc.1049T>A (p.Val350Asp)
c.956T>A (p.Val319Asp)
n.324T>A
c.551T>A (p.Val184Asp)
c.-463+16910A>T (n.-463+16910A>T)
17g.44006662T>CCA399726437NAGS,PYYc.1049T>C (p.Val350Ala)
c.956T>C (p.Val319Ala)
n.324T>C
c.551T>C (p.Val184Ala)
c.-463+16910A>G (n.-463+16910A>G)
17g.44006662T>GCA399726438NAGS,PYYc.1049T>G (p.Val350Gly)
c.956T>G (p.Val319Gly)
n.324T>G
c.551T>G (p.Val184Gly)
c.-463+16910A>C (n.-463+16910A>C)
17g.44006662_44006668delCA399726439NAGS,PYYc.1049_1055del (p.Val350AlafsTer?)
c.956_962del (p.Val319AlafsTer?)
n.324_330del
c.551_557del (p.Val184AlafsTer?)
c.-463+16904_-463+16910del (n.-463+16904_-463+16910del)
17g.44006663C>ACA500241243NAGS,PYYc.1050C>A (p.Val350=)
c.957C>A (p.Val319=)
n.325C>A
c.552C>A (p.Val184=)
c.-463+16909G>T (n.-463+16909G>T)
17g.44006663C>GCA500241244NAGS,PYYc.1050C>G (p.Val350=)
c.957C>G (p.Val319=)
n.325C>G
c.552C>G (p.Val184=)
c.-463+16909G>C (n.-463+16909G>C)
17g.44006663C>TCA500241245NAGS,PYYc.1050C>T (p.Val350=)
c.957C>T (p.Val319=)
n.325C>T
c.552C>T (p.Val184=)
c.-463+16909G>A (n.-463+16909G>A)
17g.44006664A>CCA399726441NAGS,PYYc.1051A>C (p.Ile351Leu)
c.958A>C (p.Ile320Leu)
n.326A>C
c.553A>C (p.Ile185Leu)
c.-463+16908T>G (n.-463+16908T>G)
 gnomAD v4
17g.44006664A>GCA399726442NAGS,PYYc.1051A>G (p.Ile351Val)
c.958A>G (p.Ile320Val)
n.326A>G
c.553A>G (p.Ile185Val)
c.-463+16908T>C (n.-463+16908T>C)
 gnomAD v4
17g.44006664A>TCA399726444NAGS,PYYc.1051A>T (p.Ile351Phe)
c.958A>T (p.Ile320Phe)
n.326A>T
c.553A>T (p.Ile185Phe)
c.-463+16908T>A (n.-463+16908T>A)
17g.44006664_44006665delCA2638146955NAGS,PYYc.1051_1052del (p.Ile351HisfsTer4)
c.958_959del (p.Ile320HisfsTer4)
n.326_327del
c.553_554del (p.Ile185HisfsTer4)
c.-463+16907_-463+16908del (n.-463+16907_-463+16908del)
 gnomAD v4
17g.44006665T>ACA399726446NAGS,PYYc.1052T>A (p.Ile351Asn)
c.959T>A (p.Ile320Asn)
n.327T>A
c.554T>A (p.Ile185Asn)
c.-463+16907A>T (n.-463+16907A>T)
17g.44006665T>CCA399726448NAGS,PYYc.1052T>C (p.Ile351Thr)
c.959T>C (p.Ile320Thr)
n.327T>C
c.554T>C (p.Ile185Thr)
c.-463+16907A>G (n.-463+16907A>G)
17g.44006665T>GCA399726450NAGS,PYYc.1052T>G (p.Ile351Ser)
c.959T>G (p.Ile320Ser)
n.327T>G
c.554T>G (p.Ile185Ser)
c.-463+16907A>C (n.-463+16907A>C)
17g.44006666C>ACA500241248NAGS,PYYc.1053C>A (p.Ile351=)
c.960C>A (p.Ile320=)
n.328C>A
c.555C>A (p.Ile185=)
c.-463+16906G>T (n.-463+16906G>T)
 ClinVar gnomAD v4
17g.44006666C>GCA399726452NAGS,PYYc.1053C>G (p.Ile351Met)
c.960C>G (p.Ile320Met)
n.328C>G
c.555C>G (p.Ile185Met)
c.-463+16906G>C (n.-463+16906G>C)
17g.44006666C>TCA500241249NAGS,PYYc.1053C>T (p.Ile351=)
c.960C>T (p.Ile320=)
n.328C>T
c.555C>T (p.Ile185=)
c.-463+16906G>A (n.-463+16906G>A)
 ClinVar dbSNP
17g.44006667A=CA2261182245NAGS,PYYc.1054A= (p.Thr352=)
c.961A= (p.Thr321=)
n.329A=
c.556A= (p.Thr186=)
c.-463+16905T= (n.-463+16905T=)
17g.44006667A>CCA8595298NAGS,PYYc.1054A>C (p.Thr352Pro)
c.961A>C (p.Thr321Pro)
n.329A>C
c.556A>C (p.Thr186Pro)
c.-463+16905T>G (n.-463+16905T>G)
 dbSNP ExAC gnomAD v2 gnomAD v4
17g.44006667A>GCA399726454NAGS,PYYc.1054A>G (p.Thr352Ala)
c.961A>G (p.Thr321Ala)
n.329A>G
c.556A>G (p.Thr186Ala)
c.-463+16905T>C (n.-463+16905T>C)
 gnomAD v4
17g.44006667A>TCA399726455NAGS,PYYc.1054A>T (p.Thr352Ser)
c.961A>T (p.Thr321Ser)
n.329A>T
c.556A>T (p.Thr186Ser)
c.-463+16905T>A (n.-463+16905T>A)
17g.44006668C>ACA399726460NAGS,PYYc.1055C>A (p.Thr352Asn)
c.962C>A (p.Thr321Asn)
n.330C>A
c.557C>A (p.Thr186Asn)
c.-463+16904G>T (n.-463+16904G>T)
17g.44006668C=CA2261182246NAGS,PYYc.1055C= (p.Thr352=)
c.962C= (p.Thr321=)
n.330C=
c.557C= (p.Thr186=)
c.-463+16904G= (n.-463+16904G=)
17g.44006668C>GCA290853208NAGS,PYYc.1055C>G (p.Thr352Ser)
c.962C>G (p.Thr321Ser)
n.330C>G
c.557C>G (p.Thr186Ser)
c.-463+16904G>C (n.-463+16904G>C)
 dbSNP gnomAD v4
17g.44006668C>TCA399726458NAGS,PYYc.1055C>T (p.Thr352Ile)
c.962C>T (p.Thr321Ile)
n.330C>T
c.557C>T (p.Thr186Ile)
c.-463+16904G>A (n.-463+16904G>A)
 gnomAD v4
17g.44006669C>ACA500241250NAGS,PYYc.1056C>A (p.Thr352=)
c.963C>A (p.Thr321=)
n.331C>A
c.558C>A (p.Thr186=)
c.-463+16903G>T (n.-463+16903G>T)
17g.44006669C=CA2261182247NAGS,PYYc.1056C= (p.Thr352=)
c.963C= (p.Thr321=)
n.331C=
c.558C= (p.Thr186=)
c.-463+16903G= (n.-463+16903G=)
17g.44006669C>GCA500241251NAGS,PYYc.1056C>G (p.Thr352=)
c.963C>G (p.Thr321=)
n.331C>G
c.558C>G (p.Thr186=)
c.-463+16903G>C (n.-463+16903G>C)
17g.44006669C>TCA500241252NAGS,PYYc.1056C>T (p.Thr352=)
c.963C>T (p.Thr321=)
n.331C>T
c.558C>T (p.Thr186=)
c.-463+16903G>A (n.-463+16903G>A)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.44006670G>ACA399726462NAGS,PYYc.1057G>A (p.Ala353Thr)
c.964G>A (p.Ala322Thr)
n.332G>A
c.559G>A (p.Ala187Thr)
c.-463+16902C>T (n.-463+16902C>T)
 dbSNP gnomAD v2 gnomAD v4
17g.44006670G>CCA399726463NAGS,PYYc.1057G>C (p.Ala353Pro)
c.964G>C (p.Ala322Pro)
n.332G>C
c.559G>C (p.Ala187Pro)
c.-463+16902C>G (n.-463+16902C>G)
17g.44006670G=CA2261182248NAGS,PYYc.1057G= (p.Ala353=)
c.964G= (p.Ala322=)
n.332G=
c.559G= (p.Ala187=)
c.-463+16902C= (n.-463+16902C=)
17g.44006670G>TCA399726465NAGS,PYYc.1057G>T (p.Ala353Ser)
c.964G>T (p.Ala322Ser)
n.332G>T
c.559G>T (p.Ala187Ser)
c.-463+16902C>A (n.-463+16902C>A)
 ClinVar dbSNP gnomAD v2 gnomAD v4
17g.44006671C>ACA399726467NAGS,PYYc.1058C>A (p.Ala353Asp)
c.965C>A (p.Ala322Asp)
n.333C>A
c.560C>A (p.Ala187Asp)
c.-463+16901G>T (n.-463+16901G>T)
 gnomAD v4
17g.44006671C=CA2261182249NAGS,PYYc.1058C= (p.Ala353=)
c.965C= (p.Ala322=)
n.333C=
c.560C= (p.Ala187=)
c.-463+16901G= (n.-463+16901G=)
17g.44006671C>GCA399726468NAGS,PYYc.1058C>G (p.Ala353Gly)
c.965C>G (p.Ala322Gly)
n.333C>G
c.560C>G (p.Ala187Gly)
c.-463+16901G>C (n.-463+16901G>C)
 gnomAD v4
17g.44006671C>TCA399726470NAGS,PYYc.1058C>T (p.Ala353Val)
c.965C>T (p.Ala322Val)
n.333C>T
c.560C>T (p.Ala187Val)
c.-463+16901G>A (n.-463+16901G>A)
 dbSNP gnomAD v2 gnomAD v4
17g.44006672C>ACA500241253NAGS,PYYc.1059C>A (p.Ala353=)
c.966C>A (p.Ala322=)
n.334C>A
c.561C>A (p.Ala187=)
c.-463+16900G>T (n.-463+16900G>T)
 dbSNP gnomAD v2 gnomAD v4
17g.44006672C=CA2261182250NAGS,PYYc.1059C= (p.Ala353=)
c.966C= (p.Ala322=)
n.334C=
c.561C= (p.Ala187=)
c.-463+16900G= (n.-463+16900G=)
17g.44006672C>GCA500241254NAGS,PYYc.1059C>G (p.Ala353=)
c.966C>G (p.Ala322=)
n.334C>G
c.561C>G (p.Ala187=)
c.-463+16900G>C (n.-463+16900G>C)
17g.44006672C>TCA500241255NAGS,PYYc.1059C>T (p.Ala353=)
c.966C>T (p.Ala322=)
n.334C>T
c.561C>T (p.Ala187=)
c.-463+16900G>A (n.-463+16900G>A)
 ClinVar dbSNP gnomAD v4

Number of alleles fetched