Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.44006540C>ACA399726030NAGS,PYYc.927C>A (p.Asn309Lys)
c.834C>A (p.Asn278Lys)
n.202C>A
c.429C>A (p.Asn143Lys)
c.-463+17032G>T (n.-463+17032G>T)
17g.44006540C=CA2261182177NAGS,PYYc.927C= (p.Asn309=)
c.834C= (p.Asn278=)
n.202C=
c.429C= (p.Asn143=)
c.-463+17032G= (n.-463+17032G=)
17g.44006540C>GCA8595275NAGS,PYYc.927C>G (p.Asn309Lys)
c.834C>G (p.Asn278Lys)
n.202C>G
c.429C>G (p.Asn143Lys)
c.-463+17032G>C (n.-463+17032G>C)
 dbSNP ExAC gnomAD v3 gnomAD v4
17g.44006540C>TCA290853077NAGS,PYYc.927C>T (p.Asn309=)
c.834C>T (p.Asn278=)
n.202C>T
c.429C>T (p.Asn143=)
c.-463+17032G>A (n.-463+17032G>A)
 ClinVar dbSNP gnomAD v3 gnomAD v4
17g.44006541G>ACA399726033NAGS,PYYc.928G>A (p.Val310Met)
c.835G>A (p.Val279Met)
n.203G>A
c.430G>A (p.Val144Met)
c.-463+17031C>T (n.-463+17031C>T)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.44006541G>CCA399726032NAGS,PYYc.928G>C (p.Val310Leu)
c.835G>C (p.Val279Leu)
n.203G>C
c.430G>C (p.Val144Leu)
c.-463+17031C>G (n.-463+17031C>G)
17g.44006541G=CA2261182178NAGS,PYYc.928G= (p.Val310=)
c.835G= (p.Val279=)
n.203G=
c.430G= (p.Val144=)
c.-463+17031C= (n.-463+17031C=)
17g.44006541G>TCA399726031NAGS,PYYc.928G>T (p.Val310Leu)
c.835G>T (p.Val279Leu)
n.203G>T
c.430G>T (p.Val144Leu)
c.-463+17031C>A (n.-463+17031C>A)
 gnomAD v4
17g.44006542T>ACA399726034NAGS,PYYc.929T>A (p.Val310Glu)
c.836T>A (p.Val279Glu)
n.204T>A
c.431T>A (p.Val144Glu)
c.-463+17030A>T (n.-463+17030A>T)
17g.44006542T>CCA399726035NAGS,PYYc.929T>C (p.Val310Ala)
c.836T>C (p.Val279Ala)
n.204T>C
c.431T>C (p.Val144Ala)
c.-463+17030A>G (n.-463+17030A>G)
17g.44006542T>GCA399726036NAGS,PYYc.929T>G (p.Val310Gly)
c.836T>G (p.Val279Gly)
n.204T>G
c.431T>G (p.Val144Gly)
c.-463+17030A>C (n.-463+17030A>C)
17g.44006543G>ACA500241057NAGS,PYYc.930G>A (p.Val310=)
c.837G>A (p.Val279=)
n.205G>A
c.432G>A (p.Val144=)
c.-463+17029C>T (n.-463+17029C>T)
17g.44006543G>CCA500241058NAGS,PYYc.930G>C (p.Val310=)
c.837G>C (p.Val279=)
n.205G>C
c.432G>C (p.Val144=)
c.-463+17029C>G (n.-463+17029C>G)
17g.44006543G>TCA500241059NAGS,PYYc.930G>T (p.Val310=)
c.837G>T (p.Val279=)
n.205G>T
c.432G>T (p.Val144=)
c.-463+17029C>A (n.-463+17029C>A)
 gnomAD v4
17g.44006544A>CCA399726037NAGS,PYYc.931A>C (p.Asn311His)
c.838A>C (p.Asn280His)
n.206A>C
c.433A>C (p.Asn145His)
c.-463+17028T>G (n.-463+17028T>G)
 gnomAD v4
17g.44006544A>GCA399726038NAGS,PYYc.931A>G (p.Asn311Asp)
c.838A>G (p.Asn280Asp)
n.206A>G
c.433A>G (p.Asn145Asp)
c.-463+17028T>C (n.-463+17028T>C)
 gnomAD v4
17g.44006544A>TCA399726039NAGS,PYYc.931A>T (p.Asn311Tyr)
c.838A>T (p.Asn280Tyr)
n.206A>T
c.433A>T (p.Asn145Tyr)
c.-463+17028T>A (n.-463+17028T>A)
17g.44006545A=CA2261182179NAGS,PYYc.932A= (p.Asn311=)
c.839A= (p.Asn280=)
n.207A=
c.434A= (p.Asn145=)
c.-463+17027T= (n.-463+17027T=)
17g.44006545A>CCA399726040NAGS,PYYc.932A>C (p.Asn311Thr)
c.839A>C (p.Asn280Thr)
n.207A>C
c.434A>C (p.Asn145Thr)
c.-463+17027T>G (n.-463+17027T>G)
 dbSNP
17g.44006545A>GCA399726042NAGS,PYYc.932A>G (p.Asn311Ser)
c.839A>G (p.Asn280Ser)
n.207A>G
c.434A>G (p.Asn145Ser)
c.-463+17027T>C (n.-463+17027T>C)
17g.44006545A>TCA399726041NAGS,PYYc.932A>T (p.Asn311Ile)
c.839A>T (p.Asn280Ile)
n.207A>T
c.434A>T (p.Asn145Ile)
c.-463+17027T>A (n.-463+17027T>A)
17g.44006546C>ACA399726043NAGS,PYYc.933C>A (p.Asn311Lys)
c.840C>A (p.Asn280Lys)
n.208C>A
c.435C>A (p.Asn145Lys)
c.-463+17026G>T (n.-463+17026G>T)
 gnomAD v4
17g.44006546C>GCA399726044NAGS,PYYc.933C>G (p.Asn311Lys)
c.840C>G (p.Asn280Lys)
n.208C>G
c.435C>G (p.Asn145Lys)
c.-463+17026G>C (n.-463+17026G>C)
17g.44006546C>TCA500241060NAGS,PYYc.933C>T (p.Asn311=)
c.840C>T (p.Asn280=)
n.208C>T
c.435C>T (p.Asn145=)
c.-463+17026G>A (n.-463+17026G>A)
 ClinVar dbSNP
17g.44006547C>ACA399726045NAGS,PYYc.934C>A (p.Leu312Met)
c.841C>A (p.Leu281Met)
n.209C>A
c.436C>A (p.Leu146Met)
c.-463+17025G>T (n.-463+17025G>T)
17g.44006547C>GCA399726046NAGS,PYYc.934C>G (p.Leu312Val)
c.841C>G (p.Leu281Val)
n.209C>G
c.436C>G (p.Leu146Val)
c.-463+17025G>C (n.-463+17025G>C)
17g.44006547C>TCA500241063NAGS,PYYc.934C>T (p.Leu312=)
c.841C>T (p.Leu281=)
n.209C>T
c.436C>T (p.Leu146=)
c.-463+17025G>A (n.-463+17025G>A)
17g.44006548T>ACA399726047NAGS,PYYc.935T>A (p.Leu312Gln)
c.842T>A (p.Leu281Gln)
n.210T>A
c.437T>A (p.Leu146Gln)
c.-463+17024A>T (n.-463+17024A>T)
17g.44006548T>CCA8595276NAGS,PYYc.935T>C (p.Leu312Pro)
c.842T>C (p.Leu281Pro)
n.210T>C
c.437T>C (p.Leu146Pro)
c.-463+17024A>G (n.-463+17024A>G)
 dbSNP ExAC gnomAD v2 gnomAD v4
17g.44006548T>GCA399726048NAGS,PYYc.935T>G (p.Leu312Arg)
c.842T>G (p.Leu281Arg)
n.210T>G
c.437T>G (p.Leu146Arg)
c.-463+17024A>C (n.-463+17024A>C)
17g.44006548T=CA2261182180NAGS,PYYc.935T= (p.Leu312=)
c.842T= (p.Leu281=)
n.210T=
c.437T= (p.Leu146=)
c.-463+17024A= (n.-463+17024A=)
17g.44006549G>ACA8595277NAGS,PYYc.936G>A (p.Leu312=)
c.843G>A (p.Leu281=)
n.211G>A
c.438G>A (p.Leu146=)
c.-463+17023C>T (n.-463+17023C>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.44006549G>CCA500241065NAGS,PYYc.936G>C (p.Leu312=)
c.843G>C (p.Leu281=)
n.211G>C
c.438G>C (p.Leu146=)
c.-463+17023C>G (n.-463+17023C>G)
17g.44006549G=CA2261182181NAGS,PYYc.936G= (p.Leu312=)
c.843G= (p.Leu281=)
n.211G=
c.438G= (p.Leu146=)
c.-463+17023C= (n.-463+17023C=)
17g.44006549G>TCA500241066NAGS,PYYc.936G>T (p.Leu312=)
c.843G>T (p.Leu281=)
n.211G>T
c.438G>T (p.Leu146=)
c.-463+17023C>A (n.-463+17023C>A)
 gnomAD v4
17g.44006550C>ACA399726049NAGS,PYYc.937C>A (p.Pro313Thr)
c.844C>A (p.Pro282Thr)
n.212C>A
c.439C>A (p.Pro147Thr)
c.-463+17022G>T (n.-463+17022G>T)
 gnomAD v4
17g.44006550C>GCA399726050NAGS,PYYc.937C>G (p.Pro313Ala)
c.844C>G (p.Pro282Ala)
n.212C>G
c.439C>G (p.Pro147Ala)
c.-463+17022G>C (n.-463+17022G>C)
17g.44006550C>TCA399726051NAGS,PYYc.937C>T (p.Pro313Ser)
c.844C>T (p.Pro282Ser)
n.212C>T
c.439C>T (p.Pro147Ser)
c.-463+17022G>A (n.-463+17022G>A)
 gnomAD v4
17g.44006551C>ACA399726054NAGS,PYYc.938C>A (p.Pro313His)
c.845C>A (p.Pro282His)
n.213C>A
c.440C>A (p.Pro147His)
c.-463+17021G>T (n.-463+17021G>T)
 gnomAD v4
17g.44006551C>GCA399726053NAGS,PYYc.938C>G (p.Pro313Arg)
c.845C>G (p.Pro282Arg)
n.213C>G
c.440C>G (p.Pro147Arg)
c.-463+17021G>C (n.-463+17021G>C)
17g.44006551C>TCA399726052NAGS,PYYc.938C>T (p.Pro313Leu)
c.845C>T (p.Pro282Leu)
n.213C>T
c.440C>T (p.Pro147Leu)
c.-463+17021G>A (n.-463+17021G>A)
 gnomAD v4
17g.44006552C>ACA500241067NAGS,PYYc.939C>A (p.Pro313=)
c.846C>A (p.Pro282=)
n.214C>A
c.441C>A (p.Pro147=)
c.-463+17020G>T (n.-463+17020G>T)
 gnomAD v4
17g.44006552C=CA2261182182NAGS,PYYc.939C= (p.Pro313=)
c.846C= (p.Pro282=)
n.214C=
c.441C= (p.Pro147=)
c.-463+17020G= (n.-463+17020G=)
17g.44006552C>GCA500241068NAGS,PYYc.939C>G (p.Pro313=)
c.846C>G (p.Pro282=)
n.214C>G
c.441C>G (p.Pro147=)
c.-463+17020G>C (n.-463+17020G>C)
 ClinVar gnomAD v4
17g.44006552C>TCA8595278NAGS,PYYc.939C>T (p.Pro313=)
c.846C>T (p.Pro282=)
n.214C>T
c.441C>T (p.Pro147=)
c.-463+17020G>A (n.-463+17020G>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.44006553G>ACA8595279NAGS,PYYc.940G>A (p.Ala314Thr)
c.847G>A (p.Ala283Thr)
n.215G>A
c.442G>A (p.Ala148Thr)
c.-463+17019C>T (n.-463+17019C>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.44006553G>CCA399726056NAGS,PYYc.940G>C (p.Ala314Pro)
c.847G>C (p.Ala283Pro)
n.215G>C
c.442G>C (p.Ala148Pro)
c.-463+17019C>G (n.-463+17019C>G)
17g.44006553G=CA2261182183NAGS,PYYc.940G= (p.Ala314=)
c.847G= (p.Ala283=)
n.215G=
c.442G= (p.Ala148=)
c.-463+17019C= (n.-463+17019C=)
17g.44006553G>TCA399726055NAGS,PYYc.940G>T (p.Ala314Ser)
c.847G>T (p.Ala283Ser)
n.215G>T
c.442G>T (p.Ala148Ser)
c.-463+17019C>A (n.-463+17019C>A)
 gnomAD v4
17g.44006554C>ACA399726057NAGS,PYYc.941C>A (p.Ala314Asp)
c.848C>A (p.Ala283Asp)
n.216C>A
c.443C>A (p.Ala148Asp)
c.-463+17018G>T (n.-463+17018G>T)
17g.44006554C>GCA399726058NAGS,PYYc.941C>G (p.Ala314Gly)
c.848C>G (p.Ala283Gly)
n.216C>G
c.443C>G (p.Ala148Gly)
c.-463+17018G>C (n.-463+17018G>C)
 gnomAD v4
17g.44006554C>TCA399726059NAGS,PYYc.941C>T (p.Ala314Val)
c.848C>T (p.Ala283Val)
n.216C>T
c.443C>T (p.Ala148Val)
c.-463+17018G>A (n.-463+17018G>A)
 gnomAD v4
17g.44006555C>ACA500241072NAGS,PYYc.942C>A (p.Ala314=)
c.849C>A (p.Ala283=)
n.217C>A
c.444C>A (p.Ala148=)
c.-463+17017G>T (n.-463+17017G>T)
17g.44006555C=CA2261182184NAGS,PYYc.942C= (p.Ala314=)
c.849C= (p.Ala283=)
n.217C=
c.444C= (p.Ala148=)
c.-463+17017G= (n.-463+17017G=)
17g.44006555C>GCA500241073NAGS,PYYc.942C>G (p.Ala314=)
c.849C>G (p.Ala283=)
n.217C>G
c.444C>G (p.Ala148=)
c.-463+17017G>C (n.-463+17017G>C)
17g.44006555C>TCA500241074NAGS,PYYc.942C>T (p.Ala314=)
c.849C>T (p.Ala283=)
n.217C>T
c.444C>T (p.Ala148=)
c.-463+17017G>A (n.-463+17017G>A)
 ClinVar dbSNP gnomAD v2 gnomAD v4
17g.44006556G>ACA8595280NAGS,PYYc.943G>A (p.Asp315Asn)
c.850G>A (p.Asp284Asn)
n.218G>A
c.445G>A (p.Asp149Asn)
c.-463+17016C>T (n.-463+17016C>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.44006556G>CCA399726060NAGS,PYYc.943G>C (p.Asp315His)
c.850G>C (p.Asp284His)
n.218G>C
c.445G>C (p.Asp149His)
c.-463+17016C>G (n.-463+17016C>G)
17g.44006556G=CA2261182185NAGS,PYYc.943G= (p.Asp315=)
c.850G= (p.Asp284=)
n.218G=
c.445G= (p.Asp149=)
c.-463+17016C= (n.-463+17016C=)
17g.44006556G>TCA399726061NAGS,PYYc.943G>T (p.Asp315Tyr)
c.850G>T (p.Asp284Tyr)
n.218G>T
c.445G>T (p.Asp149Tyr)
c.-463+17016C>A (n.-463+17016C>A)
 gnomAD v4
17g.44006557A>CCA399726062NAGS,PYYc.944A>C (p.Asp315Ala)
c.851A>C (p.Asp284Ala)
n.219A>C
c.446A>C (p.Asp149Ala)
c.-463+17015T>G (n.-463+17015T>G)
17g.44006557A>GCA399726063NAGS,PYYc.944A>G (p.Asp315Gly)
c.851A>G (p.Asp284Gly)
n.219A>G
c.446A>G (p.Asp149Gly)
c.-463+17015T>C (n.-463+17015T>C)
17g.44006557A>TCA399726064NAGS,PYYc.944A>T (p.Asp315Val)
c.851A>T (p.Asp284Val)
n.219A>T
c.446A>T (p.Asp149Val)
c.-463+17015T>A (n.-463+17015T>A)
 COSMIC
17g.44006558C>ACA399726065NAGS,PYYc.945C>A (p.Asp315Glu)
c.852C>A (p.Asp284Glu)
n.220C>A
c.447C>A (p.Asp149Glu)
c.-463+17014G>T (n.-463+17014G>T)
 gnomAD v4
17g.44006558C>GCA399726067NAGS,PYYc.945C>G (p.Asp315Glu)
c.852C>G (p.Asp284Glu)
n.220C>G
c.447C>G (p.Asp149Glu)
c.-463+17014G>C (n.-463+17014G>C)
17g.44006558C>TCA500241075NAGS,PYYc.945C>T (p.Asp315=)
c.852C>T (p.Asp284=)
n.220C>T
c.447C>T (p.Asp149=)
c.-463+17014G>A (n.-463+17014G>A)
17g.44006559C>ACA399726069NAGS,PYYc.946C>A (p.Leu316Met)
c.853C>A (p.Leu285Met)
n.221C>A
c.448C>A (p.Leu150Met)
c.-463+17013G>T (n.-463+17013G>T)
 gnomAD v4
17g.44006559C>GCA399726071NAGS,PYYc.946C>G (p.Leu316Val)
c.853C>G (p.Leu285Val)
n.221C>G
c.448C>G (p.Leu150Val)
c.-463+17013G>C (n.-463+17013G>C)
17g.44006559C>TCA500241076NAGS,PYYc.946C>T (p.Leu316=)
c.853C>T (p.Leu285=)
n.221C>T
c.448C>T (p.Leu150=)
c.-463+17013G>A (n.-463+17013G>A)
17g.44006560T>ACA399726072NAGS,PYYc.947T>A (p.Leu316Gln)
c.854T>A (p.Leu285Gln)
n.222T>A
c.449T>A (p.Leu150Gln)
c.-463+17012A>T (n.-463+17012A>T)
 gnomAD v4
17g.44006560T>CCA399726077NAGS,PYYc.947T>C (p.Leu316Pro)
c.854T>C (p.Leu285Pro)
n.222T>C
c.449T>C (p.Leu150Pro)
c.-463+17012A>G (n.-463+17012A>G)
 gnomAD v4
17g.44006560T>GCA399726074NAGS,PYYc.947T>G (p.Leu316Arg)
c.854T>G (p.Leu285Arg)
n.222T>G
c.449T>G (p.Leu150Arg)
c.-463+17012A>C (n.-463+17012A>C)
17g.44006561G>ACA500241077NAGS,PYYc.948G>A (p.Leu316=)
c.855G>A (p.Leu285=)
n.223G>A
c.450G>A (p.Leu150=)
c.-463+17011C>T (n.-463+17011C>T)
 dbSNP gnomAD v3 gnomAD v4
17g.44006561G>CCA500241078NAGS,PYYc.948G>C (p.Leu316=)
c.855G>C (p.Leu285=)
n.223G>C
c.450G>C (p.Leu150=)
c.-463+17011C>G (n.-463+17011C>G)
17g.44006561G=CA2261182186NAGS,PYYc.948G= (p.Leu316=)
c.855G= (p.Leu285=)
n.223G=
c.450G= (p.Leu150=)
c.-463+17011C= (n.-463+17011C=)
17g.44006561G>TCA500241079NAGS,PYYc.948G>T (p.Leu316=)
c.855G>T (p.Leu285=)
n.223G>T
c.450G>T (p.Leu150=)
c.-463+17011C>A (n.-463+17011C>A)
 gnomAD v4
17g.44006562G>ACA399726079NAGS,PYYc.949G>A (p.Asp317Asn)
c.856G>A (p.Asp286Asn)
n.224G>A
c.451G>A (p.Asp151Asn)
c.-463+17010C>T (n.-463+17010C>T)
 ClinVar dbSNP gnomAD v3 gnomAD v4
17g.44006562G>CCA399726081NAGS,PYYc.949G>C (p.Asp317His)
c.856G>C (p.Asp286His)
n.224G>C
c.451G>C (p.Asp151His)
c.-463+17010C>G (n.-463+17010C>G)
17g.44006562G=CA2261182187NAGS,PYYc.949G= (p.Asp317=)
c.856G= (p.Asp286=)
n.224G=
c.451G= (p.Asp151=)
c.-463+17010C= (n.-463+17010C=)
17g.44006562G>TCA399726083NAGS,PYYc.949G>T (p.Asp317Tyr)
c.856G>T (p.Asp286Tyr)
n.224G>T
c.451G>T (p.Asp151Tyr)
c.-463+17010C>A (n.-463+17010C>A)
 gnomAD v4
17g.44006563A>CCA399726084NAGS,PYYc.950A>C (p.Asp317Ala)
c.857A>C (p.Asp286Ala)
n.225A>C
c.452A>C (p.Asp151Ala)
c.-463+17009T>G (n.-463+17009T>G)
 gnomAD v4
17g.44006563A>GCA399726086NAGS,PYYc.950A>G (p.Asp317Gly)
c.857A>G (p.Asp286Gly)
n.225A>G
c.452A>G (p.Asp151Gly)
c.-463+17009T>C (n.-463+17009T>C)
17g.44006563A>TCA399726088NAGS,PYYc.950A>T (p.Asp317Val)
c.857A>T (p.Asp286Val)
n.225A>T
c.452A>T (p.Asp151Val)
c.-463+17009T>A (n.-463+17009T>A)
17g.44006564C>ACA399726090NAGS,PYYc.951C>A (p.Asp317Glu)
c.858C>A (p.Asp286Glu)
n.226C>A
c.453C>A (p.Asp151Glu)
c.-463+17008G>T (n.-463+17008G>T)
17g.44006564C>GCA399726091NAGS,PYYc.951C>G (p.Asp317Glu)
c.858C>G (p.Asp286Glu)
n.226C>G
c.453C>G (p.Asp151Glu)
c.-463+17008G>C (n.-463+17008G>C)
17g.44006564C>TCA500241080NAGS,PYYc.951C>T (p.Asp317=)
c.858C>T (p.Asp286=)
n.226C>T
c.453C>T (p.Asp151=)
c.-463+17008G>A (n.-463+17008G>A)
 ClinVar dbSNP gnomAD v4
17g.44006565C>ACA399726093NAGS,PYYc.952C>A (p.Leu318Met)
c.859C>A (p.Leu287Met)
n.227C>A
c.454C>A (p.Leu152Met)
c.-463+17007G>T (n.-463+17007G>T)
 gnomAD v4
17g.44006565C>GCA399726095NAGS,PYYc.952C>G (p.Leu318Val)
c.859C>G (p.Leu287Val)
n.227C>G
c.454C>G (p.Leu152Val)
c.-463+17007G>C (n.-463+17007G>C)
17g.44006565C>TCA500241081NAGS,PYYc.952C>T (p.Leu318=)
c.859C>T (p.Leu287=)
n.227C>T
c.454C>T (p.Leu152=)
c.-463+17007G>A (n.-463+17007G>A)
 gnomAD v4
17g.44006566T>ACA399726101NAGS,PYYc.953T>A (p.Leu318Gln)
c.860T>A (p.Leu287Gln)
n.228T>A
c.455T>A (p.Leu152Gln)
c.-463+17006A>T (n.-463+17006A>T)
17g.44006566T>CCA399726100NAGS,PYYc.953T>C (p.Leu318Pro)
c.860T>C (p.Leu287Pro)
n.228T>C
c.455T>C (p.Leu152Pro)
c.-463+17006A>G (n.-463+17006A>G)
 gnomAD v4
17g.44006566T>GCA399726098NAGS,PYYc.953T>G (p.Leu318Arg)
c.860T>G (p.Leu287Arg)
n.228T>G
c.455T>G (p.Leu152Arg)
c.-463+17006A>C (n.-463+17006A>C)
17g.44006567G>ACA500241082NAGS,PYYc.954G>A (p.Leu318=)
c.861G>A (p.Leu287=)
n.229G>A
c.456G>A (p.Leu152=)
c.-463+17005C>T (n.-463+17005C>T)
17g.44006567G>CCA500241083NAGS,PYYc.954G>C (p.Leu318=)
c.861G>C (p.Leu287=)
n.229G>C
c.456G>C (p.Leu152=)
c.-463+17005C>G (n.-463+17005C>G)
17g.44006567G>TCA500241084NAGS,PYYc.954G>T (p.Leu318=)
c.861G>T (p.Leu287=)
n.229G>T
c.456G>T (p.Leu152=)
c.-463+17005C>A (n.-463+17005C>A)
17g.44006568G>ACA399726104NAGS,PYYc.955G>A (p.Val319Met)
c.862G>A (p.Val288Met)
n.230G>A
c.457G>A (p.Val153Met)
c.-463+17004C>T (n.-463+17004C>T)
 dbSNP gnomAD v2 gnomAD v4
17g.44006568G>CCA399726105NAGS,PYYc.955G>C (p.Val319Leu)
c.862G>C (p.Val288Leu)
n.230G>C
c.457G>C (p.Val153Leu)
c.-463+17004C>G (n.-463+17004C>G)
17g.44006568G=CA2261182188NAGS,PYYc.955G= (p.Val319=)
c.862G= (p.Val288=)
n.230G=
c.457G= (p.Val153=)
c.-463+17004C= (n.-463+17004C=)
17g.44006568G>TCA399726107NAGS,PYYc.955G>T (p.Val319Leu)
c.862G>T (p.Val288Leu)
n.230G>T
c.457G>T (p.Val153Leu)
c.-463+17004C>A (n.-463+17004C>A)
 gnomAD v4
17g.44006569T>ACA399726108NAGS,PYYc.956T>A (p.Val319Glu)
c.863T>A (p.Val288Glu)
n.231T>A
c.458T>A (p.Val153Glu)
c.-463+17003A>T (n.-463+17003A>T)
17g.44006569T>CCA399726109NAGS,PYYc.956T>C (p.Val319Ala)
c.863T>C (p.Val288Ala)
n.231T>C
c.458T>C (p.Val153Ala)
c.-463+17003A>G (n.-463+17003A>G)
 dbSNP gnomAD v2 gnomAD v4 COSMIC
17g.44006569T>GCA399726111NAGS,PYYc.956T>G (p.Val319Gly)
c.863T>G (p.Val288Gly)
n.231T>G
c.458T>G (p.Val153Gly)
c.-463+17003A>C (n.-463+17003A>C)
17g.44006569T=CA2261182189NAGS,PYYc.956T= (p.Val319=)
c.863T= (p.Val288=)
n.231T=
c.458T= (p.Val153=)
c.-463+17003A= (n.-463+17003A=)
17g.44006570G>ACA500241085NAGS,PYYc.957G>A (p.Val319=)
c.864G>A (p.Val288=)
n.232G>A
c.459G>A (p.Val153=)
c.-463+17002C>T (n.-463+17002C>T)
 ClinVar gnomAD v4
17g.44006570G>CCA500241086NAGS,PYYc.957G>C (p.Val319=)
c.864G>C (p.Val288=)
n.232G>C
c.459G>C (p.Val153=)
c.-463+17002C>G (n.-463+17002C>G)
 gnomAD v4
17g.44006570G>TCA500241087NAGS,PYYc.957G>T (p.Val319=)
c.864G>T (p.Val288=)
n.232G>T
c.459G>T (p.Val153=)
c.-463+17002C>A (n.-463+17002C>A)
17g.44006570_44006571delinsGTCA2261182190NAGS,PYYc.957_958delinsGT (p.Val319=)
c.864_865delinsGT (p.Val288=)
n.232_233delinsGT
c.459_460delinsGT (p.Val153=)
c.-463+17001_-463+17002delinsAC (n.-463+17001_-463+17002delinsAC)
17g.44006571delCA626222676NAGS,PYYc.958del (p.Cys320AlafsTer6)
c.865del (p.Cys289AlafsTer6)
n.233del
c.460del (p.Cys154AlafsTer6)
c.-463+17001del (n.-463+17001del)
 dbSNP gnomAD v2 gnomAD v4
17g.44006571T>ACA399726116NAGS,PYYc.958T>A (p.Cys320Ser)
c.865T>A (p.Cys289Ser)
n.233T>A
c.460T>A (p.Cys154Ser)
c.-463+17001A>T (n.-463+17001A>T)
17g.44006571T>CCA399726113NAGS,PYYc.958T>C (p.Cys320Arg)
c.865T>C (p.Cys289Arg)
n.233T>C
c.460T>C (p.Cys154Arg)
c.-463+17001A>G (n.-463+17001A>G)
17g.44006571T>GCA399726115NAGS,PYYc.958T>G (p.Cys320Gly)
c.865T>G (p.Cys289Gly)
n.233T>G
c.460T>G (p.Cys154Gly)
c.-463+17001A>C (n.-463+17001A>C)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.44006571T=CA2261182191NAGS,PYYc.958T= (p.Cys320=)
c.865T= (p.Cys289=)
n.233T=
c.460T= (p.Cys154=)
c.-463+17001A= (n.-463+17001A=)
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

Number of alleles fetched