Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.75582084A>CCA367726930HIP1c.533T>G (p.Val178Gly)
c.446T>G (p.Val149Gly)
c.431T>G (p.Val144Gly)
c.491T>G (p.Val164Gly)
7g.75582084A>GCA367726931HIP1c.533T>C (p.Val178Ala)
c.446T>C (p.Val149Ala)
c.431T>C (p.Val144Ala)
c.491T>C (p.Val164Ala)
7g.75582084A>TCA367726932HIP1c.533T>A (p.Val178Glu)
c.446T>A (p.Val149Glu)
c.431T>A (p.Val144Glu)
c.491T>A (p.Val164Glu)
7g.75582085C>ACA4302597HIP1c.532G>T (p.Val178Leu)
c.445G>T (p.Val149Leu)
c.430G>T (p.Val144Leu)
c.490G>T (p.Val164Leu)
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.75582085C=CA1717985595HIP1c.532G= (p.Val178=)
c.445G= (p.Val149=)
c.430G= (p.Val144=)
c.490G= (p.Val164=)
7g.75582085C>GCA367726937HIP1c.532G>C (p.Val178Leu)
c.445G>C (p.Val149Leu)
c.430G>C (p.Val144Leu)
c.490G>C (p.Val164Leu)
7g.75582085C>TCA4302598HIP1c.532G>A (p.Val178Met)
c.445G>A (p.Val149Met)
c.430G>A (p.Val144Met)
c.490G>A (p.Val164Met)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.75582086G>ACA4302599HIP1c.531C>T (p.Asp177=)
c.444C>T (p.Asp148=)
c.429C>T (p.Asp143=)
c.489C>T (p.Asp163=)
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.75582086G>CCA367726944HIP1c.531C>G (p.Asp177Glu)
c.444C>G (p.Asp148Glu)
c.429C>G (p.Asp143Glu)
c.489C>G (p.Asp163Glu)
7g.75582086G=CA1717985597HIP1c.531C= (p.Asp177=)
c.444C= (p.Asp148=)
c.429C= (p.Asp143=)
c.489C= (p.Asp163=)
7g.75582086G>TCA367726947HIP1c.531C>A (p.Asp177Glu)
c.444C>A (p.Asp148Glu)
c.429C>A (p.Asp143Glu)
c.489C>A (p.Asp163Glu)
7g.75582087T>ACA367726954HIP1c.530A>T (p.Asp177Val)
c.443A>T (p.Asp148Val)
c.428A>T (p.Asp143Val)
c.488A>T (p.Asp163Val)
7g.75582087T>CCA367726949HIP1c.530A>G (p.Asp177Gly)
c.443A>G (p.Asp148Gly)
c.428A>G (p.Asp143Gly)
c.488A>G (p.Asp163Gly)
7g.75582087T>GCA367726952HIP1c.530A>C (p.Asp177Ala)
c.443A>C (p.Asp148Ala)
c.428A>C (p.Asp143Ala)
c.488A>C (p.Asp163Ala)
7g.75582088C>ACA367726956HIP1c.529G>T (p.Asp177Tyr)
c.442G>T (p.Asp148Tyr)
c.427G>T (p.Asp143Tyr)
c.487G>T (p.Asp163Tyr)
7g.75582088C>GCA367726958HIP1c.529G>C (p.Asp177His)
c.442G>C (p.Asp148His)
c.427G>C (p.Asp143His)
c.487G>C (p.Asp163His)
7g.75582088C>TCA367726965HIP1c.529G>A (p.Asp177Asn)
c.442G>A (p.Asp148Asn)
c.427G>A (p.Asp143Asn)
c.487G>A (p.Asp163Asn)
7g.75582089A>CCA367726968HIP1c.528T>G (p.Ser176Arg)
c.441T>G (p.Ser147Arg)
c.426T>G (p.Ser142Arg)
c.486T>G (p.Ser162Arg)
7g.75582089A>GCA455709779HIP1c.528T>C (p.Ser176=)
c.441T>C (p.Ser147=)
c.426T>C (p.Ser142=)
c.486T>C (p.Ser162=)
7g.75582089A>TCA367726976HIP1c.528T>A (p.Ser176Arg)
c.441T>A (p.Ser147Arg)
c.426T>A (p.Ser142Arg)
c.486T>A (p.Ser162Arg)
7g.75582090C>ACA4302600HIP1c.527G>T (p.Ser176Ile)
c.440G>T (p.Ser147Ile)
c.425G>T (p.Ser142Ile)
c.485G>T (p.Ser162Ile)
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.75582090C=CA1717985600HIP1c.527G= (p.Ser176=)
c.440G= (p.Ser147=)
c.425G= (p.Ser142=)
c.485G= (p.Ser162=)
7g.75582090C>GCA367726986HIP1c.527G>C (p.Ser176Thr)
c.440G>C (p.Ser147Thr)
c.425G>C (p.Ser142Thr)
c.485G>C (p.Ser162Thr)
7g.75582090C>TCA367726987HIP1c.527G>A (p.Ser176Asn)
c.440G>A (p.Ser147Asn)
c.425G>A (p.Ser142Asn)
c.485G>A (p.Ser162Asn)
7g.75582091T>ACA367726989HIP1c.526A>T (p.Ser176Cys)
c.439A>T (p.Ser147Cys)
c.424A>T (p.Ser142Cys)
c.484A>T (p.Ser162Cys)
7g.75582091T>CCA367726993HIP1c.526A>G (p.Ser176Gly)
c.439A>G (p.Ser147Gly)
c.424A>G (p.Ser142Gly)
c.484A>G (p.Ser162Gly)
 dbSNP
7g.75582091T>GCA367726994HIP1c.526A>C (p.Ser176Arg)
c.439A>C (p.Ser147Arg)
c.424A>C (p.Ser142Arg)
c.484A>C (p.Ser162Arg)
7g.75582091T=CA1717985604HIP1c.526A= (p.Ser176=)
c.439A= (p.Ser147=)
c.424A= (p.Ser142=)
c.484A= (p.Ser162=)
7g.75582092T>ACA367727004HIP1c.525A>T (p.Glu175Asp)
c.438A>T (p.Glu146Asp)
c.423A>T (p.Glu141Asp)
c.483A>T (p.Glu161Asp)
7g.75582092T>CCA455709852HIP1c.525A>G (p.Glu175=)
c.438A>G (p.Glu146=)
c.423A>G (p.Glu141=)
c.483A>G (p.Glu161=)
7g.75582092T>GCA367726998HIP1c.525A>C (p.Glu175Asp)
c.438A>C (p.Glu146Asp)
c.423A>C (p.Glu141Asp)
c.483A>C (p.Glu161Asp)
7g.75582093T>ACA367727010HIP1c.524A>T (p.Glu175Val)
c.437A>T (p.Glu146Val)
c.422A>T (p.Glu141Val)
c.482A>T (p.Glu161Val)
7g.75582093T>CCA367727014HIP1c.524A>G (p.Glu175Gly)
c.437A>G (p.Glu146Gly)
c.422A>G (p.Glu141Gly)
c.482A>G (p.Glu161Gly)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.75582093T>GCA367727022HIP1c.524A>C (p.Glu175Ala)
c.437A>C (p.Glu146Ala)
c.422A>C (p.Glu141Ala)
c.482A>C (p.Glu161Ala)
7g.75582093T=CA1717985607HIP1c.524A= (p.Glu175=)
c.437A= (p.Glu146=)
c.422A= (p.Glu141=)
c.482A= (p.Glu161=)
7g.75582094C>ACA367727033HIP1c.523G>T (p.Glu175Ter)
c.436G>T (p.Glu146Ter)
c.421G>T (p.Glu141Ter)
c.481G>T (p.Glu161Ter)
7g.75582094C>GCA367727038HIP1c.523G>C (p.Glu175Gln)
c.436G>C (p.Glu146Gln)
c.421G>C (p.Glu141Gln)
c.481G>C (p.Glu161Gln)
7g.75582094C>TCA367727041HIP1c.523G>A (p.Glu175Lys)
c.436G>A (p.Glu146Lys)
c.421G>A (p.Glu141Lys)
c.481G>A (p.Glu161Lys)
7g.75582095T>ACA455709895HIP1c.522A>T (p.Gly174=)
c.435A>T (p.Gly145=)
c.420A>T (p.Gly140=)
c.480A>T (p.Gly160=)
7g.75582095T>CCA455709899HIP1c.522A>G (p.Gly174=)
c.435A>G (p.Gly145=)
c.420A>G (p.Gly140=)
c.480A>G (p.Gly160=)
 gnomAD v4
7g.75582095T>GCA455709902HIP1c.522A>C (p.Gly174=)
c.435A>C (p.Gly145=)
c.420A>C (p.Gly140=)
c.480A>C (p.Gly160=)
7g.75582096C>ACA367727046HIP1c.521G>T (p.Gly174Val)
c.434G>T (p.Gly145Val)
c.419G>T (p.Gly140Val)
c.479G>T (p.Gly160Val)
7g.75582096C>GCA367727052HIP1c.521G>C (p.Gly174Ala)
c.434G>C (p.Gly145Ala)
c.419G>C (p.Gly140Ala)
c.479G>C (p.Gly160Ala)
7g.75582096C>TCA367727056HIP1c.521G>A (p.Gly174Glu)
c.434G>A (p.Gly145Glu)
c.419G>A (p.Gly140Glu)
c.479G>A (p.Gly160Glu)
7g.75582097C>ACA367727057HIP1c.520G>T (p.Gly174Ter)
c.433G>T (p.Gly145Ter)
c.418G>T (p.Gly140Ter)
c.478G>T (p.Gly160Ter)
7g.75582097C=CA1717985609HIP1c.520G= (p.Gly174=)
c.433G= (p.Gly145=)
c.418G= (p.Gly140=)
c.478G= (p.Gly160=)
7g.75582097C>GCA367727060HIP1c.520G>C (p.Gly174Arg)
c.433G>C (p.Gly145Arg)
c.418G>C (p.Gly140Arg)
c.478G>C (p.Gly160Arg)
7g.75582097C>TCA4302601HIP1c.520G>A (p.Gly174Arg)
c.433G>A (p.Gly145Arg)
c.418G>A (p.Gly140Arg)
c.478G>A (p.Gly160Arg)
 dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
7g.75582098A=CA1717985611HIP1c.519T= (p.Ala173=)
c.432T= (p.Ala144=)
c.417T= (p.Ala139=)
c.477T= (p.Ala159=)
7g.75582098A>CCA455709951HIP1c.519T>G (p.Ala173=)
c.432T>G (p.Ala144=)
c.417T>G (p.Ala139=)
c.477T>G (p.Ala159=)
 dbSNP
7g.75582098A>GCA4302602HIP1c.519T>C (p.Ala173=)
c.432T>C (p.Ala144=)
c.417T>C (p.Ala139=)
c.477T>C (p.Ala159=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.75582098A>TCA455709958HIP1c.519T>A (p.Ala173=)
c.432T>A (p.Ala144=)
c.417T>A (p.Ala139=)
c.477T>A (p.Ala159=)
 dbSNP
7g.75582099G>ACA367727078HIP1c.518C>T (p.Ala173Val)
c.431C>T (p.Ala144Val)
c.416C>T (p.Ala139Val)
c.476C>T (p.Ala159Val)
 COSMIC
7g.75582099G>CCA367727070HIP1c.518C>G (p.Ala173Gly)
c.431C>G (p.Ala144Gly)
c.416C>G (p.Ala139Gly)
c.476C>G (p.Ala159Gly)
7g.75582099G>TCA367727067HIP1c.518C>A (p.Ala173Asp)
c.431C>A (p.Ala144Asp)
c.416C>A (p.Ala139Asp)
c.476C>A (p.Ala159Asp)
7g.75582100C>ACA367727081HIP1c.517G>T (p.Ala173Ser)
c.430G>T (p.Ala144Ser)
c.415G>T (p.Ala139Ser)
c.475G>T (p.Ala159Ser)
7g.75582100C=CA1717985614HIP1c.517G= (p.Ala173=)
c.430G= (p.Ala144=)
c.415G= (p.Ala139=)
c.475G= (p.Ala159=)
7g.75582100C>GCA367727082HIP1c.517G>C (p.Ala173Pro)
c.430G>C (p.Ala144Pro)
c.415G>C (p.Ala139Pro)
c.475G>C (p.Ala159Pro)
7g.75582100C>TCA367727084HIP1c.517G>A (p.Ala173Thr)
c.430G>A (p.Ala144Thr)
c.415G>A (p.Ala139Thr)
c.475G>A (p.Ala159Thr)
 dbSNP
7g.75582101C>ACA367727092HIP1c.516G>T (p.Glu172Asp)
c.429G>T (p.Glu143Asp)
c.414G>T (p.Glu138Asp)
c.474G>T (p.Glu158Asp)
7g.75582101C>GCA367727095HIP1c.516G>C (p.Glu172Asp)
c.429G>C (p.Glu143Asp)
c.414G>C (p.Glu138Asp)
c.474G>C (p.Glu158Asp)
7g.75582101C>TCA455709995HIP1c.516G>A (p.Glu172=)
c.429G>A (p.Glu143=)
c.414G>A (p.Glu138=)
c.474G>A (p.Glu158=)
 gnomAD v4
7g.75582102T>ACA367727099HIP1c.515A>T (p.Glu172Val)
c.428A>T (p.Glu143Val)
c.413A>T (p.Glu138Val)
c.473A>T (p.Glu158Val)
7g.75582102T>CCA367727100HIP1c.515A>G (p.Glu172Gly)
c.428A>G (p.Glu143Gly)
c.413A>G (p.Glu138Gly)
c.473A>G (p.Glu158Gly)
7g.75582102T>GCA367727101HIP1c.515A>C (p.Glu172Ala)
c.428A>C (p.Glu143Ala)
c.413A>C (p.Glu138Ala)
c.473A>C (p.Glu158Ala)
7g.75582103C>ACA367727104HIP1c.514G>T (p.Glu172Ter)
c.427G>T (p.Glu143Ter)
c.412G>T (p.Glu138Ter)
c.472G>T (p.Glu158Ter)
7g.75582103C=CA1717985617HIP1c.514G= (p.Glu172=)
c.427G= (p.Glu143=)
c.412G= (p.Glu138=)
c.472G= (p.Glu158=)
7g.75582103C>GCA367727106HIP1c.514G>C (p.Glu172Gln)
c.427G>C (p.Glu143Gln)
c.412G>C (p.Glu138Gln)
c.472G>C (p.Glu158Gln)
7g.75582103C>TCA4302603HIP1c.514G>A (p.Glu172Lys)
c.427G>A (p.Glu143Lys)
c.412G>A (p.Glu138Lys)
c.472G>A (p.Glu158Lys)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.75582104G>ACA4302605HIP1c.513C>T (p.Asp171=)
c.426C>T (p.Asp142=)
c.411C>T (p.Asp137=)
c.471C>T (p.Asp157=)
 dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
7g.75582104G>CCA367727109HIP1c.513C>G (p.Asp171Glu)
c.426C>G (p.Asp142Glu)
c.411C>G (p.Asp137Glu)
c.471C>G (p.Asp157Glu)
7g.75582104G=CA1717985619HIP1c.513C= (p.Asp171=)
c.426C= (p.Asp142=)
c.411C= (p.Asp137=)
c.471C= (p.Asp157=)
7g.75582104G>TCA4302604HIP1c.513C>A (p.Asp171Glu)
c.426C>A (p.Asp142Glu)
c.411C>A (p.Asp137Glu)
c.471C>A (p.Asp157Glu)
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.75582105T>ACA367727134HIP1c.512A>T (p.Asp171Val)
c.425A>T (p.Asp142Val)
c.410A>T (p.Asp137Val)
c.470A>T (p.Asp157Val)
7g.75582105T>CCA367727139HIP1c.512A>G (p.Asp171Gly)
c.425A>G (p.Asp142Gly)
c.410A>G (p.Asp137Gly)
c.470A>G (p.Asp157Gly)
7g.75582105T>GCA367727125HIP1c.512A>C (p.Asp171Ala)
c.425A>C (p.Asp142Ala)
c.410A>C (p.Asp137Ala)
c.470A>C (p.Asp157Ala)
7g.75582106C>ACA367727141HIP1c.511G>T (p.Asp171Tyr)
c.424G>T (p.Asp142Tyr)
c.409G>T (p.Asp137Tyr)
c.469G>T (p.Asp157Tyr)
7g.75582106C>GCA367727143HIP1c.511G>C (p.Asp171His)
c.424G>C (p.Asp142His)
c.409G>C (p.Asp137His)
c.469G>C (p.Asp157His)
 gnomAD v4
7g.75582106C>TCA367727146HIP1c.511G>A (p.Asp171Asn)
c.424G>A (p.Asp142Asn)
c.409G>A (p.Asp137Asn)
c.469G>A (p.Asp157Asn)
7g.75582107C>ACA455710090HIP1c.510G>T (p.Leu170=)
c.423G>T (p.Leu141=)
c.408G>T (p.Leu136=)
c.468G>T (p.Leu156=)
7g.75582107C=CA1717985621HIP1c.510G= (p.Leu170=)
c.423G= (p.Leu141=)
c.408G= (p.Leu136=)
c.468G= (p.Leu156=)
7g.75582107C>GCA455710095HIP1c.510G>C (p.Leu170=)
c.423G>C (p.Leu141=)
c.408G>C (p.Leu136=)
c.468G>C (p.Leu156=)
7g.75582107C>TCA455710107HIP1c.510G>A (p.Leu170=)
c.423G>A (p.Leu141=)
c.408G>A (p.Leu136=)
c.468G>A (p.Leu156=)
 dbSNP gnomAD v2
7g.75582108A>CCA367727148HIP1c.509T>G (p.Leu170Arg)
c.422T>G (p.Leu141Arg)
c.407T>G (p.Leu136Arg)
c.467T>G (p.Leu156Arg)
7g.75582108A>GCA367727149HIP1c.509T>C (p.Leu170Pro)
c.422T>C (p.Leu141Pro)
c.407T>C (p.Leu136Pro)
c.467T>C (p.Leu156Pro)
7g.75582108A>TCA367727151HIP1c.509T>A (p.Leu170Gln)
c.422T>A (p.Leu141Gln)
c.407T>A (p.Leu136Gln)
c.467T>A (p.Leu156Gln)
7g.75582109G>ACA4302606HIP1c.508C>T (p.Leu170=)
c.421C>T (p.Leu141=)
c.406C>T (p.Leu136=)
c.466C>T (p.Leu156=)
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.75582109G>CCA367727153HIP1c.508C>G (p.Leu170Val)
c.421C>G (p.Leu141Val)
c.406C>G (p.Leu136Val)
c.466C>G (p.Leu156Val)
7g.75582109G=CA1717985623HIP1c.508C= (p.Leu170=)
c.421C= (p.Leu141=)
c.406C= (p.Leu136=)
c.466C= (p.Leu156=)
7g.75582109G>TCA367727154HIP1c.508C>A (p.Leu170Met)
c.421C>A (p.Leu141Met)
c.406C>A (p.Leu136Met)
c.466C>A (p.Leu156Met)
7g.75582110C>ACA367727161HIP1c.507G>T (p.Gln169His)
c.420G>T (p.Gln140His)
c.405G>T (p.Gln135His)
c.465G>T (p.Gln155His)
 gnomAD v4
7g.75582110C>GCA367727167HIP1c.507G>C (p.Gln169His)
c.420G>C (p.Gln140His)
c.405G>C (p.Gln135His)
c.465G>C (p.Gln155His)
7g.75582110C>TCA455710168HIP1c.507G>A (p.Gln169=)
c.420G>A (p.Gln140=)
c.405G>A (p.Gln135=)
c.465G>A (p.Gln155=)
7g.75582111T>ACA367727169HIP1c.506A>T (p.Gln169Leu)
c.419A>T (p.Gln140Leu)
c.404A>T (p.Gln135Leu)
c.464A>T (p.Gln155Leu)
7g.75582111T>CCA367727170HIP1c.506A>G (p.Gln169Arg)
c.419A>G (p.Gln140Arg)
c.404A>G (p.Gln135Arg)
c.464A>G (p.Gln155Arg)
7g.75582111T>GCA367727171HIP1c.506A>C (p.Gln169Pro)
c.419A>C (p.Gln140Pro)
c.404A>C (p.Gln135Pro)
c.464A>C (p.Gln155Pro)
7g.75582112G>ACA367727173HIP1c.505C>T (p.Gln169Ter)
c.418C>T (p.Gln140Ter)
c.403C>T (p.Gln135Ter)
c.463C>T (p.Gln155Ter)
7g.75582112G>CCA367727176HIP1c.505C>G (p.Gln169Glu)
c.418C>G (p.Gln140Glu)
c.403C>G (p.Gln135Glu)
c.463C>G (p.Gln155Glu)
7g.75582112G>TCA367727174HIP1c.505C>A (p.Gln169Lys)
c.418C>A (p.Gln140Lys)
c.403C>A (p.Gln135Lys)
c.463C>A (p.Gln155Lys)
7g.75582113G>ACA455710206HIP1c.504C>T (p.Arg168=)
c.417C>T (p.Arg139=)
c.402C>T (p.Arg134=)
c.462C>T (p.Arg154=)
7g.75582113G>CCA455710209HIP1c.504C>G (p.Arg168=)
c.417C>G (p.Arg139=)
c.402C>G (p.Arg134=)
c.462C>G (p.Arg154=)
7g.75582113G>TCA455710215HIP1c.504C>A (p.Arg168=)
c.417C>A (p.Arg139=)
c.402C>A (p.Arg134=)
c.462C>A (p.Arg154=)
7g.75582114C>ACA367727179HIP1c.503G>T (p.Arg168Leu)
c.416G>T (p.Arg139Leu)
c.401G>T (p.Arg134Leu)
c.461G>T (p.Arg154Leu)
7g.75582114C=CA1717985625HIP1c.503G= (p.Arg168=)
c.416G= (p.Arg139=)
c.401G= (p.Arg134=)
c.461G= (p.Arg154=)
7g.75582114C>GCA367727180HIP1c.503G>C (p.Arg168Pro)
c.416G>C (p.Arg139Pro)
c.401G>C (p.Arg134Pro)
c.461G>C (p.Arg154Pro)
 dbSNP
7g.75582114C>TCA4302607HIP1c.503G>A (p.Arg168His)
c.416G>A (p.Arg139His)
c.401G>A (p.Arg134His)
c.461G>A (p.Arg154His)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.75582115G>ACA4302608HIP1c.502C>T (p.Arg168Cys)
c.415C>T (p.Arg139Cys)
c.400C>T (p.Arg134Cys)
c.460C>T (p.Arg154Cys)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.75582115G>CCA367727181HIP1c.502C>G (p.Arg168Gly)
c.415C>G (p.Arg139Gly)
c.400C>G (p.Arg134Gly)
c.460C>G (p.Arg154Gly)
7g.75582115G=CA1717985627HIP1c.502C= (p.Arg168=)
c.415C= (p.Arg139=)
c.400C= (p.Arg134=)
c.460C= (p.Arg154=)
7g.75582115G>TCA367727184HIP1c.502C>A (p.Arg168Ser)
c.415C>A (p.Arg139Ser)
c.400C>A (p.Arg134Ser)
c.460C>A (p.Arg154Ser)
7g.75582116G>ACA455710248HIP1c.501C>T (p.Asp167=)
c.414C>T (p.Asp138=)
c.399C>T (p.Asp133=)
c.459C>T (p.Asp153=)
 dbSNP gnomAD v2 gnomAD v4
7g.75582116G>CCA367727187HIP1c.501C>G (p.Asp167Glu)
c.414C>G (p.Asp138Glu)
c.399C>G (p.Asp133Glu)
c.459C>G (p.Asp153Glu)
7g.75582116G=CA1717985629HIP1c.501C= (p.Asp167=)
c.414C= (p.Asp138=)
c.399C= (p.Asp133=)
c.459C= (p.Asp153=)
7g.75582116G>TCA367727188HIP1c.501C>A (p.Asp167Glu)
c.414C>A (p.Asp138Glu)
c.399C>A (p.Asp133Glu)
c.459C>A (p.Asp153Glu)
 dbSNP gnomAD v4
7g.75582116_75582117insGACCA2578914549HIP1c.500_501insGTC (p.Asp167delinsGluSer)
c.413_414insGTC (p.Asp138delinsGluSer)
c.398_399insGTC (p.Asp133delinsGluSer)
c.458_459insGTC (p.Asp153delinsGluSer)
7g.75582117T>ACA367727189HIP1c.500A>T (p.Asp167Val)
c.413A>T (p.Asp138Val)
c.398A>T (p.Asp133Val)
c.458A>T (p.Asp153Val)
7g.75582117T>CCA367727190HIP1c.500A>G (p.Asp167Gly)
c.413A>G (p.Asp138Gly)
c.398A>G (p.Asp133Gly)
c.458A>G (p.Asp153Gly)
7g.75582117T>GCA367727192HIP1c.500A>C (p.Asp167Ala)
c.413A>C (p.Asp138Ala)
c.398A>C (p.Asp133Ala)
c.458A>C (p.Asp153Ala)
7g.75582118C>ACA367727196HIP1c.499G>T (p.Asp167Tyr)
c.412G>T (p.Asp138Tyr)
c.397G>T (p.Asp133Tyr)
c.457G>T (p.Asp153Tyr)
 gnomAD v4
7g.75582118C>GCA367727198HIP1c.499G>C (p.Asp167His)
c.412G>C (p.Asp138His)
c.397G>C (p.Asp133His)
c.457G>C (p.Asp153His)
7g.75582118C>TCA367727195HIP1c.499G>A (p.Asp167Asn)
c.412G>A (p.Asp138Asn)
c.397G>A (p.Asp133Asn)
c.457G>A (p.Asp153Asn)
7g.75582119A>CCA367727204HIP1c.498T>G (p.Ser166Arg)
c.411T>G (p.Ser137Arg)
c.396T>G (p.Ser132Arg)
c.456T>G (p.Ser152Arg)
7g.75582119A>GCA455710317HIP1c.498T>C (p.Ser166=)
c.411T>C (p.Ser137=)
c.396T>C (p.Ser132=)
c.456T>C (p.Ser152=)
7g.75582119A>TCA367727200HIP1c.498T>A (p.Ser166Arg)
c.411T>A (p.Ser137Arg)
c.396T>A (p.Ser132Arg)
c.456T>A (p.Ser152Arg)
7g.75582120C>ACA367727211HIP1c.497G>T (p.Ser166Ile)
c.410G>T (p.Ser137Ile)
c.395G>T (p.Ser132Ile)
c.455G>T (p.Ser152Ile)
7g.75582120C=CA1717985631HIP1c.497G= (p.Ser166=)
c.410G= (p.Ser137=)
c.395G= (p.Ser132=)
c.455G= (p.Ser152=)
7g.75582120C>GCA367727207HIP1c.497G>C (p.Ser166Thr)
c.410G>C (p.Ser137Thr)
c.395G>C (p.Ser132Thr)
c.455G>C (p.Ser152Thr)
 gnomAD v4
7g.75582120C>TCA367727209HIP1c.497G>A (p.Ser166Asn)
c.410G>A (p.Ser137Asn)
c.395G>A (p.Ser132Asn)
c.455G>A (p.Ser152Asn)
 dbSNP
7g.75582121T>ACA367727214HIP1c.496A>T (p.Ser166Cys)
c.409A>T (p.Ser137Cys)
c.394A>T (p.Ser132Cys)
c.454A>T (p.Ser152Cys)
7g.75582121T>CCA367727217HIP1c.496A>G (p.Ser166Gly)
c.409A>G (p.Ser137Gly)
c.394A>G (p.Ser132Gly)
c.454A>G (p.Ser152Gly)
7g.75582121T>GCA367727220HIP1c.496A>C (p.Ser166Arg)
c.409A>C (p.Ser137Arg)
c.394A>C (p.Ser132Arg)
c.454A>C (p.Ser152Arg)
7g.75582122C>ACA367727221HIP1c.495G>T (p.Met165Ile)
c.408G>T (p.Met136Ile)
c.393G>T (p.Met131Ile)
c.453G>T (p.Met151Ile)
7g.75582122C=CA1717985633HIP1c.495G= (p.Met165=)
c.408G= (p.Met136=)
c.393G= (p.Met131=)
c.453G= (p.Met151=)
7g.75582122C>GCA367727222HIP1c.495G>C (p.Met165Ile)
c.408G>C (p.Met136Ile)
c.393G>C (p.Met131Ile)
c.453G>C (p.Met151Ile)
 dbSNP gnomAD v4
7g.75582122C>TCA367727223HIP1c.495G>A (p.Met165Ile)
c.408G>A (p.Met136Ile)
c.393G>A (p.Met131Ile)
c.453G>A (p.Met151Ile)
7g.75582123A>CCA367727227HIP1c.494T>G (p.Met165Arg)
c.407T>G (p.Met136Arg)
c.392T>G (p.Met131Arg)
c.452T>G (p.Met151Arg)
7g.75582123A>GCA367727228HIP1c.494T>C (p.Met165Thr)
c.407T>C (p.Met136Thr)
c.392T>C (p.Met131Thr)
c.452T>C (p.Met151Thr)
7g.75582123A>TCA367727229HIP1c.494T>A (p.Met165Lys)
c.407T>A (p.Met136Lys)
c.392T>A (p.Met131Lys)
c.452T>A (p.Met151Lys)
7g.75582124T>ACA367727233HIP1c.493A>T (p.Met165Leu)
c.406A>T (p.Met136Leu)
c.391A>T (p.Met131Leu)
c.451A>T (p.Met151Leu)
7g.75582124T>CCA367727236HIP1c.493A>G (p.Met165Val)
c.406A>G (p.Met136Val)
c.391A>G (p.Met131Val)
c.451A>G (p.Met151Val)
 dbSNP
7g.75582124T>GCA367727238HIP1c.493A>C (p.Met165Leu)
c.406A>C (p.Met136Leu)
c.391A>C (p.Met131Leu)
c.451A>C (p.Met151Leu)
7g.75582124T=CA1717985635HIP1c.493A= (p.Met165=)
c.406A= (p.Met136=)
c.391A= (p.Met131=)
c.451A= (p.Met151=)
7g.75582125C>ACA367727244HIP1c.492G>T (p.Gln164His)
c.405G>T (p.Gln135His)
c.390G>T (p.Gln130His)
c.450G>T (p.Gln150His)
7g.75582125C>GCA367727241HIP1c.492G>C (p.Gln164His)
c.405G>C (p.Gln135His)
c.390G>C (p.Gln130His)
c.450G>C (p.Gln150His)
 gnomAD v4
7g.75582125C>TCA455710387HIP1c.492G>A (p.Gln164=)
c.405G>A (p.Gln135=)
c.390G>A (p.Gln130=)
c.450G>A (p.Gln150=)
 gnomAD v4
7g.75582126T>ACA367727249HIP1c.491A>T (p.Gln164Leu)
c.404A>T (p.Gln135Leu)
c.389A>T (p.Gln130Leu)
c.449A>T (p.Gln150Leu)
7g.75582126T>CCA367727252HIP1c.491A>G (p.Gln164Arg)
c.404A>G (p.Gln135Arg)
c.389A>G (p.Gln130Arg)
c.449A>G (p.Gln150Arg)
7g.75582126T>GCA367727255HIP1c.491A>C (p.Gln164Pro)
c.404A>C (p.Gln135Pro)
c.389A>C (p.Gln130Pro)
c.449A>C (p.Gln150Pro)
7g.75582127G>ACA367727256HIP1c.490C>T (p.Gln164Ter)
c.403C>T (p.Gln135Ter)
c.388C>T (p.Gln130Ter)
c.448C>T (p.Gln150Ter)
7g.75582127G>CCA367727257HIP1c.490C>G (p.Gln164Glu)
c.403C>G (p.Gln135Glu)
c.388C>G (p.Gln130Glu)
c.448C>G (p.Gln150Glu)
7g.75582127G>TCA367727258HIP1c.490C>A (p.Gln164Lys)
c.403C>A (p.Gln135Lys)
c.388C>A (p.Gln130Lys)
c.448C>A (p.Gln150Lys)
7g.75582128C>ACA455710408HIP1c.489G>T (p.Leu163=)
c.402G>T (p.Leu134=)
c.387G>T (p.Leu129=)
c.447G>T (p.Leu149=)
7g.75582128C=CA1717985637HIP1c.489G= (p.Leu163=)
c.402G= (p.Leu134=)
c.387G= (p.Leu129=)
c.447G= (p.Leu149=)
7g.75582128C>GCA455710410HIP1c.489G>C (p.Leu163=)
c.402G>C (p.Leu134=)
c.387G>C (p.Leu129=)
c.447G>C (p.Leu149=)
7g.75582128C>TCA159888443HIP1c.489G>A (p.Leu163=)
c.402G>A (p.Leu134=)
c.387G>A (p.Leu129=)
c.447G>A (p.Leu149=)
 dbSNP gnomAD v4
7g.75582129A>CCA367727259HIP1c.488T>G (p.Leu163Arg)
c.401T>G (p.Leu134Arg)
c.386T>G (p.Leu129Arg)
c.446T>G (p.Leu149Arg)
7g.75582129A>GCA367727262HIP1c.488T>C (p.Leu163Pro)
c.401T>C (p.Leu134Pro)
c.386T>C (p.Leu129Pro)
c.446T>C (p.Leu149Pro)
7g.75582129A>TCA367727264HIP1c.488T>A (p.Leu163Gln)
c.401T>A (p.Leu134Gln)
c.386T>A (p.Leu129Gln)
c.446T>A (p.Leu149Gln)
7g.75582130G>ACA455710442HIP1c.487C>T (p.Leu163=)
c.400C>T (p.Leu134=)
c.385C>T (p.Leu129=)
c.445C>T (p.Leu149=)
7g.75582130G>CCA367727267HIP1c.487C>G (p.Leu163Val)
c.400C>G (p.Leu134Val)
c.385C>G (p.Leu129Val)
c.445C>G (p.Leu149Val)
7g.75582130G>TCA367727272HIP1c.487C>A (p.Leu163Met)
c.400C>A (p.Leu134Met)
c.385C>A (p.Leu129Met)
c.445C>A (p.Leu149Met)
7g.75582131G>ACA455710451HIP1c.486C>T (p.Asn162=)
c.399C>T (p.Asn133=)
c.384C>T (p.Asn128=)
c.444C>T (p.Asn148=)
7g.75582131G>CCA367727275HIP1c.486C>G (p.Asn162Lys)
c.399C>G (p.Asn133Lys)
c.384C>G (p.Asn128Lys)
c.444C>G (p.Asn148Lys)
7g.75582131G>TCA367727281HIP1c.486C>A (p.Asn162Lys)
c.399C>A (p.Asn133Lys)
c.384C>A (p.Asn128Lys)
c.444C>A (p.Asn148Lys)
7g.75582132T>ACA367727284HIP1c.485A>T (p.Asn162Ile)
c.398A>T (p.Asn133Ile)
c.383A>T (p.Asn128Ile)
c.443A>T (p.Asn148Ile)
7g.75582132T>CCA367727301HIP1c.485A>G (p.Asn162Ser)
c.398A>G (p.Asn133Ser)
c.383A>G (p.Asn128Ser)
c.443A>G (p.Asn148Ser)
7g.75582132T>GCA367727290HIP1c.485A>C (p.Asn162Thr)
c.398A>C (p.Asn133Thr)
c.383A>C (p.Asn128Thr)
c.443A>C (p.Asn148Thr)
7g.75582133T>ACA367727303HIP1c.484A>T (p.Asn162Tyr)
c.397A>T (p.Asn133Tyr)
c.382A>T (p.Asn128Tyr)
c.442A>T (p.Asn148Tyr)
7g.75582133T>CCA367727304HIP1c.484A>G (p.Asn162Asp)
c.397A>G (p.Asn133Asp)
c.382A>G (p.Asn128Asp)
c.442A>G (p.Asn148Asp)
7g.75582133T>GCA367727305HIP1c.484A>C (p.Asn162His)
c.397A>C (p.Asn133His)
c.382A>C (p.Asn128His)
c.442A>C (p.Asn148His)
7g.75582134G>ACA455710494HIP1c.483C>T (p.Gly161=)
c.396C>T (p.Gly132=)
c.381C>T (p.Gly127=)
c.441C>T (p.Gly147=)
 gnomAD v4
7g.75582134G>CCA455710502HIP1c.483C>G (p.Gly161=)
c.396C>G (p.Gly132=)
c.381C>G (p.Gly127=)
c.441C>G (p.Gly147=)
7g.75582134G>TCA455710626HIP1c.483C>A (p.Gly161=)
c.396C>A (p.Gly132=)
c.381C>A (p.Gly127=)
c.441C>A (p.Gly147=)
7g.75582135C>ACA367727308HIP1c.482G>T (p.Gly161Val)
c.395G>T (p.Gly132Val)
c.380G>T (p.Gly127Val)
c.440G>T (p.Gly147Val)
7g.75582135C>GCA367727310HIP1c.482G>C (p.Gly161Ala)
c.395G>C (p.Gly132Ala)
c.380G>C (p.Gly127Ala)
c.440G>C (p.Gly147Ala)
7g.75582135C>TCA367727312HIP1c.482G>A (p.Gly161Asp)
c.395G>A (p.Gly132Asp)
c.380G>A (p.Gly127Asp)
c.440G>A (p.Gly147Asp)
7g.75582136C>ACA367727315HIP1c.481G>T (p.Gly161Cys)
c.394G>T (p.Gly132Cys)
c.379G>T (p.Gly127Cys)
c.439G>T (p.Gly147Cys)
7g.75582136C>GCA367727320HIP1c.481G>C (p.Gly161Arg)
c.394G>C (p.Gly132Arg)
c.379G>C (p.Gly127Arg)
c.439G>C (p.Gly147Arg)
7g.75582136C>TCA367727325HIP1c.481G>A (p.Gly161Ser)
c.394G>A (p.Gly132Ser)
c.379G>A (p.Gly127Ser)
c.439G>A (p.Gly147Ser)
7g.75582137T>ACA455710666HIP1c.480A>T (p.Pro160=)
c.393A>T (p.Pro131=)
c.378A>T (p.Pro126=)
c.438A>T (p.Pro146=)
7g.75582137T>CCA455710669HIP1c.480A>G (p.Pro160=)
c.393A>G (p.Pro131=)
c.378A>G (p.Pro126=)
c.438A>G (p.Pro146=)
7g.75582137T>GCA455710673HIP1c.480A>C (p.Pro160=)
c.393A>C (p.Pro131=)
c.378A>C (p.Pro126=)
c.438A>C (p.Pro146=)
7g.75582137_75582138delinsTGCA1717985638HIP1c.479_480delinsCA (p.Pro160=)
c.392_393delinsCA (p.Pro131=)
c.377_378delinsCA (p.Pro126=)
c.437_438delinsCA (p.Pro146=)
7g.75582138G>ACA367727334HIP1c.479C>T (p.Pro160Leu)
c.392C>T (p.Pro131Leu)
c.377C>T (p.Pro126Leu)
c.437C>T (p.Pro146Leu)
7g.75582138G>CCA367727337HIP1c.479C>G (p.Pro160Arg)
c.392C>G (p.Pro131Arg)
c.377C>G (p.Pro126Arg)
c.437C>G (p.Pro146Arg)
7g.75582138G>TCA367727340HIP1c.479C>A (p.Pro160Gln)
c.392C>A (p.Pro131Gln)
c.377C>A (p.Pro126Gln)
c.437C>A (p.Pro146Gln)
7g.75582140delCA1717985640HIP1c.479del (p.Pro160GlnfsTer6)
c.392del (p.Pro131GlnfsTer6)
c.377del (p.Pro126GlnfsTer6)
c.437del (p.Pro146GlnfsTer6)
 dbSNP gnomAD v4
7g.75582139G>ACA367727344HIP1c.478C>T (p.Pro160Ser)
c.391C>T (p.Pro131Ser)
c.376C>T (p.Pro126Ser)
c.436C>T (p.Pro146Ser)
7g.75582139G>CCA367727342HIP1c.478C>G (p.Pro160Ala)
c.391C>G (p.Pro131Ala)
c.376C>G (p.Pro126Ala)
c.436C>G (p.Pro146Ala)
7g.75582139G>TCA367727343HIP1c.478C>A (p.Pro160Thr)
c.391C>A (p.Pro131Thr)
c.376C>A (p.Pro126Thr)
c.436C>A (p.Pro146Thr)
7g.75582140G>ACA455710706HIP1c.477C>T (p.Phe159=)
c.390C>T (p.Phe130=)
c.375C>T (p.Phe125=)
c.435C>T (p.Phe145=)
7g.75582140G>CCA367727347HIP1c.477C>G (p.Phe159Leu)
c.390C>G (p.Phe130Leu)
c.375C>G (p.Phe125Leu)
c.435C>G (p.Phe145Leu)
 dbSNP
7g.75582140G=CA1717985642HIP1c.477C= (p.Phe159=)
c.390C= (p.Phe130=)
c.375C= (p.Phe125=)
c.435C= (p.Phe145=)
7g.75582140G>TCA367727366HIP1c.477C>A (p.Phe159Leu)
c.390C>A (p.Phe130Leu)
c.375C>A (p.Phe125Leu)
c.435C>A (p.Phe145Leu)
7g.75582141A>CCA367727373HIP1c.476T>G (p.Phe159Cys)
c.389T>G (p.Phe130Cys)
c.374T>G (p.Phe125Cys)
c.434T>G (p.Phe145Cys)
7g.75582141A>GCA367727374HIP1c.476T>C (p.Phe159Ser)
c.389T>C (p.Phe130Ser)
c.374T>C (p.Phe125Ser)
c.434T>C (p.Phe145Ser)
7g.75582141A>TCA367727375HIP1c.476T>A (p.Phe159Tyr)
c.389T>A (p.Phe130Tyr)
c.374T>A (p.Phe125Tyr)
c.434T>A (p.Phe145Tyr)
7g.75582142A>CCA367727379HIP1c.475T>G (p.Phe159Val)
c.388T>G (p.Phe130Val)
c.373T>G (p.Phe125Val)
c.433T>G (p.Phe145Val)
7g.75582142A>GCA367727385HIP1c.475T>C (p.Phe159Leu)
c.388T>C (p.Phe130Leu)
c.373T>C (p.Phe125Leu)
c.433T>C (p.Phe145Leu)
7g.75582142A>TCA367727389HIP1c.475T>A (p.Phe159Ile)
c.388T>A (p.Phe130Ile)
c.373T>A (p.Phe125Ile)
c.433T>A (p.Phe145Ile)
7g.75582143C>ACA367727394HIP1c.474G>T (p.Arg158Ser)
c.387G>T (p.Arg129Ser)
c.372G>T (p.Arg124Ser)
c.432G>T (p.Arg144Ser)
 gnomAD v4
7g.75582143C=CA1717985644HIP1c.474G= (p.Arg158=)
c.387G= (p.Arg129=)
c.372G= (p.Arg124=)
c.432G= (p.Arg144=)
7g.75582143C>GCA367727398HIP1c.474G>C (p.Arg158Ser)
c.387G>C (p.Arg129Ser)
c.372G>C (p.Arg124Ser)
c.432G>C (p.Arg144Ser)
 gnomAD v4
7g.75582143C>TCA4302609HIP1c.474G>A (p.Arg158=)
c.387G>A (p.Arg129=)
c.372G>A (p.Arg124=)
c.432G>A (p.Arg144=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.75582144C>ACA367727408HIP1c.473G>T (p.Arg158Met)
c.386G>T (p.Arg129Met)
c.371G>T (p.Arg124Met)
c.431G>T (p.Arg144Met)
 gnomAD v4
7g.75582144C=CA1717985647HIP1c.473G= (p.Arg158=)
c.386G= (p.Arg129=)
c.371G= (p.Arg124=)
c.431G= (p.Arg144=)
7g.75582144C>GCA4302610HIP1c.473G>C (p.Arg158Thr)
c.386G>C (p.Arg129Thr)
c.371G>C (p.Arg124Thr)
c.431G>C (p.Arg144Thr)
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.75582144C>TCA367727406HIP1c.473G>A (p.Arg158Lys)
c.386G>A (p.Arg129Lys)
c.371G>A (p.Arg124Lys)
c.431G>A (p.Arg144Lys)
 dbSNP gnomAD v3 gnomAD v4
7g.75582145T>ACA367727440HIP1c.472A>T (p.Arg158Trp)
c.385A>T (p.Arg129Trp)
c.370A>T (p.Arg124Trp)
c.430A>T (p.Arg144Trp)
7g.75582145T>CCA4302612HIP1c.472A>G (p.Arg158Gly)
c.385A>G (p.Arg129Gly)
c.370A>G (p.Arg124Gly)
c.430A>G (p.Arg144Gly)
 dbSNP ExAC gnomAD v2
7g.75582145T>GCA4302611HIP1c.472A>C (p.Arg158=)
c.385A>C (p.Arg129=)
c.370A>C (p.Arg124=)
c.430A>C (p.Arg144=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.75582145T=CA1717985649HIP1c.472A= (p.Arg158=)
c.385A= (p.Arg129=)
c.370A= (p.Arg124=)
c.430A= (p.Arg144=)
7g.75582146G>ACA455710799HIP1c.471C>T (p.Pro157=)
c.384C>T (p.Pro128=)
c.369C>T (p.Pro123=)
c.429C>T (p.Pro143=)
7g.75582146G>CCA455710808HIP1c.471C>G (p.Pro157=)
c.384C>G (p.Pro128=)
c.369C>G (p.Pro123=)
c.429C>G (p.Pro143=)
7g.75582146G>TCA455710833HIP1c.471C>A (p.Pro157=)
c.384C>A (p.Pro128=)
c.369C>A (p.Pro123=)
c.429C>A (p.Pro143=)
7g.75582147G>ACA367727443HIP1c.470C>T (p.Pro157Leu)
c.383C>T (p.Pro128Leu)
c.368C>T (p.Pro123Leu)
c.428C>T (p.Pro143Leu)
7g.75582147G>CCA367727444HIP1c.470C>G (p.Pro157Arg)
c.383C>G (p.Pro128Arg)
c.368C>G (p.Pro123Arg)
c.428C>G (p.Pro143Arg)
 gnomAD v4
7g.75582147G>TCA367727445HIP1c.470C>A (p.Pro157His)
c.383C>A (p.Pro128His)
c.368C>A (p.Pro123His)
c.428C>A (p.Pro143His)
7g.75582148G>ACA367727449HIP1c.469C>T (p.Pro157Ser)
c.382C>T (p.Pro128Ser)
c.367C>T (p.Pro123Ser)
c.427C>T (p.Pro143Ser)
 gnomAD v4
7g.75582148G>CCA367727461HIP1c.469C>G (p.Pro157Ala)
c.382C>G (p.Pro128Ala)
c.367C>G (p.Pro123Ala)
c.427C>G (p.Pro143Ala)
7g.75582148G>TCA367727462HIP1c.469C>A (p.Pro157Thr)
c.382C>A (p.Pro128Thr)
c.367C>A (p.Pro123Thr)
c.427C>A (p.Pro143Thr)
7g.75582149A>CCA367727465HIP1c.468T>G (p.Asn156Lys)
c.381T>G (p.Asn127Lys)
c.366T>G (p.Asn122Lys)
c.426T>G (p.Asn142Lys)
7g.75582149A>GCA455710849HIP1c.468T>C (p.Asn156=)
c.381T>C (p.Asn127=)
c.366T>C (p.Asn122=)
c.426T>C (p.Asn142=)
7g.75582149A>TCA367727466HIP1c.468T>A (p.Asn156Lys)
c.381T>A (p.Asn127Lys)
c.366T>A (p.Asn122Lys)
c.426T>A (p.Asn142Lys)
7g.75582150T>ACA367727467HIP1c.467A>T (p.Asn156Ile)
c.380A>T (p.Asn127Ile)
c.365A>T (p.Asn122Ile)
c.425A>T (p.Asn142Ile)
7g.75582150T>CCA367727471HIP1c.467A>G (p.Asn156Ser)
c.380A>G (p.Asn127Ser)
c.365A>G (p.Asn122Ser)
c.425A>G (p.Asn142Ser)
7g.75582150T>GCA367727473HIP1c.467A>C (p.Asn156Thr)
c.380A>C (p.Asn127Thr)
c.365A>C (p.Asn122Thr)
c.425A>C (p.Asn142Thr)
7g.75582151T>ACA367727489HIP1c.466A>T (p.Asn156Tyr)
c.379A>T (p.Asn127Tyr)
c.364A>T (p.Asn122Tyr)
c.424A>T (p.Asn142Tyr)
 gnomAD v4
7g.75582151T>CCA367727478HIP1c.466A>G (p.Asn156Asp)
c.379A>G (p.Asn127Asp)
c.364A>G (p.Asn122Asp)
c.424A>G (p.Asn142Asp)
7g.75582151T>GCA367727486HIP1c.466A>C (p.Asn156His)
c.379A>C (p.Asn127His)
c.364A>C (p.Asn122His)
c.424A>C (p.Asn142His)
7g.75582152C>ACA367727491HIP1c.466-1G>T (n.466-1G>T)
c.379-1G>T (n.379-1G>T)
c.364-1G>T (n.364-1G>T)
c.424-1G>T (n.424-1G>T)
7g.75582152C>GCA367727493HIP1c.466-1G>C (n.466-1G>C)
c.379-1G>C (n.379-1G>C)
c.364-1G>C (n.364-1G>C)
c.424-1G>C (n.424-1G>C)
 gnomAD v4
7g.75582152C>TCA367727494HIP1c.466-1G>A (n.466-1G>A)
c.379-1G>A (n.379-1G>A)
c.364-1G>A (n.364-1G>A)
c.424-1G>A (n.424-1G>A)
7g.75582153T>ACA367727498HIP1c.466-2A>T (n.466-2A>T)
c.379-2A>T (n.379-2A>T)
c.364-2A>T (n.364-2A>T)
c.424-2A>T (n.424-2A>T)
7g.75582153T>CCA367727500HIP1c.466-2A>G (n.466-2A>G)
c.379-2A>G (n.379-2A>G)
c.364-2A>G (n.364-2A>G)
c.424-2A>G (n.424-2A>G)
7g.75582153T>GCA367727503HIP1c.466-2A>C (n.466-2A>C)
c.379-2A>C (n.379-2A>C)
c.364-2A>C (n.364-2A>C)
c.424-2A>C (n.424-2A>C)
7g.75582154G>ACA2683363509HIP1c.466-3C>T (n.466-3C>T)
c.379-3C>T (n.379-3C>T)
c.364-3C>T (n.364-3C>T)
c.424-3C>T (n.424-3C>T)
 gnomAD v4
7g.75582154G=CA1717985651HIP1c.466-3C= (n.466-3C=)
c.379-3C= (n.379-3C=)
c.364-3C= (n.364-3C=)
c.424-3C= (n.424-3C=)
7g.75582154G>TCA575556922HIP1c.466-3C>A (n.466-3C>A)
c.379-3C>A (n.379-3C>A)
c.364-3C>A (n.364-3C>A)
c.424-3C>A (n.424-3C>A)
 dbSNP gnomAD v2 gnomAD v4
7g.75582163_75582176delCA2683363507HIP1c.466-16_466-3del (n.466-16_466-3del)
c.379-16_379-3del (n.379-16_379-3del)
c.364-16_364-3del (n.364-16_364-3del)
c.424-16_424-3del (n.424-16_424-3del)
 gnomAD v4
7g.75582155G>ACA2683363517HIP1c.466-4C>T (n.466-4C>T)
c.379-4C>T (n.379-4C>T)
c.364-4C>T (n.364-4C>T)
c.424-4C>T (n.424-4C>T)
 gnomAD v4
7g.75582155G=CA1717985653HIP1c.466-4C= (n.466-4C=)
c.379-4C= (n.379-4C=)
c.364-4C= (n.364-4C=)
c.424-4C= (n.424-4C=)
7g.75582155G>TCA4302613HIP1c.466-4C>A (n.466-4C>A)
c.379-4C>A (n.379-4C>A)
c.364-4C>A (n.364-4C>A)
c.424-4C>A (n.424-4C>A)
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.75582158G>ACA1717985654HIP1c.466-7C>T (n.466-7C>T)
c.379-7C>T (n.379-7C>T)
c.364-7C>T (n.364-7C>T)
c.424-7C>T (n.424-7C>T)
 dbSNP
7g.75582158G=CA1717985656HIP1c.466-7C= (n.466-7C=)
c.379-7C= (n.379-7C=)
c.364-7C= (n.364-7C=)
c.424-7C= (n.424-7C=)
7g.75582158G>TCA2683363519HIP1c.466-7C>A (n.466-7C>A)
c.379-7C>A (n.379-7C>A)
c.364-7C>A (n.364-7C>A)
c.424-7C>A (n.424-7C>A)
 gnomAD v4
7g.75582159G=CA1717985657HIP1c.466-8C= (n.466-8C=)
c.379-8C= (n.379-8C=)
c.364-8C= (n.364-8C=)
c.424-8C= (n.424-8C=)
7g.75582159G>TCA4302614HIP1c.466-8C>A (n.466-8C>A)
c.379-8C>A (n.379-8C>A)
c.364-8C>A (n.364-8C>A)
c.424-8C>A (n.424-8C>A)
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.75582162G>ACA4302615HIP1c.466-11C>T (n.466-11C>T)
c.379-11C>T (n.379-11C>T)
c.364-11C>T (n.364-11C>T)
c.424-11C>T (n.424-11C>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.75582162G=CA1717985658HIP1c.466-11C= (n.466-11C=)
c.379-11C= (n.379-11C=)
c.364-11C= (n.364-11C=)
c.424-11C= (n.424-11C=)
7g.75582163G>ACA4302616HIP1c.466-12C>T (n.466-12C>T)
c.379-12C>T (n.379-12C>T)
c.364-12C>T (n.364-12C>T)
c.424-12C>T (n.424-12C>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.75582163G=CA1717985660HIP1c.466-12C= (n.466-12C=)
c.379-12C= (n.379-12C=)
c.364-12C= (n.364-12C=)
c.424-12C= (n.424-12C=)
7g.75582163G>TCA575556929HIP1c.466-12C>A (n.466-12C>A)
c.379-12C>A (n.379-12C>A)
c.364-12C>A (n.364-12C>A)
c.424-12C>A (n.424-12C>A)
 dbSNP gnomAD v2 gnomAD v4
7g.75582164C=CA1717985663HIP1c.466-13G= (n.466-13G=)
c.379-13G= (n.379-13G=)
c.364-13G= (n.364-13G=)
c.424-13G= (n.424-13G=)
7g.75582164C>GCA651266522HIP1c.466-13G>C (n.466-13G>C)
c.379-13G>C (n.379-13G>C)
c.364-13G>C (n.364-13G>C)
c.424-13G>C (n.424-13G>C)
 COSMIC
7g.75582164C>TCA575556931HIP1c.466-13G>A (n.466-13G>A)
c.379-13G>A (n.379-13G>A)
c.364-13G>A (n.364-13G>A)
c.424-13G>A (n.424-13G>A)
 dbSNP gnomAD v2 gnomAD v4
7g.75582167_75582180delCA2683363528HIP1c.466-26_466-13del (n.466-26_466-13del)
c.379-26_379-13del (n.379-26_379-13del)
c.364-26_364-13del (n.364-26_364-13del)
c.424-26_424-13del (n.424-26_424-13del)
 gnomAD v4
7g.75582165A>GCA2776533414HIP1c.466-14T>C (n.466-14T>C)
c.379-14T>C (n.379-14T>C)
c.364-14T>C (n.364-14T>C)
c.424-14T>C (n.424-14T>C)
7g.75582166G>TCA2683363530HIP1c.466-15C>A (n.466-15C>A)
c.379-15C>A (n.379-15C>A)
c.364-15C>A (n.364-15C>A)
c.424-15C>A (n.424-15C>A)
 gnomAD v4
7g.75582167A>TCA2578914550HIP1c.466-16T>A (n.466-16T>A)
c.379-16T>A (n.379-16T>A)
c.364-16T>A (n.364-16T>A)
c.424-16T>A (n.424-16T>A)
7g.75582168G>ACA4302617HIP1c.466-17C>T (n.466-17C>T)
c.379-17C>T (n.379-17C>T)
c.364-17C>T (n.364-17C>T)
c.424-17C>T (n.424-17C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.75582168G>CCA2776533416HIP1c.466-17C>G (n.466-17C>G)
c.379-17C>G (n.379-17C>G)
c.364-17C>G (n.364-17C>G)
c.424-17C>G (n.424-17C>G)
7g.75582168G=CA1717985664HIP1c.466-17C= (n.466-17C=)
c.379-17C= (n.379-17C=)
c.364-17C= (n.364-17C=)
c.424-17C= (n.424-17C=)
7g.75582172G>CCA2776533417HIP1c.466-21C>G (n.466-21C>G)
c.379-21C>G (n.379-21C>G)
c.364-21C>G (n.364-21C>G)
c.424-21C>G (n.424-21C>G)
7g.75582172G=CA1717985666HIP1c.466-21C= (n.466-21C=)
c.379-21C= (n.379-21C=)
c.364-21C= (n.364-21C=)
c.424-21C= (n.424-21C=)
7g.75582172G>TCA4302618HIP1c.466-21C>A (n.466-21C>A)
c.379-21C>A (n.379-21C>A)
c.364-21C>A (n.364-21C>A)
c.424-21C>A (n.424-21C>A)
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.75582173G>ACA2683363536HIP1c.466-22C>T (n.466-22C>T)
c.379-22C>T (n.379-22C>T)
c.364-22C>T (n.364-22C>T)
c.424-22C>T (n.424-22C>T)
 gnomAD v4
7g.75582174G>CCA1103244765HIP1c.466-23C>G (n.466-23C>G)
c.379-23C>G (n.379-23C>G)
c.364-23C>G (n.364-23C>G)
c.424-23C>G (n.424-23C>G)
 gnomAD v3 gnomAD v4
7g.75582174G>TCA2683363537HIP1c.466-23C>A (n.466-23C>A)
c.379-23C>A (n.379-23C>A)
c.364-23C>A (n.364-23C>A)
c.424-23C>A (n.424-23C>A)
 gnomAD v4
7g.75582175A=CA1717985667HIP1c.466-24T= (n.466-24T=)
c.379-24T= (n.379-24T=)
c.364-24T= (n.364-24T=)
c.424-24T= (n.424-24T=)
7g.75582175A>GCA455710967HIP1c.466-24T>C (n.466-24T>C)
c.379-24T>C (n.379-24T>C)
c.364-24T>C (n.364-24T>C)
c.424-24T>C (n.424-24T>C)
 dbSNP gnomAD v2 gnomAD v4
7g.75582176G>TCA2683363539HIP1c.466-25C>A (n.466-25C>A)
c.379-25C>A (n.379-25C>A)
c.364-25C>A (n.364-25C>A)
c.424-25C>A (n.424-25C>A)
 gnomAD v4
7g.75582178C>ACA2683363541HIP1c.466-27G>T (n.466-27G>T)
c.379-27G>T (n.379-27G>T)
c.364-27G>T (n.364-27G>T)
c.424-27G>T (n.424-27G>T)
 gnomAD v4
7g.75582178C=CA1717985669HIP1c.466-27G= (n.466-27G=)
c.379-27G= (n.379-27G=)
c.364-27G= (n.364-27G=)
c.424-27G= (n.424-27G=)
7g.75582178C>TCA575556940HIP1c.466-27G>A (n.466-27G>A)
c.379-27G>A (n.379-27G>A)
c.364-27G>A (n.364-27G>A)
c.424-27G>A (n.424-27G>A)
 dbSNP gnomAD v2 gnomAD v4
7g.75582179A=CA1717985670HIP1c.466-28T= (n.466-28T=)
c.379-28T= (n.379-28T=)
c.364-28T= (n.364-28T=)
c.424-28T= (n.424-28T=)
7g.75582179A>GCA1717985671HIP1c.466-28T>C (n.466-28T>C)
c.379-28T>C (n.379-28T>C)
c.364-28T>C (n.364-28T>C)
c.424-28T>C (n.424-28T>C)
 dbSNP gnomAD v4
7g.75582180G>ACA842236286HIP1c.466-29C>T (n.466-29C>T)
c.379-29C>T (n.379-29C>T)
c.364-29C>T (n.364-29C>T)
c.424-29C>T (n.424-29C>T)
 dbSNP gnomAD v3 gnomAD v4
7g.75582180G=CA1717985672HIP1c.466-29C= (n.466-29C=)
c.379-29C= (n.379-29C=)
c.364-29C= (n.364-29C=)
c.424-29C= (n.424-29C=)
7g.75582180G>TCA2683363547HIP1c.466-29C>A (n.466-29C>A)
c.379-29C>A (n.379-29C>A)
c.364-29C>A (n.364-29C>A)
c.424-29C>A (n.424-29C>A)
 gnomAD v4
7g.75582181G>ACA2578914551HIP1c.466-30C>T (n.466-30C>T)
c.379-30C>T (n.379-30C>T)
c.364-30C>T (n.364-30C>T)
c.424-30C>T (n.424-30C>T)
 gnomAD v4
7g.75582181G>CCA2683363554HIP1c.466-30C>G (n.466-30C>G)
c.379-30C>G (n.379-30C>G)
c.364-30C>G (n.364-30C>G)
c.424-30C>G (n.424-30C>G)
 gnomAD v4
7g.75582181G>TCA2683363552HIP1c.466-30C>A (n.466-30C>A)
c.379-30C>A (n.379-30C>A)
c.364-30C>A (n.364-30C>A)
c.424-30C>A (n.424-30C>A)
 gnomAD v4
7g.75582182G>ACA2683363558HIP1c.466-31C>T (n.466-31C>T)
c.379-31C>T (n.379-31C>T)
c.364-31C>T (n.364-31C>T)
c.424-31C>T (n.424-31C>T)
 gnomAD v4
7g.75582182G>TCA2683363556HIP1c.466-31C>A (n.466-31C>A)
c.379-31C>A (n.379-31C>A)
c.364-31C>A (n.364-31C>A)
c.424-31C>A (n.424-31C>A)
 gnomAD v4

Number of alleles fetched