Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.159034623C>ACA459008423VIPR2c.837G>T (p.Val279=)
c.789G>T (p.Val263=)
c.1260G>T (p.Val420=)
c.597G>T (p.Val199=)
n.1023G>T
c.912G>T (p.Val304=)
c.648G>T (p.Val216=)
c.423G>T (p.Val141=)
n.1232G>T
n.933G>T
7g.159034623C>GCA459008424VIPR2c.837G>C (p.Val279=)
c.789G>C (p.Val263=)
c.1260G>C (p.Val420=)
c.597G>C (p.Val199=)
n.1023G>C
c.912G>C (p.Val304=)
c.648G>C (p.Val216=)
c.423G>C (p.Val141=)
n.1232G>C
n.933G>C
7g.159034623C>TCA459008425VIPR2c.837G>A (p.Val279=)
c.789G>A (p.Val263=)
c.1260G>A (p.Val420=)
c.597G>A (p.Val199=)
n.1023G>A
c.912G>A (p.Val304=)
c.648G>A (p.Val216=)
c.423G>A (p.Val141=)
n.1232G>A
n.933G>A
7g.159034624A>CCA369941406VIPR2c.836T>G (p.Val279Gly)
c.788T>G (p.Val263Gly)
c.1259T>G (p.Val420Gly)
c.596T>G (p.Val199Gly)
n.1022T>G
c.911T>G (p.Val304Gly)
c.647T>G (p.Val216Gly)
c.422T>G (p.Val141Gly)
n.1231T>G
n.932T>G
7g.159034624A>GCA369941408VIPR2c.836T>C (p.Val279Ala)
c.788T>C (p.Val263Ala)
c.1259T>C (p.Val420Ala)
c.596T>C (p.Val199Ala)
n.1022T>C
c.911T>C (p.Val304Ala)
c.647T>C (p.Val216Ala)
c.422T>C (p.Val141Ala)
n.1231T>C
n.932T>C
7g.159034624A>TCA369941411VIPR2c.836T>A (p.Val279Glu)
c.788T>A (p.Val263Glu)
c.1259T>A (p.Val420Glu)
c.596T>A (p.Val199Glu)
n.1022T>A
c.911T>A (p.Val304Glu)
c.647T>A (p.Val216Glu)
c.422T>A (p.Val141Glu)
n.1231T>A
n.932T>A
7g.159034625C>ACA369941413VIPR2c.835G>T (p.Val279Leu)
c.787G>T (p.Val263Leu)
c.1258G>T (p.Val420Leu)
c.595G>T (p.Val199Leu)
n.1021G>T
c.910G>T (p.Val304Leu)
c.646G>T (p.Val216Leu)
c.421G>T (p.Val141Leu)
n.1230G>T
n.931G>T
7g.159034625C=CA1756436852VIPR2c.835G= (p.Val279=)
c.787G= (p.Val263=)
c.1258G= (p.Val420=)
c.595G= (p.Val199=)
n.1021G=
c.910G= (p.Val304=)
c.646G= (p.Val216=)
c.421G= (p.Val141=)
n.1230G=
n.931G=
7g.159034625C>GCA369941417VIPR2c.835G>C (p.Val279Leu)
c.787G>C (p.Val263Leu)
c.1258G>C (p.Val420Leu)
c.595G>C (p.Val199Leu)
n.1021G>C
c.910G>C (p.Val304Leu)
c.646G>C (p.Val216Leu)
c.421G>C (p.Val141Leu)
n.1230G>C
n.931G>C
7g.159034625C>TCA4595437VIPR2c.835G>A (p.Val279Met)
c.787G>A (p.Val263Met)
c.1258G>A (p.Val420Met)
c.595G>A (p.Val199Met)
n.1021G>A
c.910G>A (p.Val304Met)
c.646G>A (p.Val216Met)
c.421G>A (p.Val141Met)
n.1230G>A
n.931G>A
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.159034626A=CA1756436855VIPR2c.834T= (p.Ser278=)
c.786T= (p.Ser262=)
c.1257T= (p.Ser419=)
c.594T= (p.Ser198=)
n.1020T=
c.909T= (p.Ser303=)
c.645T= (p.Ser215=)
c.420T= (p.Ser140=)
n.1229T=
n.930T=
7g.159034626A>CCA369941437VIPR2c.834T>G (p.Ser278Arg)
c.786T>G (p.Ser262Arg)
c.1257T>G (p.Ser419Arg)
c.594T>G (p.Ser198Arg)
n.1020T>G
c.909T>G (p.Ser303Arg)
c.645T>G (p.Ser215Arg)
c.420T>G (p.Ser140Arg)
n.1229T>G
n.930T>G
7g.159034626A>GCA459008426VIPR2c.834T>C (p.Ser278=)
c.786T>C (p.Ser262=)
c.1257T>C (p.Ser419=)
c.594T>C (p.Ser198=)
n.1020T>C
c.909T>C (p.Ser303=)
c.645T>C (p.Ser215=)
c.420T>C (p.Ser140=)
n.1229T>C
n.930T>C
 dbSNP gnomAD v4
7g.159034626A>TCA369941435VIPR2c.834T>A (p.Ser278Arg)
c.786T>A (p.Ser262Arg)
c.1257T>A (p.Ser419Arg)
c.594T>A (p.Ser198Arg)
n.1020T>A
c.909T>A (p.Ser303Arg)
c.645T>A (p.Ser215Arg)
c.420T>A (p.Ser140Arg)
n.1229T>A
n.930T>A
7g.159034627C>ACA369941440VIPR2c.833G>T (p.Ser278Ile)
c.785G>T (p.Ser262Ile)
c.1256G>T (p.Ser419Ile)
c.593G>T (p.Ser198Ile)
n.1019G>T
c.908G>T (p.Ser303Ile)
c.644G>T (p.Ser215Ile)
c.419G>T (p.Ser140Ile)
n.1228G>T
n.929G>T
7g.159034627C=CA1756436859VIPR2c.833G= (p.Ser278=)
c.785G= (p.Ser262=)
c.1256G= (p.Ser419=)
c.593G= (p.Ser198=)
n.1019G=
c.908G= (p.Ser303=)
c.644G= (p.Ser215=)
c.419G= (p.Ser140=)
n.1228G=
n.929G=
7g.159034627C>GCA170113012VIPR2c.833G>C (p.Ser278Thr)
c.785G>C (p.Ser262Thr)
c.1256G>C (p.Ser419Thr)
c.593G>C (p.Ser198Thr)
n.1019G>C
c.908G>C (p.Ser303Thr)
c.644G>C (p.Ser215Thr)
c.419G>C (p.Ser140Thr)
n.1228G>C
n.929G>C
 dbSNP gnomAD v4
7g.159034627C>TCA369941451VIPR2c.833G>A (p.Ser278Asn)
c.785G>A (p.Ser262Asn)
c.1256G>A (p.Ser419Asn)
c.593G>A (p.Ser198Asn)
n.1019G>A
c.908G>A (p.Ser303Asn)
c.644G>A (p.Ser215Asn)
c.419G>A (p.Ser140Asn)
n.1228G>A
n.929G>A
 gnomAD v4
7g.159034628T>ACA369941468VIPR2c.832A>T (p.Ser278Cys)
c.784A>T (p.Ser262Cys)
c.1255A>T (p.Ser419Cys)
c.592A>T (p.Ser198Cys)
n.1018A>T
c.907A>T (p.Ser303Cys)
c.643A>T (p.Ser215Cys)
c.418A>T (p.Ser140Cys)
n.1227A>T
n.928A>T
7g.159034628T>CCA369941472VIPR2c.832A>G (p.Ser278Gly)
c.784A>G (p.Ser262Gly)
c.1255A>G (p.Ser419Gly)
c.592A>G (p.Ser198Gly)
n.1018A>G
c.907A>G (p.Ser303Gly)
c.643A>G (p.Ser215Gly)
c.418A>G (p.Ser140Gly)
n.1227A>G
n.928A>G
7g.159034628T>GCA369941480VIPR2c.832A>C (p.Ser278Arg)
c.784A>C (p.Ser262Arg)
c.1255A>C (p.Ser419Arg)
c.592A>C (p.Ser198Arg)
n.1018A>C
c.907A>C (p.Ser303Arg)
c.643A>C (p.Ser215Arg)
c.418A>C (p.Ser140Arg)
n.1227A>C
n.928A>C
7g.159034629G>ACA459008427VIPR2c.831C>T (p.His277=)
c.783C>T (p.His261=)
c.1254C>T (p.His418=)
c.591C>T (p.His197=)
n.1017C>T
c.906C>T (p.His302=)
c.642C>T (p.His214=)
c.417C>T (p.His139=)
n.1226C>T
n.927C>T
7g.159034629G>CCA369941483VIPR2c.831C>G (p.His277Gln)
c.783C>G (p.His261Gln)
c.1254C>G (p.His418Gln)
c.591C>G (p.His197Gln)
n.1017C>G
c.906C>G (p.His302Gln)
c.642C>G (p.His214Gln)
c.417C>G (p.His139Gln)
n.1226C>G
n.927C>G
7g.159034629G>TCA369941484VIPR2c.831C>A (p.His277Gln)
c.783C>A (p.His261Gln)
c.1254C>A (p.His418Gln)
c.591C>A (p.His197Gln)
n.1017C>A
c.906C>A (p.His302Gln)
c.642C>A (p.His214Gln)
c.417C>A (p.His139Gln)
n.1226C>A
n.927C>A
7g.159034630T>ACA369941487VIPR2c.830A>T (p.His277Leu)
c.782A>T (p.His261Leu)
c.1253A>T (p.His418Leu)
c.590A>T (p.His197Leu)
n.1016A>T
c.905A>T (p.His302Leu)
c.641A>T (p.His214Leu)
c.416A>T (p.His139Leu)
n.1225A>T
n.926A>T
7g.159034630T>CCA4595438VIPR2c.830A>G (p.His277Arg)
c.782A>G (p.His261Arg)
c.1253A>G (p.His418Arg)
c.590A>G (p.His197Arg)
n.1016A>G
c.905A>G (p.His302Arg)
c.641A>G (p.His214Arg)
c.416A>G (p.His139Arg)
n.1225A>G
n.926A>G
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.159034630T>GCA369941493VIPR2c.830A>C (p.His277Pro)
c.782A>C (p.His261Pro)
c.1253A>C (p.His418Pro)
c.590A>C (p.His197Pro)
n.1016A>C
c.905A>C (p.His302Pro)
c.641A>C (p.His214Pro)
c.416A>C (p.His139Pro)
n.1225A>C
n.926A>C
7g.159034630T=CA1756436864VIPR2c.830A= (p.His277=)
c.782A= (p.His261=)
c.1253A= (p.His418=)
c.590A= (p.His197=)
n.1016A=
c.905A= (p.His302=)
c.641A= (p.His214=)
c.416A= (p.His139=)
n.1225A=
n.926A=
7g.159034631G>ACA369941495VIPR2c.829C>T (p.His277Tyr)
c.781C>T (p.His261Tyr)
c.1252C>T (p.His418Tyr)
c.589C>T (p.His197Tyr)
n.1015C>T
c.904C>T (p.His302Tyr)
c.640C>T (p.His214Tyr)
c.415C>T (p.His139Tyr)
n.1224C>T
n.925C>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.159034631G>CCA369941497VIPR2c.829C>G (p.His277Asp)
c.781C>G (p.His261Asp)
c.1252C>G (p.His418Asp)
c.589C>G (p.His197Asp)
n.1015C>G
c.904C>G (p.His302Asp)
c.640C>G (p.His214Asp)
c.415C>G (p.His139Asp)
n.1224C>G
n.925C>G
7g.159034631G=CA1756436870VIPR2c.829C= (p.His277=)
c.781C= (p.His261=)
c.1252C= (p.His418=)
c.589C= (p.His197=)
n.1015C=
c.904C= (p.His302=)
c.640C= (p.His214=)
c.415C= (p.His139=)
n.1224C=
n.925C=
7g.159034631G>TCA369941500VIPR2c.829C>A (p.His277Asn)
c.781C>A (p.His261Asn)
c.1252C>A (p.His418Asn)
c.589C>A (p.His197Asn)
n.1015C>A
c.904C>A (p.His302Asn)
c.640C>A (p.His214Asn)
c.415C>A (p.His139Asn)
n.1224C>A
n.925C>A
7g.159034632G>ACA4595439VIPR2c.828C>T (p.Asp276=)
c.780C>T (p.Asp260=)
c.1251C>T (p.Asp417=)
c.588C>T (p.Asp196=)
n.1014C>T
c.903C>T (p.Asp301=)
c.639C>T (p.Asp213=)
c.414C>T (p.Asp138=)
n.1223C>T
n.924C>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.159034632G>CCA369941507VIPR2c.828C>G (p.Asp276Glu)
c.780C>G (p.Asp260Glu)
c.1251C>G (p.Asp417Glu)
c.588C>G (p.Asp196Glu)
n.1014C>G
c.903C>G (p.Asp301Glu)
c.639C>G (p.Asp213Glu)
c.414C>G (p.Asp138Glu)
n.1223C>G
n.924C>G
7g.159034632G=CA1756436873VIPR2c.828C= (p.Asp276=)
c.780C= (p.Asp260=)
c.1251C= (p.Asp417=)
c.588C= (p.Asp196=)
n.1014C=
c.903C= (p.Asp301=)
c.639C= (p.Asp213=)
c.414C= (p.Asp138=)
n.1223C=
n.924C=
7g.159034632G>TCA369941503VIPR2c.828C>A (p.Asp276Glu)
c.780C>A (p.Asp260Glu)
c.1251C>A (p.Asp417Glu)
c.588C>A (p.Asp196Glu)
n.1014C>A
c.903C>A (p.Asp301Glu)
c.639C>A (p.Asp213Glu)
c.414C>A (p.Asp138Glu)
n.1223C>A
n.924C>A
7g.159034633T>ACA369941509VIPR2c.827A>T (p.Asp276Val)
c.779A>T (p.Asp260Val)
c.1250A>T (p.Asp417Val)
c.587A>T (p.Asp196Val)
n.1013A>T
c.902A>T (p.Asp301Val)
c.638A>T (p.Asp213Val)
c.413A>T (p.Asp138Val)
n.1222A>T
n.923A>T
7g.159034633T>CCA369941510VIPR2c.827A>G (p.Asp276Gly)
c.779A>G (p.Asp260Gly)
c.1250A>G (p.Asp417Gly)
c.587A>G (p.Asp196Gly)
n.1013A>G
c.902A>G (p.Asp301Gly)
c.638A>G (p.Asp213Gly)
c.413A>G (p.Asp138Gly)
n.1222A>G
n.923A>G
7g.159034633T>GCA369941511VIPR2c.827A>C (p.Asp276Ala)
c.779A>C (p.Asp260Ala)
c.1250A>C (p.Asp417Ala)
c.587A>C (p.Asp196Ala)
n.1013A>C
c.902A>C (p.Asp301Ala)
c.638A>C (p.Asp213Ala)
c.413A>C (p.Asp138Ala)
n.1222A>C
n.923A>C
7g.159034634C>ACA369941513VIPR2c.826G>T (p.Asp276Tyr)
c.778G>T (p.Asp260Tyr)
c.1249G>T (p.Asp417Tyr)
c.586G>T (p.Asp196Tyr)
n.1012G>T
c.901G>T (p.Asp301Tyr)
c.637G>T (p.Asp213Tyr)
c.412G>T (p.Asp138Tyr)
n.1221G>T
n.922G>T
 dbSNP gnomAD v3 gnomAD v4
7g.159034634C=CA1756436876VIPR2c.826G= (p.Asp276=)
c.778G= (p.Asp260=)
c.1249G= (p.Asp417=)
c.586G= (p.Asp196=)
n.1012G=
c.901G= (p.Asp301=)
c.637G= (p.Asp213=)
c.412G= (p.Asp138=)
n.1221G=
n.922G=
7g.159034634C>GCA369941514VIPR2c.826G>C (p.Asp276His)
c.778G>C (p.Asp260His)
c.1249G>C (p.Asp417His)
c.586G>C (p.Asp196His)
n.1012G>C
c.901G>C (p.Asp301His)
c.637G>C (p.Asp213His)
c.412G>C (p.Asp138His)
n.1221G>C
n.922G>C
7g.159034634C>TCA170113026VIPR2c.826G>A (p.Asp276Asn)
c.778G>A (p.Asp260Asn)
c.1249G>A (p.Asp417Asn)
c.586G>A (p.Asp196Asn)
n.1012G>A
c.901G>A (p.Asp301Asn)
c.637G>A (p.Asp213Asn)
c.412G>A (p.Asp138Asn)
n.1221G>A
n.922G>A
 dbSNP gnomAD v3 gnomAD v4
7g.159034635G>ACA4595440VIPR2c.825C>T (p.Asn275=)
c.777C>T (p.Asn259=)
c.1248C>T (p.Asn416=)
c.585C>T (p.Asn195=)
n.1011C>T
c.900C>T (p.Asn300=)
c.636C>T (p.Asn212=)
c.411C>T (p.Asn137=)
n.1220C>T
n.921C>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.159034635G>CCA369941520VIPR2c.825C>G (p.Asn275Lys)
c.777C>G (p.Asn259Lys)
c.1248C>G (p.Asn416Lys)
c.585C>G (p.Asn195Lys)
n.1011C>G
c.900C>G (p.Asn300Lys)
c.636C>G (p.Asn212Lys)
c.411C>G (p.Asn137Lys)
n.1220C>G
n.921C>G
7g.159034635G=CA1756436882VIPR2c.825C= (p.Asn275=)
c.777C= (p.Asn259=)
c.1248C= (p.Asn416=)
c.585C= (p.Asn195=)
n.1011C=
c.900C= (p.Asn300=)
c.636C= (p.Asn212=)
c.411C= (p.Asn137=)
n.1220C=
n.921C=
7g.159034635G>TCA369941523VIPR2c.825C>A (p.Asn275Lys)
c.777C>A (p.Asn259Lys)
c.1248C>A (p.Asn416Lys)
c.585C>A (p.Asn195Lys)
n.1011C>A
c.900C>A (p.Asn300Lys)
c.636C>A (p.Asn212Lys)
c.411C>A (p.Asn137Lys)
n.1220C>A
n.921C>A
 dbSNP
7g.159034636T>ACA369941527VIPR2c.824A>T (p.Asn275Ile)
c.776A>T (p.Asn259Ile)
c.1247A>T (p.Asn416Ile)
c.584A>T (p.Asn195Ile)
n.1010A>T
c.899A>T (p.Asn300Ile)
c.635A>T (p.Asn212Ile)
c.410A>T (p.Asn137Ile)
n.1219A>T
n.920A>T
 dbSNP
7g.159034636T>CCA369941528VIPR2c.824A>G (p.Asn275Ser)
c.776A>G (p.Asn259Ser)
c.1247A>G (p.Asn416Ser)
c.584A>G (p.Asn195Ser)
n.1010A>G
c.899A>G (p.Asn300Ser)
c.635A>G (p.Asn212Ser)
c.410A>G (p.Asn137Ser)
n.1219A>G
n.920A>G
7g.159034636T>GCA369941529VIPR2c.824A>C (p.Asn275Thr)
c.776A>C (p.Asn259Thr)
c.1247A>C (p.Asn416Thr)
c.584A>C (p.Asn195Thr)
n.1010A>C
c.899A>C (p.Asn300Thr)
c.635A>C (p.Asn212Thr)
c.410A>C (p.Asn137Thr)
n.1219A>C
n.920A>C

Number of alleles fetched