Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.150959584_150959605delinsAGCTGGTGGGGGGGCCCCGGTGCA1752419800KCNH2n.1272_1293delinsCACCGGGGCCCCCCCACCAGCT
c.439_460delinsCACCGGGGCCCCCCCACCAGCT (p.His147=)
c.234+28_234+49delinsCACCGGGGCCCCCCCACCAGCT (n.234+28_234+49delinsCACCGGGGCCCCCCCACCAGCT)
n.662_683delinsCACCGGGGCCCCCCCACCAGCT
c.139_160delinsCACCGGGGCCCCCCCACCAGCT (p.His47=)
c.289_310delinsCACCGGGGCCCCCCCACCAGCT (p.His97=)
c.262_283delinsCACCGGGGCCCCCCCACCAGCT (p.His88=)
7g.150959586_150959606delCA579075484KCNH2n.1272_1292del
c.439_459del (p.His147_Ser153del)
c.234+28_234+48del (n.234+28_234+48del)
n.662_682del
c.139_159del (p.His47_Ser53del)
c.289_309del (p.His97_Ser103del)
c.262_282del (p.His88_Ser94del)
 dbSNP gnomAD v2 gnomAD v4
7g.150959587_150959649delinsTGGTGGGGGGGCCCCGGTGGTTGGTGTCATGAGCCGGGGACCCCACCATGTCCTTCTCCATCACA1752419809KCNH2n.1228_1290delinsTGATGGAGAAGGACATGGTGGGGTCCCCGGCTCATGACACCAACCACCGGGGCCCCCCCACCA
c.395_457delinsTGATGGAGAAGGACATGGTGGGGTCCCCGGCTCATGACACCAACCACCGGGGCCCCCCCACCA (p.Val132=)
c.218_234+46delinsTGATGGAGAAGGACATGGTGGGGTCCCCGGCTCATGACACCAACCACCGGGGCCCCCCCACCA
n.618_680delinsTGATGGAGAAGGACATGGTGGGGTCCCCGGCTCATGACACCAACCACCGGGGCCCCCCCACCA
c.95_157delinsTGATGGAGAAGGACATGGTGGGGTCCCCGGCTCATGACACCAACCACCGGGGCCCCCCCACCA (p.Val32=)
c.245_307delinsTGATGGAGAAGGACATGGTGGGGTCCCCGGCTCATGACACCAACCACCGGGGCCCCCCCACCA (p.Val82=)
c.218_280delinsTGATGGAGAAGGACATGGTGGGGTCCCCGGCTCATGACACCAACCACCGGGGCCCCCCCACCA (p.Val73=)
7g.150959588_150959649delCA16618415KCNH2n.1228_1289del
c.395_456del (p.Val132GlufsTer?)
c.218_234+45del
n.618_679del
c.95_156del (p.Val32GlufsTer?)
c.245_306del (p.Val82GlufsTer?)
c.218_279del (p.Val73GlufsTer?)
 ClinVar dbSNP
7g.150959605G>ACA369863648KCNH2n.1272C>T
c.439C>T (p.His147Tyr)
c.234+28C>T (n.234+28C>T)
n.662C>T
c.139C>T (p.His47Tyr)
c.289C>T (p.His97Tyr)
c.262C>T (p.His88Tyr)
 ClinVar
7g.150959605G>CCA369863649KCNH2n.1272C>G
c.439C>G (p.His147Asp)
c.234+28C>G (n.234+28C>G)
n.662C>G
c.139C>G (p.His47Asp)
c.289C>G (p.His97Asp)
c.262C>G (p.His88Asp)
7g.150959605G>TCA369863650KCNH2n.1272C>A
c.439C>A (p.His147Asn)
c.234+28C>A (n.234+28C>A)
n.662C>A
c.139C>A (p.His47Asn)
c.289C>A (p.His97Asn)
c.262C>A (p.His88Asn)
7g.150959606G>ACA458646905KCNH2n.1271C>T
c.438C>T (p.Asn146=)
c.234+27C>T (n.234+27C>T)
n.661C>T
c.138C>T (p.Asn46=)
c.288C>T (p.Asn96=)
c.261C>T (p.Asn87=)
7g.150959606G>CCA369863651KCNH2n.1271C>G
c.438C>G (p.Asn146Lys)
c.234+27C>G (n.234+27C>G)
n.661C>G
c.138C>G (p.Asn46Lys)
c.288C>G (p.Asn96Lys)
c.261C>G (p.Asn87Lys)
 gnomAD v4
7g.150959606G=CA1752419879KCNH2n.1271C=
c.438C= (p.Asn146=)
c.234+27C= (n.234+27C=)
n.661C=
c.138C= (p.Asn46=)
c.288C= (p.Asn96=)
c.261C= (p.Asn87=)
7g.150959606G>TCA369863652KCNH2n.1271C>A
c.438C>A (p.Asn146Lys)
c.234+27C>A (n.234+27C>A)
n.661C>A
c.138C>A (p.Asn46Lys)
c.288C>A (p.Asn96Lys)
c.261C>A (p.Asn87Lys)
 dbSNP
7g.150959607T>ACA369863653KCNH2n.1270A>T
c.437A>T (p.Asn146Ile)
c.234+26A>T (n.234+26A>T)
n.660A>T
c.137A>T (p.Asn46Ile)
c.287A>T (p.Asn96Ile)
c.260A>T (p.Asn87Ile)
 gnomAD v4
7g.150959607T>CCA369863654KCNH2n.1270A>G
c.437A>G (p.Asn146Ser)
c.234+26A>G (n.234+26A>G)
n.660A>G
c.137A>G (p.Asn46Ser)
c.287A>G (p.Asn96Ser)
c.260A>G (p.Asn87Ser)
7g.150959607T>GCA369863655KCNH2n.1270A>C
c.437A>C (p.Asn146Thr)
c.234+26A>C (n.234+26A>C)
n.660A>C
c.137A>C (p.Asn46Thr)
c.287A>C (p.Asn96Thr)
c.260A>C (p.Asn87Thr)
7g.150959608T>ACA369863656KCNH2n.1269A>T
c.436A>T (p.Asn146Tyr)
c.234+25A>T (n.234+25A>T)
n.659A>T
c.136A>T (p.Asn46Tyr)
c.286A>T (p.Asn96Tyr)
c.259A>T (p.Asn87Tyr)
 gnomAD v4
7g.150959608T>CCA369863657KCNH2n.1269A>G
c.436A>G (p.Asn146Asp)
c.234+25A>G (n.234+25A>G)
n.659A>G
c.136A>G (p.Asn46Asp)
c.286A>G (p.Asn96Asp)
c.259A>G (p.Asn87Asp)
 dbSNP gnomAD v3 gnomAD v4
7g.150959608T>GCA369863658KCNH2n.1269A>C
c.436A>C (p.Asn146His)
c.234+25A>C (n.234+25A>C)
n.659A>C
c.136A>C (p.Asn46His)
c.286A>C (p.Asn96His)
c.259A>C (p.Asn87His)
7g.150959608T=CA1752419882KCNH2n.1269A=
c.436A= (p.Asn146=)
c.234+25A= (n.234+25A=)
n.659A=
c.136A= (p.Asn46=)
c.286A= (p.Asn96=)
c.259A= (p.Asn87=)
7g.150959609G>ACA169082123KCNH2n.1268C>T
c.435C>T (p.Thr145=)
c.234+24C>T (n.234+24C>T)
n.658C>T
c.135C>T (p.Thr45=)
c.285C>T (p.Thr95=)
c.258C>T (p.Thr86=)
 ClinVar dbSNP gnomAD v4
7g.150959609G>CCA458646906KCNH2n.1268C>G
c.435C>G (p.Thr145=)
c.234+24C>G (n.234+24C>G)
n.658C>G
c.135C>G (p.Thr45=)
c.285C>G (p.Thr95=)
c.258C>G (p.Thr86=)
7g.150959609G=CA1752419887KCNH2n.1268C=
c.435C= (p.Thr145=)
c.234+24C= (n.234+24C=)
n.658C=
c.135C= (p.Thr45=)
c.285C= (p.Thr95=)
c.258C= (p.Thr86=)
7g.150959609G>TCA458646907KCNH2n.1268C>A
c.435C>A (p.Thr145=)
c.234+24C>A (n.234+24C>A)
n.658C>A
c.135C>A (p.Thr45=)
c.285C>A (p.Thr95=)
c.258C>A (p.Thr86=)
7g.150959610G>ACA369863661KCNH2n.1267C>T
c.434C>T (p.Thr145Ile)
c.234+23C>T (n.234+23C>T)
n.657C>T
c.134C>T (p.Thr45Ile)
c.284C>T (p.Thr95Ile)
c.257C>T (p.Thr86Ile)
 ClinVar dbSNP gnomAD v4
7g.150959610G>CCA369863660KCNH2n.1267C>G
c.434C>G (p.Thr145Ser)
c.234+23C>G (n.234+23C>G)
n.657C>G
c.134C>G (p.Thr45Ser)
c.284C>G (p.Thr95Ser)
c.257C>G (p.Thr86Ser)
7g.150959610G=CA1752419890KCNH2n.1267C=
c.434C= (p.Thr145=)
c.234+23C= (n.234+23C=)
n.657C=
c.134C= (p.Thr45=)
c.284C= (p.Thr95=)
c.257C= (p.Thr86=)
7g.150959610G>TCA369863659KCNH2n.1267C>A
c.434C>A (p.Thr145Asn)
c.234+23C>A (n.234+23C>A)
n.657C>A
c.134C>A (p.Thr45Asn)
c.284C>A (p.Thr95Asn)
c.257C>A (p.Thr86Asn)
7g.150959611T>ACA369863663KCNH2n.1266A>T
c.433A>T (p.Thr145Ser)
c.234+22A>T (n.234+22A>T)
n.656A>T
c.133A>T (p.Thr45Ser)
c.283A>T (p.Thr95Ser)
c.256A>T (p.Thr86Ser)
7g.150959611T>CCA369863662KCNH2n.1266A>G
c.433A>G (p.Thr145Ala)
c.234+22A>G (n.234+22A>G)
n.656A>G
c.133A>G (p.Thr45Ala)
c.283A>G (p.Thr95Ala)
c.256A>G (p.Thr86Ala)
 gnomAD v4
7g.150959611T>GCA369863664KCNH2n.1266A>C
c.433A>C (p.Thr145Pro)
c.234+22A>C (n.234+22A>C)
n.656A>C
c.133A>C (p.Thr45Pro)
c.283A>C (p.Thr95Pro)
c.256A>C (p.Thr86Pro)
7g.150959612G>ACA039409KCNH2n.1265C>T
c.432C>T (p.Asp144=)
c.234+21C>T (n.234+21C>T)
n.655C>T
c.132C>T (p.Asp44=)
c.282C>T (p.Asp94=)
c.255C>T (p.Asp85=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.150959612G>CCA369863665KCNH2n.1265C>G
c.432C>G (p.Asp144Glu)
c.234+21C>G (n.234+21C>G)
n.655C>G
c.132C>G (p.Asp44Glu)
c.282C>G (p.Asp94Glu)
c.255C>G (p.Asp85Glu)
7g.150959612G=CA1752419897KCNH2n.1265C=
c.432C= (p.Asp144=)
c.234+21C= (n.234+21C=)
n.655C=
c.132C= (p.Asp44=)
c.282C= (p.Asp94=)
c.255C= (p.Asp85=)
7g.150959612G>TCA369863666KCNH2n.1265C>A
c.432C>A (p.Asp144Glu)
c.234+21C>A (n.234+21C>A)
n.655C>A
c.132C>A (p.Asp44Glu)
c.282C>A (p.Asp94Glu)
c.255C>A (p.Asp85Glu)
7g.150959613T>ACA039396KCNH2n.1264A>T
c.431A>T (p.Asp144Val)
c.234+20A>T (n.234+20A>T)
n.654A>T
c.131A>T (p.Asp44Val)
c.281A>T (p.Asp94Val)
c.254A>T (p.Asp85Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.150959613T>CCA369863667KCNH2n.1264A>G
c.431A>G (p.Asp144Gly)
c.234+20A>G (n.234+20A>G)
n.654A>G
c.131A>G (p.Asp44Gly)
c.281A>G (p.Asp94Gly)
c.254A>G (p.Asp85Gly)
 dbSNP gnomAD v3 gnomAD v4
7g.150959613T>GCA369863668KCNH2n.1264A>C
c.431A>C (p.Asp144Ala)
c.234+20A>C (n.234+20A>C)
n.654A>C
c.131A>C (p.Asp44Ala)
c.281A>C (p.Asp94Ala)
c.254A>C (p.Asp85Ala)
7g.150959613T=CA1752419899KCNH2n.1264A=
c.431A= (p.Asp144=)
c.234+20A= (n.234+20A=)
n.654A=
c.131A= (p.Asp44=)
c.281A= (p.Asp94=)
c.254A= (p.Asp85=)
7g.150959614C>ACA369863669KCNH2n.1263G>T
c.430G>T (p.Asp144Tyr)
c.234+19G>T (n.234+19G>T)
n.653G>T
c.130G>T (p.Asp44Tyr)
c.280G>T (p.Asp94Tyr)
c.253G>T (p.Asp85Tyr)
 COSMIC COSMIC
7g.150959614C>GCA369863670KCNH2n.1263G>C
c.430G>C (p.Asp144His)
c.234+19G>C (n.234+19G>C)
n.653G>C
c.130G>C (p.Asp44His)
c.280G>C (p.Asp94His)
c.253G>C (p.Asp85His)
7g.150959614C>TCA369863671KCNH2n.1263G>A
c.430G>A (p.Asp144Asn)
c.234+19G>A (n.234+19G>A)
n.653G>A
c.130G>A (p.Asp44Asn)
c.280G>A (p.Asp94Asn)
c.253G>A (p.Asp85Asn)
 gnomAD v4
7g.150959615A>CCA369863672KCNH2n.1262T>G
c.429T>G (p.His143Gln)
c.234+18T>G (n.234+18T>G)
n.652T>G
c.129T>G (p.His43Gln)
c.279T>G (p.His93Gln)
c.252T>G (p.His84Gln)
7g.150959615A>GCA458646908KCNH2n.1262T>C
c.429T>C (p.His143=)
c.234+18T>C (n.234+18T>C)
n.652T>C
c.129T>C (p.His43=)
c.279T>C (p.His93=)
c.252T>C (p.His84=)
7g.150959615A>TCA369863673KCNH2n.1262T>A
c.429T>A (p.His143Gln)
c.234+18T>A (n.234+18T>A)
n.652T>A
c.129T>A (p.His43Gln)
c.279T>A (p.His93Gln)
c.252T>A (p.His84Gln)
7g.150959616T>ACA369863676KCNH2n.1261A>T
c.428A>T (p.His143Leu)
c.234+17A>T (n.234+17A>T)
n.651A>T
c.128A>T (p.His43Leu)
c.278A>T (p.His93Leu)
c.251A>T (p.His84Leu)
7g.150959616T>CCA369863675KCNH2n.1261A>G
c.428A>G (p.His143Arg)
c.234+17A>G (n.234+17A>G)
n.651A>G
c.128A>G (p.His43Arg)
c.278A>G (p.His93Arg)
c.251A>G (p.His84Arg)
 gnomAD v4
7g.150959616T>GCA369863674KCNH2n.1261A>C
c.428A>C (p.His143Pro)
c.234+17A>C (n.234+17A>C)
n.651A>C
c.128A>C (p.His43Pro)
c.278A>C (p.His93Pro)
c.251A>C (p.His84Pro)
7g.150959617G>ACA369863677KCNH2n.1260C>T
c.427C>T (p.His143Tyr)
c.234+16C>T (n.234+16C>T)
n.650C>T
c.127C>T (p.His43Tyr)
c.277C>T (p.His93Tyr)
c.250C>T (p.His84Tyr)
 gnomAD v4 COSMIC COSMIC
7g.150959617G>CCA369863678KCNH2n.1260C>G
c.427C>G (p.His143Asp)
c.234+16C>G (n.234+16C>G)
n.650C>G
c.127C>G (p.His43Asp)
c.277C>G (p.His93Asp)
c.250C>G (p.His84Asp)
7g.150959617G>TCA369863679KCNH2n.1260C>A
c.427C>A (p.His143Asn)
c.234+16C>A (n.234+16C>A)
n.650C>A
c.127C>A (p.His43Asn)
c.277C>A (p.His93Asn)
c.250C>A (p.His84Asn)
7g.150959618A>CCA458646909KCNH2n.1259T>G
c.426T>G (p.Ala142=)
c.234+15T>G (n.234+15T>G)
n.649T>G
c.126T>G (p.Ala42=)
c.276T>G (p.Ala92=)
c.249T>G (p.Ala83=)

Number of alleles fetched