Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.56863765_56872392delCA1139664706 ClinVar
16g.56869796C>ACA495602932SLC12A3c.573C>A (p.Ala191=)
c.570C>A (p.Ala190=)
16g.56869796C>GCA495602933SLC12A3c.573C>G (p.Ala191=)
c.570C>G (p.Ala190=)
16g.56869796C>TCA495602934SLC12A3c.573C>T (p.Ala191=)
c.570C>T (p.Ala190=)
16g.56869797A=CA2224349107SLC12A3c.574A= (p.Ile192=)
c.571A= (p.Ile191=)
16g.56869797A>CCA395981080SLC12A3c.574A>C (p.Ile192Leu)
c.571A>C (p.Ile191Leu)
16g.56869797A>GCA395981084SLC12A3c.574A>G (p.Ile192Val)
c.571A>G (p.Ile191Val)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.56869797A>TCA395981088SLC12A3c.574A>T (p.Ile192Phe)
c.571A>T (p.Ile191Phe)
16g.56869798T>ACA395981091SLC12A3c.575T>A (p.Ile192Asn)
c.572T>A (p.Ile191Asn)
16g.56869798T>CCA395981098SLC12A3c.575T>C (p.Ile192Thr)
c.572T>C (p.Ile191Thr)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.56869798T>GCA395981100SLC12A3c.575T>G (p.Ile192Ser)
c.572T>G (p.Ile191Ser)
16g.56869798T=CA2224349108SLC12A3c.575T= (p.Ile192=)
c.572T= (p.Ile191=)
16g.56869799C>ACA495602935SLC12A3c.576C>A (p.Ile192=)
c.573C>A (p.Ile191=)
16g.56869799C>GCA395981105SLC12A3c.576C>G (p.Ile192Met)
c.573C>G (p.Ile191Met)
 gnomAD v4
16g.56869799C>TCA495602936SLC12A3c.576C>T (p.Ile192=)
c.573C>T (p.Ile191=)
16g.56869800T>ACA395981112SLC12A3c.577T>A (p.Ser193Thr)
c.574T>A (p.Ser192Thr)
16g.56869800T>CCA395981109SLC12A3c.577T>C (p.Ser193Pro)
c.574T>C (p.Ser192Pro)
16g.56869800T>GCA395981114SLC12A3c.577T>G (p.Ser193Ala)
c.574T>G (p.Ser192Ala)
16g.56869801C>ACA395981117SLC12A3c.578C>A (p.Ser193Tyr)
c.575C>A (p.Ser192Tyr)
 gnomAD v4
16g.56869801C=CA2224349109SLC12A3c.578C= (p.Ser193=)
c.575C= (p.Ser192=)
16g.56869801C>GCA395981120SLC12A3c.578C>G (p.Ser193Cys)
c.575C>G (p.Ser192Cys)
16g.56869801C>TCA395981121SLC12A3c.578C>T (p.Ser193Phe)
c.575C>T (p.Ser192Phe)
 dbSNP gnomAD v3 gnomAD v4
16g.56869804_56869806delCA2695223668SLC12A3c.581_583del (p.Thr194del)
c.578_580del (p.Thr193del)
16g.56869802C>ACA495602937SLC12A3c.579C>A (p.Ser193=)
c.576C>A (p.Ser192=)
16g.56869802C>GCA495602938SLC12A3c.579C>G (p.Ser193=)
c.576C>G (p.Ser192=)
16g.56869802C>TCA495602939SLC12A3c.579C>T (p.Ser193=)
c.576C>T (p.Ser192=)
16g.56869803A>CCA395981122SLC12A3c.580A>C (p.Thr194Pro)
c.577A>C (p.Thr193Pro)
16g.56869803A>GCA395981124SLC12A3c.580A>G (p.Thr194Ala)
c.577A>G (p.Thr193Ala)
16g.56869803A>TCA395981128SLC12A3c.580A>T (p.Thr194Ser)
c.577A>T (p.Thr193Ser)
16g.56869804C>ACA395981130SLC12A3c.581C>A (p.Thr194Asn)
c.578C>A (p.Thr193Asn)
16g.56869804C>GCA395981133SLC12A3c.581C>G (p.Thr194Ser)
c.578C>G (p.Thr193Ser)
16g.56869804C>TCA395981135SLC12A3c.581C>T (p.Thr194Ile)
c.578C>T (p.Thr193Ile)
 ClinVar gnomAD v4
16g.56869805C>ACA495602940SLC12A3c.582C>A (p.Thr194=)
c.579C>A (p.Thr193=)
 gnomAD v4
16g.56869805C>GCA495602941SLC12A3c.582C>G (p.Thr194=)
c.579C>G (p.Thr193=)
 ClinVar
16g.56869805C>TCA495602942SLC12A3c.582C>T (p.Thr194=)
c.579C>T (p.Thr193=)
16g.56869806A=CA2224349110SLC12A3c.583A= (p.Asn195=)
c.580A= (p.Asn194=)
16g.56869806A>CCA395981137SLC12A3c.583A>C (p.Asn195His)
c.580A>C (p.Asn194His)
16g.56869806A>GCA395981139SLC12A3c.583A>G (p.Asn195Asp)
c.580A>G (p.Asn194Asp)
 dbSNP
16g.56869806A>TCA395981140SLC12A3c.583A>T (p.Asn195Tyr)
c.580A>T (p.Asn194Tyr)
16g.56869807A>CCA395981151SLC12A3c.584A>C (p.Asn195Thr)
c.581A>C (p.Asn194Thr)
16g.56869807A>GCA395981141SLC12A3c.584A>G (p.Asn195Ser)
c.581A>G (p.Asn194Ser)
16g.56869807A>TCA395981143SLC12A3c.584A>T (p.Asn195Ile)
c.581A>T (p.Asn194Ile)
16g.56869808T>ACA395981154SLC12A3c.585T>A (p.Asn195Lys)
c.582T>A (p.Asn194Lys)
16g.56869808T>CCA495602943SLC12A3c.585T>C (p.Asn195=)
c.582T>C (p.Asn194=)
 dbSNP
16g.56869808T>GCA395981158SLC12A3c.585T>G (p.Asn195Lys)
c.582T>G (p.Asn194Lys)
16g.56869808T=CA2224349111SLC12A3c.585T= (p.Asn195=)
c.582T= (p.Asn194=)
16g.56869809G>ACA395981162SLC12A3c.586G>A (p.Gly196Ser)
c.583G>A (p.Gly195Ser)
 gnomAD v4
16g.56869809G>CCA395981171SLC12A3c.586G>C (p.Gly196Arg)
c.583G>C (p.Gly195Arg)
16g.56869809G>TCA395981174SLC12A3c.586G>T (p.Gly196Cys)
c.583G>T (p.Gly195Cys)
16g.56869810G>ACA395981178SLC12A3c.587G>A (p.Gly196Asp)
c.584G>A (p.Gly195Asp)
 gnomAD v4
16g.56869810G>CCA395981179SLC12A3c.587G>C (p.Gly196Ala)
c.584G>C (p.Gly195Ala)
16g.56869810G=CA2224349112SLC12A3c.587G= (p.Gly196=)
c.584G= (p.Gly195=)
16g.56869810G>TCA395981182SLC12A3c.587G>T (p.Gly196Val)
c.584G>T (p.Gly195Val)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.56869811C>ACA495602944SLC12A3c.588C>A (p.Gly196=)
c.585C>A (p.Gly195=)
 gnomAD v4
16g.56869811C>GCA495602945SLC12A3c.588C>G (p.Gly196=)
c.585C>G (p.Gly195=)
16g.56869811C>TCA495602946SLC12A3c.588C>T (p.Gly196=)
c.585C>T (p.Gly195=)
16g.56869812A>CCA395981194SLC12A3c.589A>C (p.Lys197Gln)
c.586A>C (p.Lys196Gln)
16g.56869812A>GCA395981195SLC12A3c.589A>G (p.Lys197Glu)
c.586A>G (p.Lys196Glu)
16g.56869812A>TCA395981199SLC12A3c.589A>T (p.Lys197Ter)
c.586A>T (p.Lys196Ter)
16g.56869813A>CCA395981205SLC12A3c.590A>C (p.Lys197Thr)
c.587A>C (p.Lys196Thr)
16g.56869813A>GCA395981208SLC12A3c.590A>G (p.Lys197Arg)
c.587A>G (p.Lys196Arg)
16g.56869813A>TCA395981203SLC12A3c.590A>T (p.Lys197Met)
c.587A>T (p.Lys196Met)
16g.56869814G>ACA495602947SLC12A3c.591G>A (p.Lys197=)
c.588G>A (p.Lys196=)
16g.56869814G>CCA395981211SLC12A3c.591G>C (p.Lys197Asn)
c.588G>C (p.Lys196Asn)
16g.56869814G=CA2224349113SLC12A3c.591G= (p.Lys197=)
c.588G= (p.Lys196=)
16g.56869814G>TCA395981214SLC12A3c.591G>T (p.Lys197Asn)
c.588G>T (p.Lys196Asn)
 dbSNP gnomAD v2 gnomAD v4 COSMIC
16g.56869815G>ACA8069104SLC12A3c.592G>A (p.Val198Ile)
c.589G>A (p.Val197Ile)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.56869815G>CCA395981218SLC12A3c.592G>C (p.Val198Leu)
c.589G>C (p.Val197Leu)
16g.56869815G=CA2224349114SLC12A3c.592G= (p.Val198=)
c.589G= (p.Val197=)
16g.56869815G>TCA395981219SLC12A3c.592G>T (p.Val198Phe)
c.589G>T (p.Val197Phe)
 gnomAD v4
16g.56869816T>ACA395981220SLC12A3c.593T>A (p.Val198Asp)
c.590T>A (p.Val197Asp)
16g.56869816T>CCA395981221SLC12A3c.593T>C (p.Val198Ala)
c.590T>C (p.Val197Ala)
16g.56869816T>GCA395981223SLC12A3c.593T>G (p.Val198Gly)
c.590T>G (p.Val197Gly)
16g.56869817C>ACA495602950SLC12A3c.594C>A (p.Val198=)
c.591C>A (p.Val197=)
16g.56869817C>GCA495602949SLC12A3c.594C>G (p.Val198=)
c.591C>G (p.Val197=)
16g.56869817C>TCA495602948SLC12A3c.594C>T (p.Val198=)
c.591C>T (p.Val197=)
16g.56869817_56869819delinsCAACA2224349115SLC12A3c.594_596delinsCAA (p.Val198=)
c.591_593delinsCAA (p.Val197=)
16g.56869818A>CCA395981227SLC12A3c.595A>C (p.Lys199Gln)
c.592A>C (p.Lys198Gln)
 gnomAD v4
16g.56869818A>GCA395981230SLC12A3c.595A>G (p.Lys199Glu)
c.592A>G (p.Lys198Glu)
16g.56869818A>TCA395981232SLC12A3c.595A>T (p.Lys199Ter)
c.592A>T (p.Lys198Ter)
16g.56869818_56869819delCA977637953SLC12A3c.595_596del (p.Lys199ValfsTer?)
c.592_593del (p.Lys198ValfsTer?)
 ClinVar dbSNP gnomAD v3 gnomAD v4
16g.56869819delCA2633370362SLC12A3c.596del (p.Lys199SerfsTer?)
c.593del (p.Lys198SerfsTer?)
 gnomAD v4
16g.56869819A=CA2224349116SLC12A3c.596A= (p.Lys199=)
c.593A= (p.Lys198=)
16g.56869819A>CCA395981234SLC12A3c.596A>C (p.Lys199Thr)
c.593A>C (p.Lys198Thr)
16g.56869819A>GCA8069105SLC12A3c.596A>G (p.Lys199Arg)
c.593A>G (p.Lys198Arg)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.56869819A>TCA395981235SLC12A3c.596A>T (p.Lys199Met)
c.593A>T (p.Lys198Met)
16g.56869820G>ACA495602951SLC12A3c.597G>A (p.Lys199=)
c.594G>A (p.Lys198=)
 gnomAD v4
16g.56869820G>CCA395981238SLC12A3c.597G>C (p.Lys199Asn)
c.594G>C (p.Lys198Asn)
16g.56869820G>TCA395981243SLC12A3c.597G>T (p.Lys199Asn)
c.594G>T (p.Lys198Asn)
16g.56869821_56869829delCA645573538SLC12A3c.598_601+5del
c.595_598+5del
 COSMIC
16g.56869821T>ACA395981247SLC12A3c.598T>A (p.Ser200Thr)
c.595T>A (p.Ser199Thr)
16g.56869821T>CCA395981250SLC12A3c.598T>C (p.Ser200Pro)
c.595T>C (p.Ser199Pro)
16g.56869821T>GCA395981253SLC12A3c.598T>G (p.Ser200Ala)
c.595T>G (p.Ser199Ala)
16g.56869822C>ACA395981256SLC12A3c.599C>A (p.Ser200Ter)
c.596C>A (p.Ser199Ter)
16g.56869822C>GCA395981268SLC12A3c.599C>G (p.Ser200Ter)
c.596C>G (p.Ser199Ter)
16g.56869822C>TCA395981270SLC12A3c.599C>T (p.Ser200Leu)
c.596C>T (p.Ser199Leu)
16g.56869823A=CA2224349117SLC12A3c.600A= (p.Ser200=)
c.597A= (p.Ser199=)
16g.56869823A>CCA495602952SLC12A3c.600A>C (p.Ser200=)
c.597A>C (p.Ser199=)
16g.56869823A>GCA8069106SLC12A3c.600A>G (p.Ser200=)
c.597A>G (p.Ser199=)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.56869823A>TCA495602953SLC12A3c.600A>T (p.Ser200=)
c.597A>T (p.Ser199=)
16g.56869824G>ACA395981282SLC12A3c.601G>A (p.Gly201Ser)
c.598G>A (p.Gly200Ser)
16g.56869824G>CCA395981284SLC12A3c.601G>C (p.Gly201Arg)
c.598G>C (p.Gly200Arg)
16g.56869824G>TCA395981289SLC12A3c.601G>T (p.Gly201Cys)
c.598G>T (p.Gly200Cys)
16g.56869825G>ACA395981294SLC12A3c.601+1G>A (n.601+1G>A)
c.598+1G>A (n.598+1G>A)
16g.56869825G>CCA395981298SLC12A3c.601+1G>C (n.601+1G>C)
c.598+1G>C (n.598+1G>C)
 ClinVar
16g.56869825G>TCA395981299SLC12A3c.601+1G>T (n.601+1G>T)
c.598+1G>T (n.598+1G>T)
16g.56869826T>ACA395981310SLC12A3c.601+2T>A (n.601+2T>A)
c.598+2T>A (n.598+2T>A)
 gnomAD v4
16g.56869826T>CCA395981307SLC12A3c.601+2T>C (n.601+2T>C)
c.598+2T>C (n.598+2T>C)
16g.56869826T>GCA395981303SLC12A3c.601+2T>G (n.601+2T>G)
c.598+2T>G (n.598+2T>G)
16g.56869827G=CA2224349118SLC12A3c.601+3G= (n.601+3G=)
c.598+3G= (n.598+3G=)
16g.56869827G>TCA8069107SLC12A3c.601+3G>T (n.601+3G>T)
c.598+3G>T (n.598+3G>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.56869828G>ACA912996055SLC12A3c.601+4G>A (n.601+4G>A)
c.598+4G>A (n.598+4G>A)
16g.56869828_56869829insCACCTACTTCCTCATCTCCCGGAGTCTGGGCCCAGAGCTTCA2633370381SLC12A3c.601+4_601+5insCACCTACTTCCTCATCTCCCGGAGTCTGGGCCCAGAGCTT (n.601+4_601+5insCACCTACTTCCTCATCTCCCGGAGTCTGGGCCCAGAGCTT)
c.598+4_598+5insCACCTACTTCCTCATCTCCCGGAGTCTGGGCCCAGAGCTT (n.598+4_598+5insCACCTACTTCCTCATCTCCCGGAGTCTGGGCCCAGAGCTT)
 gnomAD v4
16g.56869830C>ACA2633370383SLC12A3c.601+6C>A (n.601+6C>A)
c.598+6C>A (n.598+6C>A)
 gnomAD v4
16g.56869830C>TCA2633370385SLC12A3c.601+6C>T (n.601+6C>T)
c.598+6C>T (n.598+6C>T)
 gnomAD v4
16g.56869831_56869832insTTGGTGGAAAGGGGGCA2633370390SLC12A3c.601+7_601+8insTTGGTGGAAAGGGGG (n.601+7_601+8insTTGGTGGAAAGGGGG)
c.598+7_598+8insTTGGTGGAAAGGGGG (n.598+7_598+8insTTGGTGGAAAGGGGG)
 gnomAD v4
16g.56869832A=CA2224349119SLC12A3c.601+8A= (n.601+8A=)
c.598+8A= (n.598+8A=)
16g.56869832A>GCA722004783SLC12A3c.601+8A>G (n.601+8A>G)
c.598+8A>G (n.598+8A>G)
 ClinVar dbSNP gnomAD v3 gnomAD v4
16g.56869832A>TCA2573152448SLC12A3c.601+8A>T (n.601+8A>T)
c.598+8A>T (n.598+8A>T)
 ClinVar dbSNP gnomAD v4
16g.56869833T>CCA2499223587SLC12A3c.601+9T>C (n.601+9T>C)
c.598+9T>C (n.598+9T>C)
 ClinVar dbSNP gnomAD v4
16g.56869838_56869900delCA2633370394SLC12A3c.601+14_601+76del (n.601+14_601+76del)
c.598+14_598+76del (n.598+14_598+76del)
 gnomAD v4
16g.56869833_56869834insGGCA2633370398SLC12A3c.601+9_601+10insGG (n.601+9_601+10insGG)
c.598+9_598+10insGG (n.598+9_598+10insGG)
 gnomAD v4
16g.56869834C=CA2224349120SLC12A3c.601+10C= (n.601+10C=)
c.598+10C= (n.598+10C=)
16g.56869834C>GCA622333568SLC12A3c.601+10C>G (n.601+10C>G)
c.598+10C>G (n.598+10C>G)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.56869834C>TCA2807159803SLC12A3c.601+10C>T (n.601+10C>T)
c.598+10C>T (n.598+10C>T)
16g.56869835C=CA2224349121SLC12A3c.601+11C= (n.601+11C=)
c.598+11C= (n.598+11C=)
16g.56869835C>TCA622333569SLC12A3c.601+11C>T (n.601+11C>T)
c.598+11C>T (n.598+11C>T)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.56869836C=CA2224349122SLC12A3c.601+12C= (n.601+12C=)
c.598+12C= (n.598+12C=)
16g.56869836C>TCA622333570SLC12A3c.601+12C>T (n.601+12C>T)
c.598+12C>T (n.598+12C>T)
 ClinVar dbSNP gnomAD v2 gnomAD v4
16g.56869837C=CA2224349123SLC12A3c.601+13C= (n.601+13C=)
c.598+13C= (n.598+13C=)
16g.56869837C>GCA2739266786SLC12A3c.601+13C>G (n.601+13C>G)
c.598+13C>G (n.598+13C>G)
 ClinVar
16g.56869837C>TCA2224349124SLC12A3c.601+13C>T (n.601+13C>T)
c.598+13C>T (n.598+13C>T)
 dbSNP gnomAD v4
16g.56869838C>ACA2633370401SLC12A3c.601+14C>A (n.601+14C>A)
c.598+14C>A (n.598+14C>A)
 gnomAD v4
16g.56869838C=CA2224349125SLC12A3c.601+14C= (n.601+14C=)
c.598+14C= (n.598+14C=)
16g.56869838C>GCA2633370404SLC12A3c.601+14C>G (n.601+14C>G)
c.598+14C>G (n.598+14C>G)
 gnomAD v4
16g.56869838C>TCA622333571SLC12A3c.601+14C>T (n.601+14C>T)
c.598+14C>T (n.598+14C>T)
 ClinVar dbSNP gnomAD v2 gnomAD v4
16g.56869841delCA2633370406SLC12A3c.601+17del (n.601+17del)
c.598+17del (n.598+17del)
 gnomAD v4
16g.56869840T>GCA2633370407SLC12A3c.601+16T>G (n.601+16T>G)
c.598+16T>G (n.598+16T>G)
 gnomAD v4
16g.56869841T>ACA2633370409SLC12A3c.601+17T>A (n.601+17T>A)
c.598+17T>A (n.598+17T>A)
 gnomAD v4
16g.56869841_56869842delinsTCCA2224349126SLC12A3c.601+17_601+18delinsTC (n.601+17_601+18delinsTC)
c.598+17_598+18delinsTC (n.598+17_598+18delinsTC)
16g.56869842C>TCA2739266787SLC12A3c.601+18C>T (n.601+18C>T)
c.598+18C>T (n.598+18C>T)
 ClinVar
16g.56869843delCA8069108SLC12A3c.601+19del (n.601+19del)
c.598+19del (n.598+19del)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.56869843C>ACA2633370412SLC12A3c.601+19C>A (n.601+19C>A)
c.598+19C>A (n.598+19C>A)
 gnomAD v4
16g.56869845C>ACA2633370414SLC12A3c.601+21C>A (n.601+21C>A)
c.598+21C>A (n.598+21C>A)
 gnomAD v4
16g.56869845C=CA2224349127SLC12A3c.601+21C= (n.601+21C=)
c.598+21C= (n.598+21C=)
16g.56869845C>TCA8069109SLC12A3c.601+21C>T (n.601+21C>T)
c.598+21C>T (n.598+21C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.56869846C>ACA2576001861SLC12A3c.601+22C>A (n.601+22C>A)
c.598+22C>A (n.598+22C>A)
 gnomAD v4
16g.56869846C>TCA2576001860SLC12A3c.601+22C>T (n.601+22C>T)
c.598+22C>T (n.598+22C>T)
 gnomAD v4
16g.56869848A>CCA2633370415SLC12A3c.601+24A>C (n.601+24A>C)
c.598+24A>C (n.598+24A>C)
 gnomAD v4
16g.56869849G>ACA8069110SLC12A3c.601+25G>A (n.601+25G>A)
c.598+25G>A (n.598+25G>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.56869849G=CA2224349128SLC12A3c.601+25G= (n.601+25G=)
c.598+25G= (n.598+25G=)
16g.56869851C>ACA2633370420SLC12A3c.601+27C>A (n.601+27C>A)
c.598+27C>A (n.598+27C>A)
 gnomAD v4
16g.56869851C=CA2224349129SLC12A3c.601+27C= (n.601+27C=)
c.598+27C= (n.598+27C=)
16g.56869851C>TCA977637963SLC12A3c.601+27C>T (n.601+27C>T)
c.598+27C>T (n.598+27C>T)
 dbSNP gnomAD v3 gnomAD v4
16g.56869853delCA2576001863SLC12A3c.601+29del (n.601+29del)
c.598+29del (n.598+29del)
16g.56869852C=CA2224349130SLC12A3c.601+28C= (n.601+28C=)
c.598+28C= (n.598+28C=)
16g.56869852C>TCA977637967SLC12A3c.601+28C>T (n.601+28C>T)
c.598+28C>T (n.598+28C>T)
 dbSNP gnomAD v3 gnomAD v4
16g.56869853C>ACA2576001864SLC12A3c.601+29C>A (n.601+29C>A)
c.598+29C>A (n.598+29C>A)
16g.56869853_56869854insACGAGAGGAGGGCCTTGGCA2633370422SLC12A3c.601+29_601+30insACGAGAGGAGGGCCTTGG (n.601+29_601+30insACGAGAGGAGGGCCTTGG)
c.598+29_598+30insACGAGAGGAGGGCCTTGG (n.598+29_598+30insACGAGAGGAGGGCCTTGG)
 gnomAD v4
16g.56869855C>ACA622333572SLC12A3c.601+31C>A (n.601+31C>A)
c.598+31C>A (n.598+31C>A)
 dbSNP gnomAD v2 gnomAD v4
16g.56869855C=CA2224349131SLC12A3c.601+31C= (n.601+31C=)
c.598+31C= (n.598+31C=)
16g.56869855C>TCA8069111SLC12A3c.601+31C>T (n.601+31C>T)
c.598+31C>T (n.598+31C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.56869856C=CA2224349132SLC12A3c.601+32C= (n.601+32C=)
c.598+32C= (n.598+32C=)
16g.56869856C>GCA622333573SLC12A3c.601+32C>G (n.601+32C>G)
c.598+32C>G (n.598+32C>G)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.56869859_56869860delCA2633370430SLC12A3c.601+35_601+36del (n.601+35_601+36del)
c.598+35_598+36del (n.598+35_598+36del)
 gnomAD v4
16g.56869857T>CCA2633370434SLC12A3c.601+33T>C (n.601+33T>C)
c.598+33T>C (n.598+33T>C)
 gnomAD v4
16g.56869860C>ACA622333574SLC12A3c.601+36C>A (n.601+36C>A)
c.598+36C>A (n.598+36C>A)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.56869860C=CA2224349133SLC12A3c.601+36C= (n.601+36C=)
c.598+36C= (n.598+36C=)
16g.56869860C>GCA622333575SLC12A3c.601+36C>G (n.601+36C>G)
c.598+36C>G (n.598+36C>G)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.56869860C>TCA8069112SLC12A3c.601+36C>T (n.601+36C>T)
c.598+36C>T (n.598+36C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.56869861G>ACA8069113SLC12A3c.601+37G>A (n.601+37G>A)
c.598+37G>A (n.598+37G>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.56869861G=CA2224349134SLC12A3c.601+37G= (n.601+37G=)
c.598+37G= (n.598+37G=)
16g.56869861G>TCA622333576SLC12A3c.601+37G>T (n.601+37G>T)
c.598+37G>T (n.598+37G>T)
 dbSNP gnomAD v2 gnomAD v4
16g.56869862T>CCA8069114SLC12A3c.601+38T>C (n.601+38T>C)
c.598+38T>C (n.598+38T>C)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.56869862T>GCA722004812SLC12A3c.601+38T>G (n.601+38T>G)
c.598+38T>G (n.598+38T>G)
 dbSNP gnomAD v3 gnomAD v4
16g.56869862T=CA2224349135SLC12A3c.601+38T= (n.601+38T=)
c.598+38T= (n.598+38T=)
16g.56869863G>ACA622333577SLC12A3c.601+39G>A (n.601+39G>A)
c.598+39G>A (n.598+39G>A)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.56869863G=CA2224349136SLC12A3c.601+39G= (n.601+39G=)
c.598+39G= (n.598+39G=)
16g.56869863G>TCA8069115SLC12A3c.601+39G>T (n.601+39G>T)
c.598+39G>T (n.598+39G>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.56869864G=CA2224349137SLC12A3c.601+40G= (n.601+40G=)
c.598+40G= (n.598+40G=)
16g.56869864G>TCA8069116SLC12A3c.601+40G>T (n.601+40G>T)
c.598+40G>T (n.598+40G>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.56869865G>ACA622333580SLC12A3c.601+41G>A (n.601+41G>A)
c.598+41G>A (n.598+41G>A)
 dbSNP gnomAD v2
16g.56869865G>CCA2576001871SLC12A3c.601+41G>C (n.601+41G>C)
c.598+41G>C (n.598+41G>C)
16g.56869865G=CA2224349138SLC12A3c.601+41G= (n.601+41G=)
c.598+41G= (n.598+41G=)
16g.56869865G>TCA2633370451SLC12A3c.601+41G>T (n.601+41G>T)
c.598+41G>T (n.598+41G>T)
 gnomAD v4
16g.56869866C>ACA2576001872SLC12A3c.601+42C>A (n.601+42C>A)
c.598+42C>A (n.598+42C>A)
 gnomAD v4
16g.56869866C>TCA2633370452SLC12A3c.601+42C>T (n.601+42C>T)
c.598+42C>T (n.598+42C>T)
 gnomAD v4
16g.56869868C>GCA2576001874SLC12A3c.601+44C>G (n.601+44C>G)
c.598+44C>G (n.598+44C>G)
16g.56869868C>TCA2633370453SLC12A3c.601+44C>T (n.601+44C>T)
c.598+44C>T (n.598+44C>T)
 gnomAD v4
16g.56869869C>TCA2576001875SLC12A3c.601+45C>T (n.601+45C>T)
c.598+45C>T (n.598+45C>T)
16g.56869871A=CA2224349139SLC12A3c.601+47A= (n.601+47A=)
c.598+47A= (n.598+47A=)
16g.56869871A>TCA622333582SLC12A3c.601+47A>T (n.601+47A>T)
c.598+47A>T (n.598+47A>T)
 dbSNP gnomAD v2 gnomAD v4
16g.56869872A=CA2224349140SLC12A3c.601+48A= (n.601+48A=)
c.598+48A= (n.598+48A=)
16g.56869872A>CCA2224349141SLC12A3c.601+48A>C (n.601+48A>C)
c.598+48A>C (n.598+48A>C)
 dbSNP gnomAD v4
16g.56869874C>ACA2633370457SLC12A3c.601+50C>A (n.601+50C>A)
c.598+50C>A (n.598+50C>A)
 gnomAD v4
16g.56869874C=CA2224349142SLC12A3c.601+50C= (n.601+50C=)
c.598+50C= (n.598+50C=)
16g.56869874C>GCA2224349143SLC12A3c.601+50C>G (n.601+50C>G)
c.598+50C>G (n.598+50C>G)
 dbSNP gnomAD v4
16g.56869874C>TCA622333584SLC12A3c.601+50C>T (n.601+50C>T)
c.598+50C>T (n.598+50C>T)
 dbSNP gnomAD v2
16g.56869875C>GCA2633370459SLC12A3c.601+51C>G (n.601+51C>G)
c.598+51C>G (n.598+51C>G)
 gnomAD v4
16g.56869877G>TCA2633370461SLC12A3c.601+53G>T (n.601+53G>T)
c.598+53G>T (n.598+53G>T)
 gnomAD v4
16g.56869877_56869878insTTCCCACA2633370462SLC12A3c.601+53_601+54insTTCCCA (n.601+53_601+54insTTCCCA)
c.598+53_598+54insTTCCCA (n.598+53_598+54insTTCCCA)
 gnomAD v4
16g.56869878G>ACA722004819SLC12A3c.601+54G>A (n.601+54G>A)
c.598+54G>A (n.598+54G>A)
 dbSNP gnomAD v3 gnomAD v4
16g.56869878G=CA2224349144SLC12A3c.601+54G= (n.601+54G=)
c.598+54G= (n.598+54G=)
16g.56869878G>TCA2633370465SLC12A3c.601+54G>T (n.601+54G>T)
c.598+54G>T (n.598+54G>T)
 gnomAD v4
16g.56869879G>TCA2633370479SLC12A3c.601+55G>T (n.601+55G>T)
c.598+55G>T (n.598+55G>T)
 gnomAD v4
16g.56869881A>CCA2633370481SLC12A3c.601+57A>C (n.601+57A>C)
c.598+57A>C (n.598+57A>C)
 gnomAD v4
16g.56869881A>TCA2633370482SLC12A3c.601+57A>T (n.601+57A>T)
c.598+57A>T (n.598+57A>T)
 gnomAD v4
16g.56869882C>ACA281496699SLC12A3c.601+58C>A (n.601+58C>A)
c.598+58C>A (n.598+58C>A)
 dbSNP gnomAD v3 gnomAD v4
16g.56869882C=CA2224349145SLC12A3c.601+58C= (n.601+58C=)
c.598+58C= (n.598+58C=)
16g.56869882C>TCA281496701SLC12A3c.601+58C>T (n.601+58C>T)
c.598+58C>T (n.598+58C>T)
 dbSNP gnomAD v3 gnomAD v4
16g.56869883A=CA2224349146SLC12A3c.601+59A= (n.601+59A=)
c.598+59A= (n.598+59A=)
16g.56869883A>CCA2576001877SLC12A3c.601+59A>C (n.601+59A>C)
c.598+59A>C (n.598+59A>C)
16g.56869883A>GCA722004821SLC12A3c.601+59A>G (n.601+59A>G)
c.598+59A>G (n.598+59A>G)
 dbSNP gnomAD v4
16g.56869884G=CA2224349147SLC12A3c.601+60G= (n.601+60G=)
c.598+60G= (n.598+60G=)
16g.56869884G>TCA2224349148SLC12A3c.601+60G>T (n.601+60G>T)
c.598+60G>T (n.598+60G>T)
 dbSNP gnomAD v4
16g.56869885G>ACA2633370490SLC12A3c.601+61G>A (n.601+61G>A)
c.598+61G>A (n.598+61G>A)
 gnomAD v4
16g.56869886A>GCA2576001879SLC12A3c.601+62A>G (n.601+62A>G)
c.598+62A>G (n.598+62A>G)
16g.56869887C>ACA2576001880SLC12A3c.601+63C>A (n.601+63C>A)
c.598+63C>A (n.598+63C>A)
 gnomAD v4
16g.56869887C>TCA2576001881SLC12A3c.601+63C>T (n.601+63C>T)
c.598+63C>T (n.598+63C>T)
 gnomAD v4
16g.56869888T>CCA977637985SLC12A3c.601+64T>C (n.601+64T>C)
c.598+64T>C (n.598+64T>C)
 dbSNP gnomAD v3 gnomAD v4
16g.56869888T=CA2224349149SLC12A3c.601+64T= (n.601+64T=)
c.598+64T= (n.598+64T=)
16g.56869889C=CA2224349150SLC12A3c.601+65C= (n.601+65C=)
c.598+65C= (n.598+65C=)
16g.56869889C>TCA2224349151SLC12A3c.601+65C>T (n.601+65C>T)
c.598+65C>T (n.598+65C>T)
 dbSNP
16g.56869890C=CA2224349152SLC12A3c.601+66C= (n.601+66C=)
c.598+66C= (n.598+66C=)
16g.56869890C>TCA2224349153SLC12A3c.601+66C>T (n.601+66C>T)
c.598+66C>T (n.598+66C>T)
 dbSNP gnomAD v4
16g.56869891C>ACA2633370496SLC12A3c.601+67C>A (n.601+67C>A)
c.598+67C>A (n.598+67C>A)
 gnomAD v4
16g.56869891C=CA2224349154SLC12A3c.601+67C= (n.601+67C=)
c.598+67C= (n.598+67C=)
16g.56869891C>TCA722004823SLC12A3c.601+67C>T (n.601+67C>T)
c.598+67C>T (n.598+67C>T)
 dbSNP gnomAD v4
16g.56869892A>GCA2633370500SLC12A3c.601+68A>G (n.601+68A>G)
c.598+68A>G (n.598+68A>G)
 gnomAD v4
16g.56869893A>CCA2633370502SLC12A3c.601+69A>C (n.601+69A>C)
c.598+69A>C (n.598+69A>C)
 gnomAD v4
16g.56869893A>GCA2633370503SLC12A3c.601+69A>G (n.601+69A>G)
c.598+69A>G (n.598+69A>G)
 gnomAD v4
16g.56869893_56869894insACACA2807159808SLC12A3c.601+69_601+70insACA (n.601+69_601+70insACA)
c.598+69_598+70insACA (n.598+69_598+70insACA)
16g.56869894C>ACA2576001882SLC12A3c.601+70C>A (n.601+70C>A)
c.598+70C>A (n.598+70C>A)
16g.56869895T>ACA2807159811SLC12A3c.601+71T>A (n.601+71T>A)
c.598+71T>A (n.598+71T>A)
16g.56869895_56869896delCA2807159810SLC12A3c.601+71_601+72del (n.601+71_601+72del)
c.598+71_598+72del (n.598+71_598+72del)
16g.56869896T>ACA2807159812SLC12A3c.601+72T>A (n.601+72T>A)
c.598+72T>A (n.598+72T>A)
16g.56869896T>CCA2224349156SLC12A3c.601+72T>C (n.601+72T>C)
c.598+72T>C (n.598+72T>C)
 dbSNP
16g.56869896T=CA2224349155SLC12A3c.601+72T= (n.601+72T=)
c.598+72T= (n.598+72T=)

Number of alleles fetched