Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.56894558T>ACA395997337SLC12A3c.2549T>A (p.Leu850His)
c.2546T>A (p.Leu849His)
c.2576T>A (p.Leu859His)
c.2573T>A (p.Leu858His)
16g.56894558T>CCA250046SLC12A3c.2549T>C (p.Leu850Pro)
c.2546T>C (p.Leu849Pro)
c.2576T>C (p.Leu859Pro)
c.2573T>C (p.Leu858Pro)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.56894558T>GCA395997340SLC12A3c.2549T>G (p.Leu850Arg)
c.2546T>G (p.Leu849Arg)
c.2576T>G (p.Leu859Arg)
c.2573T>G (p.Leu858Arg)
16g.56894558T=CA2224361221SLC12A3c.2549T= (p.Leu850=)
c.2546T= (p.Leu849=)
c.2576T= (p.Leu859=)
c.2573T= (p.Leu858=)
16g.56894559T>ACA495612747SLC12A3c.2550T>A (p.Leu850=)
c.2547T>A (p.Leu849=)
c.2577T>A (p.Leu859=)
c.2574T>A (p.Leu858=)
16g.56894559T>CCA8069965SLC12A3c.2550T>C (p.Leu850=)
c.2547T>C (p.Leu849=)
c.2577T>C (p.Leu859=)
c.2574T>C (p.Leu858=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.56894559T>GCA495612748SLC12A3c.2550T>G (p.Leu850=)
c.2547T>G (p.Leu849=)
c.2577T>G (p.Leu859=)
c.2574T>G (p.Leu858=)
16g.56894559T=CA2224361222SLC12A3c.2550T= (p.Leu850=)
c.2547T= (p.Leu849=)
c.2577T= (p.Leu859=)
c.2574T= (p.Leu858=)
16g.56894560G>ACA395997351SLC12A3c.2551G>A (p.Gly851Ser)
c.2548G>A (p.Gly850Ser)
c.2578G>A (p.Gly860Ser)
c.2575G>A (p.Gly859Ser)
16g.56894560G>CCA395997349SLC12A3c.2551G>C (p.Gly851Arg)
c.2548G>C (p.Gly850Arg)
c.2578G>C (p.Gly860Arg)
c.2575G>C (p.Gly859Arg)
16g.56894560G>TCA395997346SLC12A3c.2551G>T (p.Gly851Cys)
c.2548G>T (p.Gly850Cys)
c.2578G>T (p.Gly860Cys)
c.2575G>T (p.Gly859Cys)
16g.56894561G>ACA395997352SLC12A3c.2552G>A (p.Gly851Asp)
c.2549G>A (p.Gly850Asp)
c.2579G>A (p.Gly860Asp)
c.2576G>A (p.Gly859Asp)
16g.56894561G>CCA395997354SLC12A3c.2552G>C (p.Gly851Ala)
c.2549G>C (p.Gly850Ala)
c.2579G>C (p.Gly860Ala)
c.2576G>C (p.Gly859Ala)
16g.56894561G>TCA395997355SLC12A3c.2552G>T (p.Gly851Val)
c.2549G>T (p.Gly850Val)
c.2579G>T (p.Gly860Val)
c.2576G>T (p.Gly859Val)
16g.56894562C>ACA495612749SLC12A3c.2553C>A (p.Gly851=)
c.2550C>A (p.Gly850=)
c.2580C>A (p.Gly860=)
c.2577C>A (p.Gly859=)
ClinVar dbSNP gnomAD v2 gnomAD v4
16g.56894562C=CA2224361223SLC12A3c.2553C= (p.Gly851=)
c.2550C= (p.Gly850=)
c.2580C= (p.Gly860=)
c.2577C= (p.Gly859=)
16g.56894562C>GCA495612750SLC12A3c.2553C>G (p.Gly851=)
c.2550C>G (p.Gly850=)
c.2580C>G (p.Gly860=)
c.2577C>G (p.Gly859=)
16g.56894562C>TCA495612751SLC12A3c.2553C>T (p.Gly851=)
c.2550C>T (p.Gly850=)
c.2580C>T (p.Gly860=)
c.2577C>T (p.Gly859=)
16g.56894563C>ACA395997358SLC12A3c.2554C>A (p.Arg852Ser)
c.2551C>A (p.Arg851Ser)
c.2581C>A (p.Arg861Ser)
c.2578C>A (p.Arg860Ser)
dbSNP
16g.56894563C=CA2224361224SLC12A3c.2554C= (p.Arg852=)
c.2551C= (p.Arg851=)
c.2581C= (p.Arg861=)
c.2578C= (p.Arg860=)
16g.56894563C>GCA395997362SLC12A3c.2554C>G (p.Arg852Gly)
c.2551C>G (p.Arg851Gly)
c.2581C>G (p.Arg861Gly)
c.2578C>G (p.Arg860Gly)
16g.56894563C>TCA8069966SLC12A3c.2554C>T (p.Arg852Cys)
c.2551C>T (p.Arg851Cys)
c.2581C>T (p.Arg861Cys)
c.2578C>T (p.Arg860Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.56894564G>ACA8069967SLC12A3c.2555G>A (p.Arg852His)
c.2552G>A (p.Arg851His)
c.2582G>A (p.Arg861His)
c.2579G>A (p.Arg860His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
16g.56894564G>CCA395997375SLC12A3c.2555G>C (p.Arg852Pro)
c.2552G>C (p.Arg851Pro)
c.2582G>C (p.Arg861Pro)
c.2579G>C (p.Arg860Pro)
16g.56894564G=CA2224361225SLC12A3c.2555G= (p.Arg852=)
c.2552G= (p.Arg851=)
c.2582G= (p.Arg861=)
c.2579G= (p.Arg860=)
16g.56894564G>TCA395997370SLC12A3c.2555G>T (p.Arg852Leu)
c.2552G>T (p.Arg851Leu)
c.2582G>T (p.Arg861Leu)
c.2579G>T (p.Arg860Leu)
dbSNP gnomAD v4
16g.56894565C>ACA495612752SLC12A3c.2556C>A (p.Arg852=)
c.2553C>A (p.Arg851=)
c.2583C>A (p.Arg861=)
c.2580C>A (p.Arg860=)
gnomAD v4
16g.56894565C>GCA495612753SLC12A3c.2556C>G (p.Arg852=)
c.2553C>G (p.Arg851=)
c.2583C>G (p.Arg861=)
c.2580C>G (p.Arg860=)
16g.56894565C>TCA495612754SLC12A3c.2556C>T (p.Arg852=)
c.2553C>T (p.Arg851=)
c.2583C>T (p.Arg861=)
c.2580C>T (p.Arg860=)
16g.56894566A=CA2224361226SLC12A3c.2557A= (p.Lys853=)
c.2554A= (p.Lys852=)
c.2584A= (p.Lys862=)
c.2581A= (p.Lys861=)
16g.56894566A>CCA395997377SLC12A3c.2557A>C (p.Lys853Gln)
c.2554A>C (p.Lys852Gln)
c.2584A>C (p.Lys862Gln)
c.2581A>C (p.Lys861Gln)
16g.56894566A>GCA395997379SLC12A3c.2557A>G (p.Lys853Glu)
c.2554A>G (p.Lys852Glu)
c.2584A>G (p.Lys862Glu)
c.2581A>G (p.Lys861Glu)
dbSNP gnomAD v4
16g.56894566A>TCA395997381SLC12A3c.2557A>T (p.Lys853Ter)
c.2554A>T (p.Lys852Ter)
c.2584A>T (p.Lys862Ter)
c.2581A>T (p.Lys861Ter)
16g.56894567A>CCA395997383SLC12A3c.2558A>C (p.Lys853Thr)
c.2555A>C (p.Lys852Thr)
c.2585A>C (p.Lys862Thr)
c.2582A>C (p.Lys861Thr)
16g.56894567A>GCA395997386SLC12A3c.2558A>G (p.Lys853Arg)
c.2555A>G (p.Lys852Arg)
c.2585A>G (p.Lys862Arg)
c.2582A>G (p.Lys861Arg)
16g.56894567A>TCA395997388SLC12A3c.2558A>T (p.Lys853Met)
c.2555A>T (p.Lys852Met)
c.2585A>T (p.Lys862Met)
c.2582A>T (p.Lys861Met)
16g.56894568G>ACA8069968SLC12A3c.2559G>A (p.Lys853=)
c.2556G>A (p.Lys852=)
c.2586G>A (p.Lys862=)
c.2583G>A (p.Lys861=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.56894568G>CCA395997393SLC12A3c.2559G>C (p.Lys853Asn)
c.2556G>C (p.Lys852Asn)
c.2586G>C (p.Lys862Asn)
c.2583G>C (p.Lys861Asn)
16g.56894568G=CA2224361227SLC12A3c.2559G= (p.Lys853=)
c.2556G= (p.Lys852=)
c.2586G= (p.Lys862=)
c.2583G= (p.Lys861=)
16g.56894568G>TCA395997396SLC12A3c.2559G>T (p.Lys853Asn)
c.2556G>T (p.Lys852Asn)
c.2586G>T (p.Lys862Asn)
c.2583G>T (p.Lys861Asn)
16g.56894569A=CA2224361228SLC12A3c.2560A= (p.Arg854=)
c.2557A= (p.Arg853=)
c.2587A= (p.Arg863=)
c.2584A= (p.Arg862=)
16g.56894569A>CCA495612755SLC12A3c.2560A>C (p.Arg854=)
c.2557A>C (p.Arg853=)
c.2587A>C (p.Arg863=)
c.2584A>C (p.Arg862=)
16g.56894569A>GCA395997399SLC12A3c.2560A>G (p.Arg854Gly)
c.2557A>G (p.Arg853Gly)
c.2587A>G (p.Arg863Gly)
c.2584A>G (p.Arg862Gly)
dbSNP gnomAD v3 gnomAD v4
16g.56894569A>TCA395997402SLC12A3c.2560A>T (p.Arg854Trp)
c.2557A>T (p.Arg853Trp)
c.2587A>T (p.Arg863Trp)
c.2584A>T (p.Arg862Trp)
16g.56894570G>ACA281514318SLC12A3c.2561G>A (p.Arg854Lys)
c.2558G>A (p.Arg853Lys)
c.2588G>A (p.Arg863Lys)
c.2585G>A (p.Arg862Lys)
dbSNP
16g.56894570G>CCA395997408SLC12A3c.2561G>C (p.Arg854Thr)
c.2558G>C (p.Arg853Thr)
c.2588G>C (p.Arg863Thr)
c.2585G>C (p.Arg862Thr)
16g.56894570G=CA2224361229SLC12A3c.2561G= (p.Arg854=)
c.2558G= (p.Arg853=)
c.2588G= (p.Arg863=)
c.2585G= (p.Arg862=)
16g.56894570G>TCA395997406SLC12A3c.2561G>T (p.Arg854Met)
c.2558G>T (p.Arg853Met)
c.2588G>T (p.Arg863Met)
c.2585G>T (p.Arg862Met)
16g.56894571G>ACA495612756SLC12A3c.2562G>A (p.Arg854=)
c.2559G>A (p.Arg853=)
c.2589G>A (p.Arg863=)
c.2586G>A (p.Arg862=)
ClinVar dbSNP
16g.56894571G>CCA395997409SLC12A3c.2562G>C (p.Arg854Ser)
c.2559G>C (p.Arg853Ser)
c.2589G>C (p.Arg863Ser)
c.2586G>C (p.Arg862Ser)

Number of alleles fetched