Chr Mutation (hg38) CAid Gene Transcript Linkouts
20g.763779_763780delinsAACA310677314SLC52A3c.791_792delinsTT (p.Ser264Phe)
c.567+1428_567+1429delinsTT (n.567+1428_567+1429delinsTT)
n.618+1428_618+1429delinsTT
dbSNP
20g.763779_763780delinsGGCA2345349387SLC52A3c.791_792delinsCC (p.Ser264=)
c.567+1428_567+1429delinsCC (n.567+1428_567+1429delinsCC)
n.618+1428_618+1429delinsCC
20g.763780G>ACA407963088SLC52A3c.791C>T (p.Ser264Phe)
c.567+1428C>T (n.567+1428C>T)
n.618+1428C>T
20g.763780G>CCA407963089SLC52A3c.791C>G (p.Ser264Cys)
c.567+1428C>G (n.567+1428C>G)
n.618+1428C>G
20g.763780G>TCA407963087SLC52A3c.791C>A (p.Ser264Tyr)
c.567+1428C>A (n.567+1428C>A)
n.618+1428C>A
20g.763781_763782delCA2739277024SLC52A3c.790_791del (p.Ser264HisfsTer8)
c.567+1427_567+1428del (n.567+1427_567+1428del)
n.618+1427_618+1428del
ClinVar
20g.763781A>CCA407963090SLC52A3c.790T>G (p.Ser264Ala)
c.567+1427T>G (n.567+1427T>G)
n.618+1427T>G
20g.763781A>GCA407963092SLC52A3c.790T>C (p.Ser264Pro)
c.567+1427T>C (n.567+1427T>C)
n.618+1427T>C
20g.763781A>TCA407963091SLC52A3c.790T>A (p.Ser264Thr)
c.567+1427T>A (n.567+1427T>A)
n.618+1427T>A
20g.763782G>ACA509542406SLC52A3c.789C>T (p.His263=)
c.567+1426C>T (n.567+1426C>T)
n.618+1426C>T
gnomAD v4
20g.763782G>CCA9724682SLC52A3c.789C>G (p.His263Gln)
c.567+1426C>G (n.567+1426C>G)
n.618+1426C>G
dbSNP ExAC gnomAD v2 gnomAD v4
20g.763782G=CA2345349388SLC52A3c.789C= (p.His263=)
c.567+1426C= (n.567+1426C=)
n.618+1426C=
20g.763782G>TCA407963093SLC52A3c.789C>A (p.His263Gln)
c.567+1426C>A (n.567+1426C>A)
n.618+1426C>A
20g.763783T>ACA407963094SLC52A3c.788A>T (p.His263Leu)
c.567+1425A>T (n.567+1425A>T)
n.618+1425A>T
20g.763783T>CCA407963095SLC52A3c.788A>G (p.His263Arg)
c.567+1425A>G (n.567+1425A>G)
n.618+1425A>G
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
20g.763783T>GCA407963096SLC52A3c.788A>C (p.His263Pro)
c.567+1425A>C (n.567+1425A>C)
n.618+1425A>C
gnomAD v4
20g.763783T=CA2345349389SLC52A3c.788A= (p.His263=)
c.567+1425A= (n.567+1425A=)
n.618+1425A=
20g.763784G>ACA9724683SLC52A3c.787C>T (p.His263Tyr)
c.567+1424C>T (n.567+1424C>T)
n.618+1424C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.763784G>CCA407963097SLC52A3c.787C>G (p.His263Asp)
c.567+1424C>G (n.567+1424C>G)
n.618+1424C>G
20g.763784G=CA2345349390SLC52A3c.787C= (p.His263=)
c.567+1424C= (n.567+1424C=)
n.618+1424C=
20g.763784G>TCA407963098SLC52A3c.787C>A (p.His263Asn)
c.567+1424C>A (n.567+1424C>A)
n.618+1424C>A
20g.763785G>ACA509542410SLC52A3c.786C>T (p.Leu262=)
c.567+1423C>T (n.567+1423C>T)
n.618+1423C>T
dbSNP gnomAD v4
20g.763785G>CCA509542412SLC52A3c.786C>G (p.Leu262=)
c.567+1423C>G (n.567+1423C>G)
n.618+1423C>G
20g.763785G=CA2345349391SLC52A3c.786C= (p.Leu262=)
c.567+1423C= (n.567+1423C=)
n.618+1423C=
20g.763785G>TCA509542411SLC52A3c.786C>A (p.Leu262=)
c.567+1423C>A (n.567+1423C>A)
n.618+1423C>A
20g.763786A>CCA407963099SLC52A3c.785T>G (p.Leu262Arg)
c.567+1422T>G (n.567+1422T>G)
n.618+1422T>G
20g.763786A>GCA407963100SLC52A3c.785T>C (p.Leu262Pro)
c.567+1422T>C (n.567+1422T>C)
n.618+1422T>C
20g.763786A>TCA407963101SLC52A3c.785T>A (p.Leu262His)
c.567+1422T>A (n.567+1422T>A)
n.618+1422T>A
20g.763787G>ACA407963102SLC52A3c.784C>T (p.Leu262Phe)
c.567+1421C>T (n.567+1421C>T)
n.618+1421C>T
20g.763787G>CCA407963104SLC52A3c.784C>G (p.Leu262Val)
c.567+1421C>G (n.567+1421C>G)
n.618+1421C>G
gnomAD v4
20g.763787G>TCA407963103SLC52A3c.784C>A (p.Leu262Ile)
c.567+1421C>A (n.567+1421C>A)
n.618+1421C>A
20g.763789_763797delCA2815001780SLC52A3c.776_784del (p.Gln259_Thr261del)
c.567+1413_567+1421del (n.567+1413_567+1421del)
n.618+1413_618+1421del
20g.763788G>ACA509542418SLC52A3c.783C>T (p.Thr261=)
c.567+1420C>T (n.567+1420C>T)
n.618+1420C>T
dbSNP gnomAD v2 gnomAD v4
20g.763788G>CCA509542417SLC52A3c.783C>G (p.Thr261=)
c.567+1420C>G (n.567+1420C>G)
n.618+1420C>G
gnomAD v4
20g.763788G=CA2345349392SLC52A3c.783C= (p.Thr261=)
c.567+1420C= (n.567+1420C=)
n.618+1420C=
20g.763788G>TCA509542416SLC52A3c.783C>A (p.Thr261=)
c.567+1420C>A (n.567+1420C>A)
n.618+1420C>A
20g.763789G>ACA9724684SLC52A3c.782C>T (p.Thr261Ile)
c.567+1419C>T (n.567+1419C>T)
n.618+1419C>T
dbSNP ExAC gnomAD v2
20g.763789G>CCA407963105SLC52A3c.782C>G (p.Thr261Ser)
c.567+1419C>G (n.567+1419C>G)
n.618+1419C>G
dbSNP
20g.763789G=CA2345349393SLC52A3c.782C= (p.Thr261=)
c.567+1419C= (n.567+1419C=)
n.618+1419C=
20g.763789G>TCA407963106SLC52A3c.782C>A (p.Thr261Asn)
c.567+1419C>A (n.567+1419C>A)
n.618+1419C>A
20g.763790T>ACA407963107SLC52A3c.781A>T (p.Thr261Ser)
c.567+1418A>T (n.567+1418A>T)
n.618+1418A>T
20g.763790T>CCA407963108SLC52A3c.781A>G (p.Thr261Ala)
c.567+1418A>G (n.567+1418A>G)
n.618+1418A>G
dbSNP
20g.763790T>GCA407963109SLC52A3c.781A>C (p.Thr261Pro)
c.567+1418A>C (n.567+1418A>C)
n.618+1418A>C
dbSNP gnomAD v2 gnomAD v4
20g.763790T=CA2345349394SLC52A3c.781A= (p.Thr261=)
c.567+1418A= (n.567+1418A=)
n.618+1418A=
20g.763791G>ACA509542422SLC52A3c.780C>T (p.Val260=)
c.567+1417C>T (n.567+1417C>T)
n.618+1417C>T
20g.763791G>CCA509542424SLC52A3c.780C>G (p.Val260=)
c.567+1417C>G (n.567+1417C>G)
n.618+1417C>G
20g.763791G>TCA509542423SLC52A3c.780C>A (p.Val260=)
c.567+1417C>A (n.567+1417C>A)
n.618+1417C>A
20g.763792A>CCA407963110SLC52A3c.779T>G (p.Val260Gly)
c.567+1416T>G (n.567+1416T>G)
n.618+1416T>G
20g.763792A>GCA407963111SLC52A3c.779T>C (p.Val260Ala)
c.567+1416T>C (n.567+1416T>C)
n.618+1416T>C
20g.763792A>TCA407963112SLC52A3c.779T>A (p.Val260Asp)
c.567+1416T>A (n.567+1416T>A)
n.618+1416T>A
20g.763793C>ACA407963114SLC52A3c.778G>T (p.Val260Phe)
c.567+1415G>T (n.567+1415G>T)
n.618+1415G>T
20g.763793C>GCA407963115SLC52A3c.778G>C (p.Val260Leu)
c.567+1415G>C (n.567+1415G>C)
n.618+1415G>C
20g.763793C>TCA407963113SLC52A3c.778G>A (p.Val260Ile)
c.567+1415G>A (n.567+1415G>A)
n.618+1415G>A
20g.763794C>ACA407963116SLC52A3c.777G>T (p.Gln259His)
c.567+1414G>T (n.567+1414G>T)
n.618+1414G>T
20g.763794C>GCA407963117SLC52A3c.777G>C (p.Gln259His)
c.567+1414G>C (n.567+1414G>C)
n.618+1414G>C
20g.763794C>TCA509542428SLC52A3c.777G>A (p.Gln259=)
c.567+1414G>A (n.567+1414G>A)
n.618+1414G>A
gnomAD v4
20g.763795T>ACA407963118SLC52A3c.776A>T (p.Gln259Leu)
c.567+1413A>T (n.567+1413A>T)
n.618+1413A>T
20g.763795T>CCA407963119SLC52A3c.776A>G (p.Gln259Arg)
c.567+1413A>G (n.567+1413A>G)
n.618+1413A>G
20g.763795T>GCA407963120SLC52A3c.776A>C (p.Gln259Pro)
c.567+1413A>C (n.567+1413A>C)
n.618+1413A>C
20g.763796G>ACA9724685SLC52A3c.775C>T (p.Gln259Ter)
c.567+1412C>T (n.567+1412C>T)
n.618+1412C>T
ClinVar dbSNP ExAC gnomAD v3 gnomAD v4
20g.763796G>CCA407963121SLC52A3c.775C>G (p.Gln259Glu)
c.567+1412C>G (n.567+1412C>G)
n.618+1412C>G
20g.763796G=CA2345349395SLC52A3c.775C= (p.Gln259=)
c.567+1412C= (n.567+1412C=)
n.618+1412C=
20g.763796G>TCA407963122SLC52A3c.775C>A (p.Gln259Lys)
c.567+1412C>A (n.567+1412C>A)
n.618+1412C>A
20g.763797G>ACA9724686SLC52A3c.774C>T (p.Asp258=)
c.567+1411C>T (n.567+1411C>T)
n.618+1411C>T
ClinVar dbSNP ExAC gnomAD v2
20g.763797G>CCA407963123SLC52A3c.774C>G (p.Asp258Glu)
c.567+1411C>G (n.567+1411C>G)
n.618+1411C>G
20g.763797G=CA2345349396SLC52A3c.774C= (p.Asp258=)
c.567+1411C= (n.567+1411C=)
n.618+1411C=
20g.763797G>TCA407963124SLC52A3c.774C>A (p.Asp258Glu)
c.567+1411C>A (n.567+1411C>A)
n.618+1411C>A
20g.763798T>ACA407963126SLC52A3c.773A>T (p.Asp258Val)
c.567+1410A>T (n.567+1410A>T)
n.618+1410A>T
20g.763798T>CCA407963127SLC52A3c.773A>G (p.Asp258Gly)
c.567+1410A>G (n.567+1410A>G)
n.618+1410A>G
20g.763798T>GCA407963125SLC52A3c.773A>C (p.Asp258Ala)
c.567+1410A>C (n.567+1410A>C)
n.618+1410A>C
20g.763799C>ACA407963128SLC52A3c.772G>T (p.Asp258Tyr)
c.567+1409G>T (n.567+1409G>T)
n.618+1409G>T
gnomAD v4
20g.763799C=CA2345349397SLC52A3c.772G= (p.Asp258=)
c.567+1409G= (n.567+1409G=)
n.618+1409G=
20g.763799C>GCA407963129SLC52A3c.772G>C (p.Asp258His)
c.567+1409G>C (n.567+1409G>C)
n.618+1409G>C
dbSNP gnomAD v3 gnomAD v4
20g.763799C>TCA407963130SLC52A3c.772G>A (p.Asp258Asn)
c.567+1409G>A (n.567+1409G>A)
n.618+1409G>A
20g.763800A=CA2345349398SLC52A3c.771T= (p.Asn257=)
c.567+1408T= (n.567+1408T=)
n.618+1408T=
20g.763800A>CCA407963131SLC52A3c.771T>G (p.Asn257Lys)
c.567+1408T>G (n.567+1408T>G)
n.618+1408T>G
20g.763800A>GCA509542432SLC52A3c.771T>C (p.Asn257=)
c.567+1408T>C (n.567+1408T>C)
n.618+1408T>C
ClinVar dbSNP
20g.763800A>TCA407963132SLC52A3c.771T>A (p.Asn257Lys)
c.567+1408T>A (n.567+1408T>A)
n.618+1408T>A
20g.763801T>ACA407963135SLC52A3c.770A>T (p.Asn257Ile)
c.567+1407A>T (n.567+1407A>T)
n.618+1407A>T
gnomAD v4
20g.763801T>CCA407963133SLC52A3c.770A>G (p.Asn257Ser)
c.567+1407A>G (n.567+1407A>G)
n.618+1407A>G
dbSNP gnomAD v4
20g.763801T>GCA407963134SLC52A3c.770A>C (p.Asn257Thr)
c.567+1407A>C (n.567+1407A>C)
n.618+1407A>C
20g.763801T=CA2345349399SLC52A3c.770A= (p.Asn257=)
c.567+1407A= (n.567+1407A=)
n.618+1407A=
20g.763802T>ACA407963136SLC52A3c.769A>T (p.Asn257Tyr)
c.567+1406A>T (n.567+1406A>T)
n.618+1406A>T
COSMIC COSMIC
20g.763802T>CCA407963137SLC52A3c.769A>G (p.Asn257Asp)
c.567+1406A>G (n.567+1406A>G)
n.618+1406A>G
dbSNP gnomAD v3 gnomAD v4
20g.763802T>GCA407963138SLC52A3c.769A>C (p.Asn257His)
c.567+1406A>C (n.567+1406A>C)
n.618+1406A>C
20g.763802T=CA2345349400SLC52A3c.769A= (p.Asn257=)
c.567+1406A= (n.567+1406A=)
n.618+1406A=
20g.763803G>ACA509542435SLC52A3c.768C>T (p.Leu256=)
c.567+1405C>T (n.567+1405C>T)
n.618+1405C>T
gnomAD v4
20g.763803G>CCA509542436SLC52A3c.768C>G (p.Leu256=)
c.567+1405C>G (n.567+1405C>G)
n.618+1405C>G
20g.763803G>TCA509542437SLC52A3c.768C>A (p.Leu256=)
c.567+1405C>A (n.567+1405C>A)
n.618+1405C>A
gnomAD v4
20g.763804A>CCA407963139SLC52A3c.767T>G (p.Leu256Arg)
c.567+1404T>G (n.567+1404T>G)
n.618+1404T>G
20g.763804A>GCA407963140SLC52A3c.767T>C (p.Leu256Pro)
c.567+1404T>C (n.567+1404T>C)
n.618+1404T>C
dbSNP
20g.763804A>TCA407963141SLC52A3c.767T>A (p.Leu256His)
c.567+1404T>A (n.567+1404T>A)
n.618+1404T>A
20g.763805G>ACA407963143SLC52A3c.766C>T (p.Leu256Phe)
c.567+1403C>T (n.567+1403C>T)
n.618+1403C>T
20g.763805G>CCA407963144SLC52A3c.766C>G (p.Leu256Val)
c.567+1403C>G (n.567+1403C>G)
n.618+1403C>G
dbSNP
20g.763805G=CA2345349401SLC52A3c.766C= (p.Leu256=)
c.567+1403C= (n.567+1403C=)
n.618+1403C=
20g.763805G>TCA407963142SLC52A3c.766C>A (p.Leu256Ile)
c.567+1403C>A (n.567+1403C>A)
n.618+1403C>A
20g.763806G>ACA9724687SLC52A3c.765C>T (p.Leu255=)
c.567+1402C>T (n.567+1402C>T)
n.618+1402C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.763806G>CCA509542440SLC52A3c.765C>G (p.Leu255=)
c.567+1402C>G (n.567+1402C>G)
n.618+1402C>G
ClinVar dbSNP
20g.763806G=CA2345349402SLC52A3c.765C= (p.Leu255=)
c.567+1402C= (n.567+1402C=)
n.618+1402C=
20g.763806G>TCA509542439SLC52A3c.765C>A (p.Leu255=)
c.567+1402C>A (n.567+1402C>A)
n.618+1402C>A
20g.763807A=CA2345349403SLC52A3c.764T= (p.Leu255=)
c.567+1401T= (n.567+1401T=)
n.618+1401T=
20g.763807A>CCA407963145SLC52A3c.764T>G (p.Leu255Arg)
c.567+1401T>G (n.567+1401T>G)
n.618+1401T>G
20g.763807A>GCA9724688SLC52A3c.764T>C (p.Leu255Pro)
c.567+1401T>C (n.567+1401T>C)
n.618+1401T>C
dbSNP ExAC gnomAD v2 gnomAD v4
20g.763807A>TCA407963146SLC52A3c.764T>A (p.Leu255His)
c.567+1401T>A (n.567+1401T>A)
n.618+1401T>A
20g.763808G>ACA407963147SLC52A3c.763C>T (p.Leu255Phe)
c.567+1400C>T (n.567+1400C>T)
n.618+1400C>T
ClinVar dbSNP gnomAD v4
20g.763808G>CCA407963148SLC52A3c.763C>G (p.Leu255Val)
c.567+1400C>G (n.567+1400C>G)
n.618+1400C>G
20g.763808G=CA2345349404SLC52A3c.763C= (p.Leu255=)
c.567+1400C= (n.567+1400C=)
n.618+1400C=
20g.763808G>TCA407963149SLC52A3c.763C>A (p.Leu255Ile)
c.567+1400C>A (n.567+1400C>A)
n.618+1400C>A
20g.763809G>ACA509542442SLC52A3c.762C>T (p.Asp254=)
c.567+1399C>T (n.567+1399C>T)
n.618+1399C>T
20g.763809G>CCA407963150SLC52A3c.762C>G (p.Asp254Glu)
c.567+1399C>G (n.567+1399C>G)
n.618+1399C>G
20g.763809G=CA2345349405SLC52A3c.762C= (p.Asp254=)
c.567+1399C= (n.567+1399C=)
n.618+1399C=
20g.763809G>TCA9724689SLC52A3c.762C>A (p.Asp254Glu)
c.567+1399C>A (n.567+1399C>A)
n.618+1399C>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.763810T>ACA9724690SLC52A3c.761A>T (p.Asp254Val)
c.567+1398A>T (n.567+1398A>T)
n.618+1398A>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
20g.763810T>CCA407963151SLC52A3c.761A>G (p.Asp254Gly)
c.567+1398A>G (n.567+1398A>G)
n.618+1398A>G
gnomAD v4
20g.763810T>GCA407963152SLC52A3c.761A>C (p.Asp254Ala)
c.567+1398A>C (n.567+1398A>C)
n.618+1398A>C
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
20g.763810T=CA2345349406SLC52A3c.761A= (p.Asp254=)
c.567+1398A= (n.567+1398A=)
n.618+1398A=
20g.763811C>ACA407963153SLC52A3c.760G>T (p.Asp254Tyr)
c.567+1397G>T (n.567+1397G>T)
n.618+1397G>T
20g.763811C>GCA407963154SLC52A3c.760G>C (p.Asp254His)
c.567+1397G>C (n.567+1397G>C)
n.618+1397G>C
20g.763811C>TCA407963155SLC52A3c.760G>A (p.Asp254Asn)
c.567+1397G>A (n.567+1397G>A)
n.618+1397G>A
gnomAD v4
20g.763812T>ACA407963156SLC52A3c.759A>T (p.Glu253Asp)
c.567+1396A>T (n.567+1396A>T)
n.618+1396A>T
20g.763812T>CCA509542445SLC52A3c.759A>G (p.Glu253=)
c.567+1396A>G (n.567+1396A>G)
n.618+1396A>G
20g.763812T>GCA407963157SLC52A3c.759A>C (p.Glu253Asp)
c.567+1396A>C (n.567+1396A>C)
n.618+1396A>C
20g.763813T>ACA407963158SLC52A3c.758A>T (p.Glu253Val)
c.567+1395A>T (n.567+1395A>T)
n.618+1395A>T
20g.763813T>CCA407963159SLC52A3c.758A>G (p.Glu253Gly)
c.567+1395A>G (n.567+1395A>G)
n.618+1395A>G
20g.763813T>GCA407963160SLC52A3c.758A>C (p.Glu253Ala)
c.567+1395A>C (n.567+1395A>C)
n.618+1395A>C
20g.763814C>ACA407963161SLC52A3c.757G>T (p.Glu253Ter)
c.567+1394G>T (n.567+1394G>T)
n.618+1394G>T
20g.763814C>GCA407963162SLC52A3c.757G>C (p.Glu253Gln)
c.567+1394G>C (n.567+1394G>C)
n.618+1394G>C
20g.763814C>TCA407963163SLC52A3c.757G>A (p.Glu253Lys)
c.567+1394G>A (n.567+1394G>A)
n.618+1394G>A
20g.763815C>ACA509542447SLC52A3c.756G>T (p.Val252=)
c.567+1393G>T (n.567+1393G>T)
n.618+1393G>T
20g.763815C>GCA509542448SLC52A3c.756G>C (p.Val252=)
c.567+1393G>C (n.567+1393G>C)
n.618+1393G>C
20g.763815C>TCA509542449SLC52A3c.756G>A (p.Val252=)
c.567+1393G>A (n.567+1393G>A)
n.618+1393G>A
20g.763816A>CCA407963164SLC52A3c.755T>G (p.Val252Gly)
c.567+1392T>G (n.567+1392T>G)
n.618+1392T>G
20g.763816A>GCA407963165SLC52A3c.755T>C (p.Val252Ala)
c.567+1392T>C (n.567+1392T>C)
n.618+1392T>C
20g.763816A>TCA407963166SLC52A3c.755T>A (p.Val252Glu)
c.567+1392T>A (n.567+1392T>A)
n.618+1392T>A
20g.763817C>ACA407963167SLC52A3c.754G>T (p.Val252Leu)
c.567+1391G>T (n.567+1391G>T)
n.618+1391G>T
20g.763817C=CA2345349407SLC52A3c.754G= (p.Val252=)
c.567+1391G= (n.567+1391G=)
n.618+1391G=
20g.763817C>GCA407963168SLC52A3c.754G>C (p.Val252Leu)
c.567+1391G>C (n.567+1391G>C)
n.618+1391G>C
20g.763817C>TCA9724691SLC52A3c.754G>A (p.Val252Met)
c.567+1391G>A (n.567+1391G>A)
n.618+1391G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
20g.763817_763818delinsCGCA2345349408SLC52A3c.753_754delinsCG (p.Ser251=)
c.567+1390_567+1391delinsCG (n.567+1390_567+1391delinsCG)
n.618+1390_618+1391delinsCG
20g.763818G>ACA9724692SLC52A3c.753C>T (p.Ser251=)
c.567+1390C>T (n.567+1390C>T)
n.618+1390C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.763818G>CCA509542450SLC52A3c.753C>G (p.Ser251=)
c.567+1390C>G (n.567+1390C>G)
n.618+1390C>G
20g.763818G=CA2345349409SLC52A3c.753C= (p.Ser251=)
c.567+1390C= (n.567+1390C=)
n.618+1390C=
20g.763818G>TCA509542451SLC52A3c.753C>A (p.Ser251=)
c.567+1390C>A (n.567+1390C>A)
n.618+1390C>A
gnomAD v4
20g.763819delCA913190710SLC52A3c.753del (p.Val252TrpfsTer?)
c.567+1390del (n.567+1390del)
n.618+1390del
ClinVar dbSNP gnomAD v4
20g.763819G>ACA407963169SLC52A3c.752C>T (p.Ser251Phe)
c.567+1389C>T (n.567+1389C>T)
n.618+1389C>T
COSMIC
20g.763819G>CCA407963171SLC52A3c.752C>G (p.Ser251Cys)
c.567+1389C>G (n.567+1389C>G)
n.618+1389C>G
20g.763819G>TCA407963170SLC52A3c.752C>A (p.Ser251Tyr)
c.567+1389C>A (n.567+1389C>A)
n.618+1389C>A
20g.763820A>CCA407963172SLC52A3c.751T>G (p.Ser251Ala)
c.567+1388T>G (n.567+1388T>G)
n.618+1388T>G
20g.763820A>GCA407963173SLC52A3c.751T>C (p.Ser251Pro)
c.567+1388T>C (n.567+1388T>C)
n.618+1388T>C
20g.763820A>TCA407963174SLC52A3c.751T>A (p.Ser251Thr)
c.567+1388T>A (n.567+1388T>A)
n.618+1388T>A
20g.763821A>CCA509542457SLC52A3c.750T>G (p.Ala250=)
c.567+1387T>G (n.567+1387T>G)
n.618+1387T>G
20g.763821A>GCA509542454SLC52A3c.750T>C (p.Ala250=)
c.567+1387T>C (n.567+1387T>C)
n.618+1387T>C
20g.763821A>TCA509542456SLC52A3c.750T>A (p.Ala250=)
c.567+1387T>A (n.567+1387T>A)
n.618+1387T>A
20g.763822G>ACA407963175SLC52A3c.749C>T (p.Ala250Val)
c.567+1386C>T (n.567+1386C>T)
n.618+1386C>T
20g.763822G>CCA407963176SLC52A3c.749C>G (p.Ala250Gly)
c.567+1386C>G (n.567+1386C>G)
n.618+1386C>G
20g.763822G>TCA407963177SLC52A3c.749C>A (p.Ala250Asp)
c.567+1386C>A (n.567+1386C>A)
n.618+1386C>A
20g.763823C>ACA407963180SLC52A3c.748G>T (p.Ala250Ser)
c.567+1385G>T (n.567+1385G>T)
n.618+1385G>T
20g.763823C>GCA407963178SLC52A3c.748G>C (p.Ala250Pro)
c.567+1385G>C (n.567+1385G>C)
n.618+1385G>C
20g.763823C>TCA407963179SLC52A3c.748G>A (p.Ala250Thr)
c.567+1385G>A (n.567+1385G>A)
n.618+1385G>A
gnomAD v4
20g.763824C>ACA407963181SLC52A3c.747G>T (p.Glu249Asp)
c.567+1384G>T (n.567+1384G>T)
n.618+1384G>T
COSMIC COSMIC
20g.763824C>GCA407963182SLC52A3c.747G>C (p.Glu249Asp)
c.567+1384G>C (n.567+1384G>C)
n.618+1384G>C
20g.763824C>TCA509542459SLC52A3c.747G>A (p.Glu249=)
c.567+1384G>A (n.567+1384G>A)
n.618+1384G>A
20g.763825delCA2651547673SLC52A3c.746del (p.Glu249GlyfsTer?)
c.567+1383del (n.567+1383del)
n.618+1383del
gnomAD v4
20g.763825T>ACA407963183SLC52A3c.746A>T (p.Glu249Val)
c.567+1383A>T (n.567+1383A>T)
n.618+1383A>T
20g.763825T>CCA407963184SLC52A3c.746A>G (p.Glu249Gly)
c.567+1383A>G (n.567+1383A>G)
n.618+1383A>G
ClinVar dbSNP
20g.763825T>GCA407963185SLC52A3c.746A>C (p.Glu249Ala)
c.567+1383A>C (n.567+1383A>C)
n.618+1383A>C
20g.763826C>ACA407963186SLC52A3c.745G>T (p.Glu249Ter)
c.567+1382G>T (n.567+1382G>T)
n.618+1382G>T
20g.763826C>GCA407963188SLC52A3c.745G>C (p.Glu249Gln)
c.567+1382G>C (n.567+1382G>C)
n.618+1382G>C
20g.763826C>TCA407963187SLC52A3c.745G>A (p.Glu249Lys)
c.567+1382G>A (n.567+1382G>A)
n.618+1382G>A
ClinVar gnomAD v4
20g.763827C>ACA407963189SLC52A3c.744G>T (p.Trp248Cys)
c.567+1381G>T (n.567+1381G>T)
n.618+1381G>T
20g.763827C>GCA407963190SLC52A3c.744G>C (p.Trp248Cys)
c.567+1381G>C (n.567+1381G>C)
n.618+1381G>C
20g.763827C>TCA407963191SLC52A3c.744G>A (p.Trp248Ter)
c.567+1381G>A (n.567+1381G>A)
n.618+1381G>A
20g.763828C>ACA407963192SLC52A3c.743G>T (p.Trp248Leu)
c.567+1380G>T (n.567+1380G>T)
n.618+1380G>T
20g.763828C>GCA407963193SLC52A3c.743G>C (p.Trp248Ser)
c.567+1380G>C (n.567+1380G>C)
n.618+1380G>C
20g.763828C>TCA407963194SLC52A3c.743G>A (p.Trp248Ter)
c.567+1380G>A (n.567+1380G>A)
n.618+1380G>A
20g.763829delCA2580097969SLC52A3c.742del (p.Trp248GlyfsTer?)
c.567+1379del (n.567+1379del)
n.618+1379del
ClinVar
20g.763829A>CCA407963195SLC52A3c.742T>G (p.Trp248Gly)
c.567+1379T>G (n.567+1379T>G)
n.618+1379T>G
20g.763829A>GCA407963196SLC52A3c.742T>C (p.Trp248Arg)
c.567+1379T>C (n.567+1379T>C)
n.618+1379T>C
20g.763829A>TCA407963197SLC52A3c.742T>A (p.Trp248Arg)
c.567+1379T>A (n.567+1379T>A)
n.618+1379T>A
20g.763829dupCA2577315102SLC52A3c.742dup (p.Trp248LeufsTer11)
c.567+1379dup (n.567+1379dup)
n.618+1379dup
20g.763830G>ACA509542461SLC52A3c.741C>T (p.Cys247=)
c.567+1378C>T (n.567+1378C>T)
n.618+1378C>T
20g.763830G>CCA407963198SLC52A3c.741C>G (p.Cys247Trp)
c.567+1378C>G (n.567+1378C>G)
n.618+1378C>G
dbSNP
20g.763830G=CA2345349410SLC52A3c.741C= (p.Cys247=)
c.567+1378C= (n.567+1378C=)
n.618+1378C=
20g.763830G>TCA407963199SLC52A3c.741C>A (p.Cys247Ter)
c.567+1378C>A (n.567+1378C>A)
n.618+1378C>A
20g.763831C>ACA9724693SLC52A3c.740G>T (p.Cys247Phe)
c.567+1377G>T (n.567+1377G>T)
n.618+1377G>T
dbSNP ExAC gnomAD v2 gnomAD v4
20g.763831C=CA2345349411SLC52A3c.740G= (p.Cys247=)
c.567+1377G= (n.567+1377G=)
n.618+1377G=
20g.763831C>GCA407963201SLC52A3c.740G>C (p.Cys247Ser)
c.567+1377G>C (n.567+1377G>C)
n.618+1377G>C
gnomAD v4
20g.763831C>TCA407963200SLC52A3c.740G>A (p.Cys247Tyr)
c.567+1377G>A (n.567+1377G>A)
n.618+1377G>A
20g.763832A>CCA407963202SLC52A3c.739T>G (p.Cys247Gly)
c.567+1376T>G (n.567+1376T>G)
n.618+1376T>G
20g.763832A>GCA407963204SLC52A3c.739T>C (p.Cys247Arg)
c.567+1376T>C (n.567+1376T>C)
n.618+1376T>C
20g.763832A>TCA407963203SLC52A3c.739T>A (p.Cys247Ser)
c.567+1376T>A (n.567+1376T>A)
n.618+1376T>A
COSMIC COSMIC
20g.763833C>ACA407963205SLC52A3c.738G>T (p.Arg246Ser)
c.567+1375G>T (n.567+1375G>T)
n.618+1375G>T
20g.763833C=CA2345349412SLC52A3c.738G= (p.Arg246=)
c.567+1375G= (n.567+1375G=)
n.618+1375G=
20g.763833C>GCA9724694SLC52A3c.738G>C (p.Arg246Ser)
c.567+1375G>C (n.567+1375G>C)
n.618+1375G>C
dbSNP ExAC gnomAD v2 gnomAD v4
20g.763833C>TCA509542463SLC52A3c.738G>A (p.Arg246=)
c.567+1375G>A (n.567+1375G>A)
n.618+1375G>A
20g.763834C>ACA407963206SLC52A3c.737G>T (p.Arg246Met)
c.567+1374G>T (n.567+1374G>T)
n.618+1374G>T
20g.763834C>GCA407963207SLC52A3c.737G>C (p.Arg246Thr)
c.567+1374G>C (n.567+1374G>C)
n.618+1374G>C
gnomAD v4
20g.763834C>TCA407963208SLC52A3c.737G>A (p.Arg246Lys)
c.567+1374G>A (n.567+1374G>A)
n.618+1374G>A
gnomAD v4
20g.763835T>ACA407963209SLC52A3c.736A>T (p.Arg246Trp)
c.567+1373A>T (n.567+1373A>T)
n.618+1373A>T
20g.763835T>CCA407963210SLC52A3c.736A>G (p.Arg246Gly)
c.567+1373A>G (n.567+1373A>G)
n.618+1373A>G
20g.763835T>GCA509542466SLC52A3c.736A>C (p.Arg246=)
c.567+1373A>C (n.567+1373A>C)
n.618+1373A>C
20g.763836G>ACA509542467SLC52A3c.735C>T (p.Pro245=)
c.567+1372C>T (n.567+1372C>T)
n.618+1372C>T
20g.763836G>CCA509542468SLC52A3c.735C>G (p.Pro245=)
c.567+1372C>G (n.567+1372C>G)
n.618+1372C>G
gnomAD v4
20g.763836G>TCA509542469SLC52A3c.735C>A (p.Pro245=)
c.567+1372C>A (n.567+1372C>A)
n.618+1372C>A
20g.763838delCA2651547674SLC52A3c.735del (p.Arg246GlyfsTer?)
c.567+1372del (n.567+1372del)
n.618+1372del
gnomAD v4
20g.763837G>ACA407963211SLC52A3c.734C>T (p.Pro245Leu)
c.567+1371C>T (n.567+1371C>T)
n.618+1371C>T
20g.763837G>CCA407963212SLC52A3c.734C>G (p.Pro245Arg)
c.567+1371C>G (n.567+1371C>G)
n.618+1371C>G
20g.763837G>TCA407963213SLC52A3c.734C>A (p.Pro245His)
c.567+1371C>A (n.567+1371C>A)
n.618+1371C>A
20g.763838G>ACA407963214SLC52A3c.733C>T (p.Pro245Ser)
c.567+1370C>T (n.567+1370C>T)
n.618+1370C>T
gnomAD v4
20g.763838G>CCA407963215SLC52A3c.733C>G (p.Pro245Ala)
c.567+1370C>G (n.567+1370C>G)
n.618+1370C>G
20g.763838G=CA2345349413SLC52A3c.733C= (p.Pro245=)
c.567+1370C= (n.567+1370C=)
n.618+1370C=
20g.763838G>TCA9724695SLC52A3c.733C>A (p.Pro245Thr)
c.567+1370C>A (n.567+1370C>A)
n.618+1370C>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.763839T>ACA407963216SLC52A3c.732A>T (p.Gln244His)
c.567+1369A>T (n.567+1369A>T)
n.618+1369A>T
20g.763839T>CCA509542473SLC52A3c.732A>G (p.Gln244=)
c.567+1369A>G (n.567+1369A>G)
n.618+1369A>G
20g.763839T>GCA407963217SLC52A3c.732A>C (p.Gln244His)
c.567+1369A>C (n.567+1369A>C)
n.618+1369A>C
20g.763840T>ACA407963218SLC52A3c.731A>T (p.Gln244Leu)
c.567+1368A>T (n.567+1368A>T)
n.618+1368A>T
20g.763840T>CCA407963219SLC52A3c.731A>G (p.Gln244Arg)
c.567+1368A>G (n.567+1368A>G)
n.618+1368A>G
20g.763840T>GCA407963220SLC52A3c.731A>C (p.Gln244Pro)
c.567+1368A>C (n.567+1368A>C)
n.618+1368A>C
20g.763841G>ACA407963221SLC52A3c.730C>T (p.Gln244Ter)
c.567+1367C>T (n.567+1367C>T)
n.618+1367C>T
20g.763841G>CCA407963222SLC52A3c.730C>G (p.Gln244Glu)
c.567+1367C>G (n.567+1367C>G)
n.618+1367C>G
20g.763841G>TCA407963223SLC52A3c.730C>A (p.Gln244Lys)
c.567+1367C>A (n.567+1367C>A)
n.618+1367C>A
20g.763842A>CCA509542479SLC52A3c.729T>G (p.Arg243=)
c.567+1366T>G (n.567+1366T>G)
n.618+1366T>G
20g.763842A>GCA509542477SLC52A3c.729T>C (p.Arg243=)
c.567+1366T>C (n.567+1366T>C)
n.618+1366T>C
20g.763842A>TCA509542478SLC52A3c.729T>A (p.Arg243=)
c.567+1366T>A (n.567+1366T>A)
n.618+1366T>A
20g.763843C>ACA407963224SLC52A3c.728G>T (p.Arg243Leu)
c.567+1365G>T (n.567+1365G>T)
n.618+1365G>T
20g.763843C=CA2345349414SLC52A3c.728G= (p.Arg243=)
c.567+1365G= (n.567+1365G=)
n.618+1365G=
20g.763843C>GCA407963225SLC52A3c.728G>C (p.Arg243Pro)
c.567+1365G>C (n.567+1365G>C)
n.618+1365G>C
20g.763843C>TCA9724696SLC52A3c.728G>A (p.Arg243His)
c.567+1365G>A (n.567+1365G>A)
n.618+1365G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.763844G>ACA407963226SLC52A3c.727C>T (p.Arg243Cys)
c.567+1364C>T (n.567+1364C>T)
n.618+1364C>T
dbSNP gnomAD v4
20g.763844G>CCA407963227SLC52A3c.727C>G (p.Arg243Gly)
c.567+1364C>G (n.567+1364C>G)
n.618+1364C>G
20g.763844G=CA2345349415SLC52A3c.727C= (p.Arg243=)
c.567+1364C= (n.567+1364C=)
n.618+1364C=
20g.763844G>TCA407963228SLC52A3c.727C>A (p.Arg243Ser)
c.567+1364C>A (n.567+1364C>A)
n.618+1364C>A
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
20g.763845C>ACA407963229SLC52A3c.726G>T (p.Gln242His)
c.567+1363G>T (n.567+1363G>T)
n.618+1363G>T
20g.763845C=CA2345349416SLC52A3c.726G= (p.Gln242=)
c.567+1363G= (n.567+1363G=)
n.618+1363G=
20g.763845C>GCA407963230SLC52A3c.726G>C (p.Gln242His)
c.567+1363G>C (n.567+1363G>C)
n.618+1363G>C
20g.763845C>TCA509542482SLC52A3c.726G>A (p.Gln242=)
c.567+1363G>A (n.567+1363G>A)
n.618+1363G>A
ClinVar dbSNP gnomAD v4
20g.763846T>ACA407963231SLC52A3c.725A>T (p.Gln242Leu)
c.567+1362A>T (n.567+1362A>T)
n.618+1362A>T
20g.763846T>CCA407963232SLC52A3c.725A>G (p.Gln242Arg)
c.567+1362A>G (n.567+1362A>G)
n.618+1362A>G
20g.763846T>GCA407963233SLC52A3c.725A>C (p.Gln242Pro)
c.567+1362A>C (n.567+1362A>C)
n.618+1362A>C
20g.763847G>ACA407963234SLC52A3c.724C>T (p.Gln242Ter)
c.567+1361C>T (n.567+1361C>T)
n.618+1361C>T
COSMIC COSMIC
20g.763847G>CCA407963235SLC52A3c.724C>G (p.Gln242Glu)
c.567+1361C>G (n.567+1361C>G)
n.618+1361C>G
20g.763847G>TCA407963236SLC52A3c.724C>A (p.Gln242Lys)
c.567+1361C>A (n.567+1361C>A)
n.618+1361C>A
20g.763848G>ACA509542483SLC52A3c.723C>T (p.Leu241=)
c.567+1360C>T (n.567+1360C>T)
n.618+1360C>T
20g.763848G>CCA509542484SLC52A3c.723C>G (p.Leu241=)
c.567+1360C>G (n.567+1360C>G)
n.618+1360C>G
20g.763848G=CA2345349417SLC52A3c.723C= (p.Leu241=)
c.567+1360C= (n.567+1360C=)
n.618+1360C=
20g.763848G>TCA509542485SLC52A3c.723C>A (p.Leu241=)
c.567+1360C>A (n.567+1360C>A)
n.618+1360C>A
dbSNP gnomAD v2 gnomAD v4
20g.763849A>CCA407963237SLC52A3c.722T>G (p.Leu241Arg)
c.567+1359T>G (n.567+1359T>G)
n.618+1359T>G
20g.763849A>GCA407963238SLC52A3c.722T>C (p.Leu241Pro)
c.567+1359T>C (n.567+1359T>C)
n.618+1359T>C
20g.763849A>TCA407963239SLC52A3c.722T>A (p.Leu241His)
c.567+1359T>A (n.567+1359T>A)
n.618+1359T>A
20g.763850G>ACA407963240SLC52A3c.721C>T (p.Leu241Phe)
c.567+1358C>T (n.567+1358C>T)
n.618+1358C>T
gnomAD v4
20g.763850G>CCA407963241SLC52A3c.721C>G (p.Leu241Val)
c.567+1358C>G (n.567+1358C>G)
n.618+1358C>G
20g.763850G>TCA407963242SLC52A3c.721C>A (p.Leu241Ile)
c.567+1358C>A (n.567+1358C>A)
n.618+1358C>A
20g.763851G>ACA509542488SLC52A3c.720C>T (p.Val240=)
c.567+1357C>T (n.567+1357C>T)
n.618+1357C>T
gnomAD v4
20g.763851G>CCA509542489SLC52A3c.720C>G (p.Val240=)
c.567+1357C>G (n.567+1357C>G)
n.618+1357C>G
20g.763851G>TCA509542490SLC52A3c.720C>A (p.Val240=)
c.567+1357C>A (n.567+1357C>A)
n.618+1357C>A
20g.763852A>CCA407963245SLC52A3c.719T>G (p.Val240Gly)
c.567+1356T>G (n.567+1356T>G)
n.618+1356T>G
20g.763852A>GCA407963244SLC52A3c.719T>C (p.Val240Ala)
c.567+1356T>C (n.567+1356T>C)
n.618+1356T>C
gnomAD v4
20g.763852A>TCA407963243SLC52A3c.719T>A (p.Val240Asp)
c.567+1356T>A (n.567+1356T>A)
n.618+1356T>A
gnomAD v4
20g.763853C>ACA407963246SLC52A3c.718G>T (p.Val240Phe)
c.567+1355G>T (n.567+1355G>T)
n.618+1355G>T
gnomAD v4
20g.763853C=CA2345349418SLC52A3c.718G= (p.Val240=)
c.567+1355G= (n.567+1355G=)
n.618+1355G=
20g.763853C>GCA407963247SLC52A3c.718G>C (p.Val240Leu)
c.567+1355G>C (n.567+1355G>C)
n.618+1355G>C
20g.763853C>TCA407963248SLC52A3c.718G>A (p.Val240Ile)
c.567+1355G>A (n.567+1355G>A)
n.618+1355G>A
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
20g.763854A>CCA407963249SLC52A3c.717T>G (p.Phe239Leu)
c.567+1354T>G (n.567+1354T>G)
n.618+1354T>G
20g.763854A>GCA509542494SLC52A3c.717T>C (p.Phe239=)
c.567+1354T>C (n.567+1354T>C)
n.618+1354T>C
20g.763854A>TCA407963250SLC52A3c.717T>A (p.Phe239Leu)
c.567+1354T>A (n.567+1354T>A)
n.618+1354T>A
20g.763855A>CCA407963251SLC52A3c.716T>G (p.Phe239Cys)
c.567+1353T>G (n.567+1353T>G)
n.618+1353T>G
20g.763855A>GCA407963252SLC52A3c.716T>C (p.Phe239Ser)
c.567+1353T>C (n.567+1353T>C)
n.618+1353T>C
20g.763855A>TCA407963253SLC52A3c.716T>A (p.Phe239Tyr)
c.567+1353T>A (n.567+1353T>A)
n.618+1353T>A
20g.763855_763857delinsAAGCA2345349419SLC52A3c.714_716delinsCTT (p.Phe238=)
c.567+1351_567+1353delinsCTT (n.567+1351_567+1353delinsCTT)
n.618+1351_618+1353delinsCTT
20g.763856A>CCA407963254SLC52A3c.715T>G (p.Phe239Val)
c.567+1352T>G (n.567+1352T>G)
n.618+1352T>G
20g.763856A>GCA407963255SLC52A3c.715T>C (p.Phe239Leu)
c.567+1352T>C (n.567+1352T>C)
n.618+1352T>C
20g.763856A>TCA407963256SLC52A3c.715T>A (p.Phe239Ile)
c.567+1352T>A (n.567+1352T>A)
n.618+1352T>A
20g.763857_763858delCA2345349420SLC52A3c.714_715del (p.Phe239CysfsTer19)
c.567+1351_567+1352del (n.567+1351_567+1352del)
n.618+1351_618+1352del
dbSNP
20g.763857G>ACA509542497SLC52A3c.714C>T (p.Phe238=)
c.567+1351C>T (n.567+1351C>T)
n.618+1351C>T
20g.763857G>CCA407963257SLC52A3c.714C>G (p.Phe238Leu)
c.567+1351C>G (n.567+1351C>G)
n.618+1351C>G
20g.763857G>TCA407963258SLC52A3c.714C>A (p.Phe238Leu)
c.567+1351C>A (n.567+1351C>A)
n.618+1351C>A
20g.763858A>CCA407963260SLC52A3c.713T>G (p.Phe238Cys)
c.567+1350T>G (n.567+1350T>G)
n.618+1350T>G
20g.763858A>GCA407963261SLC52A3c.713T>C (p.Phe238Ser)
c.567+1350T>C (n.567+1350T>C)
n.618+1350T>C
20g.763858A>TCA407963259SLC52A3c.713T>A (p.Phe238Tyr)
c.567+1350T>A (n.567+1350T>A)
n.618+1350T>A
20g.763859A>CCA407963263SLC52A3c.712T>G (p.Phe238Val)
c.567+1349T>G (n.567+1349T>G)
n.618+1349T>G
20g.763859A>GCA407963262SLC52A3c.712T>C (p.Phe238Leu)
c.567+1349T>C (n.567+1349T>C)
n.618+1349T>C
20g.763859A>TCA407963264SLC52A3c.712T>A (p.Phe238Ile)
c.567+1349T>A (n.567+1349T>A)
n.618+1349T>A
20g.763860C>ACA509542498SLC52A3c.711G>T (p.Ala237=)
c.567+1348G>T (n.567+1348G>T)
n.618+1348G>T
20g.763860C=CA2345349421SLC52A3c.711G= (p.Ala237=)
c.567+1348G= (n.567+1348G=)
n.618+1348G=
20g.763860C>GCA509542499SLC52A3c.711G>C (p.Ala237=)
c.567+1348G>C (n.567+1348G>C)
n.618+1348G>C
20g.763860C>TCA9724697SLC52A3c.711G>A (p.Ala237=)
c.567+1348G>A (n.567+1348G>A)
n.618+1348G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.763861G>ACA9724698SLC52A3c.710C>T (p.Ala237Val)
c.567+1347C>T (n.567+1347C>T)
n.618+1347C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
20g.763861G>CCA407963265SLC52A3c.710C>G (p.Ala237Gly)
c.567+1347C>G (n.567+1347C>G)
n.618+1347C>G
20g.763861G=CA2345349422SLC52A3c.710C= (p.Ala237=)
c.567+1347C= (n.567+1347C=)
n.618+1347C=
20g.763861G>TCA407963266SLC52A3c.710C>A (p.Ala237Glu)
c.567+1347C>A (n.567+1347C>A)
n.618+1347C>A
20g.763862C>ACA407963267SLC52A3c.709G>T (p.Ala237Ser)
c.567+1346G>T (n.567+1346G>T)
n.618+1346G>T
gnomAD v4
20g.763862C>GCA407963268SLC52A3c.709G>C (p.Ala237Pro)
c.567+1346G>C (n.567+1346G>C)
n.618+1346G>C
20g.763862C>TCA407963269SLC52A3c.709G>A (p.Ala237Thr)
c.567+1346G>A (n.567+1346G>A)
n.618+1346G>A
20g.763863C>ACA509542505SLC52A3c.708G>T (p.Val236=)
c.567+1345G>T (n.567+1345G>T)
n.618+1345G>T
20g.763863C>GCA509542503SLC52A3c.708G>C (p.Val236=)
c.567+1345G>C (n.567+1345G>C)
n.618+1345G>C
20g.763863C>TCA509542504SLC52A3c.708G>A (p.Val236=)
c.567+1345G>A (n.567+1345G>A)
n.618+1345G>A
20g.763864A>CCA407963270SLC52A3c.707T>G (p.Val236Gly)
c.567+1344T>G (n.567+1344T>G)
n.618+1344T>G
20g.763864A>GCA407963271SLC52A3c.707T>C (p.Val236Ala)
c.567+1344T>C (n.567+1344T>C)
n.618+1344T>C
20g.763864A>TCA407963272SLC52A3c.707T>A (p.Val236Glu)
c.567+1344T>A (n.567+1344T>A)
n.618+1344T>A
20g.763865C>ACA407963273SLC52A3c.706G>T (p.Val236Leu)
c.567+1343G>T (n.567+1343G>T)
n.618+1343G>T
20g.763865C=CA2345349423SLC52A3c.706G= (p.Val236=)
c.567+1343G= (n.567+1343G=)
n.618+1343G=
20g.763865C>GCA407963274SLC52A3c.706G>C (p.Val236Leu)
c.567+1343G>C (n.567+1343G>C)
n.618+1343G>C
20g.763865C>TCA310677361SLC52A3c.706G>A (p.Val236Met)
c.567+1343G>A (n.567+1343G>A)
n.618+1343G>A
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
20g.763866G>ACA9724699SLC52A3c.705C>T (p.Leu235=)
c.567+1342C>T (n.567+1342C>T)
n.618+1342C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.763866G>CCA310677392SLC52A3c.705C>G (p.Leu235=)
c.567+1342C>G (n.567+1342C>G)
n.618+1342C>G
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
20g.763866G=CA2345349424SLC52A3c.705C= (p.Leu235=)
c.567+1342C= (n.567+1342C=)
n.618+1342C=
20g.763866G>TCA9724700SLC52A3c.705C>A (p.Leu235=)
c.567+1342C>A (n.567+1342C>A)
n.618+1342C>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.763867A>CCA407963275SLC52A3c.704T>G (p.Leu235Arg)
c.567+1341T>G (n.567+1341T>G)
n.618+1341T>G
20g.763867A>GCA407963276SLC52A3c.704T>C (p.Leu235Pro)
c.567+1341T>C (n.567+1341T>C)
n.618+1341T>C
ClinVar
20g.763867A>TCA407963277SLC52A3c.704T>A (p.Leu235His)
c.567+1341T>A (n.567+1341T>A)
n.618+1341T>A
20g.763868G>ACA9724701SLC52A3c.703C>T (p.Leu235Phe)
c.567+1340C>T (n.567+1340C>T)
n.618+1340C>T
dbSNP ExAC gnomAD v2 gnomAD v4
20g.763868G>CCA407963278SLC52A3c.703C>G (p.Leu235Val)
c.567+1340C>G (n.567+1340C>G)
n.618+1340C>G
dbSNP gnomAD v4
20g.763868G=CA2345349425SLC52A3c.703C= (p.Leu235=)
c.567+1340C= (n.567+1340C=)
n.618+1340C=
20g.763868G>TCA407963279SLC52A3c.703C>A (p.Leu235Ile)
c.567+1340C>A (n.567+1340C>A)
n.618+1340C>A
COSMIC
20g.763869G>ACA509542512SLC52A3c.702C>T (p.Cys234=)
c.567+1339C>T (n.567+1339C>T)
n.618+1339C>T
gnomAD v4 COSMIC COSMIC
20g.763869G>CCA407963280SLC52A3c.702C>G (p.Cys234Trp)
c.567+1339C>G (n.567+1339C>G)
n.618+1339C>G
20g.763869G>TCA407963281SLC52A3c.702C>A (p.Cys234Ter)
c.567+1339C>A (n.567+1339C>A)
n.618+1339C>A
20g.763870C>ACA407963282SLC52A3c.701G>T (p.Cys234Phe)
c.567+1338G>T (n.567+1338G>T)
n.618+1338G>T
dbSNP
20g.763870C=CA2345349426SLC52A3c.701G= (p.Cys234=)
c.567+1338G= (n.567+1338G=)
n.618+1338G=
20g.763870C>GCA407963283SLC52A3c.701G>C (p.Cys234Ser)
c.567+1338G>C (n.567+1338G>C)
n.618+1338G>C
20g.763870C>TCA407963284SLC52A3c.701G>A (p.Cys234Tyr)
c.567+1338G>A (n.567+1338G>A)
n.618+1338G>A
20g.763871A>CCA407963287SLC52A3c.700T>G (p.Cys234Gly)
c.567+1337T>G (n.567+1337T>G)
n.618+1337T>G
20g.763871A>GCA407963286SLC52A3c.700T>C (p.Cys234Arg)
c.567+1337T>C (n.567+1337T>C)
n.618+1337T>C
20g.763871A>TCA407963285SLC52A3c.700T>A (p.Cys234Ser)
c.567+1337T>A (n.567+1337T>A)
n.618+1337T>A
20g.763872G>ACA509542516SLC52A3c.699C>T (p.Cys233=)
c.567+1336C>T (n.567+1336C>T)
n.618+1336C>T
20g.763872G>CCA407963289SLC52A3c.699C>G (p.Cys233Trp)
c.567+1336C>G (n.567+1336C>G)
n.618+1336C>G
20g.763872G>TCA407963288SLC52A3c.699C>A (p.Cys233Ter)
c.567+1336C>A (n.567+1336C>A)
n.618+1336C>A
20g.763873C>ACA407963290SLC52A3c.698G>T (p.Cys233Phe)
c.567+1335G>T (n.567+1335G>T)
n.618+1335G>T
20g.763873C>GCA407963291SLC52A3c.698G>C (p.Cys233Ser)
c.567+1335G>C (n.567+1335G>C)
n.618+1335G>C
20g.763873C>TCA407963292SLC52A3c.698G>A (p.Cys233Tyr)
c.567+1335G>A (n.567+1335G>A)
n.618+1335G>A
20g.763874A=CA2345349427SLC52A3c.697T= (p.Cys233=)
c.567+1334T= (n.567+1334T=)
n.618+1334T=
20g.763874A>CCA407963293SLC52A3c.697T>G (p.Cys233Gly)
c.567+1334T>G (n.567+1334T>G)
n.618+1334T>G
20g.763874A>GCA407963294SLC52A3c.697T>C (p.Cys233Arg)
c.567+1334T>C (n.567+1334T>C)
n.618+1334T>C
dbSNP gnomAD v2
20g.763874A>TCA407963295SLC52A3c.697T>A (p.Cys233Ser)
c.567+1334T>A (n.567+1334T>A)
n.618+1334T>A
20g.763875G>ACA9724702SLC52A3c.696C>T (p.Ala232=)
c.567+1333C>T (n.567+1333C>T)
n.618+1333C>T
dbSNP ExAC gnomAD v2 gnomAD v4
20g.763875G>CCA509542518SLC52A3c.696C>G (p.Ala232=)
c.567+1333C>G (n.567+1333C>G)
n.618+1333C>G
20g.763875G=CA2345349428SLC52A3c.696C= (p.Ala232=)
c.567+1333C= (n.567+1333C=)
n.618+1333C=
20g.763875G>TCA509542519SLC52A3c.696C>A (p.Ala232=)
c.567+1333C>A (n.567+1333C>A)
n.618+1333C>A
20g.763876G>ACA407963296SLC52A3c.695C>T (p.Ala232Val)
c.567+1332C>T (n.567+1332C>T)
n.618+1332C>T
20g.763876G>CCA407963297SLC52A3c.695C>G (p.Ala232Gly)
c.567+1332C>G (n.567+1332C>G)
n.618+1332C>G
gnomAD v4
20g.763876G>TCA407963298SLC52A3c.695C>A (p.Ala232Asp)
c.567+1332C>A (n.567+1332C>A)
n.618+1332C>A
20g.763877C>ACA9724703SLC52A3c.694G>T (p.Ala232Ser)
c.567+1331G>T (n.567+1331G>T)
n.618+1331G>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
20g.763877C=CA2345349429SLC52A3c.694G= (p.Ala232=)
c.567+1331G= (n.567+1331G=)
n.618+1331G=
20g.763877C>GCA407963299SLC52A3c.694G>C (p.Ala232Pro)
c.567+1331G>C (n.567+1331G>C)
n.618+1331G>C
20g.763877C>TCA407963300SLC52A3c.694G>A (p.Ala232Thr)
c.567+1331G>A (n.567+1331G>A)
n.618+1331G>A
20g.763878C>ACA407963301SLC52A3c.693G>T (p.Met231Ile)
c.567+1330G>T (n.567+1330G>T)
n.618+1330G>T
20g.763878C=CA2345349430SLC52A3c.693G= (p.Met231=)
c.567+1330G= (n.567+1330G=)
n.618+1330G=
20g.763878C>GCA310677410SLC52A3c.693G>C (p.Met231Ile)
c.567+1330G>C (n.567+1330G>C)
n.618+1330G>C
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
20g.763878C>TCA407963302SLC52A3c.693G>A (p.Met231Ile)
c.567+1330G>A (n.567+1330G>A)
n.618+1330G>A
20g.763879A=CA2345349431SLC52A3c.692T= (p.Met231=)
c.567+1329T= (n.567+1329T=)
n.618+1329T=
20g.763879A>CCA407963303SLC52A3c.692T>G (p.Met231Arg)
c.567+1329T>G (n.567+1329T>G)
n.618+1329T>G
20g.763879A>GCA407963304SLC52A3c.692T>C (p.Met231Thr)
c.567+1329T>C (n.567+1329T>C)
n.618+1329T>C
20g.763879A>TCA9724704SLC52A3c.692T>A (p.Met231Lys)
c.567+1329T>A (n.567+1329T>A)
n.618+1329T>A
dbSNP ExAC gnomAD v2 gnomAD v4
20g.763880T>ACA407963305SLC52A3c.691A>T (p.Met231Leu)
c.567+1328A>T (n.567+1328A>T)
n.618+1328A>T
20g.763880T>CCA407963306SLC52A3c.691A>G (p.Met231Val)
c.567+1328A>G (n.567+1328A>G)
n.618+1328A>G
gnomAD v4
20g.763880T>GCA407963307SLC52A3c.691A>C (p.Met231Leu)
c.567+1328A>C (n.567+1328A>C)
n.618+1328A>C

Number of alleles fetched