Chr Mutation (hg38) CAid Gene Transcript Linkouts
18g.36114161G>ACA298700925SLC39A6c.1779C>T (p.Ala593=)
c.954C>T (p.Ala318=)
c.480C>T (p.Ala160=)
 dbSNP gnomAD v4
18g.36114161G>CCA503640316SLC39A6c.1779C>G (p.Ala593=)
c.954C>G (p.Ala318=)
c.480C>G (p.Ala160=)
 gnomAD v4
18g.36114161G=CA2295937416SLC39A6c.1779C= (p.Ala593=)
c.954C= (p.Ala318=)
c.480C= (p.Ala160=)
18g.36114161G>TCA503640318SLC39A6c.1779C>A (p.Ala593=)
c.954C>A (p.Ala318=)
c.480C>A (p.Ala160=)
18g.36114162G>ACA402204939SLC39A6c.1778C>T (p.Ala593Val)
c.953C>T (p.Ala318Val)
c.479C>T (p.Ala160Val)
18g.36114162G>CCA402204941SLC39A6c.1778C>G (p.Ala593Gly)
c.953C>G (p.Ala318Gly)
c.479C>G (p.Ala160Gly)
18g.36114162G>TCA402204942SLC39A6c.1778C>A (p.Ala593Asp)
c.953C>A (p.Ala318Asp)
c.479C>A (p.Ala160Asp)
18g.36114163C>ACA402204944SLC39A6c.1777G>T (p.Ala593Ser)
c.952G>T (p.Ala318Ser)
c.478G>T (p.Ala160Ser)
18g.36114163C=CA2295937417SLC39A6c.1777G= (p.Ala593=)
c.952G= (p.Ala318=)
c.478G= (p.Ala160=)
18g.36114163C>GCA402204946SLC39A6c.1777G>C (p.Ala593Pro)
c.952G>C (p.Ala318Pro)
c.478G>C (p.Ala160Pro)
18g.36114163C>TCA8939020SLC39A6c.1777G>A (p.Ala593Thr)
c.952G>A (p.Ala318Thr)
c.478G>A (p.Ala160Thr)
 dbSNP ExAC gnomAD v2 gnomAD v4
18g.36114164G>ACA8939021SLC39A6c.1776C>T (p.Val592=)
c.951C>T (p.Val317=)
c.477C>T (p.Val159=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
18g.36114164G>CCA503640322SLC39A6c.1776C>G (p.Val592=)
c.951C>G (p.Val317=)
c.477C>G (p.Val159=)
18g.36114164G=CA2295937418SLC39A6c.1776C= (p.Val592=)
c.951C= (p.Val317=)
c.477C= (p.Val159=)
18g.36114164G>TCA503640324SLC39A6c.1776C>A (p.Val592=)
c.951C>A (p.Val317=)
c.477C>A (p.Val159=)
18g.36114165A>CCA402204947SLC39A6c.1775T>G (p.Val592Gly)
c.950T>G (p.Val317Gly)
c.476T>G (p.Val159Gly)
18g.36114165A>GCA402204949SLC39A6c.1775T>C (p.Val592Ala)
c.950T>C (p.Val317Ala)
c.476T>C (p.Val159Ala)
18g.36114165A>TCA402204950SLC39A6c.1775T>A (p.Val592Asp)
c.950T>A (p.Val317Asp)
c.476T>A (p.Val159Asp)
18g.36114166C>ACA402204954SLC39A6c.1774G>T (p.Val592Phe)
c.949G>T (p.Val317Phe)
c.475G>T (p.Val159Phe)
18g.36114166C=CA2295937419SLC39A6c.1774G= (p.Val592=)
c.949G= (p.Val317=)
c.475G= (p.Val159=)
18g.36114166C>GCA402204952SLC39A6c.1774G>C (p.Val592Leu)
c.949G>C (p.Val317Leu)
c.475G>C (p.Val159Leu)
18g.36114166C>TCA8939022SLC39A6c.1774G>A (p.Val592Ile)
c.949G>A (p.Val317Ile)
c.475G>A (p.Val159Ile)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.36114167G>ACA503640334SLC39A6c.1773C>T (p.Gly591=)
c.948C>T (p.Gly316=)
c.474C>T (p.Gly158=)
 dbSNP gnomAD v2 gnomAD v4
18g.36114167G>CCA503640332SLC39A6c.1773C>G (p.Gly591=)
c.948C>G (p.Gly316=)
c.474C>G (p.Gly158=)
18g.36114167G=CA2295937420SLC39A6c.1773C= (p.Gly591=)
c.948C= (p.Gly316=)
c.474C= (p.Gly158=)
18g.36114167G>TCA503640330SLC39A6c.1773C>A (p.Gly591=)
c.948C>A (p.Gly316=)
c.474C>A (p.Gly158=)
18g.36114168C>ACA402204956SLC39A6c.1772G>T (p.Gly591Val)
c.947G>T (p.Gly316Val)
c.473G>T (p.Gly158Val)
 dbSNP gnomAD v2
18g.36114168C=CA2295937421SLC39A6c.1772G= (p.Gly591=)
c.947G= (p.Gly316=)
c.473G= (p.Gly158=)
18g.36114168C>GCA402204958SLC39A6c.1772G>C (p.Gly591Ala)
c.947G>C (p.Gly316Ala)
c.473G>C (p.Gly158Ala)
18g.36114168C>TCA298700970SLC39A6c.1772G>A (p.Gly591Asp)
c.947G>A (p.Gly316Asp)
c.473G>A (p.Gly158Asp)
 dbSNP gnomAD v4
18g.36114169C>ACA402204959SLC39A6c.1771G>T (p.Gly591Cys)
c.946G>T (p.Gly316Cys)
c.472G>T (p.Gly158Cys)
18g.36114169C=CA2295937422SLC39A6c.1771G= (p.Gly591=)
c.946G= (p.Gly316=)
c.472G= (p.Gly158=)
18g.36114169C>GCA402204961SLC39A6c.1771G>C (p.Gly591Arg)
c.946G>C (p.Gly316Arg)
c.472G>C (p.Gly158Arg)
18g.36114169C>TCA8939023SLC39A6c.1771G>A (p.Gly591Ser)
c.946G>A (p.Gly316Ser)
c.472G>A (p.Gly158Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
18g.36114170G>ACA298700976SLC39A6c.1770C>T (p.Ala590=)
c.945C>T (p.Ala315=)
c.471C>T (p.Ala157=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
18g.36114170G>CCA503640342SLC39A6c.1770C>G (p.Ala590=)
c.945C>G (p.Ala315=)
c.471C>G (p.Ala157=)
18g.36114170G=CA2295937423SLC39A6c.1770C= (p.Ala590=)
c.945C= (p.Ala315=)
c.471C= (p.Ala157=)
18g.36114170G>TCA503640343SLC39A6c.1770C>A (p.Ala590=)
c.945C>A (p.Ala315=)
c.471C>A (p.Ala157=)
18g.36114171G>ACA402204963SLC39A6c.1769C>T (p.Ala590Val)
c.944C>T (p.Ala315Val)
c.470C>T (p.Ala157Val)
18g.36114171G>CCA402204965SLC39A6c.1769C>G (p.Ala590Gly)
c.944C>G (p.Ala315Gly)
c.470C>G (p.Ala157Gly)
18g.36114171G>TCA402204966SLC39A6c.1769C>A (p.Ala590Asp)
c.944C>A (p.Ala315Asp)
c.470C>A (p.Ala157Asp)
18g.36114172C>ACA402204968SLC39A6c.1768G>T (p.Ala590Ser)
c.943G>T (p.Ala315Ser)
c.469G>T (p.Ala157Ser)
18g.36114172C>GCA402204969SLC39A6c.1768G>C (p.Ala590Pro)
c.943G>C (p.Ala315Pro)
c.469G>C (p.Ala157Pro)
18g.36114172C>TCA402204971SLC39A6c.1768G>A (p.Ala590Thr)
c.943G>A (p.Ala315Thr)
c.469G>A (p.Ala157Thr)
18g.36114173A=CA2295937424SLC39A6c.1767T= (p.Asp589=)
c.942T= (p.Asp314=)
c.468T= (p.Asp156=)
18g.36114173A>CCA402204973SLC39A6c.1767T>G (p.Asp589Glu)
c.942T>G (p.Asp314Glu)
c.468T>G (p.Asp156Glu)
18g.36114173A>GCA503640350SLC39A6c.1767T>C (p.Asp589=)
c.942T>C (p.Asp314=)
c.468T>C (p.Asp156=)
18g.36114173A>TCA402204974SLC39A6c.1767T>A (p.Asp589Glu)
c.942T>A (p.Asp314Glu)
c.468T>A (p.Asp156Glu)
 dbSNP
18g.36114174T>ACA402204976SLC39A6c.1766A>T (p.Asp589Val)
c.941A>T (p.Asp314Val)
c.467A>T (p.Asp156Val)
18g.36114174T>CCA402204977SLC39A6c.1766A>G (p.Asp589Gly)
c.941A>G (p.Asp314Gly)
c.467A>G (p.Asp156Gly)

Number of alleles fetched