Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.189564090C>ACA349988180SLC40A1c.896G>T (p.Trp299Leu)
c.776G>T (p.Trp259Leu)
2g.189564090C>GCA349988178SLC40A1c.896G>C (p.Trp299Ser)
c.776G>C (p.Trp259Ser)
2g.189564090C>TCA349988179SLC40A1c.896G>A (p.Trp299Ter)
c.776G>A (p.Trp259Ter)
COSMIC
2g.189564091A>CCA349988181SLC40A1c.895T>G (p.Trp299Gly)
c.775T>G (p.Trp259Gly)
2g.189564091A>GCA349988182SLC40A1c.895T>C (p.Trp299Arg)
c.775T>C (p.Trp259Arg)
2g.189564091A>TCA349988183SLC40A1c.895T>A (p.Trp299Arg)
c.775T>A (p.Trp259Arg)
2g.189564092T>ACA430502575SLC40A1c.894A>T (p.Gly298=)
c.774A>T (p.Gly258=)
dbSNP gnomAD v4
2g.189564092T>CCA430502576SLC40A1c.894A>G (p.Gly298=)
c.774A>G (p.Gly258=)
2g.189564092T>GCA430502577SLC40A1c.894A>C (p.Gly298=)
c.774A>C (p.Gly258=)
2g.189564092T=CA1315654373SLC40A1c.894A= (p.Gly298=)
c.774A= (p.Gly258=)
2g.189564093C>ACA349988184SLC40A1c.893G>T (p.Gly298Val)
c.773G>T (p.Gly258Val)
dbSNP
2g.189564093C=CA1315654375SLC40A1c.893G= (p.Gly298=)
c.773G= (p.Gly258=)
2g.189564093C>GCA349988185SLC40A1c.893G>C (p.Gly298Ala)
c.773G>C (p.Gly258Ala)
2g.189564093C>TCA349988186SLC40A1c.893G>A (p.Gly298Glu)
c.773G>A (p.Gly258Glu)
COSMIC
2g.189564094C>ACA349988187SLC40A1c.892G>T (p.Gly298Ter)
c.772G>T (p.Gly258Ter)
2g.189564094C>GCA349988188SLC40A1c.892G>C (p.Gly298Arg)
c.772G>C (p.Gly258Arg)
2g.189564094C>TCA349988189SLC40A1c.892G>A (p.Gly298Arg)
c.772G>A (p.Gly258Arg)
2g.189564095A=CA1315654377SLC40A1c.891T= (p.Asp297=)
c.771T= (p.Asp257=)
2g.189564095A>CCA2024132SLC40A1c.891T>G (p.Asp297Glu)
c.771T>G (p.Asp257Glu)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.189564095A>GCA430502580SLC40A1c.891T>C (p.Asp297=)
c.771T>C (p.Asp257=)
dbSNP gnomAD v2 gnomAD v4
2g.189564095A>TCA349988190SLC40A1c.891T>A (p.Asp297Glu)
c.771T>A (p.Asp257Glu)
2g.189564096T>ACA349988193SLC40A1c.890A>T (p.Asp297Val)
c.770A>T (p.Asp257Val)
2g.189564096T>CCA349988192SLC40A1c.890A>G (p.Asp297Gly)
c.770A>G (p.Asp257Gly)
2g.189564096T>GCA349988191SLC40A1c.890A>C (p.Asp297Ala)
c.770A>C (p.Asp257Ala)
2g.189564097C>ACA349988194SLC40A1c.889G>T (p.Asp297Tyr)
c.769G>T (p.Asp257Tyr)
2g.189564097C>GCA349988195SLC40A1c.889G>C (p.Asp297His)
c.769G>C (p.Asp257His)
2g.189564097C>TCA349988196SLC40A1c.889G>A (p.Asp297Asn)
c.769G>A (p.Asp257Asn)
gnomAD v4
2g.189564098T>ACA430502587SLC40A1c.888A>T (p.Arg296=)
c.768A>T (p.Arg256=)
ClinVar gnomAD v4
2g.189564098T>CCA430502588SLC40A1c.888A>G (p.Arg296=)
c.768A>G (p.Arg256=)
2g.189564098T>GCA430502589SLC40A1c.888A>C (p.Arg296=)
c.768A>C (p.Arg256=)
2g.189564099C>ACA349988197SLC40A1c.887G>T (p.Arg296Leu)
c.767G>T (p.Arg256Leu)
2g.189564099C=CA1315654381SLC40A1c.887G= (p.Arg296=)
c.767G= (p.Arg256=)
2g.189564099C>GCA349988198SLC40A1c.887G>C (p.Arg296Pro)
c.767G>C (p.Arg256Pro)
2g.189564099C>TCA2024133SLC40A1c.887G>A (p.Arg296Gln)
c.767G>A (p.Arg256Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
2g.189564100G>ACA349988199SLC40A1c.886C>T (p.Arg296Ter)
c.766C>T (p.Arg256Ter)
gnomAD v4
2g.189564100G>CCA2024134SLC40A1c.886C>G (p.Arg296Gly)
c.766C>G (p.Arg256Gly)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.189564100G=CA1315654385SLC40A1c.886C= (p.Arg296=)
c.766C= (p.Arg256=)
2g.189564100G>TCA430502593SLC40A1c.886C>A (p.Arg296=)
c.766C>A (p.Arg256=)
2g.189564101G>ACA430502594SLC40A1c.885C>T (p.Phe295=)
c.765C>T (p.Phe255=)
2g.189564101G>CCA349988200SLC40A1c.885C>G (p.Phe295Leu)
c.765C>G (p.Phe255Leu)
2g.189564101G>TCA349988201SLC40A1c.885C>A (p.Phe295Leu)
c.765C>A (p.Phe255Leu)
2g.189564102A>CCA349988202SLC40A1c.884T>G (p.Phe295Cys)
c.764T>G (p.Phe255Cys)
2g.189564102A>GCA349988203SLC40A1c.884T>C (p.Phe295Ser)
c.764T>C (p.Phe255Ser)
2g.189564102A>TCA349988204SLC40A1c.884T>A (p.Phe295Tyr)
c.764T>A (p.Phe255Tyr)
2g.189564103A>CCA349988207SLC40A1c.883T>G (p.Phe295Val)
c.763T>G (p.Phe255Val)
2g.189564103A>GCA349988205SLC40A1c.883T>C (p.Phe295Leu)
c.763T>C (p.Phe255Leu)
2g.189564103A>TCA349988206SLC40A1c.883T>A (p.Phe295Ile)
c.763T>A (p.Phe255Ile)
2g.189564104G>ACA430502596SLC40A1c.882C>T (p.Thr294=)
c.762C>T (p.Thr254=)
dbSNP
2g.189564104G>CCA430502597SLC40A1c.882C>G (p.Thr294=)
c.762C>G (p.Thr254=)
2g.189564104G=CA1315654387SLC40A1c.882C= (p.Thr294=)
c.762C= (p.Thr254=)

Number of alleles fetched