Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.189562125C>ACA349986945SLC40A1c.1469G>T (p.Gly490Val)
c.1349G>T (p.Gly450Val)
2g.189562125C=CA1315652896SLC40A1c.1469G= (p.Gly490=)
c.1349G= (p.Gly450=)
2g.189562125C>GCA349986946SLC40A1c.1469G>C (p.Gly490Ala)
c.1349G>C (p.Gly450Ala)
2g.189562125C>TCA16610657SLC40A1c.1469G>A (p.Gly490Asp)
c.1349G>A (p.Gly450Asp)
ClinVar dbSNP COSMIC
2g.189562126C>ACA349986947SLC40A1c.1468G>T (p.Gly490Cys)
c.1348G>T (p.Gly450Cys)
2g.189562126C=CA1315652900SLC40A1c.1468G= (p.Gly490=)
c.1348G= (p.Gly450=)
2g.189562126C>GCA349986948SLC40A1c.1468G>C (p.Gly490Arg)
c.1348G>C (p.Gly450Arg)
2g.189562126C>TCA349986949SLC40A1c.1468G>A (p.Gly490Ser)
c.1348G>A (p.Gly450Ser)
ClinVar dbSNP
2g.189562127T>ACA349986950SLC40A1c.1467A>T (p.Arg489Ser)
c.1347A>T (p.Arg449Ser)
2g.189562127T>CCA430502661SLC40A1c.1467A>G (p.Arg489=)
c.1347A>G (p.Arg449=)
gnomAD v4
2g.189562127T>GCA349986951SLC40A1c.1467A>C (p.Arg489Ser)
c.1347A>C (p.Arg449Ser)
dbSNP
2g.189562127T=CA1315652904SLC40A1c.1467A= (p.Arg489=)
c.1347A= (p.Arg449=)
2g.189562128C>ACA349986952SLC40A1c.1466G>T (p.Arg489Ile)
c.1346G>T (p.Arg449Ile)
2g.189562128C=CA1315652907SLC40A1c.1466G= (p.Arg489=)
c.1346G= (p.Arg449=)
2g.189562128C>GCA349986953SLC40A1c.1466G>C (p.Arg489Thr)
c.1346G>C (p.Arg449Thr)
2g.189562128C>TCA349986954SLC40A1c.1466G>A (p.Arg489Lys)
c.1346G>A (p.Arg449Lys)
dbSNP
2g.189562129T>ACA349986955SLC40A1c.1465A>T (p.Arg489Ter)
c.1345A>T (p.Arg449Ter)
2g.189562129T>CCA349986956SLC40A1c.1465A>G (p.Arg489Gly)
c.1345A>G (p.Arg449Gly)
2g.189562129T>GCA430502663SLC40A1c.1465A>C (p.Arg489=)
c.1345A>C (p.Arg449=)
2g.189562130T>ACA349986957SLC40A1c.1464A>T (p.Glu488Asp)
c.1344A>T (p.Glu448Asp)
2g.189562130T>CCA430502665SLC40A1c.1464A>G (p.Glu488=)
c.1344A>G (p.Glu448=)
2g.189562130T>GCA349986958SLC40A1c.1464A>C (p.Glu488Asp)
c.1344A>C (p.Glu448Asp)
2g.189562131T>ACA349986961SLC40A1c.1463A>T (p.Glu488Val)
c.1343A>T (p.Glu448Val)
dbSNP
2g.189562131T>CCA349986960SLC40A1c.1463A>G (p.Glu488Gly)
c.1343A>G (p.Glu448Gly)
2g.189562131T>GCA349986959SLC40A1c.1463A>C (p.Glu488Ala)
c.1343A>C (p.Glu448Ala)
2g.189562131T=CA1315652909SLC40A1c.1463A= (p.Glu488=)
c.1343A= (p.Glu448=)
2g.189562132C>ACA349986963SLC40A1c.1462G>T (p.Glu488Ter)
c.1342G>T (p.Glu448Ter)
2g.189562132C>GCA349986962SLC40A1c.1462G>C (p.Glu488Gln)
c.1342G>C (p.Glu448Gln)
2g.189562132C>TCA349986964SLC40A1c.1462G>A (p.Glu488Lys)
c.1342G>A (p.Glu448Lys)
2g.189562133A>CCA430502671SLC40A1c.1461T>G (p.Ser487=)
c.1341T>G (p.Ser447=)
2g.189562133A>GCA430502673SLC40A1c.1461T>C (p.Ser487=)
c.1341T>C (p.Ser447=)
COSMIC
2g.189562133A>TCA430502672SLC40A1c.1461T>A (p.Ser487=)
c.1341T>A (p.Ser447=)
2g.189562134G>ACA349986965SLC40A1c.1460C>T (p.Ser487Phe)
c.1340C>T (p.Ser447Phe)
2g.189562134G>CCA349986966SLC40A1c.1460C>G (p.Ser487Cys)
c.1340C>G (p.Ser447Cys)
2g.189562134G>TCA349986967SLC40A1c.1460C>A (p.Ser487Tyr)
c.1340C>A (p.Ser447Tyr)
2g.189562135A>CCA349986968SLC40A1c.1459T>G (p.Ser487Ala)
c.1339T>G (p.Ser447Ala)
2g.189562135A>GCA349986969SLC40A1c.1459T>C (p.Ser487Pro)
c.1339T>C (p.Ser447Pro)
2g.189562135A>TCA349986970SLC40A1c.1459T>A (p.Ser487Thr)
c.1339T>A (p.Ser447Thr)
2g.189562136T>ACA349986971SLC40A1c.1458A>T (p.Glu486Asp)
c.1338A>T (p.Glu446Asp)
2g.189562136T>CCA430502674SLC40A1c.1458A>G (p.Glu486=)
c.1338A>G (p.Glu446=)
2g.189562136T>GCA349986972SLC40A1c.1458A>C (p.Glu486Asp)
c.1338A>C (p.Glu446Asp)
2g.189562137T>ACA349986973SLC40A1c.1457A>T (p.Glu486Val)
c.1337A>T (p.Glu446Val)
2g.189562137T>CCA349986975SLC40A1c.1457A>G (p.Glu486Gly)
c.1337A>G (p.Glu446Gly)
2g.189562137T>GCA349986974SLC40A1c.1457A>C (p.Glu486Ala)
c.1337A>C (p.Glu446Ala)
2g.189562138C>ACA349986976SLC40A1c.1456G>T (p.Glu486Ter)
c.1336G>T (p.Glu446Ter)
gnomAD v4
2g.189562138C=CA1315652911SLC40A1c.1456G= (p.Glu486=)
c.1336G= (p.Glu446=)
2g.189562138C>GCA349986977SLC40A1c.1456G>C (p.Glu486Gln)
c.1336G>C (p.Glu446Gln)
dbSNP gnomAD v4
2g.189562138C>TCA349986978SLC40A1c.1456G>A (p.Glu486Lys)
c.1336G>A (p.Glu446Lys)
gnomAD v4
2g.189562139A>CCA349986979SLC40A1c.1455T>G (p.Ile485Met)
c.1335T>G (p.Ile445Met)
2g.189562139A>GCA430502678SLC40A1c.1455T>C (p.Ile485=)
c.1335T>C (p.Ile445=)

Number of alleles fetched