Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.49448850T>ACA364397976MMUTc.1410A>T (p.Glu470Asp)
6g.49448850T>CCA3846889MMUTc.1410A>G (p.Glu470=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.49448850T>GCA364397978MMUTc.1410A>C (p.Glu470Asp)
6g.49448850T=CA1627388109MMUTc.1410A= (p.Glu470=)
6g.49448851T>ACA364397980MMUTc.1409A>T (p.Glu470Val)
6g.49448851T>CCA3846890MMUTc.1409A>G (p.Glu470Gly)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.49448851T>GCA364397982MMUTc.1409A>C (p.Glu470Ala)
6g.49448851T=CA1627388110MMUTc.1409A= (p.Glu470=)
6g.49448852C>ACA364397984MMUTc.1408G>T (p.Glu470Ter)
dbSNP
6g.49448852C=CA1627388111MMUTc.1408G= (p.Glu470=)
6g.49448852C>GCA364397985MMUTc.1408G>C (p.Glu470Gln)
6g.49448852C>TCA364397987MMUTc.1408G>A (p.Glu470Lys)
6g.49448853T>ACA364397988MMUTc.1407A>T (p.Glu469Asp)
6g.49448853T>CCA450398404MMUTc.1407A>G (p.Glu469=)
6g.49448853T>GCA364397990MMUTc.1407A>C (p.Glu469Asp)
6g.49448854T>ACA364397992MMUTc.1406A>T (p.Glu469Val)
6g.49448854T>CCA364397993MMUTc.1406A>G (p.Glu469Gly)
6g.49448854T>GCA364397995MMUTc.1406A>C (p.Glu469Ala)
6g.49448855C>ACA364397997MMUTc.1405G>T (p.Glu469Ter)
6g.49448855C=CA1627388112MMUTc.1405G= (p.Glu469=)
6g.49448855C>GCA364397998MMUTc.1405G>C (p.Glu469Gln)
6g.49448855C>TCA3846891MMUTc.1405G>A (p.Glu469Lys)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.49448856A>CCA364398001MMUTc.1404T>G (p.Ile468Met)
6g.49448856A>GCA450398405MMUTc.1404T>C (p.Ile468=)
gnomAD v4
6g.49448856A>TCA450398406MMUTc.1404T>A (p.Ile468=)
6g.49448857A=CA1627388113MMUTc.1403T= (p.Ile468=)
6g.49448857A>CCA364398002MMUTc.1403T>G (p.Ile468Ser)
6g.49448857A>GCA364398004MMUTc.1403T>C (p.Ile468Thr)
dbSNP gnomAD v2 gnomAD v4
6g.49448857A>TCA364398005MMUTc.1403T>A (p.Ile468Asn)
6g.49448858T>ACA364398009MMUTc.1402A>T (p.Ile468Phe)
dbSNP gnomAD v4
6g.49448858T>CCA138795917MMUTc.1402A>G (p.Ile468Val)
dbSNP
6g.49448858T>GCA364398007MMUTc.1402A>C (p.Ile468Leu)
6g.49448858T=CA1627388114MMUTc.1402A= (p.Ile468=)
6g.49448859T>ACA450398410MMUTc.1401A>T (p.Arg467=)
gnomAD v4
6g.49448859T>CCA450398411MMUTc.1401A>G (p.Arg467=)
6g.49448859T>GCA450398412MMUTc.1401A>C (p.Arg467=)
6g.49448860C>ACA364398011MMUTc.1400G>T (p.Arg467Leu)
6g.49448860C=CA1627388115MMUTc.1400G= (p.Arg467=)
6g.49448860C>GCA364398012MMUTc.1400G>C (p.Arg467Pro)
6g.49448860C>TCA3846892MMUTc.1400G>A (p.Arg467Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
6g.49448861G>ACA3846893MMUTc.1399C>T (p.Arg467Ter)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
6g.49448861G>CCA364398016MMUTc.1399C>G (p.Arg467Gly)
6g.49448861G=CA1627388116MMUTc.1399C= (p.Arg467=)
6g.49448861G>TCA450398416MMUTc.1399C>A (p.Arg467=)
6g.49448862A>CCA450398417MMUTc.1398T>G (p.Leu466=)
6g.49448862A>GCA450398418MMUTc.1398T>C (p.Leu466=)
6g.49448862A>TCA450398419MMUTc.1398T>A (p.Leu466=)
6g.49448863A>CCA364398017MMUTc.1397T>G (p.Leu466Arg)
6g.49448863A>GCA364398018MMUTc.1397T>C (p.Leu466Pro)
6g.49448863A>TCA364398019MMUTc.1397T>A (p.Leu466His)

Number of alleles fetched