Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.49448850T>A | CA364397976 | MMUT | c.1410A>T (p.Glu470Asp) | |
6 | g.49448850T>C | CA3846889 | MMUT | c.1410A>G (p.Glu470=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49448850T>G | CA364397978 | MMUT | c.1410A>C (p.Glu470Asp) | |
6 | g.49448850T= | CA1627388109 | MMUT | c.1410A= (p.Glu470=) | |
6 | g.49448851T>A | CA364397980 | MMUT | c.1409A>T (p.Glu470Val) | |
6 | g.49448851T>C | CA3846890 | MMUT | c.1409A>G (p.Glu470Gly) | dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.49448851T>G | CA364397982 | MMUT | c.1409A>C (p.Glu470Ala) | |
6 | g.49448851T= | CA1627388110 | MMUT | c.1409A= (p.Glu470=) | |
6 | g.49448852C>A | CA364397984 | MMUT | c.1408G>T (p.Glu470Ter) | dbSNP |
6 | g.49448852C= | CA1627388111 | MMUT | c.1408G= (p.Glu470=) | |
6 | g.49448852C>G | CA364397985 | MMUT | c.1408G>C (p.Glu470Gln) | |
6 | g.49448852C>T | CA364397987 | MMUT | c.1408G>A (p.Glu470Lys) | |
6 | g.49448853T>A | CA364397988 | MMUT | c.1407A>T (p.Glu469Asp) | |
6 | g.49448853T>C | CA450398404 | MMUT | c.1407A>G (p.Glu469=) | |
6 | g.49448853T>G | CA364397990 | MMUT | c.1407A>C (p.Glu469Asp) | |
6 | g.49448854T>A | CA364397992 | MMUT | c.1406A>T (p.Glu469Val) | |
6 | g.49448854T>C | CA364397993 | MMUT | c.1406A>G (p.Glu469Gly) | |
6 | g.49448854T>G | CA364397995 | MMUT | c.1406A>C (p.Glu469Ala) | |
6 | g.49448855C>A | CA364397997 | MMUT | c.1405G>T (p.Glu469Ter) | |
6 | g.49448855C= | CA1627388112 | MMUT | c.1405G= (p.Glu469=) | |
6 | g.49448855C>G | CA364397998 | MMUT | c.1405G>C (p.Glu469Gln) | |
6 | g.49448855C>T | CA3846891 | MMUT | c.1405G>A (p.Glu469Lys) | dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.49448856A>C | CA364398001 | MMUT | c.1404T>G (p.Ile468Met) | |
6 | g.49448856A>G | CA450398405 | MMUT | c.1404T>C (p.Ile468=) | gnomAD v4 |
6 | g.49448856A>T | CA450398406 | MMUT | c.1404T>A (p.Ile468=) | |
6 | g.49448857A= | CA1627388113 | MMUT | c.1403T= (p.Ile468=) | |
6 | g.49448857A>C | CA364398002 | MMUT | c.1403T>G (p.Ile468Ser) | |
6 | g.49448857A>G | CA364398004 | MMUT | c.1403T>C (p.Ile468Thr) | dbSNP gnomAD v2 gnomAD v4 |
6 | g.49448857A>T | CA364398005 | MMUT | c.1403T>A (p.Ile468Asn) | |
6 | g.49448858T>A | CA364398009 | MMUT | c.1402A>T (p.Ile468Phe) | dbSNP gnomAD v4 |
6 | g.49448858T>C | CA138795917 | MMUT | c.1402A>G (p.Ile468Val) | dbSNP |
6 | g.49448858T>G | CA364398007 | MMUT | c.1402A>C (p.Ile468Leu) | |
6 | g.49448858T= | CA1627388114 | MMUT | c.1402A= (p.Ile468=) | |
6 | g.49448859T>A | CA450398410 | MMUT | c.1401A>T (p.Arg467=) | gnomAD v4 |
6 | g.49448859T>C | CA450398411 | MMUT | c.1401A>G (p.Arg467=) | |
6 | g.49448859T>G | CA450398412 | MMUT | c.1401A>C (p.Arg467=) | |
6 | g.49448860C>A | CA364398011 | MMUT | c.1400G>T (p.Arg467Leu) | |
6 | g.49448860C= | CA1627388115 | MMUT | c.1400G= (p.Arg467=) | |
6 | g.49448860C>G | CA364398012 | MMUT | c.1400G>C (p.Arg467Pro) | |
6 | g.49448860C>T | CA3846892 | MMUT | c.1400G>A (p.Arg467Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
6 | g.49448861G>A | CA3846893 | MMUT | c.1399C>T (p.Arg467Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
6 | g.49448861G>C | CA364398016 | MMUT | c.1399C>G (p.Arg467Gly) | |
6 | g.49448861G= | CA1627388116 | MMUT | c.1399C= (p.Arg467=) | |
6 | g.49448861G>T | CA450398416 | MMUT | c.1399C>A (p.Arg467=) | |
6 | g.49448862A>C | CA450398417 | MMUT | c.1398T>G (p.Leu466=) | |
6 | g.49448862A>G | CA450398418 | MMUT | c.1398T>C (p.Leu466=) | |
6 | g.49448862A>T | CA450398419 | MMUT | c.1398T>A (p.Leu466=) | |
6 | g.49448863A>C | CA364398017 | MMUT | c.1397T>G (p.Leu466Arg) | |
6 | g.49448863A>G | CA364398018 | MMUT | c.1397T>C (p.Leu466Pro) | |
6 | g.49448863A>T | CA364398019 | MMUT | c.1397T>A (p.Leu466His) |